Genetic locus and neurodegenerative disease disease susceptibility. Medical search. Frequent questions

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Anatomy28

Brain Neurons Inclusion Bodies Microglia Cells, Cultured Mitochondria Cell Line Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 2 Neurofibrillary Tangles Astrocytes Central Nervous System Lewy Bodies Hippocampus Motor Neurons Chromosomes, Human, Pair 5 Cerebral Cortex Chromosomes, Mammalian Chromosomes, Human Neuroglia Substantia Nigra Spinal Cord Chromosomes, Human, Pair 1 Axons Dopaminergic Neurons Corpus Striatum Intranuclear Inclusion Bodies Cerebellum

Organisms14

Mice, Transgenic Mice, Inbred C57BL Mice, Inbred Strains Mice, Congenic Mice, Knockout Arabidopsis Animals, Genetically Modified Cycas Mice, Inbred BALB C Drosophila melanogaster Pseudomonas syringae Mice, Inbred DBA Escherichia coli Peronospora

Diseases50

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

Chemicals and Drugs52

Genetic Markers tau Proteins alpha-Synuclein Nerve Tissue Proteins Prions Neuroprotective Agents Synucleins Amyloid beta-Peptides HLA-DQ Antigens Nod2 Signaling Adaptor Protein HLA-DRB1 Chains HLA-DQ beta-Chains Anti-Bacterial Agents HLA-DR3 Antigen HLA-DR Antigens Peptides Complement C4a Amyloid RNA, Messenger DNA Primers Superoxide Dismutase Neurotoxins Membrane Proteins DNA Salicylic Acid DNA-Binding Proteins Carrier Proteins Nuclear Proteins HLA Antigens Ubiquitin Proteasome Endopeptidase Complex Iron-Binding Proteins Transcription Factors Reactive Oxygen Species Bacterial Proteins RNA-Binding Protein FUS Peptide Fragments Molecular Chaperones PrPSc Proteins Proteins Antioxidants Biological Markers beta-Synuclein Cyclin-Dependent Kinase 5 Autoantibodies Amino Acids, Diamino PrPC Proteins DNA, Bacterial Amyloid beta-Protein Precursor Arabidopsis Proteins Neurofilament Proteins DNA Transposable Elements

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

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

Psychiatry and Psychology8

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

Phenomena and Processes78

Disease Susceptibility Genetic Loci Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genotype Genetic Linkage Quantitative Trait Loci Alleles Phenotype Mutation Polymorphism, Genetic Genetic Markers Haplotypes Gene Frequency Genetic Variation Linkage Disequilibrium Genome, Human Lod Score Microsatellite Repeats Base Sequence Amino Acid Sequence Gene Expression Regulation Epistasis, Genetic Cell Death Oxidative Stress Immunity, Innate Species Specificity Signal Transduction Aging Trinucleotide Repeat Expansion Quantitative Trait, Heritable Heterozygote Plant Diseases Autophagy Homozygote Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 2 Gene Expression Protein Folding Genes, Dominant Genetic Heterogeneity Genes, MHC Class II Time Factors Polymorphism, Restriction Fragment Length Exons Major Histocompatibility Complex Multifactorial Inheritance Apoptosis Trinucleotide Repeats Protein Binding Genes, Bacterial Axonal Transport Cell Survival Gene Dosage Genes Promoter Regions, Genetic Chromosomes, Human, Pair 5 Drug Resistance, Microbial Plant Immunity Epigenesis, Genetic Chromosomes, Mammalian Genome Transcription, Genetic Chromosomes, Human Mutagenesis, Insertional Phylogeny Disease Resistance Mutation, Missense Genes, Plant Selection, Genetic Algorithms Chromosomes, Human, Pair 1 Recombination, Genetic Evolution, Molecular DNA Repeat Expansion Multigene Family Amino Acid Substitution DNA Transposable Elements

Disciplines and Occupations4

Genetics, Population Immunohistochemistry Genomics Computational Biology

Information Science7

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Algorithms Databases, Genetic Computer Simulation

Named Groups2

European Continental Ancestry Group Asian Continental Ancestry Group

Health Care9

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

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 Loci Genetic Predisposition to Disease Chromosome Mapping Polymorphism, Single Nucleotide Genotype Genetic Linkage Genome-Wide Association Study Quantitative Trait Loci Alleles Phenotype Mutation Nerve Degeneration Polymorphism, Genetic Genetic Markers Haplotypes Alzheimer Disease Brain Amyotrophic Lateral Sclerosis Neurons Gene Frequency Genetic Variation Disease Models, Animal Molecular Sequence Data Huntington Disease tau Proteins Parkinson Disease alpha-Synuclein Linkage Disequilibrium Case-Control Studies Crosses, Genetic Mice, Transgenic Nerve Tissue Proteins Mice, Inbred C57BL Pedigree Models, Genetic Prions Tauopathies Neuroprotective Agents Prion Diseases Genome, Human Lod Score Microsatellite Repeats Base Sequence Inclusion Bodies Heredodegenerative Disorders, Nervous System Amino Acid Sequence Proteostasis Deficiencies Microglia Genetic Association Studies Gene Expression Regulation Microbial Sensitivity Tests Sequence Analysis, DNA Epistasis, Genetic Cells, Cultured Synucleins Cell Death Oxidative Stress Amyloid beta-Peptides Spinocerebellar Ataxias Polymerase Chain Reaction Immunity, Innate Frontotemporal Lobar Degeneration Species Specificity Signal Transduction Aging Models, Biological Mice, Inbred Strains Trinucleotide Repeat Expansion Mitochondria HLA-DQ Antigens Quantitative Trait, Heritable Frontotemporal Dementia Friedreich Ataxia Mice, Congenic Genetics, Population Heterozygote Age of Onset Mice, Knockout Cell Line Crohn Disease Plant Diseases Nod2 Signaling Adaptor Protein HLA-DRB1 Chains Genetic Testing Autophagy HLA-DQ beta-Chains Homozygote Chromosomes, Human, Pair 6 Anti-Bacterial Agents HLA-DR3 Antigen Gene Expression Profiling European Continental Ancestry Group HLA-DR Antigens Peptides Guam Complement C4a Neuronal Ceroid-Lipofuscinoses Amyloid

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