p62, the Receptor for Selective Autophagy, Contributes in ATXN3 Aggregate Formation in Spinocerebellar Ataxia Type 3
Anna J. Zimmer(University of Tübingen), Jeannette Hübener‐Schmid(Universitätsklinikum Tübingen)
Cited by 0
Related Papers
Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3)
|Human Molecular Genetics|2012|78
From Pathways to Targets: Understanding the Mechanisms behind Polyglutamine Disease
|BioMed Research International|2014|70
A combinatorial approach to identify calpain cleavage sites in the Machado-Joseph disease protein ataxin-3
|Brain|2017|44
Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3
|Frontiers in Molecular Neuroscience|2018|43
<i>In vivo</i> assessment of riluzole as a potential therapeutic drug for spinocerebellar ataxia type 3
|Journal of Neurochemistry|2016|34