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Mitochondrial dysfunction in Parkinson's disease
scientific article published on 27 April 2007
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
review article
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stated in
Europe PubMed Central
title
Mitochondrial dysfunction in Parkinson's disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
main subject
Parkinson's disease
1 reference
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inferred from title
author
Anthony H V Schapira
series ordinal
1
object named as
A H V Schapira
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Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
publication date
27 April 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Cell Death & Differentiation
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
14
1 reference
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Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
1261-1266
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/sj.cdd.4402160
0 references
cites work
Mitochondrial complex I deficiency in Parkinson's disease
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Complex I, iron, and ferritin in Parkinson's disease substantia nigra
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Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease
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L-dihydroxyphenylalanine and complex I deficiency in Parkinson's disease brain
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Mitochondrial respiratory chain function in multiple system atrophy
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Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisal
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A 31P magnetic resonance spectroscopy study of mitochondrial function in skeletal muscle of patients with Parkinson's disease
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Generalized mitochondrial dysfunction in Parkinson's disease detected by magnetic resonance spectroscopy of muscle
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7 January 2021
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Abnormalities of the electron transport chain in idiopathic Parkinson's disease
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Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group
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Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease
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Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence
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7 January 2021
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Mitochondrial DNA analysis in Parkinson's disease
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Crossref
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7 January 2021
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Mitochondrial DNA in postmortem brain from patients with Parkinson's disease.
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7 January 2021
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Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.
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High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
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Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease
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Point mutations of mitochondrial genome in Parkinson's disease
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7 January 2021
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Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.
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7 January 2021
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Absence of the mitochondrial A7237T mutation in Parkinson's disease
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7 January 2021
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Novel mitochondrial DNA mutations in Parkinson's disease
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7 January 2021
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Sequence analysis of the entire mitochondrial genome in Parkinson's disease
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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease
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Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.
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mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish
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Origin and functional consequences of the complex I defect in Parkinson's disease
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Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease
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Mitochondrial ND5 mutations in idiopathic Parkinson's disease
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Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
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A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
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Analysis of the trinucleotide CAG repeat from the DNA polymerase gamma gene (POLG) in patients with Parkinson's disease.
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7 January 2021
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Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.
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Proteome analysis reveals phosphorylation of ATP synthase beta -subunit in human skeletal muscle and proteins with potential roles in type 2 diabetes.
1 reference
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Analysis of steady-state protein phosphorylation in mitochondria using a novel fluorescent phosphosensor dye.
1 reference
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7 January 2021
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1 reference
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inferred from DOI database lookup
Characterization of dynamic and steady-state protein phosphorylation using a fluorescent phosphoprotein gel stain and mass spectrometry
1 reference
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reference URL
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7 January 2021
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1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.CDD.4402160
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7 January 2021
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inferred from DOI database lookup
Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons
1 reference
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reference URL
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7 January 2021
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inferred from DOI database lookup
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FSJ.CDD.4402160
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7 January 2021
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inferred from DOI database lookup
Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants
1 reference
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reference URL
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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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7 January 2021
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1 reference
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Crossref
reference URL
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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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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
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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
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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/10.1038%2FSJ.CDD.4402160
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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/10.1038%2FSJ.CDD.4402160
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7 January 2021
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inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.CDD.4402160
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.CDD.4402160
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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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7 January 2021
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inferred from DOI database lookup
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1 reference
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reference URL
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7 January 2021
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reference URL
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7 January 2021
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1 reference
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7 January 2021
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1 reference
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7 January 2021
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Interactions of the neurotoxic amine 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine with monoamine oxidases
1 reference
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7 January 2021
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1 reference
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7 January 2021
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1 reference
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reference URL
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7 January 2021
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inferred from DOI database lookup
Active uptake of MPP+, a metabolite of MPTP, by brain synaptosomes.
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Uptake of MPP(+) by dopamine neurons explains selectivity of parkinsonism-inducing neurotoxin, MPTP.
1 reference
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reference URL
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7 January 2021
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1 reference
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7 January 2021
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Protection against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism by the catecholamine uptake inhibitor nomifensine: behavioral analysis in monkeys with partial striatal dopamine depletions
1 reference
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1 reference
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7 January 2021
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7 January 2021
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7 January 2021
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7 January 2021
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CHILD CARE IN GENERAL PRACTICE: MENTALLY SUBNORMAL CHILDREN.
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7 January 2021
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7 January 2021
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7 January 2021
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Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FSJ.CDD.4402160
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7 January 2021
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Mitochondrial involvement in Parkinson's disease
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.CDD.4402160
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7 January 2021
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Identifiers
DOI
10.1038/SJ.CDD.4402160
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Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PubMed publication ID
17464321
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17464321
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17464321%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
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