The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
about
Behavioral models of impulsivity in relation to ADHD: translation between clinical and preclinical studiesExpanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes?Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorderAttention-deficit hyperactivity disorder (ADHD).Molecular genetics of attention deficit hyperactivity disorder.Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.Test of variables of attention (TOVA) as a predictor of early attention complaints, an antecedent to dementia.Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.A common polymorphism in serotonin receptor 1B mRNA moderates regulation by miR-96 and associates with aggressive human behaviorsFunctional polymorphisms in the serotonin 1B receptor gene (HTR1B) predict self-reported anger and hostility among young men.Studying the effects of dietary body weight-adjusted acute tryptophan depletion on punishment-related behavioral inhibition.Attention deficit/hyperactivity disorder symptoms and depression symptoms as mediators in the intergenerational transmission of smokingThe genetics of attention deficit hyperactivity disorder.Role of the serotonin system in ADHD: treatment implications.High-resolution imaging of brain 5-HT 1B receptors in the rhesus monkey using [11C]P943.Molecular genetics of attention-deficit/hyperactivity disorder: an overviewPharmacokinetic evaluation of eltoprazine.Serotonin and molecular neuroimaging in humans using PET.Genetic and epigenetic dysregulation of imprinted genes in the brain.Biochemical and genetic analyses of childhood attention deficit/hyperactivity disorder.Lack of association of polymorphisms in six candidate genes in colombian adhd patients.The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample.Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.Allelic association of a dopamine transporter gene polymorphism with antisocial behaviour in heroin-dependent patients.Parent-of-origin effects in ADHD: distinct influences of paternal and maternal ADHD on neuropsychological functioning in offspring.Loss of neuronal 3D chromatin organization causes transcriptional and behavioural deficits related to serotonergic dysfunction.
P2860
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P2860
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
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
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@ast
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@en
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@nl
type
label
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@ast
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@en
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@nl
prefLabel
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@ast
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@en
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
@nl
P2093
P2860
P921
P356
P1433
P1476
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder
@en
P2093
Beitchman J
Kennedy JL
P2860
P2888
P304
P356
10.1038/SJ.MP.4001244
P407
P577
2003-01-01T00:00:00Z