Art

J-GLOBAL ID：200902179920757601   Reference number：99A0803258

Gene Amplification as a Common Cause of Inherited Thyroxine-Binding Globulin Excess. Analysis of One Familial and Two Sporadic Cases.

遺伝性チロキシン結合グロブリン過剰の共通原因としての遺伝子増幅 1家族と2特発症例の分析

Author (8)： MORI Y (Aichi Medical Univ., Nagakute, JPN) ,  JING P (Aichi Medical Univ., Nagakute, JPN) ,  FUJIEDA K (Hokkaido Univ. School of Medicine, Sapporo, JPN) ,  HASEGAWA T (Tokyo Metropolitan Kiyose Children’s Hospital, Tokyo, JPN) ,  KAYAMA M (Aichi Medical Univ., Nagakute, JPN) ,  NOGIMORI T (Konanshowa Hospital, Konan, JPN) ,  HIROOKA Y (Aichi Medical Univ., Nagakute, JPN) ,  MITSUMA T (Aichi Medical Univ., Nagakute, JPN)
Material： Endocrine Journal  (Endocr J)
Volume： 46  Issue： 4  Page： 613-619  Publication year： Aug. 1999 
JST Material Number： F0625A  ISSN： 0918-8959  Document type： Article
Article type： 短報  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： LOH ,...
Semi thesaurus term： thyroxine binding globulin ,...

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JST classification (2)： Endocrine diseases  (GL03000I) ,  Structure and chemistry of genes  (EC02020U)

Reference (32)：

• 1). Refetoff S, Larsen R (1989) Transport, cellular uptake, and metabolism of thyroid hormone. In: DeGroot LJ (ed) Endocrinology. 2nd ed. Saunders, Philadelphia, 541-561.
• 2). Trent JM, Flink IL, Morkin E, Tuinen PV, Ledbetter DH (1987) Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22). Am J Hum Genet 41: 428-435.
• 3). Mori Y, Miura Y Oiso Y, Seo H, Takazumi K (1995) Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization. Human Genetics 96: 481-482.
• 4). Refetoff S (1989) Inherited thyroxine-binding globulin abnormalities in man. Endocr Rev 10: 275-293.
• 5). Lyon MF (1961) Genetic, gene action in the X-chromosome of the mouse (Mus musculus L). Nature 190:372-373.

Terms in the title (6)： 遺伝性チロキシン結合グロブリン過剰 ,  原因 ,  遺伝子増幅 ,  家族 ,  症例 ,  分析