Keywords: هتروپلاسم; CVD; cardiovascular disease; BMI; body mass index; SBP; systolic blood pressure; DBP; diastolic blood pressure; MI; myocardial infarction; HDL; high-density lipoproteins; LDL; low-density lipoproteins; TG; triglycerides; Mitochondrial mutations; Heteropla
مقالات ISI هتروپلاسم (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: هتروپلاسم; Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS syndrome); kidney biopsy; renal; Fanconi syndrome; focal segmental glomerulosclerosis (FSGS); proteinuria; heteroplasmy;
Keywords: هتروپلاسم; Mitochondria; Heteroplasmy; SNP; RNA editing; Blood cell;
Keywords: هتروپلاسم; Next generation sequencing; mtDNA; mtGenomes; Heteroplasmy; Forensic science;
Keywords: هتروپلاسم; Anisogamy; Bilateral nuclear migration; Heteroplasmy; Isogamy; Mating type genes; mtDNA mosaics; mtDNA recombination; Unilateral nuclear migration;
Keywords: هتروپلاسم; UPRmt; Sexual antagonistic pleiotropy; Sexual conflict; Mother’s curse; Heteroplasmy; Dosage compensation
Keywords: هتروپلاسم; Leigh syndrome; Complex I deficiency; Heteroplasmy; mDNA mutation
Keywords: هتروپلاسم; Mitochondrial DNA; Heteroplasmy; Oxidative phosphorylation; Human diseases; Tissue specificity; OXPHOS; oxidative phosphorylation pathway; mtDNA; mitochondrial DNA;
Keywords: هتروپلاسم; Mitochondrion; Adaptation; Mitochondrial genome evolution; Mitochondrial disease; Heteroplasmy; Male health;
Keywords: هتروپلاسم; mtDNA; 454 sequencing; SGS; NGS; heteroplasmy; SRM-2392;
Keywords: هتروپلاسم; Mitochondrial DNA quantification; Heteroplasmy; Hair DNA extraction; Next generation sequencing; Clinical;
Keywords: هتروپلاسم; Mitochondrial mutations; Heteroplasmy; Coronary heart disease; Infarction; Atherosclerosis
Renal Involvement in Neuropathy, Ataxia, Retinitis Pigmentosa (NARP) Syndrome: A Case Report
Keywords: هتروپلاسم; NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome; mitochondrial cytopathy; focal segmental glomerulosclerosis (FSGS); reduced kidney function; end-stage renal disease (ESRD); heteroplasmy; proteinuria; dialysis; renal biopsy; case report;
Massive parallel sequencing of mitochondrial DNA genomes from mother-child pairs using the ion torrent personal genome machine (PGM)
Keywords: هتروپلاسم; mtDNA; Population genetics; Heteroplasmy; Massively parallel sequencing (MPS);
Pathologies liées à des mutations de l'ADN mitochondrial
Keywords: هتروپلاسم; ADN mitochondrial; chaîne respiratoire; hétéroplasmie; maladies mitochondriales; ségrégation mitotique; prestation de conseil; traçabilité; heteroplasmy; mitochondrial disorders; mitochondrial DNA; mitotic segregation; respiratory chain;
Tri-allelic heteroplasmies, DNA-RNA differences and their polynucleotide tract associations in the mitochondrial genome
Keywords: هتروپلاسم; SNP; Heteroplasmy; Polytract;
High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy
Keywords: هتروپلاسم; Progressive hearing loss; Infant; Mitochondrial DNA; Heteroplasmy;
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load
Keywords: هتروپلاسم; Mitochondrial encephalomyopathy; Lactic acidosis and stroke-like episodes (MELAS); Leigh syndrome (LS); Mitochondrial DNA; Heteroplasmy; Neuropathology;
The MELAS mutation m.3243A>G promotes reactivation of fetal cardiac genes and an epithelial-mesenchymal transition-like program via dysregulation of miRNAs
