Receptors, Oxytocin
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Subject Areas on Research
- Age and sex differences in oxytocin and vasopressin V1a receptor binding densities in the rat brain: focus on the social decision-making network.
- An oxytocin receptor polymorphism predicts amygdala reactivity and antisocial behavior in men.
- Associations between oxytocin receptor gene (OXTR) methylation, plasma oxytocin, and attachment across adulthood.
- Central hemodynamic effects of an oxytocin receptor antagonist (atosiban) in the isolated, perfused rat heart.
- Early nurture epigenetically tunes the oxytocin receptor.
- Effects of oxytocin administration on spirituality and emotional responses to meditation.
- Enhanced Uterine Contractility and Stillbirth in Mice Lacking G Protein-Coupled Receptor Kinase 6 (GRK6): Implications for Oxytocin Receptor Desensitization.
- Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders.
- Genetic predisposition of behavioral response.
- Genetic, epigenetic, and environmental factors controlling oxytocin receptor gene expression.
- Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.
- Molecular determinants underlying the formation of stable intracellular G protein-coupled receptor-beta-arrestin complexes after receptor endocytosis*.
- Neural correlates of mating system diversity: oxytocin and vasopressin receptor distributions in monogamous and non-monogamous Eulemur.
- The Pan social brain: An evolutionary history of neurochemical receptor genes and their potential impact on sociocognitive differences.
- The association of single-nucleotide polymorphisms in the oxytocin receptor and G protein-coupled receptor kinase 6 (GRK6) genes with oxytocin dosing requirements and labor outcomes.
- The influence of maternal body mass index on myometrial oxytocin receptor expression in pregnancy.
- Universal nomenclature for oxytocin-vasotocin ligand and receptor families.
- β-Arrestin mediates oxytocin receptor signaling, which regulates uterine contractility and cellular migration.