Tyrosine hydroxylase and Parkinson's disease
Data up to Jan 2025
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Abstract
References (188)
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
1997 • 7,814 citations
Oxidative Stress, Glutamate, and Neurodegenerative Disorders
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Formation of Neuronal Intranuclear Inclusions Underlies the Neurological Dysfunction in Mice Transgenic for the HD Mutation
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Tyrosine Hydroxylase
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Basal Lipid Peroxidation in Substantia Nigra Is Increased in Parkinson's Disease
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Transition Metals, Ferritin, Glutathione, and Ascorbic Acid in Parkinsonian Brains
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Huntingtin-Encoded Polyglutamine Expansions Form Amyloid-like Protein Aggregates In Vitro and In Vivo
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Increased Nigral Iron Content and Alterations in Other Metal Ions Occurring in Brain in Parkinson's Disease
1989 • 1,117 citations
Oxidative pathways for catecholamines in the genesis of neuromelanin and cytotoxic quinones.
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Parallel signal processing among mammalian MAPKs
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Oxidative stress and the pathogenesis of Parkinson's disease
1996 • 967 citations
Effect of Deprenyl on the Progression of Disability in Early Parkinson's Disease
1989 • 913 citations
Oxidative damage to mitochondrial DNA shows marked age‐dependent increases in human brain
1993 • 759 citations
Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23
1996 • 759 citations
Psychopharmacology: The Fourth Generation of Progress
1996 • 755 citations
Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene
1994 • 751 citations
Protein kinase cascades activated by stress and inflammatory cytokines
1996 • 722 citations
Altered Brain Metabolism of Iron as a Cause of Neurodegenerative Diseases?
1994 • 701 citations
Intricate Regulation of Tyrosine Hydroxylase Activity and Gene Expression
1996 • 673 citations
Selective Increase of Iron in Substantia Nigra Zona Compacta of Parkinsonian Brains
1991 • 516 citations
B. TYROSINE HYDROXYLASE
1966 • 493 citations
Apoptosis Induced by Withdrawal of Trophic Factors Is Mediated by p38 Mitogen-activated Protein Kinase
1997 • 471 citations
Glutathione peroxidase, glial cells and Parkinson's disease
1993 • 448 citations
Free radicals in brain metabolism and pathology
1993 • 443 citations
Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development
1995 • 441 citations
Mammalian tyrosinase—The critical regulatory control point in melanocyte pigmentation
1987 • 439 citations
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
1992 • 416 citations
Fetal Nigral Transplantation as a Therapy for Parkinson’s Disease
2006 • 411 citations
A large kindred with autosomal dominant Parkinson's disease
1990 • 411 citations
A single human gene encoding multiple tyrosine hydroxylases with different predicted functional characteristics
1987 • 353 citations
Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence
1990 • 345 citations
Oxidative stress and antioxidant therapy in Parkinson's disease
1996 • 342 citations
The effect of age on the activity and molecular properties of human brain monoamine oxidase
1980 • 342 citations
Long-Term Behavioral Recovery in Parkinsonian Rats by an HSV Vector Expressing Tyrosine Hydroxylase
1994 • 333 citations
Pterin-Dependent Amino Acid Hydroxylases
1996 • 318 citations
Biological origin of free radicals, and mechanisms of antioxidant protection
1994 • 308 citations
Crystal Structure of the Biphenyl-Cleaving Extradiol Dioxygenase from a PCB-Degrading Pseudomonad
1995 • 297 citations
Transport of Iron in the Blood‐Brain‐Cerebrospinal Fluid System
1997 • 272 citations
Intrastriatal implantation of fibroblasts genetically engineered to produce brain-derived neurotrophic factor prevents degeneration of dopaminergic neurons in a rat model of Parkinson's disease
1995 • 269 citations
Hypoxia increases rate of transcription and stability of tyrosine hydroxylase mRNA in pheochromocytoma (PC12) cells.
1994 • 264 citations
Survival and function of intrastriatally grafted primary fibroblasts genetically modified to produce l-dopa
1991 • 261 citations
Grafting fibroblasts genetically modified to produce L-dopa in a rat model of Parkinson disease.
1989 • 258 citations
Crystal structure of tyrosine hydroxylase at 2.3 Å and its implications for inherited neurodegenerative diseases
1997 • 252 citations
Human gene for torsion dystonia located on chromosome 9q32-q34
1989 • 245 citations
Induction of apoptosis in catecholaminergic PC12 cells by L-DOPA. Implications for the treatment of Parkinson's disease.
