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Human Mutation|February 10, 2011
Heterogeneity in the processing of CLCN5 mutants related to Dent diseaseTeddy Grand, Sébastien L'Hoste, David Mordasini, et al.Human Mutation|May 11, 2021
New insights into the role of endoplasmic reticulum-associated degradation in Bartter Syndrome Type 1Irfan Shaukat, Dalal Bakhos-Douaihy, Yingying Zhu, et al.The Journal of Biological Chemistry|September 13, 2007
NKCC2 surface expression in mammalian cells: down-regulation by novel interaction with aldolase BBoubacar Benziane, Sylvie Demaretz, Nadia Defontaine, et al.Pflugers Archiv : European Journal of Physiology|July 2, 2003
Differentiated thick ascending limb (TAL) cultured cells derived from SV40 transgenic mice express functional apical NHE2 isoform: effect of nitric oxideSoline Bourgeois, Patrick Rossignol, Françoise Grelac, et al.Journal of the American Society of Nephrology : JASN|February 9, 2013
SPAK differentially mediates vasopressin effects on sodium cotransportersTurgay Saritas, Aljona Borschewski, James A McCormick, et al.Nature Medicine|November 5, 2013
Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expressionMatteo Trudu, Sylvie Janas, Chiara Lanzani, et al.The Journal of Clinical Investigation|August 14, 2012
PTH-independent regulation of blood calcium concentration by the calcium-sensing receptorAlexandre Loupy, Suresh Krishna Ramakrishnan, Bharath Wootla, et al.The New England Journal of Medicine|April 28, 2016
Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 MutationsKamel Laghmani, Bodo B Beck, Sung-Sen Yang, et al.Pageof 3