Promoter polymorphism gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy3

Intranuclear Inclusion Bodies Cell Line Chromosomes, Human, X

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases20

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

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Fragile X Mental Retardation Protein Iron-Binding Proteins DNA Nerve Tissue Proteins Flap Endonucleases DNA Primers Nuclear Proteins Genetic Markers DNA-Binding Proteins RNA-Binding Proteins Serotonin Plasma Membrane Transport Proteins RNA, Messenger Proteins Peptides Receptors, Androgen Transcription Factors Interleukin-10 MutS Homolog 2 Protein Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Proteins Oligodeoxyribonucleotides Matrix Metalloproteinase 3 RNA Interleukin-6

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Polymerase Chain Reaction Case-Control Studies Sequence Analysis, DNA Pedigree Genetic Association Studies Models, Genetic DNA Mutational Analysis Genetic Testing Risk Factors Chromosome Mapping Cohort Studies Disease Models, Animal Cloning, Molecular Electrophoretic Mobility Shift Assay

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes47

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Polymorphism, Genetic Alleles Promoter Regions, Genetic Polymorphism, Single Nucleotide Genotype Gene Frequency Mutation Base Sequence Genetic Predisposition to Disease Repetitive Sequences, Nucleic Acid Haplotypes Microsatellite Repeats Genomic Instability Minisatellite Repeats Anticipation, Genetic Nucleic Acid Conformation Phenotype Tandem Repeat Sequences Inverted Repeat Sequences Transcription, Genetic Genetic Variation Heterozygote Chromosome Fragility Genetic Markers Linkage Disequilibrium Exons Dinucleotide Repeats Gene Expression Regulation Homozygote DNA Repair Amino Acid Sequence Genome, Human Genetic Linkage Genes, Dominant Polymorphism, Restriction Fragment Length Gene Expression Binding Sites Sequence Deletion DNA Replication Repetitive Sequences, Amino Acid Recombination, Genetic Genes, Reporter Introns Chromosomes, Human, X

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

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Asian Continental Ancestry Group European Continental Ancestry Group

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Case-Control Studies Age of Onset Genetic Testing Risk Factors Cohort Studies

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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 Named Groups Health Care Geographicals

Trinucleotide Repeat Expansion Trinucleotide Repeats Friedreich Ataxia DNA Repeat Expansion Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Huntington Disease Fragile X Mental Retardation Protein Polymorphism, Genetic Alleles Promoter Regions, Genetic Iron-Binding Proteins Polymorphism, Single Nucleotide Genotype Gene Frequency Mutation Base Sequence Genetic Predisposition to Disease Repetitive Sequences, Nucleic Acid Haplotypes Molecular Sequence Data Polymerase Chain Reaction Spinocerebellar Ataxias DNA Machado-Joseph Disease Case-Control Studies Microsatellite Repeats Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Age of Onset Genomic Instability Frontotemporal Dementia Flap Endonucleases Minisatellite Repeats Anticipation, Genetic Nucleic Acid Conformation Phenotype Tandem Repeat Sequences Sequence Analysis, DNA Pedigree Inverted Repeat Sequences DNA Primers Transcription, Genetic Genetic Variation Genetic Association Studies Cerebellar Ataxia Nuclear Proteins Intranuclear Inclusion Bodies Heterozygote Chromosome Fragility Genetic Markers Muscular Dystrophy, Oculopharyngeal DNA-Binding Proteins Genetic Diseases, Inborn RNA-Binding Proteins Linkage Disequilibrium Asian Continental Ancestry Group Serotonin Plasma Membrane Transport Proteins RNA, Messenger Exons Models, Genetic Dinucleotide Repeats DNA Mutational Analysis Amyotrophic Lateral Sclerosis Gene Expression Regulation Neurodegenerative Diseases Proteins Homozygote Cell Line DNA Repair Peptides Amino Acid Sequence Receptors, Androgen Genome, Human Genetic Testing Transcription Factors Risk Factors Chromosome Mapping Genetic Linkage Mice, Transgenic Genes, Dominant Polymorphism, Restriction Fragment Length Gene Expression Saccharomyces cerevisiae Binding Sites Sequence Deletion DNA Replication Interleukin-10 China Myoclonic Epilepsies, Progressive Cohort Studies MutS Homolog 2 Protein Repetitive Sequences, Amino Acid Nucleic Acid Heteroduplexes Disease Models, Animal European Continental Ancestry Group Saccharomyces cerevisiae Proteins Oligodeoxyribonucleotides Recombination, Genetic

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