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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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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2009
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| Soggetti: | |
| Accesso online: | 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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