(Q40873200)

English

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.

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scholarly article

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7 November 2019

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 (English)

1 reference

Europe PubMed Central

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7 November 2019

lactic acidosis

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

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based on heuristic

inferred from title

José Antonio Enríquez

2

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7 November 2019

3

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7 November 2019

Patricio Fernández-Silva

4

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7 November 2019

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Chomyn A

1

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7 November 2019

Attardi G

5

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7 November 2019

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1 June 2000

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7 November 2019

Journal of Biological Chemistry

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7 November 2019

275

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7 November 2019

19198-19209

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7 November 2019

25

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7 November 2019

Mitochondrial DNA mutations and pathogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Mitochondrial mutation associated with nonsyndromic deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Pathophysiology of the MELAS 3243 transition mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Functional analysis of in vivo and in organello footprinting of HeLa cell mitochondrial DNA in relationship to ATP and ethidium bromide effects on transcription.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Production of Microcell Hybrids

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

57 Sequencing end-labeled DNA with base-specific chemical cleavages

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Analysis of aminoacylation of human mitochondrial tRNAs

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

In vivo labeling and analysis of human mitochondrial translation products

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Expression of the mitochondrial genome in HeLa cells. X. Properties of mitochondrial polysomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

An operational RNA code for amino acids and possible relationship to genetic code

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

The transfer RNA identity problem: a search for rules

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

An unusual RNA tertiary interaction has a role for the specific aminoacylation of a transfer RNA.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Influence of tRNA tertiary structure and stability on aminoacylation by yeast aspartyl-tRNA synthetase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Yeast tRNA(Met) recognition by methionyl-tRNA synthetase requires determinants from the primary, secondary and tertiary structure: a review

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

A protein complex mediating mRNA degradation in Escherichia coli.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Cloning and sequence analysis of the human mitochondrial translational initiation factor 2 cDNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Relaxation of a transfer RNA specificity by removal of modified nucleotides

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M908734199

21 January 2018

Identifiers

10.1074/JBC.M908734199

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10858457%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10858457%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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