HuGE Literature Finder
Records 1-13
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Study on the correlation between KCNJ11 gene polymorphism and metabolic syndrome in the elderly.
Experimental and therapeutic medicine 2017 Sep 14 (3): 2031-2035. Jiang Fan, Liu Ning, Chen Xiao Zhuang, Han Kun Yuan, Zhu Cai Zho |
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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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Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy.
Epilepsy research 2015 Oct 118 22-28. Schoeler Natasha E, Leu Costin, White Jon, Plagnol Vincent, Ellard Sian, Matarin Mar, Yellen Gary, Thiele Elizabeth A, Mackay Mark, McMahon Jacinta M, Scheffer Ingrid E, Sander Josemir W, Cross J Helen, Sisodiya Sanjay |
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Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach.
Molecular genetics and metabolism 2014 Dec 113 (4): 315-20. Alkorta-Aranburu G, Carmody D, Cheng Y W, Nelakuditi V, Ma L, Dickens Jazzmyne T, Das S, Greeley S A W, del Gaudio |
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Genetic association study with metabolic syndrome and metabolic-related traits in a cross-sectional sample and a 10-year longitudinal sample of chinese elderly population.
PloS one 2014 9 (6): e100548. Yang Jinghui, Liu Jianwei, Liu Jing, Li Wenyuan, Li Xiaoying, He Yao, Ye Li |
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Polycystic ovary syndrome is not associated with genetic variants that mark risk of type 2 diabetes.
Acta diabetologica 2013 Jun 50 (3): 451-7. Saxena R, Welt C |
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Polycystic ovary syndrome is not associated with polymorphisms of the TCF7L2, CDKAL1, HHEX, KCNJ11, FTO and SLC30A8 genes.
Clinical endocrinology 2012 Sep 77 (3): 439-45. Kim Jin Ju, Choi Young Min, Cho Young Min, Hong Min A, Chae Soo Jin, Hwang Kyu Ri, Hwang Seung Sik, Yoon Sang Ho, Moon Shin Yo |
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Candidate gene association study conditioning on individual ancestry in patients with type 2 diabetes and metabolic syndrome from Mexico City.
Diabetes/metabolism research and reviews 2010 May 26 (4): 261-70. Cruz M, Valladares-Salgado A, Garcia-Mena J, Ross K, Edwards M, Angeles-Martinez J, Ortega-Camarillo C, de la Peña J Escobedo, Burguete-Garcia A I, Wacher-Rodarte N, Ambriz R, Rivera R, D'artote A L, Peralta J, Parra Esteban J, Kumate |
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Genetic variants associated with insulin resistance and metabolic syndrome in young Asian Indians with myocardial infarction.
Metabolic syndrome and related disorders 2008 Sep 6 (3): 209-14. Ranjith Naresh, Pegoraro Rosemary J, Naidoo Datshana P, Shanmugam Rebecca, Rom L |
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Genetic variants in TCF7L2 and KCNJ11 genes in a Greek population with polycystic ovary syndrome.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2008 Sep 24 (9): 486-90. Christopoulos Panagiotis, Mastorakos George, Gazouli Maria, Panidis Dimitrios, Deligeoroglou Efthimios, Katsikis Ilias, Papadias Konstantinos, Diamandi-Kandarakis Evanthia, Creatsas Geor |
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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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Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels.
European journal of human genetics : EJHG 2007 Jun 15 (6): 679-84. Barber Thomas M, Bennett Amanda J, Gloyn Anna L, Groves Christopher J, Sovio Ulla, Ruokonen Aimo, Martikainen Hannu, Pouta Anneli, Taponen Saara, Weedon Michael N, Hartikainen Anna-Liisa, Wass John A H, Järvelin Marjo-Riitta, Zeggini Eleftheria, Franks Stephen, McCarthy Mark |
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Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.
Diabetologia 2006 Jun 49 (6): 1190-7. Flanagan S E, Edghill E L, Gloyn A L, Ellard S, Hattersley A |
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- Page last updated:Jul 10, 2020
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