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The inositol polyphosphate 5-phosphatase Ocrl associates with endosomes that are partially coated with clathrin

The subcellular localization of Ocrl, the inositol polyphosphate 5-phosphatase that is mutated in Lowe syndrome, was investigated by fluorescence microscopy. Ocrl was localized to endosomes and Golgi membranes along with clathrin, giantin, the mannose 6-phosphate receptor, transferrin, and the early...

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Bibliografski detalji
Glavni autori: Ungewickell, Alexander, Ward, Michael E., Ungewickell, Ernst, Majerus, Philip W.
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 2004
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC518786/
https://ncbi.nlm.nih.gov/pubmed/15353600
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0405664101
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