Genetic variation of serotonin receptor function affects prepulse inhibition of the startle

Journal of Neural Transmission

Volumn 116, Issue 5, 2009, Pages 607-613

  Bräuer, David ^a   Strobel, Alexander ^a,b   Hensch, Tilman ^a   Diers, Kersten ^a   Lesch, Klaus Peter ^c   Brocke, Burkhard ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^b GOETHE UNIVERSITY   (Germany)

^c UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

5 HTR1A C 1019G; 5 HTR2A T102C; Polymorphism; Prepulse inhibition; Serotonin

Indexed keywords

AUTORECEPTOR; SEROTONIN 1A RECEPTOR; SEROTONIN 2A RECEPTOR;

ADULT; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; FEMALE; GENE EXPRESSION; GENE INTERACTION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN EXPERIMENT; MALE; MOLECULAR GENETICS; NORMAL HUMAN; PREPULSE INHIBITION; PRIORITY JOURNAL; RECEPTOR INTRINSIC ACTIVITY; SCHIZOPHRENIA; SEROTONINERGIC NERVE CELL; STARTLE REFLEX;

ADOLESCENT; ADULT; BRAIN CHEMISTRY; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HUMANS; MALE; POLYMORPHISM, GENETIC; RECEPTOR, SEROTONIN, 5-HT1A; RECEPTOR, SEROTONIN, 5-HT2A; SCHIZOPHRENIA; SENSORY GATING; SEROTONIN; YOUNG ADULT;

EID: 67349285128     PISSN: 03009564     EISSN: 14351463     Source Type: Journal    
DOI: 10.1007/s00702-009-0222-0     Document Type: Article

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