Activation of the MEK5/ERK5 Cascade Is Responsible for Biliary Dysgenesis in a Rat Model of Caroli’s Disease

Polycystic kidney (PCK) rats exhibit a multiorgan cyst pathology similar to human autosomal recessive polycystic kidney disease, and are proposed as an animal model of Caroli’s disease with congenital hepatic fibrosis (CHF). This study investigated the expression and function of selected components...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Sato, Yasunori, Harada, Kenichi, Kizawa, Kazuo, Sanzen, Takahiro, Furubo, Shinichi, Yasoshima, Mitsue, Ozaki, Satoru, Ishibashi, Masahiko, Nakanuma, Yasuni
פורמט: Artigo
שפה:Inglês
יצא לאור: American Society for Investigative Pathology 2005
נושאים:
Original Research Paper
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1602300/
https://ncbi.nlm.nih.gov/pubmed/15631999
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