Human tyrosine hydroxylase in Parkinson’s disease and in related disorders

Neuroscience

• Tyrosine Hydroxylase 100%
• Parkinson's Disease 100%
• Catecholamine 16%
• Striatum 16%
• Neurodegeneration 16%
• Stereotypic Movement Disorder 8%
• Norepinephrine 8%
• Neurotransmitter 8%
• DNA Polymorphism 8%
• DOPA 8%
• Tetrahydrobiopterin 8%
• Anabolism 8%
• GTP Cyclohydrolase I 8%
• Dystonia 8%
• Epinephrine 8%
• Tyrosine 8%
• Familial Parkinson's Disease 8%
• L-DOPA 8%
• Unspecific Monooxygenase 8%

Biochemistry, Genetics and Molecular Biology

• Tyrosine Hydroxylase 100%
• Catecholamine 16%
• Genetics 8%
• Tyrosine 8%
• Neurotransmitter 8%
• Genetic Divergence 8%
• Gene Polymorphism 8%
• Anabolism 8%
• Tetrahydrobiopterin 8%
• GTP Cyclohydrolase I 8%
• Epinephrine 8%
• Unspecific Monooxygenase 8%

Keyphrases

• Familial PD 11%
• Monooxygenase 11%
• Iron-based Materials 11%
• Neurotransmitter Dopamine 11%