Pages that link to "Q43937103"

The following pages link to The 7472insC mitochondrial DNA mutation impairs the synthesis and extent of aminoacylation of tRNASer(UCN) but not its structure or rate of turnover (Q43937103):

Displaying 24 items.

• A new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations (Q24810699) (← links)
• A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs (Q33791275) (← links)
• A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential. (Q33843127) (← links)
• Dual-mode recognition of noncanonical tRNAs(Ser) by seryl-tRNA synthetase in mammalian mitochondria (Q34116221) (← links)
• Pathology-related substitutions in human mitochondrial tRNA(Ile) reduce precursor 3' end processing efficiency in vitro (Q34905523) (← links)
• Alterations to the expression level of mitochondrial transcription factor A, TFAM, modify the mode of mitochondrial DNA replication in cultured human cells (Q35128105) (← links)
• Disorders of mitochondrial protein synthesis (Q35203201) (← links)
• Noncanonical secondary structure stabilizes mitochondrial tRNA(Ser(UCN)) by reducing the entropic cost of tertiary folding. (Q35447374) (← links)
• Mitochondrial tRNA 3' end metabolism and human disease. (Q35914830) (← links)
• Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome. (Q36024220) (← links)
• Mitochondrial rRNA and tRNA and hearing function (Q36697530) (← links)
• Mitochondrial disease--its impact, etiology, and pathology. (Q36707793) (← links)
• Human mitochondrial disease-like symptoms caused by a reduced tRNA aminoacylation activity in flies. (Q37013006) (← links)
• Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness (Q37071065) (← links)
• Human mitochondrial tRNA quality control in health and disease: a channelling mechanism? (Q37976956) (← links)
• The yeast counterparts of human 'MELAS' mutations cause mitochondrial dysfunction that can be rescued by overexpression of the mitochondrial translation factor EF-Tu. (Q40663427) (← links)
• Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment (Q43784130) (← links)
• A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one? (Q44842993) (← links)
• Fatal neonatal lactic acidosis caused by a novel de novo mitochondrial G7453A tRNA-Serine ((UCN)) mutation (Q47976366) (← links)
• The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients (Q50433773) (← links)
• Polyadenylation and degradation of structurally abnormal mitochondrial tRNAs in human cells. (Q55252555) (← links)
• Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness (Q87905099) (← links)
• FICC-Seq: a method for enzyme-specified profiling of methyl-5-uridine in cellular RNA (Q92287277) (← links)
• Complete chemical structures of human mitochondrial tRNAs (Q98784800) (← links)