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Polycystin‐1: a key player in hereditary cystic kidney and liver disorders
Author(s) -
Skotte NH
Publication year - 2011
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2011.01780.x
Subject(s) - polycystic kidney disease , endoplasmic reticulum , polycystic kidney , kidney , liver disease , polycystic liver disease , cyst , kidney disorder , biology , cystic fibrosis , genetics , endocrinology , medicine , bioinformatics , pathology , transplantation , liver transplantation
References 1. Drenth JP , Martina JA , van de Kerkhof R , Bonifacino JS , Jansen JB. Polycystic liver disease is a disorder of cotranslational protein processing. Trends Mol Med 2005 : 11 : 37 – 42.2. Vembar SS , Brodsky JL. One step at a time: endoplasmic reticulum‐associated degradation. Nat Rev Mol Cell Biol 2008 : 9 : 944 – 957.3. Harris PC , Torres VE. Polycystic kidney disease. Annu. Rev. Med 2009 : 60 : 321 – 337. A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin‐1 as the central determinant of cyst formation. Fedeles et al. (2011) Nature Genetics 43(7):639–647.
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