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Article

Craniofacial shape variation in Twist1+/- mutant mice.

Anatomical record (Hoboken, N.J. : 2007) - 1 May 2014

Parsons Trish E, Weinberg Seth M, Khaksarfard Kameron, Howie R Nicole, Elsalanty Mohammed, Yu Jack C, Cray James J

Abstract excerpt

Craniosynostosis (CS) is a relatively common birth defect resulting from the premature fusion of one or more cranial sutures. Human genetic studies have identified several genes in association with CS. One such gene that has been implicated in both syndromic (Saethre-Chotzen syndrome) and nonsyndromic forms of CS in humans is TWIST1. In this study, a heterozygous Twist1 knock out (Twist1(+/-) ) mouse model was...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24585549
DOI: 10.1002/ar.22899

Genes

TWIST1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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