(Q47729944)

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Genetically driven variation in serotonin uptake: is there a link to affective spectrum, neurodevelopmental, and neurodegenerative disorders?

scientific article published in August 1998

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

1 reference

Europe PubMed Central

Genetically driven variation in serotonin uptake: is there a link to affective spectrum, neurodevelopmental, and neurodegenerative disorders? (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

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neurodegeneration

1 reference

based on heuristic

inferred from title

affective spectrum

1 reference

based on heuristic

inferred from title

author name string

Lesch KP

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

Mössner R

2

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

language of work or name

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publication date

1 August 1998

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

Biological Psychiatry

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

44

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

179-192

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

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Gene structure and 5'-flanking regulatory region of the murine serotonin transporter

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Prenatal development of the serotonin transporter in mouse brain

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Evidence of linkage between the serotonin transporter and autistic disorder

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Functional promoter polymorphism of the human serotonin transporter

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Dopamine D4 receptor and serotonin transporter promoter in the determination of neonatal temperament

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Association of short alleles of a VNTR of the serotonin transporter gene with anxiety symptoms in patients presenting after deliberate self harm

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Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African- and European-American and Japanese populations and in alcohol-dependent subjects

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Serotonin Transporter and Seasonal Variation in Blood Serotonin in Families with Obsessive-Compulsive Disorder

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

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Abnormal expression of serotonin transporter mRNA in the frontal and temporal cortex of schizophrenics

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Studies of a neurochemical link between depression, anxiety, and stress from [3H]imipramine and [3H]paroxetine binding on human platelets

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Serotonin uptake sites and serotonin receptors are altered in the limbic system of schizophrenics

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m-Chlorophenylpiperazine as a probe of serotonin function

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Serotonin1A receptors are expressed by a subpopulation of cholinergic neurons in the rat medial septum and diagonal band of Broca--a double immunocytochemical study

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Serotonin transporter (5-HTT) gene variants associated with autism?

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Serotonin transporter gene polymorphisms: ethnic difference and possible association with bipolar affective disorder

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Genetic dissection of complex traits

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Ontogeny of the serotonergic system in the rat: serotonin as a developmental signal

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Neurotransmitters as growth regulatory signals: role of receptors and second messengers

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Transient uptake and storage of serotonin in developing thalamic neurons

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Review : Serotonin Transporter and Psychiatric Disorders: Listening to the Gene

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Organization of the human serotonin transporter gene

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Primary structure of the serotonin transporter in unipolar depression and bipolar disorder

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Identifiers

10.1016/S0006-3223(98)00121-8

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/9693390

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