Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registry
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Rebecca E Hardman-KavanaughInterdisciplinary Graduate Program in Cell and Molecular Biology, University of Arkansas, Fayetteville, Arkansas 72701, United States of America.
Aaron J StoreyDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States of America.
Tara N StueckerDepartment of Biological Sciences, University of Arkansas, Fayetteville, Arkansas 72701, United States of America.
Stephanie E HoodDepartment of Biological Sciences, University of Arkansas, Fayetteville, Arkansas 72701, United States of America.ORCID 0000-0002-9857-5392
Gregory A Barrett-WiltBiotechnology Center, University of Wisconsin, Madison, WI, 53706, United States of America.ORCID 0000-0002-3583-8642
Venkata R KrishnamurthiDepartment of Physics, University of Arkansas, Fayetteville 72701, AR, United States of America.
Yong WangInterdisciplinary Graduate Program in Cell and Molecular Biology, University of Arkansas, Fayetteville, Arkansas 72701, United States of America.
Stephanie D ByrumDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States of America.ORCID 0000-0002-1783-3610
Samuel G MackintoshDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States of America.
Rick D EdmondsonCollege of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States of America.
Wayne P WahlsDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States of America.ORCID 0000-0002-1338-1610
Alan J TackettDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States of America.ORCID 0000-0002-3672-4460
Jeffrey A LewisDepartment of Biological Sciences, University of Arkansas, Fayetteville, Arkansas 72701, United States of America.ORCID 0000-0003-2952-9701
Funding
Understanding Hesitant AdoptersP20GM103429 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Lawrence E Cornett, JERRY WARE · 2012 to 2026
$60.9M
Translational Regulation in Normal Erythropoiesis and Diamond Blackfan AnemiaP20GM121293 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI Alan Tackett, Sean D. Taverna · 2017 to 2026
$27.6M
Supplement for Google cloud build-outR24GM137786 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Alan Tackett · 2020 to 2026
$15.4M
Biochemistry of recombination in meiosisR01GM081766 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI WAHLS, WAYNE P · 2007 to 2018
$2.5M
Melanoma Resistance Evolution Atlas (MREA) for identifying combinatorial targets to prevent and reverse MAPKi resistanceR01CA282198 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROGER S LO, Alan Tackett · 2024 to 2026
$2.0M
Systematic elucidation of DNA sequence codes that regulate meiotic recombinationR01GM145834 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI WAHLS, WAYNE P · 2022 to 2025
All organisms experience stress and must rapidly respond to changing conditions. Thus, cells have evolved sophisticated rapid-response mechanisms such as post-translational protein modification to rapidly and reversibly modulate protein activity. One such post-translational modification is reversible lysine acetylation, where proteomic studies have identified thousands of acetylated proteins across diverse organisms. While the sheer size of the 'acetylome' is striking, the function of acetylation for the vast majority of proteins remains largely obscure. Here, we show that global acetylation plays a previously unappreciated role in the heat shock response of
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.
Dynamic global acetylation remodeling during the yeast heat shock response. · full record | OpenQuestion