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Prion-like properties of Tau assemblies

Current opinion in neurobiology, 2020-04, Vol.61, p.49-57

2020

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Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

Lancet neurology, 2021-03, Vol.20 (3), p.235-246

2021

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Conserved meningeal lymphatic drainage circuits in mice and humans

The Journal of experimental medicine, 2022-08, Vol.219 (8)

2022

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Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study

Annals of neurology, 2016-07, Vol.80 (1), p.160-165

2016

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The role of environmental factors on sporadic Creutzfeldt-Jakob disease mortality: evidence from an age-period-cohort analysis

European journal of epidemiology, 2023-07, Vol.38 (7), p.757-764

2023

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

Nature Medicine, 2013-09, Vol.19 (9), p.1124-1131

2013

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Automated deep learning segmentation of neuritic plaques and neurofibrillary tangles in Alzheimer disease brain sections using a proprietary software

Journal of neuropathology and experimental neurology, 2024-09, Vol.83 (9), p.752-762

2024

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Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice

Journal of virology, 2016-12, Vol.90 (23), p.10867-10874

2016

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Neuropathology of iatrogenic Creutzfeldt–Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathology

Acta neuropathologica, 2018-02, Vol.135 (2), p.201-212

2018

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Variant Creutzfeldt–Jakob Disease Diagnosed 7.5 Years after Occupational Exposure

The New England journal of medicine, 2020-07, Vol.383 (1), p.83-85

2020

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Effects of a New Natural Catechol‑O‑methyl Transferase Inhibitor on Two In Vivo Models of Parkinson’s Disease

ACS chemical neuroscience, 2022-12, Vol.13 (23), p.3303-3313

2022

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Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD

PloS one, 2008-01, Vol.3 (1), p.e1419-e1419

2008

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Factors Influencing the Incubation of an Infectious Form of Creutzfeldt-Jakob Disease

Clinical infectious diseases, 2020-03, Vol.70 (7), p.1487-1490

2020

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Hemoglobin mRNA Changes in the Frontal Cortex of Patients with Neurodegenerative Diseases

Frontiers in neuroscience, 2018-01, Vol.12, p.8-8

2018

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Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms

Euro surveillance : bulletin européen sur les maladies transmissibles, 2023-12, Vol.28 (50), p.15

2023

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Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains

The Journal of biological chemistry, 2017-10, Vol.292 (40), p.16688-16696

2017

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An in vivo Caenorhabditis elegans model for therapeutic research in human prion diseases

Brain (London, England : 1878), 2021-10, Vol.144 (9), p.2745-2758

2021

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Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque

Nature communications, 2017-11, Vol.8 (1), p.1268-13, Article 1268

2017

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Validation of the Medical Research Council prion disease rating scale in France

Brain communications, 2023-11, Vol.5 (6), p.fcad267-fcad267

2023

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Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

Lancet neurology, 2020-10, Vol.19 (10), p.840-848

2020

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Prion Propagation and Toxicity Occur In Vitro with Two-Phase Kinetics Specific to Strain and Neuronal Type

Journal of Virology, 2013-03, Vol.87 (5), p.2535-2548

2013

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Autoantibodies against the prion protein in individuals with PRNP mutations

Neurology, 2020-10, Vol.95 (14), p.e2028

2020

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Glycoform-selective prion formation in sporadic and familial forms of prion disease

PloS one, 2013-03, Vol.8 (3), p.e58786-e58786

2013

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Neuroinvasion of SARS-CoV-2 in human and mouse brain

Prion-like properties of Tau assemblies

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

Conserved meningeal lymphatic drainage circuits in mice and humans

Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study

The role of environmental factors on sporadic Creutzfeldt-Jakob disease mortality: evidence from an age-period-cohort analysis

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

Automated deep learning segmentation of neuritic plaques and neurofibrillary tangles in Alzheimer disease brain sections using a proprietary software

Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice

Neuropathology of iatrogenic Creutzfeldt–Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathology

Variant Creutzfeldt–Jakob Disease Diagnosed 7.5 Years after Occupational Exposure

Effects of a New Natural Catechol‑O‑methyl Transferase Inhibitor on Two In Vivo Models of Parkinson’s Disease

Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD

Factors Influencing the Incubation of an Infectious Form of Creutzfeldt-Jakob Disease

Hemoglobin mRNA Changes in the Frontal Cortex of Patients with Neurodegenerative Diseases

Age at onset in genetic prion disease and the design of preventive clinical trials

Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms

Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains

An in vivo Caenorhabditis elegans model for therapeutic research in human prion diseases

Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque

Validation of the Medical Research Council prion disease rating scale in France

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

Prion Propagation and Toxicity Occur In Vitro with Two-Phase Kinetics Specific to Strain and Neuronal Type

Autoantibodies against the prion protein in individuals with PRNP mutations

Glycoform-selective prion formation in sporadic and familial forms of prion disease

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