Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
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Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndromeGenes other than BRCA1 and BRCA2 involved in breast cancer susceptibilityNo evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control studyCan we observe epigenetic effects on human brain function?The role of the catechol-O-methyltransferase (COMT) gene in personality and related psychopathological disordersCatechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responsesThe Role of Human Aldo-Keto Reductases in the Metabolic Activation and Detoxication of Polycyclic Aromatic Hydrocarbons: Interconversion of PAH Catechols and PAH o-QuinonesDetoxication of structurally diverse polycyclic aromatic hydrocarbon (PAH) o-quinones by human recombinant catechol-O-methyltransferase (COMT) via O-methylation of PAH catecholsMeta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.Polymorphisms in genes encoding dopamine signalling pathway and risk of alcohol dependence: a systematic review.Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels.Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women.Genetics of psychosis in Alzheimer's disease: a reviewGenetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study.A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.Race moderates the association of Catechol-O-methyltransferase genotype and posttraumatic stress disorder in preschool children.Association of COMT Val158Met polymorphism and breast cancer risk: an updated meta-analysisPolymorphism of the catechol-O-methyltransferase gene in Han Chinese patients with psoriasis vulgaris.Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome.Review and meta-analysis of antidepressant pharmacogenetic findings in major depressive disorder.Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response.Dopamine genes and attention-deficit hyperactivity disorder: a review.Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.Differential regulation of catechol-O-methyltransferase expression in a mouse model of aggression.A Genetic Variant (COMT) Coding Dopaminergic Activity Predicts Personality Traits in Healthy Elderly.Genetic Variation in the Catechol-O-Methyl Transferase Val108/158Met Is Linked to the Caudate and Posterior Cingulate Cortex Volume in Healthy Subjects: Voxel-Based Morphometry Analysis of Brain Magnetic Resonance Imaging.Estrogen metabolism and breast cancer.No association between Val158Met of the COMT gene and susceptibility to schizophrenia in the Syrian population.Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder.Association between the COMT Val158Met polymorphism and risk of cancer: evidence from 99 case-control studies.Pharmacogenetic tools for the development of target-oriented cognitive-enhancing drugs.The Role of the Catechol-o-Methyltransferase (COMT) GeneVal158Met in Aggressive Behavior, a Review of Genetic Studies.Breast cancer risk reduction and membrane-bound catechol O-methyltransferase genetic polymorphisms.Impact of interacting functional variants in COMT on regional gray matter volume in human brain.Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.Polymorphism of the COMT, MAO, DAT, NET and 5-HTT Genes, and Biogenic Amines in Parkinson's Disease
P2860
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P2860
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
description
1992 nî lūn-bûn
@nan
1992 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@ast
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@en
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@nl
type
label
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@ast
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@en
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@nl
prefLabel
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@ast
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@en
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@nl
P2093
P1433
P1476
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.
@en
P2093
Emanuel BS
Grossman MH
P304
P356
10.1016/0888-7543(92)90316-K
P577
1992-04-01T00:00:00Z