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