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10.1152/physiol.00032.2014 http://scihub22266oqcxt.onion/10.1152/physiol.00032.2014 C4422974!4422974!25933820     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Physiology+(Bethesda) 2015 ; 30 (3): 195-207 Nephropedia Template TP {{tp|p=25933820|t=2015. Molecular Pathways and Therapies in Autosomal-Dominant Polycystic Kidney Disease |pdf=|usr=}}{{25933820}} gab.com Text Molecular Pathways and Therapies in Autosomal-Dominant Polycystic Kidney Disease JO: Physiology (Bethesda) http://www.kidney.de/pget.php?&tw=1&pmid=25933820 #FOAvip Autosomal-dominant polycystic kidney disease (ADPKD) is the most prevalent inherited renal disease, characterized by multiple cysts that can eventually lead to kidney failure. Studies investigating the role of primary cilia and polycystins have significantly advanced our understanding of the pathogenesis of PKD. This review will present clinical and basic aspects of ADPKD, review current concepts of PKD pathogenesis, evaluate potential therapeutic targets, and highlight challenges for future clinical studies. Twit Text FOAVip Molecular Pathways and Therapies in Autosomal-Dominant Polycystic Kidney Disease ????Physiology (Bethesda) http://www.kidney.de/pget.php?&tw=1&pmid=25933820 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25933820 #FOAvip English Wikipedia <ref>{{Cite pmid|25933820}}</ref> Molecular Pathways and Therapies in Autosomal-Dominant Polycystic Kidney Disease #MMPMID25933820 Saigusa T; Bell PD Physiology (Bethesda) 2015[May]; 30 (3): 195-207 PMID25933820show ga Autosomal-dominant polycystic kidney disease (ADPKD) is the most prevalent inherited renal disease, characterized by multiple cysts that can eventually lead to kidney failure. Studies investigating the role of primary cilia and polycystins have significantly advanced our understanding of the pathogenesis of PKD. This review will present clinical and basic aspects of ADPKD, review current concepts of PKD pathogenesis, evaluate potential therapeutic targets, and highlight challenges for future clinical studies. äMolecular Pathways and Therapies in Autosomal-Dominant Polycystic Kidn(epmc).pdf DeepDyve Pubget Overpricing