Evidence map›Paper›PMID 22761038›Full record

ReviewWiley interdisciplinary reviews. Systems biology and medicine

The molecular circuitry underlying pluripotency in embryonic stem cells.

Aryeh Warmflash, Brigitte L Arduini, Ali H Brivanlou

Abstract readReview
In one paragraph

Review in Wiley interdisciplinary reviews. Systems biology and medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. International journal of biological sciences · 2023
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Regulatory non-coding RNAs in pluripotent stem cells.International journal of molecular sciences · 2013
    Review
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

3 authors.

Aryeh WarmflashLaboratory of Molecular Vertebrate Embryology, The Rockefeller University, New York, NY, USA.
Brigitte L Arduini
Ali H Brivanlou

Funding

Dynamic readout of TGFb signaling and modeling of cell fate specification in humaR01GM101653 · NIGMS · ROCKEFELLER UNIVERSITY · PI BRIVANLOU, ALI H, SIGGIA, ERIC D. · 2012 to 2020
$2.6M
Dissecting embryonic axis formation using micropatterned hESC colony architectureR01HD080699 · NICHD · ROCKEFELLER UNIVERSITY · PI BRIVANLOU, ALI H, SIGGIA, ERIC D. · 2014 to 2018
$1.7M
NICHD NIH HHS R01 HD080699NIGMS NIH HHS R01 GM101653
6 · The paper itself

Abstract

Cells in the pluripotent state have the ability to self-renew indefinitely and to differentiate to all the cells of the embryo. These cells provide an in vitro window into development, including human development, as well as holding extraordinary promise for cell-based therapies in regenerative medicine. The recent demonstration that somatic cells can be reprogrammed to the pluripotent state has raised the possibility of patient and disease-specific induced pluripotent cells. In this article, we review the molecular underpinning of pluripotency. We focus on the transcriptional and signaling networks that underlie the state of pluripotency and control differentiation. In general, the action of each of the molecular components and pathways is dose and context dependent highlighting the need for a systems approach to understanding pluripotency.

Indexed as

AnimalsCell DifferentiationCellular ReprogrammingEmbryonic Stem CellsHumansRegenerative MedicineSignal TransductionTranscription FactorsTranscription Factors

Identifiers

PMID22761038
PMCPMC5872147

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.