HuGE Literature Finder
Records 1-29
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Changes of the echocardiographic parameters in chronic heart failure patients with Ile337val, Glu23lys, and Ser1369ala polymorphisms of genes encoding the ATP-sensitive potassium channels subunits in the Ukrainian population.
Annals of human genetics 2018 Jul . Strutynskyi R B, Voronkov L G, Nagibin V S, Mazur I D, Stroy D, Dosenko V |
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Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies.
Placenta 2018 Jun 66 8-16. Workalemahu Tsegaselassie, Enquobahrie Daniel A, Gelaye Bizu, Sanchez Sixto E, Garcia Pedro J, Tekola-Ayele Fasil, Hajat Anjum, Thornton Timothy A, Ananth Cande V, Williams Michelle |
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KCNJ11 variants and their effect on the association between serum potassium and diabetes risk in the Atherosclerosis Risk in Communities (ARIC) Study and Jackson Heart Study (JHS) cohorts.
PloS one 2018 13 (8): e0203213. Chatterjee Ranee, Davenport Clemontina A, Raffield Laura M, Maruthur Nisa, Lange Leslie, Selvin Elizabeth, Butler Kenneth, Yeh Hsin-Chieh, Wilson James G, Correa Adolfo, Edelman David, Hauser Elizabe |
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[Association of the polymorphic marker Glu23Lys in the KCNJ11 gene with hypertension in Kyrgyz patients].
Terapevticheskii arkhiv 2017 89 (1): 14-18. Isakova Zh T, Talaibekova E T, Asambaeva D A, Kerimkulova A S, Lunegova O S, Aldashev A |
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Interactive Effect of the KCNJ11 Ile337Val Polymorphism and Cigarette Smoking on the Antihypertensive Response to Irbesartan in Chinese Hypertensive Patients.
American journal of hypertension 2015 Aug . Jiang Shanqun, Venners Scott Alan, Hsu Yi-Hsiang, Weinstock Justin, Wang Binyan, Xing Houxun, Wang Xiaobin, Xu Xipi |
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An analysis of the association between a polymorphism of KCNJ11 and diabetic retinopathy in a Chinese Han population.
European journal of medical research 2015 20 (1): 3. Liu Nai-Jia, Wu Hui-Hui, Li Yan-Liang, Yang Zhen, Tao Xiao-Ming, Du Yan-Ping, Wang Xuan-Chun, Lu Bin, Zhang Zhao-Yun, Hu Ren-Ming, Wen J |
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Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease.
Basic research in cardiology 2013 Nov 108 (6): 387. Fedele Francesco, Mancone Massimo, Chilian William M, Severino Paolo, Canali Emanuele, Logan Suzanna, De Marchis Maria Laura, Volterrani Maurizio, Palmirotta Raffaele, Guadagni Fiorel |
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Association study of genetic variants of 17 diabetes-related genes/loci and cardiovascular risk and diabetic nephropathy in the Chinese She population.
Journal of diabetes 2013 Jun 5 (2): 136-45. Chen Gang, Xu Yuan, Lin Yinghua, Lai Xiaolan, Yao Jin, Huang Baoying, Chen Zichun, Huang Huibin, Fu Xianguo, Lin Lixiang, Lai Shenghan, Wen Junpi |
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Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations.
Cerebrovascular diseases (Basel, Switzerland) 2013 36 (3): 181-8. Chou S H-Y, Shulman J M, Keenan B T, Secor E A, Buchman A S, Schneider J, Bennett D A, De Jager P |
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Relationship between dilated cardiomyopathy and the E23K and I337V polymorphisms in the Kir6.2 subunit of the KATP channel.
Genetics and molecular research : GMR 2013 12 (4): 4383-92. Xi H L, Liu J F, Li L, Wan |
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Association of the antihypertensive response of iptakalim with KCNJ11 (Kir6.2 gene) polymorphisms in Chinese Han hypertensive patients.
Acta pharmacologica Sinica 2011 Aug 32 (8): 1078-84. Duan Rui-feng, Cui Wen-yu, Wang H |
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Association of KCNJ11 with impaired glucose regulation in essential hypertension.
