Mtdna mutations. Medical search. Frequent questions

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Anatomy13

Mitochondria Hybrid Cells Mitochondria, Muscle Cell Line Muscle, Skeletal Cell Nucleus Fibroblasts Cells, Cultured Cell Line, Tumor COS Cells Chromosomes, Human, Y HeLa Cells X Chromosome

Organisms11

Escherichia coli Mice, Inbred C57BL Saccharomyces cerevisiae Drosophila melanogaster Mice, Mutant Strains Mice, Transgenic Drosophila Cercopithecus aethiops Cricetinae HIV-1 Mice, Knockout

Diseases26

Mitochondrial Diseases Optic Atrophy, Hereditary, Leber MELAS Syndrome Mitochondrial Myopathies Optic Atrophies, Hereditary Mitochondrial Encephalomyopathies MERRF Syndrome Leigh Disease Ophthalmoplegia, Chronic Progressive External Hearing Loss, Sensorineural Deafness Hearing Loss Syndrome Neoplasms Genetic Predisposition to Disease Retinitis Pigmentosa Genetic Diseases, X-Linked Cytochrome-c Oxidase Deficiency Abnormalities, Multiple Eye Abnormalities Chromosome Deletion Ataxia Genetic Diseases, Inborn Disease Models, Animal Osteochondrodysplasias Colorectal Neoplasms

Chemicals and Drugs62

DNA, Mitochondrial RNA, Transfer, Leu NADH Dehydrogenase Electron Transport Complex I RNA, Transfer, Ser Electron Transport Complex IV Mitochondrial Proton-Translocating ATPases Mitochondrial Proteins RNA, Transfer, Arg Reactive Oxygen Species DNA-Directed DNA Polymerase DNA Primers Codon, Nonsense Codon DNA-Binding Proteins Transcription Factors DNA Membrane Proteins Mutant Proteins Bacterial Proteins Nuclear Proteins DNA, Neoplasm RNA, Messenger Proto-Oncogene Proteins B-raf Carrier Proteins Saccharomyces cerevisiae Proteins Cytochromes b Recombinant Proteins Genetic Markers Proteins Eye Proteins Fungal Proteins Mutagens Proto-Oncogene Proteins DNA, Fungal Recombinant Fusion Proteins Ethylnitrosourea RNA Splice Sites Tumor Suppressor Protein p53 Repressor Proteins ras Proteins Codon, Terminator DNA, Complementary BRCA2 Protein Drosophila Proteins DNA Transposable Elements Escherichia coli Proteins DNA, Bacterial Adenosine Triphosphatases Trans-Activators RNA, Transfer RNA Protein-Serine-Threonine Kinases Ethyl Methanesulfonate DNA Helicases Arginine Succinate Dehydrogenase Homeodomain Proteins Alanine Membrane Transport Proteins Tumor Suppressor Proteins Neoplasm Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

DNA Mutational Analysis Pedigree Polymerase Chain Reaction Sequence Analysis, DNA Models, Genetic Amino Acid Substitution Mutagenesis, Site-Directed Genetic Testing Chromosome Mapping Models, Molecular Sequence Alignment Genetic Complementation Test Cloning, Molecular Transfection Heterozygote Detection Mutagenesis, Insertional Crosses, Genetic Restriction Mapping Blotting, Southern Reverse Transcriptase Polymerase Chain Reaction Models, Biological Blotting, Western Genetic Association Studies Immunohistochemistry Case-Control Studies Disease Models, Animal

