Literature DB >> 10469319

A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia.

W Ahmad, K Nomura, J A McGrath, I Hashimoto, A M Christiano.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1999        PMID： 10469319     DOI： 10.1046/j.1523-1747.1999.00686.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


× No keyword cloud information.
  3 in total

1.  Molecular basis for hair loss in mice carrying a novel nonsense mutation (Hrrh-R ) in the hairless gene (Hr).

Authors:  Y Liu; J P Sundberg; S Das; D Carpenter; K T Cain; E J Michaud; B H Voy
Journal:  Vet Pathol       Date:  2010-01       Impact factor: 2.221

2.  A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis.

Authors:  In Cheol Baek; Jeong Ki Kim; Kyu-Hyuk Cho; Dal-Sun Cha; Jae-Woo Cho; Jong Keun Park; Chang-Woo Song; Sungjoo Kim Yoon
Journal:  Mamm Genome       Date:  2009-06-10       Impact factor: 2.957

3.  Mutations in the hairless gene underlie APL in three families of Pakistani origin.

Authors:  Liv Kraemer; Muhammad Wajid; Yutaka Shimomura; Angela M Christiano
Journal:  J Dermatol Sci       Date:  2008-04       Impact factor: 4.563
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.