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Journal of Neurochemistry|May 13, 2020
The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cellsElena De Cecco, Luigi Celauro, Silvia Vanni, et al.
Viruses|August 28, 2021
The Cellular Prion Protein Increases the Uptake and Toxicity of TDP-43 FibrilsCarlo Scialò, Luigi Celauro, Marco Zattoni, et al.
The Journal of Biological Chemistry|July 16, 2023
Different tau fibril types reduce prion level in chronically and de novo infected cellsLuigi Celauro, Anna Burato, Marco Zattoni, 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.
Neuron|March 29, 2025
Seeded aggregation of TDP-43 induces its loss of function and reveals early pathological signaturesCarlo Scialò, Weijia Zhong, Somanath Jagannath, et al.
Elife|April 14, 2021
PMCA-generated prions from the olfactory mucosa of patients with Fatal Familial Insomnia cause prion disease in miceEdoardo Bistaffa, Alba Marín-Moreno, Juan Carlos Espinosa, et al.
Veterinary Research|July 29, 2024
Transmission of Norwegian reindeer CWD to sheep by intracerebral inoculation results in an unusual phenotype and prion distributionErez Harpaz, Federico Angelo Cazzaniga, Linh Tran, et al.
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