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    <title>Recent ics_cs items</title>
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    <description>Recent eScholarship items from Department of Computer Science</description>
    <pubDate>Fri, 15 May 2026 03:52:11 +0000</pubDate>
    <item>
      <title>Genetic Variation and Stroke Recovery: The STRONG Study</title>
      <link>https://escholarship.org/uc/item/8184b81p</link>
      <description>BACKGROUND: Genetic association studies can reveal biology and treatment targets but have received limited attention for stroke recovery. STRONG (Stroke, Stress, Rehabilitation, and Genetics) was a prospective, longitudinal (1-year), genetic study in adults with stroke at 28 US stroke centers. The primary aim was to examine the association that candidate genetic variants have with (1) motor/functional outcomes and (2) stress-related outcomes.
METHODS: For motor/functional end points, 3 candidate gene variants (ApoE ε4, BDNF [brain-derived neurotrophic factor], and a dopamine polygenic score) were analyzed for associations with change in grip strength (3 months-baseline), function (3-month Stroke Impact Scale-Activities of Daily Living), mood (3-month Patient Health Questionnaire-8), and cognition (12-month telephone-Montreal Cognitive Assessment). For stress-related outcomes, 7 variants (serotonin transporter gene-linked promoter region, ACE [angiotensin-converting enzyme], oxytocin...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8184b81p</guid>
      <pubDate>Tue, 12 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cramer, Steven C</name>
      </author>
      <author>
        <name>Parodi, Livia</name>
      </author>
      <author>
        <name>Moslemi, Zahra</name>
      </author>
      <author>
        <name>Braun, Robynne G</name>
      </author>
      <author>
        <name>Aldridge, Chad M</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Rosand, Jonathan</name>
      </author>
      <author>
        <name>Holman, E Alison</name>
        <uri>https://orcid.org/0000-0001-5076-8403</uri>
      </author>
      <author>
        <name>Shah, Shreyansh</name>
      </author>
      <author>
        <name>Griessenauer, Christoph J</name>
      </author>
      <author>
        <name>Patel, Nirav</name>
      </author>
      <author>
        <name>Anderson, Christopher</name>
      </author>
      <author>
        <name>Henry, Jonathan</name>
      </author>
      <author>
        <name>Kourkoulis, Christina</name>
      </author>
      <author>
        <name>Lin, David J</name>
      </author>
      <author>
        <name>Zaba, Natalie</name>
      </author>
      <author>
        <name>Gee, Joey</name>
      </author>
      <author>
        <name>Moon, Johnson</name>
      </author>
      <author>
        <name>Schwertfeger, Julie</name>
      </author>
      <author>
        <name>Jayaraman, Arun</name>
      </author>
      <author>
        <name>Lee, Robert</name>
      </author>
      <author>
        <name>Lansberg, Maarten G</name>
      </author>
      <author>
        <name>Kemp, Stephanie</name>
      </author>
      <author>
        <name>Huang, Emily</name>
      </author>
      <author>
        <name>Bingham, Elijah</name>
      </author>
      <author>
        <name>Lugo, Leonel</name>
      </author>
      <author>
        <name>Eun, Da Eun Katie</name>
      </author>
      <author>
        <name>Payne, Jeremy</name>
      </author>
      <author>
        <name>Patten, Carolynn</name>
        <uri>https://orcid.org/0000-0002-9948-0045</uri>
      </author>
      <author>
        <name>Ng, Kwan</name>
      </author>
      <author>
        <name>Cao, Madelyn</name>
      </author>
      <author>
        <name>Jubb, Ashley</name>
      </author>
      <author>
        <name>McGee, Breann</name>
      </author>
      <author>
        <name>Shahbaba, Ryan</name>
      </author>
      <author>
        <name>Agrawal, Kunal</name>
      </author>
      <author>
        <name>Kissela, Brett</name>
      </author>
      <author>
        <name>DeJong, Stacey</name>
      </author>
      <author>
        <name>Cole, John</name>
      </author>
      <author>
        <name>Silver, Brian</name>
      </author>
      <author>
        <name>Manxhari, Christina</name>
      </author>
      <author>
        <name>Cucchiara, Brett</name>
      </author>
      <author>
        <name>Busza, Ania</name>
      </author>
      <author>
        <name>Hepple, Jennifer Paige</name>
      </author>
      <author>
        <name>Liew, Sook-Lei</name>
      </author>
      <author>
        <name>Alderman, Susan</name>
      </author>
      <author>
        <name>Beauchamp, Jennifer</name>
      </author>
      <author>
        <name>Mathew, Nitha Joseph</name>
      </author>
      <author>
        <name>Hayes, Heather</name>
      </author>
      <author>
        <name>Majersik, Jennifer J</name>
      </author>
      <author>
        <name>Worrall, Bradford B</name>
      </author>
      <author>
        <name>Tirschwell, David</name>
      </author>
      <author>
        <name>Bushnell, Cheryl</name>
      </author>
      <author>
        <name>Husseini, Nada El</name>
      </author>
      <author>
        <name>Lee, Jin-Moo</name>
      </author>
      <author>
        <name>Falcone, Guido J</name>
      </author>
    </item>
    <item>
      <title>Neurodatascience: Past, Present, and Future</title>
      <link>https://escholarship.org/uc/item/9d3867jx</link>
      <description>The study of the brain is a compelling example of the power of convergent science. Over the last few decades, advances in neuroscience techniques and experimentation, as well as in data science tools to analyze the resulting data, have dramatically furthered our understanding of fundamental brain functions. Historically, it has been common for analytical approaches to have a considerable lag in development following the availability of new neuroscience techniques. However, this relationship has not simply been unidirectional, as there have been examples in which analytical developments have directly led to new scientific questions and experiments. Here we review how this interplay between neuroscience and data science advances has unfolded in the past and into the present, with a focus on electrophysiology and calcium imaging. Applying lessons learned from the past and present, we then discuss expected developments, challenges, and opportunities in the future. We end by providing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9d3867jx</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cooper, Keiland W</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Fortin, Norbert J</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
    </item>
    <item>
      <title>Hippocampal ensembles represent sequential relationships among discrete nonspatial events</title>
      <link>https://escholarship.org/uc/item/93c9q82h</link>
      <description>ABSTRACT The hippocampus is critical to the temporal organization of our experiences, including the ability to remember past event sequences and predict future ones. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain poorly understood. Here we recorded hippocampal ensemble activity as rats remembered a sequence of nonspatial events (5 odor presentations unfolding over several seconds), using a task with established parallels in humans. Using novel statistical methods and deep learning techniques, we then identified new forms of sequential organization in hippocampal activity linked with task performance. We discovered that sequential firing fields (“time cells”) provided temporal information within and across events in the sequence, and that distinct types of task-critical information (stimulus identity, temporal order, and trial outcome) were also sequentially differentiated within event presentations. Finally,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/93c9q82h</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Li, Lingge</name>
      </author>
      <author>
        <name>Agostinelli, Forest</name>
      </author>
      <author>
        <name>Saraf, Mansi</name>
      </author>
      <author>
        <name>Elias, Gabriel A</name>
      </author>
      <author>
        <name>Baldi, Pierre</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Fortin, Norbert J</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
    </item>
    <item>
      <title>Unity by Diversity: Improved Representation Learning for Multimodal VAEs</title>
      <link>https://escholarship.org/uc/item/5vb1n9mb</link>
      <description>Variational Autoencoders for multimodal data hold promise for many tasks in data analysis, such as representation learning, conditional generation, and imputation. Current architectures either share the encoder output, decoder input, or both across modalities to learn a shared representation. Such architectures impose hard constraints on the model. In this work, we show that a better latent representation can be obtained by replacing these hard constraints with a soft constraint. We propose a new mixture-of-experts prior, softly guiding each modality's latent representation towards a shared aggregate posterior. This approach results in a superior latent representation and allows each encoding to preserve information better from its uncompressed original features. In extensive experiments on multiple benchmark datasets and two challenging real-world datasets, we show improved learned latent representations and imputation of missing data modalities compared to existing methods.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5vb1n9mb</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sutter, TM</name>
      </author>
      <author>
        <name>Meng, Y</name>
      </author>
      <author>
        <name>Agostini, A</name>
      </author>
      <author>
        <name>Chopard, D</name>
      </author>
      <author>
        <name>Fortin, N</name>
      </author>
      <author>
        <name>Vogt, JE</name>
      </author>
      <author>
        <name>Shahbaba, B</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Mandt, S</name>
      </author>
    </item>
    <item>
      <title>A Model-Agnostic Graph Neural Network for Integrating Local and Global Information</title>
      <link>https://escholarship.org/uc/item/54c5s9m8</link>
      <description>Graph Neural Networks (GNNs) have achieved promising performance in a variety of graph-focused tasks. Despite their success, however, existing GNNs suffer from two significant limitations: a lack of interpretability in their results due to their black-box nature, and an inability to learn representations of varying orders. To tackle these issues, we propose a novel &lt;b&gt;M&lt;/b&gt;odel-&lt;b&gt;a&lt;/b&gt;gnostic &lt;b&gt;G&lt;/b&gt;raph Neural &lt;b&gt;Net&lt;/b&gt;work (MaGNet) framework, which is able to effectively integrate information of various orders, extract knowledge from high-order neighbors, and provide meaningful and interpretable results by identifying influential compact graph structures. In particular, MaGNet consists of two components: an estimation model for the latent representation of complex relationships under graph topology, and an interpretation model that identifies influential nodes, edges, and node features. Theoretically, we establish the generalization error bound for MaGNet via empirical Rademacher...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/54c5s9m8</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Zhou, Wenzhuo</name>
      </author>
      <author>
        <name>Qu, Annie</name>
      </author>
      <author>
        <name>Cooper, Keiland W</name>
      </author>
      <author>
        <name>Fortin, Norbert</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
    </item>
    <item>
      <title>A scalable reinforcement learning framework inspired by hippocampal memory mechanisms for efficient contextual and sequential decision making</title>
      <link>https://escholarship.org/uc/item/4zm8452k</link>
      <description>Efficient decision-making in context-dependent, sequential tasks remains a fundamental challenge in reinforcement learning (RL). Inspired by the function of the brain’s hippocampal system, we introduce Hippocampal-Augmented Memory Integration (HAMI), a biologically inspired memory-based RL framework that leverages symbolic indexing, hierarchical memory refinement, and structured episodic retrieval to enhance both learning efficiency and adaptability. We also propose Hierarchical Contextual Sequences (HiCoS), a structured RL environment grounded in neuroscience studies on episodic and sequence memory and context-driven decision-making, which serves as a controlled testbed for evaluating biologically inspired memory-based decision-making systems. Our experimental results demonstrate that HAMI achieves high decision accuracy and improved sample efficiency while maintaining low memory utilization. HAMI’s architecture exhibits significantly lower inference latency than baseline memory-based...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4zm8452k</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Poursiami, Hamed</name>
      </author>
      <author>
        <name>Moshruba, Ayana</name>
      </author>
      <author>
        <name>Cooper, Keiland W</name>
      </author>
      <author>
        <name>Gobin, Derek</name>
      </author>
      <author>
        <name>Kaiser, Md Abdullah-Al</name>
      </author>
      <author>
        <name>Singh, Ankur</name>
      </author>
      <author>
        <name>Noor, Rouhan</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Jaiswal, Akhilesh</name>
      </author>
      <author>
        <name>Fortin, Norbert J</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Parsa, Maryam</name>
      </author>
    </item>
    <item>
      <title>Optimal Transport based Cross-Domain Integration for Heterogeneous Data</title>
      <link>https://escholarship.org/uc/item/47t8571q</link>
      <description>Detecting dynamic patterns shared across heterogeneous datasets is a critical yet challenging task in many scientific domains, particularly within the biomedical sciences. Systematic heterogeneity inherent in diverse data sources can significantly hinder the effectiveness of existing machine learning methods in uncovering shared underlying dynamics. Additionally, practical and technical constraints in real-world experimental designs often limit data collection to only a small number of subjects, even when rich, time-dependent measurements are available for each individual. These limited sample sizes further diminish the power to detect common dynamic patterns across subjects. In this article, we propose a novel heterogeneous data integration framework based on optimal transport to extract shared patterns in the conditional mean dynamics of target responses. The key advantage of the proposed method is its ability to enhance discriminative power by reducing heterogeneity unrelated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/47t8571q</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yuan, Yubai</name>
      </author>
      <author>
        <name>Zhang, Yijiao</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Fortin, Norbert</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Cooper, Keiland</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Qu, Annie</name>
      </author>
    </item>
    <item>
      <title>STABLE-MATCHING VORONOI DIAGRAMS: COMBINATORIAL COMPLEXITY AND ALGORITHMS</title>
      <link>https://escholarship.org/uc/item/7mp39529</link>
      <description>We study algorithms and combinatorial complexity bounds for stable-matching Voronoi diagrams, where a set, S, of n point sites in the plane determines a stable matching between the points in R&lt;sup&gt;2&lt;/sup&gt; and the sites in S such that (i) the points prefer sites closer to them and sites prefer points closer to them, and (ii) each site has a quota or "appetite" indicating the area of the set of points that can be matched to it. Thus, a stable-matching Voronoi diagram is a solution to the well-known post office problem with the added (realistic) constraint that each post office has a limit on the size of its jurisdiction. Previous work on the stable-matching Voronoi diagram provided existence and uniqueness proofs, but did not analyze its combinatorial or algorithmic complexity. In this paper, we show that a stable-matching Voronoi diagram of n point sites has O(n&lt;sup&gt;2+ε&lt;/sup&gt;) faces and edges, for any ε &amp;gt; 0, and show that this bound is almost tight by giving a family of diagrams...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7mp39529</guid>
      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Barequet, Gill</name>
      </author>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Goodrich, Michael</name>
      </author>
      <author>
        <name>Mamano, Nil</name>
      </author>
    </item>
    <item>
      <title>Folding a paper strip to minimize thickness</title>
      <link>https://escholarship.org/uc/item/6xb4c6c8</link>
      <description>In this paper, we study how to fold a specified origami crease pattern in order to minimize the impact of paper thickness. Specifically, origami designs are often expressed by a mountain–valley pattern (plane graph of creases with relative fold orientations), but in general this specification is consistent with exponentially many possible folded states. We analyze the complexity of finding the best consistent folded state according to two metrics: minimizing the total number of layers in the folded state (so that a “flat folding” is indeed close to flat), and minimizing the total amount of paper required to execute the folding (where “thicker” creases consume more paper). We prove both problems strongly NP-complete even for 1D folding. On the other hand, we prove both problems fixed-parameter tractable in 1D with respect to the number of layers.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6xb4c6c8</guid>
      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Demaine, Erik D</name>
      </author>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Hesterberg, Adam</name>
      </author>
      <author>
        <name>Ito, Hiro</name>
      </author>
      <author>
        <name>Lubiw, Anna</name>
      </author>
      <author>
        <name>Uehara, Ryuhei</name>
      </author>
      <author>
        <name>Uno, Yushi</name>
      </author>
    </item>
    <item>
      <title>NON-EUCLIDEAN ERDŐS-ANNING THEOREMS</title>
      <link>https://escholarship.org/uc/item/47n916hw</link>
      <description>NON-EUCLIDEAN ERDŐS-ANNING THEOREMS</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/47n916hw</guid>
      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>FamilyBloom: Examining Ecologies of Collaboration in Family-Centered Health Tracking</title>
      <link>https://escholarship.org/uc/item/2hs1f70b</link>
      <description>Family health informatics tools can help support well-being with shared data tracking. Prior work typically focused on shared data review, but often in specific moments, like bedtime, or centered on caregiving of children or elderly members. To investigate how tracking can support mutual health collaboration between family members pervasively across daily contexts, we designed and deployed FamilyBloom, a glanceable smartwatch and home display system for mood and goal tracking. Twelve families with both neurotypical and ADHD members used FamilyBloom for three months on average. Our findings reveal how family-centered tracking created collaboration opportunities and tensions across multiple ecological systems: individual self-regulation, collaborations within family dynamics, involvement of care networks with varying trust levels, institutional school constraints and cultural stigma, and temporality of regular routines and crisis periods. We discuss an ecosystem-aware approach to...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2hs1f70b</guid>
      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Silva, Lucas M</name>
      </author>
      <author>
        <name>Min, Aehong</name>
        <uri>https://orcid.org/0000-0002-3790-2126</uri>
      </author>
      <author>
        <name>Stefanidi, Evropi</name>
      </author>
      <author>
        <name>Cibrian, Franceli L</name>
      </author>
      <author>
        <name>Beltran, Jesus A</name>
      </author>
      <author>
        <name>Zeiler, Cassie</name>
      </author>
      <author>
        <name>Schuck, Sabrina</name>
      </author>
      <author>
        <name>Lakes, Kimberley D</name>
      </author>
      <author>
        <name>Hayes, Gillian R</name>
      </author>
      <author>
        <name>Epstein, Daniel A</name>
        <uri>https://orcid.org/0000-0002-2657-6345</uri>
      </author>
    </item>
    <item>
      <title>Efficacy of Full-Packet Encryption in Mitigating Protocol Detection for Evasive VPNs</title>
      <link>https://escholarship.org/uc/item/2781r51d</link>
      <description>Full-packet encryption is a technique used by modern evasive Virtual Private Networks (VPNs) to avoid protocol-based flagging from censorship models by disguising their traffic as random noise on the network. Traditional methods for censoring full-packet-encryption based VPN protocols requires assuming a substantial amount of collateral damage, as other non-VPN network traffic that appears random will be blocked. We tested several machine learning-based classification models against the Aggressive Circumvention of Censorship (ACC) protocol, a fully-encrypted evasive VPN protocol which merges strategies from a wide variety of currently in-use evasive VPN protocols. Our testing found that while ACC was able to survive our models when compared to random noise, it was easily detectable with minimal collateral damage using several different machine learning models when within a stream of regular network traffic. While resistant to the current techniques deployed by nation-state censors,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2781r51d</guid>
      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Parker, Amy I</name>
      </author>
    </item>
    <item>
      <title>Towards Verifying Crash Consistency</title>
      <link>https://escholarship.org/uc/item/94b298fs</link>
      <description>Compute Express Link (CXL) memory sharing, persistent memory, and other related technologies allow data to survive crash events. A key challenge is ensuring that data is consistent after crashes such that it can be safely accessed. While there has been much work on bug-finding tools for persistent memory programs, these tools cannot guarantee that a program is crash-consistent. In this paper, we present a language, CrashLang, and its type system, that together guarantee that well-typed data structure implementations written in CrashLang are crash-consistent. CrashLang leverages the well-known commit-store pattern in which a single store logically commits an entire data structure operation. In this paper, we prove that well-typed CrashLang programs are crash-consistent, and provide a prototype implementation of the CrashLang compiler. We have evaluated CrashLang on five benchmarks: the Harris linked list, the Treiber stack, the Michael–Scott queue, a Read-Copy-Update binary search...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94b298fs</guid>
