Keywords: جهش mtDNA; Non-syndromic deafness; Molecular diagnosis; GJB2; GJB6 deletion; mtDNA mutation; Nigeria
مقالات ISI جهش mtDNA (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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.
Disruption of the human COQ5-containing protein complex is associated with diminished coenzyme Q10 levels under two different conditions of mitochondrial energy deficiency
Keywords: جهش mtDNA; 2D BN-PAGE; two-dimensional blue native-polyacrylamide gel electrophoresis; BHA; butylated hydroxyanisole; CoQ; coenzyme Q; FCCP; carbonyl cyanide-p-trifluoromethoxyphenylhydrazone; HPLC; high-performance liquid chromatography; m-COQ5; mature form of COQ5
Defining the impact on yeast ATP synthase of two pathogenic human mitochondrial DNA mutations, T9185C and T9191C
Keywords: جهش mtDNA; ATP synthase; ATP6; Mitochondria; Energetics; Disease; mtDNA mutation;
Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice
Keywords: جهش mtDNA; mtDNA polymerase γ; mtDNA mutation; Parkinson's disease; Dopamine; Behavioral deficits; Metabolic deficits;
Defining the pathogenesis of human mtDNA mutations using a yeast model: The case of T8851C
Keywords: جهش mtDNA; ATP synthase; ATP6; Mitochondria; Energetics; Disease; mtDNA mutation;
Partial tandem duplication of mtDNA–tRNAPhe impairs mtDNA translation in late-onset mitochondrial myopathy
Keywords: جهش mtDNA; Mitochondrial myopathy; Oxidative phosphorylation; mtDNA; Cytochrome c oxidase; mtDNA translation; mtDNA mutation
Current molecular diagnostic algorithm for mitochondrial disorders
Keywords: جهش mtDNA; Mitochondrial disorder; mtDNA mutation; mtDNA depletion; mtDNA deletion
Identification of novel mutations in five patients with mitochondrial encephalomyopathy
Keywords: جهش mtDNA; Mitochondrial DNA; Respiratory chain complex deficiency; mtDNA Sequence analysis; mtDNA mutation;
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases
Keywords: جهش mtDNA; Complex I; NDUFS4; NDUFS1; ROS balance; mtDNA mutation; Mitochondrial encephalopathy; PINK1; Familiar Parkinsonism; Chronic epilepsy;
The study of the pathogenic mechanism of mitochondrial diseases provides information on basic bioenergetics
Keywords: جهش mtDNA; Mitochondria; ATP synthase; ATPase 6 subunit; Proton transport; mtDNA mutation;
Reversible regulation of metastasis by ROS-generating mtDNA mutations
Keywords: جهش mtDNA; mtDNA mutation; ROS overproduction; Nuclear-gene regulation; Metastasis; mtDNA transfer technology
Mitochondrial myopathy associated with a novel mutation in mtDNA
Keywords: جهش mtDNA; mtDNA mutation; tRNA-Arginine; Mitochondrial encephalomyopathy;
Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations
Keywords: جهش mtDNA; Deafness; Mitochondrial 12S rRNA; Nuclear modifier gene; tRNA modification; Modulate; mtDNA mutation; Linkage; Expression
Mitochondrial DNA involvement in human longevity
Keywords: جهش mtDNA; Mitochondrial DNA; Longevity; mtDNA mutation; mtDNA haplogroup; Centenarian; Nuclear–mitochondrial interaction; Alzheimer's Disease
Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy
Keywords: جهش mtDNA; LHON; ND4 G11778A mutation; Halpotype; Mitochondrial genome; Visual loss; mtDNA mutation; Modifier genes; Chinese;