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Anatomy36

Neurons Brain Inclusion Bodies Microglia Mitochondria Neurofibrillary Tangles Cells, Cultured Lewy Bodies Astrocytes Hippocampus Substantia Nigra Intranuclear Inclusion Bodies Cerebral Cortex Dopaminergic Neurons Neuroglia Central Nervous System Motor Neurons Corpus Striatum Cerebellum Axons Cell Line Lysosomes Spinal Cord PC12 Cells Blood-Brain Barrier Purkinje Cells Neural Stem Cells Neurites Neostriatum Synapses HEK293 Cells Oligodendroglia Neuropil Threads Mesencephalon Endoplasmic Reticulum Nervous System

Organisms13

Mice, Transgenic Mice, Inbred C57BL Animals, Genetically Modified Mice, Knockout Cycas Rats, Sprague-Dawley Mice, Neurologic Mutants Drosophila Drosophila melanogaster Animals, Newborn Caenorhabditis elegans Rats, Wistar Banisteriopsis

Diseases71

Neurodegenerative Diseases Nerve Degeneration Huntington Disease Alzheimer Disease Parkinson Disease Amyotrophic Lateral Sclerosis Heredodegenerative Disorders, Nervous System Tauopathies Disease Models, Animal Spinocerebellar Ataxias Prion Diseases Proteostasis Deficiencies Neuronal Ceroid-Lipofuscinoses Frontotemporal Dementia Frontotemporal Lobar Degeneration Parkinsonian Disorders Friedreich Ataxia Lewy Body Disease Dementia Ataxia Multiple System Atrophy Supranuclear Palsy, Progressive Mitochondrial Diseases Pick Disease of the Brain Machado-Joseph Disease Atrophy Central Nervous System Diseases Nervous System Diseases Gliosis Motor Neuron Disease Spinocerebellar Degenerations Plaque, Amyloid Muscular Atrophy, Spinal Creutzfeldt-Jakob Syndrome Encephalitis Neurotoxicity Syndromes Parkinson Disease, Secondary Brain Diseases Niemann-Pick Disease, Type C Lysosomal Storage Diseases, Nervous System Myoclonic Epilepsies, Progressive TDP-43 Proteinopathies Scrapie Neuroaxonal Dystrophies Wallerian Degeneration MPTP Poisoning Inflammation Disease Progression Spastic Paraplegia, Hereditary Gangliosidosis, GM1 Tremor Aphasia, Primary Progressive Insomnia, Fatal Familial Cerebellar Ataxia Adrenoleukodystrophy Leigh Disease Fragile X Syndrome Trauma, Nervous System Lafora Disease Multiple Sclerosis Neuroblastoma REM Sleep Behavior Disorder Apraxias Lysosomal Storage Diseases Neuritis Wolfram Syndrome Memory Disorders Postmortem Changes Menkes Kinky Hair Syndrome Niemann-Pick Diseases Genetic Predisposition to Disease

Chemicals and Drugs70

alpha-Synuclein tau Proteins Nerve Tissue Proteins Neuroprotective Agents Synucleins Amyloid beta-Peptides Prions Amyloid Neurotoxins Peptides beta-Synuclein Superoxide Dismutase Ubiquitin Nuclear Proteins Proteasome Endopeptidase Complex Amyloid beta-Protein Precursor Iron-Binding Proteins PrPSc Proteins PrPC Proteins Molecular Chaperones Reactive Oxygen Species Nitro Compounds Cyclin-Dependent Kinase 5 Dopamine 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Glial Fibrillary Acidic Protein RNA-Binding Protein FUS Thiolester Hydrolases Antioxidants Neurofilament Proteins Oxidopamine Peptide Fragments Mutant Proteins gamma-Synuclein Quinolinic Acid Glutamic Acid 1-Methyl-4-phenylpyridinium Mitochondrial Proteins Microtubule-Associated Proteins Brain-Derived Neurotrophic Factor Amyloidogenic Proteins Amino Acids, Diamino Rotenone Serine Proteases Green Fluorescent Proteins Ubiquitin-Protein Ligases RNA, Messenger Proteins Tyrosine 3-Monooxygenase Presenilin-1 Biological Markers Central Nervous System Agents DNA-Binding Proteins Drosophila Proteins Membrane Proteins Glycogen Synthase Kinase 3 Iron Thiazoles HSP70 Heat-Shock Proteins Enzyme Inhibitors Caspase 3 Nerve Growth Factors Survival of Motor Neuron 1 Protein Protein Isoforms HSP40 Heat-Shock Proteins Fragile X Mental Retardation Protein Heat-Shock Proteins Propionates Hydrogen Peroxide Receptors, N-Methyl-D-Aspartate

