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Items: 1 to 20 of 146

1.

Alopecia universalis associated with a mutation in the human hairless gene.

Ahmad W, Faiyaz ul Haque M, Brancolini V, Tsou HC, ul Haque S, Lam H, Aita VM, Owen J, deBlaquiere M, Frank J, Cserhalmi-Friedman PB, Leask A, McGrath JA, Peacocke M, Ahmad M, Ott J, Christiano AM.

Science. 1998 Jan 30;279(5351):720-4.

2.

[Mutation of the human hairless gene in atrichia universalis].

Trüeb RM.

Hautarzt. 1998 Sep;49(9):687-9. German.

PMID:
9794156
3.

A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

Ahmad W, Irvine AD, Lam H, Buckley C, Bingham EA, Panteleyev AA, Ahmad M, McGrath JA, Christiano AM.

Am J Hum Genet. 1998 Oct;63(4):984-91.

4.

Atrichia with papular lesions maps to 8p in the region containing the human hairless gene.

Sprecher E, Bergman R, Szargel R, Raz T, Labay V, Ramon M, Baruch-Gershoni R, Friedman-Birnbaum R, Cohen N.

Am J Med Genet. 1998 Dec 28;80(5):546-50.

PMID:
9880231
5.

A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions.

Aita VM, Ahmad W, Panteleyev AA, Kozlowska U, Kozlowska A, Gilliam TC, Jablonska S, Christiano AM.

Exp Dermatol. 2000 Apr;9(2):157-62.

PMID:
10772391
6.

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.

Cichon S, Anker M, Vogt IR, Rohleder H, Pützstück M, Hillmer A, Farooq SA, Al-Dhafri KS, Ahmad M, Haque S, Rietschel M, Propping P, Kruse R, Nöthen MM.

Hum Mol Genet. 1998 Oct;7(11):1671-9. Erratum in: Hum Mol Genet 1998 Nov;7(12):1987-8.

7.

A novel missense mutation in the mouse hairless gene causes irreversible hair loss: genetic and molecular analyses of Hr m1Enu.

Nam Y, Kim JK, Cha DS, Cho JW, Cho KH, Yoon S, Yoon JB, Oh YS, Suh JG, Han SS, Song CW, Yoon SK.

Genomics. 2006 Apr;87(4):520-6. Epub 2006 Feb 7.

8.

Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene.

Paradisi M, Chuang GS, Angelo C, Pedicelli C, Martinez-Mir A, Christiano AM.

Clin Exp Dermatol. 2003 Sep;28(5):535-8.

PMID:
12950347
9.

Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene.

Ahmad W, Ratterree MS, Panteleyev AA, Aita VM, Sundberg JP, Christiano AM.

Lab Anim. 2002 Jan;36(1):61-7.

PMID:
11831740
10.
11.

Structure and expression of the hairless gene of mice.

Cachon-Gonzalez MB, Fenner S, Coffin JM, Moran C, Best S, Stoye JP.

Proc Natl Acad Sci U S A. 1994 Aug 2;91(16):7717-21.

12.
13.
14.

Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.

Lefevre P, Rochat A, Bodemer C, Vabres P, Barrandon Y, de Prost Y, Garner C, Hovnanian A.

Eur J Hum Genet. 2000 Apr;8(4):273-9.

15.

A gene for universal congenital alopecia maps to chromosome 8p21-22.

Nöthen MM, Cichon S, Vogt IR, Hemmer S, Kruse R, Knapp M, Höller T, Faiyaz ul Haque M, Haque S, Propping P, Ahmad M, Rietschel M.

Am J Hum Genet. 1998 Feb;62(2):386-90.

16.

Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family.

Ahmad W, Zlotogorski A, Panteleyev AA, Lam H, Ahmad M, Faiyaz ul Haque M, Abdallah HM, Dragan L, Christiano AM.

Genomics. 1999 Mar 1;56(2):141-8.

PMID:
10051399
17.

Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions.

Djabali K, Zlotogorski A, Metzker A, Ben-Amitai D, Christiano AM.

Exp Dermatol. 2004 Apr;13(4):251-6.

PMID:
15086341
18.

Identification of a novel splice site mutation in the human hairless gene underlying atrichia with papular lesions.

Paradisi M, Massé M, Martinez-Mir A, Lam H, Pedicelli C, Christiano AM.

Eur J Dermatol. 2005 Sep-Oct;15(5):332-8.

PMID:
16172039
19.

Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.

Panteleyev AA, Paus R, Ahmad W, Sundberg JP, Christiano AM.

Exp Dermatol. 1998 Oct;7(5):249-67. Review.

PMID:
9832313
20.

Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.

Scott DA, Greinwald JH Jr, Marietta JR, Drury S, Swiderski RE, Viñas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K, Skworak AB, Friedman RA, Srikumari Srisailapathy CR, Verhoeven K, Van Gamp G, Lovett M, Deininger PL, Batzer MA, Morton CC, Keats BJ, Smith RJ, Sheffield VC.

Gene. 1998 Jul 30;215(2):461-9.

PMID:
9758550
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