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Microtubule stability, Golgi organization, and transport flux require dystonin-a2–MAP1B interaction
Loss of function of dystonin cytoskeletal linker proteins causes neurodegeneration in dystonia musculorum (dt) mutant mice. Although much investigation has focused on understanding dt pathology, the diverse cellular functions of dystonin isoforms remain poorly characterized. In this paper, we highli...
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| Auteurs principaux: | , , , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
The Rockefeller University Press
2012
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3308695/ https://ncbi.nlm.nih.gov/pubmed/22412020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201107096 |
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