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TorsinA in PC12 cells: localization in the endoplasmic reticulum and response to stress.
Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells.
TorsinB--perinuclear location and association with torsinA.
TorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton.
Inducible release of TRAIL fusion proteins from a proapoptotic form for tumor therapy.
A highly sensitive assay for monitoring the secretory pathway and ER stress.
Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells.
The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress response.
TorsinA participates in endoplasmic reticulum-associated degradation.
Inhibition of N-linked glycosylation prevents inclusion formation by the dystonia-related mutant form of torsinA.
Biochemical and cellular analysis of human variants of the DYT1 dystonia protein, TorsinA/TOR1A.
Characterization of Dystonia Gene and Protein
Molecular etiology of early onset torsion dystonia