Evidence map›Paper›PMID 24172249›Full record

ArticleCell & bioscience2013

Histone H3 lysine 4 methyltransferases and demethylases in self-renewal and differentiation of stem cells.

Bingnan Gu, Min Gyu Lee

Abstract read
In one paragraph

Article in Cell & bioscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

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  12. Senescent CD8Cancer science · 2023
    Article
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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

2 authors.

Bingnan Gu
Min Gyu Lee

Funding

Role of the Histone demethylase JARID1d in Epigenetic Events of Prostate CancerR01CA157919 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LEE, MIN GYU · 2011 to 2015
$1.5M
Role of the Histone Modifier KDM6A in Stem Cell DifferentiationR01GM095659 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LEE, MIN GYU · 2011 to 2014
$1.2M
NCI NIH HHS R01 CA157919NIGMS NIH HHS R01 GM095659
6 · The paper itself

Abstract

Epigenetic mechanisms are fundamental to understanding the regulatory networks of gene expression that govern stem cell maintenance and differentiation. Methylated histone H3 lysine 4 (H3K4) has emerged as a key epigenetic signal for gene transcription; it is dynamically modulated by several specific H3K4 methyltransferases and demethylases. Recent studies have described new epigenetic mechanisms by which H3K4 methylation modifiers control self-renewal and lineage commitments of stem cells. Such advances in stem cell biology would have a high impact on the research fields of cancer stem cell and regenerative medicine. In this review, we discuss the recent progress in understanding the roles of H3K4 methylation modifiers in regulating embryonic and adult stem cells' fates.

Identifiers

PMID24172249
PMCPMC3953348

What OpenQuestion holds

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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.