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

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Anatomy26

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

Organisms15

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

Diseases53

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 Friedreich Ataxia Frontotemporal Dementia Crohn Disease Genetic Diseases, Inborn Neuronal Ceroid-Lipofuscinoses Dementia Disease Lewy Body Disease Parkinsonian Disorders Autoimmune Diseases Diabetes Mellitus, Type 1 Lupus Erythematosus, Systemic Mitochondrial Diseases Motor Neuron Disease Supranuclear Palsy, Progressive Central Nervous System Diseases Multiple Sclerosis Inflammation Muscular Atrophy, Spinal Pick Disease of the Brain Disease Progression Nervous System Diseases Gliosis Disease Resistance Plaque, Amyloid Multiple System Atrophy Encephalomyelitis, Autoimmune, Experimental Atrophy Inflammatory Bowel Diseases Parkinson Disease, Secondary Encephalitis Creutzfeldt-Jakob Syndrome TDP-43 Proteinopathies Scrapie Neuroaxonal Dystrophies Ataxia Spinocerebellar Degenerations Arthritis, Rheumatoid

Chemicals and Drugs50

Genetic Markers tau Proteins alpha-Synuclein Nerve Tissue Proteins Prions Neuroprotective Agents Synucleins Amyloid beta-Peptides HLA-DQ Antigens HLA-DRB1 Chains HLA-DQ beta-Chains Nod2 Signaling Adaptor Protein HLA-DR Antigens HLA-DR3 Antigen Complement C4a Amyloid Peptides Anti-Bacterial Agents Superoxide Dismutase RNA, Messenger DNA-Binding Proteins HLA Antigens Neurotoxins DNA Primers Salicylic Acid Nuclear Proteins DNA Carrier Proteins Membrane Proteins Ubiquitin Proteasome Endopeptidase Complex Iron-Binding Proteins Transcription Factors Reactive Oxygen Species RNA-Binding Protein FUS Peptide Fragments Molecular Chaperones PrPSc Proteins Arabidopsis Proteins Antioxidants Biological Markers Cyclin-Dependent Kinase 5 Proteins beta-Synuclein Amino Acids, Diamino PrPC Proteins Amyloid beta-Protein Precursor Neurofilament Proteins Dopamine Complement C4

Analytical, Diagnostic and Therapeutic Techniques and Equipment31

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

Psychiatry and Psychology9

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

Phenomena and Processes74

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

Disciplines and Occupations4

Genetics, Population Immunohistochemistry Computational Biology Genomics

Anthropology, Education, Sociology and Social Phenomena1

Information Science7

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

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 Analysis of Variance Cohort Studies Reproducibility of Results Family Health

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

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