A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat model
- 1 December 2004
- journal article
- Published by Elsevier in Differentiation
- Vol. 72 (9-10) , 541-547
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” ratDifferentiation, 2004
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive HypotrichosisJournal of Investigative Dermatology, 2004
- A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive HypotrichosisJournal of Investigative Dermatology, 2004
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 geneGenomics, 2004
- Genetic Evidence for a Novel Human Desmosomal Cadherin, Desmoglein 4Journal of Investigative Dermatology, 2003
- Desmoglein 4 in Hair Follicle Differentiation and Epidermal AdhesionCell, 2003
- C-Cadherin Ectodomain Structure and Implications for Cell Adhesion MechanismsScience, 2002
- The Catalog of Human Hair KeratinsJournal of Biological Chemistry, 2001
- Lanceolate hair‐J (lahJ): A mouse model for human hair disordersExperimental Dermatology, 2000
- Complexity and expression patterns of the desmosomal cadherins.Proceedings of the National Academy of Sciences, 1992