Evidence map›Paper›PMID 34615475›Full record

ArticleBMC developmental biology2021

Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype.

Ramada R Khasawneh, Ralf Kist, Rachel Queen, Rafiqul Hussain, Jonathan Coxhead, Jürgen E Schneider, Timothy J Mohun, Stéphane Zaffran, Heiko Peters, Helen M Phillips and 1 more

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. PAX Genes in Cardiovascular Development.International journal of molecular sciences · 2022
    Review
  7. PAX9 in Cancer Development.International journal of molecular sciences · 2022
    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

11 authors at 6 institutions in 3 countries.

Ramada R KhasawnehNewcastle University Biosciences Institute, Centre for Life, Newcastle, NE1 3BZ, UK.
Ralf KistNewcastle University Biosciences Institute, Centre for Life, Newcastle, NE1 3BZ, UK.
Rachel QueenBioinformatics Support Unit, Newcastle University, Newcastle, NE1 3BZ, UK.
Rafiqul HussainGenomics Core Facility, Newcastle University, Newcastle, NE1 3BZ, UK.
Jonathan CoxheadGenomics Core Facility, Newcastle University, Newcastle, NE1 3BZ, UK.
Jürgen E SchneiderBiomedical Imaging, University of Leeds, Leeds, LS2 9JT, UK.
Timothy J MohunThe Francis Crick Institute, London, NW1 1AT, UK.
Stéphane ZaffranINSERM, Marseille Medical Genetics, U1251, Aix Marseille University, Marseille, France.
Heiko PetersNewcastle University Biosciences Institute, Centre for Life, Newcastle, NE1 3BZ, UK.
Helen M PhillipsNewcastle University Biosciences Institute, Centre for Life, Newcastle, NE1 3BZ, UK.
Simon D BamforthNewcastle University Biosciences Institute, Centre for Life, Newcastle, NE1 3BZ, UK. simon.bamforth@newcastle.ac.uk.
Newcastle University · GBCentre for Life · GBGenomics (United Kingdom) · GBInserm · FRThe Francis Crick Institute · GBUniversity of Leeds · GB

Funding

British Heart Foundation PG/16/39/32115British Heart Foundation PG/20/15/35041British Heart Foundation SI/14/1/30718
6 · The paper itself

Abstract

backgroundSuccessful embryogenesis relies on the coordinated interaction between genes and tissues. The transcription factors Pax9 and Msx1 genetically interact during mouse craniofacial morphogenesis, and mice deficient for either gene display abnormal tooth and palate development. Pax9 is expressed specifically in the pharyngeal endoderm at mid-embryogenesis, and mice deficient for Pax9 on a C57Bl/6 genetic background also have cardiovascular defects affecting the outflow tract and aortic arch arteries giving double-outlet right ventricle, absent common carotid arteries and interruption of the aortic arch.

resultsIn this study we have investigated both the effect of a different genetic background and Msx1 haploinsufficiency on the presentation of the Pax9-deficient cardiovascular phenotype. Compared to mice on a C57Bl/6 background, congenic CD1-Pax9

conclusionsMsx1 haploinsufficiency mitigates the arch artery defects in Pax9

Indexed as

Cardiovascular SystemHaploinsufficiencyMSX1 Transcription FactorAnimalsBranchial RegionMiceMice, KnockoutNeural CrestPAX9 Transcription FactorPhenotypeMsx1 protein, mouseMSX1 Transcription FactorPax9 protein, mousePAX9 Transcription FactorCardiovascular developmentMsx1Neural crestPax9Pharyngeal endoderm

Identifiers

PMID34615475
PMCPMC8493722
OpenAlexW3172467193

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.