Polycystic liver diseases: advanced insights into the molecular mechanisms-Reference-Cited by-同舟云学术

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Polycystic liver diseases: advanced insights into the molecular mechanisms

Published:2014-09-30 Issue:12 Volume:11 Page:750-761
ISSN:1759-5045
Container-title:Nature Reviews Gastroenterology & Hepatology
language:en
Short-container-title:Nat Rev Gastroenterol Hepatol

Author:

Perugorria Maria J.,Masyuk Tatyana V.,Marin Jose J.,Marzioni Marco,Bujanda Luis,LaRusso Nicholas F.,Banales Jesus M.

Publisher

Springer Science and Business Media LLC

Subject

Gastroenterology,Hepatology

Link

http://www.nature.com/articles/nrgastro.2014.155.pdf

Reference122 articles.

1. Gevers, T. J. & Drenth, J. P. Diagnosis and management of polycystic liver disease. Nat. Rev. Gastroenterol. Hepatol. 10, 101–108 (2013).

2. Drenth, J. P., te Morsche, R. H., Smink, R., Bonifacino, J. S. & Jansen, J. B. Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease. Nat. Genet. 33, 345–347 (2003).

3. Li, A. et al. Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease. Am. J. Hum. Genet. 72, 691–703 (2003).

4. Davila, S. et al. Mutations in SEC63 cause autosomal dominant polycystic liver disease. Nat. Genet. 36, 575–577 (2004).

5. Cnossen, W. R. et al. Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis. Proc. Natl Acad. Sci. USA 111, 5343–5348 (2014).

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