tTorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton

A specific mutation (ΔE) in torsinA underlies most cases of the dominantly inherited movement disorder, early-onset torsion dystonia (DYT1). TorsinA, a member of the AAA+ ATPase superfamily, is located within the lumen of the nuclear envelope (NE) and endoplasmic reticulum (ER). We investigated an a...

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Detalhes bibliográficos
Main Authors: Nery, Flavia C., Zeng, Juan, Niland, Brian P., Hewett, Jeffrey, Farley, Jonathan, Irimia, Daniel, Li, Yuqing, Wiche, Gerhard, Sonnenberg, Arnoud, Breakefield, Xandra O.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3539201/
https://ncbi.nlm.nih.gov/pubmed/18827015
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.029454
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