Protein amyloid tau proteins. Medical search. Frequent questions

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Anatomy14

Neurofibrillary Tangles Brain Neurofibrils Microtubules Neurons Neuropil Threads Hippocampus Cerebral Cortex Neurites Chromosomes, Human, Pair 17 PC12 Cells Inclusion Bodies Axons Cells, Cultured

Organisms2

Mice, Transgenic Cattle

Diseases17

Prion Diseases Alzheimer Disease Tauopathies Plaque, Amyloid Amyloidosis Cerebral Amyloid Angiopathy Amyloid Neuropathies Pick Disease of the Brain Nerve Degeneration Amyloid Neuropathies, Familial Neurodegenerative Diseases Disease Models, Animal Dementia Cerebral Amyloid Angiopathy, Familial Creutzfeldt-Jakob Syndrome Supranuclear Palsy, Progressive Amyloidosis, Familial

Chemicals and Drugs34

tau Proteins Amyloid Prions Amyloid beta-Peptides Serum Amyloid A Protein Amyloid beta-Protein Precursor Islet Amyloid Polypeptide Cyclin-Dependent Kinase 5 Serum Amyloid P-Component Microtubule-Associated Proteins Amyloid Precursor Protein Secretases Glycogen Synthase Kinase 3 Peptide Fragments Congo Red Tubulin Nerve Tissue Proteins Thiazoles Prealbumin S100 Calcium Binding Protein beta Subunit Protein Isoforms Glycogen Synthase Kinases Recombinant Proteins Presenilin-1 Aspartic Acid Endopeptidases Sarcosine Okadaic Acid Proline-Directed Protein Kinases Neurofilament Proteins Proline Serine Protein Phosphatase 2 Peptides Biological Markers Calcium-Calmodulin-Dependent Protein Kinases

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

Microscopy, Electron Disease Models, Animal Blotting, Western Immunohistochemistry Microscopy, Electron, Transmission Electrophoresis, Polyacrylamide Gel Immunoblotting Microscopy, Atomic Force Models, Molecular Amino Acid Substitution

Psychiatry and Psychology4

Alzheimer Disease Pick Disease of the Brain Dementia Creutzfeldt-Jakob Syndrome

Phenomena and Processes18

Phosphorylation Brain Chemistry Amino Acid Sequence Protein Binding Protein Structure, Secondary Mutation Protein Multimerization Solubility Protein Conformation Protein Folding Kinetics Chromosomes, Human, Pair 17 Protein Structure, Tertiary Axonal Transport Amino Acid Substitution Time Factors Repetitive Sequences, Amino Acid Aging

Disciplines and Occupations1

Immunohistochemistry

Information Science2

Amino Acid Sequence Molecular Sequence Data

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 Geographicals

tau Proteins Amyloid Prions Prion Diseases Amyloid beta-Peptides Neurofibrillary Tangles Alzheimer Disease Serum Amyloid A Protein Amyloid beta-Protein Precursor Tauopathies Plaque, Amyloid Islet Amyloid Polypeptide Amyloidosis Brain Cerebral Amyloid Angiopathy Neurofibrils Cyclin-Dependent Kinase 5 Microtubules Serum Amyloid P-Component Phosphorylation Microtubule-Associated Proteins Amyloid Neuropathies Amyloid Precursor Protein Secretases Glycogen Synthase Kinase 3 Pick Disease of the Brain Peptide Fragments Congo Red Mice, Transgenic Neurons Tubulin Brain Chemistry Neuropil Threads Nerve Degeneration Amyloid Neuropathies, Familial Neurodegenerative Diseases Amino Acid Sequence Molecular Sequence Data Nerve Tissue Proteins Thiazoles Prealbumin Microscopy, Electron Disease Models, Animal Dementia S100 Calcium Binding Protein beta Subunit Hippocampus Guam Protein Isoforms Glycogen Synthase Kinases Protein Binding Recombinant Proteins Presenilin-1 Protein Structure, Secondary Mutation Aspartic Acid Endopeptidases Sarcosine Blotting, Western Cattle Immunohistochemistry Cerebral Cortex Microscopy, Electron, Transmission Electrophoresis, Polyacrylamide Gel Protein Multimerization Immunoblotting Solubility Protein Conformation Microscopy, Atomic Force Okadaic Acid Proline-Directed Protein Kinases Neurofilament Proteins Proline Protein Folding Kinetics Serine Neurites Cerebral Amyloid Angiopathy, Familial Creutzfeldt-Jakob Syndrome Protein Phosphatase 2 Chromosomes, Human, Pair 17 Protein Structure, Tertiary Supranuclear Palsy, Progressive PC12 Cells Inclusion Bodies Peptides Axons Biological Markers Cells, Cultured Axonal Transport Amyloidosis, Familial Calcium-Calmodulin-Dependent Protein Kinases Models, Molecular Amino Acid Substitution Time Factors Repetitive Sequences, Amino Acid Aging

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