(Q44287861)

English

The serotonin transporter intronic VNTR enhancer correlated with a predisposition to affective disorders has distinct regulatory elements within the domain based on the primary DNA sequence of the repeat unit

scientific article published in January 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

The serotonin transporter intronic VNTR enhancer correlated with a predisposition to affective disorders has distinct regulatory elements within the domain based on the primary DNA sequence of the repeat unit (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

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5

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Europe PubMed Central

PubMed publication ID

1 December 2017

author name string

Lovejoy EA

1

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Europe PubMed Central

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1 December 2017

Scott AC

2

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Europe PubMed Central

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1 December 2017

Fiskerstrand CE

3

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Europe PubMed Central

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1 December 2017

Bubb VJ

4

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Europe PubMed Central

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1 December 2017

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publication date

1 January 2003

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Europe PubMed Central

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1 December 2017

European Journal of Neuroscience

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Europe PubMed Central

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1 December 2017

17

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Europe PubMed Central

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1 December 2017

2

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Europe PubMed Central

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1 December 2017

417-420

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Europe PubMed Central

PubMed publication ID

1 December 2017

An intronic polymorphic domain often associated with susceptibility to affective disorders has allele dependent differential enhancer activity in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Serotonin transporter gene and risk for bipolar affective disorder: an association study in Spanish population

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Functional promoter and polyadenylation site mapping of the human serotonin (5-HT) transporter gene

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

A new mouse embryonic stem cell line with good germ line contribution and gene targeting frequency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

The dopamine transporter gene (SLC6A3) variable number of tandem repeats domain enhances transcription in dopamine neurons

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Single nucleotide polymorphisms distinguish multiple dopamine transporter alleles in primates: implications for association with attention deficit hyperactivity disorder and other neuropsychiatric disorders

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Enhancement of serotonin transporter function by tumor necrosis factor alpha but not by interleukin-6.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT).

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Variability in the serotonin transporter gene and increased risk for major depression with melancholia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02446.X

21 January 2018

Identifiers

10.1046/J.1460-9568.2003.02446.X

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

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