      <pubDate>Thu, 23 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Keonho</name>
      </author>
      <author>
        <name>Truong, Conan</name>
      </author>
      <author>
        <name>Demsky, Brian</name>
      </author>
    </item>
    <item>
      <title>Automated Insertion of Flushes and Fences for Persistency</title>
      <link>https://escholarship.org/uc/item/5pw0t40p</link>
      <description>CXL shared memory and persistent memory allow the contents of memory to persist beyond crashes. Stores to persistent or CXL memory are typically not immediately made persistent; developers must manually flush the corresponding cache lines to force the data to be written to the underlying storage. Correctly using flush and fence operations is known to be challenging. While state-of-the-art tools can find missing flush instructions, they often require bug-revealing test cases. No existing tools can ensure the absence of missing flush bugs. In this paper, we present PMRobust, a compiler that automatically inserts flush and fence operations to ensure that code using persistent memory is free from missing flush and fence bugs. PMRobust employs a novel static analysis with optimizations that target newly allocated objects. We have evaluated PMRobust on persistent memory libraries and several persistent memory data structures and measured a geometric mean overhead of 0.26% relative to...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5pw0t40p</guid>
      <pubDate>Thu, 23 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Guo, Yutong</name>
      </author>
      <author>
        <name>Luo, Weiyu</name>
      </author>
      <author>
        <name>Demsky, Brian</name>
      </author>
    </item>
    <item>
      <title>HyperXite 9</title>
      <link>https://escholarship.org/uc/item/532817sx</link>
      <description>The overall objective for HyperXite 9 was to design and build a more robust, and reliable pod, capable of proving the feasibility of a high-speed transportation system. We are working to improve a linear induction motor as the pod's propulsion system. We are also designing and implementing a thermal cooling system to actively dissipate the heat generated by this propulsion system. Our team is comprised of the following 7 subteams: Static Structures, Braking &amp;amp; Pneumatics, Dynamic Structures, Propulsion, Power Systems, Control Systems, and Outreach.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/532817sx</guid>
      <pubDate>Wed, 15 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Antony, Jacob</name>
      </author>
      <author>
        <name>Chin, Anthony</name>
      </author>
      <author>
        <name>Whaley, Christopher</name>
      </author>
      <author>
        <name>Hsing, Allen</name>
      </author>
      <author>
        <name>Eslava, Aaron</name>
      </author>
      <author>
        <name>Trauger, Andrew</name>
      </author>
      <author>
        <name>Diaz, Angel</name>
      </author>
      <author>
        <name>Licos, Angelina</name>
      </author>
      <author>
        <name>Chau, Brian</name>
      </author>
      <author>
        <name>Chung, Brigitte</name>
      </author>
      <author>
        <name>Kang, Calvin</name>
      </author>
      <author>
        <name>Parker, Crew</name>
      </author>
      <author>
        <name>Pena, Daniel</name>
      </author>
      <author>
        <name>Kim, Dillon</name>
      </author>
      <author>
        <name>Li, Harbour</name>
      </author>
      <author>
        <name>Ng, Jefferson</name>
      </author>
      <author>
        <name>Nguyen, Joshua</name>
      </author>
      <author>
        <name>Nguyen, Kaitlyn</name>
      </author>
      <author>
        <name>Haddad, Marc</name>
      </author>
      <author>
        <name>Stark, Max</name>
      </author>
      <author>
        <name>Veloya, Nicol</name>
      </author>
      <author>
        <name>Koo, Rachael</name>
      </author>
      <author>
        <name>Goja, Riya</name>
      </author>
      <author>
        <name>Mawlawi, Ryan</name>
      </author>
      <author>
        <name>Quach, Ryan</name>
      </author>
      <author>
        <name>Scholin, Rye</name>
      </author>
      <author>
        <name>Der, Sam</name>
      </author>
      <author>
        <name>Mehra, Syona</name>
      </author>
      <author>
        <name>Hwang, Taesung</name>
      </author>
      <author>
        <name>Ngo, Timothy</name>
      </author>
      <author>
        <name>Anand, Vrushang</name>
      </author>
      <author>
        <name>Ning, Oscar</name>
      </author>
      <author>
        <name>Solorzano, Diego</name>
      </author>
      <author>
        <name>Nomura, Kaydi</name>
      </author>
      <author>
        <name>Ko, Michelle</name>
      </author>
    </item>
    <item>
      <title>Biometric Advanced Driver Assistance System (ADAS)</title>
      <link>https://escholarship.org/uc/item/3vk1x6p6</link>
      <description>This project focuses on the development of a human-aware advanced driver assistance system (ADAS) that helps promote safe driving based on a driver's biometrics and driving behavior. The system uses biometric signals from the driver using BioHarness Belt and Galvanic Skin Response (GSR) sensors to monitor the driver's heart rate, breathing rate, ECG and GSR signals. These sensory information are then analyzed by machine learning models to determine whether the driver is stressed or drowsy. The project extended the current state-of-the-art driving simulator CARLA to not only include the driver's brake intensity,  speed, throttle and steering but also the driver's biometric state. The vehicle controls and biometrics are then plotted and analyzed for correlations that could imply a driver is driving aggressively, assertively, or defensively. Based on these correlations, the driver will be displayed a warning on the simulation which advises them to drive carefully. The output from...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3vk1x6p6</guid>
      <pubDate>Wed, 15 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Bayoumi, Ismail</name>
      </author>
      <author>
        <name>Tirumala, Rithvik</name>
      </author>
      <author>
        <name>Rodriguez, Citlali</name>
      </author>
    </item>
    <item>
      <title>2025 UCI CanSat Annual Design Review Poster</title>
      <link>https://escholarship.org/uc/item/1mn1h6px</link>
      <description>The UCI CanSat team is a senior design team that competes in the international CanSat competition, an annual design-build-launch competition held by the American Astronautical Society focused on space-type systems. Each year, a ten-person team designs a “CanSat,” following competition requirements. This year, the CanSat is required to operate in 4 main phases: ascent, apogee, descent, and landing. During ascent, the CanSat must act as the nose cone of the rocket. At apogee, an ejection charge releases the CanSat from the rocket, and the CanSat must activate a parachute to begin a safe descent. At three-quarters of the peak altitude, the CanSat must deploy its payload. The payload consists of two cameras, one to film payload deployment, while the other is spin-stabilized to film the north side of the CanSat. In addition, while the container descends with a parachute, the payload must descend with an auto-gyro system. The auto-gyro system must significantly decrease the descent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1mn1h6px</guid>
      <pubDate>Wed, 15 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Nguyen, Carolynn</name>
      </author>
      <author>
        <name>Otsuka, Kaitlin</name>
      </author>
      <author>
        <name>Kim, Kaylee</name>
      </author>
      <author>
        <name>Gupta, Khushi</name>
      </author>
      <author>
        <name>Ho, Sarah</name>
      </author>
      <author>
        <name>Cason, Brady</name>
      </author>
      <author>
        <name>Ruan, Zhanhao</name>
      </author>
      <author>
        <name>Yoon, Diane</name>
      </author>
      <author>
        <name>Darjuan, Andrei</name>
      </author>
      <author>
        <name>Fajarito, Naethan</name>
      </author>
      <author>
        <name>Yee, Timothy</name>
      </author>
      <author>
        <name>Jing, Felix</name>
      </author>
    </item>
    <item>
      <title>Summary the Savior: Harmful Keyword and Query-based Summarization for LLM Jailbreak Defense</title>
      <link>https://escholarship.org/uc/item/4qk7v7jv</link>
      <description>Summary the Savior: Harmful Keyword and Query-based Summarization for LLM Jailbreak Defense</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4qk7v7jv</guid>
      <pubDate>Wed, 8 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Rahman, Shagoto</name>
      </author>
      <author>
        <name>Harris, Ian</name>
      </author>
    </item>
    <item>
      <title>Evaluating the potential of acupuncture for Alzheimer’s disease treatment: A meta-analysis and systematic review of mouse model studies</title>
      <link>https://escholarship.org/uc/item/0sd9c8sj</link>
      <description>Acupuncture is an ancient practice that was developed within the framework of traditional Chinese medicine. While acupuncture has been recently proposed as a therapy for Alzheimer’s disease (AD), acupuncture effects are not well understood in terms of neural mechanisms. Here, we review and examine the studies that used AD mouse models and analyze the experiments where researchers administered electroacupuncture (EA) to AD mice to assess the potential therapeutic impact of acupuncture on disease pathology and cognitive function in controlled laboratory settings. We analyzed 29 relevant PubMed articles published between January 2014 and July 2025. Our results reveal that EA significantly reduces both amyloid-beta (Aβ) and phosphorylated tau (p-tau) levels and neuroinflammatory biomarkers, including molecular signatures for activated microglia and astrocytes in the brain. EA also enhances cognitive functions. While no study directly compared acupoint strategies, the indirect comparisons...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0sd9c8sj</guid>
      <pubDate>Wed, 8 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yang, Mohan</name>
      </author>
      <author>
        <name>Tong, Liqi</name>
      </author>
      <author>
        <name>Guo, Zhiling</name>
      </author>
      <author>
        <name>Tan, Zhiqun</name>
      </author>
      <author>
        <name>Holmes, Todd C</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
    </item>
    <item>
      <title>An Expert Guide to Planning Experimental Tasks For Evidence-Accumulation Modeling</title>
      <link>https://escholarship.org/uc/item/8mn5z2kf</link>
      <description>Evidence-accumulation models (EAMs) are powerful tools for making sense of human and animal decision-making behavior. EAMs have generated significant theoretical advances in psychology, behavioral economics, and cognitive neuroscience and are increasingly used as a measurement tool in clinical research and other applied settings. Obtaining valid and reliable inferences from EAMs depends on knowing how to establish a close match between model assumptions and features of the task/data to which the model is applied. However, this knowledge is rarely articulated in the EAM literature, leaving beginners to rely on the private advice of mentors and colleagues and inefficient trial-and-error learning. In this article, we provide practical guidance for designing tasks appropriate for EAMs, relating experimental manipulations to EAM parameters, planning appropriate sample sizes, and preparing data and conducting an EAM analysis. Our advice is based on prior methodological studies and the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8mn5z2kf</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Boag, Russell J</name>
      </author>
      <author>
        <name>Innes, Reilly J</name>
      </author>
      <author>
        <name>Stevenson, Niek</name>
      </author>
      <author>
        <name>Bahg, Giwon</name>
      </author>
      <author>
        <name>Busemeyer, Jerome R</name>
      </author>
      <author>
        <name>Cox, Gregory E</name>
      </author>
      <author>
        <name>Donkin, Chris</name>
      </author>
      <author>
        <name>Frank, Michael J</name>
      </author>
      <author>
        <name>Hawkins, Guy E</name>
      </author>
      <author>
        <name>Heathcote, Andrew</name>
      </author>
      <author>
        <name>Hedge, Craig</name>
      </author>
      <author>
        <name>Lerche, Veronika</name>
      </author>
      <author>
        <name>Lilburn, Simon D</name>
      </author>
      <author>
        <name>Logan, Gordon D</name>
      </author>
      <author>
        <name>Matzke, Dora</name>
      </author>
      <author>
        <name>Miletić, Steven</name>
      </author>
      <author>
        <name>Osth, Adam F</name>
      </author>
      <author>
        <name>Palmeri, Thomas J</name>
      </author>
      <author>
        <name>Sederberg, Per B</name>
      </author>
      <author>
        <name>Singmann, Henrik</name>
      </author>
      <author>
        <name>Smith, Philip L</name>
      </author>
      <author>
        <name>Stafford, Tom</name>
      </author>
      <author>
        <name>Steyvers, Mark</name>
      </author>
      <author>
        <name>Strickland, Luke</name>
      </author>
      <author>
        <name>Trueblood, Jennifer S</name>
      </author>
      <author>
        <name>Tsetsos, Konstantinos</name>
      </author>
      <author>
        <name>Turner, Brandon M</name>
      </author>
      <author>
        <name>Usher, Marius</name>
      </author>
      <author>
        <name>van Maanen, Leendert</name>
      </author>
      <author>
        <name>van Ravenzwaaij, Don</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Voss, Andreas</name>
      </author>
      <author>
        <name>Weichart, Emily R</name>
      </author>
      <author>
        <name>Weindel, Gabriel</name>
      </author>
      <author>
        <name>White, Corey N</name>
      </author>
      <author>
        <name>Evans, Nathan J</name>
      </author>
      <author>
        <name>Brown, Scott D</name>
      </author>
      <author>
        <name>Forstmann, Birte U</name>
      </author>
    </item>
    <item>
      <title>Computational Complexities of Folding</title>
      <link>https://escholarship.org/uc/item/7z5601k3</link>
      <description>We prove several hardness results on folding origami crease patterns. Flat-folding finite crease patterns is fixed-parameter tractable in the ply of the folded pattern (how many layers overlap at any point) and the treewidth of an associated cell adjacency graph. Under the exponential time hypothesis, the singly-exponential dependence of our algorithm on treewidth is necessary, even for bounded ply. Improving the dependence on ply would require progress on the unsolved map folding problem. Finding the shape of a polyhedron folded from a net with triangular faces and integer edge lengths is not possible in algebraic computation tree models of computation that at each tree node allow either the computation of arbitrary integer roots of real numbers, or the extraction of roots of polynomials with bounded degree and integer coefficients. For a model of reconfigurable origami with origami squares are attached at one edge by a hinge to a rigid surface, moving from one flat-folded state...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7z5601k3</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>String Graph Obstacles of High Girth and of Bounded Degree</title>
      <link>https://escholarship.org/uc/item/7j69r6m4</link>
      <description>A string graph is the intersection graph of curves in the plane. Kratochvíl previously showed the existence of infinitely many obstacles: graphs that are not string graphs but for which any edge contraction or vertex deletion produces a string graph. Kratochvíl's obstacles contain arbitrarily large cliques, so they have girth three and unbounded degree. We extend this line of working by studying obstacles among graphs of restricted girth and/or degree. We construct an infinite family of obstacles of girth four; in addition, our construction is K2,3-subgraph-free and near-planar (planar plus one edge). Furthermore, we prove that there is a subcubic obstacle of girth three, and that there are no subcubic obstacles of high girth. We characterize the subcubic string graphs as having a matching whose contraction yields a planar graph, and based on this characterization we find a linear-time algorithm for recognizing subcubic string graphs of bounded treewidth.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7j69r6m4</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chudnovsky, M</name>
        <uri>https://orcid.org/0000-0002-8920-4944</uri>
      </author>
      <author>
        <name>Eppstein, D</name>
      </author>
      <author>
        <name>Fischer, D</name>
        <uri>https://orcid.org/0009-0009-3488-838X</uri>
      </author>
    </item>
    <item>
      <title>The Complexity of Iterated Reversible Computation</title>
      <link>https://escholarship.org/uc/item/70d126n1</link>
      <description>We study a class of functional problems reducible to computing $f^{(n)}(x)$ for inputs $n$ and $x$, where $f$ is a polynomial-time bijection. As we prove, the definition is robust against variations in the type of reduction used in its definition, and in whether we require $f$ to have a polynomial-time inverse or to be computible by a reversible logic circuit. These problems are characterized by the complexity class $\mathsf{FP}^{\mathsf{PSPACE}}$, and include natural $\mathsf{FP}^{\mathsf{PSPACE}}$-complete problems in circuit complexity, cellular automata, graph algorithms, and the dynamical systems described by piecewise-linear transformations.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/70d126n1</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>Distributed Construction of Lightweight Spanners for Unit Ball Graphs</title>
      <link>https://escholarship.org/uc/item/69m9x7t0</link>
      <description>Resolving an open question from 2006 [14], we prove the existence of light-weight bounded-degree spanners for unit ball graphs in the metrics of bounded doubling dimension, and we design a simple O(log&lt;sup&gt;∗&lt;/sup&gt; n)-round distributed algorithm in the LOCAL model of computation, that given a unit ball graph G with n vertices and a positive constant ϵ &amp;lt; 1 finds a (1+ϵ)-spanner with constant bounds on its maximum degree and its lightness using only 2-hop neighborhood information. This immediately improves the best prior lightness bound, the algorithm of Damian, Pandit, and Pemmaraju [13], which runs in O(log&lt;sup&gt;∗&lt;/sup&gt; n) rounds in the LOCAL model, but has a O(log ∆) bound on its lightness, where ∆ is the ratio of the length of the longest edge to the length of the shortest edge in the unit ball graph. Next, we adjust our algorithm to work in the CONGEST model, without changing its round complexity, hence proposing the first spanner construction for unit ball graphs in the CONGEST...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/69m9x7t0</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Khodabandeh, Hadi</name>
      </author>
    </item>
    <item>
      <title>Brief Announcement: Distributed Lightweight Spanner Construction for Unit Ball Graphs in Doubling Metrics</title>
      <link>https://escholarship.org/uc/item/4z38v63d</link>
      <description>Resolving an open question from 2006, we prove the existence of light-weight bounded-degree (1+ε)-spanners for unit ball graphs in the metrics of bounded doubling dimension, and we design a simple O(log*n)-round distributed algorithm in the LOCAL model for finding such spanners using only 2-hop neighborhood information. We further study the problem in the two dimensional Euclidean plane and we propose a construction with similar properties that has a low-intersection property as well. Lastly, we provide experimental results that confirm the performance of our algorithms.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4z38v63d</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Khodabandeh, Hadi</name>
      </author>
    </item>
    <item>
      <title>Visualizing Treewidth</title>
      <link>https://escholarship.org/uc/item/4v97s3sk</link>
      <description>A witness drawing of a graph is a visualization that clearly shows a given property of a graph. We study and implement various drawing paradigms for witness drawings to clearly show that graphs have bounded pathwidth or treewidth. Our approach draws the tree decomposition or path decomposition as a tree of bags, with induced subgraphs shown in each bag, and with “tracks” for each graph vertex connecting its copies in multiple bags. Within bags, we optimize the vertex layout to avoid crossings of edges and tracks. We implement a visualization prototype for crossing minimization using dynamic programming for graphs of small width and heuristic approaches for graphs of larger width. We introduce a taxonomy of drawing styles, which render the subgraph for each bag as an arc diagram with one or two pages or as a circular layout with straight-line edges, and we render tracks either with straight lines or with orbital-radial paths.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4v97s3sk</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chiu, A</name>
        <uri>https://orcid.org/0009-0009-6863-859X</uri>
      </author>
      <author>
        <name>Depian, T</name>
        <uri>https://orcid.org/0009-0003-7498-6271</uri>
      </author>
      <author>
        <name>Eppstein, D</name>
      </author>
      <author>
        <name>Goodrich, MT</name>
        <uri>https://orcid.org/0000-0002-8943-191X</uri>
      </author>
      <author>
        <name>Nöllenburg, M</name>
      </author>
    </item>
    <item>
      <title>A Stronger Lower Bound on Parametric Minimum Spanning Trees</title>
      <link>https://escholarship.org/uc/item/3c79s8db</link>
      <description>We prove that, for an undirected graph with n vertices and m edges, each labeled with a linear function of a parameter λ$$\lambda $$, the number of different minimum spanning trees obtained as the parameter varies can be Ω(mlogn)$$\Omega (m\log n)$$.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3c79s8db</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>On the treewidth of Hanoi graphs</title>
      <link>https://escholarship.org/uc/item/1jd9s728</link>
      <description>The objective of the well-known Tower of Hanoi puzzle is to move a set of discs one at a time from one of a set of pegs to another, while keeping the discs sorted on each peg. We propose an adversarial variation in which the first player forbids a set of states in the puzzle, and the second player must then convert one randomly-selected state to another without passing through forbidden states. Analyzing this version raises the question of the treewidth of Hanoi graphs. We find this number exactly for three-peg puzzles and provide nearly-tight asymptotic bounds for larger numbers of pegs.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1jd9s728</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Frishberg, Daniel</name>
