Art

J-GLOBAL ID：200902226540831564   Reference number：06A0406763

Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1

刷込み遺伝子KCNQ1のイントロン1aにおける短鎖縦列反復遺伝子座での親刷込み対立遺伝子タイピング

Author (7)： XU Hong-de (Div. of Legal Medicine, Inst. of Medicine and Dentistry, Niigata Univ. Academic Assembly, 1-757 Asahimachidori ...) ,  NAITO Emiko (Div. of Legal Medicine, Inst. of Medicine and Dentistry, Niigata Univ. Academic Assembly, 1-757 Asahimachidori ...) ,  DEWA Koji (Div. of Legal Medicine, Inst. of Medicine and Dentistry, Niigata Univ. Academic Assembly, 1-757 Asahimachidori ...) ,  FUKUDA Masaaki (Div. of Legal Medicine, Inst. of Medicine and Dentistry, Niigata Univ. Academic Assembly, 1-757 Asahimachidori ...) ,  SUMI Hirokazu (Scientific Investigation Lab., Niigata Pref. Police HQ, 4-1 Shinkocho, Niigata 950-8553, JPN) ,  YUASA Isao (Div. of Legal Medicine, Fac. of Medicine, Tottori Univ., Yonago 683-8503, JPN) ,  YAMANOUCHI Haruo (Div. of Legal Medicine, Inst. of Medicine and Dentistry, Niigata Univ. Academic Assembly, 1-757 Asahimachidori ...)
Material： Legal Medicine  (Leg Med)
Volume： 8  Issue： 3  Page： 139-143  Publication year： May. 2006 
JST Material Number： W1412A  ISSN： 1344-6223  Document type： Article
Article type： 原著論文  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： human(primates) ,...
Semi thesaurus term： *ヒトKCNQ1遺伝子 ,...

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JST classification (2)： Forensic medicine  (GA03000B) ,  Research methods in genetics  (EC01020N)

Reference (20)：

• REEDER, DJ. Impact of DNA typing on standards and practice in the forensic community. Arch Pathol Lab Med. 1999, 123, 1063-1065
• NAITO, E. Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene. J Forensic Sci. 2003, 48, 275-279
• SUMI, H. Applicability of the parentally imprinted allele (PIA) typing of a VNTR upstream the H19 gene to forensic samples of different tissues. Legal Med. 2005, 7, 179-182
• LEE, MP. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KvLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc Natl Acad Sci USA. 1999, 96, 5203-5208
• ROMEY, G. Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity. J Biol Chem. 1997, 272, 16713-16716

Terms in the title (7)： 刷込み ,  遺伝子 ,  KCNQ1 ,  イントロン ,  反復 ,  遺伝子座 ,  遺伝子タイピング