Distinct pathways for the involvement of WNK4 in the signaling of hypertonicity and EGF

WNK4 kinase mutations produce the autosomal dominant disorder familial hyperkalemia and hypertension (FHH), also known as pseudohypoaldosteronism type II, by a molecular mechanism that is not completely understood. In vitro experiments in frog oocytes showed that WNK4 affects ion transport systems s...

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Bibliographic Details
Published inThe FEBS journal Vol. 275; no. 8; pp. 1631 - 1642
Main Authors Shaharabany, Miriam, Holtzman, Eliezer J, Mayan, Haim, Hirschberg, Koret, Seger, Rony, Farfel, Zvi
Format Journal Article
LanguageEnglish
Published Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.04.2008
Blackwell Publishing Ltd
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