      </author>
      <author>
        <name>Maxwell, William</name>
      </author>
    </item>
    <item>
      <title>Stabbing Faces by a Convex Curve</title>
      <link>https://escholarship.org/uc/item/11k047cd</link>
      <description>We prove that, for every plane graph G and every smooth convex curve C not on a single line, there exists a straight-line drawing of G for which every face is crossed by C.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/11k047cd</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, D</name>
      </author>
    </item>
    <item>
      <title>What is... Treewidth?</title>
      <link>https://escholarship.org/uc/item/0mc7w5m5</link>
      <description>What is... Treewidth?</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mc7w5m5</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>On the complexity of embedding in graph products</title>
      <link>https://escholarship.org/uc/item/0gb5v73f</link>
      <description>Graph embedding, especially as a subgraph of a grid, is an old topic in VLSI design and graph drawing. In this paper, we investigate related questions concerning the complexity of embedding a graph G in a host graph that is the strong product of a path P with a graph H that satisfies some properties, such as having small treewidth, pathwidth or treedepth. We show that this is NP-hard, even under numerous restrictions on both G and H. In particular, computing the row pathwidth and the row treedepth is NP-hard even for a tree of small pathwidth, while computing the row treewidth is NP-hard even for series-parallel graphs.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0gb5v73f</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Biedl, T</name>
      </author>
      <author>
        <name>Eppstein, D</name>
      </author>
      <author>
        <name>Ueckerdt, T</name>
      </author>
    </item>
    <item>
      <title>Spatial and temporal evaluations of the liquid argon purity in ProtoDUNE-SP</title>
      <link>https://escholarship.org/uc/item/2ks5b3d4</link>
      <description>Liquid argon time projection chambers (LArTPCs) rely on highly pure argon to ensure that ionization electrons produced by charged particles reach readout arrays. ProtoDUNE Single-Phase (ProtoDUNE-SP) was an approximately 700-ton liquid argon detector intended to prototype the Deep Underground Neutrino Experiment (DUNE) Far Detector Horizontal Drift module. It contains two drift volumes bisected by the cathode plane assembly, which is biased to create an almost uniform electric field in both volumes. The DUNE Far Detector modules must have robust cryogenic systems capable of filtering argon and supplying the TPC with clean liquid. This paper will explore comparisons of the argon purity measured by the purity monitors with those measured using muons in the TPC from October 2018 to November 2018. A new method is introduced to measure the liquid argon purity in the TPC using muons crossing both drift volumes of ProtoDUNE-SP. For extended periods on the timescale of weeks, the drift...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2ks5b3d4</guid>
      <pubDate>Mon, 16 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Abbaslu, S</name>
      </author>
      <author>
        <name>Abud, A Abed</name>
      </author>
      <author>
        <name>Acciarri, R</name>
      </author>
      <author>
        <name>Accorsi, LP</name>
      </author>
      <author>
        <name>Acero, MA</name>
      </author>
      <author>
        <name>Adames, MR</name>
      </author>
      <author>
        <name>Adamov, G</name>
      </author>
      <author>
        <name>Adamowski, M</name>
      </author>
      <author>
        <name>Adriano, C</name>
      </author>
      <author>
        <name>Akbar, F</name>
      </author>
      <author>
        <name>Alemanno, F</name>
      </author>
      <author>
        <name>Alex, NS</name>
      </author>
      <author>
        <name>Allison, K</name>
      </author>
      <author>
        <name>Alrashed, M</name>
      </author>
      <author>
        <name>Alton, A</name>
      </author>
      <author>
        <name>Alvarez, R</name>
      </author>
      <author>
        <name>Alves, T</name>
      </author>
      <author>
        <name>Aman, A</name>
      </author>
      <author>
        <name>Amar, H</name>
      </author>
      <author>
        <name>Amedo, P</name>
      </author>
      <author>
        <name>Anderson, J</name>
      </author>
      <author>
        <name>Andrade, DA</name>
      </author>
      <author>
        <name>Andreopoulos, C</name>
      </author>
      <author>
        <name>Andreotti, M</name>
      </author>
      <author>
        <name>Andrews, MP</name>
      </author>
      <author>
        <name>Andrianala, F</name>
      </author>
      <author>
        <name>Andringa, S</name>
      </author>
      <author>
        <name>Anjarazafy, F</name>
      </author>
      <author>
        <name>Ansarifard, S</name>
      </author>
      <author>
        <name>Antic, D</name>
      </author>
      <author>
        <name>Antoniassi, M</name>
      </author>
      <author>
        <name>Aranda-Fernandez, A</name>
      </author>
      <author>
        <name>Arellano, L</name>
      </author>
      <author>
        <name>Diaz, E Arrieta</name>
      </author>
      <author>
        <name>Arroyave, MA</name>
      </author>
      <author>
        <name>Arteropons, M</name>
      </author>
      <author>
        <name>Asaadi, J</name>
      </author>
      <author>
        <name>Ascencio, M</name>
      </author>
      <author>
        <name>Ashkenazi, A</name>
      </author>
      <author>
        <name>Asner, D</name>
      </author>
      <author>
        <name>Asquith, L</name>
      </author>
      <author>
        <name>Atkin, E</name>
      </author>
      <author>
        <name>Auguste, D</name>
      </author>
      <author>
        <name>Aurisano, A</name>
      </author>
      <author>
        <name>Aushev, V</name>
      </author>
      <author>
        <name>Autiero, D</name>
      </author>
      <author>
        <name>Gómez, D Ávila</name>
      </author>
      <author>
        <name>Azam, MB</name>
      </author>
      <author>
        <name>Azfar, F</name>
      </author>
      <author>
        <name>Back, A</name>
      </author>
      <author>
        <name>Back, JJ</name>
      </author>
      <author>
        <name>Bae, Y</name>
      </author>
      <author>
        <name>Bagaturia, I</name>
      </author>
      <author>
        <name>Bagby, L</name>
      </author>
      <author>
        <name>Baigarashev, D</name>
      </author>
      <author>
        <name>Balasubramanian, S</name>
      </author>
      <author>
        <name>Balboni, A</name>
      </author>
      <author>
        <name>Baldi, P</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Baldini, W</name>
      </author>
      <author>
        <name>Baldonedo, J</name>
      </author>
      <author>
        <name>Baller, B</name>
      </author>
      <author>
        <name>Bambah, B</name>
      </author>
      <author>
        <name>Barao, F</name>
      </author>
      <author>
        <name>Barbu, D</name>
      </author>
      <author>
        <name>Barenboim, G</name>
      </author>
      <author>
        <name>Alzás, P Barham</name>
      </author>
      <author>
        <name>Barker, GJ</name>
      </author>
      <author>
        <name>Barkhouse, W</name>
      </author>
      <author>
        <name>Barr, G</name>
      </author>
      <author>
        <name>Barros, A</name>
      </author>
      <author>
        <name>Barros, N</name>
      </author>
      <author>
        <name>Barrow, D</name>
      </author>
      <author>
        <name>Barrow, JL</name>
      </author>
      <author>
        <name>Basharina-Freshville, A</name>
      </author>
      <author>
        <name>Bashyal, A</name>
      </author>
      <author>
        <name>Basque, V</name>
      </author>
      <author>
        <name>Bassani, M</name>
      </author>
      <author>
        <name>Basu, D</name>
      </author>
      <author>
        <name>Batchelor, C</name>
      </author>
      <author>
        <name>Bathe-Peters, L</name>
      </author>
      <author>
        <name>Battat, JBR</name>
      </author>
      <author>
        <name>Battisti, F</name>
      </author>
      <author>
        <name>Bautista, J</name>
      </author>
      <author>
        <name>Bay, F</name>
      </author>
      <author>
        <name>Alba, JLL Bazo</name>
      </author>
      <author>
        <name>Beacom, JF</name>
      </author>
      <author>
        <name>Bechetoille, E</name>
      </author>
      <author>
        <name>Behera, B</name>
      </author>
      <author>
        <name>Belchior, E</name>
      </author>
      <author>
        <name>Bell, B</name>
      </author>
      <author>
        <name>Bell, G</name>
      </author>
      <author>
        <name>Bellantoni, L</name>
      </author>
      <author>
        <name>Bellettini, G</name>
      </author>
      <author>
        <name>Bellini, V</name>
      </author>
      <author>
        <name>Beltramello, O</name>
      </author>
      <author>
        <name>Belyaev, A</name>
      </author>
      <author>
        <name>Montiel, C Benitez</name>
      </author>
      <author>
        <name>Benjamin, D</name>
      </author>
      <author>
        <name>Neves, F Bento</name>
      </author>
      <author>
        <name>Berger, J</name>
      </author>
    </item>
    <item>
      <title>Radiative, Hydrologic, and Circulation Responses to Warming in Cess‐Potter Simulations Using the Global 3.25‐km SCREAM</title>
      <link>https://escholarship.org/uc/item/5t65r0x2</link>
      <description>Abstract Using the global 3.25‐km Simple Cloud Resolving E3SM Atmosphere Model (SCREAM 3&amp;nbsp;km), a pair of 13‐month Cess‐Potter simulations are performed to quantify the radiative feedbacks and the hydrologic and circulation responses to warming. Large‐scale aspects of SCREAM 3&amp;nbsp;km's top‐of‐atmosphere radiative fluxes, precipitation rates, and circulations are in good agreement with observations and reanalysis, with notable differences, including a drier lower free‐troposphere in the Tropics, reduced precipitation and humidity over the Tropical West Pacific, and poleward shifted Southern Hemisphere midlatitude jet. In response to warming, SCREAM 3&amp;nbsp;km predicts a total radiative feedback within the top 15% of the CMIP5 and CMIP6 models, which puts it substantially higher than the feedback reported by other kilometer‐scale models. SCREAM 3&amp;nbsp;km's high radiative feedback stems from a strongly positive shortwave cloud feedback, most prominent over the mid‐ and high‐latitudes....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5t65r0x2</guid>
      <pubDate>Tue, 10 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Terai, CR</name>
      </author>
      <author>
        <name>Keen, ND</name>
        <uri>https://orcid.org/0000-0003-3607-3554</uri>
      </author>
      <author>
        <name>Caldwell, PM</name>
      </author>
      <author>
        <name>Beydoun, H</name>
      </author>
      <author>
        <name>Bogenschutz, PA</name>
      </author>
      <author>
        <name>Chao, L‐W</name>
      </author>
      <author>
        <name>Hillman, BR</name>
      </author>
      <author>
        <name>Ma, H‐Y</name>
      </author>
      <author>
        <name>Zelinka, MD</name>
      </author>
      <author>
        <name>Bertagna, L</name>
      </author>
      <author>
        <name>Bradley, AM</name>
      </author>
      <author>
        <name>Clevenger, TC</name>
      </author>
      <author>
        <name>Donahue, AS</name>
      </author>
      <author>
        <name>Foucar, J</name>
      </author>
      <author>
        <name>Golaz, J‐C</name>
      </author>
      <author>
        <name>Guba, O</name>
      </author>
      <author>
        <name>Hannah, W</name>
      </author>
      <author>
        <name>Lee, J</name>
      </author>
      <author>
        <name>Lin, W</name>
      </author>
      <author>
        <name>Mahfouz, N</name>
      </author>
      <author>
        <name>Mülmenstädt, J</name>
      </author>
      <author>
        <name>Salinger, AG</name>
      </author>
      <author>
        <name>Singh, B</name>
      </author>
      <author>
        <name>Sreepathi, S</name>
      </author>
      <author>
        <name>Qin, Y</name>
      </author>
      <author>
        <name>Taylor, MA</name>
      </author>
      <author>
        <name>Ullrich, PA</name>
        <uri>https://orcid.org/0000-0003-4118-4590</uri>
      </author>
      <author>
        <name>Wu, W‐Y</name>
      </author>
      <author>
        <name>Yuan, X</name>
      </author>
      <author>
        <name>Zender, CS</name>
        <uri>https://orcid.org/0000-0003-0129-8024</uri>
      </author>
      <author>
        <name>Zhang, Y</name>
      </author>
    </item>
    <item>
      <title>Revisiting Reconfigurable Acceleration of Vision Transformer with Patch Pruning</title>
      <link>https://escholarship.org/uc/item/4tt9n3gq</link>
      <description>Vision Transformers (ViTs) have become the backbone of numerous cutting-edge vision applications. The attention modules within ViTs play a crucial role in modeling spatial relationships between pixels. Although these attention modules enhance the accuracy of ViT models, they also increase computational demands, limiting the deployment of ViTs in edge computing environments. To address this issue, prior research has focused on optimizing ViTs from both software and hardware perspectives. A notable software optimization technique is reducing the image patches involved in attention computations. Two common methods to achieve this are window attention and patch pruning. However, they introduce new challenges for existing hardware platforms regarding attention computation. Therefore, it is essential to develop new hardware modules to simultaneously support pruned attention computations and efficient window shifts. In this study, we introduce an FPGA-based token reduction vision transformer...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4tt9n3gq</guid>
      <pubDate>Wed, 25 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Hanning</name>
      </author>
      <author>
        <name>Ni, Yang</name>
      </author>
      <author>
        <name>Huang, Wenjun</name>
      </author>
      <author>
        <name>Oh, Hyunwoo</name>
      </author>
      <author>
        <name>Das, Tamoghno</name>
      </author>
      <author>
        <name>Wen, Fei</name>
      </author>
      <author>
        <name>Imani, Mohsen</name>
      </author>
    </item>
    <item>
      <title>NUDGING: Inference-time Alignment of LLMs via Guided Decoding</title>
      <link>https://escholarship.org/uc/item/4ht09133</link>
      <description>Large language models (LLMs) require alignment to effectively and safely follow user instructions. This process necessitates training an aligned version for every base model, resulting in significant computational overhead. In this work, we propose NUDGING, a simple, training-free algorithm that aligns any base model at inference time using a small aligned model. NUDGING is motivated by recent findings that alignment primarily alters the model's behavior on a small subset of stylistic tokens (e.g., discourse markers). We find that base models are significantly more uncertain when generating these tokens. Building on this insight, NUDGING employs a small aligned model to generate nudging tokens to guide the base model's output during decoding when the base model's uncertainty is high, with only a minor additional inference overhead. We evaluate NUDGING across 3 model families on a diverse range of open-instruction tasks. Without any training, nudging a large base model with a 7×-14×...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4ht09133</guid>
      <pubDate>Wed, 11 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Fei, Yu</name>
      </author>
      <author>
        <name>Razeghi, Yasaman</name>
      </author>
      <author>
        <name>Singh, Sameer</name>
        <uri>https://orcid.org/0000-0003-0621-6323</uri>
      </author>
    </item>
    <item>
      <title>Episodic-like memory in a simulation of cuttlefish behavior.</title>
      <link>https://escholarship.org/uc/item/0zx7016p</link>
      <description>Episodic memory involves remembering the what, when, and where components of an event. It has been observed in humans, other vertebrates, and the invertebrate cuttlefish. In clever behavioral experiments, cuttlefish have been shown to have episodic-like memory, where they demonstrate the ability to remember when and where a preferred food source will appear. The present work replicates this behavior with a parsimonious model of episodic memory. To further test this model and explore episodic-like memory, we introduce a predator-prey scenario in which the agent must remember what creatures (e.g. predator, desirable prey, or less desirable prey) appear at a given time and region of the model environment. This simulates similar situations that cuttlefish face in the wild. They will typically hide when predators are in the area, and hunt for prey when available. When the memory model is queried for an action (e.g., hunt or hide), the cuttlefish agent hunts for preferred food, like...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0zx7016p</guid>
      <pubDate>Sat, 31 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kandimalla, Sriskandha</name>
      </author>
      <author>
        <name>Wong, Qian</name>
      </author>
      <author>
        <name>Zheng, Kary</name>
      </author>
      <author>
        <name>Krichmar, Jeffrey</name>
      </author>
    </item>
    <item>
      <title>A New Online Fault Detection Mechanism for Neural Network Applications</title>
      <link>https://escholarship.org/uc/item/6qg5w3z2</link>
      <description>A New Online Fault Detection Mechanism for Neural Network Applications</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6qg5w3z2</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Paola, Luca De</name>
      </author>
      <author>
        <name>Esposito, Giuseppe</name>
      </author>
      <author>
        <name>Guerrero-Balaguera, Juan-David</name>
      </author>
      <author>
        <name>Reorda, Matteo Sonza</name>
      </author>
    </item>
    <item>
      <title>Enhancing the Reliability of Split Computing Deep Neural Networks</title>
      <link>https://escholarship.org/uc/item/3xq5m8rq</link>
      <description>Artificial intelligence is becoming increasingly popular for IoT applications in safety-critical fields (e.g., autonomous systems and biomedical, robots). Unfortunately, the inference’s workload process alone increases as the model size grows. To meet the computational power limitations of mobile devices running IoT applications, modern services sometimes resort to the Split Computing paradigm. Split Computing divides the inference process of a Neural Network into Head and Tail for their execution in a mobile device and a server, respectively, which also allows the reduction of the overall IoT device’s computational cost. Nonetheless, Split Computing can be used in safety-critical fields where reliability is crucial, especially when mobile devices have computational and cost restrictions. This paper introduces hardening techniques acting on the software to mitigate the effects of hardware faults on Split Computing models. The proposed hardening techniques consist of i) a bounded...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3xq5m8rq</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Esposito, Giuseppe</name>
      </author>
      <author>
        <name>Guerrero-Balaguera, Juan-David</name>
      </author>
      <author>
        <name>Condia, Josie E Rodriguez</name>
      </author>
      <author>
        <name>Levorato, Marco</name>
        <uri>https://orcid.org/0000-0002-6920-4189</uri>
      </author>
      <author>
        <name>Reorda, Matteo Sonza</name>
      </author>
    </item>
    <item>
      <title>AI-Based Classification of Adversarial Attacks vs. Hardware Fault Corruptions in the Split Computing Context</title>
      <link>https://escholarship.org/uc/item/0kb5q35c</link>
      <description>Split Computing has emerged as a promising paradigm for deploying Deep Neural Networks in Edge and Inter-net of Things systems, enabling inference tasks to be distributed between resource-constrained edge devices and cloud servers. This approach is particularly attractive for autonomous systems, where security and reliability may be critical. However, interme-diate feature maps transmitted between devices are vulnerable to corruption, which may result from intentional adversarial attacks or unintentional hardware faults. Distinguishing whether corruption originates from an external adversary or an inherent system fault is crucial for implementing appropriate counter-measures-reinforcing security mechanisms against attacks or improving system reliability to mitigate the effects of hardware-related faults. To the best of our knowledge, this work is the first to propose a machine learning-based classification mechanism capable of differentiating adversarial attacks from hardware...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0kb5q35c</guid>
      <pubDate>Thu, 29 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Esposito, G</name>
      </author>
      <author>
        <name>Magliano, E</name>
      </author>
      <author>
        <name>Scarano, N</name>
      </author>
      <author>
        <name>Eltaras, T Ahmed</name>
      </author>
      <author>
        <name>Balaguera, JD Guerrero</name>
      </author>
      <author>
        <name>Mannella, L</name>
      </author>
      <author>
        <name>Condia, JE Rodriguez</name>
      </author>
      <author>
        <name>Ruospo, A</name>
      </author>
      <author>
        <name>Di Carlo, S</name>
      </author>
      <author>
        <name>Levorato, M</name>
        <uri>https://orcid.org/0000-0002-6920-4189</uri>
      </author>
      <author>
        <name>Savino, A</name>
      </author>
      <author>
        <name>Reorda, M Sonza</name>
      </author>
    </item>
    <item>
      <title>Analysis of yeast's ORF upstream regions by parallel processing, microarrays, and computational methods.</title>
      <link>https://escholarship.org/uc/item/52h1r6jd</link>
      <description>We use a network of workstations to compute all pairwise alignments of the 500 bp upstream regions of 6,225 yeast ORFs (Open Reading Frames). We correlate the alignments with DNA microarray expression data from budding yeast cells over an oxidative stress time course. We confirm on a genomic scale that, in general, genes with extremely similar upstream regions have similar activity levels, even when located on different chromosomes. As the difference in upstream regions increases, the correlation rapidly drops towards zero. Divergent ORFs with overlapping upstream regions do not seem to be correlated in any way. The pairwise alignments coupled with the expression data, together with other computational techniques, suggest a few new putative regulatory binding sites that can be tested experimentally. Finally, we investigate the inherent symmetry present in the two strands of the yeast genome. We show that it extends at least all the way up to 9-mers and is likely to result from...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/52h1r6jd</guid>
