首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Alpha-2-macroglobulin intronic polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's disease.
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Alpha-2-macroglobulin intronic polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's disease.

机译:Alpha-2-巨球蛋白内含子多态性与尸检确认的迟发性阿尔茨海默氏病无关。

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摘要

Alpha-2-macroglobulin (A2M) intronic polymorphism has recently been reported to be associated with late-onset Alzheimer's disease (LOAD). To corroborate this association, we analysed the A2M and apolipoprotein E (APOE) polymorphisms in autopsy cases of the MRC Alzheimer's Disease Brain Bank, Institute of Psychiatry, London. The frequencies of the insertion and deletion alleles in AD were 0.81 and 0.19, respectively, and these were not significantly different from control frequencies. After pooling the AD cases in epsilon4 positive and negative subgroups, there was again no significant difference between the A2M allele frequency in the two subgroups. In our present study, we were unable to corroborate the association between A2M intronic polymorphism and LOAD in autopsy cases.
机译:最近有报道称α-2-巨球蛋白(A2M)内含子多态性与迟发性阿尔茨海默氏病(LOAD)有关。为了证实这种关联,我们在伦敦精神病研究所的MRC阿尔茨海默氏病脑库的尸检病例中分析了A2M和载脂蛋白E(APOE)多态性。 AD中插入和缺失等位基因的频率分别为0.81和0.19,与控制频率无显着差异。将epsilon4阳性和阴性亚组的AD病例合并后,两个亚组的A2M等位基因频率再次没有显着差异。在我们目前的研究中,我们无法证实尸检病例中A2M内含子多态性与LOAD之间的关联。

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