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印度人群中与2型糖尿病相关候选基因内单核苷酸多态性的宏基因组学研究。

Metagenomic study of single-nucleotide polymorphism within candidate genes associated with type 2 diabetes in an Indian population.

作者信息

Mukhopadhyaya P N, Acharya A, Chavan Y, Purohit S S, Mutha A

机构信息

Medical Genetics Division, geneOmbio Technologies, Pashan, Pune, Maharashtra, India.

出版信息

Genet Mol Res. 2010 Oct 19;9(4):2060-8. doi: 10.4238/vol9-4gmr883.

Abstract

A population-based study was undertaken to evaluate linkage between single-nucleotide polymorphisms known as risk factors and type 2 diabetes in an Indian population. The study population was comprised of 40 normal glucose-tolerant individuals (21 males and 19 females) and 40 type 2 diabetes patients (21 males and 19 females). The genes and their corresponding single-nucleotide polymorphisms that we screened were VDR (rs 731236 and rs 1544410), IL-6 (rs 1800795), TCF7L2 (rs 7903146) and TNF-α (rs 1800629). The risk alleles were more frequent in the subjects with type 2 diabetes, except for the TNF-α gene, which was very infrequent in the population; the normal allele occurred at high and similar frequencies in both normal and diabetic individuals.

摘要

开展了一项基于人群的研究,以评估在印度人群中已知作为风险因素的单核苷酸多态性与2型糖尿病之间的联系。研究人群包括40名糖耐量正常个体(21名男性和19名女性)和40名2型糖尿病患者(21名男性和19名女性)。我们筛查的基因及其相应的单核苷酸多态性为维生素D受体(VDR,rs 731236和rs 1544410)、白细胞介素-6(IL-6,rs 1800795)、转录因子7样蛋白2(TCF7L2,rs 7903146)和肿瘤坏死因子-α(TNF-α,rs 1800629)。除了TNF-α基因(该基因在人群中非常罕见)外,风险等位基因在2型糖尿病患者中更为常见;正常等位基因在正常个体和糖尿病个体中出现的频率较高且相似。

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