Evidence map›Paper›PMID 38001317›Full record

ReviewNature reviews. Genetics2024

Context-specific functions of chromatin remodellers in development and disease.

Sai Gourisankar, Andrey Krokhotin, Wendy Wenderski, Gerald R Crabtree

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
11.4field-weighted citation impact, top 1% of its field
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

51 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. CHD8-Dependent Chromatin Licensing Sustains Trophoblast Stem Cell Transcriptional Programs.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  11. Comprehensive genomics and functional analyses identifyTranslational cancer research · 2026
    Article
  12. Review
  13. Article
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  19. Review
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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

4 authors at 1 institution in 1 country.

Sai GourisankarDepartment of Pathology, Stanford University, Stanford, CA, USA.
Andrey KrokhotinDepartment of Pathology, Stanford University, Stanford, CA, USA.
Wendy WenderskiDepartment of Pathology, Stanford University, Stanford, CA, USA.
Gerald R CrabtreeDepartment of Pathology, Stanford University, Stanford, CA, USA. crabtree@stanford.edu.ORCID http://orcid.org/0000-0001-9685-7911
Stanford University · US

Funding

ATP-Dependent Chromatin Remodeling in Human MalignancyR01CA163915 · NCI · STANFORD UNIVERSITY · PI Gerald R. Crabtree · 2012 to 2026
$5.4M
Signaling by Calcineurin and NFAT in Axonal OutgrowthR01NS046789 · NINDS · STANFORD UNIVERSITY · PI CRABTREE, GERALD R. · 2003 to 2012
$3.4M
HIJACKING CANCER DRIVERS TO ACTIVATE PROAPOPTOTIC GENES IN DLBCLR01CA276167 · NCI · STANFORD UNIVERSITY · PI Gerald R. Crabtree, NATHANAEL Schiander GRAY · 2023 to 2026
$2.2M
Small molecule regulation of endogenous transcription factors for circuit-specific neuromodulationRF1MH126720 · NIMH · STANFORD UNIVERSITY · PI CRABTREE, GERALD R. · 2021 to 2021
$1.3M
Discovery of a cerebellar-specific BAF chromatin remodeler that is necessary for social inhibition: molecular and circuit mechanismsK00MH135633 · NIMH · STANFORD UNIVERSITY · PI WENDERSKI, WENDY · 2023 to 2025
$331k
Mutations in ACTL6B cause recessive autism: affected families, mouse model, molecular and circuit mechanismsF99NS118735 · NINDS · STANFORD UNIVERSITY · PI WENDERSKI, WENDY · 2020 to 2021
$54k
NCI NIH HHS R01 CA163915NCI NIH HHS R01 CA276167NIMH NIH HHS K00 MH135633NIMH NIH HHS RF1 MH126720NINDS NIH HHS F99 NS118735NINDS NIH HHS R01 NS046789
6 · The paper itself

Abstract

Chromatin remodellers were once thought to be highly redundant and nonspecific in their actions. However, recent human genetic studies demonstrate remarkable biological specificity and dosage sensitivity of the thirty-two adenosine triphosphate (ATP)-dependent chromatin remodellers encoded in the human genome. Mutations in remodellers produce many human developmental disorders and cancers, motivating efforts to investigate their distinct functions in biologically relevant settings. Exquisitely specific biological functions seem to be an emergent property in mammals, and in many cases are based on the combinatorial assembly of subunits and the generation of stable, composite surfaces. Critical interactions between remodelling complex subunits, the nucleosome and other transcriptional regulators are now being defined from structural and biochemical studies. In addition, in vivo analyses of remodellers at relevant genetic loci have provided minute-by-minute insights into their dynamics. These studies are proposing new models for the determinants of remodeller localization and function on chromatin.

Indexed as

ChromatinTranscription FactorsAnimalsChromatin Assembly and DisassemblyGenome, HumanHumansMammalsNucleosomesChromatinNucleosomesTranscription Factors

Identifiers

PMID38001317
PMCPMC11867214
OpenAlexW4388977940

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.