Mutations in mtdna mitochondrial. Medical search. Frequent questions

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Anatomy14

Mitochondria Cell Line Cell Nucleus Cells, Cultured COS Cells Chromosomes, Human, Y Fibroblasts HeLa Cells Mitochondria, Muscle X Chromosome Cell Line, Tumor Muscle, Skeletal HEK293 Cells Oocytes

Organisms11

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

Diseases26

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

Chemicals and Drugs61

DNA, Mitochondrial Codon, Nonsense DNA Primers Codon DNA-Binding Proteins Transcription Factors DNA Mitochondrial Proteins Electron Transport Complex IV RNA, Transfer, Leu Membrane Proteins Mutant Proteins Bacterial Proteins Nuclear Proteins DNA, Neoplasm RNA, Messenger NADH Dehydrogenase Proto-Oncogene Proteins B-raf Carrier Proteins Saccharomyces cerevisiae Proteins Cytochromes b Recombinant Proteins Genetic Markers Proteins DNA-Directed DNA Polymerase 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 Mitochondrial Proton-Translocating ATPases Protein-Serine-Threonine Kinases Ethyl Methanesulfonate DNA Helicases Arginine Succinate Dehydrogenase Homeodomain Proteins Alanine Membrane Transport Proteins Tumor Suppressor Proteins Neoplasm Proteins Nerve Tissue Proteins Glycine Protein Subunits

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

Pedigree Polymerase Chain Reaction DNA Mutational Analysis Sequence Analysis, DNA Amino Acid Substitution Mutagenesis, Site-Directed Genetic Testing Models, Genetic 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 Processes111

Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Base Sequence Mutation Rate Heterozygote Exons Amino Acid Substitution Alleles Genome, Mitochondrial Polymorphism, Single-Stranded Conformational Genotype Genetic Variation Amino Acid Sequence Sequence Deletion Mutagenesis Codon, Nonsense Homozygote Phylogeny Phenotype Genes, Recessive Founder Effect Gene Deletion Genes, Dominant Codon Protein Structure, Tertiary Suppression, Genetic Evolution, Molecular Haplotypes Genes, Mitochondrial Polymorphism, Genetic Binding Sites Sequence Homology, Amino Acid Polymorphism, Restriction Fragment Length Gene Frequency Genetic Predisposition to Disease Microsatellite Repeats 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 Selection, Genetic Genes Penetrance 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 Oxidative Phosphorylation 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 Aging Genome Base Pair Mismatch Gene Rearrangement Genes, APC

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 Amino Acid Sequence Phylogeny

Named Groups4

Jews Asian Continental Ancestry Group Infant, Newborn Indians, Central American

Health Care7

Genetic Testing Family Health Age of Onset 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

Point Mutation DNA, Mitochondrial Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Pedigree Base Sequence Mutation Rate Molecular Sequence Data Polymerase Chain Reaction DNA Mutational Analysis Sequence Analysis, DNA Heterozygote Exons Amino Acid Substitution Alleles Genome, Mitochondrial Polymorphism, Single-Stranded Conformational Genotype Genetic Variation Amino Acid Sequence Mutagenesis, Site-Directed Sequence Deletion Mutagenesis Codon, Nonsense Homozygote Mitochondria Phylogeny DNA Primers Mitochondrial Myopathies Phenotype Genes, Recessive Founder Effect Genetic Testing Gene Deletion Genes, Dominant Codon MELAS Syndrome Cell Line Protein Structure, Tertiary Suppression, Genetic Models, Genetic Evolution, Molecular Chromosome Mapping Haplotypes DNA-Binding Proteins Escherichia coli Genes, Mitochondrial Models, Molecular Transcription Factors Polymorphism, Genetic Syndrome Binding Sites Genetics, Population Sequence Homology, Amino Acid DNA Sequence Alignment Saccharomyces cerevisiae Polymorphism, Restriction Fragment Length Genetic Complementation Test Cloning, Molecular Mitochondrial Encephalomyopathies Gene Frequency Genetic Predisposition to Disease Microsatellite Repeats Protein Binding Mitochondrial Proteins Genetic Linkage Genes, p53 Electron Transport Complex IV RNA, Transfer, Leu Membrane Proteins Optic Atrophy, Hereditary, Leber Transcription, Genetic Plasmids Ophthalmoplegia, Chronic Progressive External Mutant Proteins Recombination, Genetic Consanguinity Bacterial Proteins Transfection Nuclear Proteins Genes, Lethal Introns Heterozygote Detection Mutagenesis, Insertional Exome Crosses, Genetic MERRF Syndrome DNA, Neoplasm RNA, Messenger NADH Dehydrogenase DNA Replication Gene Dosage Family Health Optic Atrophies, Hereditary Proto-Oncogene Proteins B-raf Promoter Regions, Genetic Genes, BRCA1

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