Evidence map›Paper›PMID 24710206›Full record

ArticleGenes2011

Understanding the molecular circuitry of cell lineage specification in the early mouse embryo.

Anna Bergsmedh, Mary E Donohoe, Rebecca-Ayme Hughes, Anna-Katerina Hadjantonakis

Abstract read
In one paragraph

Article in Genes, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. 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

4 authors.

Anna BergsmedhCenter for Reproductive Medicine and Infertility, Weill Cornell Medical College, New York, NY 10065, USA. anna.bergsmedh@me.com.
Mary E DonohoeBurke Medical Research Institute, White Plains, NY 10605, USA. med2008@med.cornell.edu.
Rebecca-Ayme HughesBurke Medical Research Institute, White Plains, NY 10605, USA. reh2010@med.cornell.edu.
Anna-Katerina HadjantonakisDevelopmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA. hadj@mskcc.org.

Funding

Morphogenesis of the paraxial mesoderm in miceR01HD052115 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI HADJANTONAKIS, ANNA-KATERINA · 2006 to 2015
$4.1M
Morphogenesis of mammalian gut endodermR01DK084391 · NIDDK · SLOAN-KETTERING INST CAN RESEARCH · PI HADJANTONAKIS, ANNA-KATERINA · 2009 to 2018
$4.1M
Allelic Choice in Rett SyndromeR01MH090267 · NIMH · WINIFRED MASTERSON BURKE MED RES INST · PI DONOHOE, MARY E · 2010 to 2014
$1.9M
NICHD NIH HHS R01 HD052115NIDDK NIH HHS R01 DK084391NIMH NIH HHS R01 MH090267
6 · The paper itself

Abstract

Pluripotent stem cells hold great promise for cell-based therapies in regenerative medicine. However, critical to understanding and exploiting mechanisms of cell lineage specification, epigenetic reprogramming, and the optimal environment for maintaining and differentiating pluripotent stem cells is a fundamental knowledge of how these events occur in normal embryogenesis. The early mouse embryo has provided an excellent model to interrogate events crucial in cell lineage commitment and plasticity, as well as for embryo-derived lineage-specific stem cells and induced pluripotent stem (iPS) cells. Here we provide an overview of cell lineage specification in the early (preimplantation) mouse embryo focusing on the transcriptional circuitry and epigenetic marks necessary for successive differentiation events leading to the formation of the blastocyst.

Identifiers

PMID24710206
PMCPMC3927619

What OpenQuestion holds

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Registered trials

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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.