Pages that link to "Q33757397"

The following pages link to Disease-related versus polymorphic mutations in human mitochondrial tRNAs. Where is the difference? (Q33757397):

Displaying 32 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 T-stem slip in human mitochondrial tRNALeu(CUN) governs its charging capacity (Q24811807) (← links)
• Functional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defects. (Q30476620) (← links)
• A manually curated database of tetrapod mitochondrially encoded tRNA sequences and secondary structures (Q30838656) (← links)
• Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants (Q34365724) (← links)
• Cancer as a complex genetic trait: tumor susceptibility in humans and mouse models (Q34520426) (← links)
• Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia (Q34785735) (← links)
• Pathology-related substitutions in human mitochondrial tRNA(Ile) reduce precursor 3' end processing efficiency in vitro (Q34905523) (← links)
• Mutation in the mitochondrial tRNAVal causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (Q35028334) (← 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)
• Pathogenesis-related mutations in the T-loops of human mitochondrial tRNAs affect 3' end processing and tRNA structure (Q36062606) (← links)
• Decreased aminoacylation in pathology-related mutants of mitochondrial tRNATyr is associated with structural perturbations in tRNA architecture. (Q36503796) (← links)
• Human mitochondrial transfer RNAs: role of pathogenic mutation in disease (Q36999837) (← links)
• Is tRNA only a translation factor or also a regulator of other processes? (Q37080816) (← links)
• Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders (Q37206617) (← links)
• Non-coding RNAs and disease: the classical ncRNAs make a comeback. (Q38830955) (← links)
• Multilevel functional and structural defects induced by two pathogenic mitochondrial tRNA mutations. (Q39427538) (← links)
• Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution (Q40062641) (← links)
• Mamit-tRNA, a database of mammalian mitochondrial tRNA primary and secondary structures (Q42530161) (← links)
• Pathology-related mutation A7526G (A9G) helps in the understanding of the 3D structural core of human mitochondrial tRNA(Asp). (Q42566131) (← links)
• Length variation in the mouse mitochondrial tRNA(Arg) DHU loop size promotes oxidative phosphorylation functional differences. (Q42815614) (← links)
• Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. (Q44452930) (← links)
• Mitochondrial Aminoacyl-tRNA Synthetase Single-Nucleotide Polymorphisms That Lead to Defects in Refolding but Not Aminoacylation (Q45388652) (← links)
• Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects (Q45746327) (← links)
• Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case study. (Q46009324) (← links)
• Mechanisms and convergence of compensatory evolution in mammalian mitochondrial tRNAs (Q46163391) (← links)
• Prediction of pathogenic mutations in mitochondrially encoded human tRNAs (Q46804048) (← links)
• Decreased CCA-addition in human mitochondrial tRNAs bearing a pathogenic A4317G or A10044G mutation (Q50336111) (← links)
• Sequence variation in the tRNA genes of human mitochondrial DNA. (Q54358494) (← links)
• Sequence analysis of the complete mitochondrial DNA in 10 commonly used inbred rat strains (Q57783158) (← links)
• Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases (Q94958142) (← links)