Neurodegeneration prion diseases. Medical search. Frequent questions

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Anatomy15

Brain Neurons Microglia Hippocampus Astrocytes Dendritic Cells, Follicular Dopaminergic Neurons Cells, Cultured Cerebellum Substantia Nigra Inclusion Bodies Central Nervous System Neurofibrillary Tangles Cell Line Mitochondria

Organisms10

Deer Mice, Transgenic Mesocricetus Sheep Mice, Inbred C57BL Cricetinae Cattle Mice, Knockout Ruminants Animals, Genetically Modified

Diseases29

Prion Diseases Creutzfeldt-Jakob Syndrome Scrapie Nerve Degeneration Neurodegenerative Diseases Insomnia, Fatal Familial Gerstmann-Straussler-Scheinker Disease Wasting Disease, Chronic Encephalopathy, Bovine Spongiform Kuru Disease Models, Animal Pantothenate Kinase-Associated Neurodegeneration Proteostasis Deficiencies Alzheimer Disease Gliosis Heredodegenerative Disorders, Nervous System Parkinson Disease Tauopathies Huntington Disease Plaque, Amyloid Slow Virus Diseases Neuroblastoma Parkinsonian Disorders Neurotoxicity Syndromes Dementia Disease Progression Spinocerebellar Ataxias Neuroaxonal Dystrophies Amyotrophic Lateral Sclerosis

Chemicals and Drugs32

Prions PrPSc Proteins PrPC Proteins Endopeptidase K Amyloid tau Proteins Amyloidogenic Proteins Amyloid beta-Peptides Quinacrine PrP 27-30 Protein Nerve Tissue Proteins Neuroprotective Agents alpha-Synuclein Bentonite Protein Isoforms Peptide Fragments Copper Glial Fibrillary Acidic Protein Neurotoxins Peptides Codon Pentosan Sulfuric Polyester Glycosylphosphatidylinositols Recombinant Proteins Congo Red Mutant Proteins 14-3-3 Proteins Amyloid beta-Protein Precursor GPI-Linked Proteins Dopamine Detergents 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

Disease Models, Animal Blotting, Western Immunohistochemistry Models, Biological Models, Molecular Microscopy, Electron, Transmission Circular Dichroism

Psychiatry and Psychology5

Creutzfeldt-Jakob Syndrome Alzheimer Disease Huntington Disease Behavior, Animal Dementia

Phenomena and Processes25

Protein Folding Mutation Cell Death Brain Chemistry Protein Conformation Phenotype Time Factors Amino Acid Sequence Protein Binding Species Specificity Oxidative Stress Repetitive Sequences, Amino Acid Protein Structure, Secondary Codon Protein Structure, Tertiary Autophagy Apoptosis Protein Structure, Quaternary Protein Transport Proteolysis Gene Expression Regulation Glycosylation Aging Cell Survival Signal Transduction

Disciplines and Occupations1

Immunohistochemistry

Technology, Industry, Agriculture1

Information Science2

Molecular Sequence Data Amino Acid Sequence

Health Care1

Infectious Disease Incubation Period

Geographicals1

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

Prion Diseases Prions PrPSc Proteins PrPC Proteins Creutzfeldt-Jakob Syndrome Scrapie Nerve Degeneration Neurodegenerative Diseases Endopeptidase K Insomnia, Fatal Familial Gerstmann-Straussler-Scheinker Disease Brain Wasting Disease, Chronic Encephalopathy, Bovine Spongiform Kuru Amyloid Neurons Deer Mice, Transgenic Infectious Disease Incubation Period Disease Models, Animal Protein Folding Pantothenate Kinase-Associated Neurodegeneration Mesocricetus Proteostasis Deficiencies Microglia Sheep tau Proteins Alzheimer Disease Mice, Inbred C57BL Cricetinae Mutation Gliosis Blotting, Western Amyloidogenic Proteins Cell Death Brain Chemistry Amyloid beta-Peptides Quinacrine PrP 27-30 Protein Immunohistochemistry Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Protein Conformation Neuroprotective Agents alpha-Synuclein Parkinson Disease Cattle Mice, Knockout Tauopathies Bentonite Hippocampus Phenotype Protein Isoforms Astrocytes Huntington Disease Dendritic Cells, Follicular Ruminants Peptide Fragments Time Factors Copper Dopaminergic Neurons Cells, Cultured Plaque, Amyloid Libya Molecular Sequence Data Slow Virus Diseases Cerebellum Neuroblastoma Substantia Nigra Inclusion Bodies Glial Fibrillary Acidic Protein Central Nervous System Amino Acid Sequence Neurotoxins Models, Biological Protein Binding Peptides Parkinsonian Disorders Animals, Genetically Modified Species Specificity Oxidative Stress Repetitive Sequences, Amino Acid Protein Structure, Secondary Codon Pentosan Sulfuric Polyester Glycosylphosphatidylinositols Protein Structure, Tertiary Recombinant Proteins Neurofibrillary Tangles Behavior, Animal Autophagy Cell Line Congo Red Neurotoxicity Syndromes Apoptosis Mutant Proteins Protein Structure, Quaternary Dementia 14-3-3 Proteins

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