Myosin Va mutation in rats is an animal model for the human hereditary neurological disease, griscelli syndrome type 1

Annals of the New York Academy of Sciences

Volumn 1086, Issue , 2006, Pages 66-80

  Takagishi, Yoshiko ^a   Murata, Yoshiharu ^a  

^a NAGOYA UNIVERSITY   (Japan)

Author keywords

Calcium; Cerebellum; Mutant; Purkinje cells; Smooth endoplasmic reticulum; Synaptic plasticity

Indexed keywords

COMPLEMENTARY DNA; MOLECULAR MOTOR; MYOSIN; INOSITOL 1,4,5 TRISPHOSPHATE RECEPTOR; MYO5A PROTEIN, RAT; MYOSIN HEAVY CHAIN; MYOSIN V;

BREEDING; CALCIUM CELL LEVEL; CEREBELLUM; CLONIC SEIZURE; CONFERENCE PAPER; DENDRITIC SPINE; EXON; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENOMICS; GRISCELLI SYNDROME; LEARNING; LONG TERM DEPRESSION; MORPHOLOGY; NERVE CELL PLASTICITY; NONHUMAN; PROTEIN EXPRESSION; PURKINJE CELL; SMOOTH ENDOPLASMIC RETICULUM; SYNAPSE; SYNAPTIC TRANSMISSION; AMINO ACID SEQUENCE; ANIMAL; BRAIN; DENDRITE; DISEASE MODEL; GENETICS; METABOLISM; MOLECULAR GENETICS; MUTATION; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; PATHOLOGY; PHYSIOLOGY; RAT; REVIEW; SYNDROME; WISTAR RAT;

ANIMALIA; EPICOCCUM; RATTUS; RATTUS NORVEGICUS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BRAIN; DENDRITES; DISEASE MODELS, ANIMAL; ENDOPLASMIC RETICULUM, SMOOTH; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; MOLECULAR SEQUENCE DATA; MUTATION; MYOSIN HEAVY CHAINS; MYOSIN TYPE V; NERVOUS SYSTEM DISEASES; PURKINJE CELLS; RATS; RATS, WISTAR; SYNAPTIC TRANSMISSION; SYNDROME;

EID: 34447523840     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1196/annals.1377.006     Document Type: Conference Paper

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