Exosome-dependent and independent mechanisms are involved in prion-like transmission of propagated Cu/Zn superoxide dismutase misfolding

Prion

Volumn 8, Issue 5, 2014, Pages 331-335

  Grad, Leslie I ^a   Pokrishevsky, Edward ^a   Silverman, Judith M ^a   Cashman, Neil R ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Amyotrophic lateral sclerosis; Exosome; Intercellular transmission; Prion like; Protein misfolding; Superoxide dismutase

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; PRION PROTEIN; PRION; SUPEROXIDE DISMUTASE;

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CELL GROWTH; CELL TRANSPORT; CELL VACUOLE; CYTOTOXICITY; DISEASE TRANSMISSION; ENDOPLASMIC RETICULUM; EXOSOME; EXTRACELLULAR SPACE; GOLGI MEMBRANE; HUMAN; HUMAN CELL CULTURE; LYSOSOME; MUTANT; MUTATION; NERVOUS SYSTEM; NEUROMUSCULAR DISEASE; NEUROMUSCULAR PROTEINOPATHY; NONHUMAN; PINOCYTOSIS; PRION DISEASE; PROTEIN AGGREGATION; PROTEIN CONFORMATION; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FOLDING; QUANTITATIVE ANALYSIS; METABOLISM; PHYSIOLOGY; PRION;

EXOSOMES; PRIONS; PROTEIN FOLDING; SUPEROXIDE DISMUTASE;

EID: 84920768238     PISSN: 19336896     EISSN: 1933690X     Source Type: Journal    
DOI: 10.4161/19336896.2014.983398     Document Type: Article

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