Keywords: جهش DNA DNA میتوکندریایی; Mitochondrial cardiomyopathy; Mitochondrial syndrome; Mitochondrial DNA mutation; Diabetic cardiomyopathy; Arrhythmia mechanisms; Arrhythmia management;
مقالات ISI جهش DNA DNA میتوکندریایی (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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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.
A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members
Keywords: جهش DNA DNA میتوکندریایی; Neurogenetics; Mitochondrial DNA mutation; Genotype-driven treatment; Klinefelter syndrome; MERRF/Leigh-like syndrome;
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241Â TÂ >Â G mutation
Keywords: جهش DNA DNA میتوکندریایی; Mitochondrial inherited diabetes and deafness; Retinopathy; Family; Mitochondrial DNA mutation; Haplotype;
Mitochondrial ND5 mutation mediated elevated ROS regulates apoptotic pathway epigenetically in a P53 dependent manner for generating pro-cancerous phenotypes
Keywords: جهش DNA DNA میتوکندریایی; mtND5; Mitochondrial DNA mutation; Reactive oxygen species; Apoptotic pathway; Differential methylation;
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families
Keywords: جهش DNA DNA میتوکندریایی; Leber's hereditary optic neuropathy; Mitochondrial DNA mutation; ND6; Penetrance; Haplogroup; Chinese;
Leigh syndrome caused by a novel m.4296GÂ >Â A mutation in mitochondrial tRNA isoleucine
Keywords: جهش DNA DNA میتوکندریایی; Leigh syndrome; tRNA isoleucine; Mitochondrial DNA mutation; Heteroplasmy;
A new mitochondrial point mutation in the transfer RNALys gene associated with progressive external ophthalmoplegia with impaired respiratory regulation
Keywords: جهش DNA DNA میتوکندریایی; Progressive external ophthalmoplegia; Mitochondrial disorders; Mitochondrial tRNA; Mitochondrial DNA mutation; Respiratory insufficiency;
Mitochondrial DNA mutations and depletion in pediatric medicine
Keywords: جهش DNA DNA میتوکندریایی; Mitochondrial DNA depletion; Neonatal pathology; Mitochondrial DNA mutation
Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation
Keywords: جهش DNA DNA میتوکندریایی; Atypical Leigh syndrome; Leber hereditary optic neuropathy; Mitochondrial DNA mutation; Phenotypic variation;
Analysis of mitochondrial DNA mutations in D-loop region in thyroid lesions
Keywords: جهش DNA DNA میتوکندریایی; Mitochondrial DNA mutation; Mitochondrial microsatellite instability; D-loop region; Thyroid; Tumor progression
Genotype-phenotype correlations in Leber hereditary optic neuropathy
Keywords: جهش DNA DNA میتوکندریایی; Leber hereditary optic neuropathy; Optic nerve; Mitochondrial DNA mutation; Apoptosis; ROS;
Left ventricular noncompaction is associated with mutations in the mitochondrial genome
Keywords: جهش DNA DNA میتوکندریایی; Noncompaction; Mitochondrial DNA mutation; Apoptosis; MitoMaster; Illumina parallel sequencing
Mitochondrial functional complementation in mitochondrial DNA-based diseases
Keywords: جهش DNA DNA میتوکندریایی; Mitochondrial DNA; Mitochondrial DNA mutation; Mitochondrial respiratory function; Mitochondrial respiration defects; Trans-mitochondrial models;
Oxidative stress in prostate cancer
Keywords: جهش DNA DNA میتوکندریایی; Reactive oxygen species; Oxidative stress; Prostate cancer; Aging; Mitochondrial DNA mutation
The search of ‘novel’ mtDNA mutations in hypertrophic cardiomyopathy: MITOMAPping as a risk factor
Keywords: جهش DNA DNA میتوکندریایی; Hypertrophic cardiomyopathy; Noonan syndrome; Mitochondrial DNA mutation; Haplogroup; MITOMAP
Does strong hypertrophic condition induce fast mitochondrial DNA mutation of rabbit heart?
Keywords: جهش DNA DNA میتوکندریایی; Mitochondrial DNA mutation; Cardiac hypertrophy; Left ventricle; Isoproterenol; Respiratory chain gene; White male New Zealand rabbit
Inappropriate intracranial hemodynamics in the natural course of MELAS
Keywords: جهش DNA DNA میتوکندریایی; MELAS; Mitochondrial disorders; Mitochondrial DNA mutation; SPM SPECT; Strokelike episodes; Endothelial dysfunction; Mitochondrial angiopathy
Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family
Keywords: جهش DNA DNA میتوکندریایی; Vision loss; Mitochondrial DNA mutation; Penetrance; Expressivity; HaplotypemtDNA, mitochondrial DNA; LHON, Leber’s hereditary optic neuropathy; PCR, polymerase chain reaction
Leber's hereditary optic neuropathy with dystonia in a Japanese family
Keywords: جهش DNA DNA میتوکندریایی; Leber's disease; Hereditary; Optic neuropathy; Dystonia; Mitochondrial disease; Mitochondrial DNA mutation; Striatal degeneration; Japanese family;
The mitochondrial tRNAThr A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family
Keywords: جهش DNA DNA میتوکندریایی; DIG, digoxigenin; mtDNA, mitochondrial DNA; LHON, Leber's hereditary optic neuropathy; PCR, Polymerase Chain ReactionVision loss; Mitochondrial DNA mutation; tRNA metabolism; Penetrance; Expressivity; Haplotype
Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families
Keywords: جهش DNA DNA میتوکندریایی; Hearing loss; Mitochondrial DNA mutation; tRNA; Aminoglycoside; Non-syndromic; CO1; Processing; ND6; Penetrance; Haplogroup; Chinese
Visualizing common deletion of mitochondrial DNA-augmented mitochondrial reactive oxygen species generation and apoptosis upon oxidative stress
Keywords: جهش DNA DNA میتوکندریایی; Apoptosis; Electron transport chain; Mitochondrial DNA mutation; Mitochondrial membrane potential; Mitochondrial permeability transition pore; Mitochondrial reactive oxygen specie
Single cell quantification of the 8993TÂ >Â G NARP mitochondrial DNA mutation by fluorescent PCR
Keywords: جهش DNA DNA میتوکندریایی; Leigh syndrome; Mitochondrial DNA mutation; NARP syndrome; Quantification; Single-cell PCR; Preimplantation genetic diagnosis;
Degree of heteroplasmy reflects oxidant damage in a large family with the mitochondrial DNA A8344G mutation
Keywords: جهش DNA DNA میتوکندریایی; MERRF; inherited myoclonic epilepsy and ragged red fibers; Heteroplasmy; Oxidant injury; F2-isoprostanes; Mitochondrial DNA mutation; mtA8344G;