Evidence map›Paper›PMID 23092754›Full record

ReviewCurrent opinion in cell biology2013

Signaling networks in human pluripotent stem cells.

Stephen Dalton

Abstract readReview
In one paragraph

Review in Current opinion in cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
–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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  15. Cell stemness is maintained upon concurrent expression of RB and the mitochondrial ribosomal protein S18-2.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Article
  17. PI3K in stemness regulation: from development to cancer.Biochemical Society transactions · 2020
    Review
  18. Article
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  20. 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

1 author.

Stephen DaltonPaul D. Coverdell Center for Biomedical and Health Science, Department of Biochemistry and Molecular Biology, University of Georgia, 500 DW Brooks Drive, Athens, GA 30602, United States. sdalton@uga.edu

Funding

UNDERSTANDING MECHANISMS OF hESC SELF-RENEWAL AND CELL FATE COMMITMENTP01GM085354 · NIGMS · UNIVERSITY OF GEORGIA · PI DALTON, STEPHEN · 2008 to 2018
$18.3M
Embryonic stem cell renewal-Myc transcription factorsR01HD049647 · NICHD · UNIVERSITY OF GEORGIA · PI DALTON, STEPHEN · 2006 to 2010
$1.5M
NICHD NIH HHS R01 HD049647NIGMS NIH HHS P01 GM085354
6 · The paper itself

Abstract

Maintaining a finely-balanced network of signaling inputs is critical for the maintenance of pluripotent stem cells. Together, signaling pathways achieve this by maintaining a long-term, proliferative state while suppressing differentiation. Although the major pathways involved in pluripotency have been known for some time, it was not previously clear how they function in concert to maintain stem cell identity. Recent work has identified a signaling network involving cross-talk between PI3K, TGFβ, MAPK and Wnt pathways that culminate in a finely-balanced molecular switch that determines the fate of pluripotent cells.

Indexed as

Signal TransductionActivinsAnimalsCell DifferentiationFibroblast Growth Factor 2HumansInsulinMAP Kinase Signaling SystemPhosphatidylinositol 3-KinasesPluripotent Stem CellsProto-Oncogene Proteins c-aktSmad ProteinsTransforming Growth Factor betaWnt Signaling PathwayActivinsFibroblast Growth Factor 2InsulinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSmad ProteinsTransforming Growth Factor beta

Identifiers

PMID23092754
PMCPMC3570582

What OpenQuestion holds

Textmetadata
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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.