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    <title>Recent ucsf items</title>
    <link>https://escholarship.org/uc/ucsf/rss</link>
    <description>Recent eScholarship items from UCSF</description>
    <pubDate>Thu, 18 Jun 2026 04:12:37 +0000</pubDate>
    <item>
      <title>A phase 2 study of olutasidenib in combination with azacitidine followed by olutasidenib maintenance after venetoclax plus a hypomethylating agent regimen for IDH1-mutated acute myeloid leukemia (University of California Hematologic Malignancies Consortium Study 2441).</title>
      <link>https://escholarship.org/uc/item/8wg0r7m6</link>
      <description>TPS6603   Background: Acute myeloid leukemia (AML) with isocitrate dehydrogenase-1 (IDH1) mutations represents a subset of up to approximately 7-14% of patients. For patients with IDH1m AML ineligible for first line intensive induction, the combination of a hypomethylating agent (HMA) and venetoclax (VEN) is a standard of care based on the VIALE-A study. In patients with IDH1m, the HMA azacitidine (AZA) plus VEN regimen leads to a complete remission (CR) plus CR with incomplete count recovery (CRi) rate of 66.7%, duration of remission (DoR) 21.9 months, and median overall survival (OS) of 15.2 months. However, one of the limiting features of HMA-VEN is myelosuppression, leading to dose delays and reductions, and adverse events (AEs) led to discontinuation in up to 30% of patients on the VIALE-A study. Approaches to increase tolerability and improve outcomes are of interest. Olutasidenib (OLU) is a potent, oral and selective small-molecule IDH1m inhibitor currently approved for...</description>
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      <pubDate>Wed, 17 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Jonas, Brian Andrew</name>
        <uri>https://orcid.org/0000-0002-4921-5809</uri>
      </author>
      <author>
        <name>Bukari, Mohammad</name>
      </author>
      <author>
        <name>Ferng, Timothy</name>
      </author>
      <author>
        <name>Jeyakumar, Deepa</name>
      </author>
      <author>
        <name>Oliai, Caspian</name>
      </author>
      <author>
        <name>Tanaka, Tiffany N</name>
      </author>
      <author>
        <name>Huang, Chiung-Yu</name>
        <uri>https://orcid.org/0000-0003-2313-3562</uri>
      </author>
      <author>
        <name>Socola, Francisco</name>
      </author>
    </item>
    <item>
      <title>Metformin Is Associated With Reduced Odds for Colorectal Cancer Among Persons With Diabetes</title>
      <link>https://escholarship.org/uc/item/6m40k0gc</link>
      <description>INTRODUCTION: Metformin may be associated with reduced colorectal cancer (CRC) risk, but findings from previous studies have been inconsistent and had insufficient sample sizes to examine whether the association differs by anatomic site. This study examined whether metformin was associated with reduced CRC risk, both overall and stratified by anatomic site, in a large sample of persons with diabetes who underwent colonoscopy.
METHODS: We performed a case-control study of US Veterans with prevalent diabetes who underwent colonoscopy between 1999 and 2014 using Department of Veterans Affairs electronic health record data. Cases were defined by presence of CRC at colonoscopy, while controls had normal colonoscopy. The primary exposure was metformin use at time of colonoscopy (yes/no). Association of metformin exposure with CRC (further stratified by proximal, distal, or rectal subsite) was examined using multivariable and multinomial logistic regression and summarized by odds ratios...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6m40k0gc</guid>
      <pubDate>Wed, 17 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Demb, Joshua</name>
      </author>
      <author>
        <name>Yaseyyedi, Armaan</name>
      </author>
      <author>
        <name>Liu, Lin</name>
      </author>
      <author>
        <name>Bustamante, Ranier</name>
      </author>
      <author>
        <name>Earles, Ashley</name>
      </author>
      <author>
        <name>Ghosh, Pradipta</name>
        <uri>https://orcid.org/0000-0002-8917-3201</uri>
      </author>
      <author>
        <name>Gutkind, J Silvio</name>
        <uri>https://orcid.org/0000-0002-5150-4482</uri>
      </author>
      <author>
        <name>Gawron, Andrew J</name>
      </author>
      <author>
        <name>Kaltenbach, Tonya R</name>
      </author>
      <author>
        <name>Martinez, Maria Elena</name>
      </author>
      <author>
        <name>Gupta, Samir</name>
        <uri>https://orcid.org/0000-0003-4192-5002</uri>
      </author>
    </item>
    <item>
      <title>Simulated Reasoning and Self-Verification for Psychiatric Diagnosis in Generalist Large Language Models: Comparative Evaluation.</title>
      <link>https://escholarship.org/uc/item/3c51f39z</link>
      <description>&lt;h4&gt;Background&lt;/h4&gt;Large language models (LLMs) and, more recently, large reasoning models (LRMs) have rapidly garnered significant interest for application in psychiatry and behavioral health. However, recent studies have identified significant shortcomings and potential risks in the performance of LLM-based systems, complicating their application to psychiatric diagnosis. Two promising approaches to addressing these challenges and improving the efficacy of these models are simulated reasoning (SR) and self-verification (SV), in which additional reasoning tokens are used to guide model output, either during or after inference.&lt;h4&gt;Objective&lt;/h4&gt;We aimed to explore how the use of SR (via LRMs) and SV (via supplemental prompting) affects the psychiatric diagnostic performance of LLMs.&lt;h4&gt;Methods&lt;/h4&gt;106 case vignettes and associated diagnoses were extracted from the DSM-5-TR (Diagnostic and Statistical Manual, Version 5, Text Revision) Clinical Cases book, with permission. Both...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3c51f39z</guid>
      <pubDate>Wed, 17 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sarma, Karthik</name>
      </author>
      <author>
        <name>Hanss, Kaitlin</name>
      </author>
      <author>
        <name>Halls, Andrew</name>
      </author>
      <author>
        <name>Becker, Daniel</name>
      </author>
      <author>
        <name>Glowinski, Anne</name>
      </author>
      <author>
        <name>Krystal, Andrew</name>
      </author>
    </item>
    <item>
      <title>Changes in and Remission of Body Weight and Eating Disorder Psychopathology in Adolescents with Anorexia Nervosa During and Four Weeks Post Inpatient Treatment.</title>
      <link>https://escholarship.org/uc/item/05n7r2bk</link>
      <description>&lt;h4&gt;Objectives&lt;/h4&gt;To assess associations between body weight metrics and eating disorder (ED)-psychopathology in adolescents with anorexia nervosa (AN) at baseline and four weeks post-discharge (4-week follow-up) from inpatient psychiatric multimodal treatment (IMT), calculating full and partial body mass index (BMI) percentile/ED-psychopathology remission rates.&lt;h4&gt;Methods&lt;/h4&gt;Secondary analysis of a prospective observational cohort study in adolescents (12-18 years) with AN-restricting (AN-R)/-binge-purge (AN-BP), and atypical AN (AAN). Body weight metrics and ED-psychopathology (Eating Disorder Examination Questionnaire, EDE-Q) were assessed at baseline and 4-week follow-up. Remission at 4-week follow-up was calculated by applying German-AN-S3-guidelines-based vs. DSM-5 criteria.&lt;h4&gt;Results&lt;/h4&gt;In 40 adolescents (mean age = 15.6 ± 1.5 years; females = 90%; BMI &lt;i&gt;z&lt;/i&gt;-score = -2.59 ± 1.07) receiving IMT (median duration = 118 (IQR = 90-150) days), BMI &lt;i&gt;z&lt;/i&gt;-score increased...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/05n7r2bk</guid>
      <pubDate>Wed, 17 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Neumeier, Elisabeth</name>
      </author>
      <author>
        <name>Imken, Linus</name>
      </author>
      <author>
        <name>Kaiser, Vivien</name>
      </author>
      <author>
        <name>Le Grange, Daniel</name>
      </author>
      <author>
        <name>Haas, Verena</name>
      </author>
      <author>
        <name>Correll, Christoph</name>
      </author>
    </item>
    <item>
      <title>Association Between Age at Kidney Transplantation and Risk of Early Graft Loss.</title>
      <link>https://escholarship.org/uc/item/9490m93h</link>
      <description>&lt;h4&gt;Background&lt;/h4&gt;Adolescence has been identified as a high-risk period for graft failure. However, existing knowledge on this topic is largely limited to long-term graft outcomes. The aim of this study was to examine the association between age at kidney transplantation and early graft loss, defined as graft failure within 3 years post-transplantation in the contemporary era.&lt;h4&gt;Methods&lt;/h4&gt;This study was a retrospective analysis of 55 973 first-time kidney transplant recipients identified in the U.S. Renal Data System from January 1, 2005, to December 31, 2021. Adjusted Cox proportional hazards regression models were used to evaluate the association between age at transplantation and early graft failure including an interaction term for race/ethnicity.&lt;h4&gt;Results&lt;/h4&gt;Adolescents (12 to &amp;lt; 18 years) and young adults (18 to &amp;lt; 26 years) were at the highest risk of early death-censored graft loss compared to young adults (26 to &amp;lt; 40 years), with hazard ratios of 1.95 (95%...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9490m93h</guid>
      <pubDate>Mon, 15 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Marroquin, Karina</name>
      </author>
      <author>
        <name>Frazier, Krystle</name>
      </author>
      <author>
        <name>Mcculloch, Chuck</name>
      </author>
      <author>
        <name>Grimes, Barbara</name>
      </author>
      <author>
        <name>Ku, Elaine</name>
      </author>
    </item>
    <item>
      <title>A Prodrug Strategy to Conditionally Trap Therapeutic Payloads for Improved Tumor Retention</title>
      <link>https://escholarship.org/uc/item/7st7q7dt</link>
      <description>Altered extracellular proteolysis has been exploited to selectively activate therapeutics in diseases such as cancer; however, once activated, extracellular drugs can diffuse away, limiting efficacy. We address this challenge by coupling proteolytic activation with membrane tethering to retain drugs within diseased tissue. To accomplish this, we developed “restricted interaction peptides” (RIPs), a delivery platform that leverages elevated proteolytic activity to activate membrane-interacting peptides, localizing cargos near the site of proteolysis. We demonstrate that RIPs can deliver diverse therapeutic cargos, including cytotoxins and radioisotopes. As proof of concept, we engineered “FRIP,” a RIP designed for cleavage by fibroblast activation protein (FAP), an endoprotease upregulated in solid tumors and fibrosis. Efficient P4–P4’ substrate sequences were identified and incorporated into FRIPs. Cell-based studies showed that, upon activation, the peptide adhered to membranes...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7st7q7dt</guid>
      <pubDate>Mon, 15 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kang, Deokhee</name>
      </author>
      <author>
        <name>Pandey, Apurva</name>
      </author>
      <author>
        <name>Kumar, Garima</name>
      </author>
      <author>
        <name>Mehta, Abijeet Singh</name>
      </author>
      <author>
        <name>Detomasi, Tyler C</name>
      </author>
      <author>
        <name>Anderson, Dashiell</name>
      </author>
      <author>
        <name>Bardine, Conner</name>
      </author>
      <author>
        <name>Asper, Garrison</name>
      </author>
      <author>
        <name>Qi, Junyang</name>
      </author>
      <author>
        <name>Nadig, Isha</name>
      </author>
      <author>
        <name>Cui, Yifan</name>
      </author>
      <author>
        <name>Quimby, Fiona M</name>
      </author>
      <author>
        <name>Ling, Jesse</name>
      </author>
      <author>
        <name>Seo, Youngho</name>
        <uri>https://orcid.org/0000-0001-5908-6636</uri>
      </author>
      <author>
        <name>Cohen, Bruce E</name>
      </author>
      <author>
        <name>Anwar, Mekhail</name>
      </author>
      <author>
        <name>Evans, Michael J</name>
      </author>
      <author>
        <name>Craik, Charles S</name>
        <uri>https://orcid.org/0000-0001-7704-9185</uri>
      </author>
    </item>
    <item>
      <title>Launching an innovative program to enhance patient care and physician productivity in Multiple Myeloma</title>
      <link>https://escholarship.org/uc/item/5nr0992r</link>
      <description>https://ucsf.app.box.com/s/a6f0eh4w5wjh31eu55bn5ku92kq0sfi4</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5nr0992r</guid>
      <pubDate>Thu, 11 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shabbir, Zain</name>
      </author>
      <author>
        <name>Shagun, Arora</name>
      </author>
      <author>
        <name>Dunn, Lisa</name>
      </author>
      <author>
        <name>Ghaskadbi, Pranav</name>
      </author>
      <author>
        <name>Le, Victoria</name>
      </author>
      <author>
        <name>Jimenez Rodriguez, Jimena</name>
      </author>
      <author>
        <name>Aldana, Mario</name>
      </author>
      <author>
        <name>Zhu, Ryan</name>
      </author>
      <author>
        <name>Zou, Charisse</name>
      </author>
      <author>
        <name>Wang, Livia</name>
      </author>
      <author>
        <name>Alvarez, Mae</name>
      </author>
      <author>
        <name>Chung, Alfred</name>
      </author>
      <author>
        <name>Kumar, Anupama</name>
      </author>
      <author>
        <name>Lipof, Jodi</name>
      </author>
      <author>
        <name>Pan, Darren</name>
      </author>
      <author>
        <name>Martin, Thomas</name>
      </author>
      <author>
        <name>Wolf, Jeffrey</name>
      </author>
      <author>
        <name>Chari, Ajai</name>
      </author>
      <author>
        <name>Belkora, Jeffrey</name>
      </author>
    </item>
    <item>
      <title>Establishing the Fundamental Role of Somatic Cells in Age-Related Reproductive Fitness Decline</title>
      <link>https://escholarship.org/uc/item/5z10z7tj</link>
      <description>Aging is defined by a progressive deterioration of tissue and organ functionality during adulthood. Across species from invertebrates to mammals, the female reproductive system has consistently been found to be one of the first organs to lose functionality with age. While oocytes have long been assumed to be the primary cells affected by aging, growing evidence points to ovarian somatic cells as key contributors, though the molecular mechanisms driving their aging remain poorly understood. In the Drosophila ovary, a layer of somatic follicle cells surrounds each germ-cell cyst. These follicle cells are essential for guiding and supporting germ-cell cyst development into a mature oocyte. We found that aging is characterized by an accumulation of phenotypes in the somatic compartment, including failure of the follicle cells to encapsulate germ-cell cysts, an extended S phase, and increased DNA damage. These follicle encapsulation defects are associated with the lack of a germ-cell...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5z10z7tj</guid>
      <pubDate>Wed, 10 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wolfgram, Emily Allyson</name>
        <uri>https://orcid.org/0000-0003-1073-7981</uri>
      </author>
    </item>
    <item>
      <title>Workflow‑Based Information Management Framework for Multicenter Research Studies: Design and Development.</title>
      <link>https://escholarship.org/uc/item/7nf6n5wd</link>
      <description>&lt;h4&gt;Background&lt;/h4&gt;Biological and health research is increasingly data-driven, with commercial and academic institutions generating data at unprecedented rates. The rapid pace of data generation, together with lessons learned during the COVID-19 pandemic, underscores the need for nimble, transparent, and dependable data infrastructures that enable rapid study execution and timely insights to inform public health policy and practice.&lt;h4&gt;Objective&lt;/h4&gt;This paper describes the workflow-based information management (WIM) framework, a flexible research information management system designed to support diverse epidemiologic workflows and data-intensive research projects.&lt;h4&gt;Methods&lt;/h4&gt;WIM was developed as a modular, workflow-oriented framework built on the open-source R (R Foundation) programming language and its extensive ecosystem of community-developed packages. The framework emphasizes reproducibility, adaptability, and transparency, enabling users to design and manage research...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7nf6n5wd</guid>
      <pubDate>Mon, 8 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sulaeman, Hasan</name>
      </author>
      <author>
        <name>Stone, Mars</name>
      </author>
      <author>
        <name>Bruhn, Roberta</name>
      </author>
      <author>
        <name>Zurita, Karla</name>
      </author>
      <author>
        <name>Nguyen, Anh</name>
      </author>
      <author>
        <name>Chiang, Vincent</name>
      </author>
      <author>
        <name>Jones, Jefferson</name>
      </author>
      <author>
        <name>Deng, Xutao</name>
      </author>
      <author>
        <name>Custer, Brian</name>
      </author>
      <author>
        <name>Busch, Michael</name>
      </author>
      <author>
        <name>Grebe, Eduard</name>
      </author>
    </item>
    <item>
      <title>Sustainment of Hydroxyurea Adherence in Patients With Sickle Cell Disease</title>
      <link>https://escholarship.org/uc/item/7179824j</link>
      <description>Importance: Despite established treatment guidelines and strong therapeutic benefit, hydroxyurea remains underused among patients with sickle cell disease.
Objective: To assess the change in self-reported hydroxyurea use (ie, taking the medication at all) and adherence (ie, the number of days taken per week) over time and to examine factors associated with the trajectory of hydroxyurea use and adherence.
Design, Setting, and Participants: Data were collected through the Sickle Cell Disease Implementation Consortium, a longitudinal, multicenter, observational cohort study that recruited patients from 8 centers across the US. Data collection occurred from 2017 to 2022, and analyses were performed from January to October 2025. Data were collected via self-report survey at baseline and 3 follow-up surveys distributed yearly. Patients with sickle cell disease of all genotypes between the ages of 15 and 45 years were included.
Exposure: Sickle cell disease.