1995 • 241 citations
Superoxide dismutase, aging, and degenerative disease
1994 • 234 citations
Dopamine, 6-hydroxydopamine, iron, and dioxygen — their mutual interactions and possible implication in the development of Parkinson's disease
1996 • 232 citations
Lazaroids improve the survival of grafted rat embryonic dopamine neurons.
1994 • 225 citations
In vivo release of DOPA and dopamine from genetically engineered cells grafted to the denervated rat striatum
1990 • 225 citations
Targeted Disruption of the Tyrosine Hydroxylase Locus Results in Severe Catecholamine Depletion and Perinatal Lethality in Mice
1995 • 220 citations
Correspondence
1996 • 215 citations
Exposure to hydrogen peroxide induces cell death via apoptosis in cultured rat cortical neurons
1994 • 208 citations
Oxidative stress as a cause of Parkinson's disease
1991 • 203 citations
A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome
1995 • 202 citations
Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene
1995 • 200 citations
Dopa-responsive dystonia
2012 • 192 citations
DEVELOPMENT AND APPLICATION OF HERPES SIMPLEX VIRUS VECTORS FOR HUMAN GENE THERAPY
1995 • 187 citations
Regulation of Tyrosine Hydroxylase Gene Expression in the Rat Carotid Body by Hypoxia
1992 • 186 citations
Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene
1996 • 186 citations
Glial Cell Line‐Derived Neurotrophic Factor Exerts Neurotrophic Effects on Dopaminergic Neurons In Vitro and Promotes Their Survival and Regrowth After Damage by 1‐Methyl‐4‐Phenylpyridinium
1996 • 181 citations
Dopa‐responsive dystonia: Pathological and biochemical observations in a case
1994 • 180 citations
Phosphorylation and activation of human tyrosine hydroxylase in vitro by mitogen‐activated protein (MAP) kinase and MAP‐kinase‐activated kinases 1 and 2
1993 • 175 citations
Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria
1997 • 175 citations
Targeted vectors for gene therapy
1995 • 163 citations
Direct intracerebral gene transfer of an adenoviral vector expressing tyrosine hydroxylase in a rat model of Parkinsonʼs disease
1994 • 160 citations
Site-directed mutagenesis of serine 40 of rat tyrosine hydroxylase. Effects of dopamine and cAMP-dependent phosphorylation on enzyme activity.
1992 • 149 citations
Astrocytes retrovirally transduced with BDNF elicit behavioral improvement in a rat model of Parkinson's disease
1995 • 148 citations
Understanding Parkinson's Disease
1997 • 146 citations
Tyrosine hydroxylase: human isoforms, structure and regulation in physiology and pathology.
1995 • 145 citations
BDNF Enhances the Functional Reinnervation of the Striatum by Grafted Fetal Dopamine Neurons
1996 • 141 citations
Generation of DOPA-Producing Astrocytes by Retroviral Transduction of the Human Tyrosine Hydroxylase Gene:In VitroCharacterization andin VivoEffects in the Rat Parkinson Model
1996 • 140 citations
Neural-Targeted Gene Therapy for Rodent and Primate Hemiparkinsonism
1994 • 139 citations
Effects of Brain-derived Neurotrophic Factor on 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced Parkinsonism in Monkeys
1995 • 138 citations
Specific A10 Dopaminergic Nuclei in the Midbrain Degenerate in Parkinson's Disease
1997 • 126 citations
Multiple signaling pathways in bovine chromaffin cells regulate tyrosine hydroxylase phosphorylation at Ser19, Ser31, and Ser40
1993 • 124 citations
THE HISTOCHEMICAL RELATIONSHIP OF NEUROMELANIN AND LIPOFUSCIN
1969 • 124 citations
The roles of neuromelanin, binding of metal ions, and oxidative cytotoxicity in the pathogenesis of Parkinson's disease: A hypothesis
1994 • 114 citations
Dopa-responsive dystonia in British patients: new mutations of the GTP- cyclohydrolase I gene and evidence for genetic heterogeneity
1996 • 112 citations
Characterization of the Active Site Iron in Tyrosine Hydroxylase
1996 • 111 citations
Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21
1996 • 111 citations
Double transduction with GTP cyclohydrolase I and tyrosine hydroxylase is necessary for spontaneous synthesis of L-DOPA by primary fibroblasts.
