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Volumn 121, Issue 2, 2003, Pages 430-432

Compound heterozygous mutations in the hairless gene in atrichia with papular lesions [4]

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOSTEROID; MINOXIDIL;

EID: 0041742192     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1747.2003.12370.x     Document Type: Article
Times cited : (24)

References (14)
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    • Alopecia universalis associated with a mutation in the human hairless gene
    • Ahmad W, ul Haque MF, Brancolini V, et al: Alopecia universalis associated with a mutation in the human hairless gene. Science 279:720-724, 1998
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    • Ahmad, W.1    Ul Haque, M.F.2    Brancolini, V.3
  • 2
    • 0033499173 scopus 로고    scopus 로고
    • A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia
    • Ahmad W, Nomura K, McGrath JA, Hashimoto I, Christiano AM: A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia. J Invest Dermatol 113:281-283, 1999a
    • (1999) J Invest Dermatol , vol.113 , pp. 281-283
    • Ahmad, W.1    Nomura, K.2    McGrath, J.A.3    Hashimoto, I.4    Christiano, A.M.5
  • 3
    • 0033105801 scopus 로고    scopus 로고
    • Genomic organization of the human hairless gene and identification of a mutation underlying congenital atrichia in an Arab Palestinian family
    • Ahmad W, Zlotogorski A, Panteleyev A, et al: Genomic organization of the human hairless gene and identification of a mutation underlying congenital atrichia in an Arab Palestinian family. Genomics 56:141-148, 1999b
    • (1999) Genomics , vol.56 , pp. 141-148
    • Ahmad, W.1    Zlotogorski, A.2    Panteleyev, A.3
  • 4
    • 0034124694 scopus 로고    scopus 로고
    • 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, et al: A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions. Exp Dermatol 9:157-162, 2000
    • (2000) Exp Dermatol , vol.9 , pp. 157-162
    • Aita, V.M.1    Ahmad, W.2    Panteleyev, A.A.3
  • 5
    • 7344229369 scopus 로고    scopus 로고
    • Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia
    • 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 7:1671-1679, 1998
    • (1998) Hum Mol Genet , vol.7 , pp. 1671-1679
    • Cichon, S.1    Anker, M.2    Vogt, I.R.3
  • 6
    • 0036788824 scopus 로고    scopus 로고
    • Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene. A lesson for different diagnosis of alopecia universalis
    • Henn W, Zlotogorski A, Lam H, Martinez-Mir A, Zaun H, Christiano AM: Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene. A lesson for different diagnosis of alopecia universalis. J Am Acad Dermatol 47:519-523, 2002
    • (2002) J Am Acad Dermatol , vol.47 , pp. 519-523
    • Henn, W.1    Zlotogorski, A.2    Lam, H.3    Martinez-Mir, A.4    Zaun, H.5    Christiano, A.M.6
  • 7
    • 0033386222 scopus 로고    scopus 로고
    • Novel hairless mutations in two kindreds with autosomal recessive papular atrichia
    • Kruse R, Cichon S, Anker M, et al: Novel hairless mutations in two kindreds with autosomal recessive papular atrichia. J Invest Dermatol 113:954-959, 1999
    • (1999) J Invest Dermatol , vol.113 , pp. 954-959
    • Kruse, R.1    Cichon, S.2    Anker, M.3
  • 9
    • 0026664103 scopus 로고
    • Prevalence of alopecia areata in the First National Health and Nutrition Examination Survey
    • Safavi K: Prevalence of alopecia areata in the First National Health and Nutrition Examination Survey (letter). Arch Dermatol 128:702, 1992
    • (1992) Arch Dermatol , vol.128 , pp. 702
    • Safavi, K.1
  • 10
    • 0023651307 scopus 로고
    • RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression
    • Shapiro MB, Senapathy P: RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression. Nucl Acids Res 15:7155-7174, 1987
    • (1987) Nucl Acids Res , vol.15 , pp. 7155-7174
    • Shapiro, M.B.1    Senapathy, P.2
  • 11
    • 0032835805 scopus 로고    scopus 로고
    • Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene
    • 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 113:687-690, 1999
    • (1999) J Invest Dermatol , vol.113 , pp. 687-690
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  • 12
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    • Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene
    • 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 103:400-404, 1998
    • (1998) Hum Genet , vol.103 , pp. 400-404
    • Zlotogorski, A.1    Ahmad, W.2    Christiano, A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.