Effect of mouse chromosome 13 terminal fragment on liability to catalepsy and expression of tryptophane Hydroxylase-2, Serotonin transporter, and 5-HT1A receptor genes in the brain

Bulletin of Experimental Biology and Medicine

Volumn 147, Issue 5, 2009, Pages 621-624

  Kulikov, A V ^a   Naumenko, V S ^a   Bazovkina, D V ^a   Dee, V Yu ^a   Osipova, D V ^a   Popova, N K ^a  

^a INSTITUTE OF CYTOLOGY AND GENETICS   (Russian Federation)

Author keywords

5 HT transporter; 5 HT1Areceptor gene; Congenic mice; Hereditary catalepsy; Tryptophane hydroxylase 2

Indexed keywords

SEROTONIN 1A RECEPTOR; SEROTONIN TRANSPORTER; TRYPTOPHAN HYDROXYLASE 2;

AMPLICON; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CATALEPSY; CHROMOSOME 13; CONGENIC STRAIN; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENE FREQUENCY; GENE LOCUS; GENOMIC FRAGMENT; GENOTYPE; HETEROZYGOSITY; MALE; MESENCEPHALON; MOUSE; NONHUMAN; PROTEIN EXPRESSION;

ANIMALS; BRAIN; CATALEPSY; CHROMOSOMES, MAMMALIAN; GENETIC PREDISPOSITION TO DISEASE; MALE; MICE; MICE, INBRED AKR; MICE, INBRED CBA; RECEPTOR, SEROTONIN, 5-HT1A; SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS; TRYPTOPHAN HYDROXYLASE;

ANIMALIA; MUS;

EID: 70350062105     PISSN: 00074888     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10517-009-0567-2     Document Type: Article

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