Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: BSND[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 |
Functional BSND variants in essential hypertension. American journal of hypertension 2007 Nov 20 (11): 1176-1182. Sile Saba, Gillani Niloufar B, Velez Digna R, Vanoye Carlos G, Yu Chang, Byrne Loretta M, Gainer James V, Brown Nancy J, Williams Scott M, George Alfred |
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 |
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 |
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