Carboxy terminal tail of polycystin-1 regulates localization of TSC2 to repress mTOR.

Autosomal dominant polycystic kidney disease (ADPKD) is a commonly inherited renal disorder caused by defects in the PKD1 or PKD2 genes. ADPKD is associated with significant morbidity, and is a major underlying cause of end-stage renal failure (ESRF). Commonly, treatment options are limited to the m...

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Bibliographic Details
Main Authors: Ruhee Dere, Patricia D Wilson, Richard N Sandford, Cheryl Lyn Walker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-02-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2821926?pdf=render