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等位基因特异性基因探测支持DQ分子作为1型(胰岛素依赖型)糖尿病遗传易感性的一个决定因素。

Allele-specific gene probing supports the DQ molecule as a determinant of inherited susceptibility to type 1 (insulin-dependent) diabetes mellitus.

作者信息

Jenkins D, Mijovic C, Jacobs K H, Penny M A, Fletcher J, Barnett A H

机构信息

Department of Medicine, University of Birmingham, UK.

出版信息

Diabetologia. 1991 Feb;34(2):109-13. doi: 10.1007/BF00500381.

Abstract

Trans-racial analysis of disease associations has improved mapping of MHC-linked susceptibility to Type 1 (insulin-dependent) diabetes mellitus. In this study the contributions of the MHC class II DQA1 and DQB1 genes were investigated. Sequence-specific oligonucleotide gene probing in Type 1 diabetic and control subjects of North Indian origin supported the DQw1.18 allele of the DQB1 gene as a determinant of inherited protection against Type 1 diabetes (RR = 0.12, pc less than 0.05). The A3 allele of the DQA1 gene was positively associated with the disease, (RR = 3.6, pc less than 0.05), as was the DQw2 allele of the DQB1 gene (RR = 4.6, pc less than 0.01). Trans-racial comparison of these disease associations indicates that DQ alleles may directly determine an element of inherited susceptibility to Type 1 diabetes.

摘要

疾病关联的跨种族分析改进了对与MHC相关的1型(胰岛素依赖型)糖尿病易感性的定位。在本研究中,对MHCⅡ类DQA1和DQB1基因的作用进行了调查。对北印度裔1型糖尿病患者和对照受试者进行序列特异性寡核苷酸基因探测,结果支持DQB1基因的DQw1.18等位基因是对1型糖尿病遗传保护性的决定因素(相对危险度=0.12,P<0.05)。DQA1基因的A3等位基因与该病呈正相关(相对危险度=3.6,P<0.05),DQB1基因的DQw2等位基因也是如此(相对危险度=4.6,P<0.01)。这些疾病关联的跨种族比较表明,DQ等位基因可能直接决定1型糖尿病遗传易感性的一个因素。

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