Triptolide reduces cyst formation in a neonatal to adult transition Pkd1 model of ADPKD

Abstract

Background. Autosomal dominant polycystic kidney disease (ADPKD), a major cause of end-stage renal failure, results from genetic mutation of either polycystin-1 (Pkd1) or polycystin-2 (Pkd2). In order to develop novel therapies to treat the advancement of disease progression, numerous rodent models of different genetic backgrounds are available to study cyst development

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    Last time updated on 11/12/2019