Evidence map›Paper›PMID 31649239›Full record

ArticleCell death & disease2019

Severe head dysgenesis resulting from imbalance between anterior and posterior ontogenetic programs.

Emmanuelle Grall, Victor Gourain, Asmaa Naïr, Elisabeth Martin, Marie-Christine Birling, Jean-Noël Freund, Isabelle Duluc

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 3 institutions in 2 countries.

Emmanuelle GrallUniversité de Strasbourg, Inserm, IRFAC/UMR-S1113, FMTS, 67200, Strasbourg, France.
Victor GourainKarlsruhe Institute of Technology, Institute of Toxicology and Genetics, 76021, Karlsruhe, Germany.ORCID http://orcid.org/0000-0002-6483-0738
Asmaa NaïrUniversité de Strasbourg, Inserm, IRFAC/UMR-S1113, FMTS, 67200, Strasbourg, France.
Elisabeth MartinUniversité de Strasbourg, Inserm, IRFAC/UMR-S1113, FMTS, 67200, Strasbourg, France.
Marie-Christine BirlingInstitut Clinique de la Souris, 67404, Illkirch Cedex, France.
Jean-Noël FreundUniversité de Strasbourg, Inserm, IRFAC/UMR-S1113, FMTS, 67200, Strasbourg, France. jean-noel.freund@inserm.fr.ORCID http://orcid.org/0000-0002-0971-3774
Isabelle DulucUniversité de Strasbourg, Inserm, IRFAC/UMR-S1113, FMTS, 67200, Strasbourg, France. isabelle.duluc@inserm.fr.ORCID http://orcid.org/0000-0001-8396-6385
Inserm · FRInstitut Clinique de la Souris · FRKarlsruhe Institute of Technology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Head dysgenesis is a major cause of fetal demise and craniofacial malformation. Although mutations in genes of the head ontogenetic program have been reported, many cases remain unexplained. Head dysgenesis has also been related to trisomy or amplification of the chromosomal region overlapping the CDX2 homeobox gene, a master element of the trunk ontogenetic program. Hence, we investigated the repercussion on head morphogenesis of the imbalance between the head and trunk ontogenetic programs, by means of ectopic rostral expression of CDX2 at gastrulation. This caused severe malformations affecting the forebrain and optic structures, and also the frontonasal process associated with defects in neural crest cells colonization. These malformations are the result of the downregulation of genes of the head program together with the abnormal induction of trunk program genes. Together, these data indicate that the imbalance between the anterior and posterior ontogenetic programs in embryos is a new possible cause of head dysgenesis during human development, linked to defects in setting up anterior neuroectodermal structures.

Indexed as

AnimalsCDX2 Transcription FactorCraniofacial AbnormalitiesEmbryonic DevelopmentGastrulationGene Expression Regulation, DevelopmentalGenes, HomeoboxHeadHumansMiceMorphogenesisNeural CrestProsencephalonCdx2 protein, mouseCDX2 Transcription Factor

Identifiers

PMID31649239
PMCPMC6813351
OpenAlexW2981454062

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.