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The thankless task of playing genetics with mammalian mitochondrial DNA: a 30-year review.
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Europe PubMed Central
PubMed publication ID
16120305
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
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6 January 2020
title
The thankless task of playing genetics with mammalian mitochondrial DNA: a 30-year review
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
main subject
mitochondrial DNA
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author
Patricio Fernández-Silva
series ordinal
2
1 reference
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Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
José Antonio Enríquez
series ordinal
3
1 reference
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Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
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6 January 2020
author name string
M Pilar Bayona-Bafaluy
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1
1 reference
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Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
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6 January 2020
publication date
1 November 2002
1 reference
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Europe PubMed Central
PubMed publication ID
16120305
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retrieved
6 January 2020
published in
Mitochondrion
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
volume
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
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6 January 2020
page(s)
3-25
1 reference
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Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
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Relationship of genotype to phenotype in fibroblast-derived transmitochondrial cell lines carrying the 3243 mutation associated with the MELAS encephalomyopathy: shift towards mutant genotype and role of mtDNA copy number
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Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines
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Mitochondrial DNA of chloramphenicol-resistant mouse cells contains a single nucleotide change in the region encoding the 3' end of the large ribosomal RNA.
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A compilation of mutations located in the cytochrome b subunit of the bacterial and mitochondrial bc1 complex
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Genetics of the Mammalian Oxidative Phosphorylation System: Characterization of a New Oligomycin-Resistant Chinese Hamster Ovary Cell Line
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Respiration-deficient Chinese hamster cell mutants: Biochemical characterization
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Cytoplasmic inheritance of oligomycin resistance in Chinese hamster ovary cells
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MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase.
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7 January 2021
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Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation
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based on heuristic
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Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations
1 reference
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7 January 2021
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Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families
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7 January 2021
based on heuristic
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A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV.
1 reference
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7 January 2021
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Large-scale chromatographic purification of F1F0-ATPase and complex I from bovine heart mitochondria
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Cytoplasmic inheritance of chloramphenicol resistance in mouse tissue culture cells
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Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase
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7 January 2021
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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
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The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.
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An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy
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In vivo differentiation of yeast cytoplasmic and mitochondrial protein synthesis with antibiotics
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The biogenesis of mitochondria in Saccharomyces cerevisiae. A comparison between cytoplasmic respiratory-deficient mutant yeast and chlormaphenicol-inhibited wild type cells
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The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis
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7 January 2021
based on heuristic
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Conditionally lethal mutations in Chinese hamster cells. Characterization of a cell line with a possible defect in the krebs cycle
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7 January 2021
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based on heuristic
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Natural substances (acetogenins) from the family Annonaceae are powerful inhibitors of mitochondrial NADH dehydrogenase (Complex I)
1 reference
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Crossref
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7 January 2021
based on heuristic
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An established avian fibroblast cell line without mitochondrial DNA.
1 reference
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based on heuristic
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Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines
1 reference
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7 January 2021
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Cytoplasmic inheritance of erythromycin resistance in human cells
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Energy metabolism in respiration-deficient and wild type chinese hamster fibroblasts in culture
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence of the intron and flanking exons of the mitochondrial 21S rRNA gene of yeast strains having different alleles at the ω and rib-1 loci
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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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
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenone.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
A tRNA suppressor mutation in human mitochondria
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Chloramphenicol-erythromycin resistance mutations in a 23S rRNA gene of Escherichia coli
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
The same domain motif for ubiquinone reduction in mitochondrial or chloroplast NADH dehydrogenase and bacterial glucose dehydrogenase
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
The proton-pumping respiratory complex I of bacteria and mitochondria and its homologue in chloroplasts
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
On auxotrophy for pyrimidines of respiration-deficient chick embryo cells.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three-dimensional structure of NADH-dehydrogenase from Neurospora crassa by electron microscopy and conical tilt reconstruction
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional and molecular mitochondrial abnormalities associated with a C --> T transition at position 3256 of the human mitochondrial genome. The effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional and structural features of a tandem duplication of the human mtDNA promoter region
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytoplasmic transfer of resistance to antimycin A in Chinese hamster cells
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pyruvate blocks expression of sensitivity to antimycin A and chloramphenicol
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nucleotide changes in mitochondrial 16S rRNA gene from different mammalian cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel point mutations in mitochondrial 16S rRNA gene of Chinese hamster cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial electron transport and oxidative phosphorylation system
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A pathogenic 15-base pair deletion in mitochondrial DNA-encoded cytochrome c oxidase subunit III results in the absence of functional cytochrome c oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron microscopic analysis of the peripheral and membrane parts of mitochondrial NADH dehydrogenase (Complex I)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behaviour of a population of partially duplicated mitochondrial DNA molecules in cell culture: segregation, maintenance and recombination dependent upon nuclear background
