Hairless : Il s’en est fallu d’un cheveu

Medecine/Sciences

Volumn 18, Issue 3, 2002, Pages 276-280

  Bernard, Bruno A ^a  

^a L ORÉAL RECHERCHE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84996138257     PISSN: 07670974     EISSN: 19585381     Source Type: Journal    
DOI: 10.1051/medsci/2002183276     Document Type: Article

References (14)

1. Cachon-Gonzalez MB, Fenner S, Coffin JM, Moran C, Best S, Stoye JP. Strucuture and expression of the hairless gene in mice. Proc Natl Acad Sci USA 1994; 91: 7717-21.
2. Cichon S, Anker M, Vogt IR, et al.Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. Hum Mol Genet 1998; 11: 1671-79.
3. Djabali K, Aita VM, Christiano AM. Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix. J Cell Sci 2000; 114: 367-76.
4. Sprecher E, Lestringant GG, Szargel R, et al.Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene. J Invest Dermatol 1999;113: 687-90.
5. Zlotogorski A, Ahmad W, Christiano AM. Congenital atrichia in five arab palestinian families resulting from a deletion mutation in the human hairless gene. Hum Genet 1998; 103: 400-4.
6. Ahmad W, Haque MF, Brancolini V, etal. Alopecia universalis associated with a mutation in the human hairless gene. Science 1998; 279: 720-4.
7. Ahmad W, Irvine AD, Lam HM, et al. A missense mutation in the zinc-finger domain of the human hairless geneunderlies congenital atrichia in a family of irish travellers. Am J Hum Genet 1998; 63: 984-91.
8. Sprecher E, Bergman R, Szargel R, FriedmanBirnbaum R, Cohen N. Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichias. Am J Hum Genet 1999; 64:1323-29.
9. Panteleyev AA, Paus R, Christiano AM. Patterns of hairless gene expression in mouse hair follicle morphogenesis and cycling. Am J Pathol 2000; 157:1071-9.
10. Potter GB, Beaudoin GMJ, DeRenzo CL, Zarach JM, Chen SH, Thompson CC. The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor. Genes Dev 2001; 15: 2687-701.
11. Billoni N, Buan B, Gautier B, Gaillard O, Mahe YF, Bernard BA. Thyroid hormone receptor b1 is expressed in the human hair follicle. Br J Dermatol 2000; 142: 645-52.
12. Commo S, Bernard BA. Immunohistochemical analysis of tissue remodelling during the anagen-catagen transition of the human hair follicle. Br J Dermatol 1997; 137: 31-8
13. Miller J, Djabali K, Chen T, et al. Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene. J Invest Dermatol 2001; 117: 612-7.
14. Billoni N, Gautier B, Mahé YF, Bernard BA. Expression of retinoid receptor super family members in human hair follicles and its implication in hair growth. Acta Dermatol Venereol (Stockh) 1997; 77: 350-5.