Main Outcomes and Measures:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7179824j</guid>
      <pubDate>Mon, 8 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Heitzer, Andrew M</name>
      </author>
      <author>
        <name>Wooten, Zachary</name>
      </author>
      <author>
        <name>Luo, Guangjin</name>
      </author>
      <author>
        <name>Treadwell, Marsha</name>
        <uri>https://orcid.org/0000-0003-0521-1846</uri>
      </author>
      <author>
        <name>King, Allison A</name>
      </author>
      <author>
        <name>Gordeuk, Victor R</name>
      </author>
      <author>
        <name>Shah, Nirmish</name>
      </author>
      <author>
        <name>Abrams, Christina M</name>
      </author>
      <author>
        <name>McCuskee, Sarah</name>
      </author>
      <author>
        <name>Gollan, Siera</name>
      </author>
      <author>
        <name>Longoria, Jennifer</name>
      </author>
      <author>
        <name>Hankins, Jane S</name>
      </author>
    </item>
    <item>
      <title>A harmonized public resource of deeply sequenced diverse human genomes.</title>
      <link>https://escholarship.org/uc/item/7pw9j9mr</link>
      <description>Underrepresented populations are often excluded from genomic studies owing in part to a lack of resources supporting their analyses. The 1000 Genomes Project (1kGP) and Human Genome Diversity Project (HGDP), which have recently been sequenced to high coverage, are valuable genomic resources because of the global diversity they capture and their open data sharing policies. Here, we harmonized a high-quality set of 4094 whole genomes from 80 populations in the HGDP and 1kGP with data from the Genome Aggregation Database (gnomAD) and identified over 153 million high-quality SNVs, indels, and SVs. We performed a detailed ancestry analysis of this cohort, characterizing population structure and patterns of admixture across populations, analyzing site frequency spectra, and measuring variant counts at global and subcontinental levels. We also show substantial added value from this data set compared with the prior versions of the component resources, typically combined via liftOver and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7pw9j9mr</guid>
      <pubDate>Fri, 5 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Koenig, Zan</name>
      </author>
      <author>
        <name>Yohannes, Mary</name>
      </author>
      <author>
        <name>Nkambule, Lethukuthula</name>
      </author>
      <author>
        <name>Zhao, Xuefang</name>
      </author>
      <author>
        <name>Goodrich, Julia</name>
      </author>
      <author>
        <name>Kim, Heesu</name>
      </author>
      <author>
        <name>Wilson, Michael</name>
      </author>
      <author>
        <name>Tiao, Grace</name>
      </author>
      <author>
        <name>Hao, Stephanie</name>
      </author>
      <author>
        <name>Sahakian, Nareh</name>
      </author>
      <author>
        <name>Chao, Katherine</name>
      </author>
      <author>
        <name>Walker, Mark</name>
      </author>
      <author>
        <name>Lyu, Yunfei</name>
      </author>
      <author>
        <name>Rehm, Heidi</name>
      </author>
      <author>
        <name>Neale, Benjamin</name>
      </author>
      <author>
        <name>Talkowski, Michael</name>
      </author>
      <author>
        <name>Daly, Mark</name>
      </author>
      <author>
        <name>Brand, Harrison</name>
      </author>
      <author>
        <name>Karczewski, Konrad</name>
      </author>
      <author>
        <name>Atkinson, Elizabeth</name>
      </author>
      <author>
        <name>Martin, Alicia</name>
      </author>
    </item>
    <item>
      <title>Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.</title>
      <link>https://escholarship.org/uc/item/0372c6fn</link>
      <description>Pregnancy loss and perinatal death are devastating events for families. We assessed genomic autopsy as an adjunct to standard autopsy for 200 families who had experienced fetal or newborn death, providing a definitive or candidate genetic diagnosis in 105 families. Our cohort provides evidence of severe atypical in utero presentations of known genetic disorders and identifies novel phenotypes and disease genes. Inheritance of 42% of definitive diagnoses were either autosomal recessive (30.8%), X-linked recessive (3.8%) or autosomal dominant (excluding de novos, 7.7%), with risk of recurrence in future pregnancies. We report that at least ten families (5%) used their diagnosis for preimplantation (5) or prenatal diagnosis (5) of 12 pregnancies. We emphasize the clinical importance of genomic investigations of pregnancy loss and perinatal death, with short turnaround times for diagnostic reporting and followed by systematic research follow-up investigations. This approach has the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0372c6fn</guid>
      <pubDate>Fri, 5 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Byrne, Alicia</name>
      </author>
      <author>
        <name>Arts, Peer</name>
      </author>
      <author>
        <name>Ha, Thuong</name>
      </author>
      <author>
        <name>Kassahn, Karin</name>
      </author>
      <author>
        <name>Pais, Lynn</name>
      </author>
      <author>
        <name>ODonnell-Luria, Anne</name>
      </author>
      <author>
        <name>Babic, Milena</name>
      </author>
      <author>
        <name>Frank, Mahalia</name>
      </author>
      <author>
        <name>Feng, Jinghua</name>
      </author>
      <author>
        <name>Wang, Paul</name>
      </author>
      <author>
        <name>Lawrence, David</name>
      </author>
      <author>
        <name>Eshraghi, Leila</name>
      </author>
      <author>
        <name>Arriola, Luis</name>
      </author>
      <author>
        <name>Toubia, John</name>
      </author>
      <author>
        <name>Nguyen, Hung</name>
      </author>
      <author>
        <name>McGillivray, George</name>
      </author>
      <author>
        <name>Pinner, Jason</name>
      </author>
      <author>
        <name>McKenzie, Fiona</name>
      </author>
      <author>
        <name>Morrow, Rebecca</name>
      </author>
      <author>
        <name>Lipsett, Jill</name>
      </author>
      <author>
        <name>Manton, Nick</name>
      </author>
      <author>
        <name>Khong, T</name>
      </author>
      <author>
        <name>Moore, Lynette</name>
      </author>
      <author>
        <name>Liebelt, Jan</name>
      </author>
      <author>
        <name>Schreiber, Andreas</name>
      </author>
      <author>
        <name>King-Smith, Sarah</name>
      </author>
      <author>
        <name>Hardy, Tristan</name>
      </author>
      <author>
        <name>Jackson, Matilda</name>
      </author>
      <author>
        <name>Barnett, Christopher</name>
      </author>
      <author>
        <name>Scott, Hamish</name>
      </author>
    </item>
    <item>
      <title>Inadequate Support</title>
      <link>https://escholarship.org/uc/item/9hx559x0</link>
      <description>Inadequate Support A 71-year-old man presented to the emergency department with a 6-month history of melena, easy bleeding and bruising, and lightheadedness.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9hx559x0</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Pichan, Cayla</name>
      </author>
      <author>
        <name>Dhaliwal, Gurpreet</name>
      </author>
      <author>
        <name>Cusick, Alice</name>
      </author>
      <author>
        <name>Saint, Sanjay</name>
      </author>
      <author>
        <name>Houchens, Nathan</name>
      </author>
    </item>
    <item>
      <title>Rapamycin Reverses Lymphatic Abnormalities in a Transgenic Mouse Model of Pulmonary Lymphangiectasia</title>
      <link>https://escholarship.org/uc/item/9hm8q7nw</link>
      <description>Rapamycin Reverses Lymphatic Abnormalities in a Transgenic Mouse Model of Pulmonary Lymphangiectasia</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9hm8q7nw</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Baluk, Peter</name>
      </author>
      <author>
        <name>Yao, Li-Chin</name>
      </author>
      <author>
        <name>Flores, Julio</name>
      </author>
      <author>
        <name>McDonald, Donald</name>
        <uri>https://orcid.org/0000-0002-6985-9564</uri>
      </author>
    </item>
    <item>
      <title>The Lived Experience of Moral Distress Among Certified Nursing Assistants Working in Nursing Homes</title>
      <link>https://escholarship.org/uc/item/98d9b89k</link>
      <description>Purpose/Background: Moral distress among registered nurses (RNs) has been extensively examined in acute care settings, drawing increased attention during the COVID-19 pandemic. However, research has been limited for certified nursing assistants (CNAs) who comprise approximately 60% of the nursing home workforce and provide most of the direct care. Moral distress is a significant contributor to burnout and turnover. CNAs differ from RNs in education, training, and scope of practice and are predominantly women and individuals from racially and ethnically diverse, often immigrant, backgrounds, factors that may shape their professional positioning and experiences of moral distress in nursing home settings. This study aimed to explore the lived experience of moral distress among CNAs who work in nursing homes and to give voice to this population.Method: Guided by an interpretive phenomenological approach, semi-structured interviews were conducted with CNAs who currently work in, or...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/98d9b89k</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Toivanen-Atilla, Kirsi</name>
        <uri>https://orcid.org/0000-0002-2431-8385</uri>
      </author>
    </item>
    <item>
      <title>INVESTIGATING THE MECHANISMS OF NUCLEOSOME REMODELING BY THE INO80 CHROMATIN REMODELING FAMILY</title>
      <link>https://escholarship.org/uc/item/9892z9cn</link>
      <description>ATP-dependent chromatin remodelers are essential regulators of genome function. By altering histone–DNA contacts, these enzymes reposition nucleosomes, change nucleosome accessibility, and catalyze histone exchange during transcription, replication, and DNA repair. A central challenge in chromatin biology is to understand how remodelers that share a conserved Snf2-family ATPase motor nevertheless generate distinct remodeling outcomes in different chromatin contexts. This thesis investigates that question with a focus on how nucleosomal cues and family-specific regulatory elements govern remodeler specificity, with particular emphasis on the INO80 family.The first part of this thesis focuses on the mechanism by which INO80 positions nucleosomes. Precise nucleosome positioning is essential for controlling the sites of transcription and replication initiation, and INO80 is uniquely required in vivo to establish such positioning. This role can be explained by the observation that...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9892z9cn</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kaur, Upneet</name>
        <uri>https://orcid.org/0000-0002-1894-3563</uri>
      </author>
    </item>
    <item>
      <title>Runx transcription factor control of medullary thymic epithelial cell development</title>
      <link>https://escholarship.org/uc/item/8q08r9fx</link>
      <description>Runt-related transcription factors 1 and 3 (Runx1 and Runx3) have been shown to orchestrate various developmental and cellular processes in numerous cell types and are critical for proper proliferation, differentiation, and cell lineage commitment. Using a conditional knockout mouse line, we specifically deleted Runx1 and Runx3 in the thymic epithelial compartment. Our findings reveal that Runx1 and Runx3 play critical, yet unique roles in controlling the development of medullary thymic epithelial cells (mTECs). ScRNA-sequencing (scRNA-seq) analysis on Runx1 conditional knockout mice reveal alterations in mTEC cell types, with a remarkable expansion of alveolar type 2 epithelial cells (AT2), a previously unknown mimetic cell type within the thymus. Conversely our findings show Runx3 expression in medullary thymic epithelial cells (mTECs) is required for both Autoimmune Regulator+ (Aire+) mTEC development and tissue-specific antigen (TSA) gene expression. Consequently, TEC-specific...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8q08r9fx</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sin, Jun Hyung</name>
        <uri>https://orcid.org/0009-0002-7338-3877</uri>
      </author>
    </item>
    <item>
      <title>Prefrontal-insular gamma synchrony promotes modality-specific cognitive flexibility</title>
      <link>https://escholarship.org/uc/item/8852v3x4</link>
      <description>The ability to alter our behavior based on sensory inputs, such as odors or textures, is a necessity for adaptation. The medial prefrontal cortex (mPFC), important for cognitive function(Miller et al., 2001), produces gamma synchrony that is necessary for this behavioral flexibility tested in mice(Cho et al., 2015; Cho et al., 2020; Cho et al., 2023).  It is unclear what contributes to this necessary gamma synchrony. The insula is also known to be necessary for proper cognitive function (Gehrlach et al., 2020; Menon et al., 2010; Kayyal et al., 2021), and also has bidirectional connectivity with the mPFC (Gehrlach et al., 2020). Here we apply optogenetic inhibition on the medial insular cortex (mIC) to mPFC projecting (mIC-mPFC) cell bodies and terminals during a Rule-Shifting task in mice to show that this projection is necessary for texture to odor cue rule shifts. We further determine the existence of gamma synchrony between mIC and mPFC parvalbumin interneurons (PVIs) during...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8852v3x4</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hagopian, Lara Louise</name>
        <uri>https://orcid.org/0000-0003-0481-301X</uri>
      </author>
    </item>
    <item>
      <title>An Exploration of the Lived Experiences of Lesbian-Identified Black Women Seeking Sexual and Reproductive Healthcare: An Interpretative Phenomenological Study</title>
      <link>https://escholarship.org/uc/item/7ts2z0ff</link>
      <description>Background: There is a lack of research focusing exclusively on the sexual and reproductive healthcare of lesbian-identified Black women compared to studies with samples of heterosexual-identified and bisexual-identified Black women. Lesbian-identified Black women are likely to have different sexual and reproductive healthcare needs and concerns than heterosexual-identified Black women. An example of such needs includes the need for tailored safer sex options and education on alternative ways of achieving pregnancy, as well as other cultural considerations.Objectives: This dissertation sought to 1) examine and interpret how lesbian-identified Black women navigate accessing sexual and reproductive healthcare, 2) identify and interpret barriers and facilitators to accessing sexual and reproductive healthcare among lesbian-identified Black women, and 3) examine resiliency and protective factors employed by lesbian-identified Black women when navigating sexual and reproductive healthcare.Method:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7ts2z0ff</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Scott-Henderson, Daphne</name>
        <uri>https://orcid.org/0000-0003-4439-3697</uri>
      </author>
    </item>
    <item>
      <title>Deep Learning on Cardiac MRI Videos Embeds Disease-Relevant Phenotypic Features</title>
      <link>https://escholarship.org/uc/item/7h97w8r9</link>
      <description>Cardiac MRI encodes rich spatiotemporal information about cardiac structure and function, yet standard analysis pipelines reduce this signal to scalar phenotypes derived from segmentation, discarding temporal dynamics and constraining discovery to predefined traits. To address this, we fine-tuned a pretrained VideoMAE model on 4-chamber cardiac MRI videos from 60,498 UK Biobank participants using a masked autoencoding objective, generating high-dimensional embeddings without label supervision. Attention analysis revealed preferential weighting of high-motion intra-cardiac regions, consistent with the spatiotemporal reconstruction objective. The embeddings predicted sex with 95.2% accuracy and body surface area with r = 0.85, showed biologically coherent correlations with blood biomarkers including testosterone, SHBG, and HDL cholesterol, and were broadly associated with segmentation-derived cardiac phenotypes, explaining substantial variance across chamber volumes (adjusted R2...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7h97w8r9</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Saylor, Wren</name>
        <uri>https://orcid.org/0000-0002-6806-7469</uri>
      </author>
    </item>
    <item>
      <title>Intraflagellar transport trains can switch rails and move along multiple microtubules in intact primary cilia</title>
      <link>https://escholarship.org/uc/item/7bt8h9xn</link>
      <description>Structural homeostasis and proper distributions of signaling molecules in cilia require a constant flow of cargoes carried by intraflagellar transport (IFT) trains in both anterograde and retrograde directions within the thin, long ciliary shafts. In the motile cilium framework, the nine microtubule doublets of the same length serve as the transportation rails, and a preferential association to the two subtubules of the microtubule doublets prevents collisions among the IFT trains that move in opposite directions. However, this mechanism is incompatible with the primary cilia structure, where most of the nine microtubule doublets terminate in the ciliary shafts-only several of them reach the ciliary tip and only in a singlet form. Here, we demonstrate that anterograde and retrograde trains in primary cilia interact with both subtubules of the microtubule doublets without apparent preference. They can switch microtubules, and they may simultaneously interact with multiple microtubules...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7bt8h9xn</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sun, Shufeng</name>
      </author>
      <author>
        <name>Liang, Biqing</name>
      </author>
      <author>
        <name>Koplas, Adam</name>
      </author>
      <author>
        <name>Tikhonenko, Irina</name>
      </author>
      <author>
        <name>Nachury, Maxence</name>
        <uri>https://orcid.org/0000-0003-4918-1562</uri>
      </author>
      <author>
        <name>Khodjakov, Alexey</name>
      </author>
      <author>
        <name>Sui, Haixin</name>
      </author>
    </item>
    <item>
      <title>A 3D Assessment of Orthodontic Dental Decompensation and Its Relationship to Postoperative Facial Balance and Esthetics in Patients Who Underwent Orthognathic Surgery</title>
      <link>https://escholarship.org/uc/item/71r8f9vs</link>
      <description>Presurgical dental decompensation is a critical step in combined orthodontic–orthognathic treatment, as it systematically reverses natural dentoalveolar compensations across the sagittal, vertical, and transverse planes to fully unmask the underlying skeletal discrepancy. This preparatory phase enables precise surgical repositioning of the jaws, stable postoperative occlusion, and harmonious facial esthetics. Despite its importance, the direct influence of decompensation adequacy on postoperative facial profile attractiveness has remained relatively understudied. The present retrospective investigation tested the central hypothesis that greater achievement of three-dimensional ideal dental decompensation from T1 (initial records) to T2 (presurgical) would correlate with higher postoperative attractiveness ratings at T3 (postsurgical).The study included sixty-two adult patients (34 female, 28 male; mean age 26.4 ± 8.1 years) with skeletal Class III (61.3 %), Class II (25.8 %),...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/71r8f9vs</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ricupito, Michael Eaton</name>
        <uri>https://orcid.org/0009-0008-8976-9436</uri>
      </author>
    </item>
    <item>
      <title>Health Service Use and Costs During Pregnancy Among Privately Insured Individuals With Congenital Heart Disease</title>
      <link>https://escholarship.org/uc/item/6zq2f4g7</link>
      <description>Importance: Individuals with congenital heart disease (CHD) are increasingly reaching childbearing age, are more prone to adverse pregnancy events, and uncommonly undergo recommended cardiac evaluations. Data to better understand resource allocation and financial planning are lacking.
Objective: To examine health care use and costs for patients with CHD during pregnancy.
Design, Setting, and Participants: This retrospective cohort study was performed from January 1, 2010, to December 31, 2016, using Merative MarketScan commercial insurance data. Participants included patients with CHD and those without CHD matched 1:1 by age, sex, and insurance enrollment year. Pregnancy claims were identified for all participants. Data were analyzed from September 2022 to March 2024.
Exposures: Baseline characteristics (age, US region, delivery year, insurance type) and pregnancy-related events (obstetric, cardiac, and noncardiac conditions; birth outcomes; and cesarean delivery).
Main Outcomes...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6zq2f4g7</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Agarwal, Anushree</name>
        <uri>https://orcid.org/0000-0001-8535-3152</uri>
      </author>
      <author>
        <name>Duan, Rong</name>
      </author>
      <author>
        <name>Sobhani, Nasim C</name>
      </author>
      <author>
        <name>Sabanayagam, Aarthi</name>
      </author>
      <author>
        <name>Marcus, Gregory M</name>
        <uri>https://orcid.org/0000-0001-5197-7696</uri>
      </author>
      <author>
        <name>Gurvitz, Michelle</name>
      </author>
    </item>
    <item>
      <title>Neuromodulatory Control of Dentate Gyrus Granule Cells during Discrimination Learning</title>
      <link>https://escholarship.org/uc/item/6w51r8dw</link>
      <description>Animals must continuously update internal representations of the external world to guide adaptive behavior. Individual features of the environment may not initially carry meaning, but through reinforcement, animals learn which cues predict salient outcomes and whether those cues should be approached, avoided, or ignored. A central challenge, however, is that many stimuli share overlapping features despite carrying different meanings. For example, a person in a new apartment building may initially struggle to distinguish among several similar-looking doors, only one of which is their own. To behave appropriately, the brain must balance two competing demands: it must generalize across related experiences that share useful structure, while also discriminating between similar cues when small differences predict different outcomes. Too much generalization can blur important distinctions, whereas too much discrimination can prevent related experiences from being linked. One way neural...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6w51r8dw</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Choi, Hye Sun</name>
        <uri>https://orcid.org/0009-0001-4207-1486</uri>
      </author>
    </item>
    <item>
      <title>Understanding gaps in guideline-recommended adult congenital heart disease care: Data from 12 US health care centers</title>
      <link>https://escholarship.org/uc/item/6vs5h6tf</link>
      <description>BACKGROUND: Guidelines recommend lifelong care with adult congenital heart disease (ACHD) specialists for adults with congenital heart disease (CHD). However, such gaps in visits at specialized ACHD centers have not been well-characterized from diverse US settings.
METHODS: This retrospective study analyzed data from 12 centers in the national Patient-Centered Clinical Research Network. CHD conditions were classified using International Classification of Disease codes and a hierarchical algorithm. ACHD specialists were identified by investigators and encounter volumes. Data from the 'Pre-COVID' (2015-2019) and 'COVID' (2020-2022) periods were analyzed separately. Main outcome measures were: 1) Gaps in any ACHD specialist visit and recommended testing throughout the study period. 2) Gaps in recommended ACHD follow-up care.
RESULTS: During pre-COVID (N = 18,934) and COVID (N = 22,453) periods, between 55.3%-55.8% were males, 27.2%-31.0% were 40+ years, 18.2%-19.6% had severe CHD,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6vs5h6tf</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Bayne, Joseph</name>
      </author>
      <author>
        <name>Duan, Rong</name>
      </author>
      <author>
        <name>Rudov, Lindsey</name>
      </author>
      <author>
        <name>Mehta, Rittal</name>
      </author>
      <author>
        <name>Phillippi, Ruth</name>
      </author>
      <author>
        <name>Roeder, Mark</name>
      </author>
      <author>
        <name>Saraf, Sneha</name>
      </author>
      <author>
        <name>Jackson, Jamie L</name>
      </author>
      <author>
        <name>Lewis, Matthew</name>
      </author>
      <author>
        <name>Saidi, Arwa</name>
      </author>
      <author>
        <name>Kanter, Ronald</name>
      </author>
      <author>
        <name>Sandhu, Satinder</name>
      </author>
      <author>
        <name>Young, Thomas</name>
      </author>
      <author>
        <name>Jacobsen, Roni</name>
      </author>
      <author>
        <name>Ruckdeschel, Emily</name>
      </author>
      <author>
        <name>Lubert, Adam</name>
      </author>
      <author>
        <name>Singh, Harsimran</name>
      </author>
      <author>
        <name>Zaidi, Ali</name>
      </author>
      <author>
        <name>Halpern, Dan G</name>
      </author>
      <author>
        <name>Leezer, Scott</name>
      </author>
      <author>
        <name>John, Anitha S</name>
      </author>
      <author>
        <name>Carton, Thomas</name>
      </author>
      <author>
        <name>Agarwal, Anushree</name>
        <uri>https://orcid.org/0000-0001-8535-3152</uri>
      </author>
      <author>
        <name>Investigators, Congenital Heart Initiative-Redefining Outcomes and Navigation to an Adult-centered Care</name>
      </author>
    </item>
    <item>
      <title>Craniofacial Growth and the Temporomandibular Joint in Orthodontic Patients Undergoing Gender-Affirming Medical Care: A Pilot Study</title>
      <link>https://escholarship.org/uc/item/6s5236f8</link>
      <description>Adolescent patients undergoing gender-affirming medical care are being treated with gonadotropin-releasing hormone agonists (GnRHas) and gender-affirming hormone therapy (GAHT), but the effects of these medications on craniofacial growth potential or temporomandibular joint (TMJ) health have not been studied. This gap in knowledge is significant for the orthodontic clinician especially as this underrepresented population continues to grow. This retrospective pilot study examined orthodontic records and cone-beam computed tomography (CBCT) data from six transgender patients, three transgender male patients taking testosterone therapy and three transgender female patients taking estrogen and spironolactone, to generate preliminary hypotheses on the effects of GAHT on craniofacial growth and TMJ health in the orthodontic context.A transgender male adolescent demonstrated condylar length growth of 2.7 mm between ages 15 and 16, exceeding the expected female norm of 1 mm, suggesting...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6s5236f8</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>O'Neal, Yvonne</name>
        <uri>https://orcid.org/0009-0009-6476-9816</uri>
      </author>
    </item>
    <item>
      <title>Elevated AD biomarkers do not explain cognitive performance in a community‐recruited clinical trial cohort</title>
      <link>https://escholarship.org/uc/item/6pr3b9x9</link>
      <description>INTRODUCTION: To examine the generalizability of Alzheimer's disease (AD) biomarker models in real-world older adults, we examined AD biomarker relationships with cognition in two multicenter cohorts that differ with respect to recruitment approach and health risk factors but were matched on a variety of characteristics.
