Genetic neurodegenerative disease susceptibility. Medical search. Frequent questions

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Anatomy26

Brain Neurons Inclusion Bodies Microglia Cells, Cultured Mitochondria Neurofibrillary Tangles Astrocytes Cell Line Chromosomes, Human, Pair 6 Central Nervous System Lewy Bodies Hippocampus Motor Neurons Cerebral Cortex Neuroglia Substantia Nigra Axons Spinal Cord Dopaminergic Neurons Corpus Striatum Intranuclear Inclusion Bodies Cerebellum Chromosomes, Human, Pair 2 Lysosomes PC12 Cells

Organisms12

Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Cycas Mice, Inbred Strains Pseudomonas syringae Animals, Genetically Modified Arabidopsis Peronospora Rats, Sprague-Dawley Mice, Inbred BALB C Mice, Congenic

Diseases59

Neurodegenerative Diseases Disease Susceptibility Genetic Predisposition to Disease Nerve Degeneration Alzheimer Disease Amyotrophic Lateral Sclerosis Huntington Disease Parkinson Disease Disease Models, Animal Tauopathies Prion Diseases Heredodegenerative Disorders, Nervous System Proteostasis Deficiencies Spinocerebellar Ataxias Frontotemporal Lobar Degeneration Frontotemporal Dementia Friedreich Ataxia Crohn Disease Neuronal Ceroid-Lipofuscinoses Dementia Genetic Diseases, Inborn Lewy Body Disease Parkinsonian Disorders Disease Autoimmune Diseases Mitochondrial Diseases Motor Neuron Disease Supranuclear Palsy, Progressive Central Nervous System Diseases Diabetes Mellitus, Type 1 Inflammation Lupus Erythematosus, Systemic Muscular Atrophy, Spinal Multiple Sclerosis Pick Disease of the Brain Gliosis Nervous System Diseases Disease Resistance Disease Progression Plaque, Amyloid Multiple System Atrophy Encephalomyelitis, Autoimmune, Experimental Inflammatory Bowel Diseases Parkinson Disease, Secondary Atrophy Encephalitis Creutzfeldt-Jakob Syndrome TDP-43 Proteinopathies Ataxia Scrapie Neuroaxonal Dystrophies Trauma, Nervous System Machado-Joseph Disease Brain Diseases Neurotoxicity Syndromes Arthritis, Rheumatoid Spinocerebellar Degenerations Wallerian Degeneration Celiac Disease

Chemicals and Drugs61

tau Proteins alpha-Synuclein Nerve Tissue Proteins Prions Neuroprotective Agents Genetic Markers Synucleins Amyloid beta-Peptides HLA-DQ Antigens Nod2 Signaling Adaptor Protein HLA-DRB1 Chains HLA-DR3 Antigen HLA-DQ beta-Chains Amyloid Complement C4a HLA-DR Antigens Anti-Bacterial Agents Peptides Superoxide Dismutase Neurotoxins Salicylic Acid Ubiquitin HLA Antigens Iron-Binding Proteins Proteasome Endopeptidase Complex Nuclear Proteins RNA, Messenger Reactive Oxygen Species DNA-Binding Proteins RNA-Binding Protein FUS Carrier Proteins Membrane Proteins Peptide Fragments PrPSc Proteins Molecular Chaperones Antioxidants beta-Synuclein Biological Markers Amino Acids, Diamino Cyclin-Dependent Kinase 5 PrPC Proteins Amyloid beta-Protein Precursor Neurofilament Proteins DNA Primers Nitro Compounds Dopamine Glial Fibrillary Acidic Protein Receptor, EphA1 Cytokines Complement C4 Amyloidogenic Proteins Autoantibodies 1-Methyl-4-phenylpyridinium Mutant Proteins Arabidopsis Proteins Complement C2 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Mitochondrial Proteins Microtubule-Associated Proteins DNA gamma-Synuclein

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

Disease Models, Animal Genome-Wide Association Study Case-Control Studies Chromosome Mapping Microbial Sensitivity Tests Models, Genetic Genetic Association Studies Models, Biological Pedigree Genetic Testing Gene Expression Profiling Polymerase Chain Reaction Oligonucleotide Array Sequence Analysis Sequence Analysis, DNA Immunohistochemistry Blotting, Western Crosses, Genetic Risk Factors Analysis of Variance Encephalomyelitis, Autoimmune, Experimental Rotarod Performance Test Reverse Transcriptase Polymerase Chain Reaction Physical Chromosome Mapping Reproducibility of Results Cohort Studies Magnetic Resonance Imaging Amino Acid Substitution Models, Molecular DNA Mutational Analysis

