Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.
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Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Defining the blanks--pharmacochaperoning of SLC6 transporters and ABC transportersGenetic susceptibility and neurotransmitters in Tourette syndromeReduced sensitivity to both positive and negative reinforcement in mice over-expressing the 5-hydroxytryptamine transporterTrio study and meta-analysis support the association of genetic variation at the serotonin transporter with early-onset obsessive-compulsive disorder.SLC6 transporters: structure, function, regulation, disease association and therapeuticsQuantitative trait loci mapping and gene network analysis implicate protocadherin-15 as a determinant of brain serotonin transporter expression.Dopamine D4 receptor and serotonin transporter gene effects on the longitudinal development of infant temperament.Monoamine transporters: vulnerable and vital doorkeepers.Inhibition of the cortex using transcranial magnetic stimulation in psychiatric populations: current and future directions.Physical Interactions and Functional Relationships of Neuroligin 2 and Midbrain Serotonin Transporters.Neurobiology of rodent self-grooming and its value for translational neuroscienceEvidence-based pharmacotherapy for pediatric obsessive-compulsive disorder and chronic tic disordersControl of serotonin transporter phosphorylation by conformational state.Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder.Whole-genome association analysis of treatment response in obsessive-compulsive disorder.Association between serotonin transporter gene polymorphisms and increased suicidal risk among HIV positive patients in Uganda.Molecular genetics of obsessive-compulsive disorder: a comprehensive meta-analysis of genetic association studies.Serotonin transporter variants play a role in anxiety sensitivity in South African adolescents.Peripheral SLC6A4 Gene Expression in Obsessive-Compulsive Disorder in the Han Chinese PopulationRare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome.Serotonin transporter promoter polymorphism is associated with executive function impairments in patients with obsessive compulsive disorder.Appetitive and reactive aggression are differentially associated with the STin2 genetic variant in the serotonin transporter gene.
P2860
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P2860
Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.
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2009 nî lūn-bûn
@nan
2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年學術文章
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2009年學術文章
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2009年學術文章
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name
Association of SLC6A4 variants ...... e multicenter US family study.
@en
Association of SLC6A4 variants ...... e multicenter US family study.
@nl
type
label
Association of SLC6A4 variants ...... e multicenter US family study.
@en
Association of SLC6A4 variants ...... e multicenter US family study.
@nl
prefLabel
Association of SLC6A4 variants ...... e multicenter US family study.
@en
Association of SLC6A4 variants ...... e multicenter US family study.
@nl
P2093
P2860
P356
P1433
P1476
Association of SLC6A4 variants ...... ge multicenter US family study
@en
P2093
B D Greenberg
D L Murphy
E Voyiaziakis
J A Knowles
J Piacentini
P2860
P2888
P304
P356
10.1038/MP.2009.100
P407
P50
P577
2009-10-06T00:00:00Z
P5875
P6179
1012673477