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Origin, cellular expression, and cybrid transmission of mitochondrial CAP-R, PYR-IND, and OLI-R mutant phenotypes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence analysis of mitochondrial chloramphenicol resistance mutations in Chinese hamster cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence analysis of mouse mitochondrial chloramphenicol-resistant mutants.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial chloramphenicol-resistant mutants can have deficiencies in energy metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytoplasmic genetics of mammalian cells: Conditional sensitivity to mitochondrial inhibitors and isolation of new mutant phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mammalian mitochondrial mutants selected for resistance to the cytochromeb inhibitors HQNO or myxothiazol
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial genetics of mammalian cells: A mouse antimycin-resistant mutant with a probable alteration of cytochromeb
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Energy-driven subunit rotation at the interface between subunit a and the c oligomer in the F(O) sector of Escherichia coli ATP synthase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of mitochondrial DNA-less mouse cell lines and their application for trapping mouse synaptosomal mitochondrial DNA with deletion mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of mitochondrial DNA-less lines from various mammalian cell lines by application of an anticancer drug, ditercalinium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of human cell lines lacking mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
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/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oligomycin-resistant mitochondrial ATPase from mouse fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytoplasmic inheritance of rutamycin resistance in mouse fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial genetics in perspective: The derivation of a genetic and physical map of the yeast mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assembly of the mitochondrial membrane system: sequence analysis of a yeast mitochondrial ATPase gene containing the oli-2 and oli-4 loci
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in subunit 6 of the F1F0-ATP synthase cause two entirely different diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmitochondrial mice carrying resistance to chloramphenicol on mitochondrial DNA: developing the first mouse model of mitochondrial DNA disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative studies of the effects of acridines and other petite inducing drugs on the mitochondrial genome of Saccharomyces cerevisiae
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of Rattus norvegicus mtDNA in Mus musculus cells results in multiple respiratory chain defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protonmotive redox mechanism of the cytochrome b-c 1 complex in the respiratory chain: Protonmotive ubiquinone cycle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Possible molecular mechanisms of the protonmotive function of cytochrome systems
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chick embryo cells rendered respiration-deficient by chloramphenicol and ethidium bromide are auxotrophic for pyrimidines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the contribution of the mitochondrial genome to the growth of Chinese hamster embryo cells in culture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of two mitochondrially synthesized polypeptides to human mitochondrial DNA and their use in the study of intracellular mitochondrial interaction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative proteomics as a new tool for exploring human mitochondrial tRNA disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural changes linked to proton translocation by subunit c of the ATP synthase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inhibitors of respiration at energy-coupling site 2 of the respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Location of haem‐binding sites in the mitochondrial cytochrome b
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conditional lethal mutants of Chinese hamster cells: Mutants requiring exogenous carbondioxide for growth
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenesis of primary defects in mitochondrial ATP synthesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disposition of polar and nonpolar residues on outer surfaces of transmembrane helical segments of proteins involved in proton translocation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
degSegregation of Mitochondrial DNAs Carrying a Pathogenic Point Mutation (tRNAleu3243) in Cybrid Cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence analysis of mitochondrial DNA in a mouse cell line resistant to chloramphenicol and oligomycin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chloramphenicol-resistant mutants of human HeLa cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcomplementation between different types of respiration-deficient mitochondria with different pathogenic mutant mitochondrial DNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mitochondrial DNA mutation at 14577 T/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myxothiazol, a new antibiotic interfering with respiration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular Phenotype of the np 7472 Deafness-Associated Mitochondrial Mutation in Osteosarcoma Cell Cybrids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rotation of the c subunit oligomer in fully functional F1Fo ATP synthase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large conformational changes of the epsilon subunit in the bacterial F1F0 ATP synthase provide a ratchet action to regulate this rotary motor enzyme
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Both heavy strand replication origins are active in partially duplicated human mitochondrial DNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of a novel mitochondrial DNA deletion in a patient with a variant of the Pearson marrow-pancreas syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studies on the induction of petite mutants in yeast by analogues of berenil. Characterization of three mutants resistant to the compound Hoe 15,030.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Introduction of heteroplasmic mitochondrial DNA (mtDNA) from a patient with NARP into two human rho degrees cell lines is associated either with selection and maintenance of NARP mutant mtDNA or failure to maintain mtDNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Use of specific inhibitors on the mitochondrial bc1 complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the chloramphenicol resistance gene to mitochondrial deoxyribonucleic acid and analysis of its expression in cultured human cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytoplasmic transfer of chloramphenicol resistance in human tissue culture cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-7249%2802%2900044-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The respiratory-chain NADH dehydrogenase (complex I) of mitochondria
1 reference
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Mutation of a highly conserved base in the yeast mitochondrial 21S rRNA restricts ribosomal frameshifting.
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Sequence homology and structural similarity between cytochrome b of mitochondrial complex III and the chloroplast b6-f complex: position of the cytochrome b hemes in the membrane
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Reversible tenfod reduction in mitochondria DNA content of human cells treated with ethidium bromide
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Cytoplasmically inherited mutations of a human cell line resulting in deficient mitochondrial protein synthesis
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Crystal structure of the cytochrome bc1 complex from bovine heart mitochondria
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Procaryotic complex I (NDH-1), an overview
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Mice with only rat mtDNA are required as models of mitochondrial diseases
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A pathogenic point mutation reduces stability of mitochondrial mutant tRNA(Ile)
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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
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Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
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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
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Heteroplasmic mitochondrial tRNALys mutation and its complementation in MERRF patient-derived mitochondrial transformants
1 reference
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reference URL
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Elimination of mitochondrial elements and improved viability in hybrid cells.
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Identifiers
DOI
10.1016/S1567-7249(02)00044-2
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Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
PubMed publication ID
16120305
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16120305
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16120305%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
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