Extracellular potassium deprivation reversibly dephosphorylates cofilin
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference34 articles.
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3. Genetic heterogeneity of Bartter’s syndrome revealed by mutations in the K+ channel, ROMK;Simon;Nat. Genet.,1996
4. Gitelman’s syndrome (Bartter’s variant) maps to the thiazide-sensitive co-transporter gene locus on chromosome 16q13 in a large kindred;Pollack;J. Am. Soc. Nephrol.,1996
5. Hypertension in the syndrome of apparent mineralocorticoid excess due to a mutation of the 11-hydroxysteroid dehydrogenase type 2 gene;Sterwart;Lancet,1996
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