Evidence map›Paper›PMID 20800472›Full record

ReviewCurrent opinion in genetics & development2010

Control of embryonic stem cell identity by nucleosome remodeling enzymes.

Thomas G Fazzio, Barbara Panning

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in genetics & development, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Navigating the epigenetic landscape of pluripotent stem cells.Nature reviews. Molecular cell biology · 2012
    Review
  5. Article
  6. Article
  7. Review
  8. Article
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 at 2 institutions in 1 country.

Thomas G FazzioProgram in Gene Function and Expression, University of Massachusetts Medical School, United States.
Barbara Panning
Protein Express (United States) · USUniversity of California, San Francisco · US

Funding

Investigation of the Tip60-p400 complex role in embryonic stem cell self-renR01GM085186 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PANNING, BARBARA · 2009 to 2012
$1.2M
The role of chromatin regulation in normal and cancer stem cell self-renawalR00CA140854 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FAZZIO, THOMAS G · 2010 to 2012
$732k
NCI NIH HHS 4R00CA140854-02NCI NIH HHS R00 CA140854NIGMS NIH HHS R01 GM085186NIGMS NIH HHS R01GM085186
6 · The paper itself

Abstract

Embryonic stem (ES) cells are pluripotent cells that can self-renew indefinitely or be induced to differentiate into multiple cell lineages, and thus have the potential to be used in regenerative medicine. Pluripotency transcription factors (TFs), such as Oct4, Sox2, and Nanog, function in a regulatory circuit that silences the expression of key TFs required for differentiation and activates the expression of genes important for maintenance of pluripotency. In addition, proteins that remodel chromatin structure also play important roles in determining the ES cell-specific gene expression pattern. Here we review recent studies demonstrating the roles of enzymes that carry out one facet of chromatin regulation, nucleosome remodeling, in control of ES cell self-renewal and differentiation.

Indexed as

Cell DifferentiationChromatin Assembly and DisassemblyAnimalsCell LineageEmbryonic Stem CellsGene Expression ProfilingNucleosomesPluripotent Stem CellsTranscription FactorsNucleosomesTranscription Factors

Identifiers

PMID20800472
PMCPMC3001349
OpenAlexW1965931598

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.