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The genetics of attention deficit/hyperactivity disorder in adults, a reviewOxygen dependence of tyrosine hydroxylasePulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigenExpanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes?Three-dimensional structure of human tryptophan hydroxylase and its implications for the biosynthesis of the neurotransmitters serotonin and melatoninDominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune DiseasesIdentification of tyrosine hydroxylase as an autoantigen in autoimmune polyendocrine syndrome type IConformation of the substrate and pterin cofactor bound to human tryptophan hydroxylase. Important role of Phe313 in substrate specificityRegulation of tyrosine hydroxylase by stress-activated protein kinasesPhosphorylation and activation of human tyrosine hydroxylase in vitro by mitogen-activated protein (MAP) kinase and MAP-kinase-activated kinases 1 and 2Three-way interaction between 14-3-3 proteins, the N-terminal region of tyrosine hydroxylase, and negatively charged membranesA common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medicationTyrosine hydroxylase and Parkinson's diseaseIsolation and characterization of tetrahydropterin oxidation products generated in the tyrosine 3-monooxygenase (tyrosine hydroxylase) reactionSelectivity and affinity determinants for ligand binding to the aromatic amino acid hydroxylasesCharacterization of a novel pterin intermediate formed in the catalytic cycle of tyrosine hydroxylaseVitamin levels in adults with ADHD.DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorderIdentification of tryptophan hydroxylase as an intestinal autoantigen.Adult attention deficit hyperactivity disorder is associated with asthma.Phosphorylation dependence and stoichiometry of the complex formed by tyrosine hydroxylase and 14-3-3γ.A genome-wide association study of bipolar disorder and comorbid migraineLong-term efficacy and safety of treatment with stimulants and atomoxetine in adult ADHD: a review of controlled and naturalistic studies.A structural approach into human tryptophan hydroxylase and its implications for the regulation of serotonin biosynthesis.Decreased serum levels of adiponectin in adult attention deficit hyperactivity disorder.Structure/function relationships in human phenylalanine hydroxylase. Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme.Adult ADHD and Comorbid Somatic Disease: A Systematic Literature Review.Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder.Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients.Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder.Attention Network Test in adults with ADHD--the impact of affective fluctuationsDIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders.Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorderGenome-wide analysis of attention deficit hyperactivity disorder in Norway.Adults with attention-deficit/hyperactivity disorder - a brain magnetic resonance spectroscopy studyEffects of ECT in treatment of depression: study protocol for a prospective neuroradiological study of acute and longitudinal effects on brain structure and function.Adult attention deficit hyperactivity disorder is associated with migraine headaches.Common variants in the ARC gene are not associated with cognitive abilitiesSerum concentrations of kynurenines in adult patients with attention-deficit hyperactivity disorder (ADHD): a case-control study.
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description
Noors onderzoeker
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հետազոտող
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Haavik J
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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Jan Haavik
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P106
P1153
7007170106
P21
P27
P31
P496
0000-0001-7865-2808