Neurodegenerative trinucleotide. Medical search. Frequent questions

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Anatomy28

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

Organisms7

Mice, Transgenic Saccharomyces cerevisiae Mice, Inbred C57BL Escherichia coli Animals, Genetically Modified Mice, Knockout Cycas

Diseases53

Neurodegenerative Diseases Huntington Disease Friedreich Ataxia Fragile X Syndrome Spinocerebellar Degenerations Heredodegenerative Disorders, Nervous System Nerve Degeneration Machado-Joseph Disease Alzheimer Disease Parkinson Disease Disease Models, Animal Amyotrophic Lateral Sclerosis Genomic Instability Tauopathies Cerebellar Ataxia Anticipation, Genetic Muscular Dystrophy, Oculopharyngeal Ataxia Chromosome Fragility Genetic Diseases, Inborn Spinocerebellar Ataxias Muscular Atrophy, Spinal Prion Diseases Nervous System Diseases Proteostasis Deficiencies Neuronal Ceroid-Lipofuscinoses Frontotemporal Dementia Frontotemporal Lobar Degeneration Parkinsonian Disorders Lewy Body Disease Dementia Multiple System Atrophy Supranuclear Palsy, Progressive Mitochondrial Diseases Pick Disease of the Brain Atrophy Central Nervous System Diseases Gliosis Motor Neuron Disease Genetic Predisposition to Disease Plaque, Amyloid Creutzfeldt-Jakob Syndrome Encephalitis Neurotoxicity Syndromes Intellectual Disability Parkinson Disease, Secondary Brain Diseases Niemann-Pick Disease, Type C Lysosomal Storage Diseases, Nervous System Myoclonic Epilepsies, Progressive TDP-43 Proteinopathies Scrapie Neuroaxonal Dystrophies

Chemicals and Drugs66

Fragile X Mental Retardation Protein Nerve Tissue Proteins alpha-Synuclein DNA tau Proteins Iron-Binding Proteins Peptides Neuroprotective Agents Nuclear Proteins RNA-Binding Proteins Oligonucleotides Flap Endonucleases Synucleins Amyloid beta-Peptides Prions Receptors, Androgen RNA, Messenger DNA Primers Oligodeoxyribonucleotides Nucleic Acid Heteroduplexes Nucleotides RNA DNA-Binding Proteins Proteins Guanine Amyloid Neurotoxins Codon Oligoribonucleotides Genetic Markers Polydeoxyribonucleotides Saccharomyces cerevisiae Proteins Transcription Factors beta-Synuclein Superoxide Dismutase Ubiquitin DNA, Satellite Proteasome Endopeptidase Complex Amyloid beta-Protein Precursor PrPSc Proteins PrPC Proteins DNA, Complementary MutS Homolog 2 Protein Protein-Serine-Threonine Kinases Endodeoxyribonucleases Molecular Chaperones Adenine Reactive Oxygen Species Nitro Compounds DNA, Plant Cyclin-Dependent Kinase 5 Cytosine Dopamine 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Glial Fibrillary Acidic Protein DNA, Fungal RNA-Binding Protein FUS DNA, Single-Stranded Thiolester Hydrolases Antioxidants Neurofilament Proteins RNA, Transfer Repressor Proteins Oxidopamine Peptide Fragments Mutant Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Disease Models, Animal Pedigree Polymerase Chain Reaction Gene Knock-In Techniques Models, Genetic Sequence Analysis, DNA Models, Biological Models, Molecular Chromosome Mapping DNA Mutational Analysis Genetic Testing Cloning, Molecular Nucleic Acid Denaturation Rotarod Performance Test Circular Dichroism Magnetic Resonance Spectroscopy Transfection Immunohistochemistry Blotting, Western Blotting, Southern Magnetic Resonance Imaging Case-Control Studies

Psychiatry and Psychology12

Huntington Disease Alzheimer Disease Frontotemporal Dementia Frontotemporal Lobar Degeneration Lewy Body Disease Dementia Pick Disease of the Brain Creutzfeldt-Jakob Syndrome Fathers Intellectual Disability Cognition Disorders Behavior, Animal

