Neurodegenerative diseases termed tauopathies. Medical search. Frequent questions

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Anatomy18

Neurofibrillary Tangles Brain Neurons Inclusion Bodies Neurofibrils Microtubules Microglia Cells, Cultured Hippocampus Cerebral Cortex Neuroglia Mitochondria Axons Spinal Cord Astrocytes Lewy Bodies Central Nervous System Motor Neurons

Organisms4

Mice, Transgenic Animals, Genetically Modified Mice, Inbred C57BL Cycas

Diseases25

Tauopathies Neurodegenerative Diseases Pick Disease of the Brain Alzheimer Disease Nerve Degeneration Supranuclear Palsy, Progressive Heredodegenerative Disorders, Nervous System Parkinson Disease Disease Models, Animal Amyotrophic Lateral Sclerosis Frontotemporal Dementia Huntington Disease Dementia Parkinsonian Disorders Proteostasis Deficiencies Prion Diseases Spinocerebellar Ataxias Frontotemporal Lobar Degeneration Friedreich Ataxia Neuronal Ceroid-Lipofuscinoses Lewy Body Disease Motor Neuron Disease Mitochondrial Diseases Central Nervous System Diseases Muscular Atrophy, Spinal

Chemicals and Drugs22

tau Proteins alpha-Synuclein Nerve Tissue Proteins Amyloidogenic Proteins Neuroprotective Agents Protein Isoforms Cyclin-Dependent Kinase 5 Glycogen Synthase Kinase 3 Prions Synucleins Amyloid beta-Peptides Microtubule-Associated Proteins Epothilones Tubulin Modulators Amyloid Peptides Neurotoxins Superoxide Dismutase Ubiquitin Iron-Binding Proteins Proteasome Endopeptidase Complex RNA-Binding Protein FUS

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Disease Models, Animal Models, Biological Immunohistochemistry Blotting, Western Drug Evaluation, Preclinical

Psychiatry and Psychology7

Pick Disease of the Brain Alzheimer Disease Frontotemporal Dementia Huntington Disease Dementia Frontotemporal Lobar Degeneration Lewy Body Disease

Phenomena and Processes16

Mutation Phosphorylation Axonal Transport Cell Death Aging Oxidative Stress Trinucleotide Repeat Expansion Autophagy Protein Folding Protein Binding Alternative Splicing Trinucleotide Repeats Exons Signal Transduction Cell Survival Solubility

Disciplines and Occupations1

Immunohistochemistry

Geographicals1

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

Tauopathies Neurodegenerative Diseases tau Proteins Neurofibrillary Tangles Pick Disease of the Brain Alzheimer Disease Nerve Degeneration Supranuclear Palsy, Progressive Brain Neurons Inclusion Bodies Heredodegenerative Disorders, Nervous System Mice, Transgenic Parkinson Disease Disease Models, Animal alpha-Synuclein Amyotrophic Lateral Sclerosis Frontotemporal Dementia Huntington Disease Neurofibrils Nerve Tissue Proteins Dementia Mutation Phosphorylation Amyloidogenic Proteins Parkinsonian Disorders Axonal Transport Neuroprotective Agents Cell Death Proteostasis Deficiencies Microtubules Protein Isoforms Cyclin-Dependent Kinase 5 Glycogen Synthase Kinase 3 Microglia Prions Animals, Genetically Modified Prion Diseases Synucleins Amyloid beta-Peptides Models, Biological Aging Spinocerebellar Ataxias Frontotemporal Lobar Degeneration Oxidative Stress Immunohistochemistry Cells, Cultured Mice, Inbred C57BL Microtubule-Associated Proteins Hippocampus Cerebral Cortex Trinucleotide Repeat Expansion Neuroglia Epothilones Friedreich Ataxia Mitochondria Autophagy Axons Blotting, Western Spinal Cord Neuronal Ceroid-Lipofuscinoses Guam Tubulin Modulators Amyloid Protein Folding Protein Binding Lewy Body Disease Astrocytes Peptides Drug Evaluation, Preclinical Neurotoxins Superoxide Dismutase Lewy Bodies Alternative Splicing Central Nervous System Trinucleotide Repeats Motor Neuron Disease Mitochondrial Diseases Motor Neurons Ubiquitin Central Nervous System Diseases Cycas Iron-Binding Proteins Proteasome Endopeptidase Complex Exons Muscular Atrophy, Spinal Signal Transduction Cell Survival Solubility RNA-Binding Protein FUS

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