Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: CLCNKA[original query] |
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Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption. Human heredity 2008 65 (1): 33-46. Sile Saba, Velez Digna R, Gillani Niloufar B, Alexander Charles A, Alexander Charles R, George Alfred L, Williams Scott |
Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension. Human molecular genetics 2007 Jul 16 (13): 1630-8. Barlassina Cristina, Dal Fiume Chiara, Lanzani Chiara, Manunta Paolo, Guffanti Guia, Ruello Antonella, Bianchi Giuseppe, Del Vecchio Lucia, Macciardi Fabio, Cusi Danie |
Common variants in HSPB7 and FRMD4B associated with advanced heart failure. Circulation. Cardiovascular genetics 2010 Apr 3 (2): 147-54. Cappola Thomas P, Li Mingyao, He Jing, Ky Bonnie, Gilmore Joan, Qu Liming, Keating Brendan, Reilly Muredach, Kim Cecelia E, Glessner Joseph, Frackelton Edward, Hakonarson Hakon, Syed Faisel, Hindes Anna, Matkovich Scot J, Cresci Sharon, Dorn Gerald |
Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation. Proceedings of the National Academy of Sciences of the United States of America 2011 Feb 108 (6): 2456-61. Cappola Thomas P, Matkovich Scot J, Wang Wei, van Booven Derek, Li Mingyao, Wang Xuexia, Qu Liming, Sweitzer Nancy K, Fang James C, Reilly Muredach P, Hakonarson Hakon, Nerbonne Jeanne M, Dorn Gerald |
A CLCNKA polymorphism (rs10927887; p.Arg83Gly) previously linked to heart failure is associated with the estimated glomerular filtration rate in the RENASTUR cohort. Gene 2013 Sep 527 (2): 670-2. Tavira Beatriz, Gómez Juan, Ortega Francisco, Tranche Salvador, Díaz-Corte Carmen, Alvarez Francisco, Ortiz Alberto, Santos Fernando, Sánchez-Niño María D, Coto Eliec |
Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV. International journal of pediatric otorhinolaryngology 2016 12 92 17-20. Wang Hong-Han, Feng Yong, Li Hai-Bo, Wu Hong, Mei Ling-Yun, Wang Xing-Wei, Jiang Lu, He Chu-Fe |
Mutation spectrum of Chinese patients with Bartter syndrome. Oncotarget 2017 12 8 (60): 101614-101622. Han Yue, Lin Yi, Sun Qing, Wang Shujuan, Gao Yanxia, Shao Lepi |
Genetic Variation in SLC8A1 Gene Involved in Blood Pressure Responses to Acute Salt Loading. American journal of hypertension 2017 Nov . Liu Kuo, Liu Zheng, Qi Han, Liu Bin, Wu Jingjing, Liu Yezhou, Zhang Jie, Cao Han, Yan Yuxiang, He Yan, Zhang Li |
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Circulation 2018 Nov . Aragam Krishna G, Chaffin Mark, Levinson Rebecca T, McDermott Gregory, Choi Seung-Hoan, Shoemaker M Benjamin, Haas Mary E, Weng Lu-Chen, Lindsay Mark E, Smith J Gustav, Newton-Cheh Christopher, Roden Dan M, London Barry, Wells Quinn S, Ellinor Patrick T, Kathiresan Sekar, Lubitz Steven A, |
The Genetic Makeup of the Electrocardiogram.
Cell systems 2020 Sep 11 (3): 229-238.e5. Verweij Niek, Benjamins Jan-Walter, Morley Michael P, van de Vegte Yordi J, Teumer Alexander, Trenkwalder Teresa, Reinhard Wibke, Cappola Thomas P, van der Harst P |
Genetic predictors of sick sinus syndrome. Molecular biology reports 2021 7 48 (6): 5355-5362. Timasheva Yanina, Badykov Marat, Akhmadishina Leysan, Nasibullin Timur, Badykova Elena, Pushkareva Alfiya, Plechev Vladimir, Sagitov Ildus, Zagidullin Nauf |
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions. Genome medicine 2023 8 15 (1): 62. Nikolai Tschernoster, Florian Erger, Stefan Kohl, Björn Reusch, Andrea Wenzel, Stephen Walsh, Holger Thiele, Christian Becker, Marek Franitza, Malte P Bartram, Martin Kömhoff, Lena Schumacher, Christian Kukat, Tatiana Borodina, Claudia Quedenau, Peter Nürnberg, Markus M Rinschen, Jan H Driller, Bjørn P Pedersen, Karl P Schlingmann, Bruno Hüttel, Detlef Bockenhauer, Bodo Beck, Janine Altmüll |
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- Page last updated:Apr 16, 2024
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