HuGE Literature Finder
Records 1-11
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Mexican Carriers of the HNF1A p.E508K Variant Do Not Experience an Enhanced Response to Sulfonylureas.
Diabetes care 2018 May . Martagón Alexandro J, Bello-Chavolla Omar Yaxmehen, Arellano-Campos Olimpia, Almeda-Valdés Paloma, Walford Geoffrey A, Cruz-Bautista Ivette, Gómez-Velasco Donají V, Mehta Roopa, Muñoz-Hernández Liliana, Sevilla-González Magdalena, Viveros-Ruiz Tannia L, Ordoñez-Sánchez María Luisa, Rodríguez-Guillen Rosario, Florez Jose C, Tusié-Luna María Teresa, Aguilar-Salinas Carlos A, |
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels.
Nature communications 2015 6 7754. Setoh Kazuya, Terao Chikashi, Muro Shigeo, Kawaguchi Takahisa, Tabara Yasuharu, Takahashi Meiko, Nakayama Takeo, Kosugi Shinji, Sekine Akihiro, Yamada Ryo, Mishima Michiaki, Matsuda Fumihi |
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Williams-beuren syndrome is a genetic disorder associated with impaired glucose tolerance and diabetes in childhood and adolescence: new insights from a longitudinal study.
Hormone research in pædiatrics 2014 82 (1): 38-43. Stagi Stefano, Lapi Elisabetta, Cecchi Cecilia, Chiarelli Francesco, D'Avanzo Maria Gabriella, Seminara Salvatore, de Martino Mauriz |
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Type 2 diabetes risk allele near CENTD2 is associated with decreased glucose-stimulated insulin release.
Diabetologia 2011 May 54 (5): 1052-6. Nielsen T, Sparsø T, Grarup N, Jørgensen T, Pisinger C, Witte D R, , Hansen T, Pedersen |
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PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease.
Hepatology (Baltimore, Md.) 2010 Sep 52 (3): 904-12. Speliotes Elizabeth K, Butler Johannah L, Palmer Cameron D, Voight Benjamin F, , , , Hirschhorn Joel |
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Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.
Dementia and geriatric cognitive disorders 2009 27 (1): 59-68. Giedraitis Vilmantas, Kilander Lena, Degerman-Gunnarsson Malin, Sundelöf Johan, Axelsson Tomas, Syvänen Ann-Christine, Lannfelt Lars, Glaser An |
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The A98V single nucleotide polymorphism (SNP) in hepatic nuclear factor 1 alpha (HNF-1alpha) is associated with insulin sensitivity and beta-cell function.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2008 Sep 116 Suppl 1 S50-5. Bergmann A, Li J, Selisko T, Reimann M, Fischer S, Grässler J, Schulze J, Bornstein S R, Schwarz P E |
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Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
American journal of human genetics 2008 May 82 (5): 1185-92. Ridker Paul M, Pare Guillaume, Parker Alex, Zee Robert Y L, Danik Jacqueline S, Buring Julie E, Kwiatkowski David, Cook Nancy R, Miletich Joseph P, Chasman Daniel |
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The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies.
BMC medical genetics 2008 9 (1): 45. Cauchi Stéphane, Nead Kevin T, Choquet Hélène, Horber Fritz, Potoczna Natascha, Balkau Beverley, Marre Michel, Charpentier Guillaume, Froguel Philippe, Meyre Dav |
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Synergism between mutant HNF1A and the metabolic syndrome in Oji-Cree Type 2 diabetes.
Diabetic medicine : a journal of the British Diabetic Association 2005 Nov 22 (11): 1510-5. Pollex R L, Hanley A J G, Zinman B, Harris S B, Khan H M R, Hegele R |
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High frequency of mutations in the HNF-1alpha gene in non-obese patients with diabetes of youth in Japanese and identification of a case of digenic inheritance.
Diabetologia 2002 Dec 45 (12): 1709-12. Tonooka N, Tomura H, Takahashi Y, Onigata K, Kikuchi N, Horikawa Y, Mori M, Takeda |
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- Page last updated:Jun 03, 2020
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