Relationship of serotonin
transporter gene polymorphisms and haplotypes to mRNA transcription
A meta - analysis of the association between the serotonin
transporter gene polymorphism (5 - HTTLPR) and trait anxiety
An exploratory genetic analysis: Associations between parent depression symptoms, child temperament, and the serotonin
transporter gene polymorphism (5HTTLPR).
Not exact matches
Moderate level fetal alcohol exposure and serotonin
transporter gene promoter
polymorphism affect neonatal temperament and limbic - hypothalamic - pituitary - adrenal axis regulation in monkeys.
A functional
polymorphism in the promoter region of the human serotonin
transporter gene (SLC6A4) has been associated with several dimensions of neuroticism and psychopathology, especially anxiety traits, but the predictive value of this genotype against these complex behaviors has been inconsistent.
Comparative analysis of length
polymorphisms in the promoter region of the serotonin
transporter gene (SLC6A4) in Cercopithecidae [abstract].
The aim of this study was to investigate the role of serotonin in depression, searching for association of two serotoninergic
polymorphisms (T102C of serotonin receptor 5 - HT2A and serotonin
transporter linked polymorphic region -5-HTTLPR - of SLC6A4
gene) with depressive symptoms and considering their possible interactions with Apolipoprotein E... (ApoE) and between themselves, in a sample of 208 sporadic AD patients and 116 normal controls from Italy.
The aim of this study was to investigate the role of serotonin in depression, searching for association of two serotoninergic
polymorphisms (T102C of serotonin receptor 5 - HT2A and serotonin
transporter linked polymorphic region -5-HTTLPR - of SLC6A4
gene) with depressive symptoms and considering their possible interactions with Apolipoprotein E
However, response to treatment may be predicted by baseline frontal lobe blood flow, and presence of
polymorphisms of the 5 - hydroxytryptamine (5 - HT)-1 a
gene, the LL genotype of the serotonin
transporter linked polymorphic region (5 - HTTLPR)
gene, and Val / Val homozygotes of the brain - derived neurotrophic factor (BDNF)
gene.
To explore the possibility of common genetic pathways within the respective pathophysiologies, nine ADHD candidate single nucleotide
polymorphisms (SNPs) in seven
genes were tested for association with PD in 5333 cases and 12,019 healthy controls: one variant, respectively, in the
genes coding for synaptosomal - associated protein 25 k (SNAP25), the dopamine (DA)
transporter (SLC6A3; DAT1), DA receptor D4 (DRD4), serotonin receptor 1B (HTR1B), tryptophan hydroxylase 2 (TPH2), the norepinephrine
transporter SLC6A2 and three SNPs in cadherin 13 (CDH13).
In this study, measures of the quality and availability of social supports were found to moderate risk for depression associated with a history of maltreatment and the presence of the short (s) allele of the serotonin
transporter gene promoter
polymorphism (5 - HTTLPR).
We studied the well known functional
polymorphism in the 5 ′ flanking regulatory (promoter) region of the
gene (SLC6A4) coding for the serotonin
transporter protein.
However, researchers at the University of California — Berkeley wanted to find out if there might a genetic component that could predict how couple interactions affect marital satisfaction.5 Specifically, the team decided to look at the 5 - HTTLPR
polymorphism in the promoter region of the serotonin
transporter gene.
This investigation examined the extent to which
polymorphisms of the serotonin
transporter linked promoter region (5 - HTTLPR) and the dopamine receptor D4 (DRD4)
genes differentially influenced the development of attachment security and disorganization in maltreated and nonmaltreated infants at age 13 months, and the extent to which the efficacy of preventive interventions to promote attachment security were influenced by genetic variation.
