Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: SLC4A10[original query] |
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AQP1 and SLC4A10 as candidate genes for primary open-angle glaucoma. Molecular vision 2010 16 93-7. Liu Wenjing, Liu Yutao, Qin Xue-Jun, Schmidt Silke, Hauser Michael A, Allingham R Ra |
A follow-up case-control association study of tractable (druggable) genes in recurrent major depression. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Sep 156B (6): 640-50. Schosser A, Gaysina D, Cohen-Woods S, Domenici E, Perry J, Tozzi F, Korszun A, Gunasinghe C, Gray J, Jones L, Binder E B, Holsboer F, Craddock N, Owen M J, Craig I W, Farmer A E, Muglia P, McGuffin |
Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study. Journal of human hypertension 2015 Nov . Guo L, Liu F, Chen S, Yang X, Huang J, He J, Jaquish C E, Zhao Q, Gu C C, Hixson J E, Gu |
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality.
Journal of the American Society of Nephrology : JASN 2017 Mar . Böger Carsten A, Gorski Mathias, McMahon Gearoid M, Xu Huichun, Chang Yen-Pei C, van der Most Peter J, Navis Gerjan, Nolte Ilja M, de Borst Martin H, Zhang Weihua, Lehne Benjamin, Loh Marie, Tan Sian-Tsung, Boerwinkle Eric, Grams Morgan E, Sekula Peggy, Li Man, Wilmot Beth, Moon James G, Scheet Paul, Cucca Francesco, Xiao Xiangjun, Lyytikäinen Leo-Pekka, Delgado Graciela, Grammer Tanja B, Kleber Marcus E, Sedaghat Sanaz, Rivadeneira Fernando, Corre Tanguy, Kutalik Zoltan, Bergmann Sven, Nielson Carrie M, Srikanth Priya, Teumer Alexander, Müller-Nurasyid Martina, Brockhaus Anne Catharina, Pfeufer Arne, Rathmann Wolfgang, Peters Annette, Matsumoto Martha, de Andrade Mariza, Atkinson Elizabeth J, Robinson-Cohen Cassianne, de Boer Ian H, Hwang Shih-Jen, Heid Iris M, Gögele Martin, Concas Maria Pina, Tanaka Toshiko, Bandinelli Stefania, Nalls Mike A, Singleton Andrew, Tajuddin Salman M, Adeyemo Adebowale, Zhou Jie, Doumatey Ayo, McWeeney Shannon, Murabito Joanne, Franceschini Nora, Flessner Michael, Shlipak Michael, Wilson James G, Chen Guanjie, Rotimi Charles N, Zonderman Alan B, Evans Michele K, Ferrucci Luigi, Devuyst Olivier, Pirastu Mario, Shuldiner Alan, Hicks Andrew A, Pramstaller Peter Paul, Kestenbaum Bryan, Kardia Sharon L R, Turner Stephen T, Study LifeLines Cohort, Briske Tamara Ellefson, Gieger Christian, Strauch Konstantin, Meisinger Christa, Meitinger Thomas, Völker Uwe, Nauck Matthias, Völzke Henry, Vollenweider Peter, Bochud Murielle, Waeber Gerard, Kähönen Mika, Lehtimäki Terho, März Winfried, Dehghan Abbas, Franco Oscar H, Uitterlinden Andre G, Hofman Albert, Taylor Herman A, Chambers John C, Kooner Jaspal S, Fox Caroline S, Hitzemann Robert, Orwoll Eric S, Pattaro Cristian, Schlessinger David, Köttgen Anna, Snieder Harold, Parsa Afshin, Cohen David |
Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique. Balkan medical journal 2022 11 40 (1): 13-20. Atl? Engin, Gürkan Hakan, Güldiken Babürhan, Eker Damla, Yalç?ntepe Sinem, Demir Selma, Atl? Emine ?kb |
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