METHODS: We compared harmonized health and demographic data, AD and cerebrovascular biomarkers, and cognitive performance in the community-recruited U.S. Study to Protect Brain Health Through Lifestyle Intervention to Reduce Risk (U.S. POINTER) Imaging substudy and a matched sample from the Alzheimer's Disease Neuroimaging Initiative (ADNI) which recruited primarily from academic specialty clinics.
RESULTS: Elevated β-amyloid (Aβ) and tau were associated with cognitive performance in ADNI but not U.S. POINTER. Findings were consistent across different cohort matching schemes, and were not explained by discrepancies in vascular risk.
DISCUSSION: The role of Aβ...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6pr3b9x9</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Landau, Susan M</name>
      </author>
      <author>
        <name>Liu, Peiwei</name>
      </author>
      <author>
        <name>Harrison, Theresa M</name>
      </author>
      <author>
        <name>Taggett, Jacinda</name>
      </author>
      <author>
        <name>Ward, Tyler J</name>
      </author>
      <author>
        <name>Murphy, Alice</name>
      </author>
      <author>
        <name>Lockhart, Samuel N</name>
      </author>
      <author>
        <name>Lovato, Laura C</name>
      </author>
      <author>
        <name>Koeppe, Robert</name>
      </author>
      <author>
        <name>Farias, Sarah Tomaszewski</name>
      </author>
      <author>
        <name>Papp, Kathryn V</name>
      </author>
      <author>
        <name>Snyder, Heather M</name>
      </author>
      <author>
        <name>Harvey, Danielle J</name>
        <uri>https://orcid.org/0000-0002-5367-0951</uri>
      </author>
      <author>
        <name>Espeland, Mark</name>
      </author>
      <author>
        <name>Maillard, Pauline</name>
      </author>
      <author>
        <name>DeCarli, Charles</name>
      </author>
      <author>
        <name>Vemuri, Prashanthi</name>
      </author>
      <author>
        <name>Weiner, Michael</name>
        <uri>https://orcid.org/0000-0002-0877-4583</uri>
      </author>
      <author>
        <name>Baker, Laura D</name>
      </author>
      <author>
        <name>Jagust, William J</name>
      </author>
      <author>
        <name>Weiner, Michael W</name>
      </author>
      <author>
        <name>Trojanowski, John Q</name>
      </author>
      <author>
        <name>Shaw, Leslie</name>
      </author>
      <author>
        <name>Beckett, Laurel</name>
      </author>
      <author>
        <name>Aisen, Paul</name>
      </author>
      <author>
        <name>Petersen, Ronald</name>
      </author>
      <author>
        <name>Saykin, Andrew J</name>
      </author>
      <author>
        <name>Toga, Arthur W</name>
      </author>
      <author>
        <name>Jack, Clifford</name>
      </author>
      <author>
        <name>Morris, John C</name>
      </author>
      <author>
        <name>Jagust, William</name>
      </author>
      <author>
        <name>Landau, Susan M</name>
      </author>
      <author>
        <name>Baker, Laura D</name>
      </author>
      <author>
        <name>Espeland, Mark A</name>
      </author>
      <author>
        <name>Vemuri, Prashanthi</name>
      </author>
      <author>
        <name>DeCarli, Charles</name>
        <uri>https://orcid.org/0000-0003-1914-2693</uri>
      </author>
      <author>
        <name>Harrison, Theresa M</name>
      </author>
      <author>
        <name>Koeppe, Robert A</name>
      </author>
      <author>
        <name>Jagust, William J</name>
      </author>
      <author>
        <name>Maillard, Pauline</name>
        <uri>https://orcid.org/0000-0003-3516-6345</uri>
      </author>
      <author>
        <name>Jung, Youngkyoo</name>
        <uri>https://orcid.org/0000-0002-7236-8897</uri>
      </author>
      <author>
        <name>Lovato, Laura</name>
      </author>
      <author>
        <name>Harvey, Danielle J</name>
      </author>
      <author>
        <name>Toga, Arthur W</name>
      </author>
      <author>
        <name>Zamora, Ezequiel</name>
      </author>
      <author>
        <name>Cleveland, Jo</name>
      </author>
      <author>
        <name>DeCarli, Charles</name>
      </author>
      <author>
        <name>Whitmer, Rachel</name>
      </author>
      <author>
        <name>Aggarwal, Neelum</name>
      </author>
      <author>
        <name>Tangney, Christy</name>
      </author>
      <author>
        <name>Gitelman, Darren</name>
      </author>
      <author>
        <name>Masdeu, Joseph</name>
      </author>
      <author>
        <name>Pavlik, Valory</name>
      </author>
      <author>
        <name>Yu, Melissa</name>
      </author>
      <author>
        <name>Oh, Hwamee</name>
      </author>
      <author>
        <name>Huey, Edward</name>
      </author>
      <author>
        <name>Salloway, Steve</name>
      </author>
      <author>
        <name>Wing, Rena</name>
      </author>
    </item>
    <item>
      <title>Advancing Preclinical Radiotherapy through High-Throughput Automation, Deep Learning Segmentation, and Plan Optimization</title>
      <link>https://escholarship.org/uc/item/6gx6r8x2</link>
      <description>Purpose: The translation of modern clinical radiotherapy techniques to preclinical small-animal models is often hindered by hardware limitations, soft-tissue imaging deficits, and inefficient treatment planning. This dissertation aims to address these translational challenges by developing an integrated automated framework for precision preclinical radiotherapy, incorporating high throughput hardware, deep learning-based segmentation, and advanced plan optimization.
      Methods: The framework was developed across three interconnected domains. First, a custom high-throughput automated platform and a sparse orthogonal collimator were integrated into a commercial small animal irradiator to enable streamlined treatment delivery. Second, deep learning architectures were developed for micro-cone-beam computed tomography segmentation. A transformer-based network was trained for robust multi-organ contouring, and a generative adversarial network was utilized for anatomy-constrained...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6gx6r8x2</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Jiang, Lu</name>
        <uri>https://orcid.org/0000-0002-7616-1746</uri>
      </author>
    </item>
    <item>
      <title>Advanced Computational Methods for Radiation Therapy: GPU-Accelerated Photon Dose Calculation, Treatment Plan Optimization, and Statistical Modeling of Primary Proton Fluence</title>
      <link>https://escholarship.org/uc/item/6g4299xz</link>
      <description>Accurate and efficient radiation dose calculation and treatment plan optimization are central to modern radiotherapy. This dissertation addresses computational challenges in two complementary areas: GPU-accelerated photon dose calculation and 4-pi non-coplanar treatment planning, and the statistical modeling of primary proton transport as a foundation for analytical proton dose calculation.
      The first contribution is UHPP (Ultra-High Performance Parallel), a GPU-accelerated framework for 4-pi non-coplanar radiotherapy planning. 4-pi plans exploit the full solid angle of beam directions accessible to a standard linac, offering superior dose conformality compared to coplanar VMAT, but require computing dose-loading matrices for thousands of candidate beams—a task that exceeds the throughput of existing methods. UHPP addresses this through three technical innovations: a two-step TERMA computation with area rescaling that eliminates aliasing artifacts, a synchronized collapsed-cone...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6g4299xz</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Xu, Qifan</name>
        <uri>https://orcid.org/0000-0002-7155-9552</uri>
      </author>
    </item>
    <item>
      <title>The Role of KCNT1 in Ciliary Biology</title>
      <link>https://escholarship.org/uc/item/632503qb</link>
      <description>KCNT1-related epilepsy is a severe neurodevelopmental disorder caused by pathogenic variants in KCNT1, which encodes a sodium-activated potassium channel. In addition to frequent, often treatment-resistant seizures, affected individuals may experience respiratory complications, cardiac abnormalities, hypotonia, skeletal fragility, and gastrointestinal dysfunction. Standard anti-seizure medications are typically ineffective, leaving patients and their caregivers to manage a broad and complex set of symptoms. Although there has been a concerted effort to find better treatment and care for KCNT1 individuals, the underlying mechanism in which mutations in KCNT1 result in multi-organ disorder remains unclear. This dissertation focuses on the role of KCNT1 beyond the synapse, specifically on cilia. In chapter 2, we provide evidence that KCNT1 localizes to both motile and primary cilia across cell types and species and explored overexpression of KCNT1. In chapter 3, we characterized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/632503qb</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chemel, Angeline Katia</name>
        <uri>https://orcid.org/0000-0002-7040-2270</uri>
      </author>
    </item>
    <item>
      <title>Mitoredox shifts in mitochondrial dysfunction</title>
      <link>https://escholarship.org/uc/item/5vc693vm</link>
      <description>Mitoredox shifts in mitochondrial dysfunction</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5vc693vm</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moos, Walter H</name>
        <uri>https://orcid.org/0000-0001-7244-811X</uri>
      </author>
      <author>
        <name>Faller, Douglas V</name>
      </author>
      <author>
        <name>Glavas, Ioannis P</name>
      </author>
      <author>
        <name>Kanara, Iphigenia</name>
      </author>
      <author>
        <name>Kodukula, Krishna</name>
      </author>
      <author>
        <name>Pernokas, Julie</name>
      </author>
      <author>
        <name>Pernokas, Mark</name>
      </author>
      <author>
        <name>Pinkert, Carl A</name>
      </author>
      <author>
        <name>Powers, Whitney R</name>
      </author>
      <author>
        <name>Sampani, Konstantina</name>
      </author>
      <author>
        <name>Steliou, Kosta</name>
      </author>
      <author>
        <name>Vavvas, Demetrios G</name>
      </author>
    </item>
    <item>
      <title>INVESTIGATING THE EFFECTS OF CHROMATIN CONDENSATES, CHROMATIN BINDING PROTEINS, AND CHROMATIN REMODELERS ON NUCLEOSOMAL ACCESSIBILITY AND POSITIONING</title>
      <link>https://escholarship.org/uc/item/5mw247w0</link>
      <description>The genome is broadly organized into compartments of active chromatin (euchromatin) and inactive chromatin (heterochromatin). These compartments were first described by cytological staining due to differences in chromatin density (1), then later characterized via Hi-C contact maps (2). In general, heterochromatin is less accessible than euchromatin. It has been proposed that the difference in accessibility is due to nucleosomes in heterochromatin having more restricted motion compared to euchromatic nucleosomes, and heterochromatin having higher viscoelastic resistance than euchromatin (3-5).The molecular mechanisms that underlie these differences between eu- and heterochromatin are not well understood. We know that some euchromatic regions have epigenetic modifications that inherently cause chromatin de-condensation (6, 7), but this only accounts for a small set of genomic regions. Thus, it is likely that proteins enriched in euchromatin could further decondense euchromatin and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5mw247w0</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moore, Camille Marie</name>
        <uri>https://orcid.org/0000-0002-3324-789X</uri>
      </author>
    </item>
    <item>
      <title>Dynamics Of Button-Like Lymphatic Endothelial Cell Junctions In Airway Development And Inflammation</title>
      <link>https://escholarship.org/uc/item/55r534bc</link>
      <description>Dynamics Of Button-Like Lymphatic Endothelial Cell Junctions In Airway Development And Inflammation</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/55r534bc</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yao, Li-Chin</name>
      </author>
      <author>
        <name>Baluk, Peter</name>
      </author>
      <author>
        <name>McDonald, Donald M</name>
        <uri>https://orcid.org/0000-0002-6985-9564</uri>
      </author>
    </item>
    <item>
      <title>Differences in Concentration of Growth Factor Proteins in PRF among Diabetics and Non-Diabetics with Respect to Age: An Exploratory Study</title>
      <link>https://escholarship.org/uc/item/4wt407xs</link>
      <description>Platelet-rich fibrin (PRF) is an autologous biomaterial used in periodontal and oral regenerative procedures because it contains growth factors that support wound healing. Diabetes mellitus is associated with impaired healing and may affect PRF composition, but the relationships among diabetic status, age, and PRF growth factor levels are not well defined. This exploratory case-control study examined platelet-derived growth factor-BB (PDGF-BB) and vascular endothelial growth factor (VEGF) concentrations in PRF from 15 subjects: 10 healthy, non-diabetic controls and 5 subjects with diabetes. PRF was made using a standardized centrifugation protocol, and ELISA measured PDGF-BB and VEGF. Two readings were taken for each sample, and the mean value was used for analysis. Descriptive summaries and exploratory regression models were used to examine possible correlations among diabetic status, age, sex, and HbA1c. A mean PDGF-BB concentration of 4,292.6 ± 922.8 pg/mL was found in healthy...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4wt407xs</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Viets, Helena Louise</name>
        <uri>https://orcid.org/0009-0003-8584-9600</uri>
      </author>
    </item>
    <item>
      <title>Automated segmentation of soft X-ray tomography: Native cellular structure with submicron resolution at high-throughput for whole-cell quantitative imaging in yeast.</title>
      <link>https://escholarship.org/uc/item/41p6v8d6</link>
      <description>Soft X-ray tomography (SXT) is an invaluable tool for quantitatively analyzing cellular structures at suboptical isotropic resolution. However, it has traditionally depended on manual segmentation, limiting its scalability for large datasets. Here, we leverage a deep learning-based autosegmentation pipeline to segment and label cellular structures in hundreds of cells across three &lt;i&gt;Saccharomyces cerevisiae&lt;/i&gt; strains. This task-based pipeline uses manual iterative refinement to improve segmentation accuracy for key structures, including the cell body, nucleus, vacuole, and lipid droplets, enabling high-throughput and precise phenotypic analysis. Using this approach, we quantitatively compared the three-dimensional (3D) whole-cell morphometric characteristics of wild-type, VPH1-GFP, and &lt;i&gt;vac14&lt;/i&gt; strains, uncovering detailed strain-specific cell and organelle size and shape variations. We show the utility of SXT data for precise 3D curvature analysis of entire organelles...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/41p6v8d6</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Jianhua</name>
        <uri>https://orcid.org/0000-0002-7998-0878</uri>
      </author>
      <author>
        <name>Mirvis, Mary</name>
      </author>
      <author>
        <name>Ekman, Axel</name>
      </author>
      <author>
        <name>Vanslembrouck, Bieke</name>
      </author>
      <author>
        <name>Gros, Mark Le</name>
      </author>
      <author>
        <name>Larabell, Carolyn</name>
      </author>
      <author>
        <name>Marshall, Wallace F</name>
      </author>
    </item>
    <item>
      <title>Modulation of turn-related activity in the superior colliculus by ongoing behavioral and cognitive dynamics</title>
      <link>https://escholarship.org/uc/item/3xk5x1mz</link>
      <description>The superior colliculus (SC) is a highly conserved sensorimotor midbrain structure implicated in the control of orienting movements. Yet, despite decades of research, it remains unclear how neural activity in this structure unfolds during internally-driven behaviors like spatial navigation, when orienting movements need to be coordinated with other ongoing behavioral and cognitive processes. This dissertation aims to address this gap. By recording from neurons in the intermediate and deep motor layers of the SC (dSC) of mice navigating a Y-maze, it is demonstrated that: 1) About 30% of neurons fire selectively for left or right turns at the maze bifurcation (left- or right-preferring ‘turn cells’). 2) Turn cell activity is rhythmically modulated during locomotion, firing in-phase with the ongoing stepping cycle of the animal, such that left and right turn cells fire at opposite phases of the stepping cycle. 3) Simultaneous recordings from turn cells and populations of hippocampal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3xk5x1mz</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wilhite, Cameron</name>
        <uri>https://orcid.org/0000-0002-5655-2010</uri>
      </author>
    </item>
    <item>
      <title>Bytes to blood: Artificial intelligence in leukemia management—A 2025 update.</title>
      <link>https://escholarship.org/uc/item/3px3n399</link>
      <description>e18557   Background: Artificial intelligence (AI) has been proposed as a tool to aid in the diagnosis, treatment, and monitoring of leukemias given their genetic complexity, subtype heterogeneity, array of treatments, and need for relapse detection. AI has several potential applications in the management of leukemia. First, it can be used to detect leukemia. Using AI to detect subtle nuances in lab values can ensure these deadly cancers are never missed and that complications, such as disseminated intravascular coagulation, are recognized quickly. Second, AI can be used to risk-stratify patients and personalize treatments. Leukemias are among the most genetically complex cancers and, while they have well-characterized risk profiles, tailoring treatments remains a challenge despite our advances. And third, AI can be used for surveillance ( e.g. , minimal/measurable residual disease [MRD] testing) and relapse management. There is a role for AI in predicting risk of relapse and determining...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3px3n399</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Runde, Austin P</name>
      </author>
      <author>
        <name>Koo, Stephanie Mei</name>
      </author>
      <author>
        <name>Daneshpajouhnejad, Parnaz</name>
        <uri>https://orcid.org/0000-0002-8845-5813</uri>
      </author>
      <author>
        <name>Shahid, Ramzan</name>
      </author>
      <author>
        <name>Slasuraitis, Andrea</name>
      </author>
      <author>
        <name>Speisman, Melvin</name>
      </author>
    </item>
    <item>
      <title>microRNAs and TGFβ&amp;nbsp;signaling: Molecular regulators of osteocytes and bone biomechanics in appendicular and craniofacial skeleton</title>
      <link>https://escholarship.org/uc/item/3pp5p18g</link>
      <description>Bone is a unique tissue that carries both mineralized and connective components, contributing to its malleability and strength in resisting fractures and protecting internal organs. Despite the stagnant look of the tissue, bone undergoes constant remodeling to resorb and replenish its mineral and organic constituents. Of the bone cells, osteocytes contribute to bone health maintenance by orchestrating bone remodeling in response to mechanical load. Osteocytes are housed inside an intricate network of lacunae and canaliculi called the lacunocanalicular network (LCN) and serve to directly remodel the matrix surrounding LCN as well as regulate osteoclastic bone resorption and osteoblastic bone formation at the whole bone level. Mechanical load on the bone at the tissue level stimulates fluid shear stress in the lacunocanalicular network, allowing osteocytes to sense and transmit the mechanical force to downstream intracellular signaling pathways. However, specific molecular mechanisms...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3pp5p18g</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yoon, Jihee</name>
