Functional conservation of human Spastin in a Drosophila model of autosomal dominant-hereditary spastic paraplegia

Human Molecular Genetics

Volumn 19, Issue 10, 2010, Pages 1883-1896

  Du, Fang ^a   Ozdowski, Emily F ^a   Kotowski, Ingrid K ^b   Marchuk, Douglas A ^b   Sherwood, Nina Tang ^a  

^a DUKE UNIVERSITY   (United States)

^b DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; GLUTAMINE; LEUCINE; LYSINE; PROLINE; SERINE; SPASTIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CONTROLLED STUDY; DROSOPHILA; EMBRYO; GENE EXPRESSION; GENE MUTATION; GENETIC CONSERVATION; GENETIC MODEL; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOSITY; IN VITRO STUDY; MICROTUBULE; MUTANT; NONHUMAN; NONSENSE MUTATION; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; SYNAPSE; WILD TYPE;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SUBSTITUTION; ANIMALS; ANIMALS, GENETICALLY MODIFIED; DISEASE MODELS, ANIMAL; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; GENES, DOMINANT; GENOTYPE; HETEROZYGOTE; HUMANS; MODELS, GENETIC; MUTATION; PROTEIN TRANSPORT; SPASTIC PARAPLEGIA, HEREDITARY; SUBCELLULAR FRACTIONS; TRANSGENES;

DROSOPHILA MELANOGASTER;

EID: 77952504559     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddq064     Document Type: Article

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