Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome

Cell Reports

Volumn 7, Issue 4, 2014, Pages 1077-1092

  Portmann, Thomas ^a,b   Yang, Mu ^c,h   Mao, Rong ^a,b   Panagiotakos, Georgia ^a,b   Ellegood, Jacob ^d   Dolen, Gul ^e   Bader, Patrick L ^a,b   Grueter, Brad A ^b   Goold, Carleton ^a,b   Fisher, Elaine ^a,b   Clifford, Katherine ^a,b   Rengarajan, Pavitra ^a,b   Kalikhman, David ^c   Loureiro, Darren ^c   Saw, Nay L ^a   Zhengqui, Zhou ^a   Miller, Michael A ^a   Lerch, Jason P ^d,f   Henkelman, R Mark ^d,f   Shamloo, Mehrdad ^a,b   Malenka, Robert C ^b   Crawley, Jacqueline N ^c,h   Dolmetsch, Ricardo E ^a,g   more..

^a STANFORD UNIVERSITY   (United States)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF TORONTO   (Canada)

^g NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH   (United States)

^h UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE; DOPAMINE 2 RECEPTOR; RISPERIDONE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUTISM; BASAL GANGLION; BRAIN CORTEX; BRAIN NERVE CELL; CELL COUNT; CHROMOSOME DELETION; CHROMOSOME DELETION 16P11.2; CONTROLLED STUDY; CORPUS STRIATUM; FEMALE; GENE EXPRESSION; HABITUATION; HYPERACTIVITY; LOCOMOTION; MALE; MOTOR DYSFUNCTION; MOUSE; NEUROPATHOLOGY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; SOCIAL BEHAVIOR; TRANSCRIPTOMICS; BEHAVIORAL RESEARCH; BRAIN REGION; CHROMOSOME 16P; CHROMOSOME 16P11.2 DELETION SYNDROME; CHROMOSOME 7; CIRCLING BEHAVIOR; DOPAMINERGIC NERVE CELL; GENE FUNCTION; JUVENILE ANIMAL; MEDIUM SPINY NEURON; MOLECULAR PATHOLOGY; MOUSE MUTANT; NERVE CELL; PATHOLOGICAL ANATOMY; SYNAPTIC TRANSMISSION; ANIMAL; C57BL MOUSE; CHROMOSOME 16; CHROMOSOME DISORDER; CONGENITAL MALFORMATION; DISEASE MODEL; GENETICS; HUMAN; INTELLECTUAL IMPAIRMENT; MENTAL DISEASE; PATHOLOGY; TRANSGENIC MOUSE;

MUS;

ANIMALS; AUTISTIC DISORDER; BASAL GANGLIA; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 16; DISEASE MODELS, ANIMAL; FEMALE; HUMANS; INTELLECTUAL DISABILITY; MALE; MENTAL DISORDERS; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC;

EID: 84901286741     PISSN: None     EISSN: 22111247     Source Type: Journal    
DOI: 10.1016/j.celrep.2014.03.036     Document Type: Article

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