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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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Gene Expr
Κύριοι συγγραφείς: Jiang, Lu, Sun, Lina, Edwards, Genea, Manley, Michael, Wallace, Darren P., Septer, Seth, Manohar, Chirag, Pritchard, Michele T., Apte, Udayan
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Cognizant Communication Corporation 2017
Θέματα:
Διαθέσιμο Online: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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