(Q36676493)

English

Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation

scientific article published on 8 April 2008

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scholarly article

1 reference

Europe PubMed Central

15 August 2017

Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation (English)

1 reference

Europe PubMed Central

15 August 2017

1 reference

based on heuristic

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Abdul Aziz Yusoff

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Abdul Aziz Yusoff

2

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object named as

Helen Tuppen

3

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object named as

Joanna Rorbach

1

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Robert McFarland

object named as

Robert McFarland

8

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Robert William Taylor

6

object named as

Robert W Taylor

1 reference

Europe PubMed Central

15 August 2017

Douglass Matthew Turnbull

7

object named as

Douglass M Turnbull

1 reference

Europe PubMed Central

15 August 2017

Zofia M Chrzanowska-Lightowlers

5

object named as

Zofia M A Chrzanowska-Lightowlers

1 reference

Europe PubMed Central

15 August 2017

Robert N Lightowlers

9

object named as

Robert N Lightowlers

1 reference

Europe PubMed Central

15 August 2017

author name string

Dyg P Abg-Kamaludin

4

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Europe PubMed Central

15 August 2017

language of work or name

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publication date

8 April 2008

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Europe PubMed Central

15 August 2017

Nucleic Acids Research

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Europe PubMed Central

15 August 2017

36

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Europe PubMed Central

15 August 2017

9

1 reference

Europe PubMed Central

15 August 2017

3065-3074

1 reference

Europe PubMed Central

15 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2396425/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Mutations in yeast mt tRNAs: specific and general suppression by nuclear encoded tRNA interactors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396425

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Mitochondrial DNA mutations in human disease

1 reference

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30 September 2017

Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS

1 reference

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30 September 2017

Characterization of the human mitochondrial methionyl-tRNA synthetase

1 reference

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30 September 2017

Recognition of human mitochondrial tRNALeu(UUR) by its cognate leucyl-tRNA synthetase.

1 reference

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Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genome

1 reference

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Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction

1 reference

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A one-step method for in vitro production of tRNA transcripts

1 reference

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Identification and characterization of human mitochondrial tryptophanyl-tRNA synthetase

1 reference

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A missense mutation in the nuclear gene coding for the mitochondrial aspartyl-tRNA synthetase suppresses a mitochondrial tRNA(Asp) mutation

1 reference

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30 September 2017

Expression and characterization of the human mitochondrial leucyl-tRNA synthetase

1 reference

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The 2.0 A crystal structure of Thermus thermophilus methionyl-tRNA synthetase reveals two RNA-binding modules

1 reference

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Expression and characterization of a human mitochondrial phenylalanyl-tRNA synthetase

1 reference

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The presence of modified nucleotides is required for cloverleaf folding of a human mitochondrial tRNA

1 reference

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In vivo labeling and analysis of human mitochondrial translation products

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396425

30 September 2017

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

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Structure of E. coli glutaminyl-tRNA synthetase complexed with tRNA(Gln) and ATP at 2.8 A resolution

1 reference

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Effect of extreme amino acid starvation on the protein synthetic machinery of CHO cells

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Reversal of a mitochondrial DNA defect in human skeletal muscle.

1 reference

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Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells

1 reference

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A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

1 reference

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5 September 2018

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

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The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units

1 reference

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Mitochondrial disorders

1 reference

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A novel role for aminoacyl-tRNA synthetases in the regulation of polypeptide chain initiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18400783

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18400783

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based on heuristic

inferred from PubMed ID database lookup

Homoplasmy, heteroplasmy, and mitochondrial dystonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18400783

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based on heuristic

inferred from PubMed ID database lookup

The interference of chloramphenicol and thiamphenicol with the biogenesis of mitochondria in animal tissues. A possible clue to the toxic action

1 reference

https://pubmed.ncbi.nlm.nih.gov/18400783

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/GKN147

1 reference

Europe PubMed Central

15 August 2017

1 reference

Europe PubMed Central

15 August 2017

1 reference

Europe PubMed Central

15 August 2017

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