Mitochondrial tRNAThr 15909A>G mutation associated with hypertension in a Chinese Han pedigree
Keywords: tRNA میتوکندری; Hypertension; Mitochondrial tRNA; Mutation; Chinese Han;
مقالات ISI tRNA میتوکندری (ترجمه نشده)
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Novel patient missense mutations in the HSD17B10 gene affect dehydrogenase and mitochondrial tRNA modification functions of the encoded protein
Keywords: tRNA میتوکندری; HSD10; 17β-hydroxysteroid dehydrogenase type 10; MRPP1; mitochondrial ribonuclease P protein subunit 1; MRPP2; mitochondrial ribonuclease P protein subunit 2; MRPP3; mitochondrial ribonuclease P protein subunit 3; SDR; short-chain dehydrogenase/reductase
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmy
Keywords: tRNA میتوکندری; Mitochondrial tRNA; Threshold effect; Heteroplasmy; OXPHOS; Hearing loss
In vitro substrate specificities of 3′–5′ polymerases correlate with biological outcomes of tRNA 5′-editing reactions
Keywords: tRNA میتوکندری; Thg1, tRNAHis guanylyltransferase; TLP, Thg1-like protein; WC, Watson–Crick; mt-tRNA, mitochondrial-tRNA; EDTA, ethylenediamine tetraacetic acidtRNA editing; Mitochondrial tRNA; Thg1-like protein; 3′–5′ polymerase; Acanthamoeba castellanii; Dictyostelium
Mitochondrial tRNA cleavage by tRNA-targeting ribonuclease causes mitochondrial dysfunction observed in mitochondrial disease
Keywords: tRNA میتوکندری; mnm5U; 5-methylaminomethyluridine; MELAS; mitochondrial myopathy, encephalopathy, lactic acidosis, stroke-like episodes; MERRF; myoclonic epilepsy with ragged-red fibers; MTS; mitochondrial-targeting sequence; TALEN; transcription activator-like effector
A new mitochondrial point mutation in the transfer RNALys gene associated with progressive external ophthalmoplegia with impaired respiratory regulation
Keywords: tRNA میتوکندری; Progressive external ophthalmoplegia; Mitochondrial disorders; Mitochondrial tRNA; Mitochondrial DNA mutation; Respiratory insufficiency;
Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies
Keywords: tRNA میتوکندری; MD; mitochondrial disease; mtDNA; mitochondrial DNA; tRNA; transfer ribonucleic acid; MCM; mitochondrial cardiomyopathy; MELAS; mitochondrial encephalopathy, lactic acidosis and stroke-like episodes; MiMyCa; maternally inherited myopathy and cardiomyopath
Adaptation of aminoacylation identity rules to mammalian mitochondria
Keywords: tRNA میتوکندری; Identity elements; Mitochondrial tRNA; Cross-aminoacylation; Structural plasticity
Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia
Keywords: tRNA میتوکندری; Mitochondrial disease; CPEO; Mitochondrial tRNA; 3â² end processing; MT-TI;
Mitochondrial tRNALeu(UUR) gene mutation and maternally inherited diabetes mellitus in Pakistani population
Keywords: tRNA میتوکندری; Diabetes mellitus; Gene mutation; Mitochondrial tRNA
Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae
Keywords: tRNA میتوکندری; Mitochondrial tRNA; Nucleotide modification; 15S rRNA; RNA metabolism; Yeast;
Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases
Keywords: tRNA میتوکندری; Mitochondrial disease; Mitochondrial tRNA; Patient tissue; Post-transcriptional modification; Taurine;