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Biomolecules|May 27, 2023
Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted PrionsRosalia Bruno, Geraldina Riccardi, Floriana Iacobone, et al.Scientific Reports|March 16, 2016
A cationic tetrapyrrole inhibits toxic activities of the cellular prion proteinTania Massignan, Sara Cimini, Claudia Stincardini, et al.Acta Neuropathologica|June 30, 2026
Prion-like transmission and propagation of human β-amyloid to the bank vole rodent modelMichele Angelo Di Bari, Rosalia Bruno, Geraldina Riccardi, et al.Brain : a Journal of Neurology|April 18, 2020
Isolation of infectious, non-fibrillar and oligomeric prions from a genetic prion diseaseIlaria Vanni, Laura Pirisinu, Claudia Acevedo-Morantes, et al.Acta Neuropathologica|February 10, 2026
D178N prion protein mutation endows RML prions with new strain properties that do not mimic human genetic prion diseasesAntonio Masone, Anna Grasso, Liliana Comerio, et al.Plos One|August 9, 2017
An antipsychotic drug exerts anti-prion effects by altering the localization of the cellular prion proteinClaudia Stincardini, Tania Massignan, Silvia Biggi, et al.Proceedings of the National Academy of Sciences of the United States of America|November 24, 2020
Studies in bank voles reveal strain differences between chronic wasting disease prions from Norway and North AmericaRomolo Nonno, Michele A Di Bari, Laura Pirisinu, et al.Emerging Infectious Diseases|November 21, 2018
Novel Type of Chronic Wasting Disease Detected in Moose (Alces alces), NorwayLaura Pirisinu, Linh Tran, Barbara Chiappini, et al.Acta Neuropathologica|November 3, 2017
Cofactors influence the biological properties of infectious recombinant prionsNatalia Fernández-Borges, Michele A Di Bari, Hasier Eraña, et al.Emerging Infectious Diseases|July 28, 2026
Camel Prion Disease, Tataouine, Tunisia, 2019-2021Abdelkader Amara, Michele Angelo Di Bari, Kéfia Elmehatli, et al.Pageof 3