Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype. - Wikidata - awgldk - TriplyDB

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype.

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype.

http://www.wikidata.org/entity/Q34273765

about

Lack of association between the Serotonin Transporter Promoter Polymorphism (5-HTTLPR) and Panic Disorder: a systematic review and meta-analysis Genetics of autism spectrum disorder Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors Factor structure, reliability and criterion validity of the Autism-Spectrum Quotient (AQ): a study in Dutch population and patient groups Genetics of obsessive-compulsive disorder Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Defining the blanks--pharmacochaperoning of SLC6 transporters and ABC transporters Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments The serotonergic system in mood disorders and suicidal behaviour A competitive inhibitor traps LeuT in an open-to-out conformation.Binding of an octylglucoside detergent molecule in the second substrate (S2) site of LeuT establishes an inhibitor-bound conformation Regulation of the serotonin transporter in the pathogenesis of irritable bowel syndrome The serotonin system in autism spectrum disorder: From biomarker to animal models Cysteine-scanning mutagenesis of serotonin transporter intracellular loop 2 suggests an alpha-helical conformation Physical interaction between the serotonin transporter and neuronal nitric oxide synthase underlies reciprocal modulation of their activity The Development of Screening Methods to Identify Drugs to Limit ER Stress Using Wild-type and Mutant Serotonin Transporter Characterization of a functional polymorphism in the 3' UTR of SLC6A4 and its association with drinking intensity Essential role for orbitofrontal serotonin 1B receptors in obsessive-compulsive disorder-like behavior and serotonin reuptake inhibitor response in mice.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.Genetic variation in cortico-amygdala serotonin function and risk for stress-related disease Invasive circuitry-based neurotherapeutics: stereotactic ablation and deep brain stimulation for OCD Insights from molecular dynamics: the binding site of cocaine in the dopamine transporter and permeation pathways of substrates in the leucine and dopamine transporters.Novel and functional norepinephrine transporter protein variants identified in attention-deficit hyperactivity disorder Boron-Doped Diamond Microelectrodes Reveal Reduced Serotonin Uptake Rates in Lymphocytes from Adult Rhesus Monkeys Carrying the Short Allele of the 5-HTTLPR.Biological substrates underpinning diagnosis of major depression.Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase.Discovery of novel selective serotonin reuptake inhibitors through development of a protein-based pharmacophore.Discovery of novel-scaffold monoamine transporter ligands via in silico screening with the S1 pocket of the serotonin transporter A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.Myristoylation of cGMP-dependent protein kinase dictates isoform specificity for serotonin transporter regulation.Regulation of monoamine transporters: Role of transporter phosphorylation.Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder.A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders Signal attenuation as a rat model of obsessive compulsive disorder.Identification of a novel selective serotonin reuptake inhibitor by coupling monoamine transporter-based virtual screening and rational molecular hybridization Quantitative trait loci mapping and gene network analysis implicate protocadherin-15 as a determinant of brain serotonin transporter expression.Gene-environment interaction and the genetics of depression.Molecular genetics of autism spectrum disorder.

P2860

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P2860

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype.

http://www.wikidata.org/entity/Q34273765

description

2003 nî lūn-bûn

@nan

2003 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@ast

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@en

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@nl

type

label

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@ast

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@en

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@nl

prefLabel

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@ast

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@en

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@nl

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P1433

Molecular Psychiatry

P1476

Serotonin transporter missense ...... ex neuropsychiatric phenotype.

@en

P2093

Greenberg BD

http://www.w3.org/2001/XMLSchema#string

Kaye WH

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Lappalainen J

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Murphy DL

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Ozaki N

http://www.w3.org/2001/XMLSchema#string

Plotnicov K

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Rudnick G

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P2860

Genetics of austim: complex aetiology for a heterogeneous disorder

Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

Sexually dimorphic relationship of a 5-HT2A promoter polymorphism with obsessive-compulsive disorder.

The relationship of obsessive-compulsive disorder to possible spectrum disorders: results from a family study.

What is the prevalence of Asperger disorder?

The prevalence of clinically recognized obsessive-compulsive disorder in a large health maintenance organization.

Genetic perspectives on the serotonin transporter.

Cloning, expression, and localization of a chloride-facilitated, cocaine-sensitive serotonin transporter from Drosophila melanogaster.

Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.

P2888

P304

933-936

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scholarly article

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10.1038/SJ.MP.4001365

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11

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8

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2003-11-01T00:00:00Z

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9030980

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1004279529

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14593431

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