2010 Fiscal Year Final Research Report
APPLICATION OF POLYMORPHISMS AT PIGMENTATION GENES TO PERSONAL IDENTIFICATION
| Project/Area Number |
20590678
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Legal medicine
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| Research Institution | Tottori University |
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Principal Investigator |
YUASA Isao Tottori University, 医学部, 准教授 (00093633)
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| Co-Investigator(Kenkyū-buntansha) |
IRIZAWA Yoshito 鳥取大学, 医学部, 教授 (90112226)
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| Co-Investigator(Renkei-kenkyūsha) |
UMETSU Kazuo 山形大学, 医学部, 准教授 (10091828)
AKANE Atsushi 関西医科大学, 医学部, 教授 (70202520)
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| Project Period (FY) |
2008 – 2010
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| Keywords | 色素形成遺伝子 / 多型 / 個人識別 / 帰属集団 / 祖先集団 |
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| Research Abstract |
Personal identification is one of the most important investigations in forensics, and the STR polymorphisms are usually used all over the world. However, the investigation of STR does not provide information of the ancestry and population to which an individual belongs. In this study, the frequencies of pigmentation gene polymorphisms and new East Asian- and Japanese-specific alleles were investigated. On the basis of these data, methods were developed for the inference.
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[Journal Article] Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European and African populations.2011
Author(s)
Muro T, Iida R, Fujihara J, Yasuda T, Watanabe Y, Imamura S, Nakamura H, Kimura-Kataoka K, Yuasa I, Toga T, Takeshita H
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Journal Title
Legal Medicine 13(3)
Pages: 134-141
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[Journal Article] A Japanese- specific allele. at the GALNT11 gene.2010
Author(s)
Yuasa I, Umetsu K, Matsusue A, Nishimukai H, Fukumori Y, Harihara S, Saitou N, Jin F, Chattopadhyay PK, Henke L, Henke J
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Journal Title
Legal Medicine 12(4)
Pages: 208-211
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[Journal Article] Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzyme.2009
Author(s)
Ueki M, Takeshita H, Fujihara J, Iida R, Yuasa I, Kato H, Panduro A, Nakajima T, Kominato Y, Yasuda T
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Journal Title
Clinica Chimica Acta 407(1/2)
Pages: 20-24
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[Journal Article] Molecular basis of complement factor I (CFI) polymorphism : One of two polymorphic suballeles responsible for CFI A is Japanese-specific.2008
Author(s)
Yuasa I, Nakagawa M, Umetsu K, Harihara S, Matsusue A, Nishimukai H, Fukumori Y, Saitou N, Park KS, Jin F, Lucotte G, Chattopadhyay P, Henke L, Henke J
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Journal Title
Journal of Human Genetics 53(11-12)
Pages: 1016-1021
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[Journal Article] Distribution of OCA2*481Thr and OCA2*615Arg, associated with hypopigmentation, in several additional populations.
Author(s)
Yuasa I, Harihara S, Jin F, Nishimukai H, Fujihara J, Fukumori Y, Takeshita H, Umetsu K, Saitou N
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Journal Title
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[Journal Article] Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.
Author(s)
Guillard M, Wada Y, Hansikova H, Yuasa I, Vesela K, Ondruskova N, Kadoya M, Janssen A, Van den Heuvel LP, Morava E, Zeman J, Wevers RA, Lefeber DJ.
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Journal Title
Journal of Inherited Metabolic Disease (印刷中)
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