        <uri>https://orcid.org/0000-0001-9677-3419</uri>
      </author>
    </item>
    <item>
      <title>Measuring confidence for community-based childbirth in the United States: A mixed methods study with CHOICES Memphis Center for Reproductive Health</title>
      <link>https://escholarship.org/uc/item/3p65m7gq</link>
      <description>Background Fear during pregnancy and birth can worsen health care experiences and outcomes, especially among populations experiencing racism, disrespect and reproductive inequities. Far less is known about an important counterpart, confidence. Methods This dissertation aimed to elucidate the pathways through which midwifery-led care impacts prenatal confidence for physiologic birth and to inform future care, centering the perspectives of Black populations. The work includes a participatory instrument adaptation resulting in the Preparation for Community-based Labor and Birth (P-CLAB) to measure confidence for community-based birth; a mixed methods study of prenatal confidence from the perspective of birth center patients and providers; and the qualitative and psychometric evaluation of the P-CLAB. Findings The iterative development of the P-CLAB resulted in a Likert-response survey prioritizing measures of safety, dignity, and racial concordance. Through engagement with patients...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3p65m7gq</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Mitchell, Ashley</name>
        <uri>https://orcid.org/0000-0002-6351-3204</uri>
      </author>
    </item>
    <item>
      <title>BMP Signaling Coordinates the Neurogenesis of Dorsal and Ventral Fates During Spinal Cord Regeneration</title>
      <link>https://escholarship.org/uc/item/3nn3811r</link>
      <description>Zebrafish fully regenerate and recover locomotor function after spinal cord injury (SCI), but whether and/or how developmental signals are redeployed to rebuild functional circuits remains unclear. During development, Bone Morphogenetic Protein (BMP) signaling patterns dorsal neural tube fates, but whether this pathway fulfills a similar function during SCI-based regeneration is unknown. Here we show that SCI triggers a broad elevation in BMP pathway activity in the larval zebrafish spinal cord, accompanied by upregulation of the BMP receptor bmpr2b in neural progenitors. Disruption of BMP signaling impairs locomotor recovery, producing a phenotype in which larvae initiate movement but fail to sustain or propagate swimming. At the cellular level, BMP inhibition selectively reduces regeneration of dI1 and dI2 dorsal sensory-relay interneurons and v1 and v2a ventral premotor interneurons, with reduced consequences for other neuronal subclasses. Together, these findings reveal that...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3nn3811r</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Roy, Irena</name>
        <uri>https://orcid.org/0000-0002-6924-4471</uri>
      </author>
    </item>
    <item>
      <title>Neural Systems for Sensory and Social Processing</title>
      <link>https://escholarship.org/uc/item/3fv1c4tj</link>
      <description>Communication, the transfer of social information from one individual to another via sensory signals, is essential for life across animal species.  The neural circuitry that supports sending and interpreting these signals is incompletely understood.  Responding to communication signals involves sensory processing, representation of internal states such as reproductive status, and representation of the other party in an interaction.  This work addresses sensory processing systems, communication behaviors, neuromodulator control of neural responses to social behavior, and the genetics of the circuits that control these processes.  I demonstrated that amplitude modulated sounds are processed differently in laboratory mice and squirrel monkey primary auditory cortex.  I documented the evolution of prairie vole ultrasonic vocalizations across pair bonding.  I examined the neural activity associated with chemosensory investigation during pair bonding and showed that loss of oxytocin...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3fv1c4tj</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hoglen, Nerissa</name>
        <uri>https://orcid.org/0000-0002-4841-4275</uri>
      </author>
    </item>
    <item>
      <title>Prevalence and Personal and Occupational Risk Factors Associated with Postpartum Depression among Registered Nurses</title>
      <link>https://escholarship.org/uc/item/3cc0n9v7</link>
      <description>Introduction: Postpartum depression (PPD) is a common mental health condition that occurs within the first 12 months after childbirth. Complications of severe and untreated PPD are associated with increased risk of maternal mortality. Risk factors are well-established in the general population; however, far less is known about PPD in specific occupational groups, including registered nurses (RNs). The RN profession is one of the few professions dominated by women in the United States, and nurses have much higher rates of depression unrelated to pregnancy compared to the general population, which is a strong predictor for the development of PPD. The prevalence and unique risk factors of PPD among RNs are unknown. To better understand how personal and occupational factors may contribute to PPD, two theories were leveraged to create a conceptual model: 1) Teetering on the Edge: A substantive theory of postpartum depression, and 2) the Person-Environment Fit Theory. These theories,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3cc0n9v7</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Mariano, Karley</name>
        <uri>https://orcid.org/0000-0002-0933-5769</uri>
      </author>
    </item>
    <item>
      <title>Naturalistic outcomes for a day‐hospital programme in a mixed diagnostic sample of adolescents with eating disorders</title>
      <link>https://escholarship.org/uc/item/3548r21t</link>
      <description>Despite initial data suggesting positive treatment outcomes for adolescent eating disorder day-hospital programmes (DHPs), existing studies have included limited follow-up, small samples, and a focus on restricting-type eating disorders. To address these gaps, we explored naturalistic outcomes for an adolescent eating disorders DHP. Adolescent participants (N = 265) completed measurements at treatment admission, discharge (n = 170), and various lengths of follow-up (n = 126; M&lt;sub&gt;follow up&lt;/sub&gt; = 278.87 days). Results from multilevel models indicated significant increases in body weight for the anorexia nervosa group throughout treatment and maintenance of increased body weight from discharge to follow-up. In bulimic spectrum disorders, binge eating and purging significantly decreased from intake to discharge and did not change from discharge to follow-up. Across the entire sample, eating disorder symptoms decreased from intake to discharge and did not change from discharge...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3548r21t</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Reilly, Erin E</name>
        <uri>https://orcid.org/0000-0001-9269-0747</uri>
      </author>
      <author>
        <name>Rockwell, Roxanne E</name>
      </author>
      <author>
        <name>Ramirez, Ana L</name>
      </author>
      <author>
        <name>Anderson, Leslie K</name>
      </author>
      <author>
        <name>Brown, Tiffany A</name>
      </author>
      <author>
        <name>Wierenga, Christina E</name>
        <uri>https://orcid.org/0000-0002-4843-1809</uri>
      </author>
      <author>
        <name>Kaye, Walter H</name>
        <uri>https://orcid.org/0000-0002-4478-4906</uri>
      </author>
    </item>
    <item>
      <title>Predictability of a Dental Implant Prognosis System: A Retrospective Study</title>
      <link>https://escholarship.org/uc/item/344666gv</link>
      <description>Prognosis refers to the prediction of a disease’s course and outcome. While several systems exist for natural dentition, implant-specific prognosis systems remain limited. Kwok et al. 2023 proposed a dental implant prognosis system based on peri-implant supporting tissue stability and patient-related risk factors. This study aims to evaluate the predictability of this system by assessing implant survival across initial prognosis categories over a five-year period. A total of 651 implants from 291 patients were included. Baseline examinations were conducted at the time of implant-supported prosthesis delivery, with follow-up examinations at least 12 months later. Implants were categorized as favorable, questionable, unfavorable, or hopeless according to the Kwok et al. classification. Recorded variables included age, sex, follow-up duration, supportive care, history of Grade C periodontitis, smoking, diabetes, and use of intravenous bone-sparing agents. Implants initially classified...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/344666gv</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Young, Kristen Hsi</name>
        <uri>https://orcid.org/009-0000-8679-8102</uri>
      </author>
    </item>
    <item>
      <title>Metabolic MRI of Brain Function: Methods Development and Multimodal Applications</title>
      <link>https://escholarship.org/uc/item/2zz2f159</link>
      <description>Brain function depends on a tightly regulated interplay between vascular delivery, neuronal activity, glial support, and energy metabolism. Disturbances in this coupling are central to two of the most common causes of age-related cognitive decline — Alzheimer's disease (AD) and cerebral small vessel disease (cSVD) — yet the tools most commonly used to study them in vivo remain fragmented. Positron emission tomography (PET) with [¹⁸F]FDG reports glucose uptake but requires ionizing radiation and cyclotron infrastructure; magnetic resonance imaging (MRI) offers structural, vascular, and spectroscopic contrast but has historically lacked a practical, non-ionizing readout of glucose metabolism, and the multimodal datasets it produces have outpaced the analyses applied to them. This dissertation advances metabolic MRI as an integrated framework along three steps: combining established MRI contrasts to phenotype a monogenic cerebrovascular disease; developing a new MRI contrast to fill...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2zz2f159</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gao, Xiao</name>
        <uri>https://orcid.org/0000-0002-6175-5840</uri>
      </author>
    </item>
    <item>
      <title>Inadequate Support. Reply.</title>
      <link>https://escholarship.org/uc/item/2nx395g1</link>
      <description>Inadequate Support. Reply.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2nx395g1</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Pichan, Cayla</name>
      </author>
      <author>
        <name>Dhaliwal, Gurpreet</name>
      </author>
      <author>
        <name>Houchens, Nathan</name>
      </author>
    </item>
    <item>
      <title>Tissue, Teamwork, and Timing: an Exercise in Clinical Reasoning</title>
      <link>https://escholarship.org/uc/item/2j4091m5</link>
      <description>Tissue, Teamwork, and Timing: an Exercise in Clinical Reasoning</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2j4091m5</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ahmad, Tessnim R</name>
      </author>
      <author>
        <name>Kazberouk, Alexander</name>
      </author>
      <author>
        <name>Santhosh, Lekshmi</name>
        <uri>https://orcid.org/0000-0002-9897-3462</uri>
      </author>
      <author>
        <name>Hsu, Gerald</name>
      </author>
      <author>
        <name>Dhaliwal, Gurpreet</name>
      </author>
    </item>
    <item>
      <title>Diet texture, not fiber content, modulates host and microbial phenotypes linked to periodontitis</title>
      <link>https://escholarship.org/uc/item/2cf296dp</link>
      <description>The Western diet, characterized by high consumption of refined, processed grains, has been epidemiologically associated with elevated periodontal disease risk, yet the mechanisms underlying this relationship remain incompletely understood. Grain refinement simultaneously removes dietary fiber and reduces food texture, producing a soft, rapidly fermentable substrate that may promote oral biofilm dysbiosis through two distinct but potentially synergistic pathways: augmented saccharide substrate availability to saccharolytic pioneer species, and loss of the masticatory mechanical challenge that limits biofilm maturation and sustains homeostatic gingival immune signaling. Whether the protective effects of whole grain consumption are attributable to its fiber content, its structural and textural properties, or both has not been experimentally resolved.The present thesis employed a multi-diet murine experimental framework to dissociate the contributions of dietary texture and fiber...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cf296dp</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sedghi, Lea Maryam</name>
        <uri>https://orcid.org/0000-0002-0263-3683</uri>
      </author>
    </item>
    <item>
      <title>Quantitative tools for decision-making in tuberculosis drug development and utilization</title>
      <link>https://escholarship.org/uc/item/28t6r55j</link>
      <description>Tuberculosis (TB) is the deadliest infectious disease worldwide, taking the lives of 1.23 million individuals in 2024. While TB is curable, the current pharmacological standard-of-care is arduous—requiring months of strict adherence to a four-drug regimen that carries risks for significant toxicities. Thus, ongoing developmental efforts concentrate on advancing safe and effective regimens with shorter treatment durations for cure. Yet, in the past several decades, only a few novel, shortened regimens have been found successful in Phase 3 clinical trials. This paucity of new therapies is due to several facets associated with TB drug development, including the need for multi-drug regimens to prevent resistance, the presence of highly variable patient phenotypes, the prolonged final clinical endpoint of relapse-free cure, and the lack of a standardized paradigm in translational decision-making. The work presented here applies integrated preclinical and clinical modeling and simulation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/28t6r55j</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Patel, Anu</name>
        <uri>https://orcid.org/0000-0003-0628-668X</uri>
      </author>
    </item>
    <item>
      <title>Changes in Treponeme community after non-surgical therapy in patients with chronic periodontitis</title>
      <link>https://escholarship.org/uc/item/26p1j8sw</link>
      <description>Periodontitis is a chronic, multifactorial inflammatory disease affecting 42% of US adults over the age of 30, characterized by progressive destruction of tooth-supporting structures associated with dysbiotic subgingival biofilms. Treponema denticola, a member of the Red complex, is one of the identified pathogenic bacteria that is strongly associated with the progression of periodontal disease. Advances in full-length 16S rRNA sequencing now allows for high-resolution taxonomic identification of Treponema species, including uncultivable phylotypes previously undetectable by traditional methods. The aim of this study was to investigate the relationship between subgingival Treponema community composition and clinical treatment outcomes following non-surgical periodontal therapy, with the hypothesis that greater reductions in Treponema relative abundance would be associated with improved clinical outcomes.Twenty-eight patients were initially enrolled in this study. Subjects over...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/26p1j8sw</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Arroyo, Nicholas</name>
        <uri>https://orcid.org/0009-0004-7051-4821</uri>
      </author>
    </item>
    <item>
      <title>Immune Interference</title>
      <link>https://escholarship.org/uc/item/21p9k545</link>
      <description>A 62-year-old man was admitted to the hospital for malaise, anorexia, rash, and diffuse lymphadenopathy. Fatigue and anorexia began 6 months earlier. Four months before admission, a pruritic rash d...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/21p9k545</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Matsumura, Masami</name>
      </author>
      <author>
        <name>Kanda, Naoki</name>
      </author>
      <author>
        <name>Hatakeyama, Shuji</name>
      </author>
      <author>
        <name>Dhaliwal, Gurpreet</name>
      </author>
    </item>
    <item>
      <title>A Short‐Lived Crisis</title>
      <link>https://escholarship.org/uc/item/1xf8q95k</link>
      <description>A Short‐Lived Crisis</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1xf8q95k</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Saxena, Kapil</name>
        <uri>https://orcid.org/0000-0001-5393-7313</uri>
      </author>
      <author>
        <name>Dhaliwal, Gurpreet</name>
      </author>
      <author>
        <name>Rao, Madhu N</name>
      </author>
      <author>
        <name>Babik, Jennifer M</name>
      </author>
    </item>
    <item>
      <title>Medication Management Among Older Adults Living Alone With Cognitive Impairment.</title>
      <link>https://escholarship.org/uc/item/1qx8m9c3</link>
      <description>Importance: More than one-fourth of older individuals in the US with cognitive impairment live alone. These individuals often lack support for medication management and face a high risk of medication-related harm.
Objective: To elucidate barriers and facilitators to medication management experienced by older adults living alone with cognitive impairment and their social contacts.
Design, Setting, and Participants: This qualitative study was conducted between May 2016 and February 2024 among adults of diverse racial and ethnic backgrounds aged 55 years or older living alone with cognitive impairment in California, Louisiana, and Michigan (ie, participants), along with their social contacts, defined as family members or other familiar persons. Data were analyzed between February 2024 and March 2025.
Main Outcomes and Measures: As part of the Living Alone With Cognitive Impairment Project, participants' and social contacts' perspectives regarding barriers and facilitators were elicited...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1qx8m9c3</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Growdon, Matthew E</name>
        <uri>https://orcid.org/0000-0001-5997-4406</uri>
      </author>
      <author>
        <name>Harrison, Krista L</name>
        <uri>https://orcid.org/0000-0001-5373-3011</uri>
      </author>
      <author>
        <name>Steinman, Michael A</name>
        <uri>https://orcid.org/0000-0002-9564-9480</uri>
      </author>
      <author>
        <name>Hunt, Lauren J</name>
      </author>
      <author>
        <name>Stone, Robyn I</name>
      </author>
      <author>
        <name>Tran, Thi</name>
      </author>
      <author>
        <name>Johnson, Julene K</name>
      </author>
      <author>
        <name>Portacolone, Elena</name>
      </author>
    </item>
    <item>
      <title>NET Rounding: A Standardized Rounding Intervention to Improve Rounding Efficiency and Optimize the Inpatient Experience for Internal Medicine Attendings and Residents</title>
      <link>https://escholarship.org/uc/item/1qk6n6fv</link>
      <description>OBJECTIVES: There is a scarcity of published best practices for efficient and effective hospital rounds. We introduced a standardized rounding intervention (NET Rounding, or &lt;i&gt;Novel&lt;/i&gt; Rounding Practices, Shared &lt;i&gt;Expectations&lt;/i&gt;, and &lt;i&gt;Time&lt;/i&gt; Management) with the primary aims of improving rounding efficiency, reducing resident work-hour violations, and positively affecting clinician experience. Secondary aims included identifying efficient rounding practices and describing the intervention's impact on the attending and resident experience.
