(Q28217558)

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Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation

scientific article (publication date: 26 July 2002)

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scholarly article

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Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation (English)

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1 reference

based on heuristic

inferred from title

Mitochondrial tRNA translation optimization 1

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GOA release 2020-03-11

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based on heuristic

inferred from title

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based on heuristic

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author name string

Xiaoming Li

1

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Ronghua Li

2

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Xinhua Lin

3

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Min-Xin Guan

4

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language of work or name

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publication date

26 July 2002

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Journal of Biological Chemistry

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277

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30

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27256-64

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Mitochondrial DNA mutations and pathogenesis

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https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Mitochondrial diseases in man and mouse

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https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Mitochondrial deafness mutations reviewed

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https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

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.M203267200

21 January 2018

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Candidate locus for a nuclear modifier gene for maternally inherited deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Characterization of a collection of deletion mutants at the 3'-end of 16S ribosomal RNA of Escherichia coli.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Interaction of antibiotics with functional sites in 16S ribosomal RNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Effects of mutagenesis of a conserved base-paired site near the decoding region of Escherichia coli 16 S ribosomal RNA.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Nonsense suppressor and antisuppressor mutations at the 1409-1491 base pair in the decoding region of Escherichia coli 16S rRNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

MTO1 codes for a mitochondrial protein required for respiration in paromomycin-resistant mutants of Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

MSS1, a nuclear-encoded mitochondrial GTPase involved in the expression of COX1 subunit of cytochrome c oxidase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Translational misreading: a tRNA modification counteracts a +2 ribosomal frameshift

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Information content of individual genetic sequences.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

A cDNA encoding a human CCAAT-binding protein cloned by functional complementation in yeast

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Applications of high efficiency lithium acetate transformation of intact yeast cells using single-stranded nucleic acids as carrier

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

DNA sequence around the Escherichia coli unc operon. Completion of the sequence of a 17 kilobase segment containing asnA, oriC, unc, glmS and phoS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Protein sorting to mitochondria: evolutionary conservations of folding and assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Undermodification in the first position of the anticodon of supG-tRNA reduces translational efficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Novel E. coli mutants deficient in biosynthesis of 5-methylaminomethyl-2-thiouridine

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Multiple zinc finger forms resulting from developmentally regulated alternative splicing of a transcription factor gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

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.M203267200

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.M203267200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

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.M203267200

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.M203267200

21 January 2018

Two-locus mitochondrial and nuclear gene models for mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Compilation of small ribosomal subunit RNA sequences

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

The paromomycin resistance mutation (parr-454) in the 15 S rRNA gene of the yeast Saccharomyces cerevisiae is involved in ribosomal frameshifting

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Mitochondrial genetics, circular DNA and the mechanism of the petite mutation in yeast

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Aminoacylation of hypomodified tRNAGlu in vivo

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M203267200

21 January 2018

Identifiers

10.1074/JBC.M203267200

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