A tRNA suppressor mutation in human mitochondria (Q74428372)

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10 November 2019

title

A tRNA suppressor mutation in human mitochondria (English)

1 reference

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10 November 2019

6

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10 November 2019

Howard Jacobs

7

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10 November 2019

author name string

El Meziane A

1

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10 November 2019

Lehtinen SK

2

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10 November 2019

Hance N

3

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10 November 2019

Nijtmans LG

4

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10 November 2019

Dunbar D

5

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10 November 2019

publication date

1 April 1998

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10 November 2019

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10 November 2019

volume

18

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10 November 2019

issue

4

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10 November 2019

page(s)

350-353

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Molecular genetic aspects of human mitochondrial disorders

10 November 2019

cites work

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7 January 2021

Clinical spectrum of mitochondrial diseases

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7 January 2021

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

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7 January 2021

Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybrids

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7 January 2021

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

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7 January 2021

Mitochondrial DNA and RNA processing in MELAS.

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7 January 2021

Sequence and organization of the human mitochondrial genome

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7 January 2021

Glycine transfer RNA of Escherichia coli. II. Impaired GGA-recognition in strains containing a genetically altered transfer RNA; reversal by a secondary suppressor mutation

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7 January 2021

Suppression of a double missense mutation by a mutant tRNA(Phe) in Escherichia coli

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7 January 2021

A mitochondrial tRNA anticodon swap associated with a muscle disease

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7 January 2021

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

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7 January 2021

Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies

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7 January 2021

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

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7 January 2021

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

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7 January 2021

5-[[(carboxymethyl)amino]methyl]uridine is found in the anticodon of yeast mitochondrial tRNAs recognizing two-codon families ending in a purine

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7 January 2021

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

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7 January 2021

Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation.

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7 January 2021

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Assembly of mitochondrial ATP synthase in cultured human cells: implications for mitochondrial diseases

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7 January 2021

Silver stain for proteins in polyacrylamide gels: A modified procedure with enhanced uniform sensitivity

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7 January 2021

Identifiers

DOI

10.1038/NG0498-350

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10 November 2019

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