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Journal Abstract Search
453 related items for PubMed ID: 19141580
1. Association of common genetic variation in the FOXO1 gene with beta-cell dysfunction, impaired glucose tolerance, and type 2 diabetes. Müssig K, Staiger H, Machicao F, Stancáková A, Kuusisto J, Laakso M, Thamer C, Machann J, Schick F, Claussen CD, Stefan N, Fritsche A, Häring HU. J Clin Endocrinol Metab; 2009 Apr; 94(4):1353-60. PubMed ID: 19141580 [Abstract] [Full Text] [Related]
2. The impact of genetic variation in the G6PC2 gene on insulin secretion depends on glycemia. Heni M, Ketterer C, Hart LM, Ranta F, van Haeften TW, Eekhoff EM, Dekker JM, Boomsma DI, Nijpels G, Kramer MH, Diamant M, Simonis-Bik AM, Heine RJ, de Geus EJ, Schäfer SA, Machicao F, Ullrich S, Thamer C, Stefan N, Staiger H, Häring HU, Fritsche A. J Clin Endocrinol Metab; 2010 Dec; 95(12):E479-84. PubMed ID: 20826583 [Abstract] [Full Text] [Related]
3. Single-nucleotide polymorphism rs7754840 of CDKAL1 is associated with impaired insulin secretion in nondiabetic offspring of type 2 diabetic subjects and in a large sample of men with normal glucose tolerance. Stancáková A, Pihlajamäki J, Kuusisto J, Stefan N, Fritsche A, Häring H, Andreozzi F, Succurro E, Sesti G, Boesgaard TW, Hansen T, Pedersen O, Jansson PA, Hammarstedt A, Smith U, Laakso M, EUGENE2 Consortium. J Clin Endocrinol Metab; 2008 May; 93(5):1924-30. PubMed ID: 18285412 [Abstract] [Full Text] [Related]
4. Genetic variation within the NR1H2 gene encoding liver X receptor β associates with insulin secretion in subjects at increased risk for type 2 diabetes. Ketterer C, Müssig K, Machicao F, Stefan N, Fritsche A, Häring HU, Staiger H. J Mol Med (Berl); 2011 Jan; 89(1):75-81. PubMed ID: 21042792 [Abstract] [Full Text] [Related]
5. Genetic variation within the TRPM5 locus associates with prediabetic phenotypes in subjects at increased risk for type 2 diabetes. Ketterer C, Müssig K, Heni M, Dudziak K, Randrianarisoa E, Wagner R, Machicao F, Stefan N, Holst JJ, Fritsche A, Häring HU, Staiger H. Metabolism; 2011 Sep; 60(9):1325-33. PubMed ID: 21489577 [Abstract] [Full Text] [Related]
6. Polymorphisms within the novel type 2 diabetes risk locus MTNR1B determine beta-cell function. Staiger H, Machicao F, Schäfer SA, Kirchhoff K, Kantartzis K, Guthoff M, Silbernagel G, Stefan N, Häring HU, Fritsche A. PLoS One; 2008 Sep; 3(12):e3962. PubMed ID: 19088850 [Abstract] [Full Text] [Related]
7. Variants of transcription factor 7-like 2 (TCF7L2) gene predict conversion to type 2 diabetes in the Finnish Diabetes Prevention Study and are associated with impaired glucose regulation and impaired insulin secretion. Wang J, Kuusisto J, Vänttinen M, Kuulasmaa T, Lindström J, Tuomilehto J, Uusitupa M, Laakso M. Diabetologia; 2007 Jun; 50(6):1192-200. PubMed ID: 17437080 [Abstract] [Full Text] [Related]
8. Variants of the TCF7L2 gene are associated with beta cell dysfunction and confer an increased risk of type 2 diabetes mellitus in the ULSAM cohort of Swedish elderly men. Dahlgren A, Zethelius B, Jensevik K, Syvänen AC, Berne C. Diabetologia; 2007 Sep; 50(9):1852. PubMed ID: 17618413 [Abstract] [Full Text] [Related]
