Related references
Note: Only part of the references are listed.A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix Saguenay
Teisha Y. Bradshaw et al.
HUMAN MOLECULAR GENETICS (2016)
LAMP-2 is required for incorporating syntaxin-17 into autophagosomes and for their fusion with lysosomes
Virginie Hubert et al.
BIOLOGY OPEN (2016)
Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay
Chiara Criscuolo et al.
JOURNAL OF NEUROLOGY (2015)
Molecular chaperones and neuronal proteostasis
Heather L. Smith et al.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2015)
Vimentin filament organization and stress sensing depend on its single cysteine residue and zinc binding
Dolores Perez-Sala et al.
NATURE COMMUNICATIONS (2015)
Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay
Roxanne Lariviere et al.
HUMAN MOLECULAR GENETICS (2015)
Proteasome Failure Promotes Positioning of Lysosomes around the Aggresome via Local Block of Microtubule-Dependent Transport
Nava Zaarur et al.
MOLECULAR AND CELLULAR BIOLOGY (2014)
Normal role of the low-molecular-weight neurofilament protein in mitochondrial dynamics and disruption in Charcot-Marie-Tooth disease
Benoit J. Gentil et al.
FASEB JOURNAL (2012)
Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)
Martine Girard et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Regulation of autophagy by lysosomal positioning
Viktor I. Korolchuk et al.
AUTOPHAGY (2011)
Structural Basis of Defects in the Sacsin HEPN Domain Responsible for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)
Guennadi Kozlov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
The Neurodegenerative-Disease-Related Protein Sacsin Is a Molecular Chaperone
John F. Anderrson et al.
JOURNAL OF MOLECULAR BIOLOGY (2011)
Lysosomal positioning coordinates cellular nutrient responses
Viktor I. Korolchuk et al.
NATURE CELL BIOLOGY (2011)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: An overview
Yosr Bouhlal et al.
PARKINSONISM & RELATED DISORDERS (2011)
Regulation of vimentin intermediate filaments in endothelial cells by hypoxia
Tiegang Liu et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2010)
The Sacsin Repeating Region (SRR): A Novel Hsp90-Related Supra-Domain Associated with Neurodegeneration
John F. Anderson et al.
JOURNAL OF MOLECULAR BIOLOGY (2010)
Chaperone networks: Tipping the balance in protein folding diseases
Cindy Voisine et al.
NEUROBIOLOGY OF DISEASE (2010)
Mutations in SACS cause atypical and late-onset forms of ARSACS
J. Baets et al.
NEUROLOGY (2010)
Protein turnover and inclusion body formation
Siddhartha Mitra et al.
AUTOPHAGY (2009)
The cellular pathways of neuronal autophagy and their implication in neurodegenerative diseases
Zhenyu Yue et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2009)
Vimentin supports mitochondrial morphology and organization
Ho Lam Tang et al.
BIOCHEMICAL JOURNAL (2008)
Structural basis for sorting mechanism of p62 in selective autophagy
Yoshinobu Ichimura et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Ref(2) P, the Drosophila melanogaster homologue of mammalian p62, is required for the formation of protein aggregates in adult brain
Ioannis P. Nezis et al.
JOURNAL OF CELL BIOLOGY (2008)
Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice
Masaaki Komatsu et al.
CELL (2007)
p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy
Serhiy Pankiv et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
The relationship between mitochondrial shape and function and the cytoskeleton
Vasiliki Anesti et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2006)
p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death
G Bjorkoy et al.
JOURNAL OF CELL BIOLOGY (2005)
Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport
R Pérez-Ollé et al.
JOURNAL OF NEUROCHEMISTRY (2005)
The endo-lysosomal sorting machinery interacts with the intermediate filament cytoskeleton
ML Styers et al.
MOLECULAR BIOLOGY OF THE CELL (2004)
Aggregation and loss of cytokeratin filament networks inhibit golgi organization in liver-derived epithelial cell lines
H Kumemura et al.
CELL MOTILITY AND THE CYTOSKELETON (2004)
Aggresomes, inclusion bodies and protein aggregation
RR Kopito
TRENDS IN CELL BIOLOGY (2000)
Share Paper
