The Conserved Bardet-Biedl Syndrome Proteins Assemble a Coat that Traffics Membrane Proteins to Cilia-Reference-Cited by-同舟云学术

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The Conserved Bardet-Biedl Syndrome Proteins Assemble a Coat that Traffics Membrane Proteins to Cilia

Published:2010-06 Issue:7 Volume:141 Page:1208-1219
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Jin Hua,White Susan Roehl,Shida Toshinobu,Schulz Stefan,Aguiar Mike,Gygi Steven P.,Bazan J. Fernando,Nachury Maxence V.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference56 articles.

1. Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia;Berbari;Proc. Natl. Acad. Sci. USA,2008

2. Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors;Berbari;Mol. Biol. Cell,2008

3. Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies;Bielas;Nat. Genet.,2009

4. Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport;Blacque;Genes Dev.,2004

5. Coupling of coat assembly and vesicle budding to packaging of putative cargo receptors;Bremser;Cell,1999

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