Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and WNK4[original query] |
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Identification of 108 SNPs in TSC, WNK1, and WNK4 and their association with hypertension in a Japanese general population. Journal of human genetics 2004 49 (9): 507-15. Kokubo Yoshihiro, Kamide Kei, Inamoto Nozomu, Tanaka Chihiro, Banno Mariko, Takiuchi Shin, Kawano Yuhei, Tomoike Hitonobu, Miyata Toshiyu |
Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. Human mutation 2011 Jul 32 (7): 806-14. Putku Margus, Kepp Katrin, Org Elin, Sõber Siim, Comas David, Viigimaa Margus, Veldre Gudrun, Juhanson Peeter, Hallast Pille, Tõnisson Neeme, , Shaw-Hawkins Sue, Caulfield Mark J, , Khusnutdinova Elza, Kožich Viktor, Munroe Patricia B, Laan Mar |
A WNK4 gene variant relates to osteoporosis and not to hypertension in the Portuguese population. Molecular genetics and metabolism 2011 Apr 102 (4): 465-9. Mendes Ana Isabel, Mascarenhas Mário Rui, Matos Sónia, Sousa Inês, Ferreira Joana, Barbosa Ana Paula, Bicho Manuel, Jordan Pet |
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 |
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