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1
Deoxyribonucleic acid repair gene X-ray repair cross-complementing group 1 polymorphisms and non-carcinogenic disease risk in different populations: A meta-analysis.脱氧核糖核酸修复基因X射线修复交叉互补组1多态性与不同人群的非致癌性疾病风险：一项荟萃分析。
Indian J Hum Genet. 2013 Oct;19(4):494-511. doi: 10.4103/0971-6866.124385.
2
Mutation analysis of mitogen activated protein kinase 1 gene in Indian cases of 46,XY disorder of sex development.46,XY性发育障碍印度病例中丝裂原活化蛋白激酶1基因的突变分析
Indian J Hum Genet. 2013 Oct;19(4):437-42. doi: 10.4103/0971-6866.124372.
3
Promoter variants in interleukin-6 and tumor necrosis factor alpha and risk of coronary artery disease in a population from Western India.印度西部人群中白细胞介素-6和肿瘤坏死因子α的启动子变体与冠状动脉疾病风险
Indian J Hum Genet. 2013 Oct;19(4):430-6. doi: 10.4103/0971-6866.124371.
4
Distribution and genotype frequency of the C1431T and pro12ala polymorphisms of the peroxisome proliferator activator receptor gamma gene in an Iranian population.伊朗人群中过氧化物酶体增殖物激活受体γ基因C1431T和pro12ala多态性的分布及基因型频率
Indian J Hum Genet. 2013 Oct;19(4):423-9. doi: 10.4103/0971-6866.124370.
5
Prevalence of methylenetetrahydrofolate reductase 677 C-T polymorphism among mothers of Down syndrome children.唐氏综合征患儿母亲中亚甲基四氢叶酸还原酶677 C-T多态性的患病率。
Indian J Hum Genet. 2013 Oct;19(4):412-4. doi: 10.4103/0971-6866.124368.
6
Genetic polymorphisms of estrogen receptor alpha and catechol-O-methyltransferase genes in Turkish patients with familial prostate carcinoma.土耳其家族性前列腺癌患者雌激素受体α和儿茶酚-O-甲基转移酶基因的遗传多态性
Indian J Hum Genet. 2013 Oct;19(4):408-11. doi: 10.4103/0971-6866.124366.
7
Protein tyrosine phosphatase non-receptor type 22 gene polymorphism C1858T is not associated with leprosy in Azerbaijan, Northwest Iran.蛋白酪氨酸磷酸酶非受体22型基因多态性C1858T与伊朗西北部阿塞拜疆的麻风病无关。
Indian J Hum Genet. 2013 Oct;19(4):403-7. doi: 10.4103/0971-6866.124365.
8
Linking disease associations with regulatory information in the human genome.将疾病关联与人类基因组中的调控信息联系起来。
Genome Res. 2012 Sep;22(9):1748-59. doi: 10.1101/gr.136127.111.
9
Deficiencies of natural anticoagulants, protein C, protein S, and antithrombin.天然抗凝剂、蛋白C、蛋白S和抗凝血酶缺乏。
Circulation. 2011 Oct 4;124(14):e365-8. doi: 10.1161/CIRCULATIONAHA.111.044412.
10
Determinants of specific RNA interference-mediated silencing of human beta-globin alleles differing by a single nucleotide polymorphism.单核苷酸多态性导致的人类β-珠蛋白等位基因特异性RNA干扰介导沉默的决定因素。
Proc Natl Acad Sci U S A. 2006 Apr 11;103(15):5953-8. doi: 10.1073/pnas.0601309103. Epub 2006 Apr 3.

Innumerable studies on single nucleotide polymorphisms: What could be its utility?

作者信息

Ghosh K, Gorakshakar Ajit

机构信息

National Institute of Immunohaematology, Parel, Mumbai, Maharashtra, India.

出版信息

Indian J Hum Genet. 2013 Oct;19(4):381-3. doi: 10.4103/0971-6866.124354.

DOI:10.4103/0971-6866.124354
PMID:24497699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3897129/
Abstract
摘要