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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >T/G polymorphism at intron 9 of presenilin 1 gene is associated with, but not responsible for sporadic late-onset Alzheimer's disease in Japanese population.
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T/G polymorphism at intron 9 of presenilin 1 gene is associated with, but not responsible for sporadic late-onset Alzheimer's disease in Japanese population.

机译:早老素1基因内含子9的T / G多态性与日本人群零星的迟发性阿尔茨海默氏病有关,但并不负责。

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摘要

To investigate whether presenilin 1 (PS1) gene, a major causative gene of familial early-onset Alzheimer's disease (AD), also contributes to the etiology of sporadic AD, we evaluated associations between Japanese AD and polymorphisms located at 14q24.3. While the D14S43 and FOS loci showed no association with either early- or late-onset AD, late-onset AD carrying no APOE-epsilon4 allele was associated with the G allele of the T/G polymorphism located at intron 9 of the PS1 gene (P = 0.016). Considering another study showing a positive association between AD and the T allele, this polymorphism is associated with, but not responsible for sporadic late-onset Alzheimer's disease.
机译:为了研究早衰家族1的主要病因基因早老素1(PS1)基因是否也有助于散发性AD的病因,我们评估了日本AD与位于14q24.3的多态性之间的关联。虽然D14S43和FOS基因座与早发型或迟发型AD没有关联,但携带APOE-ε4等位基因的晚发型AD与位于PS1基因内含子9的T / G多态性的G等位基因相关( P = 0.016)。考虑到另一项研究显示AD与T等位基因之间存在正相关,这种多态性与零星的迟发性阿尔茨海默氏病有关,但不负责任。

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