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    题名: Genetic Variation in N-Methyl-D-Aspartate Receptor Subunit NR3A but Not NR3B Influences Susceptibility to Alzheimer's Disease
    作者: Liu, HP (Liu, Hsin-Ping);Lin, WY (Lin, Wei-Yong);Liu, SH (Liu, Shu-Hsiang);Wang, WF (Wang, Wen-Fu);Tsai, CH (Tsai, Chon-Haw);Wu, BT (Wu, Bor-Tsang);Wang, CK (Wang, Chien-Kuo);Tsai, FJ (Tsai, Fuu-Jen)
    贡献者: Department of Biotechnology
    关键词: Alzheimer's disease;NMDA receptor;Polymorphism
    日期: 2009
    上传时间: 2010-03-26 10:29:11 (UTC+8)
    出版者: Asia University
    摘要: Background: The administration of memantine, an N-methyl-D-aspartate (NMDA) receptor antagonist, has clinically improved the cognitive function of patients with Alzheimer's disease ( AD), indicating that a disturbance in glutamatergic transmission might be involved in a predisposition to developing the disease. Aim: The potential association of polymorphisms in NMDA receptor subunits NR3A and NR3B, encoded by the GRIN3A and GRIN3B genes, with AD was investigated. Methods: We performed a case-control study. Two single nucleotide polymorphisms, 3104 G/A (rs10989563) and 3723 G/A (rs3739722), in the GRIN3A gene and 2 GRIN3B gene polymorphisms, 1210 C/T (rs4807399) and 1730 C/T (rs2240158), were studied. Results: Upon genotyping of the exonic polymorphism in the GRIN3A gene, the G allele was present at a higher rate than the A allele at position 3723 in AD patients compared with normal groups ( p < 0.05). Three haplotypes (designated Ht1-3) were identified from these 2 polymorphisms (3104 G/A and 3723 G/A), and the distribution of Ht2 (AG) differed between AD patients and controls ( p < 0.05). Additionally, from the 2 GRIN3B gene variants 1210 C/T and 1730 C/T analyzed, no strong association with AD was observed. Conclusion: These observations suggest that the genetic variation of the NR3A, but not NR3B, subunit of the NMDA receptor may be a risk factor for AD pathogenesis among the Taiwanese population. Copyright (C) 2009 S. Karger AG, Basel
    显示于类别:[生物科技學系] 期刊論文


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