Interaction between familial Amyotrophic Lateral Sclerosis (ALS)-linked SOD1 mutants and the dynein complex

Journal of Biological Chemistry

Volumn 282, Issue 22, 2007, Pages 16691-16699

  Zhang, Fujian ^a   Ström, Anna Lena ^b   Fukada, Kei ^b   Lee, Sangmook ^c   Hayward, Lawrence J ^c   Zhu, Haining ^a,b,d  

^a Lexington Veterans Affairs Health Care System   (United States)

^b UNIVERSITY OF KENTUCKY   (United States)

^c UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^d NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DEATH; COMPLEXATION; MOLECULAR INTERACTIONS; MUTAGENESIS; PATHOLOGY; TOXICITY;

AMYOTROPHIC LATERAL SCLEROSIS (ALS); CYTOPLASMIC INCLUSION; MOLECULAR WEIGHT COMPLEXES;

NEURAL NETWORKS;

COPPER ZINC SUPEROXIDE DISMUTASE; DYNEIN ADENOSINE TRIPHOSPHATASE; MULTIENZYME COMPLEX; SUPEROXIDE DISMUTASE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL INCLUSION; CELL INTERACTION; CONTROLLED STUDY; DISEASE COURSE; MOLECULAR WEIGHT; MOTONEURON; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN INTERACTION; RETROGRADE NERVE FIBER TRANSPORT; TRANSGENIC MOUSE; ANIMAL; CELL LINE; DISEASE MODEL; ENZYMOLOGY; GENETIC DISORDER; GENETICS; HUMAN; METABOLISM; MUTATION; NERVE FIBER; NERVE FIBER TRANSPORT; PATHOLOGY; PROTEIN BINDING; PROTEOMICS;

ANIMALIA; RODENTIA;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; AXONAL TRANSPORT; AXONS; CELL LINE; DISEASE MODELS, ANIMAL; DYNEIN ATPASE; GENETIC DISEASES, INBORN; HUMANS; INCLUSION BODIES; MICE; MOTOR NEURONS; MULTIENZYME COMPLEXES; MUTATION; PROTEIN BINDING; PROTEOMICS; SUPEROXIDE DISMUTASE;

EID: 34447550238     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M609743200     Document Type: Article

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