Association analysis of the catechol - o - methyltransferase (COMT), serotonin
transporter (5 - HTT) and serotonin 2A receptor (5HT2A)
gene polymorphisms with obsessive - compulsive disorder
Behavioural genetics studies examining the association between
polymorphisms of the serotonin
transporter gene and affective disorders (Uher & McGuffin 2008) as well as the association between environmental interactions with the serotonin
transporter gene and affective disorders (Munafo et al. 2009; Risch et al. 2009) within a given population often produce inconsistent results, suggesting a more complex path from
gene to disease.
Obsessive - compulsive disorder and the promoter region
polymorphism (5 - HTTLPR) in the serotonin
transporter gene (SLC6A4): a negative association study in the Afrikaner population
Serotonin
transporter gene regulatory region
polymorphism and anxiety - related traits in the Japanese
In relation to the association of infant attachment with a promoter
polymorphism of the serotonin
transporter gene, we have mentioned that
gene expression may be affected by variation in the DNA sequence of the regulatory region of the
gene.
Association between Dopamine
Transporter Gene (DAT1)
Polymorphisms and Eating Disorders with Binge Eating Behavior
Here, we examined the association between cultural values of individualism — collectivism and allelic frequency of the serotonin
transporter functional
polymorphism (5 - HTTLPR) as well as the role this culture —
gene association may play in explaining global variability in prevalence of pathogens and affective disorders.
Adults who had been categorized as behaviorally inhibited at the age of 2 years exhibited a higher amygdala activation in response to unknown vs familiar faces16 compared with adults who were uninhibited as children, consistent with the notion that novel or ambiguous environmental stimuli of potential biological relevance activate the amygdala.17 Turning to
genes that can influence the neurobiological bases of the processing of emotions, 2 common alleles, the short (S) and the long (L), in a variable repeat sequence of the serotonin
transporter (5 - HTT) promoter
polymorphism (5 - HTTLPR) on human chromosome 17q11 have been differently associated with greater amygdala activity in response to angry or fearful faces18 in healthy adults.
SEROTONIN
TRANSPORTER LENGTH
POLYMORPHISM, CHILDHOOD MALTREATMENT, AND CHRONIC DEPRESSION: A SPECIFIC
GENE - ENVIRONMENT INTERACTION.
Functional
polymorphism within the promotor of the serotonin
transporter gene is associated with severe hyperkinetic disorders
A meta - analysis of association studies between the 10 - repeat allele of a VNTR
polymorphism in the 3 ′ UTR of dopamine
transporter gene and attention deficit hyperactivity disorder
Moderate level fetal alcohol exposure and serotonin
transporter gene promoter
polymorphism affect neonatal temperament and limbic - hypothalamic - pituitary - adrenal axis regulation in monkeys.
The effects of child maltreatment and
polymorphisms of the serotonin
transporter and dopamine D4 receptor
genes and infant attachment and intervention efficacy
The human serotonin
transporter gene linked
polymorphism (5 - HTTLPR) shows ten novel allelic variants
Polymorphism in serotonin
transporter gene associated with susceptibility to major depression
The present study examined
gene — environment correlations and Gene × Environment interactions for polymorphisms of three target genes, the serotonin transporter gene, the D4 dopamine receptor gene, and the monoamine oxidase A gene in relation to symptoms of anxiety, depression, and oppositional behav
gene — environment correlations and
Gene × Environment interactions for polymorphisms of three target genes, the serotonin transporter gene, the D4 dopamine receptor gene, and the monoamine oxidase A gene in relation to symptoms of anxiety, depression, and oppositional behav
Gene × Environment interactions for
polymorphisms of three target
genes, the serotonin
transporter gene, the D4 dopamine receptor gene, and the monoamine oxidase A gene in relation to symptoms of anxiety, depression, and oppositional behav
gene, the D4 dopamine receptor
gene, and the monoamine oxidase A gene in relation to symptoms of anxiety, depression, and oppositional behav
gene, and the monoamine oxidase A
gene in relation to symptoms of anxiety, depression, and oppositional behav
gene in relation to symptoms of anxiety, depression, and oppositional behavior.