1996 • 109 citations
Resonance Raman studies on the blue-green-colored bovine adrenal tyrosine 3-monooxygenase (tyrosine hydroxylase). Evidence that the feedback inhibitors adrenaline and noradrenaline are coordinated to iron.
1988 • 107 citations
7th International Symposium
2004 • 106 citations
Recombinant human tyrosine hydroxylase isozymes
1991 • 106 citations
Does Oxidative Stress Participate in Nerve Cell Death in Parkinson’s Disease?
1993 • 104 citations
Regulation of tyrosine hydroxylase gene transcription rate and tyrosine hydroxylase mRNA stability by cyclic AMP and glucocorticoid.
1992 • 101 citations
A dual role for the cAMP-dependent protein kinase in tyrosine hydroxylase gene expression.
1993 • 96 citations
Double Transduction with GTP Cyclohydrolase I and Tyrosine Hydroxylase Is Necessary for Spontaneous Synthesis ofl-DOPA by Primary Fibroblasts
1996 • 94 citations
Resonance Raman Studies of Catecholate and Phenolate Complexes of Recombinant Human Tyrosine Hydroxylase
1995 • 93 citations
Two-Locus Admixture Linkage Analysis of Bipolar and Unipolar Affective Disorder Supports the Presence of Susceptibility Loci on Chromosomes 11p15 and 21q22
1997 • 93 citations
A Novel Adenovirus—Adeno-Associated Virus Hybrid Vector That Displays Efficient Rescue and Delivery of the AAV Genome
1996 • 92 citations
Four isoforms of tyrosine hydroxylase are expressed in human brain
1993 • 91 citations
Alterations in Brain Monoamine Oxidase Activity in Aging, Alzheimer's Disease, and Pick's Disease
1991 • 90 citations
Association of the mitochondrial tRNAA4336G mutation with Alzheimer's and Parkinson's diseases
1997 • 90 citations
The stress activated protein kinase pathway.
1996 • 90 citations
Isolation and sequence of a cDNA clone which contains the complete coding region of rat phenylalanine hydroxylase. Structural homology with tyrosine hydroxylase, glucocorticoid regulation, and use of alternate polyadenylation sites.
1986 • 89 citations
Hydrogen peroxide production by monoamine oxidase in isolated rat-brain mitochondria: its effect on glutathione levels and Ca2+ efflux
1990 • 88 citations
Homospecific activity (activity per enzyme protein) of tyrosine hydroxylase increases in parkinsonian brain
1988 • 88 citations
Regulation of recombinant human tyrosine hydroxylase isozymes by catecholamine binding and phosphorylation
1992 • 87 citations
Quantitation of a mitochondrial DNA deletion in Parkinson's disease
1992 • 87 citations
Reconstruction of the Nigrostriatal Pathway by Simultaneous Intrastriatal and Intranigral Dopaminergic Transplants
1996 • 87 citations
GDNF triggers fiber outgrowth of fetal ventral mesencephalic grafts from nigra to striatum in 6-OHDA-lesioned rats
1996 • 85 citations
A Mechanism for Hydroxylation by Tyrosine Hydroxylase Based on Partitioning of Substituted Phenylalanines
1996 • 84 citations
Dystonia with marked diurnal variation associated with biopterin deficiency
1988 • 83 citations
BDNF attenuates the effects of intrastriatal injection of 6-hydroxydopamine
1995 • 82 citations
Peroxynitrite‐Mediated Inhibition of DOPA Synthesis in PC12 Cells
1995 • 79 citations
Biochemistry of Parkinson's disease with special reference to the dopaminergic systems
1994 • 78 citations
MELANIN FORMATION BY HUMAN BRAIN IN VITRO
1975 • 77 citations
Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of seven candidate genes
1994 • 77 citations
Generation of Reactive Oxygen Species by Tyrosine Hydroxylase: A Possible Contribution to the Degeneration of Dopaminergic Neurons?
1997 • 76 citations
Viral vectors for modulating gene expression in neurons
1996 • 75 citations
A novel and major isoform of tyrosine hydroxylase in Drosophila is generated by alternative RNA processing
1994 • 71 citations
Oxidative inactivation of tyrosine hydroxylase in substantia nigra of aged rat
1996 • 69 citations
Mutations in the GTP cyclohydrolase I and 6-pyruvoyl-tetrahydropterin synthase genes
1997 • 69 citations
pH‐dependent release of catecholamines from tyrosine hydroxylase and the effect of phosphorylation of Ser‐40
1990 • 68 citations
Potential of neural "stem-like" cells for gene therapy and repair of the degenerating central nervous system.