9. Common polymorphisms within the NR4A3 locus, encoding the orphan nuclear receptor Nor-1, are associated with enhanced beta-cell function in non-diabetic subjects. Weyrich P, Staiger H, Stancáková A, Schäfer SA, Kirchhoff K, Ullrich S, Ranta F, Gallwitz B, Stefan N, Machicao F, Kuusisto J, Laakso M, Fritsche A, Häring HU. BMC Med Genet; 2009 Aug 14; 10():77. PubMed ID: 19682370 [Abstract] [Full Text] [Related]
10. The influence of genetic variations in HHEX gene on insulin metabolism in the German MESYBEPO cohort. Pivovarova O, Nikiforova VJ, Pfeiffer AF, Rudovich N. Diabetes Metab Res Rev; 2009 Feb 14; 25(2):156-62. PubMed ID: 19117022 [Abstract] [Full Text] [Related]
11. Insulin secretion and insulin sensitivity in diabetic subgroups: studies in the prediabetic and diabetic state. Tripathy D, Carlsson AL, Lehto M, Isomaa B, Tuomi T, Groop L. Diabetologia; 2000 Dec 14; 43(12):1476-83. PubMed ID: 11151756 [Abstract] [Full Text] [Related]
12. Variants and haplotypes of TCF7L2 are associated with β-cell function in patients with newly diagnosed type 2 diabetes: the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 1. Bonetti S, Trombetta M, Malerba G, Boselli L, Trabetti E, Muggeo M, Stoico V, Negri C, Pignatti PF, Bonora E, Bonadonna RC. J Clin Endocrinol Metab; 2011 Feb 14; 96(2):E389-93. PubMed ID: 21159844 [Abstract] [Full Text] [Related]
13. The inhibitory effect of recent type 2 diabetes risk loci on insulin secretion is modulated by insulin sensitivity. Haupt A, Guthoff M, Schäfer SA, Kirchhoff K, Machicao F, Gallwitz B, Staiger H, Stefan N, Fritsche A, Häring HU. J Clin Endocrinol Metab; 2009 May 14; 94(5):1775-80. PubMed ID: 19258404 [Abstract] [Full Text] [Related]
14. Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion. Müssig K, Staiger H, Machicao F, Kirchhoff K, Guthoff M, Schäfer SA, Kantartzis K, Silbernagel G, Stefan N, Holst JJ, Gallwitz B, Häring HU, Fritsche A. Diabetes; 2009 Jul 14; 58(7):1715-20. PubMed ID: 19366866 [Abstract] [Full Text] [Related]
15. The vitamin D receptor (VDR) gene rs11568820 variant is associated with type 2 diabetes and impaired insulin secretion in Italian adult subjects, and associates with increased cardio-metabolic risk in children. Sentinelli F, Bertoccini L, Barchetta I, Capoccia D, Incani M, Pani MG, Loche S, Angelico F, Arca M, Morini S, Manconi E, Lenzi A, Cossu E, Leonetti F, Baroni MG, Cavallo MG. Nutr Metab Cardiovasc Dis; 2016 May 14; 26(5):407-13. PubMed ID: 27052925 [Abstract] [Full Text] [Related]
16. The rs7903146 Variant in the TCF7L2 Gene Increases the Risk of Prediabetes/Type 2 Diabetes in Obese Adolescents by Impairing β-Cell Function and Hepatic Insulin Sensitivity. Cropano C, Santoro N, Groop L, Dalla Man C, Cobelli C, Galderisi A, Kursawe R, Pierpont B, Goffredo M, Caprio S. Diabetes Care; 2017 Aug 14; 40(8):1082-1089. PubMed ID: 28611053 [Abstract] [Full Text] [Related]
17. Novel meta-analysis-derived type 2 diabetes risk loci do not determine prediabetic phenotypes. Staiger H, Machicao F, Kantartzis K, Schäfer SA, Kirchhoff K, Guthoff M, Silbernagel G, Stefan N, Fritsche A, Häring HU. PLoS One; 2008 Aug 20; 3(8):e3019. PubMed ID: 18714373 [Abstract] [Full Text] [Related]