Pages that link to "Q73066598"

The following pages link to The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate (Q73066598):

Displaying 25 items.

• Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies (Q21296841) (← links)
• Evolution meets disease: penetrance and functional epistasis of mitochondrial tRNA mutations (Q33886174) (← links)
• Human mitochondrial DNA diseases (Q34264417) (← links)
• tRNA and cytochrome c in cell death and beyond. (Q34318143) (← links)
• Structural probing of a pathogenic tRNA dimer (Q34366246) (← links)
• Hearing loss as a function of aging and diabetes mellitus: a cross sectional study (Q34456031) (← links)
• Mitochondrial diabetes mellitus (Q34660403) (← links)
• Mitochondrial disease: mutations and mechanisms. (Q35707245) (← links)
• Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS. (Q35919630) (← links)
• Aminoacyl tRNA synthetases and their connections to disease (Q36837363) (← links)
• Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene (Q36962856) (← links)
• Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR. (Q38668918) (← links)
• Mitochondrial disease and endocrine dysfunction (Q38800022) (← links)
• A pathogenic point mutation reduces stability of mitochondrial mutant tRNA(Ile) (Q39584529) (← links)
• Mitochondrial dysfunction induces aberrant insulin signalling and glucose utilisation in murine C2C12 myotube cells (Q40273568) (← links)
• Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene. (Q40489976) (← links)
• Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation. (Q40900095) (← links)
• Molecular dysfunction associated with the human mitochondrial 3302A>G mutation in the MTTL1 (mt-tRNALeu(UUR)) gene (Q41283457) (← links)
• Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes (Q43815581) (← links)
• Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness (Q44189303) (← links)
• Proteomic Consequences of a Human Mitochondrial tRNA Mutation beyond the Frame of Mitochondrial Translation (Q44417232) (← links)
• Towards understanding human mitochondrial leucine aminoacylation identity. (Q44428732) (← links)
• Wobble modification defect suppresses translational activity of tRNAs with MERRF and MELAS mutations (Q46667489) (← links)
• The mitochondrial tRNAGly T10003C mutation may not be associated with diabetes mellitus (Q58690875) (← links)
• Resolving complexity in mitochondrial disease: Towards precision medicine (Q90927931) (← links)