Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials

Proceedings of the National Academy of Sciences of the United States of America

Volumn 103, Issue 37, 2006, Pages 13860-13865

  Ferri, Alberto ^a,b   Cozzolino, Mauro ^b   Crosio, Claudia ^b,c   Nencini, Monica ^b   Casciati, Arianna ^b   Gralla, Edith Butler ^d   Rotilio, Giuseppe ^e   Valentine, Joan Selverstone ^d   Carri, Maria Teresa ^b,e  

^a CNR   (Italy)

^b IRCCS FONDAZIONE SANTA LUCIA   (Italy)

^c UNIVERSITY OF SASSARI   (Italy)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF ROME TOR VERGATA   (Italy)

Author keywords

Amyotrophic lateral sclerosis; Motor neuron; Neurodegeneration

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; CYSTEINE; MUTANT PROTEIN; MUTANT SUPEROXIDE DISMUTASE 1; OLIGOMER; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL CELL; ARTICLE; CELL DEATH; DISEASE ASSOCIATION; ENZYME ANALYSIS; FAMILIAL DISEASE; GENE MUTATION; MITOCHONDRIAL RESPIRATION; MOTONEURON; MOUSE; NONHUMAN; OLIGOMERIZATION; OXIDATION REDUCTION REACTION; PRIORITY JOURNAL; PROTEIN CROSS LINKING; WILD TYPE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; CYSTEINE; HUMANS; MICE; MITOCHONDRIA; MOTOR NEURONS; MUTATION; OXIDATION-REDUCTION; SUPEROXIDE DISMUTASE;

EID: 33748795566     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0605814103     Document Type: Article

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