Genetics and molecular research : GMR 2011 10 (2): 2. Wang Y, Zhou XO, Zhang Y, Gao PJ, Zhu DL |
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The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations.
Pediatric research 2011 Jun 69 (6): 538-43. Devaney Joseph M, Thompson Paul D, Visich Paul S, Saltarelli William A, Gordon Paul M, Orkunoglu-Suer E Funda, Gordish-Dressman Heather, Harmon Brennan T, Bradbury Margaret K, Panchapakesan Karuna, Khianey Rahul, Hubal Monica J, Clarkson Priscilla M, Pescatello Linda S, Zoeller Robert F, Moyna Niall M, Angelopoulos Theodore J, Kraus William E, Hoffman Eric |
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Genetic variants of diabetes risk and incident cardiovascular events in chronic coronary artery disease.
PloS one 2011 6 (1): e16341. Sousa André Gustavo P, Lopes Neuza H, Hueb Whady A, Krieger José Eduardo, Pereira Alexandre |
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Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease.
BMC medical genetics 2011 12 55. Ding Keyue, Kullo Iftikhar |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort.
Arteriosclerosis, thrombosis, and vascular biology 2010 Sep 30 (9): 1867-72. Pechlivanis Sonali, Scherag André, Mühleisen Thomas W, Möhlenkamp Stefan, Horsthemke Bernhard, Boes Tanja, Bröcker-Preuss Martina, Mann Klaus, Erbel Raimund, Jöckel Karl-Heinz, Nöthen Markus M, Moebus Susanne, |
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Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010 Feb 19 (2): 558-65. Meyer Tamra E, Boerwinkle Eric, Morrison Alanna C, Volcik Kelly A, Sanderson Maureen, Coker Ann L, Pankow James S, Folsom Aaron |
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Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.
BMC medical genetics 2010 11 125. Morgan Angharad R, Thompson John M D, Murphy Rinki, Black Peter N, Lam Wen-Jiun, Ferguson Lynnette R, Mitchell Ed |
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KATP channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress response.
Human genetics 2009 Dec 126 (6): 779-89. Reyes Santiago, Park Sungjo, Johnson Bruce D, Terzic Andre, Olson Timothy |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.
Human molecular genetics 2009 Jun 18 (12): 2305-16. Drenos Fotios, Talmud Philippa J, Casas Juan P, Smeeth Liam, Palmen Jutta, Humphries Steve E, Hingorani Aroon |
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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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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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K(ATP) channel polymorphism is associated with left ventricular size in hypertensive individuals: a large-scale community-based study.
Human genetics 2008 Jul 123 (6): 665-7. Reyes Santiago, Terzic Andre, Mahoney Douglas W, Redfield Margaret M, Rodeheffer Richard J, Olson Timothy |
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Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population.
Diabetic medicine : a journal of the British Diabetic Association 2007 Feb 24 (2): 178-86. Koo B K, Cho Y M, Park B L, Cheong H S, Shin H D, Jang H C, Kim S Y, Lee H K, Park K |
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Association of sixty-one non-synonymous polymorphisms in forty-one hypertension candidate genes with blood pressure variation and hypertension.
Hypertension research : official journal of the Japanese Society of Hypertension 2006 Aug 29 (8): 611-9. Kokubo Yoshihiro, Tomoike Hitonobu, Tanaka Chihiro, Banno Mariko, Okuda Tomohiko, Inamoto Nozomu, Kamide Kei, Kawano Yuhei, Miyata Toshiyu |
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The E23K polymorphism in Kir6.2 gene and coronary heart disease.
Clinica chimica acta; international journal of clinical chemistry 2006 May 367 (1-2): 93-7. Xiong Chenling, Zheng Fang, Wan Jun, Zhou Xin, Yin Zhinong, Sun Xiao |
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KCNJ11 polymorphisms and sudden cardiac death in patients with acute myocardial infarction.
Journal of molecular and cellular cardiology 2004 Feb 36 (2): 287-93. Jeron A, Hengstenberg C, Holmer S, Wollnik B, Riegger G A J, Schunkert H, Erdmann |
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- Page last updated:Jul 10, 2020
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