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NADPH oxidases as drug targets and biomarkers in neurodegenerative diseases: What is the evidence?

Free radical biology & medicine, 2017-11, Vol.112, p.387-396

2017

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Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

Proceedings of the National Academy of Sciences - PNAS, 2010-06, Vol.107 (26), p.12005-12010

2010

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The Structural Architecture of an Infectious Mammalian Prion Using Electron Cryomicroscopy

PLoS pathogens, 2016-09, Vol.12 (9), p.e1005835-e1005835

2016

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α-Synuclein Amyloids Hijack Prion Protein to Gain Cell Entry, Facilitate Cell-to-Cell Spreading and Block Prion Replication

Scientific reports, 2017-08, Vol.7 (1), p.10050-12, Article 10050

2017

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Creutzfeldt‐Jakob disease

Neuropathology, 2017-04, Vol.37 (2), p.174-188

Iwasaki, Yasushi

2017

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Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

JAMA neurology, 2020-09, Vol.77 (9), p.1141

2020

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Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients

Emerging infectious diseases, 2017-06, Vol.23 (6), p.946-956

2017

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Tau pathology in Creutzfeldt‐Jakob disease revisited

Brain pathology (Zurich, Switzerland), 2017-05, Vol.27 (3), p.332-344

2017

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CSF neurogranin as a neuronal damage marker in CJD: a comparative study with AD

Journal of neurology, neurosurgery and psychiatry, 2019-08, Vol.90 (8), p.846-853

2019

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Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Brain (London, England : 1878), 2015-11, Vol.138 (Pt 11), p.3386-3399

2015

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Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK

Acta neuropathologica, 2017-08, Vol.134 (2), p.221-240

2017

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Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone

Nature medicine, 2024-02, Vol.30 (2), p.394-402

2024

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Imaging of Creutzfeldt-Jakob Disease: Imaging Patterns and Their Differential Diagnosis

Radiographics, 2017-01, Vol.37 (1), p.234-257

2017

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Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias

Neurology, 2011-05, Vol.76 (20), p.1711-1719

2011

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Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice

PLoS pathogens, 2011-03, Vol.7 (3), p.e1001319-e1001319

2011

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Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom

Emerging infectious diseases, 2017-06, Vol.23 (6), p.893-897

2017

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Real‐time quaking‐induced conversion assay using a small‐scale substrate production workflow for the diagnosis of Creutzfeldt‐Jakob disease

Journal of neurochemistry, 2023-07, Vol.166 (2), p.403-413

2023

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A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis

Nature communications, 2020-08, Vol.11 (1), p.3960-3960, Article 3960

2020

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Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies

Expert opinion on therapeutic targets, 2023-12, Vol.ahead-of-print (ahead-of-print), p.1-14

2023

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Dura mater is a potential source of Aβ seeds

Acta neuropathologica, 2016-06, Vol.131 (6), p.911-923

2016

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Assessment of the Zoonotic Potential of Atypical Scrapie Prions in Humanized Mice Reveals Rare Phenotypic Convergence but Not Identity With Sporadic Creutzfeldt-Jakob Disease Prions

The Journal of infectious diseases, 2024-07, Vol.230 (1), p.161-171

2024

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Modelling neurodegenerative disease using brain organoids

Seminars in cell & developmental biology, 2021-03, Vol.111, p.60-66

Wray, Selina

2021

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Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease

Acta neuropathologica, 2020-08, Vol.140 (2), p.169-181

2020

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Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples

NADPH oxidases as drug targets and biomarkers in neurodegenerative diseases: What is the evidence?

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

The Structural Architecture of an Infectious Mammalian Prion Using Electron Cryomicroscopy

α-Synuclein Amyloids Hijack Prion Protein to Gain Cell Entry, Facilitate Cell-to-Cell Spreading and Block Prion Replication

Creutzfeldt‐Jakob disease

Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients

Tau pathology in Creutzfeldt‐Jakob disease revisited

CSF neurogranin as a neuronal damage marker in CJD: a comparative study with AD

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Potential human transmission of amyloid β pathology: surveillance and risks

Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK

Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone

Imaging of Creutzfeldt-Jakob Disease: Imaging Patterns and Their Differential Diagnosis

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias

Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice

Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom

Real‐time quaking‐induced conversion assay using a small‐scale substrate production workflow for the diagnosis of Creutzfeldt‐Jakob disease

A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis

Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies

Dura mater is a potential source of Aβ seeds

Assessment of the Zoonotic Potential of Atypical Scrapie Prions in Humanized Mice Reveals Rare Phenotypic Convergence but Not Identity With Sporadic Creutzfeldt-Jakob Disease Prions

Modelling neurodegenerative disease using brain organoids

Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease

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