1997 • 65 citations
Morphological Alterations in the Peripheral and Central Nervous Systems of Mice Lacking Glial Cell Line-Derived Neurotrophic Factor (GDNF): Immunohistochemical Studies
1997 • 65 citations
Expression and characterization of catalytic and regulatory domains of rat tyrosine hydroxylase
1993 • 64 citations
Increased iron in the substantia nigra of 6-OHDA induced parkinsonian rats: a nuclear microscopy study
1996 • 60 citations
Mitochondrial function in neurodegeneration and ageing
1992 • 59 citations
Participation of a Stress‐Activated Protein Kinase Cascade in the Activation of Tyrosine Hydroxylase in Chromaffin Cells
1997 • 59 citations
The metal requirement of rat tyrosine hydroxylase
1989 • 58 citations
Kinetics and mechanism of the autoxidation of the 2-amino-4-hydroxy-5,6,7,8-tetrahydropteridines
1974 • 58 citations
Reactive oxygen species: relation to aging and neurotoxic damage.
1992 • 58 citations
Cerebrospinal Fluid Homovanillic Acid in the DATATOP Study on Parkinson's Disease
1995 • 56 citations
Association of DNA polymorphism in the first intron of the tyrosine hydroxylase gene with disturbances of the catecholaminergic system in schizophrenia
1997 • 52 citations
α-synuclein—a link between Parkinson and Alzheimer diseases?
1997 • 52 citations
Isolation and characterization of tetrahydropterin oxidation products generated in the tyrosine 3-monooxygenase (tyrosine hydroxylase) reaction
1987 • 50 citations
Conversion of Tyrosine Hydroxylase to Stable and Inactive Form by the End Products
1991 • 46 citations
Monoamine oxidase, dopamine and Parkinson's disease
1991 • 45 citations
Suppression of Hydroxyl Radical Formation and Protection of Nigral Neurons by l‐Deprenyl (Selegiline)
1996 • 43 citations
Mössbauer, Electron‐Paramagnetic‐Resonance and X‐ray‐Absorption Fine‐Structure Studies of the Iron Environment in Recombinant Human Tyrosine Hydroxylase
1996 • 43 citations
Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1.
1992 • 42 citations
Genetic factors in the etiology of idiopathic Parkinson's disease
1994 • 42 citations
The incorporation of divalent metal ions into recombinant human tyrosine hydroxylase apoenzymes studied by intrinsic fluorescence and 1H‐NMR spectroscopy
1992 • 42 citations
New Species of Human Tyrosine Hydroxylase mRNA Are Produced in Variable Amounts in Adrenal Medulla and Are Overexpressed in Progressive Supranuclear Palsy
1996 • 41 citations
Regional heterogeneity of mtDNA heteroplasmy in parkinsonian brain.
1996 • 41 citations
<scp>l</scp>‐DOPA Is a Substrate for Tyrosine Hydroxylase
1997 • 41 citations
Post-transcriptional regulation of tyrosine hydroxylase gene expression by oxygen in PC12 Cells
1997 • 40 citations
Site-directed mutagenesis of tyrosine hydroxylase. Role of serine 40 in catalysis.