Psychiatry and Psychology1

Phenomena and Processes112

Point Mutation Mutation Mutation, Missense Genome, Mitochondrial Genes, Mitochondrial Base Sequence Frameshift Mutation Oxidative Phosphorylation Germ-Line Mutation Penetrance Heterozygote Phenotype Aging Haplotypes Polymorphism, Restriction Fragment Length Sequence Deletion Phylogeny Genotype Mutation Rate Cell Respiration Gene Deletion Exons Amino Acid Substitution Polymorphism, Genetic Evolution, Molecular Alleles Selection, Genetic Polymorphism, Single-Stranded Conformational Electron Transport Genetic Variation Amino Acid Sequence Mutagenesis Codon, Nonsense Homozygote Genes, Recessive Oxidative Stress Founder Effect Oxygen Consumption Genes, Dominant Codon Protein Structure, Tertiary Suppression, Genetic Binding Sites Sequence Homology, Amino Acid Gene Frequency Genetic Predisposition to Disease Microsatellite Repeats Apoptosis Protein Binding Genetic Linkage Genes, p53 Transcription, Genetic Plasmids Recombination, Genetic Consanguinity Transfection Genes, Lethal Introns Mutagenesis, Insertional Exome DNA Replication Gene Dosage Promoter Regions, Genetic Genes, BRCA1 Genes Conserved Sequence Protein Conformation Genes, Bacterial Kinetics Genetic Markers DNA Repair Genes, Fungal Polymorphism, Single Nucleotide Signal Transduction INDEL Mutation Structure-Activity Relationship Species Specificity Drug Resistance, Viral Genes, Suppressor Gene Pool Nucleic Acid Conformation Temperature Biological Evolution Genetic Heterogeneity Genes, BRCA2 Gene Expression Regulation Gene Expression Sequence Homology, Nucleic Acid Chromosomes, Human, Y RNA Splicing RNA Splice Sites Protein Structure, Secondary Codon, Terminator Extrachromosomal Inheritance Inheritance Patterns DNA Transposable Elements Mosaicism Time Factors Chromosome Deletion X Chromosome Amino Acid Motifs Protein Transport Phosphorylation Drug Resistance, Microbial Loss of Heterozygosity Drug Resistance Repetitive Sequences, Nucleic Acid Open Reading Frames Gene Expression Regulation, Bacterial Protein Biosynthesis Virus Replication Ultraviolet Rays

Disciplines and Occupations5

Genetics, Population Geography Phylogeography Immunohistochemistry Forensic Genetics

Anthropology, Education, Sociology and Social Phenomena3

Emigration and Immigration Family Forensic Genetics

Humanities1

History, Ancient

Information Science4

Base Sequence Molecular Sequence Data Phylogeny Amino Acid Sequence

Named Groups3

Jews Asian Continental Ancestry Group Infant, Newborn

Health Care7

Age of Onset Genetic Testing Family Health Temperature Case-Control Studies Emigration and Immigration Ultraviolet Rays

Geographicals2

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

DNA, Mitochondrial Point Mutation Mutation Mitochondrial Diseases Optic Atrophy, Hereditary, Leber MELAS Syndrome Mitochondrial Myopathies Mutation, Missense Optic Atrophies, Hereditary Mitochondrial Encephalomyopathies RNA, Transfer, Leu Genome, Mitochondrial DNA Mutational Analysis MERRF Syndrome NADH Dehydrogenase Pedigree Mitochondria Leigh Disease Genes, Mitochondrial Polymerase Chain Reaction Base Sequence Frameshift Mutation Electron Transport Complex I RNA, Transfer, Ser Electron Transport Complex IV Mitochondrial Proton-Translocating ATPases Molecular Sequence Data Oxidative Phosphorylation Mitochondrial Proteins Germ-Line Mutation Sequence Analysis, DNA Penetrance Ophthalmoplegia, Chronic Progressive External Heterozygote Phenotype RNA, Transfer, Arg Aging Haplotypes Hearing Loss, Sensorineural Polymorphism, Restriction Fragment Length Sequence Deletion Hybrid Cells Phylogeny Genotype Mitochondria, Muscle Mutation Rate Reactive Oxygen Species DNA-Directed DNA Polymerase Cell Respiration Deafness Gene Deletion DNA Primers Models, Genetic Exons Amino Acid Substitution Polymorphism, Genetic Evolution, Molecular Hearing Loss Alleles Cell Line Selection, Genetic Age of Onset Muscle, Skeletal Polymorphism, Single-Stranded Conformational Electron Transport Genetic Variation Amino Acid Sequence Mutagenesis, Site-Directed Mutagenesis Codon, Nonsense Homozygote Cell Nucleus Genes, Recessive Fibroblasts Oxidative Stress Founder Effect Genetic Testing Oxygen Consumption Genes, Dominant Codon Protein Structure, Tertiary Suppression, Genetic Chromosome Mapping DNA-Binding Proteins Escherichia coli Cells, Cultured Models, Molecular Mice, Inbred C57BL Transcription Factors Cell Line, Tumor Syndrome Binding Sites Genetics, Population Sequence Homology, Amino Acid DNA Sequence Alignment Saccharomyces cerevisiae Genetic Complementation Test Cloning, Molecular Neoplasms

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