Axonal transport deficits and degeneration can evolve independently in mouse models of amyotrophic lateral sclerosis

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

Volumn 109, Issue 11, 2012, Pages 4296-4301

  Marinković, Petar ^a   Reuter, Miriam S ^a   Brill, Monika S ^a   Godinho, Leanne ^a   Kerschensteiner, Martin ^b   Misgeld, Thomas ^a,c  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c GERMAN CENTER FOR NEURODEGENERATIVE DISEASES DZNE   (Germany)

Author keywords

Neuromuscular junction; Time lapse imaging

Indexed keywords

SUPEROXIDE DISMUTASE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL ORGANELLE; CONTROLLED STUDY; ENDOSOME; EXON; MALE; MITOCHONDRION; MOTONEURON; MOUSE; NERVE FIBER DEGENERATION; NERVE FIBER TRANSPORT; NONHUMAN; PRIORITY JOURNAL; SURVIVAL; WILD TYPE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; AXONAL TRANSPORT; DISEASE MODELS, ANIMAL; MICE; MICE, TRANSGENIC; MITOCHONDRIA; NERVE DEGENERATION; SUPEROXIDE DISMUTASE;

ANIMALIA; MUS;

EID: 84858259015     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1200658109     Document Type: Article

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