Polyglutamine trinucleotide repeats. Medical search. Frequent questions

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Anatomy9

Intranuclear Inclusion Bodies Inclusion Bodies Cell Line Chromosomes, Human, X Brain X Chromosome Neurons Cell Nucleus COS Cells

Organisms3

Mice, Transgenic Saccharomyces cerevisiae Animals, Genetically Modified

Diseases24

Huntington Disease Friedreich Ataxia Fragile X Syndrome Spinocerebellar Degenerations Heredodegenerative Disorders, Nervous System Myotonic Dystrophy Machado-Joseph Disease Spinocerebellar Ataxias Neurodegenerative Diseases Genomic Instability Anticipation, Genetic Chromosome Fragility Cerebellar Ataxia Muscular Disorders, Atrophic Genetic Diseases, Inborn Muscular Dystrophy, Oculopharyngeal Disease Models, Animal Myoclonic Epilepsies, Progressive Proteostasis Deficiencies Nervous System Diseases Muscular Atrophy, Spinal Bulbo-Spinal Atrophy, X-Linked Intellectual Disability Nerve Degeneration

Chemicals and Drugs31

Peptides Nerve Tissue Proteins Fragile X Mental Retardation Protein Nuclear Proteins DNA Receptors, Androgen Flap Endonucleases Iron-Binding Proteins RNA-Binding Proteins Nucleic Acid Heteroduplexes DNA Primers Saccharomyces cerevisiae Proteins DNA, Satellite Oligodeoxyribonucleotides DNA-Binding Proteins RNA, Messenger Genetic Markers MutS Homolog 2 Protein Proteins Endodeoxyribonucleases Transcription Factors RNA DNA, Complementary DNA, Fungal HSP40 Heat-Shock Proteins Repressor Proteins Protein-Serine-Threonine Kinases Proteasome Endopeptidase Complex Ubiquitin Oligonucleotides Green Fluorescent Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Polymerase Chain Reaction Pedigree Sequence Analysis, DNA Disease Models, Animal Models, Genetic Chromosome Mapping Nucleic Acid Denaturation Blotting, Southern Gene Knock-In Techniques DNA Mutational Analysis Genetic Testing Transfection Cloning, Molecular Models, Molecular

Psychiatry and Psychology2

Huntington Disease Intellectual Disability

Phenomena and Processes49

Trinucleotide Repeats Trinucleotide Repeat Expansion Repetitive Sequences, Nucleic Acid Base Sequence Alleles Microsatellite Repeats Genomic Instability Nucleic Acid Conformation Mutation Minisatellite Repeats Tandem Repeat Sequences Inverted Repeat Sequences Anticipation, Genetic Chromosome Fragility Polymorphism, Genetic DNA Repair Amino Acid Sequence Transcription, Genetic Repetitive Sequences, Amino Acid Phenotype Exons DNA Repeat Expansion Chromosomes, Human, X Dinucleotide Repeats DNA, Satellite DNA Replication Sequence Deletion Genome, Human Genotype Genetic Markers Genes, Dominant Nucleic Acid Denaturation Gene Frequency X Chromosome Heterozygote Genetic Variation Ankyrin Repeat Protein Binding Recombination, Genetic Protein Folding Promoter Regions, Genetic Gene Expression Point Mutation Protein Structure, Tertiary Cell Death Transfection Plasmids Genetic Linkage Haplotypes

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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

Trinucleotide Repeats Trinucleotide Repeat Expansion Huntington Disease Friedreich Ataxia Fragile X Syndrome Spinocerebellar Degenerations Heredodegenerative Disorders, Nervous System Myotonic Dystrophy Machado-Joseph Disease Peptides Nerve Tissue Proteins Spinocerebellar Ataxias Fragile X Mental Retardation Protein Repetitive Sequences, Nucleic Acid Base Sequence Neurodegenerative Diseases Nuclear Proteins Intranuclear Inclusion Bodies Alleles Molecular Sequence Data Microsatellite Repeats Genomic Instability Nucleic Acid Conformation Mutation Minisatellite Repeats DNA Tandem Repeat Sequences Receptors, Androgen Inverted Repeat Sequences Flap Endonucleases Anticipation, Genetic Iron-Binding Proteins Chromosome Fragility Cerebellar Ataxia Polymorphism, Genetic Inclusion Bodies Muscular Disorders, Atrophic Polymerase Chain Reaction Genetic Diseases, Inborn RNA-Binding Proteins Pedigree Age of Onset Muscular Dystrophy, Oculopharyngeal Mice, Transgenic DNA Repair Sequence Analysis, DNA Amino Acid Sequence Disease Models, Animal Transcription, Genetic Models, Genetic Repetitive Sequences, Amino Acid Saccharomyces cerevisiae Nucleic Acid Heteroduplexes Myoclonic Epilepsies, Progressive Phenotype Exons Cell Line DNA Primers DNA Repeat Expansion Chromosomes, Human, X Saccharomyces cerevisiae Proteins Proteostasis Deficiencies Dinucleotide Repeats DNA, Satellite DNA Replication Sequence Deletion Nervous System Diseases Genome, Human Genotype Oligodeoxyribonucleotides DNA-Binding Proteins Chromosome Mapping RNA, Messenger Brain Genetic Markers MutS Homolog 2 Protein Proteins Genes, Dominant Nucleic Acid Denaturation Gene Frequency Endodeoxyribonucleases X Chromosome Transcription Factors RNA Heterozygote Muscular Atrophy, Spinal Neurons Genetic Variation Ankyrin Repeat Blotting, Southern Protein Binding DNA, Complementary Recombination, Genetic Protein Folding Cell Nucleus Bulbo-Spinal Atrophy, X-Linked DNA, Fungal HSP40 Heat-Shock Proteins Intellectual Disability Repressor Proteins

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