Keywords: هتروپلاسم; OXPHOS diseases; Heteroplasmy; Hypertrophic cardiomyopathy; miR-218-5p; miR-4775;
Bilateral striatal necrosis caused by a founder mitochondrial 14459GÂ >Â A mutation in two independent Japanese families
Keywords: هتروپلاسم; Bilateral striatal necrosis; NADH dehydrogenase subunit 6; 14459GÂ >Â A; SNP; Homoplasmy; Heteroplasmy;
Mitochondrial control region and GSTP1 polymorphism associated with familial urinary bladder cancer in Karbi-Anglong tribe of Assam, Northeast India
Keywords: هتروپلاسم; Glutathione S-transferase; Urinary bladder cancer; mtDNA D-loop; Karbi-Anglong; Haplogroup; Heteroplasmy;
The phenotypic spectrum of fifty Czech m.3243A>Â G carriers
Keywords: هتروپلاسم; MELAS; m.3243AÂ >Â G; Heteroplasmy; Natural course; Fully expressed phenotype; Oligosymptomatic patients;
3697GÂ >Â A in MT-ND1 is a causative mutation in mitochondrial disease
Keywords: هتروپلاسم; Leigh disease; Mitochondrial disease; Next Generation Sequencing; Heteroplasmy; Clinical genomics;
Sequencing the hypervariable regions of human mitochondrial DNA using massively parallel sequencing: Enhanced data acquisition for DNA samples encountered in forensic testing
Keywords: هتروپلاسم; Mitochondrial DNA; HVI; HVII; Massively parallel sequencing; Sanger type sequencing; Heteroplasmy
Heteroplasmic substitutions in the entire mitochondrial genomes of human colon cells detected by ultra-deep 454 sequencing
Keywords: هتروپلاسم; Mitochondrial genome; Phylogeny; Haplogroup; Heteroplasmy; 454 Sequencing; Low-level variants;
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmy
Keywords: هتروپلاسم; Mitochondrial tRNA; Threshold effect; Heteroplasmy; OXPHOS; Hearing loss
Parkin modulates heteroplasmy of truncated mtDNA in Caenorhabditis elegans
Keywords: هتروپلاسم; Caenorhabditis elegans; Heteroplasmy; Mitochondria; mtDNA; Parkin; PINK1;
Mitochondrial DNA heteroplasmy in the emerging field of massively parallel sequencing
Keywords: هتروپلاسم; mtDNA; mtGenome; Heteroplasmy; Errors; Massively parallel sequencing;
Full mtGenome reference data: Development and characterization of 588 forensic-quality haplotypes representing three U.S. populations
Keywords: هتروپلاسم; mtDNA; mtGenome; Sequencing; Reference population database; Heteroplasmy; Haplogroup;
The mitochondrial genome of the lone star tick (Amblyomma americanum)
Keywords: هتروپلاسم; Ixodid; Heteroplasmy; Phylogenetics; Mitochondria;
Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis
Keywords: هتروپلاسم; Mitochondrial DNA (mtDNA); Heteroplasmy; Preimplantation genetic diagnosis (PGD); Blastocyst; Trophectoderm biopsy;
High-throughput sequencing in mitochondrial DNA research
Keywords: هتروپلاسم; High throughput sequencing; Next generation sequencing; Heteroplasmy; SNP; Mutation; Copy number;
DNA Commission of the International Society for Forensic Genetics: Revised and extended guidelines for mitochondrial DNA typing
Keywords: هتروپلاسم; Phylogeny; Haplogroups; Quasi-median networks; Heteroplasmy; Alignment; Database searches;
mtDNA mutations in human aging and longevity: Controversies and new perspectives opened by high-throughput technologies
Keywords: هتروپلاسم; GWAS; genome wide association study; OXPHOS; oxidative phosphorylation; ROS; reactive oxygen species; mtDNA; mitochondrial DNA; polγ; polymerase gamma; GEHA; Genetic of Healthy Aging; NGS; next generation sequencing; nDNA; nuclear DNA; 90 +; nonagenaria
