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Revisiting oxidative damage in ALS: microglia, Nox, and mutant SOD1
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
title
Revisiting oxidative damage in ALS: microglia, Nox, and mutant SOD1
(English)
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
main subject
microglia
0 references
amyotrophic lateral sclerosis
1 reference
based on heuristic
inferred from title
nitrogen oxide
0 references
author
Don W. Cleveland
series ordinal
2
object named as
Don W Cleveland
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
author name string
Séverine Boillée
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
language of work or name
English
0 references
publication date
1 February 2008
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
volume
118
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
page(s)
474-478
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
cites work
SOD1 mutations disrupt redox-sensitive Rac regulation of NADPH oxidase in a familial ALS model
1 reference
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PubMed Central
reference URL
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30 September 2017
Redox modifier genes in amyotrophic lateral sclerosis in mice.
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PubMed Central
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30 September 2017
Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity
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PubMed Central
reference URL
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30 September 2017
Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons
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PubMed Central
reference URL
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30 September 2017
Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model
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PubMed Central
reference URL
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30 September 2017
The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology
1 reference
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PubMed Central
reference URL
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30 September 2017
Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis
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PubMed Central
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30 September 2017
ALS: a disease of motor neurons and their nonneuronal neighbors
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PubMed Central
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30 September 2017
The inflammatory NADPH oxidase enzyme modulates motor neuron degeneration in amyotrophic lateral sclerosis mice
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PubMed Central
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30 September 2017
Onset and progression in inherited ALS determined by motor neurons and microglia
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PubMed Central
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30 September 2017
A key role for the microglial NADPH oxidase in APP-dependent killing of neurons
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PubMed Central
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30 September 2017
Critical role for microglial NADPH oxidase in rotenone-induced degeneration of dopaminergic neurons.
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30 September 2017
NADPH oxidase mediates oxidative stress in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease
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30 September 2017
Chronic inhibition of glutamate uptake produces a model of slow neurotoxicity
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30 September 2017
Ischemic stroke injury is reduced in mice lacking a functional NADPH oxidase.
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28 June 2018
Manganese porphyrin given at symptom onset markedly extends survival of ALS mice
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PubMed Central
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21 September 2018
Exacerbation of motor neuron disease by chronic stimulation of innate immunity in a mouse model of amyotrophic lateral sclerosis.
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21 September 2018
Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice
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PubMed Central
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21 September 2018
Minocycline slows disease progression in a mouse model of amyotrophic lateral sclerosis
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PubMed Central
reference URL
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21 September 2018
Minocycline delays disease onset and mortality in a transgenic model of ALS.
1 reference
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PubMed Central
reference URL
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retrieved
21 September 2018
Rapid disease progression correlates with instability of mutant SOD1 in familial ALS
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2213376
retrieved
5 December 2018
Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18219386
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Characteristics of the inhibition of NADPH oxidase activation in neutrophils by apocynin, a methoxy-substituted catechol
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18219386
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI34613
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
PMCID
2213376
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
PubMed ID
18219386
1 reference
stated in
Europe PubMed Central
PMCID
2213376
retrieved
14 August 2017
ResearchGate publication ID
5633122
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