Evidence map›Paper›PMID 19562686›Full record

ReviewJournal of cellular physiology2009

Stem cell pluripotency: a cellular trait that depends on transcription factors, chromatin state and a checkpoint deficient cell cycle.

Kenneth R Boheler

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cellular physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Frontiers in genetics · 2026
    Article
  3. Regulators of liver cancer stem cells.World journal of stem cells · 2021
    Review
  4. Tissue and cell-type-specific transduction using rAAV vectors in lung diseases.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  5. METTL3-mediated mStem cell research & therapy · 2021
    Article
  6. A Tale of Two States: Pluripotency Regulation of Telomeres.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
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  17. Article
  18. Article
  19. 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

1 author at 1 institution in 1 country.

Kenneth R BohelerNational Institute on Aging, NIH, Baltimore, Maryland 21224, USA. bohelerk@grc.nia.nih.gov
National Institute on Aging · US

Funding

Embryonic Stem Cell Pluripotency and Early DifferentiationZIAAG000847 · NIA · NATIONAL INSTITUTE ON AGING · PI BOHELER, KENNETH · 2009 to 2012
$2.5M
Embryonic Stem Cell Pluripotency and Early DifferentiationZ01AG000847 · NIA · NATIONAL INSTITUTE ON AGING · PI BOHELER, KENNETH · 2008 to 2008
$446k
Intramural NIH HHS Z01 AG000847
6 · The paper itself

Abstract

Embryonic stem (ES) and induced pluripotent stem (iPS) cells self-renew and are pluripotent. Differentiation of these cells can yield over 200 somatic cell types, making pluripotent cells an obvious source for regenerative medicine. Before the potential of these cells can be maximally harnessed for clinical applications, it will be necessary to understand the processes that maintain pluripotentiality and signal differentiation. Currently, three unique molecular properties distinguish pluripotent stem cells from somatic cells. These include a unique transcriptional hierarchy that sustains the pluripotent state during the process of self-renewal; a poised epigenetic state that maintains chromatin in a form ready for rapid cell fate decisions; and a cell cycle characterized by an extremely short gap 1 (G1) phase and the near absence of normal somatic cell checkpoint controls. Recently, B-MYB (MYBL2) was implicated in the gene regulation of two pluripotency factors and normal cell cycle progression. In this article, the three pluripotency properties and the potential role of B-Myb to regulate these processes will be discussed.

Indexed as

Cell CycleAnimalsChromatinEpigenesis, GeneticHumansPluripotent Stem CellsTranscription FactorsChromatinTranscription Factors

Identifiers

PMID19562686
PMCPMC3326661
OpenAlexW1967351943

What Socratic 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 Socratic graph.