Werner patient mutations. Medical search. Frequent questions

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Anatomy7

Cell Line Telomere HeLa Cells Fibroblasts Cells, Cultured Cell Nucleus Cell Nucleolus

Organisms2

Escherichia coli Saccharomyces cerevisiae

Diseases9

Werner Syndrome Bloom Syndrome Aging, Premature Progeria Rothmund-Thomson Syndrome Genomic Instability DNA Repair-Deficiency Disorders Syndrome Genetic Predisposition to Disease

Chemicals and Drugs24

RecQ Helicases DNA Helicases Exonucleases 4-Nitroquinoline-1-oxide DNA DNA-Binding Proteins Adenosine Triphosphatases Codon, Nonsense DNA Primers Telomeric Repeat Binding Protein 2 Replication Protein A Nuclear Proteins Recombinant Proteins Antigens, Nuclear Codon Transcription Factors Recombinant Fusion Proteins Mutant Proteins RNA, Messenger Membrane Proteins Bacterial Proteins DNA, Single-Stranded Telomere-Binding Proteins Flap Endonucleases

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Pedigree Amino Acid Substitution Polymerase Chain Reaction DNA Mutational Analysis Mutagenesis, Site-Directed Sequence Analysis, DNA Sequence Alignment Models, Genetic Genetic Testing Models, Molecular Chromosome Mapping Genetic Complementation Test Cloning, Molecular Transfection

Phenomena and Processes47

Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Base Sequence Mutation Rate Exons Heterozygote Amino Acid Substitution Protein Structure, Tertiary Amino Acid Sequence DNA Replication Alleles Protein Binding Telomere Polymorphism, Single-Stranded Conformational Phenotype DNA Repair Codon, Nonsense Genotype Homozygote Binding Sites Mutagenesis DNA Damage Recombination, Genetic Genes, Recessive Sequence Homology, Amino Acid Sequence Deletion Genes, Dominant Suppression, Genetic Codon Genomic Instability Kinetics Gene Deletion Founder Effect Cell Aging Genes, p53 Genetic Linkage Base Pair Mismatch Genetic Predisposition to Disease Consanguinity DNA, Single-Stranded Plasmids Nucleic Acid Conformation Transfection Genes, Lethal

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

Genetic Testing

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

Werner Syndrome RecQ Helicases Point Mutation Mutation, Missense Mutation DNA Helicases Frameshift Mutation Germ-Line Mutation Bloom Syndrome Pedigree Exonucleases Base Sequence 4-Nitroquinoline-1-oxide Aging, Premature Molecular Sequence Data DNA Mutation Rate Exons Heterozygote Amino Acid Substitution Protein Structure, Tertiary DNA-Binding Proteins Amino Acid Sequence Progeria Adenosine Triphosphatases Polymerase Chain Reaction DNA Mutational Analysis DNA Replication Alleles Cell Line Protein Binding Telomere Polymorphism, Single-Stranded Conformational Phenotype DNA Repair Mutagenesis, Site-Directed Codon, Nonsense Genotype Homozygote Binding Sites Mutagenesis Sequence Analysis, DNA DNA Primers DNA Damage HeLa Cells Rothmund-Thomson Syndrome Telomeric Repeat Binding Protein 2 Replication Protein A Recombination, Genetic Genes, Recessive Sequence Homology, Amino Acid Fibroblasts Nuclear Proteins Sequence Alignment Sequence Deletion Genes, Dominant Models, Genetic Recombinant Proteins Genetic Testing Antigens, Nuclear Escherichia coli Suppression, Genetic Models, Molecular Chromosome Mapping Codon Genomic Instability DNA Repair-Deficiency Disorders Genetic Complementation Test Kinetics Gene Deletion Cells, Cultured Founder Effect Transcription Factors Cell Aging Genes, p53 Syndrome Cloning, Molecular Recombinant Fusion Proteins Cell Nucleus Mutant Proteins RNA, Messenger Genetic Linkage Base Pair Mismatch Cell Nucleolus Genetic Predisposition to Disease Saccharomyces cerevisiae Membrane Proteins Consanguinity Bacterial Proteins DNA, Single-Stranded Plasmids Telomere-Binding Proteins Nucleic Acid Conformation Transfection Genes, Lethal Flap Endonucleases

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