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Mitochondrial DNA mutations, oxidative stress, and aging
scientific article published on 01 September 2001
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Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
title
Mitochondrial DNA mutations, oxidative stress, and aging
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author name string
T R Golden
series ordinal
1
1 reference
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Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
S Melov
series ordinal
2
1 reference
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Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
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10 November 2019
publication date
1 September 2001
1 reference
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Europe PubMed Central
PubMed publication ID
11511398
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
published in
Mechanisms of Ageing and Development
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stated in
Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
volume
122
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
issue
14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
page(s)
1577-1589
1 reference
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Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
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10 November 2019
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Determination of the production of superoxide radicals and hydrogen peroxide in mitochondria
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Oxidative stress and Alzheimer disease
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Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age
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7 January 2021
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Oxidative biochemical markers; clues to understanding aging in long-lived species
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Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction
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Lipid peroxidation: its mechanism, measurement, and significance
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Dependence of H2O2 formation by rat heart mitochondria on substrate availability and donor age.
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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
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Point mutations of mitochondrial genome in Parkinson's disease
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Unaltered aconitase activity, but decreased complex I activity in substantia nigra pars compacta of patients with Parkinson's disease
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Mitochondrial manganese superoxide dismutase prevents neural apoptosis and reduces ischemic brain injury: suppression of peroxynitrite production, lipid peroxidation, and mitochondrial dysfunction.
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Mitochondrial mutational spectra in human cells and tissues
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Rapid accumulation of deleted mitochondrial deoxyribonucleic acid in postmenopausal ovaries
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Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1
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Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin
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Multiple mitochondrial DNA deletions associated with age in skeletal muscle of rhesus monkeys.
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Mitochondrial DNA 4977 bp deletion and OH8dG levels correlate in the brain of aged subjects but not Alzheimer's disease patients.
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Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase
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Quantitative allele-specific PCR: demonstration of age-associated accumulation in human tissues of the A-->G mutation at nucleotide 3243 in mitochondrial DNA
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7 January 2021
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Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing
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7 January 2021
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Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
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7 January 2021
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Cellular actions of beta-amyloid precursor protein and its soluble and fibrillogenic derivatives
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7 January 2021
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Mitochondrial disease in superoxide dismutase 2 mutant mice
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7 January 2021
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Multi-organ characterization of mitochondrial genomic rearrangements in ad libitum and caloric restricted mice show striking somatic mitochondrial DNA rearrangements with age
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7 January 2021
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Increased frequency of deletions in the mitochondrial genome with age of Caenorhabditis elegans
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7 January 2021
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Extension of Life-Span with Superoxide Dismutase/Catalase Mimetics
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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Mitochondrial DNA rearrangements in aging human brain and in situ PCR of mtDNA
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Crossref
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7 January 2021
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A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase
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7 January 2021
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Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication
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7 January 2021
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Oxidative stress is not an obligate mediator of disease provoked by mitochondrial DNA mutations
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7 January 2021
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Human aging is associated with various point mutations in tRNA genes of mitochondrial DNA.
1 reference
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7 January 2021
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The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method
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7 January 2021
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Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
Indices of oxidative stress in Parkinson's disease, Alzheimer's disease and dementia with Lewy bodies.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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Molecular genetics and pathogenesis of Friedreich ataxia
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7 January 2021
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
Structural and replicative forms of mitochondrial DNA from human leukocytes in relation to age
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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Mitochondria, oxygen free radicals, disease and ageing
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
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Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia
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reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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Mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson's Disease Research Group
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reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial dysfunction in neurodegenerative disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High levels of mitochondrial DNA deletions in skeletal muscle of old rhesus monkeys
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA diseases: histological and cellular studies
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
Role of oxidized amino acids in protein breakdown and stability
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of mtDNA deletions in muscle by in situ hybridization
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial diseases in man and mouse
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis
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Crossref
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
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https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
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inferred from DOI database lookup
Manganese superoxide dismutase protects mitochondrial complex I against adriamycin-induced cardiomyopathy in transgenic mice
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mitochondrial DNA deletions in an elderly human individual
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Construction of transgenic mice with tissue-specific acceleration of mitochondrial DNA mutagenesis
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900288-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0047-6374(01)00288-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
PubMed publication ID
11511398
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11511398
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11511398%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
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