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Increased YAP Activation Is Associated With Hepatic Cyst Epithelial Cell Proliferation in ARPKD/CHF

Autosomal recessive polycystic kidney disease/congenital hepatic fibrosis (ARPKD/CHF) is a rare but fatal genetic disease characterized by progressive cyst development in the kidneys and liver. Liver cysts arise from aberrantly proliferative cholangiocytes accompanied by pericystic fibrosis and infl...

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Detalles Bibliográficos
Publicado en:Gene Expr
Main Authors: Jiang, Lu, Sun, Lina, Edwards, Genea, Manley, Michael, Wallace, Darren P., Septer, Seth, Manohar, Chirag, Pritchard, Michele T., Apte, Udayan
Formato: Artigo
Idioma:Inglês
Publicado: Cognizant Communication Corporation 2017
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5705408/
https://ncbi.nlm.nih.gov/pubmed/28915934
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3727/105221617X15034976037343
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