Evidence map›Paper›PMID 41125440›Full record

ArticleGenome research2025

A gene regulatory element modulates myosin expression and controls cardiomyocyte response to stress.

Taylor Anglen, Irene M Kaplow, Baekgyu Choi, Enya Dewars, Robin M Perelli, Kevin T Hagy, Duc Tran, Megan E Ramaker, Svati H Shah, Inkyung Jung and 4 more

Abstract read
In one paragraph

Article in Genome research, 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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Mechanisms and Therapeutic Potential of Human Cardiomyocyte Proliferation.Journal of cardiovascular development and disease · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Taylor AnglenDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Irene M KaplowCenter for Advanced Genomic Technologies, Duke University, Durham, North Carolina 27708, USA.
Baekgyu ChoiDepartment of Biological Science, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
Enya DewarsDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Robin M PerelliDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Kevin T HagyCenter for Advanced Genomic Technologies, Duke University, Durham, North Carolina 27708, USA.
Duc TranDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Megan E RamakerDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Svati H ShahDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Inkyung JungDepartment of Biological Science, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
Andrew P LandstromDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA.ORCID 0000-0002-1878-9631
Ravi KarraDivision of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, North Carolina 27708, USA.ORCID 0000-0001-6741-285X
Yarui DiaoDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA.
Charles A GersbachDepartment of Cell Biology, Duke University School of Medicine, Durham, North Carolina 27708, USA; charles.gersbach@duke.edu.ORCID 0000-0003-1478-4013

Funding

The Duke FUNCTION Center: Pioneering the comprehensive identification of combinatorial noncoding causes of diseaseRM1HG011123 · NHGRI · DUKE UNIVERSITY · PI GREGORY E CRAWFORD, Raluca Gordan · 2020 to 2026
$21.9M
High-Throughput Functional Annotation of Gene Regulatory Elements and Variants Critical to Complex Cellular PhenotypesUM1HG012053 · NHGRI · DUKE UNIVERSITY · PI GREGORY E CRAWFORD, Charles A. Gersbach · 2021 to 2026
$10.7M
Beyond GWAS: High Throughput Functional Genomics & Epigenome Editing to Elucidate the Effects of Genetic Associations for SchizophreniaR01MH125236 · NIMH · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, GERSBACH, CHARLES A. · 2021 to 2025
$8.1M
NHGRI NIH HHS RM1 HG011123NHGRI NIH HHS UM1 HG012053NIMH NIH HHS R01 MH125236
6 · The paper itself

Abstract

A hallmark of heart disease is gene dysregulation and reactivation of fetal gene programs. Reactivation of these fetal programs has compensatory effects during heart failure, depending on the type and stage of the underlying cardiomyopathy. Thousands of putative cardiac gene regulatory elements have been identified that may control these programs, but their functions are largely unknown. Here, we profile genome-wide changes to gene expression and chromatin structure in cardiomyocytes derived from human pluripotent stem cells. We identify and characterize a gene regulatory element essential for regulating

Indexed as

Cardiac MyosinsEnhancer Elements, GeneticGene Expression RegulationMyocytes, CardiacMyosin Heavy ChainsStress, PhysiologicalChromatinEndothelin-1HumansPluripotent Stem CellsCardiac MyosinsChromatinEndothelin-1MYH6 protein, humanMyosin Heavy Chains

Identifiers

PMID41125440
PMCPMC12581865

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.