Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder
about
Genetics of obsessive-compulsive disorderInsights to ligand binding to the monoamine transporters-from homology modeling to LeuBAT and dDATAssessing the validity of current mouse genetic models of obsessive-compulsive disorder.Chronic reductions in serotonin transporter function prevent 5-HT1B-induced behavioral effects in mice.How the serotonin story is being rewritten by new gene-based discoveries principally related to SLC6A4, the serotonin transporter gene, which functions to influence all cellular serotonin systems.Myristoylation of cGMP-dependent protein kinase dictates isoform specificity for serotonin transporter regulation.A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disordersRole of mother's genes and environment in postpartum depression.Olanzapine, but not fluoxetine, treatment increases survival in activity-based anorexia in miceFragile X syndrome and autism at the intersection of genetic and neural networks.Mechanism of Paroxetine (Paxil) Inhibition of the Serotonin Transporter.Anxiety and affective disorder comorbidity related to serotonin and other neurotransmitter systems: obsessive-compulsive disorder as an example of overlapping clinical and genetic heterogeneityGenetics of obsessive-compulsive disorder: a research update.Control of serotonin transporter phosphorylation by conformational state.Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder.Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.Modeling rare gene variation to gain insight into the oldest biomarker in autism: construction of the serotonin transporter Gly56Ala knock-in mouse.Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome.Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder.
P2860
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P2860
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder
description
2005 nî lūn-bûn
@nan
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Support for the association be ...... obsessive compulsive disorder
@ast
Support for the association be ...... obsessive compulsive disorder
@en
Support for the association be ...... obsessive compulsive disorder
@nl
type
label
Support for the association be ...... obsessive compulsive disorder
@ast
Support for the association be ...... obsessive compulsive disorder
@en
Support for the association be ...... obsessive compulsive disorder
@nl
prefLabel
Support for the association be ...... obsessive compulsive disorder
@ast
Support for the association be ...... obsessive compulsive disorder
@en
Support for the association be ...... obsessive compulsive disorder
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
Support for the association be ...... obsessive compulsive disorder
@en
P2093
C M Durand
M C Mouren-Simeoni
P2860
P2888
P304
P3181
P356
10.1038/SJ.MP.4001728
P407
P50
P577
2005-12-01T00:00:00Z
P5875
P6179
1036874164