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English
Human mitochondrial diseases: answering questions and questioning answers
scientific article published on 01 January 1999
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1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Human mitochondrial diseases: answering questions and questioning answers
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author name string
N Howell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
publication date
1 January 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
International Review of Cytology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
186
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
49-116
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
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Energy metabolism of rabbit retina as related to function: high cost of Na+ transport
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Sequence and organization of the human mitochondrial genome
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Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems
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Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation
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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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Axotomy results in delayed death and apoptosis of retinal ganglion cells in adult rats.
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Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.
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7 January 2021
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Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes
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7 January 2021
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The amyloid beta protein induces oxidative damage of mitochondrial DNA.
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7 January 2021
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Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations
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7 January 2021
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Mitochondrial DNA sequences of primates: Tempo and mode of evolution
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X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation
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Optic disk risk factors for nonarteritic anterior ischemic optic neuropathy.
1 reference
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7 January 2021
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Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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Mitochondrial DNA and human evolution
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Crossref
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7 January 2021
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Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.
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Crossref
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7 January 2021
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Leber’s Hereditary Optic Neuroretinopathy and the X-Chromosomal Susceptibility Factor: No Linkage to DXS7
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Crossref
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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
Clinical features, investigation, and management of patients with defects of mitochondrial DNA.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
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Crossref
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7 January 2021
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inferred from DOI database lookup
A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegia
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Crossref
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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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Crossref
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7 January 2021
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Reversal of a mitochondrial DNA defect in human skeletal muscle.
1 reference
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7 January 2021
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inferred from DOI database lookup
Optic neuritis with prolonged use of chloramphenicol. Case report and relationship to fundus changes in cystic fibrosis
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Crossref
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7 January 2021
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Respiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease
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Crossref
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Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study
1 reference
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Crossref
reference URL
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7 January 2021
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An oxidative damage-specific endonuclease from rat liver mitochondria.
1 reference
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Crossref
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7 January 2021
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At least two mechanisms are involved in the death of retinal ganglion cells following target ablation in neonatal rats
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Crossref
reference URL
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7 January 2021
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Leber's hereditary optic neuropathy masquerading as tobacco-alcohol amblyopia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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Threshold effects in synaptosomal and nonsynaptic mitochondria from hippocampal CA1 and paramedian neocortex brain regions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
In situ localization of mitochondrial DNA replication in intact mammalian cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Greater sensitivity of larger retinal ganglion cells to NMDA-mediated cell death
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Elevated glutamate levels in the vitreous body of humans and monkeys with glaucoma
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping frequencies of endogenous oxidative damage and the kinetic response to oxidative stress in a region of rat mtDNA.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
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1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Axonal transport blockade in the neonatal rat optic nerve induces limited retinal ganglion cell death.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanisms of optic nerve damage in primary open angle glaucoma
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pathophysiology of the MELAS 3243 transition mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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7 January 2021
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inferred from DOI database lookup
An intrinsic time limit between genesis and death of individual neurons in the developing retinal ganglion cell layer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paternal inheritance of mitochondrial DNA in mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
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%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human mitochondria and mitochondrial genome function as a single dynamic cellular unit
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal inheritance of the mouse mitochondrial genome is not mediated by a loss or gross alteration of the paternal mitochondrial DNA or by methylation of the oocyte mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fate of sperm tail components after incorporation into the hamster egg
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of constriction of optic nerve axons at the lamina cribrosa in the normotensive eye in humans and other mammals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inheritance and expression of mitochondrial DNA point mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mtDNA recombination: what do in vitro data mean?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber hereditary optic neuropathy: how do mitochondrial DNA mutations cause degeneration of the optic nerve?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Origin, transmission, and segregation of mitochondrial DNA dimers in mouse hybrid and cybrid cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of the mitochondrial 8344 MERRF mutation with maternally inherited spinocerebellar degeneration and Leigh disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mtDNA mutations that cause optic neuropathy: how do we know?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Visual recovery in a patient with Leber hereditary optic neuropathy and the 14484 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Random mitotic segregation of mitochondrial DNA in MELAS syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Visual disturbances in cystic fibrosis following chloramphenicol administration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations of mitochondrial genome in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequences attaching loops of nuclear and mitochondrial DNA to underlying structures in human cells: the role of transcription units
