COMT Val158Met genotype as a risk factor for problem behaviors in youth. - Wikidata - awgldk - TriplyDB

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

http://www.wikidata.org/entity/Q35121037

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The influence of COMT Val¹⁵⁸Met genotype on the character dimension cooperativeness in healthy females Influence of candidate genes on attention problems in children: a longitudinal study Neonatal pain and COMT Val158Met genotype in relation to serotonin transporter (SLC6A4) promoter methylation in very preterm children at school age.Polymorphism in the serotonin receptor 2a (HTR2A) gene as possible predisposal factor for aggressive traits.The enzymatic activities of brain catechol-O-methyltransferase (COMT) and methionine sulphoxide reductase are correlated in a COMT Val/Met allele-dependent fashion.Physical and verbal aggressive behavior and COMT genotype: Sensitivity to the environment.The Role of the Catechol-o-Methyltransferase (COMT) GeneVal158Met in Aggressive Behavior, a Review of Genetic Studies.Disorganization, COMT, and Children's Social Behavior: The Norwegian Hypothesis of Legacy of Disorganized Attachment Candidate gene associations with withdrawn behavior.Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome.Genetic determinants of aggression and impulsivity in humans.Genetics of aggressive behavior: An overview.Aggressive behavior in humans: Genes and pathways identified through association studies.Manic symptom severity correlates with COMT activity in the striatum: A post-mortem study.Adolescent externalizing behaviour, psychological control, and peer rejection: Transactional links and dopaminergic moderation.Monoamine Oxidase A (MAOA) and Catechol-O-Methyltransferase (COMT) Gene Polymorphisms Interact with Maternal Parenting in Association with Adolescent Reactive Aggression but not Proactive Aggression: Evidence of Differential Susceptibility.The association between the catechol-O-methyltransferase Val108/158Met polymorphism and hyperactive-impulsive and inattentive symptoms in youth.Catechol-O-methyltransferase Val158Met genotype moderates the effect of disorganized attachment on social development in young children.Study of the catechol-o-methyltransferase (COMT) gene with high aggression in children.

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P2860

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

http://www.wikidata.org/entity/Q35121037

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2010 nî lūn-bûn

@nan

2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

name

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

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COMT Val158Met genotype as a risk factor for problem behaviors in youth.

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type

label

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

@ast

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

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prefLabel

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

@ast

COMT Val158Met genotype as a risk factor for problem behaviors in youth.

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J.JAAC.2010.05.015

P1433

Journal of the American Academy of Child and Adolescent Psychiatry

P1476

COMT Val158Met genotype as a risk factor for problem behaviors in youth

@en

P2093

Catherine Stanger

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David C Rettew

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Erik A Ehli

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Gareth E Davies

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Julie Sulman

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Matthew D Albaugh

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Robert R Althoff

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Timea Lengyel-Nelson

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Valerie S Harder

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P2860

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior.

Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype

Catechol-o-methyltransferase inhibition improves set-shifting performance and elevates stimulated dopamine release in the rat prefrontal cortex

Polymorphisms in dopamine system genes are associated with individual differences in attention in infancy.

Dopamine transporter immunoreactivity in monkey cerebral cortex: regional, laminar, and ultrastructural localization.

Using a commercially available DNA extraction kit to obtain high quality human genomic DNA suitable for PCR and genotyping from 11-year-old saliva saturated cotton spit wads

Methylation pharmacogenetics: catechol O-methyltransferase, thiopurine methyltransferase, and histamine N-methyltransferase.

COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD.

Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.

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841-849

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scholarly article

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10.1016/J.JAAC.2010.05.015

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8

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James J Hudziak

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2010-07-01T00:00:00Z

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