      <pubDate>Wed, 28 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hampson, S</name>
      </author>
      <author>
        <name>Baldi, P</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Kibler, D</name>
      </author>
      <author>
        <name>Sandmeyer, SB</name>
        <uri>https://orcid.org/0000-0002-5059-9619</uri>
      </author>
    </item>
    <item>
      <title>Lower Bounds for Non-adaptive Shortest Path Relaxation</title>
      <link>https://escholarship.org/uc/item/8xf4c1sg</link>
      <description>We consider single-source shortest path algorithms that perform a sequence of relaxation steps whose ordering depends only on the input graph structure and not on its weights or the results of prior steps. Each step examines one edge of the graph, and replaces the tentative distance to the endpoint of the edge by its minimum with the tentative distance to the start of the edge, plus the edge length. As we prove, among such algorithms, the Bellman-Ford algorithm has optimal complexity for dense graphs and near-optimal complexity for sparse graphs, as a function of the number of edges and vertices in the given graph. Our analysis holds both for deterministic algorithms and for randomized algorithms that find shortest path distances with high probability.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8xf4c1sg</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>Stack-Number is Not Bounded by Queue-Number</title>
      <link>https://escholarship.org/uc/item/8vr2g2bx</link>
      <description>We describe a family of graphs with queue-number at most 4 but unbounded stack-number. This resolves open problems of Heath, Leighton and Rosenberg (1992) and Blankenship and Oporowski (1999).</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8vr2g2bx</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dujmović, Vida</name>
      </author>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Hickingbotham, Robert</name>
      </author>
      <author>
        <name>Morin, Pat</name>
      </author>
      <author>
        <name>Wood, David R</name>
      </author>
    </item>
    <item>
      <title>Orthogonal Dissection into Few Rectangles</title>
      <link>https://escholarship.org/uc/item/7vk4h9x2</link>
      <description>We describe a polynomial time algorithm that takes as input a polygon with axis-parallel sides but irrational vertex coordinates, and outputs a set of as few rectangles as possible into which it can be dissected by axis-parallel cuts and translations. The number of rectangles is the rank of the Dehn invariant of the polygon.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7vk4h9x2</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, D</name>
      </author>
    </item>
    <item>
      <title>Non-Euclidean Erdos-Anning Theorems</title>
      <link>https://escholarship.org/uc/item/6p42s47v</link>
      <description>The Erdos-Anning theorem states that every point set in the Euclidean plane with integer distances must be either collinear or finite. More strongly, for any (non-degenerate) triangle of diameter δ, at most O(δ2) points can have integer distances from all three triangle vertices. We prove the same results for any strictly convex distance function on the plane, and analogous results for every two-dimensional complete Riemannian manifold of bounded genus and for geodesic distance on the boundary of every three-dimensional Euclidean convex set. As a consequence, we resolve a 1983 question of Richard Guy on the equilateral dimension of Riemannian manifolds. Our proofs are based on the properties of additively weighted Voronoi diagrams of these distances.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6p42s47v</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, D</name>
      </author>
    </item>
    <item>
      <title>Manipulating Weights to Improve Stress-Graph Drawings of 3-Connected Planar Graphs</title>
      <link>https://escholarship.org/uc/item/5cz9305t</link>
      <description>We study methods to manipulate weights in stress-graph embeddings to improve convex straight-line planar drawings of 3-connected planar graphs. Stress-graph embeddings are weighted versions of Tutte embeddings, where solving a linear system places vertices at a minimum-energy configuration for a system of springs. A major drawback of the unweighted Tutte embedding is that it often results in drawings with exponential area. We present a number of approaches for choosing better weights. One approach constructs weights (in linear time) that uniformly spread all vertices in a chosen direction, such as parallel to the x- or y-axis. A second approach morphs x- and y-spread drawings to produce a more aesthetically pleasing and uncluttered drawing. We further explore a “kaleidoscope” paradigm for this xy-morph approach, where we rotate the coordinate axes so as to find the best spreads and morphs. A third approach chooses the weight of each edge according to its depth in a spanning tree...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5cz9305t</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chiu, Alvin</name>
      </author>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Goodrich, Michael T</name>
      </author>
    </item>
    <item>
      <title>Locked and Unlocked Smooth Embeddings of Surfaces</title>
      <link>https://escholarship.org/uc/item/4r11t4px</link>
      <description>We study the continuous motion of smooth isometric embeddings of a planar surface in three-dimensional Euclidean space, and two related discrete analogues of these embeddings, polygonal embeddings and flat foldings without interior vertices, under continuous changes of the embedding or folding. We show that every starshaped or spiral-shaped domain is unlocked: a continuous motion unfolds it to a flat embedding. However, disks with two holes can have locked embeddings that are topologically equivalent to a flat embedding but cannot reach a flat embedding by continuous motion.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4r11t4px</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, D</name>
      </author>
    </item>
    <item>
      <title>Noncrossing Longest Paths and Cycles</title>
      <link>https://escholarship.org/uc/item/4hk5n3pg</link>
      <description>Edge crossings in geometric graphs are sometimes undesirable as they could lead to unwanted situations such as collisions in motion planning and inconsistency in VLSI layout. Short geometric structures such as shortest perfect matchings, shortest spanning trees, shortest spanning paths, and shortest spanning cycles on a given point set are inherently noncrossing. However, the longest such structures need not be noncrossing. In fact, it is intuitive to expect many edge crossings in various geometric graphs that are longest.Recently, Álvarez-Rebollar, Cravioto-Lagos, Marín, Solé-Pi, and Urrutia (Graphs and Combinatorics, 2024) constructed a set of points for which the longest perfect matching is noncrossing. They raised several challenging questions in this direction. In particular, they asked whether the longest spanning path, on every finite set of points in the plane, must have a pair of crossing edges. They also conjectured that the longest spanning cycle must have a pair of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4hk5n3pg</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Aloupis, Greg</name>
      </author>
      <author>
        <name>Biniaz, Ahmad</name>
      </author>
      <author>
        <name>Bose, Prosenjit</name>
      </author>
      <author>
        <name>De Carufel, Jean-Lou</name>
      </author>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Maheshwari, Anil</name>
      </author>
      <author>
        <name>Odak, Saeed</name>
      </author>
      <author>
        <name>Smid, Michiel</name>
      </author>
      <author>
        <name>Tóth, Csaba D</name>
      </author>
      <author>
        <name>Valtr, Pavel</name>
      </author>
    </item>
    <item>
      <title>On the Biplanarity of Blowups</title>
      <link>https://escholarship.org/uc/item/4ch9d6nt</link>
      <description>The 2-blowup of a graph is obtained by replacing each vertex with two non-adjacent copies; a graph is biplanar if it is the union of two planar graphs. We disprove a conjecture of Gethner that 2-blowups of planar graphs are biplanar: iterated Kleetopes are counterexamples. Additionally, we construct biplanar drawings of 2-blowups of planar graphs whose duals have two-path induced path partitions, and drawings with split thickness two of 2-blowups of 3-chromatic planar graphs, and of graphs that can be decomposed into a Hamiltonian path and a dual Hamiltonian path.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4ch9d6nt</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>Quasipolynomiality of the Smallest Missing Induced Subgraph</title>
      <link>https://escholarship.org/uc/item/3m42661w</link>
      <description>We study the problem of finding the smallest graph that does not occur as an induced subgraph of a given graph. This missing induced subgraph has at most logarithmic size and can be found by a brute-force search, in an $n$-vertex graph, in time $n^{O(\log n)}$. We show that under the Exponential Time Hypothesis this quasipolynomial time bound is optimal. We also consider variations of the problem in which either the missing subgraph or the given graph comes from a restricted graph family; for instance, we prove that the smallest missing planar induced subgraph of a given planar graph can be found in polynomial time.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3m42661w</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
      <author>
        <name>Lincoln, Andrea</name>
      </author>
      <author>
        <name>Vassilevska Williams, Virginia</name>
      </author>
    </item>
    <item>
      <title>Bandwidth vs BFS Width in Matrix Reordering, Graph Reconstruction, and Graph Drawing</title>
      <link>https://escholarship.org/uc/item/35q5x6tf</link>
      <description>We provide the first approximation quality guarantees for the Cuthull-McKee heuristic for reordering symmetric matrices to have low bandwidth, and we provide an algorithm for reconstructing bounded-bandwidth graphs from distance oracles with near-linear query complexity. To prove these results we introduce a new width parameter, BFS width, and we prove polylogarithmic upper and lower bounds on the BFS width of graphs of bounded bandwidth. Unlike other width parameters, such as bandwidth, pathwidth, and treewidth, BFS width can easily be computed in polynomial time. Bounded BFS width implies bounded bandwidth, pathwidth, and treewidth, which in turn imply fixed-parameter tractable algorithms for many problems that are NP-hard for general graphs. In addition to their applications to matrix ordering, we also provide applications of BFS width to graph reconstruction, to reconstruct graphs from distance queries, and graph drawing, to construct arc diagrams of small height.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/35q5x6tf</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, D</name>
      </author>
      <author>
        <name>Goodrich, MT</name>
        <uri>https://orcid.org/0000-0002-8943-191X</uri>
      </author>
      <author>
        <name>Liu, S</name>
        <uri>https://orcid.org/0009-0003-1255-7156</uri>
      </author>
    </item>
    <item>
      <title>Computational Geometry with Probabilistically Noisy Primitive Operations</title>
      <link>https://escholarship.org/uc/item/2z8632j4</link>
      <description>Much prior work has been done on designing computational geometry algorithms that handle input degeneracies, data imprecision, and arithmetic round-off errors. We take a new approach, inspired by the noisy sorting literature, and study computational geometry algorithms subject to noisy Boolean primitive operations in which, e.g., the comparison “is point q above line ℓ?” returns the wrong answer with some fixed probability. We propose a novel technique called path-guided pushdown random walks that generalizes the results of noisy sorting. We apply this technique to solve point-location, plane-sweep, convex hulls in 2D and 3D, and Delaunay triangulations for noisy primitives in optimal time with high probability.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2z8632j4</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, D</name>
      </author>
      <author>
        <name>Goodrich, MT</name>
        <uri>https://orcid.org/0000-0002-8943-191X</uri>
      </author>
      <author>
        <name>Sridhar, V</name>
        <uri>https://orcid.org/0009-0009-3549-9589</uri>
      </author>
    </item>
    <item>
      <title>On Polyhedral Realization with Isosceles Triangles</title>
      <link>https://escholarship.org/uc/item/0bv8n96m</link>
      <description>Answering a question posed by Joseph Malkevitch, we prove that there exists a polyhedral graph, with triangular faces, such that every realization of it as the graph of a convex polyhedron includes at least one face that is a scalene triangle. Our construction is based on Kleetopes, and shows that there exists an integer i such that all convex i-iterated Kleetopes have a scalene face. However, we also show that all Kleetopes of triangulated polyhedral graphs have non-convex non-self-crossing realizations in which all faces are isosceles. We answer another question of Malkevitch by observing that a spherical tiling of Dawson (Renaissance Banff, Bridges Conference, pp. 489–496, 2005) leads to a fourth infinite family of convex polyhedra in which all faces are congruent isosceles triangles, adding one to the three families previously known to Malkevitch. We prove that the graphs of convex polyhedra with congruent isosceles faces have bounded diameter and have dominating sets of bounded...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0bv8n96m</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eppstein, David</name>
      </author>
    </item>
    <item>
      <title>Data-rate-aware FPGA-based Acceleration Framework for Streaming Applications</title>
      <link>https://escholarship.org/uc/item/5qc6s3rx</link>
      <description>In heterogeneous architectures, FPGAs are not only expected to provide higher performance, but also to provide a more energy efficient solution for computationally intensive tasks. While parallelism and pipelining enhance performance on FPGA platforms, the data transfer rate from/to off-chip memory can cause performance degradation. We propose an automated high-level synthesis framework for FPGA-based acceleration of nested loops on large multidimensional input data sets. Given the high-level of parallelism in such applications, our proposed data prefetching algorithm determines the data rate for each parallel datapath. The empirical results on a case study in scientific computing show that FPGA mapping of such nested loops accelerates the application compared to traditional mapping on multicores. The FPGA-accelerated computation results in 3x speedup in runtime and 27x energy-delay-product savings compared to multicore computation.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5qc6s3rx</guid>
      <pubDate>Sat, 8 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Rezaei, Siavash</name>
      </author>
      <author>
        <name>Hernandez-Calderon, Cesar-Alejandro</name>
      </author>
      <author>
        <name>Mirzamohammadi, Saeed</name>
      </author>
      <author>
        <name>Bozorgzadeh, Eli</name>
      </author>
      <author>
        <name>Veeidenbaum, Alexander</name>
      </author>
      <author>
        <name>Nicolau, Alex</name>
        <uri>https://orcid.org/0009-0003-9833-8455</uri>
      </author>
      <author>
        <name>Prather, Michael J</name>
        <uri>https://orcid.org/0000-0002-9442-8109</uri>
      </author>
    </item>
    <item>
      <title>Understanding How Personal Activities Are Shared In Short-form Videos</title>
      <link>https://escholarship.org/uc/item/5bp9q190</link>
      <description>Sharing activities that people do in everyday life, such as physical activity, health management, or hobbies, help people receive benefits like social support and positive self-presentation. Short-form videos present new opportunities for activity-sharing, which has traditionally been studied in static contexts like text- and image-sharing. We therefore aim to understand what information people incorporate into short-form activity videos, and how. We qualitatively analyzed 420 short-form activity videos on TikTok across three domains: running, studying, and sketching. We found people often present information before, during, and after activities, developing strategies for qualitatively and quantitatively incorporating activity-relevant information in each. We also uncover practices for aligning the sharing of activity-relevant information with the nature of short-form videos, such as modifying broader-scale goals into video-scale goals. We further discuss design opportunities...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5bp9q190</guid>
      <pubDate>Wed, 22 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Dennis</name>
      </author>
      <author>
        <name>Zhu, Jun</name>
      </author>
      <author>
        <name>Epstein, Daniel A</name>
        <uri>https://orcid.org/0000-0002-2657-6345</uri>
      </author>
    </item>
    <item>
      <title>SNICAR-ADv3: a community tool for modeling spectral snow albedo</title>
      <link>https://escholarship.org/uc/item/98p088qf</link>
      <description>The Snow, Ice, and Aerosol Radiative (SNICAR) model has been used in various capacities over the last 15 years to model the spectral albedo of snow with light-absorbing constituents (LACs). Recent studies have extended the model to include an adding-doubling two-stream solver and representations of non-spherical ice particles; carbon dioxide snow; snow algae; and new types of mineral dust, volcanic ash, and brown carbon. New options also exist for ice refractive indices and solar-zenith-angle-dependent surface spectral irradiances used to derive broadband albedo. The model spectral range was also extended deeper into the ultraviolet for studies of extraterrestrial and high-altitude cryospheric surfaces. Until now, however, these improvements and capabilities have not been merged into a unified code base. Here, we document the formulation and evaluation of the publicly available SNICAR-ADv3 source code, web-based model, and accompanying library of constituent optical properties....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/98p088qf</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Flanner, Mark G</name>
      </author>
      <author>
        <name>Arnheim, Julian B</name>
      </author>
      <author>
        <name>Cook, Joseph M</name>
      </author>
      <author>
        <name>Dang, Cheng</name>
      </author>
      <author>
        <name>He, Cenlin</name>
      </author>
      <author>
        <name>Huang, Xianglei</name>
      </author>
      <author>
        <name>Singh, Deepak</name>
      </author>
      <author>
        <name>Skiles, S McKenzie</name>
      </author>
      <author>
        <name>Whicker, Chloe A</name>
      </author>
      <author>
        <name>Zender, Charles S</name>
        <uri>https://orcid.org/0000-0003-0129-8024</uri>
      </author>
    </item>
    <item>
      <title>A Framework for Variational Inference and Data Assimilation of Soil Biogeochemical Models Using Normalizing Flows</title>
      <link>https://escholarship.org/uc/item/8fb053sp</link>
      <description>Soil biogeochemical models (SBMs) represent soil variables and their responses to global change. Data assimilation approaches help determine whether SBMs accurately represent soil processes consistent with soil pool and flux measurements. Bayesian inference is commonly used in data assimilation procedures that estimate posterior parameter distributions with Markov chain Monte Carlo (MCMC) methods. The ability to account for data and parameter uncertainty is a strength of MCMC inference, but the computational inefficiency of MCMC methods remains a barrier to their wider application, especially with large data sets. Given the limitations of MCMC approaches, we developed an alternative variational inference framework that uses a method called normalizing flows from the field of machine learning. Normalizing flows rely on deep learning to map probability distributions and approximate SBMs that have been discretized into state space models. As a test of our method, we fit approximated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8fb053sp</guid>
      <pubDate>Thu, 2 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Xie, HW</name>
      </author>
      <author>
        <name>Sujono, D</name>
      </author>
      <author>
        <name>Ryder, T</name>
      </author>
      <author>
        <name>Sudderth, EB</name>
      </author>
      <author>
        <name>Allison, SD</name>
        <uri>https://orcid.org/0000-0003-4629-7842</uri>
      </author>
    </item>
    <item>
      <title>Single-cell spatial transcriptomics reveals distinct patterns of dysregulation in non-neuronal and neuronal cells induced by the Trem2R47H Alzheimer’s risk gene mutation</title>
      <link>https://escholarship.org/uc/item/71v7f231</link>
      <description>The R47H missense mutation of the TREM2 gene is a known risk factor for development of Alzheimer’s Disease. In this study, we analyze the impact of the Trem2R47H mutation on specific cell types in multiple cortical and subcortical brain regions in the context of wild-type and 5xFAD mouse background. We profile 19 mouse brain sections consisting of wild-type, Trem2R47H, 5xFAD and Trem2R47H; 5xFAD genotypes using MERFISH spatial transcriptomics, a technique that enables subcellular profiling of spatial gene expression. Spatial transcriptomics and neuropathology data are analyzed using our custom pipeline to identify plaque and Trem2R47H-induced transcriptomic dysregulation. We initially analyze&amp;nbsp;cell type-specific transcriptomic alterations induced by plaque proximity. Next, we analyze spatial distributions of disease associated microglia and astrocytes, and how they vary between 5xFAD and Trem2R47H; 5xFAD mouse models. Finally, we analyze the impact of the Trem2R47H mutation&amp;nbsp;on...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/71v7f231</guid>
      <pubDate>Thu, 11 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Johnston, Kevin G</name>
      </author>
      <author>
        <name>Berackey, Bereket T</name>
      </author>
      <author>
        <name>Tran, Kristine M</name>
      </author>
      <author>
        <name>Gelber, Alon</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>MacGregor, Grant R</name>
      </author>
      <author>
        <name>Mukamel, Eran A</name>
        <uri>https://orcid.org/0000-0003-3203-9535</uri>
