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南亚人群中载脂蛋白B基因限制性片段长度多态性与冠心病的关系

Restriction fragment length polymorphisms in the Apo B gene in relation to coronary heart disease in a southern Asian population.

作者信息

Mendis S, Shepherd J, Packard C J, Gaffney D

机构信息

Department of Medicine, Faculty of Medicine, University of Peradeniya, Scotland.

出版信息

Clin Chim Acta. 1991 Feb 15;196(2-3):107-17. doi: 10.1016/0009-8981(91)90063-i.

Abstract

We have examined DNA polymorphisms associated with the apolipoprotein B gene in 95 Sri Lankan males with ischaemic heart disease and 95 matched controls. For polymorphisms detected using the XbaI or MspI enzymes the allele frequency in Sri Lankans contrasted markedly from that in Caucasians. Overall, there was no significant association of any allele studied with coronary disease cases in this sample. There was, however, a significant difference observed between the XbaI allele frequency in normotriglyceridaemic or normocholesterolaemic CHD cases compared with the allele frequency in the controls.

摘要

我们检测了95名患有缺血性心脏病的斯里兰卡男性及95名匹配的对照者中与载脂蛋白B基因相关的DNA多态性。对于使用XbaI或MspI酶检测到的多态性,斯里兰卡人的等位基因频率与高加索人有显著差异。总体而言,在该样本中,所研究的任何等位基因与冠心病病例之间均无显著关联。然而,观察到正常甘油三酯血症或正常胆固醇血症的冠心病病例的XbaI等位基因频率与对照组的等位基因频率存在显著差异。

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