Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation. (Q40900095)

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4 November 2019

title

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

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4 November 2019

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4 November 2019

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4 November 2019

T Yasukawa

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4 November 2019

N Ishii

series ordinal

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4 November 2019

S Ohta

series ordinal

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4 November 2019

K Watanabe

series ordinal

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4 November 2019

language of work or name

English

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publication date

1 February 2000

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4 November 2019

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4 November 2019

volume

467

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4 November 2019

issue

2-3

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4 November 2019

page(s)

175-178

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Diseases of the mitochondrial DNA.

4 November 2019

cites work

1 reference

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Mitochondrial DNA mutations and pathogenesis

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

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

1 reference

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Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

21 January 2018

1 reference

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

21 January 2018

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Different pattern of codon recognition by mammalian mitochondrial tRNAs

21 January 2018

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

21 January 2018

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Human mitochondrial diseases: answering questions and questioning answers

21 January 2018

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Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function

21 January 2018

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Analysis of modified nucleosides and nucleotide sequence of tRNA

21 January 2018

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Mobilities of modified ribonucleotides on two-dimensional cellulose thin-layer chromatography

21 January 2018

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The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate

21 January 2018

1 reference

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A novel wobble rule found in starfish mitochondria. Presence of 7-methylguanosine at the anticodon wobble position expands decoding capability of tRNA

21 January 2018

1 reference

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Translation of synonymous codons in family boxes by Mycoplasma capricolum tRNAs with unmodified uridine or adenosine at the first anticodon position

21 January 2018

1 reference

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10.1016/S0014-5793(00)01145-5

21 January 2018

Identifiers

DOI

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4 November 2019

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