Mitochondria in motor nerve terminals: Function in health and in mutant superoxide dismutase 1 mouse models of familial ALS

Journal of Bioenergetics and Biomembranes

Volumn 43, Issue 6, 2011, Pages 581-586

  Barrett, Ellen F ^a   Barrett, John N ^a   David, Gavriel ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Amyotrophic lateral sclerosis; Calcium; Mitochondria; Motor nerve terminal; Superoxide dismutase 1

Indexed keywords

CALCIUM ION; COPPER ZINC SUPEROXIDE DISMUTASE; MUTANT PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; CALCIUM TRANSPORT; DISEASE MODEL; FAMILIAL DISEASE; HUMAN; MEMBRANE DEPOLARIZATION; MITOCHONDRION; MOTONEURON; MOUSE; MOUSE MUTANT; NERVE CELL DEGENERATION; NERVE CELL NECROSIS; NERVE ENDING; NERVE FUNCTION; NERVE STIMULATION; NONHUMAN; PERIKARYON; REVIEW;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; CALCIUM; DISEASE MODELS, ANIMAL; GENETIC DISEASES, INBORN; HUMANS; MICE; MICE, TRANSGENIC; MITOCHONDRIA; MOTOR ENDPLATE; MOTOR NEURONS; MUTATION; MUTATION, MISSENSE; SUPEROXIDE DISMUTASE;

MUS; VERTEBRATA;

EID: 84857055792     PISSN: 0145479X     EISSN: 15736881     Source Type: Journal    
DOI: 10.1007/s10863-011-9392-1     Document Type: Review

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