Absence of neurofilaments reduces the selective vulnerability of motor neurons and slows disease caused by a familial amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutant

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

Volumn 95, Issue 16, 1998, Pages 9631-9636

  Williamson, Toni L ^a   Bruijn, Lucie I ^a   Zhu, Qinzhang ^b   Anderson, Karen L ^a   Anderson, Scott D ^a   Julien, Jean Pierre ^b   Cleveland, Don W ^a,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b MONTREAL GENERAL HOSPITAL   (Canada)

^c LUDWIG INSTITUTE FOR CANCER RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SUPEROXIDE DISMUTASE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL TISSUE; ARTICLE; GENE; IMMUNOBLOTTING; MOTONEURON; MOUSE; MUTANT; NEUROFILAMENT; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; TRANSGENE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; AXONS; DISEASE PROGRESSION; MICE; MICE, TRANSGENIC; MOTOR NEURONS; MUTATION; NEUROFILAMENT PROTEINS; SUPEROXIDE DISMUTASE;

ANIMALIA;

EID: 0032482976     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.16.9631     Document Type: Article

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