Complex proteinopathies and neurodegeneration: insights from the study of transmissible spongiform encephalopathies by Pedro Piccardo, David M. Asher

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Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation. by Salvatore Monaco, Michele Fiorini, Alessia Farinazzo, Sergio Ferrari, Matteo Gelati, Pedro Piccardo, Gianluigi Zanusso, Bernardino Ghetti

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A Naturally Occurring Bovine Tauopathy Is Geographically Widespread in the UK. by Martin Jeffrey, Pedro Piccardo, Diane L Ritchie, James W Ironside, Alison J E Green, Gillian McGovern

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Distribution of Misfolded Prion Protein Seeding Activity Alone Does Not Predict Regions of Neurodegeneration. by James Alibhai, Richard A Blanco, Marcelo A Barria, Pedro Piccardo, Byron Caughey, V Hugh Perry, Tom C Freeman, Jean C Manson

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Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid-β or Pathologic Phenotype. by Isobel J Whitehouse, Deborah Brown, Herbert Baybutt, Abigail B Diack, Katherine A B Kellett, Pedro Piccardo, Jean C Manson, Nigel M Hooper

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Host PrP glycosylation: a major factor determining the outcome of prion infection. by Nadia L Tuzi, Enrico Cancellotti, Herbert Baybutt, Lorraine Blackford, Barry Bradford, Chris Plinston, Anne Coghill, Patricia Hart, Pedro Piccardo, Rona M Barron, Jean C Manson

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TREM2 supports neuronal protection and microglial reactivity without an effect on misfolded protein deposition in chronic neurodegenerative prion disease by Sarah M. Carpanini, Barry M. Bradford, Alessio Alfieri, Pedro Piccardo, Jimena Monzón-Sandoval, Deborah Brown, Aileen Boyle, Aleksandra Pokrovskaya, Neil A. Mabbott, Jean Manson, Barry W. McColl, Barry W. McColl

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