Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content

Human Molecular Genetics

Volumn 16, Issue 22, 2007, Pages 2720-2728

  De vos, Kurt J ^a,b   Chapman, Anna L ^b   Tennant, Maria E ^a   Manser, Catherine ^a   Tudor, Elizabeth L ^a   Lau, Kwok Fai ^c   Brownlees, Janet ^a   Ackerley, Steven ^a   Shaw, Pamela J ^b   Mcloughlin, Declan M ^a   Shaw, Christopher E ^a   Leigh, P Nigel ^a   Miller, Christopher C J ^a   Grierson, Andrew J ^b  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF SHEFFIELD   (United Kingdom)

^c CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID PRECURSOR PROTEIN; COPPER ZINC SUPEROXIDE DISMUTASE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL CELL; ARTICLE; BRAIN FUNCTION; CELL FUNCTION; CELLULAR DISTRIBUTION; CONTROLLED STUDY; EMBRYO; HUMAN; MEMBRANE STRUCTURE; MITOCHONDRIAL MEMBRANE; MOTOR PERFORMANCE; MOUSE; NERVE DEGENERATION; NERVE FIBER TRANSPORT; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; AXONAL TRANSPORT; AXONS; FEMALE; FLUORESCENT ANTIBODY TECHNIQUE; HUMANS; MALE; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; MITOCHONDRIA; MUTATION; SUPEROXIDE DISMUTASE;

MUS MUSCULUS;

EID: 35548991459     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddm226     Document Type: Article

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