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A tRNA suppressor mutation in human mitochondria
scientific article published on 01 April 1998
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stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
title
A tRNA suppressor mutation in human mitochondria
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author
Ian Holt
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Howard Jacobs
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author name string
El Meziane A
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Lehtinen SK
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Hance N
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Nijtmans LG
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Dunbar D
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
publication date
1 April 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
volume
18
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
page(s)
350-353
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
cites work
Molecular genetic aspects of human mitochondrial disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical spectrum of mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybrids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA and RNA processing in MELAS.
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Sequence and organization of the human mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
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7 January 2021
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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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Crossref
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7 January 2021
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Suppression of a double missense mutation by a mutant tRNA(Phe) in Escherichia coli
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
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7 January 2021
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inferred from DOI database lookup
A mitochondrial tRNA anticodon swap associated with a muscle disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
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7 January 2021
based on heuristic
inferred from DOI database lookup
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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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies
1 reference
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Crossref
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7 January 2021
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Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Novel features in the genetic code and codon reading patterns in Neurospora crassa mitochondria based on sequences of six mitochondrial tRNAs
1 reference
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7 January 2021
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inferred from DOI database lookup
5-[[(carboxymethyl)amino]methyl]uridine is found in the anticodon of yeast mitochondrial tRNAs recognizing two-codon families ending in a purine
1 reference
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Crossref
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7 January 2021
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Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
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7 January 2021
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Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation.
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7 January 2021
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A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.
1 reference
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7 January 2021
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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
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Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa
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Crossref
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7 January 2021
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inferred from DOI database lookup
Assembly of mitochondrial ATP synthase in cultured human cells: implications for mitochondrial diseases
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Silver stain for proteins in polyacrylamide gels: A modified procedure with enhanced uniform sensitivity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0498-350
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0498-350
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
PubMed publication ID
9537417
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9537417
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9537417%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
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