Role of cilia in structural birth defects: Insights from ciliopathy mutant mouse models
Author:
Affiliation:
1. Department of Developmental Biology; University of Pittsburgh School of Medicine; Pittsburgh Pennsylvania
2. Program in Molecular Medicine; University of Massachusetts Medical School; Worcester Massachusetts
Funder
National Institutes of Health
Publisher
Wiley
Subject
Developmental Biology,Embryology,General Medicine
Reference45 articles.
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4. IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy;Beales;Nat Genet,2007
5. Abnormal development of NG2+PDGFR-alpha+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model;Carter;Nat Med,2012
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