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Biomolecules|March 11, 2020
PMCA Applications for Prion Detection in Peripheral Tissues of Patients with Variant Creutzfeldt-Jakob DiseaseGiorgio Giaccone, Fabio ModaPrion|April 21, 2018
Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseasesGiuseppe Legname, Tommaso Virgilio, Edoardo Bistaffa, et al.International Journal of Molecular Sciences|September 28, 2024
Unfolding Mechanism and Fibril Formation Propensity of Human Prion Protein in the Presence of Molecular Crowding AgentsManoj Madheswaran, Nataliia Ventserova, Gianluca D'Abrosca, et al.Progress in Molecular Biology and Translational Science|September 22, 2020
The role of the cellular prion protein in the uptake and toxic signaling of pathological neurodegenerative aggregatesCarlo Scialò, Giuseppe LegnameMolecular Neurodegeneration|August 11, 2010
Aberrant ERK 1/2 complex activation and localization in scrapie-infected GT1-1 cellsAlessandro Didonna, Giuseppe LegnameFrontiers in Cell and Developmental Biology|November 4, 2014
Prion protein and agingLisa Gasperini, Giuseppe LegnameExpert Opinion on Drug Discovery|April 29, 2026
Multi-target approaches to prion disease Drug discovery: a status updateLea Nikolić, Giuseppe LegnamePrion|March 10, 2015
New insights into structural determinants of prion protein folding and stabilityFederico Benetti, Giuseppe LegnamePrion|December 21, 2020
On the role of the cellular prion protein in the uptake and signaling of pathological aggregates in neurodegenerative diseasesGiuseppe Legname, Carlo ScialòPageof 24