A role of the Lowe syndrome protein OCRL in early steps of the endocytic pathway

Mutations in the inositol 5-phosphatase OCRL are responsible for Lowe syndrome, whose manifestations include mental retardation and renal Fanconi syndrome. OCRL has been implicated in membrane traffic, but disease mechanisms remain unclear. We show that OCRL visits late stage endocytic clathrin coat...

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Detalhes bibliográficos
Main Authors: Erdmann, Kai S., Mao, Yuxin, McCrea, Heather J., Zoncu, Roberto, Lee, Sangyoon, Paradise, Summer, Modregger, Jan, Biemesderfer, Daniel, Toomre, Derek, De Camilli, Pietro
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2025683/
https://ncbi.nlm.nih.gov/pubmed/17765681
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.devcel.2007.08.004
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