      </author>
      <author>
        <name>Tan, Zhiqun</name>
      </author>
      <author>
        <name>Green, Kim N</name>
        <uri>https://orcid.org/0000-0002-6049-6744</uri>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
    </item>
    <item>
      <title>An AAV capsid proposed as microglia-targeting directs genetic expression in forebrain excitatory neurons</title>
      <link>https://escholarship.org/uc/item/7rg946z5</link>
      <description>A newly developed capsid AAV-MG1.2 was reported to mediate specific microglial transduction. However, we find that AAV-MG1.2 actually enables specific genetic access to excitatory neurons in forebrain regions including hippocampal formation and visual cortex but does not confer expression in microglia or astrocytes in vivo. Furthermore, we find that AAV-MG1.2 specifically labels the deep layer of the CA1 pyramidal layer in a titer-dependent manner. We show that AAV-MG1.2-Cre can be used to genetically target excitatory neurons for cell-type-specific neural circuit mapping studies. We also find that AAV-MG1.2 conserves specificity for excitatory neurons in rat hippocampus. Thus, the AAV-MG1.2 presents a useful viral-genetic tool for targeting excitatory neurons in the forebrain across different species.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7rg946z5</guid>
      <pubDate>Wed, 10 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Cao, Wenhao</name>
      </author>
      <author>
        <name>Tan, Zhiqun</name>
      </author>
      <author>
        <name>Berackey, Bereket T</name>
      </author>
      <author>
        <name>Nguyen, Jason K</name>
      </author>
      <author>
        <name>Brown, Sara R</name>
      </author>
      <author>
        <name>Du, Shiyang</name>
      </author>
      <author>
        <name>Lin, Bin</name>
      </author>
      <author>
        <name>Ye, Qiao</name>
      </author>
      <author>
        <name>Seiler, Magdalene</name>
        <uri>https://orcid.org/0000-0002-0869-9923</uri>
      </author>
      <author>
        <name>Holmes, Todd C</name>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
    </item>
    <item>
      <title>Supernova pointing capabilities of DUNE</title>
      <link>https://escholarship.org/uc/item/60h5f1d3</link>
      <description>The determination of the direction of a stellar core collapse via its neutrino emission is crucial for the identification of the progenitor for a multimessenger follow-up. A highly effective method of reconstructing supernova directions within the Deep Underground Neutrino Experiment (DUNE) is introduced. The supernova neutrino pointing resolution is studied by simulating and reconstructing electron-neutrino charged-current absorption on  and elastic scattering of neutrinos on electrons. Procedures to reconstruct individual interactions, including a newly developed technique called “brems flipping,” as well as the burst direction from an ensemble of interactions are described. Performance of the burst direction reconstruction is evaluated for supernovae happening at a distance of 10&amp;nbsp;kpc for a specific supernova burst flux model. The pointing resolution is found to be 3.4&amp;nbsp;degrees at 68% coverage for a perfect interaction-channel classification and a fiducial mass of 40&amp;nbsp;kton,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/60h5f1d3</guid>
      <pubDate>Fri, 15 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Abud, A Abed</name>
      </author>
      <author>
        <name>Abi, B</name>
      </author>
      <author>
        <name>Acciarri, R</name>
      </author>
      <author>
        <name>Acero, MA</name>
      </author>
      <author>
        <name>Adames, MR</name>
      </author>
      <author>
        <name>Adamov, G</name>
      </author>
      <author>
        <name>Adamowski, M</name>
      </author>
      <author>
        <name>Adams, D</name>
      </author>
      <author>
        <name>Adinolfi, M</name>
      </author>
      <author>
        <name>Adriano, C</name>
      </author>
      <author>
        <name>Aduszkiewicz, A</name>
      </author>
      <author>
        <name>Aguilar, J</name>
      </author>
      <author>
        <name>Aimard, B</name>
      </author>
      <author>
        <name>Akbar, F</name>
      </author>
      <author>
        <name>Allison, K</name>
      </author>
      <author>
        <name>Monsalve, S Alonso</name>
      </author>
      <author>
        <name>Alrashed, M</name>
      </author>
      <author>
        <name>Alton, A</name>
      </author>
      <author>
        <name>Alvarez, R</name>
      </author>
      <author>
        <name>Alves, T</name>
      </author>
      <author>
        <name>Amar, H</name>
      </author>
      <author>
        <name>Amedo, P</name>
      </author>
      <author>
        <name>Anderson, J</name>
      </author>
      <author>
        <name>Andrade, DA</name>
      </author>
      <author>
        <name>Andreopoulos, C</name>
      </author>
      <author>
        <name>Andreotti, M</name>
      </author>
      <author>
        <name>Andrews, MP</name>
      </author>
      <author>
        <name>Andrianala, F</name>
      </author>
      <author>
        <name>Andringa, S</name>
      </author>
      <author>
        <name>Anfimov, N</name>
      </author>
      <author>
        <name>Ankowski, A</name>
      </author>
      <author>
        <name>Antoniassi, M</name>
      </author>
      <author>
        <name>Antonova, M</name>
      </author>
      <author>
        <name>Antoshkin, A</name>
      </author>
      <author>
        <name>Aranda-Fernandez, A</name>
      </author>
      <author>
        <name>Arellano, L</name>
      </author>
      <author>
        <name>Diaz, E Arrieta</name>
      </author>
      <author>
        <name>Arroyave, MA</name>
      </author>
      <author>
        <name>Asaadi, J</name>
      </author>
      <author>
        <name>Ashkenazi, A</name>
      </author>
      <author>
        <name>Asner, D</name>
      </author>
      <author>
        <name>Asquith, L</name>
      </author>
      <author>
        <name>Atkin, E</name>
      </author>
      <author>
        <name>Auguste, D</name>
      </author>
      <author>
        <name>Aurisano, A</name>
      </author>
      <author>
        <name>Aushev, V</name>
      </author>
      <author>
        <name>Autiero, D</name>
      </author>
      <author>
        <name>Azfar, F</name>
      </author>
      <author>
        <name>Back, A</name>
      </author>
      <author>
        <name>Back, H</name>
      </author>
      <author>
        <name>Back, JJ</name>
      </author>
      <author>
        <name>Bagaturia, I</name>
      </author>
      <author>
        <name>Bagby, L</name>
      </author>
      <author>
        <name>Balashov, N</name>
      </author>
      <author>
        <name>Balasubramanian, S</name>
      </author>
      <author>
        <name>Baldi, P</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Baldini, W</name>
      </author>
      <author>
        <name>Baldonedo, J</name>
      </author>
      <author>
        <name>Baller, B</name>
      </author>
      <author>
        <name>Bambah, B</name>
      </author>
      <author>
        <name>Banerjee, R</name>
      </author>
      <author>
        <name>Barao, F</name>
      </author>
      <author>
        <name>Barenboim, G</name>
      </author>
      <author>
        <name>Alzás, P Barham</name>
      </author>
      <author>
        <name>Barker, GJ</name>
      </author>
      <author>
        <name>Barkhouse, W</name>
      </author>
      <author>
        <name>Barr, G</name>
      </author>
      <author>
        <name>Monarca, J Barranco</name>
      </author>
      <author>
        <name>Barros, A</name>
      </author>
      <author>
        <name>Barros, N</name>
      </author>
      <author>
        <name>Barrow, D</name>
      </author>
      <author>
        <name>Barrow, JL</name>
      </author>
      <author>
        <name>Basharina-Freshville, A</name>
      </author>
      <author>
        <name>Bashyal, A</name>
      </author>
      <author>
        <name>Basque, V</name>
      </author>
      <author>
        <name>Batchelor, C</name>
      </author>
      <author>
        <name>Bathe-Peters, L</name>
      </author>
      <author>
        <name>Battat, JBR</name>
      </author>
      <author>
        <name>Battisti, F</name>
      </author>
      <author>
        <name>Bay, F</name>
      </author>
      <author>
        <name>Bazetto, MCQ</name>
      </author>
      <author>
        <name>Alba, JLL Bazo</name>
      </author>
      <author>
        <name>Beacom, JF</name>
      </author>
      <author>
        <name>Bechetoille, E</name>
      </author>
      <author>
        <name>Behera, B</name>
      </author>
      <author>
        <name>Belchior, E</name>
      </author>
      <author>
        <name>Bell, G</name>
      </author>
      <author>
        <name>Bellantoni, L</name>
      </author>
      <author>
        <name>Bellettini, G</name>
      </author>
      <author>
        <name>Bellini, V</name>
      </author>
      <author>
        <name>Beltramello, O</name>
      </author>
      <author>
        <name>Benekos, N</name>
      </author>
      <author>
        <name>Montiel, C Benitez</name>
      </author>
      <author>
        <name>Benjamin, D</name>
      </author>
      <author>
        <name>Neves, F Bento</name>
      </author>
      <author>
        <name>Berger, J</name>
      </author>
      <author>
        <name>Berkman, S</name>
      </author>
      <author>
        <name>Bernal, J</name>
      </author>
      <author>
        <name>Bernardini, P</name>
      </author>
      <author>
        <name>Bersani, A</name>
      </author>
    </item>
    <item>
      <title>FOVDA: A Federated Architecture for Overcoming Data Silos in Water Domain [Vision]</title>
      <link>https://escholarship.org/uc/item/27f6g9z7</link>
      <description>Effective water management relies on integrating data from diverse sources, including both static and dynamic datasets. However, the challenge of data silos, especially in cities and agencies with disparate systems, has hindered progress in this domain. To address this issue, we introduce FOVDA (Federated Ontology View Data Access), an ontology-driven federated system designed to overcome data silos in the water domain. FOVDA enables seamless data integration and querying across heterogeneous data stores by leveraging a federated architecture and a domain-specific ontology. This system supports both local and global data interoperability, allowing agencies to exchange critical water-related data while maintaining data sovereignty. FOVDA’s federated query engine facilitates complex queries across distributed datasets, enabling decision-makers to access comprehensive insights for tasks such as water resource management, infrastructure resilience analysis, and disaster response....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/27f6g9z7</guid>
      <pubDate>Wed, 30 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Luti, Malik</name>
      </author>
      <author>
        <name>Feldman, David</name>
        <uri>https://orcid.org/0000-0003-2288-5017</uri>
      </author>
      <author>
        <name>Hu, ZhengHui</name>
      </author>
      <author>
        <name>Mehrotra, Sharad</name>
      </author>
      <author>
        <name>Mendoza, Marina</name>
      </author>
      <author>
        <name>Venkatasubramanian, Nalini</name>
        <uri>https://orcid.org/0000-0001-7011-2268</uri>
      </author>
      <author>
        <name>Yus, Roberto</name>
      </author>
      <author>
        <name>Eguchi, Ronald</name>
      </author>
    </item>
    <item>
      <title>The track-length extension fitting algorithm for energy measurement of interacting particles in liquid argon TPCs and its performance with ProtoDUNE-SP data</title>
      <link>https://escholarship.org/uc/item/1rc2h91p</link>
      <description>This paper introduces a novel track-length extension fitting algorithm for measuring the kinetic energies of inelastically interacting particles in liquid argon time projection chambers (LArTPCs). The algorithm finds the most probable offset in track length for a track-like object by comparing the measured ionization density as a function of position with a theoretical prediction of the energy loss as a function of the energy, including models of electron recombination and detector response. The algorithm can be used to measure the energies of particles that interact before they stop, such as charged pions that are absorbed by argon nuclei. The algorithm's energy measurement resolutions and fractional biases are presented as functions of particle kinetic energy and number of track hits using samples of stopping secondary charged pions in data collected by the ProtoDUNE-SP detector, and also in a detailed simulation. Additional studies describe the impact of the dE/dx model on...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1rc2h91p</guid>
      <pubDate>Fri, 25 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Abud, A Abed</name>
      </author>
      <author>
        <name>Abi, B</name>
      </author>
      <author>
        <name>Acciarri, R</name>
      </author>
      <author>
        <name>Acero, MA</name>
      </author>
      <author>
        <name>Adames, MR</name>
      </author>
      <author>
        <name>Adamov, G</name>
      </author>
      <author>
        <name>Adamowski, M</name>
      </author>
      <author>
        <name>Adams, D</name>
      </author>
      <author>
        <name>Adinolfi, M</name>
      </author>
      <author>
        <name>Adriano, C</name>
      </author>
      <author>
        <name>Aduszkiewicz, A</name>
      </author>
      <author>
        <name>Aguilar, J</name>
      </author>
      <author>
        <name>Akbar, F</name>
      </author>
      <author>
        <name>Alex, NS</name>
      </author>
      <author>
        <name>Allison, K</name>
      </author>
      <author>
        <name>Monsalve, S Alonso</name>
      </author>
      <author>
        <name>Alrashed, M</name>
      </author>
      <author>
        <name>Alton, A</name>
      </author>
      <author>
        <name>Alvarez, R</name>
      </author>
      <author>
        <name>Alves, T</name>
      </author>
      <author>
        <name>Amar, H</name>
      </author>
      <author>
        <name>Amedo, P</name>
      </author>
      <author>
        <name>Anderson, J</name>
      </author>
      <author>
        <name>Andreopoulos, C</name>
      </author>
      <author>
        <name>Andreotti, M</name>
      </author>
      <author>
        <name>Andrews, MP</name>
      </author>
      <author>
        <name>Andrianala, F</name>
      </author>
      <author>
        <name>Andringa, S</name>
      </author>
      <author>
        <name>Anfimov, N</name>
      </author>
      <author>
        <name>Ankowski, A</name>
      </author>
      <author>
        <name>Antic, D</name>
      </author>
      <author>
        <name>Antoniassi, M</name>
      </author>
      <author>
        <name>Antonova, M</name>
      </author>
      <author>
        <name>Antoshkin, A</name>
      </author>
      <author>
        <name>Aranda-Fernandez, A</name>
      </author>
      <author>
        <name>Arellano, L</name>
      </author>
      <author>
        <name>Diaz, E Arrieta</name>
      </author>
      <author>
        <name>Arroyave, MA</name>
      </author>
      <author>
        <name>Asaadi, J</name>
      </author>
      <author>
        <name>Ashkenazi, A</name>
      </author>
      <author>
        <name>Asner, D</name>
      </author>
      <author>
        <name>Asquith, L</name>
      </author>
      <author>
        <name>Atkin, E</name>
      </author>
      <author>
        <name>Auguste, D</name>
      </author>
      <author>
        <name>Aurisano, A</name>
      </author>
      <author>
        <name>Aushev, V</name>
      </author>
      <author>
        <name>Autiero, D</name>
      </author>
      <author>
        <name>Azam, MB</name>
      </author>
      <author>
        <name>Azfar, F</name>
      </author>
      <author>
        <name>Back, A</name>
      </author>
      <author>
        <name>Back, H</name>
      </author>
      <author>
        <name>Back, JJ</name>
      </author>
      <author>
        <name>Bagaturia, I</name>
      </author>
      <author>
        <name>Bagby, L</name>
      </author>
      <author>
        <name>Balashov, N</name>
      </author>
      <author>
        <name>Balasubramanian, S</name>
      </author>
      <author>
        <name>Baldi, P</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Baldini, W</name>
      </author>
      <author>
        <name>Baldonedo, J</name>
      </author>
      <author>
        <name>Baller, B</name>
      </author>
      <author>
        <name>Bambah, B</name>
      </author>
      <author>
        <name>Banerjee, R</name>
      </author>
      <author>
        <name>Barao, F</name>
      </author>
      <author>
        <name>Barbu, D</name>
      </author>
      <author>
        <name>Barenboim, G</name>
      </author>
      <author>
        <name>Alzás, P Barham</name>
      </author>
      <author>
        <name>Barker, GJ</name>
      </author>
      <author>
        <name>Barkhouse, W</name>
      </author>
      <author>
        <name>Barr, G</name>
      </author>
      <author>
        <name>Monarca, J Barranco</name>
      </author>
      <author>
        <name>Barros, A</name>
      </author>
      <author>
        <name>Barros, N</name>
      </author>
      <author>
        <name>Barrow, D</name>
      </author>
      <author>
        <name>Barrow, JL</name>
      </author>
      <author>
        <name>Basharina-Freshville, A</name>
      </author>
      <author>
        <name>Bashyal, A</name>
      </author>
      <author>
        <name>Basque, V</name>
      </author>
      <author>
        <name>Batchelor, C</name>
      </author>
      <author>
        <name>Bathe-Peters, L</name>
      </author>
      <author>
        <name>Battat, JBR</name>
      </author>
      <author>
        <name>Battisti, F</name>
      </author>
      <author>
        <name>Bay, F</name>
      </author>
      <author>
        <name>Bazetto, MCQ</name>
      </author>
      <author>
        <name>Alba, JLL Bazo</name>
      </author>
      <author>
        <name>Beacom, JF</name>
      </author>
      <author>
        <name>Bechetoille, E</name>
      </author>
      <author>
        <name>Behera, B</name>
      </author>
      <author>
        <name>Belchior, E</name>
      </author>
      <author>
        <name>Bell, G</name>
      </author>
      <author>
        <name>Bellantoni, L</name>
      </author>
      <author>
        <name>Bellettini, G</name>
      </author>
      <author>
        <name>Bellini, V</name>
      </author>
      <author>
        <name>Beltramello, O</name>
      </author>
      <author>
        <name>Benekos, N</name>
      </author>
      <author>
        <name>Montiel, C Benitez</name>
      </author>
      <author>
        <name>Benjamin, D</name>
      </author>
      <author>
        <name>Neves, F Bento</name>
      </author>
      <author>
        <name>Berger, J</name>
      </author>
      <author>
        <name>Berkman, S</name>
      </author>
      <author>
        <name>Bernal, J</name>
      </author>
    </item>
    <item>
      <title>A Bayesian Time-Varying Psychophysiological Interaction Model</title>
      <link>https://escholarship.org/uc/item/0bq7z39h</link>
      <description>A Bayesian Time-Varying Psychophysiological Interaction Model</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0bq7z39h</guid>
      <pubDate>Thu, 3 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schetzsle, Brian</name>
      </author>
      <author>
        <name>Lee, Jaylen</name>
      </author>
      <author>
        <name>Bornstein, Aaron</name>
        <uri>https://orcid.org/0000-0001-6251-6000</uri>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Guindani, Michele</name>
        <uri>https://orcid.org/0000-0002-6363-9907</uri>
      </author>
    </item>
    <item>
      <title>Applying machine learning to assist in the morphometric assessment of brain arteriolosclerosis through automation</title>
      <link>https://escholarship.org/uc/item/2x61488x</link>
      <description>Objective quantification of brain arteriolosclerosis remains an area of ongoing refinement in neuropathology, with current methods primarily utilizing semi-quantitative scales completed through manual histological examination. These approaches offer modest inter-rater reliability and do not provide precise quantitative metrics. To address this gap, we present a prototype end-to-end machine learning (ML)-based algorithm, Arteriolosclerosis Segmentation (ArtSeg), followed by Vascular Morphometry (VasMorph) - to assist persons in the morphometric analysis of arteriolosclerotic vessels on whole slide images (WSIs). We digitized hematoxylin and eosin-stained glass slides (13 participants, total 42 WSIs) of human brain frontal or occipital lobe cortical and/or periventricular white matter collected from three brain banks (University of California, Davis, Irvine, and Los Angeles Alzheimer's Disease Research Centers). ArtSeg comprises three ML models for blood vessel detection, arteriolosclerosis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2x61488x</guid>
      <pubDate>Wed, 2 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lou, Jerry J</name>
      </author>
      <author>
        <name>Chang, Peter</name>
        <uri>https://orcid.org/0000-0001-7645-7865</uri>
      </author>
      <author>
        <name>Nava, Kiana D</name>
      </author>
      <author>
        <name>Chantaduly, Chanon</name>
      </author>
      <author>
        <name>Wang, Hsin-Pei</name>
      </author>
      <author>
        <name>Yong, William H</name>
        <uri>https://orcid.org/0000-0002-0879-0209</uri>
      </author>
      <author>
        <name>Patel, Viharkumar</name>
      </author>
      <author>
        <name>Chaudhari, Ajinkya J</name>
      </author>
      <author>
        <name>Vasquez, La Rissa</name>
      </author>
      <author>
        <name>Monuki, Edwin</name>
      </author>
      <author>
        <name>Head, Elizabeth</name>
        <uri>https://orcid.org/0000-0003-1115-6396</uri>
      </author>
      <author>
        <name>Vinters, Harry V</name>
      </author>
      <author>
        <name>Magaki, Shino</name>
        <uri>https://orcid.org/0000-0003-0433-5759</uri>
      </author>
      <author>
        <name>Harvey, Danielle J</name>
        <uri>https://orcid.org/0000-0002-5367-0951</uri>
      </author>
      <author>
        <name>Chuah, Chen-Nee</name>
      </author>
      <author>
        <name>DeCarli, Charles S</name>
        <uri>https://orcid.org/0000-0003-1914-2693</uri>
      </author>
      <author>
        <name>Williams, Christopher K</name>
      </author>
      <author>
        <name>Keiser, Michael</name>
      </author>
      <author>
        <name>Dugger, Brittany N</name>
        <uri>https://orcid.org/0000-0003-2141-8855</uri>
      </author>
    </item>
    <item>
      <title>Identification of the velum interpositum as a meningeal-CNS route for myeloid cell trafficking into the brain</title>