METHODS: A standardized rounding intervention was implemented February-June 2022. Attendings and residents completed preintervention surveys October 2021-January 2022 and postintervention surveys immediately after their inpatient rotation during the intervention period. Survey data were compared using qualitative thematic analysis along with χ&lt;sup&gt;2&lt;/sup&gt; and Fisher exact tests to assess intervention uptake, helpfulness of rounding strategies,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1qk6n6fv</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Insetta, Emily R</name>
      </author>
      <author>
        <name>Barish, Peter</name>
      </author>
      <author>
        <name>Baskin, Nathan</name>
      </author>
      <author>
        <name>Brusca, Rebeccah M</name>
      </author>
      <author>
        <name>Chia, David</name>
      </author>
      <author>
        <name>Oreper, Sandra</name>
      </author>
      <author>
        <name>Chan, Shirley</name>
      </author>
      <author>
        <name>Kantor, Molly A</name>
      </author>
      <author>
        <name>Conner, Stephanie M</name>
      </author>
    </item>
    <item>
      <title>Cranial base and facial morphology and severity of clefting: a geometric morphometric analysis</title>
      <link>https://escholarship.org/uc/item/1kp0z6hr</link>
      <description>Background: Cleft lip with or without cleft palate (CL/P) results from failed fusion of the facial prominences during embryogenesis. The cranial base, shaped largely by intrinsic developmental controls, serves as a practical proxy for the embryonic brain morphology that governs facial prominence positioning and fusion timing. Its relationship to CL/P severity in humans remains incompletely characterized.Objectives: To compare basicranial and facial shape between CL/P and non-cleft individuals, quantify their morphological covariation, and determine whether these parameters correlate with cleft severity.Materials and Methods: CBCT images from 30 children with non-syndromic CL/P (ages 7–11), acquired prior to alveolar bone grafting or orthodontic treatment, were compared to 29 age- and sex-matched controls. Thirty-nine basicranial and 29 facial three-dimensional landmarks were placed and analyzed using geometric morphometrics in MorphoJ, including Procrustes superimposition, PCA,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1kp0z6hr</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ran-Sukkawala, Marrina Ruomei</name>
        <uri>https://orcid.org/0009-0003-2736-7152</uri>
      </author>
    </item>
    <item>
      <title>Identification of single guide editing strategy in TNFAIP3/A20 for improving adoptive cell therapy anti-tumor efficacy</title>
      <link>https://escholarship.org/uc/item/1b71m4h3</link>
      <description>Tumors drive T cell exhaustion in both tumor-infiltrating lymphocytes and CAR T cells, marked by increased inhibitory receptor expression, impaired cytotoxicity, and reduced cytokine production, ultimately limiting durable clinical responses. In this work, I have performed a high-density base editor screen of A20/TNFAIP3, a multifunctional ubiquitin-modifying protein, to map variants to T cell functions. In addition, we performed genome-wide loss-of-function screening in repetitively stimulated human T cells and identified the multifunctional ubiquitin-modifying protein A20/TNFAIP3 as a major negative regulator of exhausted T cell persistence. Protein large language modeling, deep base-editing mutagenesis, and studies in immunocompetent mice with domain-specific inactivating mutations revealed A20’s non-enzymatic M1 ubiquitin-binding zinc finger 7 (A20ZF7) motif as critical to suppression of anti-tumor immunity. A20ZF7-deficient CD8+ tumor-infiltrating lymphocytes (TILs) resisted...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1b71m4h3</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sandoval, Luis Roberto</name>
        <uri>https://orcid.org/0000-0001-8654-7530</uri>
      </author>
    </item>
    <item>
      <title>Conceptualizing the Experience of Surgical Smoke: A Mixed Methods Inquiry</title>
      <link>https://escholarship.org/uc/item/0wr1x24z</link>
      <description>BACKGROUND: In the United States, over 500,000 perioperative team members are exposed to surgical smoke annually. Surgical smoke, a by-product of electrocautery use during operative procedures, contains particulate matter and volatile organic compounds, which are known irritants and carcinogens with mutagenic potential. Surgical smoke adversely impacts the respiratory, cardiovascular, and neurological systems. Despite the exposure to surgical smoke in the operating room, little is known about the experience of surgical smoke by perioperative team members.PURPOSE: Past research has an almost exclusively quantitative approach, with scarce conceptual development beyond descriptions of the smoke’s content, mechanism, hazards, and mitigation strategies. The purpose of this dissertation is to use a mixed methods approach to advance the understanding of the experience of surgical smoke.METHODS: A scoping review with the aims to synthesize the evidence on how perioperative teams experience...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0wr1x24z</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lewis, Merideth</name>
        <uri>https://orcid.org/0000-0002-5010-8664</uri>
      </author>
    </item>
    <item>
      <title>In situ proteomics unveils specialized domains for extrasynaptic signaling on neuronal cilia</title>
      <link>https://escholarship.org/uc/item/0jt5s8w5</link>
      <description>Neuronal cilia have emerged as crucial signaling hubs, yet their molecular composition and integration with synaptic communication remain poorly understood. Using a newly developed
                    Arl13b-TurboID
                    mouse model, we achieved robust cilia-specific biotinylation and proteomic profiling across diverse tissues and cell types. Comparative proteomics revealed notable tissue-specific specialization, with neuronal cilia uniquely enriched in synaptic proteins, adhesion molecules, and neurotransmitter receptors. Unexpectedly, several signaling and adhesion molecules localize to neuronal cilia in discrete nanodomains maintained by active retrieval mechanisms. In the mouse cortex, expansion microscopy revealed that the NMDA receptor subunit GluN1 is organized in nanodomains on neuronal ciliary membranes, which are precisely positioned to sample neurotransmitter efflux from neighboring glutamatergic synapses. These findings establish neuronal cilia as specialized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0jt5s8w5</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chang, Chia-Hsiang</name>
        <uri>https://orcid.org/0000-0003-2725-6789</uri>
      </author>
      <author>
        <name>Trinh, Van Ngu</name>
        <uri>https://orcid.org/0000-0002-5958-8975</uri>
      </author>
      <author>
        <name>Novak, Sammy Weiser</name>
        <uri>https://orcid.org/0000-0002-8344-9772</uri>
      </author>
      <author>
        <name>Lokesh, Nidhi Rani</name>
        <uri>https://orcid.org/0009-0003-8208-4673</uri>
      </author>
      <author>
        <name>Montecinos, Catalina Kretschmar</name>
        <uri>https://orcid.org/0000-0002-2365-6251</uri>
      </author>
      <author>
        <name>Boassa, Daniela</name>
        <uri>https://orcid.org/0000-0003-4631-4139</uri>
      </author>
      <author>
        <name>Pownall, Mark E</name>
        <uri>https://orcid.org/0000-0002-0560-2698</uri>
      </author>
      <author>
        <name>Kalocsay, Marian</name>
        <uri>https://orcid.org/0000-0002-4187-5829</uri>
      </author>
      <author>
        <name>Nachury, Maxence V</name>
        <uri>https://orcid.org/0000-0003-4918-1562</uri>
      </author>
    </item>
    <item>
      <title>Correlates of Fitness Tracker Ownership and Use in Cancer Survivors: Cross-Sectional Survey.</title>
      <link>https://escholarship.org/uc/item/0hs6k3bm</link>
      <description>&lt;h4&gt;Background&lt;/h4&gt;Consumer fitness tracker devices offer scalable opportunities to monitor real-world behavior and support health in cancer survivorship. However, adoption and sustained use outside structured research settings remain incompletely characterized, limiting their integration into survivorship care.&lt;h4&gt;Objective&lt;/h4&gt;The primary objectives were to describe the prevalence of fitness tracker ownership and use patterns among cancer survivors and to identify sociodemographic, psychosocial, and usability-related correlates of device ownership and frequent use.&lt;h4&gt;Methods&lt;/h4&gt;We conducted a cross-sectional survey of 893 cancer survivors enrolled in the Total Cancer Care protocol at a comprehensive cancer center. Participants completed an adapted online questionnaire assessing fitness tracker ownership, frequency of use, and perceived barriers and facilitators. Multivariable logistic regression models were used to identify sociodemographic, psychosocial, and usability-related...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0hs6k3bm</guid>
      <pubDate>Thu, 4 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Benzo, Roberto M</name>
        <uri>https://orcid.org/0000-0001-8634-6472</uri>
      </author>
      <author>
        <name>Fisher, James L</name>
        <uri>https://orcid.org/0000-0003-3211-2691</uri>
      </author>
      <author>
        <name>Tetrick, Macy K</name>
        <uri>https://orcid.org/0009-0004-2605-9614</uri>
      </author>
      <author>
        <name>Singh, Rujul</name>
        <uri>https://orcid.org/0009-0009-8757-0658</uri>
      </author>
      <author>
        <name>Osei, Alex B</name>
        <uri>https://orcid.org/0000-0001-9542-1817</uri>
      </author>
      <author>
        <name>Krok-Schoen, Jessica</name>
        <uri>https://orcid.org/0000-0003-2484-5887</uri>
      </author>
      <author>
        <name>Nickerson, Brett S</name>
        <uri>https://orcid.org/0000-0001-7919-970X</uri>
      </author>
      <author>
        <name>Paskett, Electra D</name>
        <uri>https://orcid.org/0000-0002-8247-8299</uri>
      </author>
      <author>
        <name>Kargarandehkordi, Ali</name>
        <uri>https://orcid.org/0000-0002-2714-9476</uri>
      </author>
      <author>
        <name>Kumar, Sachin</name>
        <uri>https://orcid.org/0009-0001-4400-114X</uri>
      </author>
      <author>
        <name>St George, Sara M</name>
        <uri>https://orcid.org/0000-0001-7263-4609</uri>
      </author>
      <author>
        <name>Rayo, Michael F</name>
        <uri>https://orcid.org/0000-0003-0180-058X</uri>
      </author>
      <author>
        <name>Penedo, Frank J</name>
        <uri>https://orcid.org/0000-0002-2780-0417</uri>
      </author>
      <author>
        <name>Washington, Peter</name>
        <uri>https://orcid.org/0000-0003-3276-4411</uri>
      </author>
    </item>
    <item>
      <title>Addition of pulsed electric field ablation to SBRT for lung tumors: effect on health-related quality of life</title>
      <link>https://escholarship.org/uc/item/8vx0p27z</link>
      <description>INTRODUCTION: Treatment indications for oligometastatic/oligoprogressive lung tumors are growing. Safety and lack of detrimental effect on patients' quality of life are critical for novel local therapies.
METHODS: We tested that the additive effect of pulsed electric field (PEF) ablation with lower-dose stereotactic body radiation therapy (SBRT) on health-related quality of life (HRQoL) as a secondary endpoint in a prospective clinical trial. FACT-Lung Cancer Subscale (FACT-LCS) and FACT-General domain surveys were collected at screening, 3 months, and 12 months. Functional clinical data included forced vital capacity (FVC), forced expiratory volume in one second (FEV1), and diffusing capacity of the lung for carbon monoxide (DLCO).
RESULTS: Six patients with eight tumors were enrolled. Baseline well-being domain scores were: Physical 25.9 (Std Dev 2.3), Social 21.0 (Std Dev 6.9), Emotional 17.3 (Std Dev 4.7), Functional 21.2 (Std Dev 5.8), and LCS 19.4 (Std Dev 5.3). There were...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8vx0p27z</guid>
      <pubDate>Wed, 3 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Harris, Jeremy P</name>
        <uri>https://orcid.org/0000-0003-1231-4798</uri>
      </author>
      <author>
        <name>Boyd, Christina</name>
      </author>
      <author>
        <name>Shi, Mengying</name>
      </author>
      <author>
        <name>Reilly, Michael</name>
        <uri>https://orcid.org/0000-0003-2481-6728</uri>
      </author>
      <author>
        <name>Simon, Aaron</name>
        <uri>https://orcid.org/0000-0003-4685-2711</uri>
      </author>
      <author>
        <name>Seyedin, Steven N</name>
      </author>
      <author>
        <name>Chen, Wen-Pin</name>
      </author>
      <author>
        <name>Nagasaka, Misako</name>
      </author>
      <author>
        <name>Abi-Jaoudeh, Nadine</name>
        <uri>https://orcid.org/0000-0001-6163-8524</uri>
      </author>
      <author>
        <name>Hoyt, Michael A</name>
        <uri>https://orcid.org/0000-0003-2274-1902</uri>
      </author>
    </item>
    <item>
      <title>Race, Ethnicity, and Mortality Following Major Osteoporotic Fracture: Results from the Women’s Health Initiative Study</title>
      <link>https://escholarship.org/uc/item/6600d6mx</link>
      <description>BackgroundMajor osteoporotic fracture (MOF) is associated with increased mortality; however, few studies in postmenopausal women have examined racial and ethnic differences in 1-year and 5-year mortality following MOF.ObjectiveTo assess 1-year and 5-year mortality following MOF by race and ethnicity.DesignThis prospective cohort study included postmenopausal women enrolled in the Women’s Health Initiative (WHI), a population-based, multisite US study. Participants were followed from September 1994 to February 2023. Data were analyzed between August 2023 and November 2023.ParticipantsPostmenopausal women aged 50 to 79&amp;nbsp;years old who experienced a MOF (N = 32,675 in 1&amp;nbsp;year and 29,506 in 5&amp;nbsp;years following MOF).Main MeasuresSelf-reported race and ethnicity. All-cause mortality was determined by death certificates, reports of surrogates, and the National Death Index Search.Key ResultsThe baseline mean age of participants was 77.0 [SD = 8.5] years with 31,223 [95.6%] White...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6600d6mx</guid>
      <pubDate>Wed, 3 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Juels, Michaela</name>
      </author>
      <author>
        <name>Larson, Joseph C</name>
      </author>
      <author>
        <name>Ensrud, Kristine E</name>
      </author>
      <author>
        <name>Stefanick, Marcia L</name>
      </author>
      <author>
        <name>Shadyab, Aladdin H</name>
        <uri>https://orcid.org/0000-0002-9693-0522</uri>
      </author>
      <author>
        <name>Garcia, Lorena</name>
      </author>
      <author>
        <name>Nassir, Rami</name>
      </author>
      <author>
        <name>Schnatz, Peter F</name>
      </author>
      <author>
        <name>Nelson, Rebecca</name>
      </author>
      <author>
        <name>Crandall, Carolyn J</name>
      </author>
    </item>
    <item>
      <title>&lt;strong&gt;Cross-D Conv&lt;/strong&gt;: Cross-Dimensional Transferable Knowledge Base via Fourier Shifting Operation</title>
      <link>https://escholarship.org/uc/item/1v14x65v</link>
      <description>&lt;strong&gt;Cross-D Conv&lt;/strong&gt;: Cross-Dimensional Transferable Knowledge Base via Fourier Shifting Operation</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1v14x65v</guid>
      <pubDate>Tue, 2 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yavuz, Mehmet Can</name>
      </author>
      <author>
        <name>Yang, Yang</name>
      </author>
    </item>
    <item>
      <title>AI in your Toolkit: Critical Approaches to Using AI in your Work (Lightning Talk at the 2026 Medical Library Association Annual Conference)</title>
      <link>https://escholarship.org/uc/item/7bs3z8ps</link>
      <description>&lt;p&gt;Background&amp;nbsp;&lt;/p&gt;&lt;p&gt;Over the past two years, the Library has experienced a sharp rise in questions about generative artificial intelligence (AI). Students, faculty, and staff are increasingly exposed to AI-powered databases and tools and seek guidance on whether these tools can be used responsibly. At the same time, the institution has made substantial investments in AI infrastructure and actively promotes AI adoption across a wide rangeof use cases. Within this environment, Library staff identified a need for coordinated training that moves beyond promotion and instead offers a critical and practical perspective to build AI literacy in the campus community.&lt;/p&gt;&lt;p&gt;Description&lt;/p&gt;&lt;p&gt;Between November 2025 and May 2026, the Library offered a six-session workshop series designed to support university students, faculty, and staff in critically examining the role of artificial intelligence (AI) in their professional practice. The series was taught by staff from across the Library...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7bs3z8ps</guid>
      <pubDate>Mon, 1 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Deardorff, Ariel</name>
      </author>
    </item>
    <item>
      <title>Connecting, Collaborating, Creating: Advancing Equitable Teaching in the Library (Talk at 2026 Medical Library Association Annual Conference)</title>
      <link>https://escholarship.org/uc/item/2xj478vn</link>
      <description>&lt;p&gt;Background&amp;nbsp;&lt;/p&gt;&lt;p&gt;In 2022 Library staff launched a project to enhance inclusive library teaching practices and foster collaboration among library educators. This project stemmed from a larger theme in the Library’s 2020-2025 strategic plan that aimed to build the reputation of library staff as essential campus educators. The key objectives of the project were to establish a community of practice for library educators, and develop a comprehensive guide to equitable teaching in the Library.&lt;/p&gt;&lt;p&gt;Description&amp;nbsp;&lt;/p&gt;&lt;p&gt;The project team brought together librarians and staff from across the Library, representing diverse teaching expertise and education backgrounds. The team met monthly from late 2022 to the end of 2025 to develop the project goals, plan the Library Educators Community of Practice meetings, and design and launch the Equitable Teaching Guide. The first major milestone was the creation of the Library Educators Community of Practice, a bi-monthly meeting to foster...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2xj478vn</guid>
      <pubDate>Mon, 1 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Deardorff, Ariel</name>
      </author>
      <author>
        <name>Thompson, Holly</name>
      </author>
      <author>
        <name>Leiva, Lisa</name>
      </author>
    </item>
    <item>
      <title>It's Beshert: The Life and Legacy of Dr. Jay A. Levy</title>
      <link>https://escholarship.org/uc/item/0zj0p2f2</link>
      <description>&lt;em&gt;It’s Beshert&lt;/em&gt; is a biography of Dr. Jay A. Levy, a former professor of medicine at UC San Francisco. His pathbreaking insights into the fundamentals of HIV/AIDS deepened public understanding of the condition and helped save lives. The book captures the diversity of Levy’s life, including his upbringing in Wilmington, Delaware; the research obstacles he encountered at UCSF in the 1980s; and his extensive travels (and rich experiences) throughout the world. Levy is a strong believer in &lt;em&gt;beshert&lt;/em&gt; – a Yiddish word for “destiny” or “fate” – and the concept is woven into his inspiring life story.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0zj0p2f2</guid>
      <pubDate>Mon, 1 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Rees, Matthew</name>
      </author>
    </item>
    <item>
      <title>Decision-Making in Pleural Drainage Following Lung Resection in Children: A Western Pediatric Surgery Research Consortium Survey</title>
      <link>https://escholarship.org/uc/item/8hn2p25s</link>
      <description>INTRODUCTION: Studies of adults undergoing lung resection indicated that selective omission of pleural drains is safe and advantageous. Significant practice variation exists for pleural drainage practices for children undergoing lung resection. We surveyed pediatric surgeons in a 10-hospital research consortium to understand decision-making for placement of pleural drains following lung resection in children.
METHODS: Faculty surgeons at the 10 member institutions of the Western Pediatric Surgery Research Consortium completed questionnaires using a REDCap survey platform. Descriptive statistics and bivariate analyses were used to characterize responses regarding indications and management of pleural drains following lung resection in pediatric patients.
RESULTS: We received 96 responses from 109 surgeons (88&amp;nbsp;%). Most surgeons agreed that use of a pleural drain after lung resection contributes to post-operative pain, increases narcotic use, and prolongs hospitalization. Opinions...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8hn2p25s</guid>
      <pubDate>Thu, 28 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Schnuck, Jamie K</name>
      </author>
      <author>
        <name>Acker, Shannon N</name>
      </author>
      <author>
        <name>Kelley-Quon, Lorraine I</name>
      </author>
      <author>
        <name>Lee, Justin H</name>
      </author>
      <author>
        <name>Shew, Stephen B</name>
      </author>
      <author>
        <name>Fialkowski, Elizabeth</name>
      </author>
      <author>
        <name>Ignacio, Romeo C</name>
        <uri>https://orcid.org/0000-0001-7259-8679</uri>
      </author>
      <author>
        <name>Melhado, Caroline</name>
      </author>
      <author>
        <name>Qureshi, Faisal G</name>
      </author>
      <author>
        <name>Russell, Katie W</name>
      </author>
      <author>
        <name>Rothstein, David H</name>
      </author>
      <author>
        <name>Consortium, the Western Pediatric Surgery Research</name>
      </author>
      <author>
        <name>Cairo, Sarah</name>
      </author>
      <author>
        <name>Chao, Stephanie D</name>
      </author>
      <author>
        <name>Fenton, Stephen J</name>
      </author>
      <author>
        <name>Gollin, Gerald</name>
        <uri>https://orcid.org/0000-0002-4642-3370</uri>
      </author>
      <author>
        <name>Jensen, Aaron</name>
      </author>
      <author>
        <name>Keane, Olivia A</name>
      </author>
      <author>
        <name>Nicassio, Lauren</name>
      </author>
      <author>
        <name>Ochoa, Brielle</name>
      </author>
      <author>
        <name>Pandya, Samir</name>
      </author>
      <author>
        <name>Patwardhan, Utsav M</name>
      </author>
    </item>
    <item>
      <title>Weather-Related Pediatric Fatalities in the United States: 2001 to 2021.</title>
      <link>https://escholarship.org/uc/item/8hc4r248</link>
      <description>BACKGROUND AND OBJECTIVES: Major weather and climate disasters are increasing in frequency and severity. How often these events result in child deaths is unknown. We assessed temporal and regional trends in pediatric fatalities due to weather events in the United States over the last 21&amp;nbsp;years.
METHODS: We conducted an ecological study of weather-related pediatric fatalities between 2001 and 2021 using the National Centers for Environmental Information Storm Events Database. Weather-related fatalities were compared with pediatric fatalities included in the Centers for Disease Control and Prevention Wide-ranging ONline Data for Epidemiologic Research database. The change in the proportion of all-cause pediatric fatalities associated with weather events was assessed over time. The frequency of events occurring in regions with Pediatric Disaster Care Centers of Excellence (COE) was examined.
RESULTS: Between 2001 and 2021, weather events were associated with 1423 pediatric fatalities....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8hc4r248</guid>
      <pubDate>Thu, 28 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Stephens, Caroline Q</name>
      </author>
      <author>
        <name>Cairo, Sarah B</name>
      </author>
      <author>
        <name>Fallat, Mary E</name>
      </author>
      <author>
        <name>Melhado, Caroline G</name>
      </author>
      <author>
        <name>Godfred-Cato, Shana</name>
      </author>
      <author>
        <name>Ong, Hilary</name>
      </author>
      <author>
        <name>Newton, Christopher</name>
      </author>
    </item>
    <item>
      <title>Comparative Analysis of Indices for Social Determinants of Health in Pediatric Surgical Populations</title>
      <link>https://escholarship.org/uc/item/6g7116b8</link>
      <description>Importance: Conclusions vary substantially among studies examining associations between area-based social determinants of health (SDOH) and pediatric health disparities based on the selected patient population and SDOH index. Most national studies use zip codes, which encompass a wide distribution of communities, limiting the generalizability of findings.
Objectives: To characterize the distributions of composite SDOH indices for pediatric surgical patients within a national sample of academic children's hospitals and to assess SDOH index precision in classifying patients at similar levels of disadvantage.
Design, Setting, and Participants: This multicenter retrospective cohort study included patients younger than 18 years who underwent surgery from January 1, 2016, to December 31, 2021, at 8 American College of Surgeons National Surgical Quality Improvement Program Pediatric children's hospitals. Data were analyzed November 15, 2023, to September 25, 2024.