1992 • 38 citations
Tyrosine Hydroxylase
1995 • 38 citations
Recombinant human phenylalanine hydroxylase is a substrate for the ubiquitin-conjugating enzyme system
1996 • 37 citations
Identification of iron ligands in tyrosine hydroxylase by mutagenesis of conserved histidinyl residues
1995 • 36 citations
Regulation of tyrosine hydroxylase gene expression in depolarized non-transformed bovine adrenal medullary cells: second messenger systems and promoter mechanisms
1994 • 35 citations
Thermal Stability and CD Analysis of Rat Tyrosine Hydroxylase
1995 • 34 citations
7‐Substituted pterins in humans with suspected pterin‐4a‐carbinolamine dehydratase deficiency
1992 • 34 citations
Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
1994 • 33 citations
Possible genotoxicity of melanin synthesis intermediates: Tyrosinase reaction products interact with DNA in vitro
1984 • 31 citations
Tetrahydrobiopterin administration in biopterin‐deflcient progressive dystonia with diurnal variation
1989 • 30 citations
Conformation and interaction of phenylalanine with the divalent cation at the active site of human recombinant tyrosine hydroxylase as determined by proton NMR
1993 • 30 citations
Bovine Tyrosine Hydroxylase Gene‐Promoter Regions Involved in Basal and Angiotensin II‐Stimulated Expression in Nontransformed Adrenal Medullary Cells
1994 • 29 citations
The Phenylalanine Hydroxylase Locus: A Marker for the History of Phenylketonuria and Human Genetic Diversity
2007 • 28 citations
A parkinsonian kindred
1989 • 27 citations
Neural Stem Cells for CNS Transplantation
1993 • 26 citations
Catalytic core of rat tyrosine hydroxylase: terminal deletion analysis of bacterially expressed enzyme
1994 • 26 citations
Deprenyl induces the tyrosine hydroxylase enzyme in the rat dopaminergic nigrostriatal system
1997 • 25 citations
The GTP-cyclohydrolase I gene in atypical Parkinsonian patients: a clinico-genetic study
1996 • 24 citations
The Stability of Endogenous Tyrosine Hydroxylase Protein in PC‐12 Cells Differs from That Expressed in Mouse Fibroblasts by Gene Transfer
1994 • 24 citations
Deletion mutagenesis of rat PC12 tyrosine hydroxylase regulatory and catalytic domains
1993 • 24 citations
The ‘common deletion’ is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction
1997 • 23 citations
The TiPS/TINS lecture. Catecholamines: from gene regulation to neuropsychiatric disorders
1996 • 23 citations
Environment, Genetics and Idiopathic Parkinson's Disease
1991 • 23 citations
l-Dopa and Dopamine-Producing Gene Cassettes for Gene Therapy Approaches to Parkinson's Disease
1997 • 23 citations
Transfection of human lactotroph adenoma cells with an adenovirus vector expressing tyrosine hydroxylase decreases prolactin release.
1996 • 22 citations
A Novel Rat Tyrosine Hydroxylase mRNA Species Generated by Alternative Splicing
1996 • 22 citations
Crystallization and preliminary diffraction analysis of a truncated homodimer of human phenylalanine hydroxylase
1997 • 19 citations
Transplantation of cells genetically modified and direct intracerebral gene transfer with an adenoviral vector expressing tyrosine hydroxylase in a rat model of Parkinson's disease
1995 • 18 citations
Melanin formation in the inner ear is catalyzed by a new tyrosine hydroxylase kinetically and structurally different from tyrosinase
1997 • 16 citations
Tyrosine hydroxylase gene expression in varying forms of human pheochromocytoma
1996 • 16 citations
Regulation of tyrosine hydroxylase gene expression by the m1 muscarinic acetylcholine receptor in rat pheochromocytoma cells
1996 • 14 citations
DOPA compared with dihydroxyfumarate as co-factor in peroxidase-mediated oxidation of tyrosine to melanin
1971 • 14 citations
15 A stress-activated kinase cascade can mediate the activation of tyrosine hydroxylase in chromaffin cells
1997 • 11 citations
Superoxide dismutase partially prevents sympathetic denervation by 6-hydroxydopamine
1991 • 10 citations
Brain biochemistry and brain disorders
1993 • 8 citations
Studies on the Possible Mechanism of Inactivation of Phenylalanine Hydroxylase by Destructive Oxygen Species
1984 • 7 citations
Regulation of N-terminus-deleted human tyrosine hydroxylase type 1 by end products of catecholamine biosynthetic pathway
1996 • 7 citations
DEFICIENCY OF TYROSINE HYDROXYLASE OR TRYPTOPHAN HYDROXYLASE: A POSSIBLE CAUSE OF TWO HYPOTHETICAL METABOLIC DISEASES
1983 • 5 citations
Regulation of L-DOPA production by genetically modified primary fibroblasts transfected with retrovirus vector system
1996 • 5 citations
Mutations in the Copper- and Zinc-Containing Superoxide Dismutase Gene are Associated with “Lou Gehrig's Disease”
2009 • 4 citations
[Segawa disease (hereditary progressive dystonia with marked diurnal fluctuation-HPD) and abnormalities in pteridin metabolism].
1996 • 4 citations
Deleted Work
1955 • 0 citations