Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder - Test2 - elhamkhani - TriplyDB

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

http://www.wikidata.org/entity/Q24646169

about

Genetics of obsessive-compulsive disorder Insights to ligand binding to the monoamine transporters-from homology modeling to LeuBAT and dDAT Assessing 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 disorders Role of mother's genes and environment in postpartum depression.Olanzapine, but not fluoxetine, treatment increases survival in activity-based anorexia in mice Fragile 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 heterogeneity Genetics 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

Q24645479-384EF7E0-94A5-4727-9C04-D597A2A7813A Q26781554-742F7B6A-EE6F-412D-ACB2-9FBCDBB3A07E Q30482891-79B93580-143B-4614-89A9-2DA779F8705C Q30482896-36F4B8E0-4F86-4C59-9546-69A94DD74453 Q30485725-F2D287D3-4A86-4103-B5A2-4D3E35497F6F Q34509255-7D956704-0082-43E0-BFBE-BCEF216DDC63 Q34975117-8EB2CBCF-9525-4118-A0FC-E794B55E2FDF Q35002581-91D170BD-F146-4AE7-A8C0-D9B869B4344F Q35982317-C97F0E0F-9169-4ED8-85EE-34001AEE8FD2 Q36603922-A4BDED20-56CC-4E79-958C-9985452C54FB Q36754967-99444D90-1FE6-45EB-8A11-C605BD3E5734 Q36801195-F826FD91-FF6E-4175-AE3C-824C5386255F Q36902024-7A95F3F6-69A5-4E2E-87E6-F05091715484 Q36930972-6A239C84-26B9-4216-B416-2FBD2505AF48 Q37154566-945CED6D-646E-47AE-B971-CE60B5D9EF09 Q37337244-BEEDCED5-F3B9-4ABA-9BC6-D45EDFB3F28D Q37449787-4277A0A5-6F00-43ED-88C6-F086B1F5B23D Q41854733-71CBFA7B-0E96-4750-BF49-A034E2D8613F Q45974051-1C1B263F-5401-4FFF-B049-CD10BE66565E Q55042376-11F13411-7469-4B08-B9B3-9BC9B81A9AE8

P2860

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

http://www.wikidata.org/entity/Q24646169

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

P1433

Q24646169-E6FCE08D-6DB9-42A2-9759-357AE23E17C3

P1476

Q24646169-7B0D24FF-EEFA-4F77-A966-DA383B72B2D9

P2093

Q24646169-1D58862E-DC66-43AD-BAE4-4200C2EAAE6A

Q24646169-26920C0C-2969-4223-B175-802CEDBB5E3A

Q24646169-3BB5F4FA-8C76-4E37-9D56-2B7CE9265166

Q24646169-50F3A2AB-8F80-44F3-A447-E413E58E3699

Q24646169-57DD57B0-CF49-4F48-9B90-5B44DCF5CA8B

Q24646169-5D80F012-DEE4-4C4C-AF64-153D3DF64D6A

Q24646169-86362DC8-D9C8-4CC1-9A36-2BD4AB52D72B

Q24646169-9A40FC6B-3F2A-4EE0-B526-520B67B02EEF

Q24646169-9CFEE552-6F9B-41C7-AF8D-FA0589440240

Q24646169-9DA30999-248B-4114-9B88-CD70EA058904

P2860

Q24646169-05227287-812F-4067-AB8E-9E1649D8F46B

Q24646169-34DD0B9F-308E-46A4-AB4E-7D8F4052D032

Q24646169-3AA58FDE-2F02-4928-BF3B-8F3F09F952C7

Q24646169-4BA955F4-1CCA-4115-88E4-EF00DE1F78B9

Q24646169-6EF0E8FD-D6B4-422A-A4E8-F350D3B3B01E

Q24646169-707407E3-1615-4099-8BA8-2AA2354B55BF

Q24646169-7B5B4F72-63BB-45BF-B875-40450E4E0E7B

Q24646169-F1B4F9FD-07FD-46CE-872E-4B0471DAEF22

P2888

Q24646169-AE51A8DF-172D-4D0A-8E14-A674247C88B3

P304

Q24646169-0E028486-0162-4874-A1A7-2204D0F3D69A

P31

Q24646169-63D5EC6F-A472-4F3E-8DE9-9FCE799F28B7

P3181

Q24646169-FDB00366-93C4-415B-AA48-BD302F60D12C

P356

Q24646169-4D9115D0-7941-439A-A562-EDE7CF7759A2

P407

Q24646169-E27F8401-349F-41C6-A717-02AE7906E26A

P433

Q24646169-08C885CE-C139-4DB7-AC38-341485D858DC

P478

Q24646169-FF7E62A1-501C-4832-8340-C989E0A26F96

P50

Q24646169-1F7AE896-641A-4AF0-BBEB-ED7D771ECFC5

Q24646169-4531C55E-0725-4262-BEDF-A335DDB8706A

Q24646169-56753F6A-EFFE-4C60-B405-823436D715D2

Q24646169-985CDBFF-9C5E-4F10-A9E6-BD1B0B509B83

Q24646169-B0FB4938-1C9F-4223-8F3F-C2890B3D38D8

Q24646169-C2A4D884-6426-4E83-AD9A-C4DC65FE3273

Q24646169-CDAF0F76-8483-4B88-AA92-AB50DA373A1A

Q24646169-E247CD06-F390-4830-B7AB-F15ACC53F60E

Q24646169-F4D1215C-858D-490B-9A4A-58D3C6B7A740

P577

Q24646169-54B01BA7-7D49-4980-93E1-E8912AEB0E44

P5875

Q24646169-61805861-1244-4948-9CF6-11882D2C5C12

P6179

Q24646169-29C345DA-DBA6-4B4F-AD0B-C5C8EBD05F9D

P698

Q24646169-4BC7A096-CDD6-447F-BF94-6971803DC440

P921

Q24646169-6ffba235-5376-40c9-b776-98044c4ab87e

P932

Q24646169-D9616A01-9DDE-4FF4-B851-711A1FE35495

P3181

P356

P1433

Molecular Psychiatry

P1476

Support for the association be ...... obsessive compulsive disorder

@en

P2093

A Kipman

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

B Millet

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

C M Durand

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

C Reck

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

F Buhtz

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

G Nygren

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

I Roy

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

M C Mouren-Simeoni

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

M O Krebs

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

M Råstam

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

P2860

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

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

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype.

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative.

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder.

A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.

A human serotonin transporter mutation causes constitutive activation of transport activity.

P2888

P304

1059-61

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

P31

scholarly article

P3181

4948128

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

P356

10.1038/SJ.MP.4001728

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

P407

P433

12

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

P478

10

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

P50

Christopher Gillberg

Thomas Bourgeron

Catalina Betancur

Henrik Anckarsäter

Richard Delorme

P577

2005-12-01T00:00:00Z

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

P5875

28376852

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

P6179

1036874164

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

P698

16088327

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

P921

P932

2547479

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