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Volumn 34, Issue 8, 2009, Pages

Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILD; CONTROLLED STUDY; FEMALE; FOUNDER EFFECT; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; HUMAN; HYPOTRICHOSIS; MAJOR CLINICAL STUDY; MALE; MARIE UNNA HEREDITARY HYPOTRICHOSIS; MIDDLE EAST; PRIORITY JOURNAL; SCHOOL CHILD; TURKEY (REPUBLIC); U2HR GENE;

EID: 72549102913     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2009.03644.x     Document Type: Article
Times cited : (14)

References (9)
  • 1
    • 0001539639 scopus 로고
    • Über Hypotrichosis congenita hereditaria
    • Unna M. Über Hypotrichosis congenita hereditaria. Dermatol Wochenschr 1925 81 : 1167 1178.
    • (1925) Dermatol Wochenschr , vol.81 , pp. 1167-1178
    • Unna, M.1
  • 2
    • 0342961071 scopus 로고    scopus 로고
    • Marie Unna hypotrichosis in an Asian family
    • Kim HS, Kim SC, Lee WS. Marie Unna hypotrichosis in an Asian family. J Dermatol 2001 28 : 149 152.
    • (2001) J Dermatol , vol.28 , pp. 149-152
    • Kim, H.S.1    Kim, S.C.2    Lee, W.S.3
  • 3
    • 0036285540 scopus 로고    scopus 로고
    • Marie Unna hypotrichosis in a Chinese family
    • Wong SN, Giam YC, Lee YS. Marie Unna hypotrichosis in a Chinese family. Pediatr Dermatol 2002 19 : 250 255.
    • (2002) Pediatr Dermatol , vol.19 , pp. 250-255
    • Wong, S.N.1    Giam, Y.C.2    Lee, Y.S.3
  • 4
    • 0033752012 scopus 로고    scopus 로고
    • A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
    • Cichon S, Kruse R, Hillmer AM et al. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family. Br J Dermatol 2000 143 : 811 814.
    • (2000) Br J Dermatol , vol.143 , pp. 811-814
    • Cichon, S.1    Kruse, R.2    Hillmer, A.M.3
  • 5
    • 0033362170 scopus 로고    scopus 로고
    • The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: Exclusion of the hr gene by cDNA and genomic sequencing
    • van Steensel M, Smith FJ, Steijlen PM et al. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing. Am J Hum Genet 1999 65 : 413 419.
    • (1999) Am J Hum Genet , vol.65 , pp. 413-419
    • Van Steensel, M.1    Smith, F.J.2    Steijlen, P.M.3
  • 6
    • 0034074163 scopus 로고    scopus 로고
    • 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 et al. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis. Eur J Hum Genet 2000 8 : 273 279.
    • (2000) Eur J Hum Genet , vol.8 , pp. 273-279
    • Lefevre, P.1    Rochat, A.2    Bodemer, C.3
  • 7
    • 3042780312 scopus 로고    scopus 로고
    • Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3
    • He PP, Zhang XJ, Yang Q et al. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3. Br J Dermatol 2004 150 : 837 842.
    • (2004) Br J Dermatol , vol.150 , pp. 837-842
    • He, P.P.1    Zhang, X.J.2    Yang, Q.3
  • 8
    • 34249705636 scopus 로고    scopus 로고
    • Congenital atrichia
    • In. Sprecher, E. ed). New York. Nova Science Publishers
    • Cichon S, Hillmer A, Betz RC et al. Congenital atrichia. In : Progress in Monogenic Hair Disorders (Sprecher E, ed). New York : Nova Science Publishers, 2006 77 89.
    • (2006) Progress in Monogenic Hair Disorders , pp. 77-89
    • Cichon, S.1    Hillmer, A.2    Betz, R.C.3
  • 9
    • 59149083659 scopus 로고    scopus 로고
    • Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
    • Wen Y, Liu Y, Xu Y et al. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. Nat Genet 2009 41 : 228 233.
    • (2009) Nat Genet , vol.41 , pp. 228-233
    • Wen, Y.1    Liu, Y.2    Xu, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.