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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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| Main Authors: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
National Academy of Sciences
2004
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| Ábhair: | |
| Rochtain Ar Líne: | 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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