Novel Therapeutic Strategies Targeting Molecular Pathways of Cystogenesis in Autosomal Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease that results from mutations in PKD1 or PKD2. The disease is characterized by the progressive development of fluid-filled cysts derived from renal tubular epithelial cells that destroy the architecture of...

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Bibliographic Details
Main Authors: Maurizio Salvadori, Aris Tsalouchos
Format: Article
Language:English
Published: Codon Publications 2017-03-01
Series:Journal of Renal and Hepatic Disorders
Subjects:
Online Access:https://jrenhep.com/index.php/jrenhep/article/view/10