      <link>https://escholarship.org/uc/item/1896d5br</link>
      <description>The borders of the central nervous system (CNS) host a repertoire of immune cells and mediate critical neuroimmune interactions, including the infiltration of peripheral myeloid cells into the CNS. Despite the fundamental role of leukocyte infiltration under physiological and pathological conditions, the neuroanatomical route of cell entry into the brain remains unclear. Here, we describe a specialized structure underneath the hippocampus, the velum interpositum (VI), that serves as a site for myeloid cell entry into the CNS. The VI functions as an extra-parenchymal leptomeningeal extension containing distinct myeloid cells subsets. Fate-mapping studies confirm meningeal and peripheral myeloid cell occupancy within the VI. Additionally, we highlight the distinct use of this route in the developing, irradiated, and demyelinating disease brain, indicating that myeloid cell trafficking through the VI could have important clinical implications for neurological disease.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1896d5br</guid>
      <pubDate>Thu, 19 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hohsfield, Lindsay A</name>
      </author>
      <author>
        <name>Kim, Sung Jin</name>
      </author>
      <author>
        <name>Barahona, Rocio A</name>
      </author>
      <author>
        <name>Henningfield, Caden M</name>
      </author>
      <author>
        <name>Mansour, Kimiya</name>
      </author>
      <author>
        <name>Vallejo, Kristen D</name>
      </author>
      <author>
        <name>Tsourmas, Kate I</name>
      </author>
      <author>
        <name>Kwang, Nellie E</name>
      </author>
      <author>
        <name>Ghorbanian, Yasamine</name>
      </author>
      <author>
        <name>Angulo, Julio Alejandro Ayala</name>
      </author>
      <author>
        <name>Gao, Pan</name>
      </author>
      <author>
        <name>Pachow, Collin</name>
      </author>
      <author>
        <name>Inlay, Matthew A</name>
      </author>
      <author>
        <name>Walsh, Craig M</name>
        <uri>https://orcid.org/0000-0001-7808-2817</uri>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
      <author>
        <name>Lane, Thomas E</name>
        <uri>https://orcid.org/0000-0003-0392-0825</uri>
      </author>
      <author>
        <name>Green, Kim N</name>
        <uri>https://orcid.org/0000-0002-6049-6744</uri>
      </author>
    </item>
    <item>
      <title>Miniaturized head-mount Doppler optical coherence tomography scope for freely moving mouse</title>
      <link>https://escholarship.org/uc/item/32h028c6</link>
      <description>Optical brain imaging has several advantages over other imaging techniques and was used to visualize both the structural and functional aspects of the brain, providing a more complete picture of brain activity. One of the promising techniques is optical coherence tomography (OCT), which uses low-coherence interferometry to obtain three-dimensional depth-resolved imaging of structures. In this research, we present a miniaturized head-mount Doppler OCT system tailored for high-resolution brain imaging in freely moving mice, providing an advanced non-invasive imaging tool in neuroscience research. With a maximum 4×4 mm field of view, 7.4 µm axial resolution, the system offers reliable imaging capabilities. Its compact design and comprehensive imaging capabilities make it well-suited for studying various brain regions and dynamic processes, contributing significantly to our understanding of brain function and pathology.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32h028c6</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Jingyi</name>
      </author>
      <author>
        <name>Ye, Qiao</name>
      </author>
      <author>
        <name>Chou, Lidek</name>
      </author>
      <author>
        <name>Qiu, Saijun</name>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
      <author>
        <name>Chen, Zhongping</name>
        <uri>https://orcid.org/0000-0002-4584-4560</uri>
      </author>
    </item>
    <item>
      <title>Label-Free Prediction of Fluorescently Labeled Fibrin Networks</title>
      <link>https://escholarship.org/uc/item/1h12679v</link>
      <description>While fluorescent labeling has been the standard for visualizing fibers within fibrillar scaffold models of the extracellular matrix (ECM), the use of fluorescent dyes can compromise cell viability and photobleach prematurely. The intricate fibrillar composition of ECM is crucial for its viscoelastic properties, which regulate intracellular signaling and provide structural support for cells. Naturally derived biomaterials such as fibrin and collagen replicate these fibrillar structures, but longitudinal confocal imaging of fibers using fluorescent dyes may impact cell function and photobleach the sample long before termination of the experiment. An alternative technique is reflection confocal microscopy (RCM) that provides high-resolution images of fibers. However, RCM is sensitive to fiber orientation relative to the optical axis, and consequently, many fibers are not detected. We aim to recover these fibers. Here, we propose a deep learning tool for predicting fluorescently...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1h12679v</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eldeen, Sarah</name>
      </author>
      <author>
        <name>Ramirez, Andres Felipe Guerrero</name>
      </author>
      <author>
        <name>Keresteci, Bora</name>
        <uri>https://orcid.org/0009-0006-7143-6698</uri>
      </author>
      <author>
        <name>Chang, Peter D</name>
        <uri>https://orcid.org/0000-0001-7645-7865</uri>
      </author>
      <author>
        <name>Botvinick, Elliot L</name>
      </author>
    </item>
    <item>
      <title>Full event particle-level unfolding with variable-length latent variational diffusion</title>
      <link>https://escholarship.org/uc/item/9g6271vw</link>
      <description>SciPost Journals Publication Detail SciPost Phys. 18, 117 (2025) Full event particle-level unfolding with variable-length latent variational diffusion</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9g6271vw</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Shmakov, Alexander</name>
      </author>
      <author>
        <name>Greif, Kevin Thomas</name>
      </author>
      <author>
        <name>Fenton, Michael James</name>
      </author>
      <author>
        <name>Ghosh, Aishik</name>
        <uri>https://orcid.org/0000-0003-0819-1553</uri>
      </author>
      <author>
        <name>Baldi, Pierre</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Whiteson, Daniel</name>
        <uri>https://orcid.org/0000-0002-2005-3113</uri>
      </author>
    </item>
    <item>
      <title>Computational Complexity of the Hylland–Zeckhauser Mechanism for One-Sided Matching Markets</title>
      <link>https://escholarship.org/uc/item/7sx6g52x</link>
      <description>Computational Complexity of the Hylland–Zeckhauser Mechanism for One-Sided Matching Markets</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7sx6g52x</guid>
      <pubDate>Wed, 21 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vazirani, Vijay V</name>
      </author>
      <author>
        <name>Yannakakis, Mihalis</name>
      </author>
    </item>
    <item>
      <title>A Theory of Alternating Paths and Blossoms from the Perspective of Minimum Length</title>
      <link>https://escholarship.org/uc/item/3083d90j</link>
      <description>The Micali–Vazirani (MV) algorithm for finding a maximum cardinality matching in general graphs, which was published in 1980, remains to this day the most efficient known algorithm for the problem. The current paper gives the first complete and correct proof of this algorithm. The MV algorithm resorts to finding minimum-length augmenting paths. However, such paths fail to satisfy an elementary property, called breadth first search honesty in this paper. In the absence of this property, an exponential time algorithm appears to be called for—just for finding one such path. On the other hand, the MV algorithm accomplishes this and additional tasks in linear time. The saving grace is the various “footholds” offered by the underlying structure, which the algorithm uses in order to perform its key tasks efficiently. The theory expounded in this paper elucidates this rich structure and yields a proof of correctness of the algorithm. It may also be of independent interest as a set of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3083d90j</guid>
      <pubDate>Wed, 21 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vazirani, Vijay V</name>
      </author>
    </item>
    <item>
      <title>Immunogenicity and safety of NVSI-06-07 as a heterologous booster after priming with BBIBP-CorV: a phase 2 trial</title>
      <link>https://escholarship.org/uc/item/9v45d7zf</link>
      <description>The increased coronavirus disease 2019 (COVID-19) breakthrough cases pose the need of booster vaccination. We conducted a randomised, double-blinded, controlled, phase 2 trial to assess the immunogenicity and safety of the heterologous prime-boost vaccination with an inactivated COVID-19 vaccine (BBIBP-CorV) followed by a recombinant protein-based vaccine (NVSI-06-07), using homologous boost with BBIBP-CorV as control. Three groups of healthy adults (600 individuals per group) who had completed two-dose BBIBP-CorV vaccinations 1–3 months, 4–6 months and ≥6 months earlier, respectively, were randomly assigned in a 1:1 ratio to receive either NVSI-06-07 or BBIBP-CorV boost. Immunogenicity assays showed that in NVSI-06-07 groups, neutralizing antibody geometric mean titers (GMTs) against the prototype SARS-CoV-2 increased by 21.01–63.85 folds on day 28 after vaccination, whereas only 4.20–16.78 folds of increases were observed in control groups. For Omicron variant, the neutralizing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9v45d7zf</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kaabi, Nawal Al</name>
      </author>
      <author>
        <name>Yang, Yun Kai</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Xu, Ke</name>
      </author>
      <author>
        <name>Liang, Yu</name>
      </author>
      <author>
        <name>Kang, Yun</name>
      </author>
      <author>
        <name>Su, Ji Guo</name>
      </author>
      <author>
        <name>Yang, Tian</name>
      </author>
      <author>
        <name>Hussein, Salah</name>
      </author>
      <author>
        <name>ElDein, Mohamed Saif</name>
      </author>
      <author>
        <name>Shao, Shuai</name>
      </author>
      <author>
        <name>Yang, Sen Sen</name>
      </author>
      <author>
        <name>Lei, Wenwen</name>
      </author>
      <author>
        <name>Gao, Xue Jun</name>
      </author>
      <author>
        <name>Jiang, Zhiwei</name>
      </author>
      <author>
        <name>Wang, Hui</name>
      </author>
      <author>
        <name>Li, Meng</name>
      </author>
      <author>
        <name>Mekki, Hanadi Mekki</name>
      </author>
      <author>
        <name>Zaher, Walid</name>
      </author>
      <author>
        <name>Mahmoud, Sally</name>
      </author>
      <author>
        <name>Zhang, Xue</name>
      </author>
      <author>
        <name>Qu, Chang</name>
      </author>
      <author>
        <name>Liu, Dan Ying</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
      </author>
      <author>
        <name>Yang, Mengjie</name>
      </author>
      <author>
        <name>Eltantawy, Islam</name>
      </author>
      <author>
        <name>Xiao, Peng</name>
      </author>
      <author>
        <name>Wang, Zhao Nian</name>
      </author>
      <author>
        <name>Yin, Jin Liang</name>
      </author>
      <author>
        <name>Mao, Xiao Yan</name>
      </author>
      <author>
        <name>Zhang, Jin</name>
      </author>
      <author>
        <name>Liu, Ning</name>
      </author>
      <author>
        <name>Shen, Fu Jie</name>
      </author>
      <author>
        <name>Qu, Liang</name>
      </author>
      <author>
        <name>Zhang, Yun Tao</name>
      </author>
      <author>
        <name>Yang, Xiao Ming</name>
      </author>
      <author>
        <name>Wu, Guizhen</name>
      </author>
      <author>
        <name>Li, Qi Ming</name>
      </author>
    </item>
    <item>
      <title>Design of a mutation-integrated trimeric RBD with broad protection against SARS-CoV-2</title>
      <link>https://escholarship.org/uc/item/9tm3w6d6</link>
      <description>The continuous emergence of SARS-CoV-2 variants highlights the need of developing vaccines with broad protection. Here, according to the immune-escape capability and evolutionary convergence, the representative SARS-CoV-2 strains carrying the hotspot mutations were selected. Then, guided by structural and computational analyses, we present a mutation-integrated trimeric form of spike receptor-binding domain (mutI-tri-RBD) as a broadly protective vaccine candidate, which combined heterologous RBDs from different representative strains into a hybrid immunogen and integrated immune-escape hotspots into a single antigen. When compared with a homo-tri-RBD vaccine candidate in the stage of phase II trial, of which all three RBDs are derived from the SARS-CoV-2 prototype strain, mutI-tri-RBD induced significantly higher neutralizing antibody titers against the Delta and Beta variants, and maintained a similar immune response against the prototype strain. Pseudo-virus neutralization assay...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9tm3w6d6</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liang, Yu</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Yuan, Run Yu</name>
      </author>
      <author>
        <name>Wang, Mei Yu</name>
      </author>
      <author>
        <name>He, Peng</name>
      </author>
      <author>
        <name>Su, Ji Guo</name>
      </author>
      <author>
        <name>Han, Zi Bo</name>
      </author>
      <author>
        <name>Jin, Yu Qin</name>
      </author>
      <author>
        <name>Hou, Jun Wei</name>
      </author>
      <author>
        <name>Zhang, Hao</name>
      </author>
      <author>
        <name>Zhang, Xue Feng</name>
      </author>
      <author>
        <name>Shao, Shuai</name>
      </author>
      <author>
        <name>Hou, Ya Nan</name>
      </author>
      <author>
        <name>Liu, Zhao Ming</name>
      </author>
      <author>
        <name>Du, Li Fang</name>
      </author>
      <author>
        <name>Shen, Fu Jie</name>
      </author>
      <author>
        <name>Zhou, Wei Min</name>
      </author>
      <author>
        <name>Xu, Ke</name>
      </author>
      <author>
        <name>Gao, Ru Qin</name>
      </author>
      <author>
        <name>Tang, Fang</name>
      </author>
      <author>
        <name>Lei, Ze Hua</name>
      </author>
      <author>
        <name>Liu, Shuo</name>
      </author>
      <author>
        <name>Zhen, Wei</name>
      </author>
      <author>
        <name>Wu, Jin Juan</name>
      </author>
      <author>
        <name>Zheng, Xiang</name>
      </author>
      <author>
        <name>Liu, Ning</name>
      </author>
      <author>
        <name>Chen, Shi</name>
      </author>
      <author>
        <name>Ma, Zhi Jing</name>
      </author>
      <author>
        <name>Zheng, Fan</name>
      </author>
      <author>
        <name>Ren, Si Yu</name>
      </author>
      <author>
        <name>Hu, Zhong Yu</name>
      </author>
      <author>
        <name>Huang, Wei Jin</name>
      </author>
      <author>
        <name>Wu, Gui Zhen</name>
      </author>
      <author>
        <name>Ke, Chang Wen</name>
      </author>
      <author>
        <name>Li, Qi Ming</name>
      </author>
    </item>
    <item>
      <title>The structure of mouse RIPK1 RHIM-containing domain as a homo-amyloid and in RIPK1/RIPK3 complex</title>
      <link>https://escholarship.org/uc/item/9tg0q2s8</link>
      <description>Receptor-interacting protein kinase 1 (RIPK1) is a therapeutic target in treating neurodegenerative diseases and cancers. RIPK1 has three distinct functional domains, with the center domain containing a receptor-interacting protein homotypic interaction motif (RHIM), which mediates amyloid formation. The functional amyloid formed by RIPK1 and/or RIPK3 is a crucial intermediate in regulating cell necroptosis. In this study, the amyloid structure of mouse RIPK1, formed by an 82-residue sequence centered at RHIM, is presented. It reveals the “N”-shaped folding of the protein subunit in the fibril with four β-strands. The folding pattern is shared by several amyloid structures formed by proteins with RHIM, with the central β-strand formed by the most conserved tetrad sequence I/VQI/VG. However, the solid-state NMR results indicate a structural difference between mouse RIPK1 and mouse RIPK3. A change in the structural rigidity is also suggested by the observation of weakened signals...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9tg0q2s8</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Jing</name>
      </author>
      <author>
        <name>Wu, Xia-lian</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Li, Bing</name>
      </author>
      <author>
        <name>Wang, Hua-yi</name>
      </author>
      <author>
        <name>Wang, Jian</name>
      </author>
      <author>
        <name>Lu, Jun-xia</name>
      </author>
    </item>
    <item>
      <title>Genomic analysis of the tribe Emesidini (Lepidoptera: Riodinidae)</title>
      <link>https://escholarship.org/uc/item/9t31785v</link>
      <description>We obtained and phylogenetically analyzed whole genome shotgun sequences of nearly all species from the tribe Emesidini Seraphim, Freitas Kaminski, 2018 (Riodinidae) and representatives from other Riodinidae tribes. We see that the recently proposed genera Neoapodemia Trujano, 2018 and Plesioarida Trujano García, 2018 are closely allied with Apodemia C. R. Felder, [1865] and are better viewed as its subgenera, new status. Overall, Emesis Fabricius, 1807 and Apodemia (even after inclusion of the two subgenera) are so phylogenetically close that several species have been previously swapped between these two genera. New combinations are: Apodemia (Neoapodemia) zela (Butler, 1870), Apodemia (Neoapodemia) ares (Edwards, 1882), and Apodemia (Neoapodemia) arnacis (Stichel, 1928) (not Emesis); and Emesis phyciodoides (Barnes Benjamin, 1924) (not Apodemia), assigned to each genus by their monophyly in genomic trees with the type species (TS) of the genus. Surprisingly, we find that Emesis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9t31785v</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>ZHANG, JING</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>SHEN, JINHUI</name>
      </author>
      <author>
        <name>CONG, QIAN</name>
      </author>
      <author>
        <name>GRISHIN, NICK V</name>
      </author>
    </item>
    <item>
      <title>High‐efficiency genome editing using a dmc1 promoter‐controlled CRISPR/Cas9 system in maize</title>
      <link>https://escholarship.org/uc/item/9nm7660d</link>
      <description>Previous studies revealed that the promoters for driving both Cas9 and sgRNAs are quite important for efficient genome editing by CRISPR/Cas9 in plants. Here, we report our results of targeted genome editing using the maize dmc1 gene promoter combined with the U3 promoter for Cas9 and sgRNA, respectively. Three loci in the maize genome were selected for targeting. The T0 plants regenerated were highly efficiently edited at the target sites with homozygous or bi-allelic mutants accounting for about 66%. The mutations in T0 plants could be stably transmitted to the T1 generation, and new mutations could be generated in gametes or zygotes. Whole-genome resequencing indicated that no off-target mutations could be detected in the predicted loci with sequence similarity to the targeted site. Our results show that the dmc1 promoter-controlled (DPC) CRISPR/Cas9 system is highly efficient in maize and provide further evidence that the optimization of the promoters used for the CRISPR/Cas9...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9nm7660d</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Feng, Chao</name>
      </author>
      <author>
        <name>Su, Handong</name>
      </author>
      <author>
        <name>Bai, Han</name>
      </author>
      <author>
        <name>Wang, Rui</name>
      </author>
      <author>
        <name>Liu, Yalin</name>
      </author>
      <author>
        <name>Guo, Xianrui</name>
      </author>
      <author>
        <name>Liu, Chang</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Yuan, Jing</name>
      </author>
      <author>
        <name>Birchler, James A</name>
      </author>
      <author>
        <name>Han, Fangpu</name>
      </author>
    </item>
    <item>
      <title>Genomes reveal drastic and recurrent phenotypic divergence in firetip skipper butterflies (Hesperiidae: Pyrrhopyginae)</title>
      <link>https://escholarship.org/uc/item/9gv997zf</link>
      <description>Biologists marvel at the powers of adaptive convergence, when distantly related animals look alike. While mimetic wing patterns of butterflies have fooled predators for millennia, entomologists inferred that mimics were distant relatives despite similar appearance. However, the obverse question has not been frequently asked. Who are the close relatives of mimetic butterflies and what are their features? As opposed to close convergence, divergence from a non-mimetic relative would also be extreme. When closely related animals look unalike, it is challenging to pair them. Genomic analysis promises to elucidate evolutionary relationships and shed light on molecular mechanisms of divergence. We chose the firetip skipper butterfly as a model due to its phenotypic diversity and abundance of mimicry. We sequenced and analysed whole genomes of nearly 120 representative species. Genomes partitioned this subfamily Pyrrhopyginae into five tribes (1 new), 23 genera and, additionally, 22 subgenera...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9gv997zf</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Shen, Jinhui</name>
      </author>
      <author>
        <name>Brockmann, Ernst</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Assessing predictions of fitness effects of missense mutations in SUMO‐conjugating enzyme UBE2I</title>
      <link>https://escholarship.org/uc/item/9d22849t</link>
      <description>The exponential growth of genomic variants uncovered by next-generation sequencing necessitates efficient and accurate computational analyses to predict their functional effects. A number of computational methods have been developed for the task, but few unbiased comparisons of their performance are available. To fill the gap, The Critical Assessment of Genome Interpretation (CAGI) comprehensively assesses phenotypic predictions on newly collected experimental datasets. Here, we present the results of the SUMO conjugase challenge where participants were predicting functional effects of missense mutations in human SUMO-conjugating enzyme UBE2I. The performance of the predictors is similar to each other and is far from perfection. Evolutionary information from sequence alignments dominates the success: deleterious mutations at conserved positions and benign mutations at variable positions are accurately predicted. Prediction accuracy of other mutations remains unsatisfactory, and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9d22849t</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Kinch, Lisa N</name>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Weile, Jochen</name>