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic neuropathy with the 11 778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The histochemical localization of cytochrome oxidase in the retina and lateral geniculate nucleus of the ferret, cat, and monkey, with particular reference to retinal mosaics and ON/OFF-center visual channels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elimination of paternal mitochondrial DNA in intraspecific crosses during early mouse embryogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Study of regulation of mitochondrial respiration in vivo
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial manganese superoxide dismutase prevents neural apoptosis and reduces ischemic brain injury: suppression of peroxynitrite production, lipid peroxidation, and mitochondrial dysfunction.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TUNEL-positive ganglion cells in human primary open-angle glaucoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial mutational spectra in human cells and tissues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial reticulum in limb skeletal muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neandertal DNA sequences and the origin of modern humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular and cellular mechanisms of mitochondrial nuclear division and mitochondriokinesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic aspects of human mitochondrial disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic neuropathy and complex I deficiency in muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apoptosis of retinal ganglion cells in anterior ischemic optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Quantitative allele-specific PCR: demonstration of age-associated accumulation in human tissues of the A-->G mutation at nucleotide 3243 in mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chloramphenicol for long-term therapy of cystic fibrosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A role for recombination junctions in the segregation of mitochondrial DNA in yeast
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by31P magnetic resonance spectroscopy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial Eve: the plot thickens
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Excitotoxicity, energy metabolism and neurodegeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation accumulation in nuclear, organelle, and prokaryotic transfer RNA genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mtDNA mutation rates--no need to panic
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Blindness in offspring of women blinded by Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber hereditary optic neuropathy in Australia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tobacco amblyopia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reply to Hofmann et al.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Catalytic activity of complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The fate of human sperm-derived mtDNA in somatic cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distribution of axonal and glial elements in the rhesus optic nerve head studied by electron microscopy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA. I. Intramitochondrial distribution and structural relations of single- and double-length circular DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of mitochondrial DNA nucleoids in wild-type and a mutant strain of Saccharomyces cerevisiae that lacks the mitochondrial HMG box protein Abf2p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A quantitative analysis of mitochondria during fetal mouse oogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial transmission during mating in Saccharomyces cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Local Supply of Energy to the Fast Axoplasmic Transport Mechanism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the many faces of Leber hereditary optic neuropathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanisms of cell death induced by the mitochondrial toxin 3-nitropropionic acid: acute excitotoxic necrosis and delayed apoptosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A high observed substitution rate in the human mitochondrial DNA control region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rethinking cell structure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Number of mitochondria and some properties of mitochondrial DNA in the mouse egg
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Confirmation that neither cyanide intoxication nor mutations commonly associated with Leber's Hereditary Optic Neuropathy are implicated in Tanzanian Epidemic Optic Neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Noninvasive diagnosis of the MELAS syndrome from blood DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ganglion cell death in glaucoma: pathology recapitulates ontogeny
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chronic human glaucoma causing selectively greater loss of large optic nerve fibers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apoptotic cell death induced by optic nerve lesion in the neonatal rat.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Anatomy of the lamina cribrosa in human eyes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electrophysiological exploration of visual function in mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adenosine triphosphate deficiency: a genre of optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal ischemia leads to apoptosis which is ameliorated by aurintricarboxylic acid
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The effect of ionic conditions on the conformations of supercoiled DNA. II. Equilibrium catenation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The nerve of glaucoma!
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the voltage dependence of the mitochondrial permeability transition pore. A critical appraisal.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA maintenance in vertebrates
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fate of sperm organelles during early embryogenesis in the rat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA diseases: histological and cellular studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heteroplasmy in Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Platelet mitochondrial function in Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic Epilepsy with Ragged‐red Fibers (MERRF): An Immunohistochemical Study of the Brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of glutamate toxicity in retinal ganglion cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fate of the sperm mitochondria, and the incorporation, conversion, and disassembly of the sperm tail structures during bovine fertilization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is all nondefinable optic atrophy Leber's hereditary optic neuropathy?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Origin and functional consequences of the complex I defect in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cybrids in Alzheimer's disease: a cellular model of the disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Treatment of mitochondrial disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The "Eve" Hypotheses: A Genetic Critique and Reanalysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mammalian mitochondria possess homologous DNA recombination activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochemical evidence of an organized microtubular cytoskeleton inXenopus laevis oocytes: Involvement in the segregation of mitochondrial populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bcl-xL regulates the membrane potential and volume homeostasis of mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LEBER'S DISEASE IN THE NETHERLANDS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct genomic copy number in mitochondria of different mammalian organs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for preserved direct pupillary light response in Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
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%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atypical Leber's hereditary optic neuropathy with molecular confirmation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic atrophy: some clinical and aetiological considerations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome oxidase in Alzheimer's disease: biochemical, histochemical, and immunohistochemical analyses of the visual and other systems
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of Ganglion Cell Loss and Cone Loss in Experimental Glaucoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevention of apoptosis by Bcl-2: release of cytochrome c from mitochondria blocked
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Among-site rate variation and its impact on phylogenetic analyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged red fibers (MERRF) syndrome: selective vulnerability of CNS neurons does not correlate with the level of mitochondrial tRNAlys mutation in individual neuronal isolates.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2961051-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0074-7696(08)61051-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
9770297
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9770297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9770297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
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