Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus

Journal of the Neurological Sciences

Volumn 173, Issue 1, 2000, Pages 53-62

  Stieber, Anna ^a   Gonatas, Jacqueline O ^a   Gonatas, Nicholas K ^a  

^a HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

13 nm Filaments; Golgi apparatus; SOD1(G93A); Ubiquitin

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; MUTANT PROTEIN; UBIQUITIN;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; GOLGI COMPLEX; HISTOPATHOLOGY; IMMUNOELECTRON MICROSCOPY; MOUSE; MUTANT; NERVE CELL DEGENERATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN AGGREGATION; SPINAL CORD; TRANSGENIC MOUSE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; DISEASE PROGRESSION; GOLGI APPARATUS; MICE; MICE, TRANSGENIC; MICROSCOPY, ELECTRON; NEURONS; SPINAL CORD; SUPEROXIDE DISMUTASE; UBIQUITINS;

EID: 0033962285     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(99)00300-7     Document Type: Article

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