(Q41085713)

26 September 2017

title

Pathophysiology of the MELAS 3243 transition mutation (English)

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26 September 2017

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Flierl A

1

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26 September 2017

Reichmann H

series ordinal

2

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26 September 2017

Seibel P

series ordinal

3

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26 September 2017

language of work or name

English

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publication date

1 October 1997

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Journal of Biological Chemistry

26 September 2017

published in

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26 September 2017

volume

272

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26 September 2017

issue

43

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26 September 2017

page(s)

27189-27196

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Diseases of the mitochondrial DNA.

26 September 2017

cites work

1 reference

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21 January 2018

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Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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Defects of oxidative phosphorylation in man.

21 January 2018

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Isolation of mitochondria from ascites tumor cells permeabilized with digitonin.

21 January 2018

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Sites of inhibition of mitochondrial electron transport in macrophage-injured neoplastic cells

21 January 2018

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

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Editing of a tRNA anticodon in marsupial mitochondria changes its codon recognition

21 January 2018

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Complexity and characterization of polyadenylated RNA in the mouse brain

21 January 2018

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Hybridization of nucleic acids immobilized on solid supports

21 January 2018

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Variation among human 28S ribosomal RNA genes

21 January 2018

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

21 January 2018

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Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

21 January 2018

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Expression of respiratory chain deficiencies in human cultured cells

21 January 2018

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Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis

21 January 2018

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Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form

21 January 2018

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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

21 January 2018

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Nucleo-Mitochondrial Interactions in Mitochondrial Gene Expression

21 January 2018

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Quantification of oxidative phosphorylation enzymes after blue native electrophoresis and two‐dimensional resolution: Normal complex I protein amounts in Parkinson's disease conflict with reduced catalytic activities

21 January 2018

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Nucleotide sequence of ornithine decarboxylase antizyme cDNA from Xenopus laevis

21 January 2018

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The glucose-starvation stimulon of Escherichia coli: induced and repressed synthesis of enzymes of central metabolic pathways and role of acetyl phosphate in gene expression and starvation survival.

21 January 2018

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Decreasing transcription elongation rate in Escherichia coli exposed to amino acid starvation

21 January 2018

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Relationship between protein synthesis and concentrations of charged and uncharged tRNATrp in Escherichia coli.

21 January 2018

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Starvation in vivo for aminoacyl-tRNA increases the spatial separation between the two ribosomal subunits.

21 January 2018

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Codon pair utilization biases influence translational elongation step times

21 January 2018

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Sequence and organization of the human mitochondrial genome

21 January 2018

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Leaky +1 and −1 frameshift mutations at the same site in a yeast mitochondrial gene

21 January 2018

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Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome

21 January 2018

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Identity of the soluble EBV-associated antigens of human lymphoid cell lines

21 January 2018

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Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain

21 January 2018

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Modified structure and kinetics of cytochrome-c oxidase in fibroblasts from patients with Leigh syndrome

21 January 2018

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Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)

21 January 2018

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Vacuum blotting enhances nucleic acid transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.43.27189

Slippery runs, shifty stops, backward steps, and forward hops: -2, -1, +1, +2, +5, and +6 ribosomal frameshifting

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.43.27189

On the mechanism of ribosomal frameshifting at hungry codons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.43.27189

Codon usage, transfer RNA availability and mistranslation in amino acid starved bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.43.27189

21 January 2018

Identifiers

DOI

10.1074/JBC.272.43.27189

1 reference

26 September 2017

1 reference