A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00335-009-9191-8.pdf
Reference31 articles.
1. Ahmad W, Faiyaz ul Haque M, Brancolini V, Tsou HC, ul Haque S et al (1998a) Alopecia universalis associated with a mutation in the human hairless gene. Science 279:720–724
2. Ahmad W, Panteleyev AA, Henson-Apollonio V, Sundberg JP, Christiano AM (1998b) Molecular basis of a novel rhino (hr(rhChr)) phenotype: a nonsense mutation in the mouse hairless gene. Exp Dermatol 7:298–301
3. Ahmad W, Panteleyev AA, Sundberg AA, Christiano AM (1998c) Molecular basis for the rhino (hrrh-8 J) phenotype: a nonsense mutation in the mouse hairless gene. Genomics 53:383–386
4. Ahmad W, Nomura K, McGrath JA, Hashimoto I, Christiano AM (1999a) A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia. J Invest Dermatol 113:281–283
5. Ahmad W, Panteleyev AA, Christiano AM (1999b) The molecular basis of congenital atrichia in humans and mice: mutations in the hairless gene. J Invest Dermatol Symp Proc 4:240–243
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