      </author>
      <author>
        <name>Sun, Song</name>
      </author>
      <author>
        <name>Cote, Atina G</name>
      </author>
      <author>
        <name>Roth, Frederick P</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Serum interleukin-6 is an indicator for severity in 901 patients with SARS-CoV-2 infection: a cohort study</title>
      <link>https://escholarship.org/uc/item/9bv752n2</link>
      <description>BackgroundInterleukin-6 (IL-6) was proposed to be associated with the severity of coronavirus disease 2019 (COVID-19). The present study aimed to explore the kinetics of IL-6 levels, validate this association in COVID-19 patients, and report preliminary data on the efficacy of IL-6 receptor blockade.MethodsWe conducted a retrospective single-institutional study of 901 consecutive confirmed cases. Serum IL-6 concentrations were tested on admission and/or during hospital stay. Tocilizumab was given to 16 patients with elevated IL-6 concentration.Results366 patients were defined as common cases, 411 patients as severe, and 124 patients as critical according to the Chinese guideline on diagnosis and treatment of COVID-19. The median concentration of IL-6 was &amp;lt; 1.5&amp;nbsp;pg/ml (IQR &amp;lt; 1.50–2.15), 1.85&amp;nbsp;pg/ml (IQR &amp;lt; 1.50–5.21), and 21.55&amp;nbsp;pg/ml (IQR 6.47–94.66) for the common, severe, and critical groups respectively (P &amp;lt; 0.001). The follow-up kinetics revealed serum...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9bv752n2</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Hao, Yiqun</name>
      </author>
      <author>
        <name>Ou, Wuling</name>
      </author>
      <author>
        <name>Ming, Fei</name>
      </author>
      <author>
        <name>Liang, Gai</name>
      </author>
      <author>
        <name>Qian, Yu</name>
      </author>
      <author>
        <name>Cai, Qian</name>
      </author>
      <author>
        <name>Dong, Shuang</name>
      </author>
      <author>
        <name>Hu, Sheng</name>
      </author>
      <author>
        <name>Wang, Weida</name>
      </author>
      <author>
        <name>Wei, Shaozhong</name>
      </author>
    </item>
    <item>
      <title>Impact of Asp/Glu‐ADP‐ribosylation on protein‐protein interaction and protein function</title>
      <link>https://escholarship.org/uc/item/99r9k3t2</link>
      <description>PARylation plays critical role in regulating multiple cellular processes such as DNA damage response and repair, transcription, RNA processing, and stress response. More than 300 human proteins have been found to be modified by PARylation on acidic residues, that is, Asp (D) and Glu (E). We used the deep-learning tool AlphaFold to predict protein-protein interactions (PPIs) and their interfaces for these proteins based on coevolution signals from joint multiple sequence alignments (MSAs). AlphaFold predicted 260 confident PPIs involving PARylated proteins, and about one quarter of these PPIs have D/E-PARylation sites in their predicted PPI interfaces. AlphaFold predictions offer novel insights into the mechanisms of PARylation regulations by providing structural details of the PPI interfaces. D/E-PARylation sites have a preference to occur in coil regions and disordered regions, and PPI interfaces containing D/E-PARylation sites tend to occur between short linear sequence motifs...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/99r9k3t2</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pei, Jimin</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Wang, Xu‐Dong</name>
      </author>
      <author>
        <name>Kim, Chiho</name>
      </author>
      <author>
        <name>Yu, Yonghao</name>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
    </item>
    <item>
      <title>Erythrina stem borer moth in California – New taxonomic status and implications for control of this emerging pest</title>
      <link>https://escholarship.org/uc/item/97f7n19f</link>
      <description>During the last 10 years, the Erythrina stem borer moth, &lt;i&gt;Terastia meticulosalis&lt;/i&gt;, emerged as a pest of cultivated coral trees (&lt;i&gt;Erythrina&lt;/i&gt; spp.) in California. Erythrina trees are valued for their moderate drought resistance and beautiful flame-like flowers. They are beloved enough to be considered Los Angeles's official "City Tree." Thus, they are a valuable horticultural crop and are grown by many nurseries and occur throughout the landscape in coastal southern California. Coral trees have been heavily affected by &lt;i&gt;T. meticulosalis&lt;/i&gt; recently. Using whole genome sequencing techniques, we analysed the origins of this and other infestations of &lt;i&gt;Erythrina&lt;/i&gt; in coastal areas and found that they have likely originated from the repeated expansions of the native range of the species in Arizona, a process possibly driven by climatic factors and/or movement of plants by humans. We also found sufficient genetic differences between the western population of the moth...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/97f7n19f</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sourakov, Andrei</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Song, Leina</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Back-spliced RNA from retrotransposon binds to centromere and regulates centromeric chromatin loops in maize</title>
      <link>https://escholarship.org/uc/item/93h884hf</link>
      <description>In most plants, centromeric DNA contains highly repetitive sequences, including tandem repeats and retrotransposons; however, the roles of these sequences in the structure and function of the centromere are unclear. Here, we found that multiple RNA sequences from centromeric retrotransposons (CRMs) were enriched in maize (Zea mays) centromeres, and back-spliced RNAs were generated from CRM1. We identified 3 types of CRM1-derived circular RNAs with the same back-splicing site based on the back-spliced sequences. These circular RNAs bound to the centromere through R-loops. Two R-loop sites inside a single circular RNA promoted the formation of chromatin loops in CRM1 regions. When RNA interference (RNAi) was used to target the back-splicing site of the circular CRM1 RNAs, the levels of R-loops and chromatin loops formed by these circular RNAs decreased, while the levels of R-loops produced by linear RNAs with similar binding sites increased. Linear RNAs with only one R-loop site...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/93h884hf</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Yalin</name>
      </author>
      <author>
        <name>Su, Handong</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Liu, Yang</name>
      </author>
      <author>
        <name>Feng, Chao</name>
      </author>
      <author>
        <name>Han, Fangpu</name>
      </author>
    </item>
    <item>
      <title>Solid State Nuclear Magnetic Resonance (SSNMR) Characterization of Osteoblasts From Mesenchymal Stromal Cell Differentiation to Osteoblast Mineralization</title>
      <link>https://escholarship.org/uc/item/90q555b1</link>
      <description>Solid-state nuclear magnetic resonance (SSNMR), a technique capable of studying solid or semisolid biological samples, was first applied to study the cell differentiation and mineralization using the whole-cell sample. Mesenchymal stromal cells (MSCs) with multipotent differentiation capacity were induced to differentiate into osteoblasts. The whole differentiation process, osteoblast mineralization and the mineral maturation, was investigated using SSNMR, providing intact, atomic level information on the cellular mineral structural transformation. Our research indicated the extent of osteoblast mineralization could vary significantly for different cell populations whereas the difference was not easily shown by other means of characterization. The SSNMR spectra revealed hydroxylapatite (or hydroxyapatite [HAP]) formation around 2 to 4 weeks after osteogenic induction for MSCs with a high differentiation potency. The early mineral phase deposit before HAP formation contained a...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/90q555b1</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Jing‐Yu</name>
      </author>
      <author>
        <name>Sun, Ming‐Hui</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Hu, Meng</name>
      </author>
      <author>
        <name>Zeng, Yu‐Teng</name>
      </author>
      <author>
        <name>Yi, Qian‐Qian</name>
      </author>
      <author>
        <name>Wang, Jian</name>
      </author>
      <author>
        <name>Bai, Yun</name>
      </author>
      <author>
        <name>Zhang, Yifeng</name>
      </author>
      <author>
        <name>Lu, Jun‐Xia</name>
      </author>
    </item>
    <item>
      <title>Safety and immunogenicity of a mosaic vaccine booster against Omicron and other SARS-CoV-2 variants: a randomized phase 2 trial</title>
      <link>https://escholarship.org/uc/item/9078d0qn</link>
      <description>An ongoing randomized, double-blind, controlled phase 2 trial was conducted to evaluate the safety and immunogenicity of a mosaic-type recombinant vaccine candidate, named NVSI-06-09, as a booster dose in subjects aged 18 years and older from the United Arab Emirates (UAE), who had administered two or three doses of inactivated vaccine BBIBP-CorV at least 6 months prior to enrollment. The participants were randomly assigned with 1:1 to receive a booster dose of NVSI-06-09 or BBIBP-CorV. The primary outcomes were immunogenicity and safety against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant, and the exploratory outcome was cross-immunogenicity against other circulating strains. Between May 25 and 30, 2022, 516 adults received booster vaccination with 260 in NVSI-06-09 group and 256 in BBIBP-CorV group. Interim results showed a similar safety profile between two booster groups, with low incidence of adverse reactions of grade 1 or 2. For immunogenicity,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9078d0qn</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kaabi, Nawal Al</name>
      </author>
      <author>
        <name>Yang, Yun Kai</name>
      </author>
      <author>
        <name>Liang, Yu</name>
      </author>
      <author>
        <name>Xu, Ke</name>
      </author>
      <author>
        <name>Zhang, Xue Feng</name>
      </author>
      <author>
        <name>Kang, Yun</name>
      </author>
      <author>
        <name>Jin, Yu Qin</name>
      </author>
      <author>
        <name>Hou, Jun Wei</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Yang, Tian</name>
      </author>
      <author>
        <name>Hussein, Salah</name>
      </author>
      <author>
        <name>ElDein, Mohamed Saif</name>
      </author>
      <author>
        <name>Lei, Ze Hua</name>
      </author>
      <author>
        <name>Zhang, Hao</name>
      </author>
      <author>
        <name>Shao, Shuai</name>
      </author>
      <author>
        <name>Liu, Zhao Ming</name>
      </author>
      <author>
        <name>Liu, Ning</name>
      </author>
      <author>
        <name>Zheng, Xiang</name>
      </author>
      <author>
        <name>Su, Ji Guo</name>
      </author>
      <author>
        <name>Yang, Sen Sen</name>
      </author>
      <author>
        <name>Cong, Xiangfeng</name>
      </author>
      <author>
        <name>Tan, Yao</name>
      </author>
      <author>
        <name>Lei, Wenwen</name>
      </author>
      <author>
        <name>Gao, Xue Jun</name>
      </author>
      <author>
        <name>Jiang, Zhiwei</name>
      </author>
      <author>
        <name>Wang, Hui</name>
      </author>
      <author>
        <name>Li, Meng</name>
      </author>
      <author>
        <name>Mekki, Hanadi Mekki</name>
      </author>
      <author>
        <name>Zaher, Walid</name>
      </author>
      <author>
        <name>Mahmoud, Sally</name>
      </author>
      <author>
        <name>Zhang, Xue</name>
      </author>
      <author>
        <name>Qu, Chang</name>
      </author>
      <author>
        <name>Liu, Dan Ying</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
      </author>
      <author>
        <name>Yang, Mengjie</name>
      </author>
      <author>
        <name>Eltantawy, Islam</name>
      </author>
      <author>
        <name>Xiao, Peng</name>
      </author>
      <author>
        <name>Shen, Fu Jie</name>
      </author>
      <author>
        <name>Wu, Jin Juan</name>
      </author>
      <author>
        <name>Han, Zi Bo</name>
      </author>
      <author>
        <name>Du, Li Fang</name>
      </author>
      <author>
        <name>Tang, Fang</name>
      </author>
      <author>
        <name>Chen, Shi</name>
      </author>
      <author>
        <name>Ma, Zhi Jing</name>
      </author>
      <author>
        <name>Zheng, Fan</name>
      </author>
      <author>
        <name>Hou, Ya Nan</name>
      </author>
      <author>
        <name>Li, Xin Yu</name>
      </author>
      <author>
        <name>Li, Xin</name>
      </author>
      <author>
        <name>Wang, Zhao Nian</name>
      </author>
      <author>
        <name>Yin, Jin Liang</name>
      </author>
      <author>
        <name>Mao, Xiao Yan</name>
      </author>
      <author>
        <name>Zhang, Jin</name>
      </author>
      <author>
        <name>Qu, Liang</name>
      </author>
      <author>
        <name>Zhang, Yun Tao</name>
      </author>
      <author>
        <name>Yang, Xiao Ming</name>
      </author>
      <author>
        <name>Wu, Guizhen</name>
      </author>
      <author>
        <name>Li, Qi Ming</name>
      </author>
    </item>
    <item>
      <title>Epigenetic modifications regulate cultivar-specific root development and metabolic adaptation to nitrogen availability in wheat</title>
      <link>https://escholarship.org/uc/item/8xg4w63s</link>
      <description>The breeding of crops with improved nitrogen use efficiency (NUE) is crucial for sustainable agriculture, but the involvement of epigenetic modifications remains unexplored. Here, we analyze the chromatin landscapes of two wheat cultivars (KN9204 and J411) that differ in NUE under varied nitrogen conditions. The expression of nitrogen metabolism genes is closely linked to variation in histone modification instead of differences in DNA sequence. Epigenetic modifications exhibit clear cultivar-specificity, which likely contributes to distinct agronomic traits. Additionally, low nitrogen (LN) induces H3K27ac and H3K27me3 to significantly enhance root growth in KN9204, while remarkably inducing NRT2 in J411. Evidence from histone deacetylase inhibitor treatment and transgenic plants with loss function of H3K27me3 methyltransferase shows that changes in epigenetic modifications could alter the strategy preference for root development or nitrogen uptake in response to LN. Here, we show...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8xg4w63s</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Hao</name>
      </author>
      <author>
        <name>Jin, Zhiyuan</name>
      </author>
      <author>
        <name>Cui, Fa</name>
      </author>
      <author>
        <name>Zhao, Long</name>
      </author>
      <author>
        <name>Zhang, Xiaoyu</name>
      </author>
      <author>
        <name>Chen, Jinchao</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Li, Yanyan</name>
      </author>
      <author>
        <name>Li, Yongpeng</name>
      </author>
      <author>
        <name>Niu, Yanxiao</name>
      </author>
      <author>
        <name>Zhang, Wenli</name>
      </author>
      <author>
        <name>Gao, Caixia</name>
      </author>
      <author>
        <name>Fu, Xiangdong</name>
      </author>
      <author>
        <name>Tong, Yiping</name>
      </author>
      <author>
        <name>Wang, Lei</name>
      </author>
      <author>
        <name>Ling, Hong-Qing</name>
      </author>
      <author>
        <name>Li, Junming</name>
      </author>
      <author>
        <name>Xiao, Jun</name>
      </author>
    </item>
    <item>
      <title>Structure classification of the proteins from Salmonella enterica pangenome revealed novel potential pathogenicity islands</title>
      <link>https://escholarship.org/uc/item/8s5890st</link>
      <description>Salmonella enterica is a pathogenic bacterium known for causing severe typhoid fever in humans, making it important to study due to its potential health risks and significant impact on public health. This study provides evolutionary classification of proteins from Salmonella enterica pangenome. We classified 17,238 domains from 13,147 proteins from 79,758 Salmonella enterica strains and studied in detail domains of 272 proteins from 14 characterized Salmonella pathogenicity islands (SPIs). Among SPIs-related proteins, 90 proteins function in the secretion machinery. 41% domains of SPI proteins have no previous sequence annotation. By comparing clinical and environmental isolates, we identified 3682 proteins that are overrepresented in clinical group that we consider as potentially pathogenic. Among domains of potentially pathogenic proteins only 50% domains were annotated by sequence methods previously. Moreover, 36% (1330 out of 3682) of potentially pathogenic proteins cannot...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8s5890st</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Medvedev, Kirill E</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Schaeffer, R Dustin</name>
      </author>
      <author>
        <name>Kinch, Lisa N</name>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Classification of domains in predicted structures of the human proteome</title>
      <link>https://escholarship.org/uc/item/8kj0k1m7</link>
      <description>Recent advances in protein structure prediction have generated accurate structures of previously uncharacterized human proteins. Identifying domains in these predicted structures and classifying them into an evolutionary hierarchy can reveal biological insights. Here, we describe the detection and classification of domains from the human proteome. Our classification indicates that only 62% of residues are located in globular domains. We further classify these globular domains and observe that the majority (65%) can be classified among known folds by sequence, with a smaller fraction (33%) requiring structural data to refine the domain boundaries and/or to support their homology. A relatively small number (966 domains) cannot be confidently assigned using our automatic pipelines, thus demanding manual inspection. We classify 47,576 domains, of which only 23% have been included in experimental structures. A portion (6.3%) of these classified globular domains lack sequence-based...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8kj0k1m7</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schaeffer, R Dustin</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Kinch, Lisa N</name>
      </author>
      <author>
        <name>Pei, Jimin</name>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) membrane (M) protein inhibits type I and III interferon production by targeting RIG-I/MDA-5 signaling</title>
      <link>https://escholarship.org/uc/item/8fw6103z</link>
      <description>Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has quickly spread worldwide and has affected more than 10 million individuals. A typical feature of COVID-19 is the suppression of type I and III interferon (IFN)-mediated antiviral immunity. However, the molecular mechanism by which SARS-CoV-2 evades antiviral immunity remains elusive. Here, we reported that the SARS-CoV-2 membrane (M) protein inhibits the production of type I and III IFNs induced by the cytosolic dsRNA-sensing pathway mediated by RIG-I/MDA-5–MAVS signaling. In addition, the SARS-CoV-2 M protein suppresses type I and III IFN induction stimulated by SeV infection or poly (I:C) transfection. Mechanistically, the SARS-CoV-2 M protein interacts with RIG-I, MAVS, and TBK1, thus preventing the formation of the multiprotein complex containing RIG-I, MAVS, TRAF3, and TBK1 and subsequently impeding the phosphorylation, nuclear translocation, and activation of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8fw6103z</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zheng, Yi</name>
      </author>
      <author>
        <name>Zhuang, Meng-Wei</name>
      </author>
      <author>
        <name>Han, Lulu</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Nan, Mei-Ling</name>
      </author>
      <author>
        <name>Zhan, Peng</name>
      </author>
      <author>
        <name>Kang, Dongwei</name>
      </author>
      <author>
        <name>Liu, Xinyong</name>
      </author>
      <author>
        <name>Gao, Chengjiang</name>
      </author>
      <author>
        <name>Wang, Pei-Hui</name>
      </author>
    </item>
    <item>
      <title>Three new subfamilies of skipper butterflies (Lepidoptera, Hesperiidae)</title>
      <link>https://escholarship.org/uc/item/8fb0q6jb</link>
      <description>We obtained and analyzed whole genome data for more than 160 representatives of skipper butterflies (family Hesperiidae) from all known subfamilies, tribes and most distinctive genera. We found that two genera, &lt;i&gt;Katreus&lt;/i&gt; Watson, 1893 and &lt;i&gt;Ortholexis&lt;/i&gt; Karsch, 1895, which are sisters, are well-separated from all other major phylogenetic lineages and originate near the base of the Hesperiidae tree, prior to the origin of some subfamilies. Due to this ancient origin compared to other subfamilies, this group is described as Katreinae Grishin, &lt;b&gt;subfam. n.&lt;/b&gt; DNA sequencing of primary type specimens reveals that &lt;i&gt;Ortholexismelichroptera&lt;/i&gt; Karsch, 1895 is not a female of &lt;i&gt;Ortholexisholocausta&lt;/i&gt; Mabille, 1891, but instead a female of &lt;i&gt;Ortholexisdimidia&lt;/i&gt; Holland, 1896. This finding establishes &lt;i&gt;O.dimidia&lt;/i&gt; as a junior subjective synonym of &lt;i&gt;O.melichroptera&lt;/i&gt;. Furthermore, we see that &lt;i&gt;Chamunda&lt;/i&gt; Evans, 1949 does not originate within Pyrginae Burmeister,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8fb0q6jb</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Shen, Jinhui</name>
      </author>
      <author>
        <name>Brockmann, Ernst</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>RIP3-mediated necroptosis is regulated by inter-filament assembly of RIP homotypic interaction motif</title>
      <link>https://escholarship.org/uc/item/8f94k4xn</link>
