(Q34682177)

3 August 2017

title

The role of the NADPH oxidase NOX2 in prion pathogenesis (English)

1 reference

3 August 2017

0 references

8

Herbert Budka

0 references

Silvia Sorce

Silvia Sorce

1

0 references

Mario Nuvolone

Mario Nuvolone

2

0 references

Annika Keller

Annika Keller

3

0 references

Adriano Aguzzi

9

Adriano Aguzzi

1 reference

3 August 2017

Jeppe Falsig

4

1 reference

3 August 2017

Ahmet Varol

5

1 reference

3 August 2017

Petra Schwarz

6

1 reference

3 August 2017

Monika Bieri

7

1 reference

3 August 2017

Herbert Budka

8

1 reference

3 August 2017

publication date

11 December 2014

1 reference

3 August 2017

1 reference

3 August 2017

volume

10

1 reference

3 August 2017

issue

12

1 reference

3 August 2017

page(s)

e1004531

1 reference

Creative Commons Attribution 4.0 International

3 August 2017

copyright license

start time

11 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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SIRPα polymorphisms, but not the prion protein, control phagocytosis of apoptotic cells

7 July 2018

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Oral treatment targeting the unfolded protein response prevents neurodegeneration and clinical disease in prion-infected mice

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The toxicity of antiprion antibodies is mediated by the flexible tail of the prion protein

7 July 2018

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Sod1 deficiency reduces incubation time in mouse models of prion disease

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7 July 2018

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Evidence for varied aetiologies regulating the transmission of prion disease: implications for understanding the heritable basis of prion incubation times

7 July 2018

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Engulfment of cerebral apoptotic bodies controls the course of prion disease in a mouse strain-dependent manner

7 July 2018

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7 July 2018

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7 July 2018

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Nox2-derived radicals contribute to neurovascular and behavioral dysfunction in mice overexpressing the amyloid precursor protein

7 July 2018

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A versatile prion replication assay in organotypic brain slices

7 July 2018

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7 July 2018

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The inflammatory NADPH oxidase enzyme modulates motor neuron degeneration in amyotrophic lateral sclerosis mice

7 July 2018

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7 July 2018

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Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

7 July 2018

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7 July 2018

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Mice devoid of PrP are resistant to scrapie

7 July 2018

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7 July 2018

1 reference

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Normal host prion protein necessary for scrapie-induced neurotoxicity

7 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

PDK1 decreases TACE-mediated α-secretase activity and promotes disease progression in prion and Alzheimer's diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Oxidative damage to nucleic acids in human prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Extracellular protein deposition correlates with glial activation and oxidative stress in Creutzfeldt-Jakob and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Oxidative stress in the brain at early preclinical stages of mouse scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Experimental autoimmune encephalomyelitis repressed by microglial paralysis.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Neuroaxonal pathology in Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Immunohistochemical study of microglia in the Creutzfeldt-Jakob diseased brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Accelerated clinical course of prion disease in mice compromised in repair of oxidative DNA damage.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4263757

Mitochondrial susceptibility to oxidative stress exacerbates cerebral infarction that follows permanent focal cerebral ischemia in mutant mice with manganese superoxide dismutase deficiency.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4263757

Correlative studies support lipid peroxidation is linked to PrPres propagation as an early primary pathogenic event in prion disease

26 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1004531

Quantitative trait loci affecting prion incubation time in mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25502554

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Reactive microglia in Creutzfeldt-Jakob disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25502554

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PPAT.1004531

1 reference

3 August 2017

1 reference

3 August 2017

1 reference