Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: SLC12A1[original query] |
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Genetic analysis of 22 candidate genes for hypertension in the Japanese population. Journal of hypertension 2004 Jun 22 (6): 1119-26. Iwai Naoharu, Tago Naomi, Yasui Naomi, Kokubo Yoshihiro, Inamoto Nozomu, Tomoike Hitonobu, Shioji Keisu |
Genetic variation in the renal sodium transporters NKCC2, NCC, and ENaC in relation to the effects of loop diuretic drugs. Clinical pharmacology and therapeutics 2007 Sep 82 (3): 300-9. Vormfelde S V, Sehrt D, Toliat M R, Schirmer M, Meineke I, Tzvetkov M, Nürnberg P, Brockmöller |
Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nature genetics 2008 May 40 (5): 592-9. Ji Weizhen, Foo Jia Nee, O'Roak Brian J, Zhao Hongyu, Larson Martin G, Simon David B, Newton-Cheh Christopher, State Matthew W, Levy Daniel, Lifton Richard |
Genetic predisposition and nongenetic risk factors of thiazolidinedione-related edema in patients with type 2 diabetes. Pharmacogenetics and genomics 2011 Dec 21 (12): 829-36. Chang Tien-Jyun, Liu Pi-Hua, Liang Yi-Chi, Chang Yi-Cheng, Jiang Yi-Der, Li Hung-Yuan, Lo Min-Tzu, Chen Harn-Shen, Chuang Lee-Mi |
Calcium intake and ion transporter genetic polymorphisms interact in human colorectal neoplasia risk in a 2-phase study. The Journal of nutrition 2014 Nov 144 (11): 1734-41. Zhu Xiangzhu, Liang Ji, Shrubsole Martha J, Ness Reid M, Cai Qiuyin, Long Jirong, Chen Zhi, Li Guoliang, Wiese Dawn, Zhang Bing, Smalley Walter E, Edwards Todd L, Giovannucci Edward, Zheng Wei, Dai |
Association of Mutations in SLC12A1 Encoding the NKCC2 Cotransporter With Neonatal Primary Hyperparathyroidism. The Journal of clinical endocrinology and metabolism 2016 Mar jc20161211. Li Dong, Tian Lifeng, Hou Cuiping, Kim Cecilia E, Hakonarson Hakon, Levine Michael |
Interactions between calcium intake and polymorphisms in genes essential for calcium reabsorption and risk of colorectal neoplasia in a two-phase study. Molecular carcinogenesis 2017 10 56 (10): 2258-2266. Zhao Jing, Zhu Xiangzhu, Shrubsole Martha J, Ness Reid M, Hibler Elizabeth A, Cai Qiuyin, Long Jirong, Chen Zhi, Jiang Ming, Kabagambe Edmond K, Zhang Bing, Hou Lifang, Smalley Walter E, Edwards Todd L, Giovannucci Edward L, Zheng Wei, Dai |
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 |
Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. Medicine 2018 Aug 97 (33): e11865. Nandakumar Priyanka, Morrison Alanna C, Grove Megan L, Boerwinkle Eric, Chakravarti Aravin |
A long-term study of the effects of SLC12A1 homozygous mutation (g.62382825G>A, p.Pro372Leu) in Japanese Black cattle. Animal science journal = Nihon chikusan Gakkaiho 2020 7 91 (1): e13415. Sakamoto Yoichi, Hasegawa Kiyotoshi, Moriwaki Shunsuke, Hara Yoko, Hamada Yuta, Sasaki Shin |
Clinical Course and Prognosis of Tubulopathies Characterized by Metabolic Alkalosis in Children. Turkish archives of pediatrics 2022 10 57 (6): 644-650. Huseynli Bahruz, Atm?? Bahriye, Cevizli Derya, Bi?gin At?l, Karabay Bayaz?t Ays |
Phenotypic and genotypic characteristics of children with Bartter syndrome. The Turkish journal of pediatrics 2022 10 64 (5): 825-838. Güven Serçin, Gökçe ?brahim, Alavanda Ceren, Çiçek Neslihan, Demirci Ece Bodur, Sak Mehtap, Pul Serim, Türkkan Özde Nisa, Y?ld?z Nurdan, Ata P?nar, Alpay Hari |
Association of polymorphisms of calcium reabsorption genes SLC12A1, KCNJ1 and SLC8A1 with colorectal adenoma. Journal of cancer research and clinical oncology 2023 4 . Xiaolian Lai, Shuoyan Lu, Jia Jiang, Hanqun Zhang, Qinglin Yang, Yuncong Liu, Libo Li, Sanming Li, Si Dai, Yanping Chen, Yan Chen, Jun Liu, Yong |
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