Psychiatry and Psychology9

Alzheimer Disease Huntington Disease Frontotemporal Lobar Degeneration Frontotemporal Dementia Dementia Lewy Body Disease Pick Disease of the Brain Creutzfeldt-Jakob Syndrome Cognition Disorders

Phenomena and Processes64

Disease Susceptibility Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genotype Alleles Haplotypes Polymorphism, Genetic Mutation Gene Frequency Phenotype Genetic Variation Linkage Disequilibrium Genetic Linkage Genetic Markers Cell Death Oxidative Stress Genome, Human Aging Trinucleotide Repeat Expansion Gene Expression Regulation Signal Transduction Immunity, Innate Epistasis, Genetic Autophagy Amino Acid Sequence Plant Diseases Genetic Loci Protein Folding Chromosomes, Human, Pair 6 Base Sequence Genes, MHC Class II Apoptosis Trinucleotide Repeats Axonal Transport Cell Survival Time Factors Quantitative Trait Loci Microsatellite Repeats Plant Immunity Species Specificity Gene Expression Protein Binding Heterozygote Homozygote Major Histocompatibility Complex Disease Resistance Exons DNA Repeat Expansion Epigenesis, Genetic Gene Dosage Lod Score Amino Acid Substitution Chromosomes, Human, Pair 2 Mutation, Missense Drug Resistance, Bacterial Promoter Regions, Genetic Neurogenesis Drug Resistance, Microbial Genetic Heterogeneity Brain Chemistry Hormesis Multifactorial Inheritance Oxidation-Reduction Protein Transport

Disciplines and Occupations3

Immunohistochemistry Genetics, Population Computational Biology

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Named Groups2

European Continental Ancestry Group Asian Continental Ancestry Group

Health Care8

Genome-Wide Association Study Case-Control Studies Age of Onset Genetic Testing Risk Factors Analysis of Variance Reproducibility of Results Cohort Studies

Geographicals2

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

Neurodegenerative Diseases Disease Susceptibility Genetic Predisposition to Disease Nerve Degeneration Polymorphism, Single Nucleotide Alzheimer Disease Genotype Brain Amyotrophic Lateral Sclerosis Alleles Neurons Haplotypes tau Proteins Huntington Disease Parkinson Disease alpha-Synuclein Polymorphism, Genetic Disease Models, Animal Mutation Genome-Wide Association Study Gene Frequency Nerve Tissue Proteins Prions Tauopathies Neuroprotective Agents Case-Control Studies Prion Diseases Mice, Transgenic Phenotype Genetic Variation Inclusion Bodies Linkage Disequilibrium Heredodegenerative Disorders, Nervous System Proteostasis Deficiencies Mice, Inbred C57BL Genetic Linkage Chromosome Mapping Microglia Microbial Sensitivity Tests Genetic Markers Molecular Sequence Data Synucleins Cell Death Oxidative Stress Amyloid beta-Peptides Spinocerebellar Ataxias Frontotemporal Lobar Degeneration Cells, Cultured Genome, Human Aging Trinucleotide Repeat Expansion Mitochondria Gene Expression Regulation Frontotemporal Dementia Friedreich Ataxia HLA-DQ Antigens Signal Transduction Immunity, Innate Models, Genetic Genetic Association Studies Nod2 Signaling Adaptor Protein Epistasis, Genetic Autophagy Crohn Disease Models, Biological HLA-DRB1 Chains Amino Acid Sequence Guam HLA-DR3 Antigen HLA-DQ beta-Chains Amyloid Neuronal Ceroid-Lipofuscinoses Complement C4a Plant Diseases Mice, Knockout HLA-DR Antigens Genetic Loci Anti-Bacterial Agents Protein Folding Peptides Pedigree Dementia Neurofibrillary Tangles Genetic Diseases, Inborn Superoxide Dismutase Astrocytes Neurotoxins Lewy Body Disease Age of Onset Parkinsonian Disorders Cell Line Bahrain Chromosomes, Human, Pair 6 Salicylic Acid Genetic Testing Disease Base Sequence Genes, MHC Class II Central Nervous System Apoptosis

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