Three routes to suppression of the neurodegenerative phenotypes caused by Kinesin Heavy Chain mutations

Genetics

Volumn 192, Issue 1, 2012, Pages 173-183

  Djagaeva, Inna ^a   Rose, Debra J ^a   Lim, Angeline ^a   Venter, Chris E ^a   Brendza, Katherine M ^a   Moua, Pangkong ^a   Saxton, William M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE DIPHOSPHATE; KINESIN; KINESIN 1; KINESIN HEAVY CHAIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL EXPERIMENT; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DIET RESTRICTION; FEMALE; GENE FREQUENCY; GENE REPRESSION; GENETIC COMPLEMENTATION; HUMAN; IN VIVO STUDY; MALE; MICROTUBULE; MISSENSE MUTATION; NERVE FIBER TRANSPORT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN STRUCTURE; SEQUENCE ANALYSIS;

ALLELES; ANIMALS; AXONAL TRANSPORT; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; FEMALE; HUMANS; KINESIN; MALE; MODELS, MOLECULAR; MUTANT PROTEINS; MUTATION; NEURODEGENERATIVE DISEASES; PHENOTYPE; PROTEIN STRUCTURE, TERTIARY;

EID: 84866060266     PISSN: 00166731     EISSN: 19432631     Source Type: Journal    
DOI: 10.1534/genetics.112.140798     Document Type: Article

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