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J-GLOBAL ID：200902195380656741   Reference number：01A0018794

A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms’ Tumors.

ヒト染色体11p15.5のWT2臨界領域中の新規すり込み遺伝子KNCQ1DNとWilms腫ようでの発現の減少

Author (9)： XIN Z (Saga Medical School, Saga) ,  SOEJIMA H (Saga Medical School, Saga) ,  HIGASHIMOTO K (Saga Medical School, Saga) ,  YATSUKI H (Saga Medical School, Saga) ,  KANEKO Y (Saitama Cancer Center Hospital, Saitama) ,  JINNO Y (Ryukyu Univ. School of Medicine, Okinawa) ,  FUKUZAWA R (Keio Univ. School of Medicine, Tokyo) ,  HATA J (Keio Univ. School of Medicine, Tokyo) ,  MUKAI T (Saga Medical School, Saga)
Material： Journal of Biochemistry  (J Biochem)
Volume： 128  Issue： 5  Page： 847-853  Publication year： Nov. 01, 2000 
JST Material Number： F0286A  ISSN： 0021-924X  CODEN： JOBIAO  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： human(primates) ,...
Semi thesaurus term： *nephroblastoma ,...

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JST classification (2)： Gene expression  (EC02040Q) ,  Carcinogenic mechanisms and factors  (GE02020C)

Reference (45)：

• SURANI, M. A. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature. 1984, 308, 548-550
• MCGRATH, J. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell. 1984, 37, 179-183
• PING, A. J. Genetic linkage of Beckwith-Wiedemann Syndrome to 11p15. Am. J. Hum. Genet. 1989, 44, 720-723
• HOOVERS, J. M. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann Syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc. Natl. Acad. Sci. USA. 1995, 92, 12456-12460
• MANNENS, M. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann Syndrome and various human neoplasia. Eur. J. Hum. Genet. 1994, 2, 3-23

Terms in the title (5)： ヒト ,  臨界 ,  遺伝子 ,  Wilms腫よう ,  発現