Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome.
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Cannabis Use during Adolescent Development: Susceptibility to Psychiatric IllnessAssessing the molecular genetics of attention networks.The structural biology of oestrogen metabolismPharmacogenetics of lithium prophylaxis in mood disorders: analysis of COMT, MAO-A, and Gbeta3 variantsMeta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.Association studies of bipolar disorder.Long-term consequences of adolescent cannabinoid exposure in adult psychopathology.Clinical, imaging, lesion, and genetic approaches toward a model of cognitive control.Velo-cardio-facial syndrome: 30 Years of study.Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).Genetics of bipolar disorder.22q11 deletion syndrome: a genetic subtype of schizophrenia.Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.COMT Val158Met, but not BDNF Val66Met, is associated with white matter abnormalities of the temporal lobe in patients with first-episode, treatment-naïve major depressive disorder: a diffusion tensor imaging study.The relationship between the val158met catechol-O-methyltransferase (COMT) polymorphism and irritable bowel syndrome.The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI studyA hotspot of inactivation: The A22S and V108M polymorphisms individually destabilize the active site structure of catechol O-methyltransferase.Genetics of psychosis in Alzheimer's disease: a reviewAnhedonia as a phenotype for the Val158Met COMT polymorphism in relatives of patients with schizophrenia.Pharmacogenetics of antidepressant response.Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study.Candidate gene studies of bipolar disorder.Normal genetic variation, cognition, and aging.Serotonin pathway polymorphisms and the treatment of major depressive disorder and anxiety disorders.The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons.Functional plasticity in childhood brain disorders: when, what, how, and whom to assess.Polymorphism of the catechol-O-methyltransferase gene in Han Chinese patients with psoriasis vulgaris.Review and meta-analysis of antidepressant pharmacogenetic findings in major depressive disorder.Dopamine genes and attention-deficit hyperactivity disorder: a review.Neural substrates of inhibitory control deficits in 22q11.2 deletion syndrome.22q11 deletion syndrome in adults with schizophrenia.Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.Lack of association between COMT gene and deficit/nondeficit schizophrenia.An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndromeMicroRNA Profiling of Neurons Generated Using Induced Pluripotent Stem Cells Derived from Patients with Schizophrenia and Schizoaffective Disorder, and 22q11.2 Del.COMT Genetic Reduction Produces Sexually Divergent Effects on Cortical Anatomy and Working Memory in Mice and Humans.Neural mechanisms of response inhibition and impulsivity in 22q11.2 deletion carriers and idiopathic attention deficit hyperactivity disorder.Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder.Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome.
P2860
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P2860
Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome.
description
1996 nî lūn-bûn
@nan
1996 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@ast
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@en
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@nl
type
label
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@ast
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@en
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@nl
prefLabel
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@ast
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@en
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@nl
P2093
P2860
P1476
Association of codon 108/158 c ...... f velo-cardio-facial syndrome.
@en
P2093
Goldberg R
Kucherlapati R
Lachman HM
Papolos DF
Shprintzen R
P2860
P304
P356
10.1002/(SICI)1096-8628(19960920)67:5<468::AID-AJMG5>3.0.CO;2-G
P577
1996-09-01T00:00:00Z