期刊文献+

SLC30A8基因单核苷酸多态性与2型糖尿病相关性的研究进展 被引量:1

Recent Progress on SLC30A8 Gene Polymorphism and Type 2 Diabetes Mellitus
下载PDF
导出
摘要 2型糖尿病具有明显的遗传倾向,是一种复杂的多基因遗传病。SLC30A8基因位于8q24.11,编码的蛋白为ZnT-8,其特异性地在胰腺内分泌细胞表达,与胰岛素的储存和分泌有关,其风险等位基因是迄今发现的与2型糖尿病的发生关联比较强的变异。近年来,许多学者致力于研究SLC30A8基因变异型增加2型糖尿病易感性的机制。 Type 2 diabetes mellitus (T2DM)has a genetic tendency obviously, it is a complicated muhi-gene heredopathia. SLC30A8 gene,located in 8q24.11 ,which encodes ZnT-8. The zinc transporter ZnT8 is specifically expressed in pancreatic endocrine cells,it was related to storage and secretion of the Insulin. It has been found that the risk allele of SLC30A8 was one of the most closely connected with T2DM up to today. Recently, many scholars have been researching the reason that variation of SLC30A8 can increase the impressionability of T2DM.
作者 李晶 王建平
出处 《医学综述》 2010年第7期989-991,共3页 Medical Recapitulate
关键词 2型糖尿病 SLC30A8基因 单核苷酸多态性 Type 2 diabetes mellitus SLC30A8 gene Single nucleotide polymorphism
  • 相关文献

参考文献18

  • 1Sladek R, Rocbeleau G, Rung J,et al. A genome-wide association study identifies novel risk loci for type 2 diabetes [ J]. Nature, 2007,445(7130) :881-885.
  • 2Staiger H, Maehieao F, Stefan N,et al. Polymorphisms within novel risk loci for type 2 diabetes determine beta-cell function[J]. PLoS ONE ,2007,2(9 ) : e832.
  • 3Scott LJ, Mohlke KL, Bonnycastle LL,et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibili- ty variants [ J 1. Science, 2007,316 ( 5829 ) : 1341-1345.
  • 4Lyssenko V, Jonsson A, Ahngren P,et al. Clinical risk factors, DNA variants,and the development of type 2 diabetes [J]. N Engl J Med,2008,359(21 ) :2220-2232.
  • 5Palmer ND, Goodarzi MO, Langefeld CD,et al. Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the insulin resistance atherosclerosis family study [ J ]. Diabetes,2008,57 (4) : 1093-100.
  • 6Lee YH, Kang ES, Kim SH, et al. Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFSI, CDKALI,KCNQI and type 2 diabetes in the Korean population [J]. J Hum Geneti ,2008,53(11/12) :991-998.
  • 7Hertel JK, Johansson S, Raeder H, et al. Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort ( the HUNT study) [ J ]. Diabetologia, 2008.51 (6) :971-977.
  • 8Omori S,Tanaka Y, Takahashi A, et al. Association of CDKAL1, IGF2BP2 ,CDKN2A/B, HHEX, SLC3OAS, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population [ J ]. Diabetes ,2008,57 ( 3 ) :791-795.
  • 9Tabara Y, Osawa H, Kawamoto R,et al. Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening[ J ]. Diabetes,2009,58 (2) :493-498.
  • 10Wu Y, Li H, Loos RJ, et al. Common variants in CDKALI, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population [ J ]. Diabetes ,2008,57 ( 10 ) :2834-2842.

同被引文献19

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部