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HNF家族基因的突变会导致青年发病的成年型糖尿病(MODY)。

[Mutations in the genes of the HNF-family cause maturity-onset diabetes of the young (MODY)].

作者信息

Takeda J

机构信息

Department of Cell Biology, Gunma University.

出版信息

Nihon Rinsho. 1998 Sep;56(9):2419-26.

PMID:9780731
Abstract

Maturity-onset diabetes of the young (MODY) is a monogenic form of non-insulin-dependent diabetes mellitus (NIDDM) characterized by an early age of onset, often in childhood or adolescence and usually < 25 years of age, and autosomal dominant inheritance. Clinical characterization of patients with MODY indicates that impaired insulin secretion is the primary defect responsible for the hyperglycemia in these patients. Genetic studies have thus far identified five MODY susceptibility genes, four of which encode transcription factors; HNF (hepatocyte nuclear factor)-1 alpha, HNF-1 beta, HNF-4 alpha, and IPF1. The association of mutations in the genes for these transcription factors with early-onset familial diabetes indicates the importance of the HNF-regulatory network in determining pancreatic beta-cell function.

摘要

青年发病的成年型糖尿病(MODY)是一种单基因形式的非胰岛素依赖型糖尿病(NIDDM),其特征为发病年龄较早,通常在儿童期或青春期,且大多小于25岁,呈常染色体显性遗传。MODY患者的临床特征表明,胰岛素分泌受损是导致这些患者高血糖的主要缺陷。迄今为止,基因研究已鉴定出五个MODY易感基因,其中四个编码转录因子:肝细胞核因子(HNF)-1α、HNF-1β、HNF-4α和胰岛素启动因子1(IPF1)。这些转录因子基因中的突变与早发型家族性糖尿病的关联表明,HNF调节网络在决定胰腺β细胞功能方面具有重要作用。

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