Phenotypic diversity associated with the MT-TV gene m.1644GÂ >Â A mutation, a matter of quantity
Keywords: هتروپلاسم; Mitochondrial DNA; Heteroplasmy; Mitochondrial diseases; Clinical diagnosis;
Development and assessment of an optimized next-generation DNA sequencing approach for the mtgenome using the Illumina MiSeq
Keywords: هتروپلاسم; MiSeq; mtDNA; NextGENe; Heteroplasmy; Next-generation sequencing; Nextera;
Changes of mitochondria in atherosclerosis: Possible determinant in the pathogenesis of the disease
Keywords: هتروپلاسم; Atherosclerosis; Mitochondria; Ultrastructure; Mitochondrial mutations; Heteroplasmy; Atherosclerotic lesions; Intima; Aorta;
Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM)
Keywords: هتروپلاسم; Next Generation Sequencing; mtDNA genomes; Heteroplasmy; Sanger-type sequencing; PGM; Forensic science;
Reprint of: Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM)
Keywords: هتروپلاسم; Next Generation Sequencing; mtDNA genomes; Heteroplasmy; Sanger-type sequencing; PGM; Forensic science;
Very Low-Level Heteroplasmy mtDNA Variations Are Inherited in Humans
Keywords: هتروپلاسم; Maternal inheritance; Next-generation sequencing; High-depth sequencing; Heteroplasmy; mtDNA mutations; Bottleneck
Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation
Keywords: هتروپلاسم; Encephalomyopathies; Mitochondrial DNA; MTTK; Heteroplasmy; Single fibre studies; Pathogenicity; Muscle biochemical analysis
Leigh syndrome caused by a novel m.4296GÂ >Â A mutation in mitochondrial tRNA isoleucine
Keywords: هتروپلاسم; Leigh syndrome; tRNA isoleucine; Mitochondrial DNA mutation; Heteroplasmy;
Whole mitochondrial genome analysis of a family with NARP/MILS caused by m.8993TÂ >Â C mutation in the MT-ATP6 gene
Keywords: هتروپلاسم; mtDNA; MT-ATP6 gene; m.8993TÂ >Â C; NARP/MILS; Heteroplasmy;
Heteroplasmy levels of mtDNA1555A>G mutation is positively associated with diverse phenotypes and mutation transmission in a Chinese family
Keywords: هتروپلاسم; Hereditary hearing loss; mtDNA 1555A>G mutation; Heteroplasmy; Eastern Asian; Clinical phenotype; Mutation transmission
The heteroplasmic 15059G>A mutation in the mitochondrial cytochrome b gene and essential hypertension in type 2 diabetes
Keywords: هتروپلاسم; Cytochrome b; Essential hypertension; Heteroplasmy; Mitochondrial DNA; 15059G>A mutation
Segregation of donor cell mitochondrial DNA in gaur-bovine interspecies somatic cell nuclear transfer embryos, fetuses and an offspring
Keywords: هتروپلاسم; Endangered species; Bovine cytoplasm; Gaur; Mitochondrial DNA; Heteroplasmy;
Mitochondrial disease – a review
Keywords: هتروپلاسم; Alpers; Barth syndrome; heteroplasmy; Kearns–Sayre syndrome; Leigh syndrome; MELAS; mitochondrial disease; MERRF; NARP; Pearson syndrome; PEO
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene
Keywords: هتروپلاسم; Encephalomyopathies; Mitochondrial DNA; tRNASer(AGY); Heteroplasmy; Single fibres studies; Pathogenicity; Muscle biochemical analysis;
Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutation
Keywords: هتروپلاسم; mtDNA; heteroplasmy; PCR-RFLP; Mutation load; Polar body analysis;
MitoBamAnnotator: A web-based tool for detecting and annotating heteroplasmy in human mitochondrial DNA sequences
Keywords: هتروپلاسم; Next generation sequence; Mitochondrial DNA; Annotation; Heteroplasmy;