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List of works by Etienne Levavasseur

Astrocytes accumulate 4-hydroxynonenal adducts in murine scrapie and human Creutzfeldt-Jakob disease

scientific article published in December 2002

Cycline efficacy on the propagation of human prions in primary cultured neurons is strain-specific

scientific article published on 21 November 2013

Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay

scientific article

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

scientific article published on 2 November 2017

Functional implication of cellular prion protein in antigen-driven interactions between T cells and dendritic cells

scientific article

High resolution fundus imaging by confocal scanning laser ophthalmoscopy in the mouse

scientific article published on 9 November 2005

In vitro Modeling of Prion Strain Tropism

article published in 2019

Molecular modeling of prion transmission to humans

scientific article

Oral scrapie infection modifies the homeostasis of Peyer’s patches’ dendritic cells

scientific article published in 2007

Phenotyping of protein-prion (PrPsc)-accumulating cells in lymphoid and neural tissues of naturally scrapie-affected sheep by double-labeling immunohistochemistry

scientific article published in October 2002

Potential role of microglia in retinal blood vessel formation

scientific article published in August 2006

Prion propagation and toxicity occur in vitro with two-phase kinetics specific to strain and neuronal type

scientific article published on 19 December 2012

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

scientific article published on 15 August 2017

Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains

scientific article

Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders

scientific article published on 10 September 2012

Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain

scientific article