      <description>Necroptosis is mediated by signaling complexes called necrosomes, which contain receptor-interacting protein 3 (RIP3) and upstream effectors, such as RIP1. In necrosomes, the RIP homotypic interaction motif (RHIM) of RIP3 and RIP1 forms amyloidal complex. But how the amyloidal necrosomes control RIP3 activation and cell necroptosis has not been determined. Here, we showed that RIP3 amyloid fibrils could further assemble into large fibrillar networks which presents as cellular puncta during necroptosis. A viral RHIM-containing necroptosis inhibitor M45 could form heteroamyloid with RIP3 in cells and prevent RIP3 puncta formation and cell necroptosis. We characterized mutual antagonism between RIP3–RHIM and M45–RHIM in necroptosis regulation, which was caused by distinct inter-filament interactions in RIP3, M45 amyloids revealed with atomic force microscopy. Moreover, double mutations Asn464 and Met468 in RIP3–RHIM to Asp disrupted RIP3 kinase-dependent necroptosis. While the mutant...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8f94k4xn</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hu, Hong</name>
      </author>
      <author>
        <name>Wu, Xialian</name>
      </author>
      <author>
        <name>Wu, Guoxiang</name>
      </author>
      <author>
        <name>Nan, Ning</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Zhu, Xinxin</name>
      </author>
      <author>
        <name>Zhang, Yu</name>
      </author>
      <author>
        <name>Shu, Zhaoqian</name>
      </author>
      <author>
        <name>Liu, Jia</name>
      </author>
      <author>
        <name>Liu, Xiaoyan</name>
      </author>
      <author>
        <name>Lu, Junxia</name>
      </author>
      <author>
        <name>Wang, Huayi</name>
      </author>
    </item>
    <item>
      <title>Refinement and curation of homologous groups facilitated by structure prediction</title>
      <link>https://escholarship.org/uc/item/88c4f939</link>
      <description>Domain classification of protein predictions released in the AlphaFold Database (AFDB) has been a recent focus of the Evolutionary Classification of protein Domains (ECOD). Although a primary focus of our recent work has been the partition and assignment of domains from these predictions, we here show how these diverse predictions can be used to examine the reference domain set more closely. Using results from DPAM, our AlphaFold-specific domain parsing algorithm, we examine hierarchical groupings that share significant levels of homologous links, both between groups that were not previously assessed to be definitively homologous and between groups that were not previously observed to share significant homologous links. Combined with manual analysis, these large datasets of structural and sequence similarities allow us to merge homologous groups in multiple cases which we detail within. These domains tend to be families of domains from families that are either small, previously...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/88c4f939</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schaeffer, Richard Dustin</name>
      </author>
      <author>
        <name>Pei, Jimin</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Nanotexture and crystal phase regulation for synergistic enhancement in re-endothelialization on medical pure titanium surface</title>
      <link>https://escholarship.org/uc/item/86k2h30t</link>
      <description>Re-endothelialization has been recognized as a promising strategy to address the tissue hyperplasia and subsequent restenosis which are major complications associated with vascular implant/interventional titanium devices. However, the uncontrollable over-proliferation of smooth muscle cells (SMCs) limits the clinical application of numerous modified strategies. Herein, a novel modified strategy involving with a two-step anodic oxidation and annealing treatment was proposed to achieve rapid re-endothelialization function regulated by regular honeycomb nanotexture and specific anatase phase on the titanium surface. Theoretical calculation revealed that the presence of nanotexture reduced the polar component of surface energy, while the generation of anatase significantly enhanced the polar component and total surface energy. Meanwhile, the modified surface with regular nanotexture and anatase phase produced positive effect on the expression of CD31, VE-Cadherin and down-regulated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/86k2h30t</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Ren, Kai</name>
      </author>
      <author>
        <name>Qiu, Jingru</name>
      </author>
      <author>
        <name>Chen, Baolan</name>
      </author>
      <author>
        <name>Duan, Weixun</name>
      </author>
      <author>
        <name>Liu, Jincheng</name>
      </author>
      <author>
        <name>Li, Guiling</name>
      </author>
      <author>
        <name>Li, Donghai</name>
      </author>
    </item>
    <item>
      <title>An antibody-based proximity labeling protocol to identify biotinylated interactors of SARS-CoV-2</title>
      <link>https://escholarship.org/uc/item/7vn1639n</link>
      <description>Elucidating the molecular interactions between virus and host is fundamental to understanding the mechanism of viral pathogenesis. Here, we present a protocol to screen SARS-CoV-2 protein interactors using an antibody-based TurboID proximity labeling approach. This technique directly identifies biotinylated peptides labeled by the TurboID-tagged viral proteins. We describe the steps to prepare biotinylated peptide samples for mass spectrometry analysis and a stringent workflow to identify biotinylated high-confidence interactors of the virus by filtering out non-specific co-purified proteins. For complete details on the use and execution of this protocol, please refer to Zhang et&amp;nbsp;al. (2022).</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7vn1639n</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Shang, Limin</name>
      </author>
      <author>
        <name>Zhang, Yuehui</name>
      </author>
      <author>
        <name>Liu, Yuchen</name>
      </author>
      <author>
        <name>Jin, Chaozhi</name>
      </author>
      <author>
        <name>Zhao, Yanan</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Wang, Pei-Hui</name>
      </author>
      <author>
        <name>Wang, Jian</name>
      </author>
    </item>
    <item>
      <title>Dynamic epigenetic states of maize centromeres</title>
      <link>https://escholarship.org/uc/item/7tp528v4</link>
      <description>The centromere is a specialized chromosomal region identified as the major constriction, upon which the kinetochore complex is formed, ensuring accurate chromosome orientation and segregation during cell division. The rapid evolution of centromere DNA sequence and the conserved centromere function are two contradictory aspects of centromere biology. Indeed, the sole presence of genetic sequence is not sufficient for centromere formation. Various dicentric chromosomes with one inactive centromere have been recognized. It has also been found that de novo centromere formation is common on fragments in which centromeric DNA sequences are lost. Epigenetic factors play important roles in centromeric chromatin assembly and maintenance. Non-disjunction of the supernumerary B chromosome centromere is independent of centromere function, but centromere pairing during early prophase of meiosis I requires an active centromere. This review discusses recent studies in maize about genetic and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7tp528v4</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Yalin</name>
      </author>
      <author>
        <name>Su, Handong</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Liu, Yang</name>
      </author>
      <author>
        <name>Han, Fangpu</name>
      </author>
      <author>
        <name>Birchler, James A</name>
      </author>
    </item>
    <item>
      <title>Insights into virulence: structure classification of the Vibrio parahaemolyticus RIMD mobilome</title>
      <link>https://escholarship.org/uc/item/7g47f154</link>
      <description>IMPORTANCE: The pandemic &lt;i&gt;Vpar&lt;/i&gt; strain RIMD causes seafood-borne illness worldwide. Previous comparative genomic studies have revealed pathogenicity islands in RIMD that contribute to the success of the strain in infection. However, not all virulence determinants have been identified, and many of the proteins encoded in known pathogenicity islands are of unknown function. Based on the EOCD database, we used evolution-based classification of structure models for the RIMD proteome to improve our functional understanding of virulence determinants acquired by the pandemic strain. We further identify and classify previously unknown mobile protein domains as well as fast evolving residue positions in structure models that contribute to virulence and adaptation with respect to a pre-pandemic strain. Our work highlights key contributions of phage in mediating seafood born illness, suggesting this strain balances its avoidance of phage predators with its successful colonization of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7g47f154</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kinch, Lisa N</name>
      </author>
      <author>
        <name>Schaeffer, R Dustin</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Orth, Kim</name>
      </author>
      <author>
        <name>Grishin, Nick</name>
      </author>
    </item>
    <item>
      <title>Evolution of the interactions between GII.4 noroviruses and histo-blood group antigens: Insights from experimental and computational studies</title>
      <link>https://escholarship.org/uc/item/7dt7t2kf</link>
      <description>Norovirus (NoV) is the major pathogen causing the outbreaks of the viral gastroenteritis across the world. Among the various genotypes of NoV, GII.4 is the most predominant over the past decades. GII.4 NoVs interact with the histo-blood group antigens (HBGAs) to invade the host cell, and it is believed that the receptor HBGAs may play important roles in selecting the predominate variants by the nature during the evolution of GII.4 NoVs. However, the evolution-induced changes in the HBGA-binding affinity for the GII.4 NoV variants and the mechanism behind the evolution of the NoV-HBGA interactions remain elusive. In the present work, the virus-like particles (VLPs) of the representative GII.4 NoV stains epidemic in the past decades were expressed by using the Hansenula polymorpha yeast expression platform constructed by our laboratory, and then the enzyme linked immunosorbent assay (ELISA)-based HBGA-binding assays as well as the molecular dynamics (MD) simulations combined with...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7dt7t2kf</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liang, Yu</name>
      </author>
      <author>
        <name>Wang, Wei Bu</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Hou, Jun Wei</name>
      </author>
      <author>
        <name>Tang, Fang</name>
      </author>
      <author>
        <name>Zhang, Xue Feng</name>
      </author>
      <author>
        <name>Du, Li Fang</name>
      </author>
      <author>
        <name>Su, Ji Guo</name>
      </author>
      <author>
        <name>Li, Qi Ming</name>
      </author>
    </item>
    <item>
      <title>A switch to feeding on cycads generates parallel accelerated evolution of toxin tolerance in two clades of Eumaeus caterpillars (Lepidoptera: Lycaenidae)</title>
      <link>https://escholarship.org/uc/item/7c8224p7</link>
      <description>We assembled a complete reference genome of &lt;i&gt;Eumaeus atala&lt;/i&gt;, an aposematic cycad-eating hairstreak butterfly that suffered near extinction in the United States in the last century. Based on an analysis of genomic sequences of &lt;i&gt;Eumaeus&lt;/i&gt; and 19 representative genera, the closest relatives of &lt;i&gt;Eumaeus&lt;/i&gt; are &lt;i&gt;Theorema&lt;/i&gt; and &lt;i&gt;Mithras&lt;/i&gt; We report natural history information for &lt;i&gt;Eumaeus&lt;/i&gt;, &lt;i&gt;Theorema&lt;/i&gt;, and &lt;i&gt;Mithras&lt;/i&gt; Using genomic sequences for each species of &lt;i&gt;Eumaeus&lt;/i&gt;, &lt;i&gt;Theorema&lt;/i&gt;, and &lt;i&gt;Mithras&lt;/i&gt; (and three outgroups), we trace the evolution of cycad feeding, coloration, gregarious behavior, and other traits. The switch to feeding on cycads and to conspicuous coloration was accompanied by little genomic change. &lt;i&gt;S&lt;/i&gt;oon after its origin, &lt;i&gt;Eumaeus&lt;/i&gt; split into two fast evolving lineages, instead of forming a clump of close relatives in the phylogenetic tree. Significant overlap of the fast evolving proteins in both clades indicates...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7c8224p7</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Robbins, Robert K</name>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Shen, Jinhui</name>
      </author>
      <author>
        <name>Riera, Julia Quer</name>
      </author>
      <author>
        <name>Murray, Debra</name>
      </author>
      <author>
        <name>Busby, Robert C</name>
      </author>
      <author>
        <name>Faynel, Christophe</name>
      </author>
      <author>
        <name>Hallwachs, Winnie</name>
      </author>
      <author>
        <name>Janzen, Daniel H</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Genomics Reveals the Origins of Historical Specimens</title>
      <link>https://escholarship.org/uc/item/78x3136s</link>
      <description>Centuries of zoological studies have amassed billions of specimens in collections worldwide. Genomics of these specimens promises to reinvigorate biodiversity research. However, because DNA degrades with age in historical specimens, it is a challenge to obtain genomic data for them and analyze degraded genomes. We developed experimental and computational protocols to overcome these challenges and applied our methods to resolve a series of long-standing controversies involving a group of butterflies. We deduced the geographical origins of several historical specimens of uncertain provenance that are at the heart of these debates. Here, genomics tackles one of the greatest problems in zoology: countless old specimens that serve as irreplaceable embodiments of species concepts cannot be confidently assigned to extant species or population due to the lack of diagnostic morphological features and clear documentation of the collection locality. The ability to determine where they were...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/78x3136s</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Shen, Jinhui</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Li, Wenlin</name>
      </author>
      <author>
        <name>Kinch, Lisa N</name>
      </author>
      <author>
        <name>Calhoun, John V</name>
      </author>
      <author>
        <name>Warren, Andrew D</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Safety and immunogenicity of a hybrid-type vaccine booster in BBIBP-CorV recipients in a randomized phase 2 trial</title>
      <link>https://escholarship.org/uc/item/7326626d</link>
      <description>NVSI-06-08 is a potential broad-spectrum recombinant COVID-19 vaccine that integrates the antigens from multiple SARS-CoV-2 strains into a single immunogen. Here, we evaluate the safety and immunogenicity of NVSI-06-08 as a heterologous booster dose in BBIBP-CorV recipients in a randomized, double-blind, controlled, phase 2 trial conducted in the United Arab Emirates (NCT05069129). Three groups of healthy adults over 18 years of age (600 participants per group) who have administered two doses of BBIBP-CorV 4-6-month, 7-9-month and &amp;gt;9-month earlier, respectively, are randomized 1:1 to receive either a homologous booster of BBIBP-CorV or a heterologous booster of NVSI-06-08. The incidence of adverse reactions is low, and the overall safety profile is quite similar between two booster regimens. Both Neutralizing and IgG antibodies elicited by NVSI-06-08 booster are significantly higher than those by BBIBP-CorV booster against not only SARS-CoV-2 prototype strain but also multiple...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7326626d</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kaabi, Nawal Al</name>
      </author>
      <author>
        <name>Yang, Yun Kai</name>
      </author>
      <author>
        <name>Du, Li Fang</name>
      </author>
      <author>
        <name>Xu, Ke</name>
      </author>
      <author>
        <name>Shao, Shuai</name>
      </author>
      <author>
        <name>Liang, Yu</name>
      </author>
      <author>
        <name>Kang, Yun</name>
      </author>
      <author>
        <name>Su, Ji Guo</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Yang, Tian</name>
      </author>
      <author>
        <name>Hussein, Salah</name>
      </author>
      <author>
        <name>ElDein, Mohamed Saif</name>
      </author>
      <author>
        <name>Yang, Sen Sen</name>
      </author>
      <author>
        <name>Lei, Wenwen</name>
      </author>
      <author>
        <name>Gao, Xue Jun</name>
      </author>
      <author>
        <name>Jiang, Zhiwei</name>
      </author>
      <author>
        <name>Cong, Xiangfeng</name>
      </author>
      <author>
        <name>Tan, Yao</name>
      </author>
      <author>
        <name>Wang, Hui</name>
      </author>
      <author>
        <name>Li, Meng</name>
      </author>
      <author>
        <name>Mekki, Hanadi Mekki</name>
      </author>
      <author>
        <name>Zaher, Walid</name>
      </author>
      <author>
        <name>Mahmoud, Sally</name>
      </author>
      <author>
        <name>Zhang, Xue</name>
      </author>
      <author>
        <name>Qu, Chang</name>
      </author>
      <author>
        <name>Liu, Dan Ying</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
      </author>
      <author>
        <name>Yang, Mengjie</name>
      </author>
      <author>
        <name>Eltantawy, Islam</name>
      </author>
      <author>
        <name>Hou, Jun Wei</name>
      </author>
      <author>
        <name>Lei, Ze Hua</name>
      </author>
      <author>
        <name>Xiao, Peng</name>
      </author>
      <author>
        <name>Wang, Zhao Nian</name>
      </author>
      <author>
        <name>Yin, Jin Liang</name>
      </author>
      <author>
        <name>Mao, Xiao Yan</name>
      </author>
      <author>
        <name>Zhang, Jin</name>
      </author>
      <author>
        <name>Qu, Liang</name>
      </author>
      <author>
        <name>Zhang, Yun Tao</name>
      </author>
      <author>
        <name>Yang, Xiao Ming</name>
      </author>
      <author>
        <name>Wu, Guizhen</name>
      </author>
      <author>
        <name>Li, Qi Ming</name>
      </author>
    </item>
    <item>
      <title>SARS‐CoV‐2 ORF10 antagonizes STING‐dependent interferon activation and autophagy</title>
      <link>https://escholarship.org/uc/item/6ws7w0xq</link>
      <description>A characteristic feature of COVID-19, the disease caused by severe acute respiratory syndrome coronavirus 2&amp;nbsp;(SARS-CoV-2) infection, is the dysregulated immune response with impaired type I and III interferon (IFN) expression and an overwhelming inflammatory cytokine storm. RIG-I-like receptors (RLRs) and cGAS-STING signaling pathways are responsible for sensing viral infection and inducing IFN production to combat invading viruses. Multiple proteins of SARS-CoV-2 have been reported to modulate the RLR signaling pathways to achieve immune evasion. Although SARS-CoV-2 infection also activates the cGAS-STING signaling by stimulating micronuclei formation during the process of syncytia, whether SARS-CoV-2 modulates the cGAS-STING pathway requires further investigation. Here, we screened 29 SARS-CoV-2-encoded viral proteins to explore the viral proteins that affect the cGAS-STING signaling pathway and found that SARS-CoV-2 open reading frame&amp;nbsp;10 (ORF10) targets STING to antagonize...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6ws7w0xq</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Han, Lulu</name>
      </author>
      <author>
        <name>Zheng, Yi</name>
      </author>
      <author>
        <name>Deng, Jian</name>
      </author>
      <author>
        <name>Nan, Mei‐Ling</name>
      </author>
      <author>
        <name>Xiao, Yang</name>
      </author>
      <author>
        <name>Zhuang, Meng‐Wei</name>
      </author>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Wang, Wei</name>
      </author>
      <author>
        <name>Gao, Chengjiang</name>
      </author>
      <author>
        <name>Wang, Pei‐Hui</name>
      </author>
    </item>
    <item>
      <title>The complete mitogenome of Euschemon rafflesia (Lepidoptera: Hesperiidae)</title>
      <link>https://escholarship.org/uc/item/6vc6w48h</link>
      <description>We assembled a complete mitochondrial genome of a unique Australian skipper butterfly &lt;i&gt;Euschemon rafflesia&lt;/i&gt; (Hesperiidae) from next generation sequencing reads. The 15,447 bp mitogenome covers 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNAs), 2 ribosomal RNA genes (rRNAs), and an A+T-rich region. Its gene order is typical for mitogenomes of Lepidoptera. Phylogenetic analysis places &lt;i&gt;Euschemon rafflesia&lt;/i&gt; as a sister to the rest of Hesperiidae except Coeliadinae.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6vc6w48h</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Cong, Qian</name>
      </author>
      <author>
        <name>Shen, Jinhui</name>
      </author>
      <author>
        <name>Fan, Xiao-Ling</name>
      </author>
      <author>
        <name>Wang, Min</name>
      </author>
      <author>
        <name>Grishin, Nick V</name>
      </author>
    </item>
    <item>
      <title>Hydroxyapatite Formation Coexists with Amyloid-like Self-Assembly of Human Amelogenin</title>
      <link>https://escholarship.org/uc/item/6g24d1zg</link>
      <description>Tooth enamel is formed in an extracellular environment. Amelogenin, the major component in the protein matrix of tooth enamel during the developing stage, could assemble into high molecular weight structures, regulating enamel formation. However, the molecular structure of amelogenin protein assembly at the functional state is still elusive. In this work, we found that amelogenin is able to induce calcium phosphate minerals into hydroxyapatite (HAP) structure in vitro at pH 6.0. Assessed using X-ray diffraction (XRD) and &lt;sup&gt;31&lt;/sup&gt;P solid-state NMR (SSNMR) evidence, the formed HAP mimics natural enamel closely. The structure of amelogenin protein assembly coexisting with the HAP was also studied using atomic force microscopy (AFM), transmission electron microscopy (TEM) and XRD, indicating the β-amyloid structure of the protein. SSNMR was proven to be an important tool in detecting both the rigid and dynamic components of the protein assembly in the sample, and the core sequence...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6g24d1zg</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Jing</name>
        <uri>https://orcid.org/0000-0002-5970-0509</uri>
      </author>
      <author>
        <name>Wang, Jian</name>
      </author>
      <author>
        <name>Ma, Chengwei</name>
      </author>
      <author>
        <name>Lu, Junxia</name>
      </author>
    </item>
  </channel>
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