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WNK4 gene

Known as: WNK4, PROTEIN KINASE, LYSINE-DEFICIENT 4, PRKWNK4 
National Institutes of Health

Papers overview

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2013
2013
The R1185C mutation in WNK4 is associated with pseudohypoaldosteronism type II (PHAII). Unlike other PHAII-causing mutations in… 
2010
2010
WNK kinase is a subfamily of serine/threonine kinases. WNK1 and WNK4 were shown to stimulate NCC activity through SPAK and OSR1… 
2010
2010
Background: It has been reported that mutations in WNK1 and WNK4 cause pseudohypoaldosteronism type II (PHA2), an autosomal… 
2010
2010
The cloning of the related sodium chloride (NCC) and sodium potassium 2 chloride (NKCC) co-transporters in the early 1990s… 
2008
2008
WNK4 kinase mutations produce the autosomal dominant disorder familial hyperkalemia and hypertension (FHH), also known as… 
2004
2004
Abstract—A polymorphism in intron 10 of the serine-threonine kinase with no lysine (K) 4 gene WNK4 (G→A, base 1156666 on… 
2003
2003
Abstract—Linkage analyses in experimental crosses of stroke-prone spontaneously hypertensive (SHRSP) and normotensive Wistar…