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Cholangiociliopathies: genetics, molecular mechanisms and potential therapies

PURPOSE OF REVIEW: The present review summarizes recent knowledge on polycystic liver diseases (PCLDs), mechanisms of hepatic cystogenesis and potential therapies for these conditions. RECENT FINDINGS: PCLD may be classified as cholangiociliopathies. In PCLD associated with polycystic kidney disease...

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Bibliografski detalji
Glavni autori: Masyuk, Tatyana, Masyuk, Anatoliy, LaRusso, Nicholas
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3831343/
https://ncbi.nlm.nih.gov/pubmed/19349863
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOG.0b013e328328f4ff
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