Polyglutamine expansion trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy7

Intranuclear Inclusion Bodies Inclusion Bodies Neurons Cell Line Brain Cell Nucleus Cells, Cultured

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases22

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

Chemicals and Drugs18

Fragile X Mental Retardation Protein Nerve Tissue Proteins Peptides Iron-Binding Proteins Nuclear Proteins Receptors, Androgen Flap Endonucleases DNA RNA-Binding Proteins Repressor Proteins Proteasome Endopeptidase Complex Proteins DNA Primers DNA-Binding Proteins RNA, Messenger Saccharomyces cerevisiae Proteins Genetic Markers MutS Homolog 2 Protein

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes29

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

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

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