Evidence map›Paper›PMID 21358755›Full record

ReviewCell research2011

ATP-dependent chromatin remodeling: genetics, genomics and mechanisms.

Diana C Hargreaves, Gerald R Crabtree

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 517 papers.

0numbers the graph read from it
0cells of the map it votes in
517citing papers in PubMed
37.8field-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

517 citing papers in PubMed, 909 citations in OpenAlex.

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  20. AAmerican journal of translational research · 2026
    Article

457 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Diana C HargreavesHoward Hughes Medical Institute, Beckman Center B211, 279 Campus Drive, Mailcode 5323, Stanford University School of Medicine, Stanford, CA 94305-5323, USA.
Gerald R Crabtree
Stanford University · US

Funding

Signaling by Calcineurin and NFAT in Axonal OutgrowthR01NS046789 · NINDS · STANFORD UNIVERSITY · PI CRABTREE, GERALD R. · 2003 to 2012
$3.4M
NFAT Signaling and Down SyndromeR01HD055391 · NICHD · STANFORD UNIVERSITY · PI CRABTREE, GERALD R. · 2008 to 2012
$1.4M
Howard Hughes Medical InstituteNICHD NIH HHS R01 HD055391NINDS NIH HHS R01 NS046789
6 · The paper itself

Abstract

Macromolecular assemblies that regulate chromatin structure using the energy of ATP hydrolysis have critical roles in development, cancer, and stem cell biology. The ATPases of this family are encoded by 27 human genes and are usually associated with several other proteins that are stable, non-exchangeable subunits. One fundamental mechanism used by these complexes is thought to be the movement or exchange of nucleosomes to regulate transcription. However, recent genetic studies indicate that chromatin remodelers may also be involved in regulating other aspects of chromatin structure during many cellular processes. The SWI/SNF family in particular appears to have undergone a substantial change in subunit composition and mechanism coincident with the evolutionary advent of multicellularity and the appearance of linking histones. The differential usage of this greater diversity of mammalian BAF subunits is essential for the development of specific cell fates, including the progression from pluripotency to multipotency to committed neurons. Recent human genetic screens have revealed that BRG1, ARID1A, BAF155, and hSNF5 are frequently mutated in tumors, indicating that BAF complexes also play a critical role in the initiation or progression of cancer. The mechanistic bases underlying the genetic requirements for BAF and other chromatin remodelers in development and cancer are relatively unexplored and will be a focus of this review.

Indexed as

ActinsAdenosine TriphosphatasesAdenosine TriphosphateChromatin Assembly and DisassemblyChromosomal Proteins, Non-HistoneHumansSaccharomyces cerevisiaeTranscription FactorsActinsAdenosine TriphosphatasesAdenosine TriphosphateChromosomal Proteins, Non-HistoneSWI-SNF-B chromatin-remodeling complexTranscription Factors

Identifiers

PMID21358755
PMCPMC3110148
OpenAlexW2080571195

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.