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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Detalles Bibliográficos
Autores principales: Ryan, Scott D., Bhanot, Kunal, Ferrier, Andrew, De Repentigny, Yves, Chu, Alphonse, Blais, Alexandre, Kothary, Rashmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2012
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308695/
https://www.ncbi.nlm.nih.gov/pubmed/22412020
http://dx.doi.org/10.1083/jcb.201107096

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308695/
https://www.ncbi.nlm.nih.gov/pubmed/22412020
http://dx.doi.org/10.1083/jcb.201107096

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