Evidence map›Paper›PMID 28654420›Full record

ArticleeLife2017

Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2.

Pierluigi Scerbo, Leslie Marchal, Laurent Kodjabachian

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

3 authors at 1 institution in 1 country.

Pierluigi ScerboInstitut de Biologie du Développement de Marseille, Aix Marseille Univ, CNRS, Marseille, France.
Leslie MarchalInstitut de Biologie du Développement de Marseille, Aix Marseille Univ, CNRS, Marseille, France.
Laurent KodjabachianInstitut de Biologie du Développement de Marseille, Aix Marseille Univ, CNRS, Marseille, France.ORCID 0000-0002-4000-612X
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During early embryogenesis, cells must exit pluripotency and commit to multiple lineages in all germ-layers. How this transition is operated in vivo is poorly understood. Here, we report that MEK1 and the Nanog-related transcription factor Ventx2 coordinate this transition. MEK1 was required to make

Indexed as

Cell DifferentiationAnimalsHomeodomain ProteinsMAP Kinase Kinase 1Pluripotent Stem CellsTranscription FactorsXenopusXenopus ProteinsHomeodomain ProteinsMAP Kinase Kinase 1Transcription Factorsventx2.1 protein, XenopusXenopus Proteinsasymmetric divisioncell biologydevelopmental biologyMEK1pluripotencystem cellsVentxxenopus

Identifiers

PMID28654420
PMCPMC5487210
OpenAlexW2731338604

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.