Exposures: Exposures...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6g7116b8</guid>
      <pubDate>Thu, 28 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Stephens, Caroline Q</name>
      </author>
      <author>
        <name>Yap, Ava</name>
      </author>
      <author>
        <name>Vu, Lan</name>
      </author>
      <author>
        <name>Saito, Jacqueline M</name>
      </author>
      <author>
        <name>Barry, Dwight</name>
      </author>
      <author>
        <name>Shui, Amy M</name>
        <uri>https://orcid.org/0000-0002-8243-6910</uri>
      </author>
      <author>
        <name>Cockrell, Hannah</name>
      </author>
      <author>
        <name>Cairo, Sarah</name>
      </author>
      <author>
        <name>Wakeman, Derek</name>
      </author>
      <author>
        <name>Berman, Loren</name>
      </author>
      <author>
        <name>Greenberg, Sarah</name>
      </author>
      <author>
        <name>Linden, Allison F</name>
      </author>
      <author>
        <name>Kohler, Jonathan</name>
        <uri>https://orcid.org/0000-0001-7509-4097</uri>
      </author>
      <author>
        <name>Tsao, KuoJen</name>
      </author>
      <author>
        <name>Wilson, Nicole A</name>
      </author>
    </item>
    <item>
      <title>Pleural drain placement following lung resection in children: A prospective observational study of the Western Pediatric Surgery Research Consortium</title>
      <link>https://escholarship.org/uc/item/3p50r0q1</link>
      <description>PURPOSE: Pleural drains are used routinely after thoracic surgery in children despite evidence that drainage is not always necessary. The purpose of this study was to assess the necessity of intraoperative drain placement after resectional lung surgery in children, provide a contemporary characterization of the use of pleural drains, and evaluate the utility of intraoperative air leak testing.
METHODS: A multi-institutional prospective cohort study was performed at 10 free-standing children's hospitals in the United States from 2023 to 2024. Patients ≤18 years old who underwent open or thoracoscopic wedge resection or lobectomy were included. Patients undergoing operation for spontaneous pneumothorax or trauma, those on extra-corporeal life support, those undergoing bi-lobectomy or pneumonectomy, and those undergoing reoperation in the affected hemithorax were excluded. Operative parameters, intra-operative air leak, length of post-operative drain placement, and number of post-operative...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3p50r0q1</guid>
      <pubDate>Thu, 28 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kahan, Anastasia M</name>
      </author>
      <author>
        <name>Kelley-Quon, Lorraine I</name>
      </author>
      <author>
        <name>Acker, Shannon N</name>
      </author>
      <author>
        <name>Vincent, Sage</name>
      </author>
      <author>
        <name>Chao, Stephanie D</name>
      </author>
      <author>
        <name>Nepomuceno, Helene</name>
      </author>
      <author>
        <name>Lee, Justin H</name>
      </author>
      <author>
        <name>Padilla, Benjamin E</name>
      </author>
      <author>
        <name>Patwardhan, Utsav M</name>
      </author>
      <author>
        <name>Gollin, Gerald</name>
      </author>
      <author>
        <name>Ignacio, Romeo C</name>
        <uri>https://orcid.org/0000-0001-7259-8679</uri>
      </author>
      <author>
        <name>Fialkowski, Elizabeth A</name>
      </author>
      <author>
        <name>Fowler, Kathryn L</name>
      </author>
      <author>
        <name>Cairo, Sarah B</name>
      </author>
      <author>
        <name>Munar, Dane</name>
      </author>
      <author>
        <name>Pandya, Samir R</name>
      </author>
      <author>
        <name>Russell, Katie W</name>
      </author>
      <author>
        <name>Fenton, Stephen J</name>
      </author>
      <author>
        <name>Lee, Steven L</name>
      </author>
      <author>
        <name>Rothstein, David H</name>
      </author>
    </item>
    <item>
      <title>Comparison of Postoperative Antibiotic Protocols for Pediatric Complicated Appendicitis: A Western Pediatric Surgery Research Consortium Study</title>
      <link>https://escholarship.org/uc/item/2v15j9s2</link>
      <description>BACKGROUND: There is no consensus on the appropriate duration of postoperative antibiotics for complicated appendicitis in children. Commonly used antibiotic endpoints include normalization of white blood cell count (WBC) or completion of a minimum number of prespecified treatment days. We compared clinical outcomes resulting from varying postoperative antibiotic protocols for complicated appendicitis in children.
METHODS: National Surgical Quality Improvement Program Pediatric (NSQIP-P) data from nine children's hospitals was used to identify a retrospective cohort of children (&amp;lt;18 years) who underwent laparoscopic appendectomy from 2021 to 2023 with intraoperative findings of complicated appendicitis. Participating hospitals were classified into four groups based on discharge protocol: 1) no discharge antibiotics, 2) oral antibiotics for elevated WBC on the day of discharge, 3) oral antibiotics to complete a minimum number of total antibiotic days, and 4) routine discharge...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2v15j9s2</guid>
      <pubDate>Thu, 28 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Patwardhan, Utsav M</name>
      </author>
      <author>
        <name>Kahan, Anastasia</name>
      </author>
      <author>
        <name>Eldredge, R Scott</name>
      </author>
      <author>
        <name>Russell, Katie W</name>
      </author>
      <author>
        <name>Lee, Justin</name>
      </author>
      <author>
        <name>Short, Scott S</name>
      </author>
      <author>
        <name>Padilla, Benjamin</name>
      </author>
      <author>
        <name>Cairo, Sarah B</name>
      </author>
      <author>
        <name>Acker, Shannon N</name>
      </author>
      <author>
        <name>Jensen, Aaron R</name>
      </author>
      <author>
        <name>Kelley-Quon, Lorraine I</name>
      </author>
      <author>
        <name>Rothstein, David H</name>
      </author>
      <author>
        <name>Fialkowski, Elizabeth A</name>
      </author>
      <author>
        <name>Chao, Stephanie D</name>
      </author>
      <author>
        <name>Gillory, Lauren</name>
      </author>
      <author>
        <name>Pandya, Samir</name>
      </author>
      <author>
        <name>Diaz-Miron, Jose</name>
      </author>
      <author>
        <name>Ignacio, Romeo C</name>
        <uri>https://orcid.org/0000-0001-7259-8679</uri>
      </author>
    </item>
    <item>
      <title>Abstract 2281: The interrelationship between maternal periconception folate nutritional intake and child’s genetic liability in the etiology of childhood acute lymphoblastic leukemia</title>
      <link>https://escholarship.org/uc/item/9517t20x</link>
      <description>Abstract  Introduction Maternal prenatal folate intake is associated with a decreased risk of acute lymphoblastic leukemia (ALL) in children. Genome-wide association studies (GWAS) show that variations in genes regulating folate metabolism impact serum folate level irrespective of nutritional intake. Polygenic risk scores (PRS) summarize the cumulative genetic liability associated with specific phenotypes. This study aimed to examine if the child PRS related to folate level interacts with maternal periconception folate intake from food and supplements, contributing to ALL risk.   Methods Data on periconceptional folate intake spanning the year prior to pregnancy were obtained from the California Childhood Leukemia Study (CCLS). Folate intake from diet and supplement was measured in dietary folate equivalents (DFE). A PRS related to folate level was constructed using summary statistics from a GWAS of serum folate levels among Europeans. After assigning genetically predicted folate...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9517t20x</guid>
      <pubDate>Tue, 26 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Xiang, Yijin</name>
      </author>
      <author>
        <name>Metayer, Catherine</name>
      </author>
      <author>
        <name>Kogan, Scott</name>
        <uri>https://orcid.org/0000-0002-2395-8479</uri>
      </author>
      <author>
        <name>Ma, Xiaomei</name>
      </author>
      <author>
        <name>Wiemels, Joseph</name>
      </author>
    </item>
    <item>
      <title>Author Correction: Mechanisms of clonal evolution in childhood acute lymphoblastic leukemia</title>
      <link>https://escholarship.org/uc/item/42q583dk</link>
      <description>Author Correction: Mechanisms of clonal evolution in childhood acute lymphoblastic leukemia</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/42q583dk</guid>
      <pubDate>Tue, 26 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Swaminathan, Srividya</name>
      </author>
      <author>
        <name>Klemm, Lars</name>
      </author>
      <author>
        <name>Park, Eugene</name>
      </author>
      <author>
        <name>Papaemmanuil, Elli</name>
      </author>
      <author>
        <name>Ford, Anthony</name>
      </author>
      <author>
        <name>Kweon, Soo-Mi</name>
      </author>
      <author>
        <name>Trageser, Daniel</name>
      </author>
      <author>
        <name>Hasselfeld, Brian</name>
      </author>
      <author>
        <name>Henke, Nadine</name>
      </author>
      <author>
        <name>Mooster, Jana</name>
      </author>
      <author>
        <name>Geng, Huimin</name>
        <uri>https://orcid.org/0000-0001-5339-5446</uri>
      </author>
      <author>
        <name>Schwarz, Klaus</name>
      </author>
      <author>
        <name>Kogan, Scott C</name>
        <uri>https://orcid.org/0000-0002-2395-8479</uri>
      </author>
      <author>
        <name>Casellas, Rafael</name>
      </author>
      <author>
        <name>Schatz, David G</name>
      </author>
      <author>
        <name>Lieber, Michael R</name>
      </author>
      <author>
        <name>Greaves, Mel F</name>
      </author>
      <author>
        <name>Müschen, Markus</name>
      </author>
    </item>
    <item>
      <title>P300/CBP inhibition with inobrodib in combination with gilteritinib and venetoclax targets leukemia stem cells in epigenetic mutant AML</title>
      <link>https://escholarship.org/uc/item/2h89g17f</link>
      <description>Acute myeloid leukemia (AML) is a fatal blood cancer with cytotoxic chemotherapy offering at best 25% 5-year survival. While targeted BCL2 and FLT3 inhibitors venetoclax and gilteritinib are used upfront in the treatment of a subset of adult patients with AML and help to extend the survival of some patients, a curative treatment combination with minimal side effects has yet to be discovered. We find that use of the dual histone acetyltransferase p300/CBP bromodomain inhibitor CCS1477 (inobrodib), together with venetoclax and gilteritinib, virtually eliminates leukemia stem cells in an aggressive preclinical model of &lt;i&gt;DNMT3A/FLT3&lt;/i&gt;-mutant AML by impairing pro-oncogenic survival and proliferation factors to effectively block leukemogenesis. This work identifies potential clinical utility of a targeted, triplet combination therapy for treatment of AML.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2h89g17f</guid>
      <pubDate>Tue, 26 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Goetz, Melanie L</name>
      </author>
      <author>
        <name>Romer-Seibert, Jennifer S</name>
      </author>
      <author>
        <name>Versace, Amanda M</name>
      </author>
      <author>
        <name>Kogan, Scott</name>
        <uri>https://orcid.org/0000-0002-2395-8479</uri>
      </author>
      <author>
        <name>Jeurkar, Chetan</name>
      </author>
      <author>
        <name>Bowman, Robert L</name>
      </author>
      <author>
        <name>Brooks, Nigel</name>
      </author>
      <author>
        <name>Frese, Kris</name>
      </author>
      <author>
        <name>Meyer, Sara E</name>
      </author>
    </item>
    <item>
      <title>The Interrelationship between Preconception Folate Nutritional Intake and Child Genetic Liability in the Risk of Childhood Acute Lymphoblastic Leukemia.</title>
      <link>https://escholarship.org/uc/item/1zb0m0sj</link>
      <description>BACKGROUND: Prenatal maternal folate intake is associated with a reduced risk of childhood acute lymphoblastic leukemia (ALL), but how this interacts with children's genetic predisposition to folate deficiency remains unclear.
METHODS: We used Mendelian randomization to investigate the causal link among serum folate, total homocysteine, and B vitamins on ALL using independent genetic instruments. These were evaluated in two independent childhood ALL genome-wide association studies: the California Childhood Cancer Record Linkage Project and the California Childhood Leukemia Study, the latter with available self-reported periconceptional nutrition data. Logistic regressions assessed the interrelationship between maternal nutrition and children's folate metabolism-related polygenic risk score (PRS) and methylenetetrahydrofolate reductase rs1801133 genotype.
RESULTS: Mendelian randomization analyses showed that higher genetically predicted serum folate was associated with reduced...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1zb0m0sj</guid>
      <pubDate>Tue, 26 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Xiang, Yijin</name>
      </author>
      <author>
        <name>Metayer, Catherine</name>
      </author>
      <author>
        <name>Kogan, Scott C</name>
        <uri>https://orcid.org/0000-0002-2395-8479</uri>
      </author>
      <author>
        <name>Ma, Xiaomei</name>
      </author>
      <author>
        <name>Nickels, Eric</name>
      </author>
      <author>
        <name>Wiemels, Joseph L</name>
      </author>
    </item>
    <item>
      <title>Psychedelic Therapy vs Antidepressants for the Treatment of Depression Under Equal Unblinding Conditions</title>
      <link>https://escholarship.org/uc/item/9k83z4gw</link>
      <description>Importance: Psychedelic-assisted therapy (PAT) trials have high levels of functional unblinding, which biases results when comparing PAT with blinded interventions. Because PAT is effectively always open label, treatment results should be compared with those of open-label traditional antidepressants (TADs), so potential benefits associated with patients knowing their treatment is equal between the interventions.
Objective: To investigate the comparative effectiveness of PAT vs open-label traditional antidepressants (TADs; such as selective serotonin and norepinephrine reuptake inhibitors) for the treatment of major depression.
Data Sources: PubMed was systematically searched in March 2024 for trials of PAT and open-label TADs for the treatment of major depression without comorbidity in adults without psychosis in the outpatient setting. Extraction was supplemented with data from a review and meta-analysis of antidepressant drugs to assess the open-label vs blinded TAD difference.
Data...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9k83z4gw</guid>
      <pubDate>Mon, 25 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Williams, Zachary J</name>
      </author>
      <author>
        <name>Barnett, Hannah</name>
      </author>
      <author>
        <name>Szigeti, Balázs</name>
        <uri>https://orcid.org/0000-0003-3809-6442</uri>
      </author>
    </item>
    <item>
      <title>Can Targeting Circadian Rhythms Help Prevent Alzheimer Disease?: Lessons From Down Syndrome.</title>
      <link>https://escholarship.org/uc/item/7st0x72x</link>
      <description>Can Targeting Circadian Rhythms Help Prevent Alzheimer Disease?: Lessons From Down Syndrome.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7st0x72x</guid>
      <pubDate>Sun, 24 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Fang, Yi</name>
        <uri>https://orcid.org/0000-0002-1199-187X</uri>
      </author>
      <author>
        <name>Leng, Yue</name>
        <uri>https://orcid.org/0000-0001-5826-4031</uri>
      </author>
    </item>
    <item>
      <title>"It's Part of Dialysis": Lived Experiences of Transportation Challenges Among Patients and Staff in In-Center Hemodialysis.</title>
      <link>https://escholarship.org/uc/item/4gx130gs</link>
      <description>Transportation insecurity significantly affects dialysis care, yet little research examines its impact from both patient and provider perspectives. This qualitative study explored how transportation challenges influence the experiences of patients receiving in-center hemodialysis and dialysis clinic staff. We conducted 78 semi-structured interviews with patients (n = 49) and staff (n = 29) across four Northern California dialysis clinics. Participants described challenges of navigating two systems, healthcare and transportation, and how this creates emotional distress for patients and staff, disrupts clinic workflows, and compromises treatment adherence. Transportation services are a major part of the patient and staff experience in dialysis clinics. Our findings highlight the need to improve transportation for dialysis patients through collaboration between healthcare systems, transportation providers, and community stakeholders.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4gx130gs</guid>
      <pubDate>Fri, 22 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Bonilla-Herrera, Bethney</name>
      </author>
      <author>
        <name>Saini, Navkirn</name>
      </author>
      <author>
        <name>Corina, Iris</name>
      </author>
      <author>
        <name>Dickerson, Bertha</name>
      </author>
      <author>
        <name>Grijalva, Maria Elena</name>
      </author>
      <author>
        <name>Pulido, Daniel Jovan</name>
      </author>
      <author>
        <name>Roshanravan, Baback</name>
      </author>
      <author>
        <name>Fenton, Joshua J</name>
      </author>
      <author>
        <name>Gottlieb, Laura M</name>
      </author>
      <author>
        <name>Razon, Na'amah</name>
        <uri>https://orcid.org/0000-0002-8785-3406</uri>
      </author>
    </item>
    <item>
      <title>Effects of a liquefied petroleum gas stove and fuel intervention on head circumference and length at birth: A multi-country household air pollution intervention network (HAPIN) trial</title>
      <link>https://escholarship.org/uc/item/9w13t71m</link>
      <description>BACKGROUND: Air pollution may impair child growth and cognitive development, with potential markers including birth length and head circumference.
METHODS: The Household Air Pollution Intervention Network (HAPIN) trial was an open label multi-country-randomized controlled trial, with 3200 pregnant women aged 18-34&amp;nbsp;years (9-19&amp;nbsp;weeks of gestation) randomly assigned in a 1:1 ratio to receive liquefied petroleum gas (LPG) stove intervention compared to women continuing to cook with solid fuels for 18&amp;nbsp;months. Particulate matter&amp;nbsp;≤&amp;nbsp;2.5&amp;nbsp;μm (PM2.5), black carbon (BC) and carbon monoxide (CO) 24-hour personal exposures were measured three times during pregnancy. Head circumference and length were measured&amp;nbsp;&amp;lt;&amp;nbsp;24&amp;nbsp;h of birth. We conducted intention-to-treat and exposure-response analyses to determine the intervention effects and associations between household air pollution (HAP) exposure during pregnancy and head circumference, head circumference-for-gestational...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9w13t71m</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Raheel, Hina</name>
      </author>
      <author>
        <name>Sinharoy, Sheela</name>
      </author>
      <author>
        <name>Diaz-Artiga, Anaité</name>
      </author>
      <author>
        <name>Garg, Sarada S</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
      <author>
        <name>Balakrishnan, Kalpana</name>
      </author>
      <author>
        <name>Chiang, Marilu</name>
      </author>
      <author>
        <name>Lovvorn, Amy</name>
      </author>
      <author>
        <name>Kirby, Miles</name>
      </author>
      <author>
        <name>Ramakrishnan, Usha</name>
      </author>
      <author>
        <name>Jabbarzadeh, Shirin</name>
      </author>
      <author>
        <name>Mukeshimana, Alexie</name>
      </author>
      <author>
        <name>Johnson, Michael</name>
      </author>
      <author>
        <name>McCracken, John P</name>
      </author>
      <author>
        <name>Naeher, Luke P</name>
      </author>
      <author>
        <name>Rosa, Ghislaine</name>
      </author>
      <author>
        <name>Wang, Jiantong</name>
      </author>
      <author>
        <name>Rosenthal, Joshua</name>
      </author>
      <author>
        <name>Checkley, William</name>
      </author>
      <author>
        <name>Clasen, Thomas F</name>
      </author>
      <author>
        <name>Peel, Jennifer L</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>investigators, Household Air Pollution Intervention Network</name>
      </author>
    </item>
    <item>
      <title>Effects of Cooking with Liquefied Petroleum Gas or Biomass on Stunting in Infants</title>
      <link>https://escholarship.org/uc/item/8wq8m0st</link>
      <description>BACKGROUND: Household air pollution is associated with stunted growth in infants. Whether the replacement of biomass fuel (e.g., wood, dung, or agricultural crop waste) with liquefied petroleum gas (LPG) for cooking can reduce the risk of stunting is unknown.
