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肝细胞核因子4A变体在2型糖尿病风险中的作用。

The role of HNF4A variants in the risk of type 2 diabetes.

作者信息

Mohlke Karen L, Boehnke Michael

机构信息

Department of Genetics, University of North Carolina, Chapel Hill, NC 27599-7264, USA.

出版信息

Curr Diab Rep. 2005 Apr;5(2):149-56. doi: 10.1007/s11892-005-0043-y.

Abstract

Genes influence susceptibility to type 2 diabetes mellitus (T2DM), and both positional cloning and candidate gene approaches have been used to identify these genes. Linkage analysis has generated evidence for T2DM-predisposing variants on chromosome 20q in studies of Caucasians, Asians, and Africans, and fine-mapping recently identified a likely susceptibility gene, hepatocyte nuclear factor 4-alpha (HNF4A). Rare loss-of-function mutations in HNF4A cause maturity-onset diabetes of the young and now common noncoding variants have been found to be associated with T2DM.

摘要

基因影响2型糖尿病(T2DM)的易感性,定位克隆和候选基因方法都已被用于鉴定这些基因。在对白种人、亚洲人和非洲人的研究中,连锁分析已为20号染色体上的T2DM易感变异提供了证据,最近的精细定位确定了一个可能的易感基因,即肝细胞核因子4α(HNF4A)。HNF4A中的罕见功能丧失突变会导致青年发病的成年型糖尿病,现在已发现常见的非编码变异与T2DM有关。

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