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Journal Abstract Search

134 related items for PubMed ID: 19753844

  • 21. The presence of the -866A/55Val/Ins haplotype in the uncoupling protein 2 (UCP2) gene is associated with decreased UCP2 gene expression in human retina.
    de Souza BM, Assmann TS, Kliemann LM, Marcon AS, Gross JL, Canani LH, Crispim D.
    Exp Eye Res; 2012 Jan; 94(1):49-55. PubMed ID: 22134120
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  • 22. Interaction between the UCP2-866G/A, mtDNA 10398G/A and PGC1alpha p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population.
    Rai E, Sharma S, Koul A, Bhat AK, Bhanwer AJ, Bamezai RN.
    Hum Genet; 2007 Dec; 122(5):535-40. PubMed ID: 17701054
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  • 35. Association between accumulation of visceral fat and the combination of β3 adrenergic receptor Trp64Arg, β2 adrenergic receptor Arg16Gly and uncoupling protein 1 -3826A>G polymorphisms detected by Smart Amplification Process 2.
    Tsunekawa K, Yanagawa Y, Aoki T, Morimura T, Araki O, Ogiwara T, Kawai Y, Mitani Y, Lezhava A, Yanagawa M, Hayashizaki Y, Murakami M.
    Endocr J; 2011 Dec; 58(12):1079-86. PubMed ID: 21959333
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  • 38. Genetic variation in UCP2 (uncoupling protein-2) is associated with energy metabolism in Pima Indians.
    Kovacs P, Ma L, Hanson RL, Franks P, Stumvoll M, Bogardus C, Baier LJ.
    Diabetologia; 2005 Nov; 48(11):2292-5. PubMed ID: 16167150
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  • 39. The uncoupling protein 2 -866G > a polymorphism is associated with the risk of ischemic stroke in Chinese type 2 diabetic patients.
    Chai Y, Gu B, Qiu JR, Yi HG, Zhu Q, Zhang L, Hu G.
    CNS Neurosci Ther; 2012 Aug; 18(8):636-40. PubMed ID: 22613561
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  • 40. Association of genetic variants with chronic kidney disease in Japanese individuals.
    Yoshida T, Kato K, Fujimaki T, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.
    Clin J Am Soc Nephrol; 2009 May; 4(5):883-90. PubMed ID: 19406964
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