Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders

Progress in Neurobiology

Volumn 96, Issue 2, 2012, Pages 220-241

  Hunsaker, Michael R ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

22q11.2 Deletion syndrome; Behavioral endophenotype; Fragile X premutation; Fragile X syndrome; Transgenic mouse

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; MESSENGER RNA; MICRORNA;

AMYGDALOID NUCLEUS; ANHEDONIA; ANIMAL BEHAVIOR; ATTENTION; AVOIDANCE BEHAVIOR; BRAIN FORNIX; BRAIN SIZE; CEREBELLUM VERMIS; CHROMOSOME DELETION 22Q11; COGNITION; COGNITIVE DEFECT; CONFLICT; CONSTRUCT VALIDITY; DECISION MAKING; DENDRITIC SPINE; DEPRESSION; DISEASE MODEL; EMOTION; ENDOPHENOTYPE; EXECUTIVE FUNCTION; FACE VALIDITY; FEAR; FRAGILE X SYNDROME; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; GENETIC RISK; HIPPOCAMPUS; HUMAN; INSTRUMENTAL CONDITIONING; INTELLIGENCE QUOTIENT; KNOCKOUT MOUSE; MAZE TEST; MICROGYRIA; MOOD DISORDER; MOTOR PERFORMANCE; NEUROANATOMY; NONHUMAN; PERCEPTIVE DISCRIMINATION; PREDICTIVE VALIDITY; PREFRONTAL CORTEX; PREPULSE INHIBITION; PRIORITY JOURNAL; PYRAMIDAL NERVE CELL; REINFORCEMENT; REVIEW; REWARD; ROTAROD TEST; SCHIZOPHRENIA; SENSORIMOTOR FUNCTION; SENSORY GATING; SEPTUM PELLUCIDUM; SOCIAL BEHAVIOR; SPATIAL MEMORY; STATE DEPENDENT LEARNING; STRIA TERMINALIS; TASK PERFORMANCE; TRANSGENIC MOUSE; WHITE MATTER; WORKING MEMORY;

ANIMALS; BEHAVIOR; CHROMOSOMES, HUMAN, PAIR 22; COGNITION; DISEASE MODELS, ANIMAL; ENDOPHENOTYPES; GENE DELETION; HUMANS; MICE;

EID: 84856413416     PISSN: 03010082     EISSN: 18735118     Source Type: Journal    
DOI: 10.1016/j.pneurobio.2011.12.001     Document Type: Review

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