Spontaneous and induced mouse mutations with cerebellar dysfunctions: Behavior and neurochemistry

Brain Research

Volumn 1140, Issue 1, 2007, Pages 51-74

  Lalonde, R ^a   Strazielle, C ^b  

^a UNIVERSITÉ DE ROUEN   (France)

^b UNIVERSITÉ DE LORRAINE   (France)

Author keywords

Amino acids; Biogenic amines; Cerebellum; Cytochrome oxidase; Equilibrium; Motor control

Indexed keywords

4 AMINOBUTYRIC ACID RECEPTOR; AMINO ACID; AMPA RECEPTOR; BIOGENIC AMINE; CALCIUM ION; CYTOCHROME C OXIDASE; IONOTROPIC RECEPTOR; MESSENGER RNA;

AGTPBP1PCD GENE; AMINO ACID METABOLISM; ANIMAL BEHAVIOR; BODY EQUILIBRIUM; BODY POSTURE; BRAIN METABOLISM; CALCIUM HOMEOSTASIS; CEREBELLAR ATAXIA; CEREBELLUM; CEREBELLUM DISEASE; CHROMOSOME 5; GENE; GENE LOCUS; GIRKSWV GENE; GRID2HO GENE; GRID2LC GENE; INDUCED MUTATION; MOTOR CONTROL; MOTOR COORDINATION; MOUSE MUTANT; NERVE CELL DEGENERATION; NEUROCHEMISTRY; NEUROPATHOLOGY; NONHUMAN; NR GENE; OPEN FIELD BEHAVIOR; PRIORITY JOURNAL; PURKINJE CELL; RELNRL GENE; REVIEW; RORASG GENE; SPONTANEOUS MUTATION;

ANIMALS; BEHAVIOR, ANIMAL; CEREBELLAR DISEASES; MICE; MICE, NEUROLOGIC MUTANTS; MUTATION; NEUROCHEMISTRY;

EID: 33847709488     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2006.01.031     Document Type: Review

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