Art

J-GLOBAL ID：200902292445952217   Reference number：05A0769918

Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations

新しい変異を速く決定するための正常に色素化したインド人と日本人におけるチロシナーゼ配列データーベースの確立

Author (10)： MIYAMURA Yoshinori (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  VERMA Ishwar C. (Dep. of Genetic Medicine, Sir Ganga Ram Hospital, New Delhi, IND) ,  SAXENA Renu (Dep. of Genetic Medicine, Sir Ganga Ram Hospital, New Delhi, IND) ,  MURASE Ayumi (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  KONO Michihiro (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  SUZUKI Tamio (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  YASUE Satoshi (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  SHIBATA Shin-ichi (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  SAKAKIBARA Akihiro (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN) ,  TOMITA Yasushi (Dep. of Dermatology, Nagoya Univ. Graduate School of Medicine, Nagoya, JPN)
Material： Journal of Dermatological Science  (J Dermatol Sci)
Volume： 39  Issue： 3  Page： 167-173  Publication year： Sep. 2005 
JST Material Number： W1280A  ISSN： 0923-1811  Document type： Article
Article type： 原著論文  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： human ,...
Semi thesaurus term： albinism

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JST classification (4)： Skin diseases  (GF03000Q) ,  Eye diseases  (GP03000U) ,  Congenital diseases,deformities in general.  (GD03010V) ,  Structure and chemistry of genes  (EC02020U)

Reference (21)：

• SHIBAHARA, S. Molecular basis for heterogeneity of human tyrosinase. Tohoku J Exp Med. 1988, 156, 403-414
• TAKEDA, A. Functional analysis of the cDNA encoding human tyrosinase precursor. Biochem Biophys Res Commun. 1989, 162, 984-990
• GIEBEL, LB. Organization and nucleotide sequence of the human tyrosinase gene and a truncated tyrosinase-related segment. Genomics. 1991, 9, 435-445
• BARTON, DE. Human tyrosinase gene, mapped to chromosome 11 (q14-q21), defines second region of homology with mouse chromosome 7. Genomics. 1988, 3, 17-24
• TOMITA, Y. Human oculocutaneous albinism caused by a single base insertion in the tyrosinase gene. Biochem Biophys Res Commun. 1989, 164, 990-996

Terms in the title (6)： 変異 ,  色素 ,  インド ,  日本人 ,  チロシナーゼ ,  データーベース