Familial amyotrophic lateral sclerosis-linked mutant SOD1 aberrantly interacts with tubulin

Biochemical and Biophysical Research Communications

Volumn 387, Issue 1, 2009, Pages 121-126

  Kabuta, Tomohiro ^a   Kinugawa, Aiko ^a   Tsuchiya, Yukihiro ^a   Kabuta, Chihana ^a   Setsuie, Rieko ^a   Tateno, Minako ^a   Araki, Toshiyuki ^a   Wada, Keiji ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

ALS; Interaction; SOD1; Tubulin

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; MUTANT PROTEIN; TUBULIN;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL STRAIN COS7; CONTROLLED STUDY; FAMILIAL DISEASE; GENE MUTATION; HELA CELL; HUMAN; HUMAN CELL; IMMUNOPRECIPITATION; MASS SPECTROMETRY; MOTONEURON; MOTOR NEURON DISEASE; MOUSE; NERVE CELL DEGENERATION; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERIZATION; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; TRANSGENIC MOUSE;

AMINO ACID SEQUENCE; AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; HELA CELLS; HUMANS; MICE; MICE, TRANSGENIC; MUTATION; SUPEROXIDE DISMUTASE; TUBULIN;

MUS MUSCULUS;

EID: 67651033222     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.06.138     Document Type: Article

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