METHODS: We conducted a randomized trial involving 3200 pregnant women 18 to 34 years of age in four low- and middle-income countries. Women at 9 to less than 20 weeks' gestation were randomly assigned to use a free LPG cookstove with continuous free fuel delivery for 18 months (intervention group) or to continue using a biomass cookstove (control group). The length of each infant was measured at 12 months of age, and personal exposures to fine particulate matter (particles with an aerodynamic diameter of ≤2.5 μm) were monitored starting at pregnancy and continuing until the infants were 1 year of age. The primary outcome for which data are presented in the current report - stunting (defined as a length-for-age z score that...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8wq8m0st</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Checkley, William</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Sinharoy, Sheela S</name>
      </author>
      <author>
        <name>Hossen, Shakir</name>
      </author>
      <author>
        <name>Moulton, Lawrence H</name>
      </author>
      <author>
        <name>Chang, Howard H</name>
      </author>
      <author>
        <name>Waller, Lance</name>
      </author>
      <author>
        <name>Steenland, Kyle</name>
      </author>
      <author>
        <name>Rosa, Ghislaine</name>
      </author>
      <author>
        <name>Mukeshimana, Alexie</name>
      </author>
      <author>
        <name>Ndagijimana, Florien</name>
      </author>
      <author>
        <name>McCracken, John P</name>
      </author>
      <author>
        <name>Díaz-Artiga, Anaité</name>
      </author>
      <author>
        <name>Balakrishnan, Kalpana</name>
      </author>
      <author>
        <name>Garg, Sarada S</name>
      </author>
      <author>
        <name>Thangavel, Gurusamy</name>
      </author>
      <author>
        <name>Aravindalochanan, Vigneswari</name>
      </author>
      <author>
        <name>Hartinger, Stella M</name>
      </author>
      <author>
        <name>Chiang, Marilú</name>
      </author>
      <author>
        <name>Kirby, Miles A</name>
      </author>
      <author>
        <name>Papageorghiou, Aris T</name>
      </author>
      <author>
        <name>Ramakrishnan, Usha</name>
      </author>
      <author>
        <name>Williams, Kendra N</name>
      </author>
      <author>
        <name>Nicolaou, Laura</name>
      </author>
      <author>
        <name>Johnson, Michael</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
      <author>
        <name>Rosenthal, Joshua</name>
      </author>
      <author>
        <name>Underhill, Lindsay J</name>
      </author>
      <author>
        <name>Wang, Jiantong</name>
      </author>
      <author>
        <name>Jabbarzadeh, Shirin</name>
      </author>
      <author>
        <name>Chen, Yunyun</name>
      </author>
      <author>
        <name>Dávila-Román, Victor G</name>
      </author>
      <author>
        <name>Naeher, Luke P</name>
      </author>
      <author>
        <name>McCollum, Eric D</name>
      </author>
      <author>
        <name>Peel, Jennifer L</name>
      </author>
      <author>
        <name>Clasen, Thomas F</name>
      </author>
    </item>
    <item>
      <title>Factors Determining Black Carbon Exposures among Pregnant Women Enrolled in the HAPIN Trial</title>
      <link>https://escholarship.org/uc/item/89v6x733</link>
      <description>Residential biomass burning is an important source of black carbon (BC) exposure among rural communities in low- and middle-income countries. We collected 7165 personal BC samples and individual/household level information from 3103 pregnant women enrolled in the Household Air Pollution Intervention Network trial. Women in the intervention arm received free liquefied petroleum gas stoves and fuel throughout pregnancy; women in the control arm continued the use of biomass stoves. Median (IQR) postintervention BC exposures were 9.6 μg/m&lt;sup&gt;3&lt;/sup&gt; (5.2-14.0) for controls and 2.8 μg/m&lt;sup&gt;3&lt;/sup&gt; (1.6-4.8) for the intervention group. Using mixed models, we characterized predictors of BC exposure and assessed how exposure contrasts differed between arms by select predictors. Primary stove type was the strongest predictor (&lt;i&gt;R&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 0.42); the models including kerosene use, kitchen location, education, occupation, or stove use hours also provided additional explanatory...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/89v6x733</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Campbell, Devan A</name>
      </author>
      <author>
        <name>Johnson, Michael</name>
      </author>
      <author>
        <name>Piedrahita, Ricardo</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
      <author>
        <name>Waller, Lance A</name>
      </author>
      <author>
        <name>Kearns, Katherine A</name>
      </author>
      <author>
        <name>Kremer, Jacob</name>
      </author>
      <author>
        <name>Mollinedo, Erick</name>
      </author>
      <author>
        <name>Sarnat, Jeremy A</name>
      </author>
      <author>
        <name>Clark, Maggie L</name>
      </author>
      <author>
        <name>Underhill, Lindsay J</name>
      </author>
      <author>
        <name>McCracken, John P</name>
      </author>
      <author>
        <name>Diaz-Artiga, Anaité</name>
      </author>
      <author>
        <name>Steenland, Kyle</name>
      </author>
      <author>
        <name>Rosa, Ghislaine</name>
      </author>
      <author>
        <name>Kirby, Miles A</name>
      </author>
      <author>
        <name>Balakrishnan, Kalpana</name>
      </author>
      <author>
        <name>Sambandam, Sankar</name>
      </author>
      <author>
        <name>Mukhopadhyay, Krishnendu</name>
      </author>
      <author>
        <name>Sendhil, Saritha</name>
      </author>
      <author>
        <name>Natarajan, Amudha</name>
      </author>
      <author>
        <name>Ndagijimana, Florien</name>
      </author>
      <author>
        <name>Dusabimana, Ephrem</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Checkley, William</name>
      </author>
      <author>
        <name>Nicolaou, Laura</name>
      </author>
      <author>
        <name>Hartinger, Stella</name>
      </author>
      <author>
        <name>Peel, Jennifer L</name>
      </author>
      <author>
        <name>Clasen, Thomas F</name>
      </author>
      <author>
        <name>Naeher, Luke P</name>
      </author>
    </item>
    <item>
      <title>When profit meets public health: private equity in methadone treatment</title>
      <link>https://escholarship.org/uc/item/7wb671hh</link>
      <description>Opioid overdose deaths in the U.S. exceed 80,000 annually and methadone, an effective treatment for opioid use disorder (OUD), remains difficult to access. Understanding how ownership structures affect access, quality, cost, and regulation in methadone treatment for opioid use disorder in the U.S. is thus a public health imperative. Private equity (PE) has rapidly consolidated opioid treatment programs (OTPs), now owning nearly one-third of all facilities that are the primary means for receiving methadone treatment. This growth is rooted in a complex federal regulatory regime and public-financing expansions that create barriers for smaller providers and predictable revenue streams for PE-owned facilities. While proponents of PE tout their capacity to infuse capital and modernize care, emerging evidence - combined with concerning patterns from PE ownership in other health sectors - suggests risks of understaffing, aggressive revenue optimization, and regulatory influence. This...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7wb671hh</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Roy, Victor</name>
      </author>
      <author>
        <name>Barsky, Benjamin A</name>
      </author>
      <author>
        <name>Fuse Brown, Erin C</name>
      </author>
      <author>
        <name>Suen, Leslie W</name>
      </author>
    </item>
    <item>
      <title>Development of personal air pollution exposure report-back materials to Household Air Pollution Intervention Network (HAPIN) trial participants in Guatemala and Rwanda: a qualitative study</title>
      <link>https://escholarship.org/uc/item/7d5790gm</link>
      <description>BACKGROUND: Report-back of individual exposure information to research participants is recognised in high-income countries as an important, yet often overlooked, component of environmental research, with many potential benefits to study communities. Nonetheless, the optimal means of communicating findings to participants in low-income countries with limited health and scientific literacy is unknown.
METHODS: Between March 2021 and May 2022, we conducted a qualitative study with 61 women and 20 of their household members (n=81) participating in the Household Air Pollution Intervention Network trial in Guatemala and Rwanda. Using participant observations and individual interviews (n=61), group interviews (n=21), dynamic working groups (n=78) and focus groups (n=45), we collaborated with study participants to iteratively develop contextually appropriate and comprehensible materials that conveyed individual air pollution exposures.
RESULTS: Posters were generated to display graphical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7d5790gm</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Quinn, Ashlinn</name>
      </author>
      <author>
        <name>Hengstermann, Mayari</name>
      </author>
      <author>
        <name>Diaz-Artiga, Anaite</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
      <author>
        <name>Clark, Maggie</name>
      </author>
      <author>
        <name>Ruiz-Aguilar, Laura</name>
      </author>
      <author>
        <name>Ndagijimana, Florien</name>
      </author>
      <author>
        <name>McCracken, John P</name>
      </author>
      <author>
        <name>Rosa, Ghislaine</name>
      </author>
      <author>
        <name>Checkley, William</name>
      </author>
      <author>
        <name>Peel, Jennifer</name>
      </author>
      <author>
        <name>Clasen, Thomas F</name>
      </author>
      <author>
        <name>Thompson, Lisa</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Aravindalochanan, Vigneswari</name>
      </author>
      <author>
        <name>Balakrishnan, Kalpana</name>
      </author>
      <author>
        <name>Bankundiye, Gloriose</name>
      </author>
      <author>
        <name>Barr, Dana Boyd</name>
      </author>
      <author>
        <name>Burrowes, Vanessa</name>
      </author>
      <author>
        <name>Bussalleu, Alejandra</name>
      </author>
      <author>
        <name>Campbell, Devan</name>
      </author>
      <author>
        <name>Canuz, Eduardo</name>
      </author>
      <author>
        <name>Castañaza, Adly</name>
      </author>
      <author>
        <name>Chang, Howard H</name>
      </author>
      <author>
        <name>Chen, Yunyun</name>
      </author>
      <author>
        <name>Chiang, Marilú</name>
      </author>
      <author>
        <name>Contreras, Carmen Lucia</name>
      </author>
      <author>
        <name>Craik, Rachel</name>
      </author>
      <author>
        <name>Crocker, Mary</name>
      </author>
      <author>
        <name>Davila-Roman, Victor G</name>
      </author>
      <author>
        <name>de las Fuentes, Lisa</name>
      </author>
      <author>
        <name>De León, Oscar</name>
      </author>
      <author>
        <name>D’Souza, Priya</name>
      </author>
      <author>
        <name>Dusabimana, Ephrem</name>
      </author>
      <author>
        <name>Elon, Lisa</name>
      </author>
      <author>
        <name>Espinoza, Juan Gabriel</name>
      </author>
    </item>
    <item>
      <title>Estimating personal exposures to household air pollution and plastic garbage burning among adolescent girls in Jalapa, Guatemala</title>
      <link>https://escholarship.org/uc/item/70z523kb</link>
      <description>Waste collection services are uncommon in rural areas of low-resource countries, causing waste accumulation and subsequent dumping and burning of garbage. Air pollution from household garbage burning, including plastics, has been observed in Jalapa, Guatemala in addition to household air pollution (HAP) from cooking. Adolescent girls often help with these cooking and household tasks, but little is known about their exposures. We characterized 24-h exposures to HAP and household garbage burning in adolescent girls by measuring fine particulate matter (PM&lt;sub&gt;2.5&lt;/sub&gt;), black carbon (BC), urinary biomarkers of polycyclic aromatic hydrocarbons (PAHs), bisphenol A (BPA), and phthalates. We recruited 60 girls between 13 and 17 years of age who helped with cooking activities and lived with participants of the Household Air Pollution Intervention Network (HAPIN) trial. We recruited n&amp;nbsp;=&amp;nbsp;30 girls each from the control (wood-burning stove) and intervention (liquefied petroleum...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/70z523kb</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kearns, Katherine A</name>
      </author>
      <author>
        <name>Naeher, Luke P</name>
      </author>
      <author>
        <name>McCracken, John P</name>
      </author>
      <author>
        <name>Barr, Dana Boyd</name>
      </author>
      <author>
        <name>Saikawa, Eri</name>
      </author>
      <author>
        <name>Hengstermann, Mayari</name>
      </author>
      <author>
        <name>Mollinedo, Erick</name>
      </author>
      <author>
        <name>Panuwet, Parinya</name>
      </author>
      <author>
        <name>Yakimavets, Volha</name>
      </author>
      <author>
        <name>Lee, Grace E</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
    </item>
    <item>
      <title>Optic Neuropathy due to an Ethmoid Mucocele: A Case Report and Literature Review.</title>
      <link>https://escholarship.org/uc/item/6jq254sn</link>
      <description>Mucoceles of the paranasal sinus commonly involve the frontal sinuses, the ethmoid sinuses, and rarely the maxillary or sphenoid sinuses. They often present with sinus pain or pressure, but rarely can present with more severe symptoms such as changes in mental status or vision due to expansion and invasion through the skull base or orbit. A 62-year-old male presented with optic neuropathy, a relative afferent pupillary defect with proptosis and lateral gaze palsy of the left eye. The patient was found to have a large mucocele extending from the left posterior ethmoid sinus into the left orbital apex. Urgent endoscopic sinus surgery was performed jointly between Oculoplastics and Otolaryngology. Post-operatively, the patient had improvement in diplopia, extraocular motion, and proptosis with stable vision. This case demonstrates the importance of early identification and intervention in a rare presentation of a sinus mucocele to prevent serious complications such as vision loss.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6jq254sn</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ting, Magdalene</name>
      </author>
      <author>
        <name>Shan, Meghan</name>
      </author>
      <author>
        <name>Gantz, Oliver</name>
      </author>
      <author>
        <name>Zhang-Nunes, Sandy</name>
      </author>
      <author>
        <name>Wrobel, Bozena</name>
      </author>
    </item>
    <item>
      <title>PRECIS-2 used as an implementation science tool for global environmental health: A cross-sectional evaluation of the Ecolectivos study protocol to reduce burning of household plastic waste in rural Guatemala</title>
      <link>https://escholarship.org/uc/item/5j95x679</link>
      <description>BACKGROUND: Randomized controlled trials (RCTs) that evaluate the efficacy of an intervention remain underutilized in community-based environmental health research. RCTs that use a pragmatic design emphasize the effectiveness of interventions in complex, real world settings. Pragmatic trials may be especially relevant when community-based interventions address social and environmental determinants that threaten health equity. The revised Pragmatic Explanatory Continuum Indicator Summary (PRECIS-2) is a validated tool developed in 2015 by trialists to ensure that clinical trials are designed to fit their intended purpose, with an assessment of applicability of the trial results to specific contexts. The purpose of this cross-sectional study was to ask Ecolectivos study investigators and external implementation scientists to evaluate the Ecolectivos study protocol using the PRECIS-2 tool prior to the launch of the trial. Ecolectivos is an implementation science study, using a village-level...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5j95x679</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Ferguson, Annalyse</name>
      </author>
      <author>
        <name>Raheel, Hina</name>
      </author>
      <author>
        <name>Lovvorn, Amy E</name>
      </author>
      <author>
        <name>Hengstermann-Artiga, Mayari</name>
      </author>
      <author>
        <name>Lopez, Maria Renee</name>
      </author>
      <author>
        <name>Higgins, Melinda</name>
      </author>
      <author>
        <name>Saikawa, Eri</name>
      </author>
      <author>
        <name>Handley, Margaret A</name>
      </author>
    </item>
    <item>
      <title>Psilocybin-Assisted Therapy for Adolescent Anorexia Nervosa: Clinical Considerations and Emerging Models of Care</title>
      <link>https://escholarship.org/uc/item/42g932b9</link>
      <description>&lt;h4&gt;Purpose of review&lt;/h4&gt;There is growing evidence that psychedelics and associated treatment modalities may offer therapeutic benefits across a range of psychiatric conditions. Anorexia nervosa (AN), a serious and often treatment-resistant illness associated with significant morbidity and mortality, is one such condition for which psilocybin-assisted therapy (PAT) may hold promise.&lt;h4&gt;Recent findings&lt;/h4&gt;To date, research on PAT for AN has focused primarily on adults, despite the fact that AN frequently begins in adolescence, and early age of onset portends poorer prognosis, including more severe AN, more lifetime psychiatric comorbidity, and greater life difficulties. Given these risks, an exploration of the theoretical potential of PAT for adolescent populations is warranted. Important considerations include biological implications, developmental stage, and consent. Adaptations to the current models of psilocybin-assisted therapy in studies of adults are proposed, and emerging...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/42g932b9</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Geller, Jamarie A</name>
      </author>
      <author>
        <name>Pacilio, Rachel</name>
      </author>
      <author>
        <name>Downey, Amanda E</name>
      </author>
      <author>
        <name>Ragnhildstveit, Anya</name>
      </author>
      <author>
        <name>Raymond-Flesch, Marissa</name>
        <uri>https://orcid.org/0000-0003-0037-8970</uri>
      </author>
      <author>
        <name>Knatz-Peck, Stephanie</name>
      </author>
      <author>
        <name>Gukasyan, Natalie</name>
      </author>
    </item>
    <item>
      <title>β-amyloid and tau drive early Alzheimer’s disease decline while glucose hypometabolism drives late decline</title>
      <link>https://escholarship.org/uc/item/4104z2rb</link>
      <description>Clinical trials focusing on therapeutic candidates that modify β-amyloid (Aβ) have repeatedly failed to treat Alzheimer’s disease (AD), suggesting that Aβ may not be the optimal target for treating AD. The evaluation of Aβ, tau, and neurodegenerative (A/T/N) biomarkers has been proposed for classifying AD. However, it remains unclear whether disturbances in each arm of the A/T/N framework contribute equally throughout the progression of AD. Here, using the random forest machine learning method to analyze participants in the Alzheimer’s Disease Neuroimaging Initiative dataset, we show that A/T/N biomarkers show varying importance in predicting AD development, with elevated biomarkers of Aβ and tau better predicting early dementia status, and biomarkers of neurodegeneration, especially glucose hypometabolism, better predicting later dementia status. Our results suggest that AD treatments may also need to be disease stage-oriented with Aβ and tau as targets in early AD and glucose...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4104z2rb</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hammond, Tyler C</name>
      </author>
      <author>
        <name>Xing, Xin</name>
      </author>
      <author>
        <name>Wang, Chris</name>
      </author>
      <author>
        <name>Ma, David</name>
      </author>
      <author>
        <name>Nho, Kwangsik</name>
      </author>
      <author>
        <name>Crane, Paul K</name>
      </author>
      <author>
        <name>Elahi, Fanny</name>
      </author>
      <author>
        <name>Ziegler, David A</name>
      </author>
      <author>
        <name>Liang, Gongbo</name>
      </author>
      <author>
        <name>Cheng, Qiang</name>
      </author>
      <author>
        <name>Yanckello, Lucille M</name>
      </author>
      <author>
        <name>Jacobs, Nathan</name>
      </author>
      <author>
        <name>Lin, Ai-Ling</name>
      </author>
    </item>
    <item>
      <title>Identification of NQO2 As a Protein Target in Small Molecule Modulation of Hepatocellular Function.</title>
      <link>https://escholarship.org/uc/item/3s65c83g</link>
      <description>The utility of &lt;i&gt;in vitro&lt;/i&gt; human disease models is mainly dependent on the availability and functional maturity of tissue-specific cell types. We have previously screened for and identified small molecules that can enhance hepatocyte function &lt;i&gt;in vitro&lt;/i&gt;. Here, we characterize the functional effects of one of the hits, FH1, on primary human hepatocytes &lt;i&gt;in vitro&lt;/i&gt;, and also &lt;i&gt;in vivo&lt;/i&gt; on primary hepatocytes in a zebrafish model. Furthermore, we conducted an analogue screen to establish the structure-activity relationship of FH1. We performed affinity-purification proteomics that identified NQO2 to be a potential binding target for this small molecule, revealing a possible link between inflammatory signaling and hepatocellular function in zebrafish and human hepatocyte model systems.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3s65c83g</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Schepers, Arnout</name>
      </author>
      <author>
        <name>Shan, Meghan</name>
      </author>
      <author>
        <name>Cox, Andrew</name>
      </author>
      <author>
        <name>Huang, Ada</name>
      </author>
      <author>
        <name>Evans, Helen</name>
      </author>
      <author>
        <name>Walesky, Chad</name>
      </author>
      <author>
        <name>Fleming, Heather</name>
      </author>
      <author>
        <name>Goessling, Wolfram</name>
      </author>
      <author>
        <name>Bhatia, Sangeeta</name>
      </author>
    </item>
    <item>
      <title>Trajectories and social determinants of child cognitive development: a prospective cohort study from infancy through middle childhood in Dhaka, Bangladesh</title>
      <link>https://escholarship.org/uc/item/3kp0v10z</link>
      <description>Background: Over a third of children globally do not meet their developmental potential, and children living in low and middle-income countries (LMICs) are most vulnerable. Understanding the contextual factors that influence cognitive development for children in LMICs is crucial to inform and develop interventions. We sought to characterize developmental trajectories of cognition in Bangladeshi children and identify salient social determinants.
Methods: We used a longitudinal design and included 542 children living in Dhaka, Bangladesh. Social determinants (maternal and paternal education, housing risks, household assets, and food security) were assessed at baseline visits using a combination of oral interviews and home assessments. Cognitive development was assessed at 6 months, 2, 3, 4, 5, and 7 years. A total of 1397 cognitive assessments were completed across all participants. Growth curve models and mixed effect models were used.
