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Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons
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17453063
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30 May 2020
title
Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons
(English)
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PubMed publication ID
17453063
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30 May 2020
author name string
Lim JE
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1
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17453063
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30 May 2020
Pinsonneault J
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2
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17453063
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30 May 2020
Sadee W
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30 May 2020
Saffen D
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publication date
12 December 2006
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30 May 2020
published in
Molecular Psychiatry
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PubMed publication ID
17453063
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30 May 2020
volume
12
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30 May 2020
issue
5
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30 May 2020
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491-501
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17453063
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30 May 2020
cites work
Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
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
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Transmission/disequilibrium tests for extended marker haplotypes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
5-HTTLPR variants not associated with autistic spectrum disorders.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Genetic variation in the serotonin transporter promoter region affects serotonin uptake in human blood platelets.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Autism: the phenotype in relatives.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Serotonin transporter (5-HTT) gene variants associated with autism?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Evidence of linkage between the serotonin transporter and autistic disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Effects of tryptophan depletion in drug-free adults with autistic disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Parametric and nonparametric linkage analysis: a unified multipoint approach
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Allelic variation of human serotonin transporter gene expression
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Organization of the human serotonin transporter gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Autism as a strongly genetic disorder: evidence from a British twin study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
A modified enzymatic-isotopic microassay for serotonin (5HT) using 5HT-N-acetyltransferase partially purified from Drosophila.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Kinetics of 3H-serotonin uptake by platelets in infantile autism and developmental language disorder (including five pairs of twins).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Whole blood serotonin in autistic and normal subjects.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Genetic control of serotonin uptake in blood platelets: a twin study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Elevated blood serotonin in autistic probands and their first-degree relatives
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Relationships of whole blood serotonin and plasma norepinephrine within families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269
retrieved
25 February 2021
Tetrahydropterin-dependent amino acid hydroxylases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The spectrum of behaviors influenced by serotonin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of serotonergic and noradrenergic systems in the pathophysiology of depression and anxiety disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synthesis of serotonin by a second tryptophan hydroxylase isoform
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of tryptophan hydroxylase I and II mRNA expression in the human brain: a post-mortem study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuronal tryptophan hydroxylase mRNA expression in the human dorsal and median raphe nuclei: major depression and suicide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of genetic variants in the neuronal form of tryptophan hydroxylase (TPH2).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional polymorphisms of the brain serotonin synthesizing enzyme tryptophan hydroxylase-2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic Variation in Human Gene Expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cis-acting variation in the expression of a high proportion of genes in human brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic expression imbalance of human mu opioid receptor (OPRM1) caused by variant A118G.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic expression of serotonin transporter (SERT) mRNA in human pons: lack of correlation with the polymorphism SERTLPR.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haploview: analysis and visualization of LD and haplotype maps
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Control elements of muscarinic receptor gene expression.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mfold web server for nucleic acid folding and hybridization prediction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Listening to silence and understanding nonsense: exonic mutations that affect splicing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Global landscape of recent inferred Darwinian selection for Homo sapiens
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recent developments and current controversies in depression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Support for the involvement of TPH2 gene in affective disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The novel brain-specific tryptophan hydroxylase-2 gene in panic disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene in suicide victims
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of the novel TPH2 gene in bipolar disorder and suicidality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Promoter polymorphism of second tryptophan hydroxylase isoform (TPH2) in schizophrenia and suicidality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The interaction between TPH2 promoter haplotypes and clinical-demographic risk factors in suicide victims with major psychoses.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of association between the serotonin transporter and tryptophan hydroxylase gene polymorphisms and completed suicide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistance.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amygdala responsiveness is modulated by tryptophan hydroxylase-2 gene variation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Additive effects of serotonin transporter and tryptophan hydroxylase-2 gene variation on emotional processing.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional promoter and polyadenylation site mapping of the human serotonin (5-HT) transporter gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serotonin and brain development: role in human developmental diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The developmental role of serotonin: news from mouse molecular genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuroticism mediates the association of the serotonin transporter gene with lifetime major depression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001923
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/SJ.MP.4001923
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17453063
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17453063%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
PMC publication ID
1896269
0 references
PubMed publication ID
17453063
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17453063
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17453063%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
11803447
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