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Journal Abstract Search

289 related items for PubMed ID: 21668369

  • 41. A functional single nucleotide polymorphism -1562C>T in the matrix metalloproteinase-9 promoter is associated with type 2 diabetes and diabetic foot ulcers.
    Singh K, Agrawal NK, Gupta SK, Singh K.
    Int J Low Extrem Wounds; 2013 Sep; 12(3):199-204. PubMed ID: 24043671
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  • 45. GLUT4 gene rs5418 polymorphism is associated with increased coronary heart disease risk in a Uygur Chinese population.
    Yu F, Liu F, Li XM, Zhao Q, Luo JY, Zhang JY, Yang YN.
    BMC Cardiovasc Disord; 2022 Apr 25; 22(1):191. PubMed ID: 35468725
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  • 46. Association study of the single-nucleotide polymorphisms -3971G/A and +276G/T in the adiponectin gene with type 2 diabetes in a North Indian Punjabi population.
    Bains V, Kaur H, Badaruddoza.
    Ann Hum Genet; 2020 May 25; 84(3):235-248. PubMed ID: 31755094
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  • 47. Effect of polymorphisms in the PPARGC1A gene on body fat in Asian Indians.
    Vimaleswaran KS, Radha V, Anjana M, Deepa R, Ghosh S, Majumder PP, Rao MR, Mohan V.
    Int J Obes (Lond); 2006 Jun 25; 30(6):884-91. PubMed ID: 16446747
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  • 48. Association of ghrelin Leu72Met polymorphism with type 2 diabetes mellitus in Chinese population.
    Liu J, Liu J, Tian LM, Liu JX, Bing YJ, Zhang JP, Wang YF, Zhang LY.
    Gene; 2012 Aug 10; 504(2):309-12. PubMed ID: 22441120
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  • 50. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians.
    Vimaleswaran KS, Radha V, Ramya K, Babu HN, Savitha N, Roopa V, Monalisa D, Deepa R, Ghosh S, Majumder PP, Rao MR, Mohan V.
    Hum Genet; 2008 Jul 10; 123(6):599-605. PubMed ID: 18465144
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  • 51. Association of TCF7L2 gene polymorphisms with susceptibility to type 2 diabetes mellitus in a Chinese Hui population.
    Yang Y, Xu JR, Wang YJ, Liu XM.
    Genet Mol Res; 2015 Aug 21; 14(3):10064-71. PubMed ID: 26345943
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  • 52. Interleukin-18 (rs187238) and glucose transporter 4 (rs5435) polymorphisms in Euro-Brazilians with type 1 diabetes.
    Al-Lahham Y, Mendes AKB, Souza EM, Alberton D, Rego FGM, Valdameri G, Picheth G.
    Genet Mol Res; 2017 Sep 21; 16(3):. PubMed ID: 28973736
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  • 54. [Association of glucose transporter 4 gene polymorphism with hypoxia caused by obstructive sleep apnea syndrome and with related inflammatory factors].
    Yin T, Li NF, Ai LG, Yao XG, Hong J, Zhou L, Kong JQ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2014 Aug 21; 36(4):400-9. PubMed ID: 25176209
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  • 55. Association of incretin receptors genetic polymorphisms with type 2 diabetes mellitus in Egyptian patients.
    Shalaby SM, Zidan HE, Shokry A, Saeed J, El-Sokkary RH.
    J Gene Med; 2017 Sep 21; 19(9-10):. PubMed ID: 28744963
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  • 58. A haplotype at the UCP1 gene locus contributes to genetic risk for type 2 diabetes in Asian Indians (CURES-72).
    Vimaleswaran KS, Radha V, Ghosh S, Majumder PP, Rao MR, Mohan V.
    Metab Syndr Relat Disord; 2010 Feb 21; 8(1):63-8. PubMed ID: 19943796
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  • 60. Associations of fibroblast growth factor 21 gene 3' untranslated region single-nucleotide polymorphisms with metabolic syndrome, obesity, and diabetes in a Han Chinese population.
    Zhang M, Zeng L, Wang YJ, An ZM, Ying BW.
    DNA Cell Biol; 2012 Apr 21; 31(4):547-52. PubMed ID: 21988350
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