Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (Q28144145)

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scientific article (publication date: 11 February 2000)

Language	Label	Description	Also known as
English	Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes	scientific article (publication date: 11 February 2000)

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scholarly article

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

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based on heuristic

inferred from title

lactic acidosis

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based on heuristic

inferred from title

mitochondrial myopathy

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based on heuristic

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author name string

T Yasukawa

1

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T Suzuki

2

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T Ueda

3

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S Ohta

4

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K Watanabe

5

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language of work or name

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publication date

11 February 2000

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Journal of Biological Chemistry

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275

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4251-7

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6

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Mitochondrial DNA mutations and pathogenesis

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https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

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.275.6.4251

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

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

1 reference

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21 January 2018

Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271.

1 reference

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21 January 2018

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

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.275.6.4251

21 January 2018

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

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.275.6.4251

21 January 2018

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

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.275.6.4251

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.275.6.4251

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.275.6.4251

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.275.6.4251

21 January 2018

Higher-order structure of bovine mitochondrial tRNA(Phe) lacking the 'conserved' GG and T psi CG sequences as inferred by enzymatic and chemical probing.

1 reference

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21 January 2018

Effects of ethidium bromide treatment of mouse cells on expression and assembly of nuclear-coded subunits of complexes involved in the oxidative phosphorylation.

1 reference

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21 January 2018

Phy M: an RNase activity specific for U and A residues useful in RNA sequence analysis

1 reference

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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

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21 January 2018

Compilation of tRNA sequences and sequences of tRNA genes

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https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

Pathophysiology of the MELAS 3243 transition mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

The 'polysemous' codon--a codon with multiple amino acid assignment caused by dual specificity of tRNA identity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

Different pattern of codon recognition by mammalian mitochondrial tRNAs

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

Novel features in the genetic code and codon reading patterns in Neurospora crassa mitochondria based on sequences of six mitochondrial tRNAs

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

7-Methylguanosine at the anticodon wobble position of squid mitochondrial tRNA(Ser)GCU: molecular basis for assignment of AGA/AGG codons as serine in invertebrate mitochondria.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

A new method for identifying the amino acid attached to a particular RNA in the cell

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.6.4251

21 January 2018

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