Phenomena and Processes82

Trinucleotide Repeats Trinucleotide Repeat Expansion Base Sequence Repetitive Sequences, Nucleic Acid Mutation Alleles Nucleic Acid Conformation Microsatellite Repeats Genomic Instability Anticipation, Genetic Polymorphism, Genetic Phenotype Chromosome Fragility Minisatellite Repeats Inverted Repeat Sequences Cell Death Amino Acid Sequence Oxidative Stress DNA Repair Transcription, Genetic Chromosome Fragile Sites Dinucleotide Repeats Genotype Exons Tandem Repeat Sequences Heterozygote Genetic Variation Autophagy Gene Expression Regulation Point Mutation Aging Genome, Human Codon Genes, Dominant Protein Binding Genetic Markers Mosaicism DNA Replication Gene Frequency Protein Folding Chromosomes, Human, X Sequence Tagged Sites Sequence Deletion Binding Sites Gene Expression Mutagenesis Expressed Sequence Tags Axonal Transport DNA, Satellite X Chromosome Cell Survival Signal Transduction Templates, Genetic Genetic Predisposition to Disease Kinetics Nucleic Acid Denaturation Apoptosis Base Pairing Genetic Loci Promoter Regions, Genetic Transfection Genetic Linkage Protein Structure, Tertiary DNA Damage Haplotypes DNA Repeat Expansion Recombination, Genetic DNA, Single-Stranded Sequence Homology, Amino Acid Substrate Specificity Conserved Sequence Thermodynamics Evolution, Molecular Base Composition Genome, Fungal Brain Chemistry Base Pair Mismatch Protein Biosynthesis Species Specificity Plasmids Protein Transport RNA Splicing

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups1

Health Care3

Age of Onset Genetic Testing Case-Control Studies

Geographicals1

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

Trinucleotide Repeats Trinucleotide Repeat Expansion Neurodegenerative Diseases Huntington Disease Friedreich Ataxia Fragile X Syndrome Spinocerebellar Degenerations Heredodegenerative Disorders, Nervous System Fragile X Mental Retardation Protein Nerve Tissue Proteins Base Sequence Nerve Degeneration Machado-Joseph Disease Repetitive Sequences, Nucleic Acid Molecular Sequence Data Brain Neurons Mutation Alleles Nucleic Acid Conformation Alzheimer Disease Parkinson Disease alpha-Synuclein DNA Disease Models, Animal tau Proteins Microsatellite Repeats Iron-Binding Proteins Mice, Transgenic Amyotrophic Lateral Sclerosis Intranuclear Inclusion Bodies Peptides Genomic Instability Tauopathies Neuroprotective Agents Cerebellar Ataxia Age of Onset Nuclear Proteins Pedigree RNA-Binding Proteins Oligonucleotides Polymerase Chain Reaction Anticipation, Genetic Inclusion Bodies Polymorphism, Genetic Flap Endonucleases Muscular Dystrophy, Oculopharyngeal Ataxia Synucleins Phenotype Chromosome Fragility Amyloid beta-Peptides Prions Genetic Diseases, Inborn Spinocerebellar Ataxias Muscular Atrophy, Spinal Microglia Prion Diseases Nervous System Diseases Receptors, Androgen Minisatellite Repeats Proteostasis Deficiencies Gene Knock-In Techniques Neuronal Ceroid-Lipofuscinoses Inverted Repeat Sequences Cell Death Amino Acid Sequence RNA, Messenger Models, Genetic Sequence Analysis, DNA DNA Primers Oxidative Stress Oligodeoxyribonucleotides DNA Repair Nucleic Acid Heteroduplexes Transcription, Genetic Nucleotides Cells, Cultured Chromosome Fragile Sites Dinucleotide Repeats Genotype Frontotemporal Dementia RNA Frontotemporal Lobar Degeneration Cell Line Parkinsonian Disorders Exons Mitochondria DNA-Binding Proteins Models, Biological Models, Molecular Tandem Repeat Sequences Heterozygote Saccharomyces cerevisiae Lewy Body Disease Genetic Variation Autophagy Gene Expression Regulation Proteins Chromosome Mapping

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