Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs (Q27027853)

Nagao Asuteka

series ordinal

2

1 reference

Suzuki Takeo

series ordinal

3

1 reference

language of work or name

1 reference

2011

1 reference

Wiley interdisciplinary reviews. RNA

published in

1 reference

volume

2

1 reference

issue

3

1 reference

page(s)

376-86

1 reference

A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

cites work

1 reference

Why do we still have a maternally inherited mitochondrial DNA? Insights from evolutionary medicine

21 January 2018

1 reference

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

21 January 2018

1 reference

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

1 reference

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

MITOMAP: a human mitochondrial genome database--2004 update

21 January 2018

1 reference

MITOMAP: a human mitochondrial genome database

21 January 2018

1 reference

Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough

21 January 2018

1 reference

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

21 January 2018

1 reference

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

21 January 2018

1 reference

Heteroplasmic mitochondrial DNA mutations in normal and tumour cells

21 January 2018

1 reference

Single-molecule LATE-PCR analysis of human mitochondrial genomic sequence variations

21 January 2018

1 reference

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication

21 January 2018

1 reference

Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication

21 January 2018

1 reference

The pathogenic A4269G mutation in human mitochondrial tRNA(Ile) alters the T-stem structure and decreases the binding affinity for elongation factor Tu.

21 January 2018

1 reference

The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation

21 January 2018

1 reference

Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome.

21 January 2018

1 reference

Effect of a mutation in the anticodon of human mitochondrial tRNAPro on its post-transcriptional modification pattern

21 January 2018

1 reference

Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants

21 January 2018

1 reference

A pathogenesis-associated mutation in human mitochondrial tRNALeu(UUR) leads to reduced 3'-end processing and CCA addition.

21 January 2018

1 reference

Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies

21 January 2018

1 reference

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

21 January 2018

1 reference

Towards understanding human mitochondrial leucine aminoacylation identity.

21 January 2018

1 reference

Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients

21 January 2018

1 reference

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

21 January 2018

1 reference

Pathophysiology of the MELAS 3243 transition mutation

21 January 2018

1 reference

Chaplet column chromatography: isolation of a large set of individual RNAs in a single step

21 January 2018

1 reference

Biogenesis of glutaminyl-mt tRNAGln in human mitochondria

21 January 2018

1 reference

Taurine as a constituent of mitochondrial tRNAs: new insights into the functions of taurine and human mitochondrial diseases

21 January 2018

1 reference

Occurrence of unmodified adenine and uracil at the first position of anticodon in threonine tRNAs in Mycoplasma capricolum

21 January 2018

1 reference

Different pattern of codon recognition by mammalian mitochondrial tRNAs

21 January 2018

1 reference

Codon recognition rules in yeast mitochondria

21 January 2018

1 reference

Molecular mechanism of codon recognition by tRNA species with modified uridine in the first position of the anticodon

21 January 2018

1 reference

1H NMR studies on the conformational characteristics of 2-thiopyrimidine nucleotides found in transfer RNAs

21 January 2018

1 reference

The nucleotide in position 32 of the tRNA anticodon loop determines ability of anticodon UCC to discriminate among glycine codons

21 January 2018

1 reference

Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

21 January 2018

1 reference

Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.

21 January 2018

1 reference

Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease

21 January 2018

1 reference

Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease

21 January 2018

1 reference

Modified uridines with C5-methylene substituents at the first position of the tRNA anticodon stabilize U.G wobble pairing during decoding

21 January 2018

1 reference

Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease

21 January 2018

1 reference

Single atom modification (O-->S) of tRNA confers ribosome binding.

21 January 2018

1 reference

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

21 January 2018

1 reference

Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.

21 January 2018

1 reference

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

21 January 2018

1 reference

An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

21 January 2018

1 reference

Mitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases

21 January 2018

1 reference

Acute infantile liver failure due to mutations in the TRMU gene.

21 January 2018

1 reference

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

21 January 2018

1 reference

A Novel Modified Nucleoside Found at the First Position of the Anticodon of Methionine tRNA from Bovine Liver Mitochondria

21 January 2018

1 reference

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/WRNA.65

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

21957023

1 reference

Consolidated OpenCitations Corpus – April 2017