Article
Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4.
Proceedings of the National Academy of Sciences of the United States of America - 7 May 2013
Shibata Shigeru, Zhang Junhui, Puthumana Jeremy, Stone Kathryn L, Lifton Richard P
Abstract excerpt
Pseudohypoaldosteronism type II (PHAII) is a rare Mendelian syndrome featuring hypertension and hyperkalemia resulting from constitutive renal salt reabsorption and impaired K(+) secretion. Recently, mutations in Kelch-like 3 (KLHL3) and Cullin 3 (CUL3), components of an E3 ubiquitin ligase complex, were found to cause PHAII, suggesting that loss of this complex's ability to target specific substrates for...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