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

Disease Models, Animal Models, Biological Rotarod Performance Test Immunohistochemistry Blotting, Western Magnetic Resonance Imaging Analysis of Variance Microscopy, Electron, Transmission Silver Staining Transfection Models, Molecular Stem Cell Transplantation Neuroimaging Pedigree Primary Cell Culture Gene Knock-In Techniques

Psychiatry and Psychology18

Huntington Disease Alzheimer Disease Frontotemporal Dementia Frontotemporal Lobar Degeneration Lewy Body Disease Dementia Pick Disease of the Brain Creutzfeldt-Jakob Syndrome Cognition Disorders Behavior, Animal Motor Activity Maze Learning Neuropsychological Tests Aphasia, Primary Progressive REM Sleep Behavior Disorder Apraxias Memory Memory Disorders

Phenomena and Processes40

Trinucleotide Repeat Expansion Cell Death Mutation Oxidative Stress Autophagy Aging Trinucleotide Repeats Protein Folding Axonal Transport Cell Survival Signal Transduction Gene Expression Regulation Apoptosis Phenotype DNA Repeat Expansion Protein Binding Brain Chemistry Amino Acid Sequence Protein Transport Neurogenesis Motor Activity Phosphorylation Time Factors Cytoprotection Mutation, Missense Protein Multimerization Mitochondrial Dynamics Oxidation-Reduction Proteolysis Protein Structure, Tertiary Gene Expression Transfection Protein Structure, Quaternary Dose-Response Relationship, Drug Up-Regulation Homeostasis Hormesis Cell Differentiation Protein Structure, Secondary Genetic Predisposition to Disease

Disciplines and Occupations1

Immunohistochemistry

Information Science2

Molecular Sequence Data Amino Acid Sequence

Health Care2

Analysis of Variance Age of Onset

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Health Care Geographicals

Neurodegenerative Diseases Nerve Degeneration Huntington Disease Alzheimer Disease Neurons Brain Parkinson Disease alpha-Synuclein tau Proteins Amyotrophic Lateral Sclerosis Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Tauopathies Neuroprotective Agents Disease Models, Animal Inclusion Bodies Synucleins Amyloid beta-Peptides Prions Spinocerebellar Ataxias Mice, Transgenic Microglia Prion Diseases Trinucleotide Repeat Expansion Proteostasis Deficiencies Neuronal Ceroid-Lipofuscinoses Cell Death Mutation Oxidative Stress Frontotemporal Dementia Frontotemporal Lobar Degeneration Parkinsonian Disorders Mitochondria Friedreich Ataxia Lewy Body Disease Autophagy Dementia Amyloid Aging Trinucleotide Repeats Neurotoxins Neurofibrillary Tangles Cells, Cultured Lewy Bodies Astrocytes Peptides Mice, Inbred C57BL Protein Folding Hippocampus Guam Substantia Nigra Ataxia Models, Biological beta-Synuclein Superoxide Dismutase Intranuclear Inclusion Bodies Cerebral Cortex Multiple System Atrophy Supranuclear Palsy, Progressive Dopaminergic Neurons Neuroglia Mitochondrial Diseases Axonal Transport Central Nervous System Ubiquitin Pick Disease of the Brain Machado-Joseph Disease Nuclear Proteins Proteasome Endopeptidase Complex Atrophy Amyloid beta-Protein Precursor Cell Survival Central Nervous System Diseases Signal Transduction Motor Neurons Nervous System Diseases Iron-Binding Proteins Gliosis PrPSc Proteins Motor Neuron Disease PrPC Proteins Corpus Striatum Rotarod Performance Test Gene Expression Regulation Apoptosis Spinocerebellar Degenerations Plaque, Amyloid Immunohistochemistry Muscular Atrophy, Spinal Phenotype Creutzfeldt-Jakob Syndrome Molecular Chaperones Animals, Genetically Modified Blotting, Western Reactive Oxygen Species Nitro Compounds Cyclin-Dependent Kinase 5 Mice, Knockout Cerebellum Axons

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