Human Genome Epidemiology Literature Finder

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Records 1 - 14 (of 14 Records)

Query Trace: Hypertension and SCNN1G[original query]
Polymorphism (-173G>A) in promoter of human epithelial sodium channel gamma subunit gene (SCNN1G) and association analysis in essential hypertension. Human mutation 2001 Feb 17 (2): 157. Morris B, Benjafield A, Ishikawa K, Iawi Similar articles in PubMed
Six missense mutations of the epithelial sodium channel beta and gamma subunits in Japanese hypertensives. Hypertension research : official journal of the Japanese Society of Hypertension 2004 May 27 (5): 333-8. Kamide Kei, Tanaka Chihiro, Takiuchi Shin, Miwa Yoshikazu, Yoshii Masayoshi, Horio Takeshi, Kawano Yuhei, Miyata Toshiyu Similar articles in PubMed
A multilocus approach to the antihypertensive pharmacogenetics of hydrochlorothiazide. Pharmacogenetics and genomics 2005 May 15 (5): 287-93. Maitland-van der Zee Anke-Hilse, Turner Stephen T, Schwartz Gary L, Chapman Arlene B, Klungel Olaf H, Boerwinkle Er Similar articles in PubMed
Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension 2008 Jun 51 (6): 1658-64. Tobin Martin D, Tomaszewski Maciej, Braund Peter S, Hajat Cother, Raleigh Stuart M, Palmer Thomas M, Caulfield Mark, Burton Paul R, Samani Nilesh Similar articles in PubMed
Genetic variations in the sodium balance-regulating genes ENaC, NEDD4L, NDFIP2 and USP2 influence blood pressure and hypertension. Kidney & blood pressure research 2010 1 33 (1): 15-23. Jin Hyun-Seok, Hong Kyung-Won, Lim Ji-Eun, Hwang Sue-Yun, Lee Sang-Ho, Shin Chol, Park Hun Kuk, Oh Bermse Similar articles in PubMed
Common variants in epithelial sodium channel genes contribute to salt sensitivity of blood pressure: The GenSalt study. Circulation. Cardiovascular genetics 2011 Aug 4 (4): 375-80. Zhao Qi, Gu Dongfeng, Hixson James E, Liu De-Pei, Rao Dabeeru C, Jaquish Cashell E, Kelly Tanika N, Lu Fanghong, Ma Jixiang, Mu Jianjun, Shimmin Lawrence C, Chen Jichun, Mei Hao, Hamm L Lee, He Jiang, Similar articles in PubMed
Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Hypertension 2012 Jun 59 (6): 1204-11. Turner Stephen T, Bailey Kent R, Schwartz Gary L, Chapman Arlene B, Chai High Seng, Boerwinkle Er Similar articles in PubMed
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation research 2012 Nov . Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freeman BI, Coresh J, Kao LW, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A Similar articles in PubMed
Variation in genes that regulate blood pressure are associated with glomerular filtration rate in Chinese. PloS one 2014 9 (3): e92468. Montasser May E, Shimmin Lawrence C, Gu Dongfeng, Chen Jing, Gu Charles, Kelly Tanika N, Jaquish Cashell E, Rice Treva K, Rao Dabeeru C, Cao Jie, Chen Jichun, De-PeLiu , Whelton Paul K, Hamm Lotuce Lee, He Jiang, Hixson James Similar articles in PubMed
Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients. Journal of hypertension 2017 Sep . Liu Kai, Qin Fang, Sun Xiaolu, Zhang Yang, Wang Jizheng, Wu Yajie, Ma Wenjun, Wang Wei, Wu Xueyi, Qin Ying, Zhang Huimin, Zhou Xianliang, Wu Haiying, Hui Rutai, Zou Yubao, Jiang Xiongjing, Song L Similar articles in PubMed
Resequencing Epithelial Sodium Channel Genes Identifies Rare Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study. American journal of hypertension 2017 10 31 (2): 205-211. Gu Xiaoying, Gu Dongfeng, He Jiang, Rao Dabeeru C, Hixson James E, Chen Jichun, Li Jianxin, Huang Jianfeng, Wu Xigui, Rice Treva K, Shimmin Lawrence C, Kelly Tanika Similar articles in PubMed
[Genetic Polymorphisms Associated with the Onset of Arterial Hypertension in a Portuguese Population]. Acta medica portuguesa 2018 Oct 31 (10): 542-550. Sousa Ana Célia, Reis Roberto Palma, Pereira Andreia, Borges Sofia, Freitas Ana Isabel, Guerra Graça, Gouveia Sara, Góis Teresa, Nóbrega Lino, Rodrigues Mariana, Henriques Eva, Freitas Sónia, Ornelas Ilídio, Pereira Décio, Brehm António, Mendonça Maria Isab Similar articles in PubMed
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia. American journal of hypertension 2019 4 32 (8): 752-758. Fan Peng, Zhao Yu-Mo, Zhang Di, Liao Ying, Yang Kun-Qi, Tian Tao, Lou Ying, Luo Fang, Ma Wen-Jun, Zhang Hui-Min, Song Lei, Cai Jun, Liu Ya-Xin, Zhou Xian-Lia Similar articles in PubMed
Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation. Kidney & blood pressure research 2020 7 45 (4): 603-611. Fan Peng, Zhang Di, Pan Xiao-Cheng, Yang Kun-Qi, Zhang Qiong-Yu, Lu Yi-Ting, Zhang Ying, Liu Xue-Ying, Ma Wen-Jun, Zhang Hui-Min, Song Lei, Cai Jun, Liu Ya-Xin, Zhou Xian-Lia Similar articles in PubMed