Hepatic Cystogenesis Is Associated with Abnormal Expression and Location of Ion Transporters and Water Channels in an Animal Model of Autosomal Recessive Polycystic Kidney Disease

Author:

Banales Jesús M.,Masyuk Tatyana V.,Bogert Pamela S.,Huang Bing Q.,Gradilone Sergio A.,Lee Seung-Ok,Stroope Angela J.,Masyuk Anatoliy I.,Medina Juan F.,LaRusso Nicholas F.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference47 articles.

1. An incredible decade for the primary cilium: a look at a once-forgotten organelle;Davenport;Am J Physiol,2005

2. Autosomal recessive and dominant polycystic kidney diseases;Sessa;Minerva Urol Nefrol,2004

3. Liver disease in autosomal recessive polycystic kidney disease;Shneider;Pediatr Transplant,2005

4. Polycystic kidney disease: new understanding in the pathogenesis;Wilson;Int J Biochem Cell Biol,2004

5. Autosomal recessive polycystic kidney disease;Zerres;J Mol Med,1998

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