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PUBMED FOR HANDHELDS

Journal Abstract Search


293 related items for PubMed ID: 17804762

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  • 2. Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
    Wu Y, Li H, Loos RJ, Yu Z, Ye X, Chen L, Pan A, Hu FB, Lin X.
    Diabetes; 2008 Oct; 57(10):2834-42. PubMed ID: 18633108
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  • 3. Beta cell glucose sensitivity is decreased by 39% in non-diabetic individuals carrying multiple diabetes-risk alleles compared with those with no risk alleles.
    Pascoe L, Frayling TM, Weedon MN, Mari A, Tura A, Ferrannini E, Walker M, RISC Consortium.
    Diabetologia; 2008 Nov; 51(11):1989-92. PubMed ID: 18719881
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  • 6. Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians.
    Ng MC, Park KS, Oh B, Tam CH, Cho YM, Shin HD, Lam VK, Ma RC, So WY, Cho YS, Kim HL, Lee HK, Chan JC, Cho NH.
    Diabetes; 2008 Aug; 57(8):2226-33. PubMed ID: 18469204
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  • 8. PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population.
    Hu C, Zhang R, Wang C, Wang J, Ma X, Lu J, Qin W, Hou X, Wang C, Bao Y, Xiang K, Jia W.
    PLoS One; 2009 Oct 28; 4(10):e7643. PubMed ID: 19862325
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  • 11. Variants of CDKAL1 and IGF2BP2 affect first-phase insulin secretion during hyperglycaemic clamps.
    Groenewoud MJ, Dekker JM, Fritsche A, Reiling E, Nijpels G, Heine RJ, Maassen JA, Machicao F, Schäfer SA, Häring HU, 't Hart LM, van Haeften TW.
    Diabetologia; 2008 Sep 28; 51(9):1659-63. PubMed ID: 18618095
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  • 13. Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population.
    Lee YH, Kang ES, Kim SH, Han SJ, Kim CH, Kim HJ, Ahn CW, Cha BS, Nam M, Nam CM, Lee HC.
    J Hum Genet; 2008 Sep 28; 53(11-12):991-998. PubMed ID: 18991055
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  • 14. HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes.
    Winkler C, Illig T, Koczwara K, Bonifacio E, Ziegler AG.
    J Clin Endocrinol Metab; 2009 Oct 28; 94(10):4113-5. PubMed ID: 19622614
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  • 15. Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population.
    Omori S, Tanaka Y, Takahashi A, Hirose H, Kashiwagi A, Kaku K, Kawamori R, Nakamura Y, Maeda S.
    Diabetes; 2008 Mar 28; 57(3):791-5. PubMed ID: 18162508
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  • 16. Polymorphisms in the TCF7L2, CDKAL1 and SLC30A8 genes are associated with impaired proinsulin conversion.
    Kirchhoff K, Machicao F, Haupt A, Schäfer SA, Tschritter O, Staiger H, Stefan N, Häring HU, Fritsche A.
    Diabetologia; 2008 Apr 28; 51(4):597-601. PubMed ID: 18264689
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  • 18. Positive Association Between Type 2 Diabetes Risk Alleles Near CDKAL1 and Reduced Birthweight in Chinese Han Individuals.
    Sun XF, Xiao XH, Zhang ZX, Liu Y, Xu T, Zhu XL, Zhang Y, Wu XP, Li WH, Zhang HB, Yu M.
    Chin Med J (Engl); 2015 Jul 20; 128(14):1873-8. PubMed ID: 26168825
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  • 20. Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program.
    Moore AF, Jablonski KA, McAteer JB, Saxena R, Pollin TI, Franks PW, Hanson RL, Shuldiner AR, Knowler WC, Altshuler D, Florez JC, Diabetes Prevention Program Research Group.
    Diabetes; 2008 Sep 20; 57(9):2503-10. PubMed ID: 18544707
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