Functional genomics of serotonin receptor 2A (HTR2A): Interaction of polymorphism, methylation, expression and disease association

NeuroMolecular Medicine

Volumn 13, Issue 1, 2011, Pages 66-76

  Falkenberg, Virginia R ^a   Gurbaxani, Brian M ^a   Unger, Elizabeth R ^a   Rajeevan, Mangalathu S ^a  

^a CENTERS FOR DISEASE CONTROL AND PREVENTION   (United States)

Author keywords

Chronic fatigue syndrome; Cortisol; DNA methylation; Gene expression; Polymorphism; Serotonergic neurotransmission; Serotonin receptor 2A (HTR2A); Structural equation modeling

Indexed keywords

GLUCOCORTICOID RECEPTOR; SEROTONIN RECEPTOR; SEROTONIN RECEPTOR 2A; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BINDING SITE; BIOTINYLATION; CONTROLLED STUDY; DISEASE ASSOCIATION; EPIGENETICS; FEMALE; FUNCTIONAL GENOMICS; GENE EXPRESSION; GENE FREQUENCY; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN BINDING; PYROSEQUENCING; SINGLE NUCLEOTIDE POLYMORPHISM; STRUCTURAL EQUATION MODELING; TRANSCRIPTION REGULATION; UPREGULATION;

ADULT; ALLELES; DNA METHYLATION; EPIGENESIS, GENETIC; FATIGUE SYNDROME, CHRONIC; FEMALE; GENE EXPRESSION REGULATION; GENOMICS; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MODELS, GENETIC; NERVOUS SYSTEM DISEASES; POLYMORPHISM, GENETIC; PROMOTER REGIONS, GENETIC; RECEPTOR, SEROTONIN, 5-HT2A;

EID: 79952706987     PISSN: 15351084     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12017-010-8138-2     Document Type: Article

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