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Brain, ISSN 0006-8950, 2010, Volume 133, Issue Part 6, pp. 1810 - 1822
Journal Article
Human Brain Mapping, ISSN 1065-9471, 03/2017, Volume 38, Issue 3, pp. 1532 - 1540
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2015, Volume 36, Issue 12, pp. 3314 - 3320
Journal Article
Journal Article
Behavioural Brain Research, ISSN 0166-4328, 06/2015, Volume 286, pp. 192 - 200
Prenatal exposure to vitamin D is thought to be critical for optimal fetal neurodevelopment, yet vitamin D deficiency is apparent in a growing proportion of... 
Neurodevelopment | Tyrosine hydroxylase | Vitamin D | Foxp2 | C57BL/6J MICE | RAT | TYROSINE-HYDROXYLASE | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | ADULT | MUTANT MICE | NEURITE OUTGROWTH | BEHAVIORAL SCIENCES | 1,25-DIHYDROXYVITAMIN D-3 | D-RECEPTOR | GROWTH-FACTOR | Brain | Vitamin D deficiency | Calcifediol | Alfacalcidol
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2011, Volume 10, Issue 1, pp. 54 - 62
Summary Background Dopamine transporter deficiency syndrome is the first identified parkinsonian disorder caused by genetic alterations of the dopamine... 
Neurology | METABOLITES | TRANSMISSION | INFANTILE PARKINSONISM-DYSTONIA | CSF | NEUROSCIENCE | DISORDERS | TYROSINE-HYDROXYLASE DEFICIENCY | MONOAMINE TRANSPORTERS | CLINICAL NEUROLOGY | Brain - diagnostic imaging | Dystonia - cerebrospinal fluid | Parkinsonian Disorders - cerebrospinal fluid | Tomography, Emission-Computed, Single-Photon - methods | Humans | Child, Preschool | Dopamine Plasma Membrane Transport Proteins - deficiency | Hydroxyindoleacetic Acid - cerebrospinal fluid | Infant | Male | Ocular Motility Disorders - genetics | Dystonia - genetics | Transfection - methods | Parkinsonian Disorders - diagnostic imaging | Female | Parkinsonian Disorders - genetics | Retrospective Studies | Homovanillic Acid - cerebrospinal fluid | Child | Parkinsonian Disorders - physiopathology | Dystonia - physiopathology | Mutation - genetics | Dopamine Plasma Membrane Transport Proteins - genetics | Brain - pathology | Ocular Motility Disorders - physiopathology | Dystonia - diagnostic imaging | Cell Line, Transformed | Cohort Studies | Medical colleges | Medical research | Neurosciences | Dopamine | Molecular genetics | Medicine, Experimental | Phenols | Genetic aspects | Biomedical engineering | Pediatrics | Basal ganglia | Congenital defects | Central nervous system diseases | homovanillic acid | Photons | Cerebrospinal fluid | Pyramidal tracts | Drug development | Hereditary diseases | Eye | Hospitals | Computed tomography | Phenotyping | Dopamine transporter | Children | Mutation | Paralysis | Age | Movement disorders | Fast track
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2017, Volume 13, Issue 7, p. e1006892
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 3/2018, Volume 55, Issue 3, pp. 2443 - 2453
Developmental vitamin D (DVD) deficiency has been proposed as an important risk factor for schizophrenia. Our previous study using Sprague Dawley rats found... 
Neurology | Neurosciences | Biomedicine | Dopamine | Vitamin D | Mesencephalon | Neurobiology | Schizophrenia | Nurr1 | Tyrosine hydroxylase | Cell Biology | PROMOTER ACTIVITY | BRAIN-DEVELOPMENT | SUBSTANTIA-NIGRA | NEUROSCIENCES | ORPHAN NUCLEAR RECEPTOR | VENTRAL TEGMENTAL AREA | GENE-EXPRESSION | ALTERS | TYROSINE-HYDROXYLASE EXPRESSION | MIDBRAIN | Gene Expression | Vitamin D Deficiency - genetics | Dopaminergic Neurons - pathology | Mesencephalon - metabolism | Rats | Tyrosine 3-Monooxygenase - antagonists & inhibitors | Nuclear Receptor Subfamily 4, Group A, Member 2 - genetics | Rats, Sprague-Dawley | Tyrosine 3-Monooxygenase - biosynthesis | Tyrosine 3-Monooxygenase - genetics | Animals | Mitosis - physiology | Dopaminergic Neurons - metabolism | Vitamin D Deficiency - pathology | Nuclear Receptor Subfamily 4, Group A, Member 2 - antagonists & inhibitors | Nuclear Receptor Subfamily 4, Group A, Member 2 - biosynthesis | Vitamin D Deficiency - metabolism | Mesencephalon - pathology | Tyrosine | Medical research | RNA | Neurons | Medicine, Experimental | Phenols | Calcifediol | Alfacalcidol | Risk factors | Ecstasy | Segmentation | Mental disorders | Substantia nigra | Confocal microscopy | Ontogeny | mRNA | Tyrosine 3-monooxygenase | Dopamine receptors | Ventral tegmentum | Nutrient deficiency | Hydroxylase | Nuclear receptors | Environmental risk | Embryos | Nurr1 protein | DVD | Microscopy | Cell number
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Journal Article