Findings: In children living above the poverty...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3kp0v10z</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Valdes, Viviane</name>
      </author>
      <author>
        <name>Sullivan, Eileen F</name>
      </author>
      <author>
        <name>Tofail, Fahmida</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Kakon, Shahria H</name>
      </author>
      <author>
        <name>Shama, Talat</name>
      </author>
      <author>
        <name>Haque, Rashidul</name>
      </author>
      <author>
        <name>Nelson, Charles A</name>
      </author>
    </item>
    <item>
      <title>Closed-Loop Systems and Real-Time Neurofeedback in Mindfulness Meditation Research</title>
      <link>https://escholarship.org/uc/item/3j40z96v</link>
      <description>Mindfulness meditation has numerous purported benefits for psychological well-being; however, problems such as adherence to mindfulness tasks, quality of mindfulness sessions, or dosage of mindfulness interventions may hinder individuals from accessing the purported benefits of mindfulness. Methodologies including closed-loop systems and real-time neurofeedback may provide tools to help bolster success in mindfulness task performance, titrate the exposure to mindfulness interventions, or improve engagement with mindfulness sessions. In this review, we explore the use of closed-loop systems and real-time neurofeedback to influence, augment, or promote mindfulness interventions. Various closed-loop neurofeedback signals from functional magnetic resonance imaging and electroencephalography have been used to provide subjective correlates of mindfulness states including functional magnetic resonance imaging region-of-interest-based signals (e.g., posterior cingulate cortex), functional...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3j40z96v</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Joseph CC</name>
        <uri>https://orcid.org/0000-0002-4166-9814</uri>
      </author>
      <author>
        <name>Ziegler, David A</name>
      </author>
    </item>
    <item>
      <title>Fidelity and adherence to a liquefied petroleum gas stove and fuel intervention: The multi-country Household Air Pollution Intervention Network (HAPIN) trial</title>
      <link>https://escholarship.org/uc/item/3d50k28z</link>
      <description>BACKGROUND: Reducing household air pollution (HAP) to levels associated with health benefits requires nearly exclusive use of clean cooking fuels and abandonment of traditional biomass fuels.
METHODS: The Household Air Pollution Intervention Network (HAPIN) trial randomized 3,195 pregnant women in Guatemala, India, Peru, and Rwanda to receive a liquefied petroleum gas (LPG) stove intervention (n&amp;nbsp;=&amp;nbsp;1,590), with controls expected to continue cooking with biomass fuels (n&amp;nbsp;=&amp;nbsp;1,605). We assessed fidelity to intervention implementation and participant adherence to the intervention starting in pregnancy through the infant's first birthday using fuel delivery and repair records, surveys, observations, and temperature-logging stove use monitors (SUMs).
RESULTS: Fidelity and adherence to the HAPIN intervention were high. Median time required to refill LPG cylinders was 1&amp;nbsp;day (interquartile range 0-2). Although 26% (n&amp;nbsp;=&amp;nbsp;410) of intervention participants...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3d50k28z</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Williams, Kendra N</name>
      </author>
      <author>
        <name>Quinn, Ashlinn</name>
      </author>
      <author>
        <name>North, Hayley</name>
      </author>
      <author>
        <name>Wang, Jiantong</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Díaz-Artiga, Anaité</name>
      </author>
      <author>
        <name>Balakrishnan, Kalpana</name>
      </author>
      <author>
        <name>Thangavel, Gurusamy</name>
      </author>
      <author>
        <name>Rosa, Ghislaine</name>
      </author>
      <author>
        <name>Ndagijimana, Florien</name>
      </author>
      <author>
        <name>Underhill, Lindsay J</name>
      </author>
      <author>
        <name>Kirby, Miles A</name>
      </author>
      <author>
        <name>Puzzolo, Elisa</name>
      </author>
      <author>
        <name>Hossen, Shakir</name>
      </author>
      <author>
        <name>Waller, Lance A</name>
      </author>
      <author>
        <name>Peel, Jennifer L</name>
      </author>
      <author>
        <name>Rosenthal, Joshua P</name>
      </author>
      <author>
        <name>Clasen, Thomas F</name>
      </author>
      <author>
        <name>Harvey, Steven A</name>
      </author>
      <author>
        <name>Checkley, William</name>
      </author>
      <author>
        <name>Investigators, for the HAPIN</name>
      </author>
    </item>
    <item>
      <title>The Environmental Costs and Geography of U.S. Data Center Expansion</title>
      <link>https://escholarship.org/uc/item/2ts9g6jj</link>
      <description>The Environmental Costs and Geography of U.S. Data Center Expansion</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2ts9g6jj</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hernandez-Cortes, Danae</name>
      </author>
      <author>
        <name>Meng, Kyle</name>
      </author>
      <author>
        <name>Weber, Paige</name>
      </author>
    </item>
    <item>
      <title>Human Milk Composition Is Associated with Maternal Body Mass Index in a Cross-Sectional, Untargeted Metabolomics Analysis of Human Milk from Guatemalan Mothers</title>
      <link>https://escholarship.org/uc/item/2gc9q3jr</link>
      <description>Background: Maternal overweight and obesity has been associated with poor lactation performance including delayed lactogenesis and reduced duration. However, the effect on human milk composition is less well understood.
Objectives: We evaluated the relationship of maternal BMI on the human milk metabolome among Guatemalan mothers.
Methods: We used data from 75 Guatemalan mothers who participated in the Household Air Pollution Intervention Network trial. Maternal BMI was measured between 9 and &amp;lt;20 weeks of gestation. Milk samples were collected at a single time point using aseptic collection from one breast at 6 mo postpartum and analyzed using high-resolution mass spectrometry. A cross-sectional untargeted high-resolution metabolomics analysis was performed by coupling hydrophilic interaction liquid chromatography (HILIC) and reverse phase C18 chromatography with mass spectrometry. Metabolic features associated with maternal BMI were determined by a metabolome-wide association...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2gc9q3jr</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sivalogan, Kasthuri</name>
      </author>
      <author>
        <name>Liang, Donghai</name>
      </author>
      <author>
        <name>Accardi, Carolyn</name>
      </author>
      <author>
        <name>Diaz-Artiga, Anaite</name>
      </author>
      <author>
        <name>Hu, Xin</name>
      </author>
      <author>
        <name>Mollinedo, Erick</name>
      </author>
      <author>
        <name>Ramakrishnan, Usha</name>
      </author>
      <author>
        <name>Teeny, Sami Nadeem</name>
      </author>
      <author>
        <name>Tran, ViLinh</name>
      </author>
      <author>
        <name>Clasen, Thomas F</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Sinharoy, Sheela S</name>
      </author>
    </item>
    <item>
      <title>Association of household air pollution exposure and anemia among pregnant women: Analysis of baseline data from ’Household Air Pollution Intervention Network (HAPIN)’ trial</title>
      <link>https://escholarship.org/uc/item/2654q9bt</link>
      <description>BACKGROUND: Anemia is common in low- and middle-income countries (LMICs), causing significant health issues and social burdens. Exposure to household air pollution from using biomass fuels for cooking and heating has been associated with anemia, but the exposure-response association has not been studied.
OBJECTIVES: We evaluated the associations between personal exposure to air pollution and both hemoglobin levels and anemia prevalence among pregnant women in a multi-country randomized controlled trial.
METHODS: We studied 3,163 pregnant women aged 18-35&amp;nbsp;years with 9-20&amp;nbsp;weeks of gestation, recruited as part of the Household Air Pollution Intervention Network (HAPIN) randomized controlled trial in Guatemala, India, Peru, and Rwanda. We assessed 24-hour personal exposures to fine particulate matter (PM&lt;sub&gt;2.5&lt;/sub&gt;), black carbon (BC), and carbon monoxide (CO), and measured hemoglobin levels at baseline (15&amp;nbsp;±&amp;nbsp;3&amp;nbsp;weeks gestation). Linear and logistic regression...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2654q9bt</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Deng, Yanling</name>
      </author>
      <author>
        <name>Steenland, Kyle</name>
      </author>
      <author>
        <name>Sinharoy, Sheela S</name>
      </author>
      <author>
        <name>Peel, Jennifer L</name>
      </author>
      <author>
        <name>Ye, Wenlu</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
      <author>
        <name>Eick, Stephanie M</name>
      </author>
      <author>
        <name>Chang, Howard H</name>
      </author>
      <author>
        <name>Wang, Jiantong</name>
      </author>
      <author>
        <name>Chen, Yunyun</name>
      </author>
      <author>
        <name>Young, Bonnie N</name>
      </author>
      <author>
        <name>Clark, Maggie L</name>
      </author>
      <author>
        <name>Barr, Dana Boyd</name>
      </author>
      <author>
        <name>Clasen, on behalf of the HAPIN Investigators Thomas F</name>
      </author>
    </item>
    <item>
      <title>Exposure Contrasts of Women Aged 40–79 Years during the Household Air Pollution Intervention Network Randomized Controlled Trial</title>
      <link>https://escholarship.org/uc/item/25q428gg</link>
      <description>Exposure to household air pollution has been linked to adverse health outcomes among women aged 40-79. Little is known about how shifting from biomass cooking to a cleaner fuel like liquefied petroleum gas (LPG) could impact exposures for this population. We report 24-h exposures to particulate matter (PM&lt;sub&gt;2.5&lt;/sub&gt;), black carbon (BC), and carbon monoxide (CO) among women aged 40 to &amp;lt;80 years participating in the Household Air Pollution Intervention Network trial. 209 participants were randomized to the intervention and received an LPG stove and continuous fuel supply; controls used biomass (&lt;i&gt;n&lt;/i&gt; = 209). Exposures were measured up to six times; we used mixed-effects models to estimate differences between intervention and control groups. Preintervention exposures between groups were comparable; median postintervention exposures were 62% (76.3 vs 29.3 μg/m&lt;sup&gt;3&lt;/sup&gt;), 73% (10.4 vs 2.8 μg/m&lt;sup&gt;3&lt;/sup&gt;), and 57% (1.4 vs 0.6 ppm) lower for PM&lt;sub&gt;2.5&lt;/sub&gt;, BC, and CO...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/25q428gg</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ye, Wenlu</name>
      </author>
      <author>
        <name>Campbell, Devan</name>
      </author>
      <author>
        <name>Johnson, Michael</name>
      </author>
      <author>
        <name>Balakrishnan, Kalpana</name>
      </author>
      <author>
        <name>Peel, Jennifer L</name>
      </author>
      <author>
        <name>Steenland, Kyle</name>
      </author>
      <author>
        <name>Underhill, Lindsay J</name>
      </author>
      <author>
        <name>Rosa, Ghislaine</name>
      </author>
      <author>
        <name>Kirby, Miles A</name>
      </author>
      <author>
        <name>Díaz-Artiga, Anaité</name>
      </author>
      <author>
        <name>McCracken, John</name>
      </author>
      <author>
        <name>Thompson, Lisa M</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>Clark, Maggie L</name>
      </author>
      <author>
        <name>Waller, Lance A</name>
      </author>
      <author>
        <name>Chang, Howard H</name>
      </author>
      <author>
        <name>Wang, Jiantong</name>
      </author>
      <author>
        <name>Dusabimana, Ephrem</name>
      </author>
      <author>
        <name>Ndagijimana, Florien</name>
      </author>
      <author>
        <name>Sambandam, Sankar</name>
      </author>
      <author>
        <name>Mukhopadhyay, Krishnendu</name>
      </author>
      <author>
        <name>Chiang, Marilu</name>
      </author>
      <author>
        <name>Hartinger, Stella M</name>
      </author>
      <author>
        <name>Nicolaou, Laura</name>
      </author>
      <author>
        <name>Williams, Kendra</name>
      </author>
      <author>
        <name>Piedrahita, Ricardo</name>
      </author>
      <author>
        <name>Kearns, Katherine A</name>
      </author>
      <author>
        <name>Kremer, Jacob</name>
      </author>
      <author>
        <name>Ghosh, Ahana</name>
      </author>
      <author>
        <name>Rosenthal, Joshua P</name>
      </author>
      <author>
        <name>Checkley, William</name>
      </author>
      <author>
        <name>Clasen, Thomas</name>
      </author>
      <author>
        <name>Naeher, Luke</name>
      </author>
      <author>
        <name>Pillarisetti, Ajay</name>
      </author>
    </item>
    <item>
      <title>Classification of hoarding and comorbid neuropsychiatric symptoms</title>
      <link>https://escholarship.org/uc/item/20v7t0rz</link>
      <description>Background: Psychiatric comorbidity and self-reported cognitive dysfunction are common among individuals with hoarding disorder (HD). However, common patterns of co-occurring neuropsychiatric symptoms, and their potential impact on the clinical manifestation of hoarding, including functional impairment, are not well-established.
Methods: Latent class analysis (LCA) was used to identify and characterize distinct neuropsychiatric symptom subgroups among 7606 adult internet-based research participants who reported experiencing social impairment due to household clutter. An additional 1129 participants who screened negative but had evidence of hoarding on additional assessment ("false negative") were identified and compared to the LCA-identified classes. Demographic and clinical characteristics associated with class membership were assessed.
Results: The best fitting model yielded five subgroups, including three subgroups characterizing individuals with hoarding symptoms: "hoarding...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/20v7t0rz</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Nutley, Sara K</name>
      </author>
      <author>
        <name>Striley, Catherine W</name>
      </author>
      <author>
        <name>Cottler, Linda B</name>
      </author>
      <author>
        <name>Eichenbaum, Joseph</name>
      </author>
      <author>
        <name>Nosheny, Rachel L</name>
      </author>
      <author>
        <name>Mackin, R Scott</name>
      </author>
      <author>
        <name>Mathews, Carol A</name>
      </author>
    </item>
    <item>
      <title>Fasting and Caloric Restriction Activate an ADIOL‐NHR‐91‐Kynurenine Pathway Signaling Axis to Promote Healthspan</title>
      <link>https://escholarship.org/uc/item/1gq1p3s2</link>
      <description>The steroid hormone 5-androstene-3β,17β-diol (ADIOL) was discovered nearly a century ago in humans, yet its physiological functions have remained poorly understood. Using C. elegans, we identify ADIOL as essential for several pro-healthspan effects of fasting and caloric restriction (CR). These dietary restriction regimens activate an ADIOL-NHR-91-kynurenic acid signaling axis, partly through transcriptional programs associated with ADIOL biosynthesis. Within this axis, ADIOL acts through NHR-91, a C. elegans homolog of estrogen receptor β, to reduce levels of kynurenic acid, a neuromodulatory metabolite, thereby enhancing healthspan. Critically, ADIOL does not extend lifespan, indicating its healthspan benefits are independent of longevity, and even late-life supplementation is effective. Collectively, this work establishes ADIOL as a physiological link between metabolic cues and neural function, promoting health during aging via the kynurenine pathway. Given that in mammals...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1gq1p3s2</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Guijarro‐Hernández, Ana</name>
      </author>
      <author>
        <name>Yoo, Shinja</name>
      </author>
      <author>
        <name>Lemieux, George A</name>
      </author>
      <author>
        <name>Komatsu, Sena</name>
      </author>
      <author>
        <name>Latiff, Abdullah Q</name>
      </author>
      <author>
        <name>Patil, Rishika R</name>
      </author>
      <author>
        <name>Ashrafi, Kaveh</name>
      </author>
    </item>
    <item>
      <title>High-Throughput Platform for Identifying Molecular Factors Involved in Phenotypic Stabilization of Primary Human Hepatocytes In Vitro.</title>
      <link>https://escholarship.org/uc/item/13b540vb</link>
      <description>Liver disease is a leading cause of morbidity worldwide and treatment options are limited, with organ transplantation being the only form of definitive management. Cell-based therapies have long held promise as alternatives to whole-organ transplantation but have been hindered by the rapid loss of liver-specific functions over a period of days in cultured hepatocytes. Hypothesis-driven studies have identified a handful of factors that modulate hepatocyte functions in vitro, but our understanding of the mechanisms involved remains incomplete. We thus report here the development of a high-throughput platform to enable systematic interrogation of liver biology in vitro. The platform is currently configured to enable genetic knockdown screens and includes an enzyme-linked immunosorbent assay-based functional assay to quantify albumin output as a surrogate marker for hepatocyte synthetic functions as well as an image-based viability assay that counts hepatocyte nuclei. Using this platform,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/13b540vb</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shan, Meghan</name>
      </author>
      <author>
        <name>Logan, David</name>
      </author>
      <author>
        <name>Root, David</name>
      </author>
      <author>
        <name>Carpenter, Anne</name>
      </author>
      <author>
        <name>Bhatia, Sangeeta</name>
      </author>
    </item>
    <item>
      <title>“It's like scratching at the door”: Experiences of outpatient buprenorphine low dose initiation among people using fentanyl</title>
      <link>https://escholarship.org/uc/item/0dh3x62v</link>
      <description>Background The fentanyl-driven overdose crisis has heightened challenges in buprenorphine initiation, as traditional methods risk precipitated withdrawal due to fentanyl's prolonged presence in the body. Buprenorphine low-dose initiation (LDI) offers a gradual approach to starting buprenorphine but requires continued full-agonist opioid use in outpatient settings, where success rates remain low and patient experiences have not been evaluated. Objectives To identify barriers and facilitators to successful LDI completion and inform strategies to improve outpatient buprenorphine treatment. Methods We conducted 19 semi-structured interviews with people with opioid use disorder using fentanyl who had attempted LDI in the past three months. Using the COM-B framework, we applied thematic analysis to identify barriers and facilitators to LDI completion from interviews until reaching thematic saturation. Results We found that barriers and facilitators to LDI completion were linked to five...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0dh3x62v</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Suen, Leslie W</name>
      </author>
      <author>
        <name>Samayoa, Elyssa</name>
      </author>
      <author>
        <name>Spinelli, Matthew A</name>
      </author>
      <author>
        <name>Scarpetta, Maia</name>
      </author>
      <author>
        <name>Knight, Kelly R</name>
      </author>
      <author>
        <name>Chael, Julia</name>
      </author>
      <author>
        <name>Soran, Christine S</name>
      </author>
      <author>
        <name>Geier, Michelle</name>
      </author>
      <author>
        <name>Snyder, Hannah R</name>
      </author>
      <author>
        <name>Coffin, Phillip O</name>
      </author>
    </item>
    <item>
      <title>Optimizing Exposure Measures in Large-Scale Household Air Pollution Studies: Results from the Multicountry HAPIN Trial</title>
      <link>https://escholarship.org/uc/item/04c579pz</link>
      <description>Repeated measurements of household air pollution may provide better estimates of average exposure but can add to costs and participant burden. In a randomized trial of gas versus biomass cookstoves in four countries, we took supplemental personal 24-h measurements on a 10% subsample for mothers and infants, interspersed between protocol samples. Mothers had up to five postrandomization protocol measurements over 16 months, while infants had three measurements over one year. For the subsample, we added up to 6 supplemental postrandomization samples for mothers and 3 for infants, measuring PM&lt;sub&gt;2.5&lt;/sub&gt;, black carbon (BC) (mothers only), and carbon monoxide (CO) at each visit. 310 mothers had both protocol (&lt;i&gt;n&lt;/i&gt; = 1026) and supplemental (&lt;i&gt;n&lt;/i&gt; = 1099) valid exposure measurements. For children, supplemental data sufficient for analysis were collected in only two countries; 94 infants had both protocol (&lt;i&gt;n&lt;/i&gt; = 317) and supplemental (&lt;i&gt;n&lt;/i&gt; = 234) samples. The geometric...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/04c579pz</guid>
      <pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Steenland, K</name>
      </author>
      <author>
        <name>Pillarisetti, A</name>
      </author>
      <author>
        <name>Johnson, M</name>
      </author>
      <author>
        <name>Rosenthal, J</name>
      </author>
      <author>
        <name>Balakrishnan, K</name>
      </author>
      <author>
        <name>Underhill, L</name>
      </author>
      <author>
        <name>Thompson, L</name>
        <uri>https://orcid.org/0000-0002-8001-2057</uri>
      </author>
      <author>
        <name>McCracken, J</name>
      </author>
      <author>
        <name>Waller, L</name>
      </author>
      <author>
        <name>Nicolaou, L</name>
      </author>
      <author>
        <name>Clark, M</name>
      </author>
      <author>
        <name>Checkley, W</name>
      </author>
      <author>
        <name>Peel, J</name>
      </author>
      <author>
        <name>Clasen, T</name>
      </author>
    </item>
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