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Altered Expression and Function of Hepatic Transporters in a Rodent Model of Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease (ADPKD) is a common form of inherited polycystic kidney disease (PKD) and is a leading cause of kidney failure. Fluid-filled cysts develop in the kidneys of patients with ADPKD, and cysts often form in their liver and other organs. Previous data have show...

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Detalhes bibliográficos
Publicado no:Drug Metab Dispos
Main Authors: Bezençon, Jacqueline, Beaudoin, James J., Ito, Katsuaki, Fu, Dong, Roth, Sharin E., Brock, William J., Brouwer, Kim L.R.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society for Pharmacology and Experimental Therapeutics 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6657211/
https://ncbi.nlm.nih.gov/pubmed/31160314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1124/dmd.119.086785
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