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Journal Abstract Search

184 related items for PubMed ID: 11508278

  • 1. Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes.
    Matsubara A, Wasson JC, Donelan SS, Welling CM, Glaser B, Permutt MA.
    Diabetologia; 2001 Jul; 44(7):910-3. PubMed ID: 11508278
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  • 2. Human calcium/calmodulin-dependent protein kinase II gamma gene (CAMK2G): cloning, genomic structure and detection of variants in subjects with type II diabetes.
    Gloyn AL, Desai M, Clark A, Levy JC, Holman RR, Frayling TM, Hattersley AT, Ashcroft SJ.
    Diabetologia; 2002 Apr; 45(4):580-3. PubMed ID: 12032636
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  • 3. Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients.
    Tsunoda K, Sanke T, Nakagawa T, Furuta H, Nanjo K.
    Diabetologia; 2001 Nov; 44(11):2092-7. PubMed ID: 11719842
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  • 4. Evaluation of apolipoprotein A-II as a positional candidate gene for familial Type II diabetes, altered lipid concentrations, and insulin resistance.
    Elbein SC, Chu W, Ren Q, Wang H, Hemphill C, Hasstedt SJ.
    Diabetologia; 2002 Jul; 45(7):1026-33. PubMed ID: 12136402
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  • 5. Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred.
    Elphinstone MS, Gordon RD, So A, Jeske YW, Stratakis CA, Stowasser M.
    Clin Endocrinol (Oxf); 2004 Dec; 61(6):716-23. PubMed ID: 15579186
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  • 6. Human cholecystokinin type A receptor gene: cytogenetic localization, physical mapping, and identification of two missense variants in patients with obesity and non-insulin-dependent diabetes mellitus (NIDDM).
    Inoue H, Iannotti CA, Welling CM, Veile R, Donis-Keller H, Permutt MA.
    Genomics; 1997 Jun 01; 42(2):331-5. PubMed ID: 9192855
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  • 11. Identification of a single nucleotide polymorphism showing no insulin-mediated suppression of the promoter activity in the human insulin receptor substrate 2 gene.
    Iwamoto K, Mori H, Okazawa H, Hashiramoto M, Kasuga M.
    Diabetologia; 2002 Aug 01; 45(8):1182-95. PubMed ID: 12189449
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  • 12. Variation in the lamin A/C gene: associations with metabolic syndrome.
    Steinle NI, Kazlauskaite R, Imumorin IG, Hsueh WC, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR.
    Arterioscler Thromb Vasc Biol; 2004 Sep 01; 24(9):1708-13. PubMed ID: 15205219
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  • 16. CD36 gene variants and their association with type 2 diabetes in an Indian population.
    Gautam S, Pirabu L, Agrawal CG, Banerjee M.
    Diabetes Technol Ther; 2013 Aug 01; 15(8):680-7. PubMed ID: 23844572
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  • 17. Isolation and characterization of the human muscle glycogen synthase gene.
    Orho M, Nikula-Ijäs P, Schalin-Jäntti C, Permutt MA, Groop LC.
    Diabetes; 1995 Sep 01; 44(9):1099-105. PubMed ID: 7657035
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  • 18. Mutation analysis of suppressor of cytokine signalling 3, a candidate gene in Type 1 diabetes and insulin sensitivity.
    Gylvin T, Nolsøe R, Hansen T, Nielsen EMD, Bergholdt R, Karlsen AE, Billestrup N, Borch-Johnsen K, Pedersen O, Mandrup-Poulsen T, Nerup J, Pociot F.
    Diabetologia; 2004 Jul 01; 47(7):1273-1277. PubMed ID: 15249995
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