Polyglutamine genetic gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy4

Intranuclear Inclusion Bodies Inclusion Bodies Cell Line Brain

Organisms4

Acinetobacter Mice, Transgenic Linaria Saccharomyces cerevisiae

Diseases22

Friedreich Ataxia Spinocerebellar Degenerations Myotonic Dystrophy Huntington Disease Fragile X Syndrome Spinocerebellar Ataxias Heredodegenerative Disorders, Nervous System Machado-Joseph Disease Neurodegenerative Diseases Genomic Instability Frontotemporal Dementia Anticipation, Genetic Cerebellar Ataxia Myoclonic Epilepsies, Progressive Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Amyotrophic Lateral Sclerosis Muscular Disorders, Atrophic Disease Models, Animal Ataxia Muscular Atrophy, Spinal

Chemicals and Drugs16

Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins Nuclear Proteins Flap Endonucleases DNA RNA-Binding Proteins Receptors, Androgen Proteins DNA Primers DNA-Binding Proteins RNA, Messenger Saccharomyces cerevisiae Proteins MutS Homolog 2 Protein Genetic Markers Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Pedigree Polymerase Chain Reaction Disease Models, Animal Sequence Analysis, DNA Models, Genetic

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes27

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Mutation Cell Death Repetitive Sequences, Nucleic Acid Base Sequence Genomic Instability Anticipation, Genetic Microsatellite Repeats Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Chromosome Fragility Polymorphism, Genetic Phenotype DNA Repair Exons Amino Acid Sequence Transcription, Genetic Genotype Genes, Dominant DNA Replication Genome, Human Genetic Markers Heterozygote

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

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

Trinucleotide Repeat Expansion Trinucleotide Repeats Friedreich Ataxia DNA Repeat Expansion Spinocerebellar Degenerations Myotonic Dystrophy Huntington Disease Fragile X Syndrome Fragile X Mental Retardation Protein Iron-Binding Proteins Alleles Spinocerebellar Ataxias Heredodegenerative Disorders, Nervous System Machado-Joseph Disease Nerve Tissue Proteins Mutation Cell Death Repetitive Sequences, Nucleic Acid Base Sequence Intranuclear Inclusion Bodies Neurodegenerative Diseases Nuclear Proteins Molecular Sequence Data Genomic Instability Frontotemporal Dementia Flap Endonucleases Anticipation, Genetic Microsatellite Repeats DNA Cerebellar Ataxia Acinetobacter Inverted Repeat Sequences Minisatellite Repeats Pedigree Tandem Repeat Sequences Age of Onset Myoclonic Epilepsies, Progressive Chromosome Fragility Muscular Dystrophy, Oculopharyngeal RNA-Binding Proteins Receptors, Androgen Genetic Diseases, Inborn Polymerase Chain Reaction Inclusion Bodies Amyotrophic Lateral Sclerosis Mice, Transgenic Polymorphism, Genetic Phenotype Proteins Linaria Muscular Disorders, Atrophic Disease Models, Animal DNA Repair Sequence Analysis, DNA Models, Genetic Exons Amino Acid Sequence Transcription, Genetic DNA Primers Saccharomyces cerevisiae Cell Line Genotype Genes, Dominant Brain DNA-Binding Proteins DNA Replication Genome, Human RNA, Messenger Saccharomyces cerevisiae Proteins MutS Homolog 2 Protein Genetic Markers Heterozygote Nucleic Acid Heteroduplexes Ataxia Muscular Atrophy, Spinal

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