Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

735 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.
Panteleyev AA, Paus R, Ahmad W, Sundberg JP, Christiano AM. Panteleyev AA, et al. Exp Dermatol. 1998 Oct;7(5):249-67. doi: 10.1111/j.1600-0625.1998.tb00295.x-i1. Exp Dermatol. 1998. PMID: 9832313 Review.
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. Ahmad W, et al. Science. 1998 Jan 30;279(5351):720-4. doi: 10.1126/science.279.5351.720. Science. 1998. PMID: 9445480
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. Ahmad W, et al. Am J Hum Genet. 1998 Oct;63(4):984-91. doi: 10.1086/302069. Am J Hum Genet. 1998. PMID: 9758627 Free PMC article.
Molecular basis for the rhino Yurlovo (hr(rhY)) phenotype: severe skin abnormalities and female reproductive defects associated with an insertion in the hairless gene.
Panteleyev AA, Ahmad W, Malashenko AM, Ignatieva EL, Paus R, Sundberg JP, Christiano AM. Panteleyev AA, et al. Exp Dermatol. 1998 Oct;7(5):281-8. doi: 10.1111/j.1600-0625.1998.tb00298.x-i1. Exp Dermatol. 1998. PMID: 9832316
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. Ahmad W, et al. Genomics. 1999 Mar 1;56(2):141-8. doi: 10.1006/geno.1998.5699. Genomics. 1999. PMID: 10051399
Identification of a de novo glycine substitution in the type VII collagen gene in a proband with mild dystrophic epidermolysis bullosa.
Cserhalmi-Friedman PB, Grossman J, Karpati S, Ahmad W, Horvath A, Christiano AM. Cserhalmi-Friedman PB, et al. Exp Dermatol. 1999 Apr;8(2):143-5. doi: 10.1111/j.1600-0625.1999.tb00363.x. Exp Dermatol. 1999. PMID: 10232407
Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies.
Frank J, Nelson J, Wang X, Yang L, Ahmad W, Lam H, Jugert FK, Kalka K, Poh-Fitzpatrick MB, Goerz G, Merk HF, Christiano AM. Frank J, et al. J Investig Med. 1999 Jul;47(6):278-84. J Investig Med. 1999. PMID: 10431482
735 results
Jump to page
Feedback