Evidence map›Paper›PMID 41500515›Full record

ArticleAmerican journal of physiology. Renal physiology2026

The response to kidney injury is epigenetically regulated through the activation of bivalent genes.

Benjamin I Tickman, Jacquelyn R McDonald, Ryan McCarthy, Kiheon Suh, Daryl M Okamura, Scott R Houghtaling, Sarah J Collins, Yeji Bae, David R Beier, Mark W Majesky and 1 more

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Benjamin I TickmanCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Jacquelyn R McDonaldCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Ryan McCarthyCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Kiheon SuhCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Daryl M OkamuraCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Scott R HoughtalingCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Sarah J CollinsCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Yeji BaeResearch Scientific Computing, Seattle Children's Research Institute, Seattle, Washington, United States.
David R BeierCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.
Mark W MajeskyCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.ORCID 0000-0003-4267-6220
Elizabeth Dong NguyenCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States.ORCID 0000-0002-2798-6581

Funding

Reprogramming of mature smooth muscle cells to vascular progenitor cellsR01HL121877 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MARK W. MAJESKY, Mary CM Weiser-Evans · 2015 to 2026
$7.8M
National Institute of Diabetes and Digestive and Kidney Diseases ATLAS (D2K-ATLAS) Center as an accessible, comprehensive data portfolio for renal and genitourinary development and diseaseU24DK135157 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI JAIN, SANJAY, VALERIUS, MICHAEL TODD · 2022 to 2023
$3.4M
Epigenetic regulation of kidney regenerationK08DK138302 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Elizabeth Dong Nguyen · 2024 to 2026
$465k
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) 2R01 HL121877HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) K08DK138302HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) U24DK135157Loie Power Robinson Stem Cell and Regenerative Medicine FundNHLBI NIH HHS R01 HL121877NIDDK NIH HHS K08 DK138302NIDDK NIH HHS U24 DK135157
6 · The paper itself

Abstract

Epigenetic regulation through histone modifications plays a crucial role in driving cellular state transitions. Regulating gene transcription through bivalency, the co-occurrence of activating histone H3 lysine 4 trimethylation (H3K4me3) and repressive histone H3 lysine 27 trimethylation (H3K27me3) histone marks, drives cell fate in development; however, its role in kidney injury is not known. Here, we investigated bivalent gene activation in the adult male

Indexed as

Acute Kidney InjuryEpigenesis, GeneticKidneyReperfusion InjuryAnimalsDisease Models, AnimalEpithelial CellsHistonesMaleMiceMice, Inbred C57BLTranscription Factorshistone H3 trimethyl Lys4HistonesTranscription Factorsbivalencyepigeneticshistonesischemia-reperfusionkidney repair

Identifiers

PMID41500515
PMCPMC12889892

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.