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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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Detalhes bibliográficos
Main Authors: Ryan, Scott D., Bhanot, Kunal, Ferrier, Andrew, De Repentigny, Yves, Chu, Alphonse, Blais, Alexandre, Kothary, Rashmi
Formato: Artigo
Idioma:Inglês
Publicado em: The Rockefeller University Press 2012
Assuntos:
Acesso em linha: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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