家族性非胰岛素依赖型糖尿病中的S20G胰岛相关多肽基因突变 - Suppr

The S20G islet-associated polypeptide gene mutation in familial NIDDM.

作者信息

Birch C L, Fagan L J, Armstrong M J, Turnbull D M, Walker M

出版信息

Diabetologia. 1997 Sep;40(9):1113.

PMID:9300251

Abstract

摘要

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The S20G islet-associated polypeptide gene mutation in familial NIDDM.

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[Amylin (IAPP) gene].

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S20G mutant amylin exhibits increased in vitro amyloidogenicity and increased intracellular cytotoxicity compared to wild-type amylin.

Am J Pathol. 2000 Dec;157(6):2101-9. doi: 10.1016/S0002-9440(10)64848-1.

引用本文的文献

Islet amyloid: a complication of islet dysfunction or an aetiological factor in Type 2 diabetes?

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Polymorphism in intron 2 of islet amyloid polypeptide gene is associated with lower low-density lipoprotein cholesterol in nondiabetic subjects and in type 2 diabetic patients.

Endocrine. 2002 Nov;19(2):185-9. doi: 10.1385/ENDO:19:2:185.

S20G mutant amylin exhibits increased in vitro amyloidogenicity and increased intracellular cytotoxicity compared to wild-type amylin.

Am J Pathol. 2000 Dec;157(6):2101-9. doi: 10.1016/S0002-9440(10)64848-1.

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The S20G islet-associated polypeptide gene mutation in familial NIDDM.

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