Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: KCNMB1[original query] |
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E65 K polymorphism in KCNMB1 gene is not associated with ischaemic heart disease in Spanish patients. Journal of human genetics 2005 50 (11): 604-6. Via Marc, Valveny Neus, López-Alomar Antonio, Athanasiadis Georgios, Pintó Xavier, Domingo Enric, Esteban Esther, González-Pérez Emili, Moral Ped |
Protective effect of the KCNMB1 E65K genetic polymorphism against diastolic hypertension in aging women and its relevance to cardiovascular risk. Circulation research 2005 Dec 97 (12): 1360-5. Sentí Mariano, Fernández-Fernández José M, Tomás Marta, Vázquez Esther, Elosua Roberto, Marrugat Jaume, Valverde Miguel |
Association analysis between hypertension and CYBA, CLCNKB, and KCNMB1 functional polymorphisms in the Japanese population--the Suita Study. Circulation journal : official journal of the Japanese Circulation Society 2005 Feb 69 (2): 138-42. Kokubo Yoshihiro, Iwai Naoharu, Tago Naomi, Inamoto Nozomu, Okayama Akira, Yamawaki Hideyuki, Naraba Hiroaki, Tomoike Hitono |
KCNMB1 genotype influences response to verapamil SR and adverse outcomes in the INternational VErapamil SR/Trandolapril STudy (INVEST). Pharmacogenetics and genomics 2007 Sep 17 (9): 719-29. Beitelshees Amber L, Gong Yan, Wang Danxin, Schork Nicholas J, Cooper-Dehoff Rhonda M, Langaee Taimour Y, Shriver Mark D, Sadee Wolfgang, Knot Harm J, Pepine Carl J, Johnson Julie A, |
Single nucleotide polymorphism discovery and haplotype analysis of Ca2+-dependent K+ channel beta-1 subunit. Pharmacogenetics and genomics 2007 Apr 17 (4): 267-75. Gong Yan, Beitelshees Amber L, Wessel Jennifer, Langaee Taimour Y, Schork Nicholas J, Johnson Julie |
An african-specific functional polymorphism in KCNMB1 shows sex-specific association with asthma severity. Human molecular genetics 2008 Sep 17 (17): 2681-90. Seibold Max A, Wang Bin, Eng Celeste, Kumar Gunjan, Beckman Kenneth B, Sen Saunak, Choudhry Shweta, Meade Kelley, Lenoir Michael, Watson H Geoffrey, Thyne Shannon, Williams L Keoki, Kumar Rajesh, Weiss Kevin B, Grammer Leslie C, Avila Pedro C, Schleimer Robert P, Burchard Esteban González, Brenner Robe |
Interactions among genetic variants from contractile pathway of vascular smooth muscle cell in essential hypertension susceptibility of Chinese Han population. Pharmacogenetics and genomics 2008 Jun 18 (6): 459-66. Zhao Qi, Wang Laiyuan, Yang Wei, Chen Shufeng, Huang Jianfeng, Fan Zhongjie, Li Hongfan, Lu Xiangfeng, Gu Dongfe |
The KCNMB1 E65K variant is associated with reduced central pulse pressure in the community-based Framingham Offspring Cohort. Journal of hypertension 2009 Jan 27 (1): 55-60. Kelley-Hedgepeth Alyson, Peter Inga, Montefusco Maria Claudia, Levy Daniel, Benjamin Emelia J, Vasan Ramachandran S, Mendelsohn Michael E, Housman David, Huggins Gordon S, Mitchell Gary |
The KCNMB1 Glu65Lys polymorphism associates with reduced systolic and diastolic blood pressure in the Inter99 study of 5729 Danes. Journal of hypertension 2008 Nov 26 (11): 2142-6. Nielsen Trine, Burgdorf Kristoffer Sølvsten, Grarup Niels, Borch-Johnsen Knut, Hansen Torben, Jørgensen Torben, Pedersen Oluf, Andersen Git |
Common charge-shift mutation Glu65Lys in K+ channel ß1-Subunit KCNMB1: pleiotropic consequences for glomerular filtration rate and progressive renal disease. American journal of nephrology 2010 32 (5): 414-24. Chen Yuqing, Salem Rany M, Rao Fangwen, Fung Maple M, Bhatnagar Vibha, Pandey Braj, Mahata Manjula, Waalen Jill, Nievergelt Caroline M, Lipkowitz Michael S, Hamilton Bruce A, Mahata Sushil K, O'Connor Daniel |
Genetic and clinical biomarkers of tocilizumab response in patients with rheumatoid arthritis. Pharmacological research 2016 09 111 264-271. Maldonado-Montoro Mar, Cañadas-Garre Marisa, González-Utrilla Alfonso, Plaza-Plaza José Cristian, Calleja-Hernández Miguel Ÿng |
Association between potassium channel SNPs and essential hypertension in Xinjiang Kazak Chinese patients. Experimental and therapeutic medicine 2017 Sep 14 (3): 1999-2006. Han Yuan-Yuan, Wang Li-Jie, Zhang Liang, Zhang Wen-Wen, Ma Ke-Tao, Li Li, Si Jun-Qia |
Cardiac arrhythmia and neuroexcitability gene variants in resected brain tissue from patients with sudden unexpected death in epilepsy (SUDEP). NPJ genomic medicine 2018 4 3 9. Friedman Daniel, Kannan Kasthuri, Faustin Arline, Shroff Seema, Thomas Cheddhi, Heguy Adriana, Serrano Jonathan, Snuderl Matija, Devinsky Orr |
The dominant models of KCNJ11 E23K and KCNMB1 E65K are associated with essential hypertension (EH) in Asian: Evidence from a meta-analysis. Medicine 2019 Jun 98 (23): e15828. Zhancheng Wang, Wenhui Ji, Yun Jiang, Lingli Wang, Huijun Huang, Yan Shen, Jin |
Genetic polymorphisms are associated with individual susceptibility to dexmedetomidine. Frontiers in genetics 2023 9 14 1187415. Yuanyuan Ding, Aiqing Liu, Yafeng Wang, Shuai Zhao, Shiqian Huang, Hongyu Zhu, Lulin Ma, Linlin Han, Shaofang Shu, Lidong Zheng, Xiangdong Ch |
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- Page last updated:Apr 16, 2024
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