HuGE Literature Finder
Records 1-17
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Identification of insulin gene variants in patients with neonatal diabetes in the Chinese population.
Journal of diabetes investigation 2019 Oct . Fu Junling, Wang Tong, Li Mingmin, Xiao Xinh |
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Clinical and Genetic Characteristics of Abnormal Glucose Tolerance in Japanese Women in the First Year after Gestational Diabetes Mellitus.
Journal of diabetes investigation 2018 Sep . Kasuga Yoshifumi, Miyakoshi Kei, Tajima Atsushi, Saisho Yoshifumi, Ikenoue Satoru, Ochiai Daigo, Matsumoto Tadashi, Arata Naoko, Hata Kenichiro, Tanaka Mamo |
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Evaluation of the pharmacokinetics of glibenclamide tablet given, off label, orally to children suffering from neonatal syndromic hyperglycemia.
European journal of clinical pharmacology 2016 Aug . Bouazza Naïm, Djerada Zoubir, Gozalo Claire, Busiah Kanetee, Beltrand Jacques, Berdugo Marianne, Urien Saik, Treluyer Jean-Marc, Polak Mich |
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Pharmacogenetics and individual responses to treatment of hyperglycemia in type 2 diabetes.
Pharmacogenetics and genomics 2015 Oct 25 (10): 475-84. Engelbrechtsen Line, Andersson Ehm, Roepstorff Soeren, Hansen Torben, Vestergaard Henr |
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[The study of the association of polymorphism rs5219 gene KCNJ11 with obesity and the risk of type 2 diabetes among residents of the Moscow Region].
Voprosy pitaniia 2015 84 (2): 4-9. Baturin A K, Sorokina E Yu, Pogozheva A V, Peskova E V, Makurina O N, Tutelyan V |
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Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men.
Diabetes 2011 May 60 (5): 1608-16. Stan?áková Alena, Paananen Jussi, Soininen Pasi, Kangas Antti J, Bonnycastle Lori L, Morken Mario A, Collins Francis S, Jackson Anne U, Boehnke Michael L, Kuusisto Johanna, Ala-Korpela Mika, Laakso Mark |
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Combined risk allele score of eight type 2 diabetes genes is associated with reduced first-phase glucose-stimulated insulin secretion during hyperglycemic clamps.
Diabetes 2010 Jan 59 (1): 287-92. 't Hart Leen M, Simonis-Bik Annemarie M, Nijpels Giel, van Haeften Timon W, Schäfer Silke A, Houwing-Duistermaat Jeanine J, Boomsma Dorret I, Groenewoud Marlous J, Reiling Erwin, van Hove Els C, Diamant Michaela, Kramer Mark H H, Heine Robert J, Maassen J Antonie, Kirchhoff Kerstin, Machicao Fausto, Häring Hans-Ulrich, Slagboom P Eline, Willemsen Gonneke, Eekhoff Elisabeth M, de Geus Eco J, Dekker Jacqueline M, Fritsche Andre |
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Improvements in glucose homeostasis in response to regular exercise are influenced by the PPARG Pro12Ala variant: results from the HERITAGE Family Study.
Diabetologia 2009 Dec . Ruchat SM, Rankinen T, Weisnagel SJ, Rice T, Rao DC, Bergman RN, Bouchard C, Pérusse L |
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Previously associated type 2 diabetes variants may interact with physical activity to modify the risk of impaired glucose regulation and type 2 diabetes: a study of 16,003 Swedish adults.
Diabetes 2009 Mar . Brito EC, Lyssenko V, Renström F, Berglund G, Nilsson PM, Groop L, Franks PW |
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Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study.
Diabetes 2008 Jan 57 (1): 244-54. Vaxillaire Martine, Veslot Jacques, Dina Christian, Proença Christine, Cauchi Stéphane, Charpentier Guillaume, Tichet Jean, Fumeron Frédéric, Marre Michel, Meyre David, Balkau Beverley, Froguel Philippe, |
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Impact of Kir6.2 E23K polymorphism on the development of type 2 diabetes in a general Japanese population: The Hisayama Study.
Diabetes 2007 Nov 56 (11): 2829-33. Doi Yasufumi, Kubo Michiaki, Ninomiya Toshiharu, Yonemoto Koji, Iwase Masanori, Arima Hisatomi, Hata Jun, Tanizaki Yumihiro, Iida Mitsuo, Kiyohara Yuta |
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Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program.
Diabetes 2007 Feb 56 (2): 531-6. Florez Jose C, Jablonski Kathleen A, Kahn Steven E, Franks Paul W, Dabelea Dana, Hamman Richard F, Knowler William C, Nathan David M, Altshuler Dav |
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The E23K variant of KCNJ11 encoding the pancreatic beta-cell adenosine 5'-triphosphate-sensitive potassium channel subunit Kir6.2 is associated with an increased risk of secondary failure to sulfonylurea in patients with type 2 diabetes.
The Journal of clinical endocrinology and metabolism 2006 Jun 91 (6): 2334-9. Sesti Giorgio, Laratta Emanuela, Cardellini Marina, Andreozzi Francesco, Del Guerra Silvia, Irace Concetta, Gnasso Agostino, Grupillo Maria, Lauro Renato, Hribal Marta Letizia, Perticone Francesco, Marchetti Pie |
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Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses.
Diabetic medicine : a journal of the British Diabetic Association 2005 May 22 (5): 590-8. van Dam R M, Hoebee B, Seidell J C, Schaap M M, de Bruin T W A, Feskens E J |
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Polymorphisms of the SUR1 (ABCC8) and Kir6.2 (KCNJ11) genes predict the conversion from impaired glucose tolerance to type 2 diabetes. The Finnish Diabetes Prevention Study.
The Journal of clinical endocrinology and metabolism 2004 Dec 89 (12): 6286-90. Laukkanen Olli, Pihlajamäki Jussi, Lindström Jaana, Eriksson Johan, Valle Timo T, Hämäläinen Helena, Ilanne-Parikka Pirjo, Keinänen-Kiukaanniemi Sirkka, Tuomilehto Jaakko, Uusitupa Matti, Laakso Markku, |
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The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes.
Diabetes 2003 Feb 52 (2): 573-7. Nielsen Eva-Maria D, Hansen Lars, Carstensen Bendix, Echwald Søren M, Drivsholm Thomas, Glümer Charlotte, Thorsteinsson Birger, Borch-Johnsen Knut, Hansen Torben, Pedersen Ol |
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The prevalent Glu23Lys polymorphism in the potassium inward rectifier 6.2 (KIR6.2) gene is associated with impaired glucagon suppression in response to hyperglycemia.
Diabetes 2002 Sep 51 (9): 2854-60. Tschritter Otto, Stumvoll Michael, Machicao Fausto, Holzwarth Martin, Weisser Melanie, Maerker Elke, Teigeler Anna, Häring Hans, Fritsche Andre |
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- Page last updated:Jul 10, 2020
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