Evidence map›Paper›PMID 34597136›Full record

ArticleScience advances2021

The ETS transcription factor ERF controls the exit from the naïve pluripotent state in a MAPK-dependent manner.

Maria Vega-Sendino, Teresa Olbrich, Desiree Tillo, Andy D Tran, Catherine N Domingo, Mariajose Franco, Peter C FitzGerald, Michael J Kruhlak, Sergio Ruiz

Abstract read
In one paragraph

Article in Science advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

9 authors.

Maria Vega-SendinoLaboratory of Genome Integrity, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0001-8179-6335
Teresa OlbrichLaboratory of Genome Integrity, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.
Desiree TilloGenetics Branch, CCR, NCI, National Institutes of Health, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-3568-6148
Andy D TranLaboratory of Cancer Biology and Genetics, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-2388-7121
Catherine N DomingoLaboratory of Genome Integrity, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.
Mariajose FrancoLaboratory of Genome Integrity, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-9512-4086
Peter C FitzGeraldGenome Analysis Unit, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.
Michael J KruhlakLaboratory of Cancer Biology and Genetics, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.
Sergio RuizLaboratory of Genome Integrity, CCR, NCI, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-0177-6965

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The naïve epiblast transitions to a pluripotent primed state during embryo implantation. Despite the relevance of the FGF pathway during this period, little is known about the downstream effectors regulating this signaling. Here, we examined the molecular mechanisms coordinating the naïve to primed transition by using inducible ESC to genetically eliminate all RAS proteins. We show that differentiated RAS

Identifiers

PMID34597136
PMCPMC10292047

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.