Prion Strain Differences in Accumulation of PrPSc on Neurons and Glia Are Associated with Similar Expression Profiles of Neuroinflammatory Genes: Comparison of Three Prion Strains von Carroll, James A, Striebel, James F, Rangel, Alejandra, Woods, Tyson, Phillips, Katie, Peterson, Karin E, Race, Brent, Chesebro, Bruce

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A Neuronal Culture System to Detect Prion Synaptotoxicity von Fang, Cheng, Imberdis, Thibaut, Garza, Maria Carmen, Wille, Holger, Harris, David A

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Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease von Bouybayoune, Ihssane, Mantovani, Susanna, Del Gallo, Federico, Bertani, Ilaria, Restelli, Elena, Comerio, Liliana, Tapella, Laura, Baracchi, Francesca, Fernández-Borges, Natalia, Mangieri, Michela, Bisighini, Cinzia, Beznoussenko, Galina V, Paladini, Alessandra, Balducci, Claudia, Micotti, Edoardo, Forloni, Gianluigi, Castilla, Joaquín, Fiordaliso, Fabio, Tagliavini, Fabrizio, Imeri, Luca, Chiesa, Roberto

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Online Machine Learning: A Practical Guide with Examples in Python von Bartz, Eva, Bartz-Beielstein, Thomas

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Prion protein polymorphisms affect chronic wasting disease progression von Johnson, Chad J, Herbst, Allen, Duque-Velasquez, Camilo, Vanderloo, Joshua P, Bochsler, Phil, Chappell, Rick, McKenzie, Debbie

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Follicular dendritic cell-specific prion protein (PrP) expression alone is sufficient to sustain prion infection in the spleen von McCulloch, Laura, Brown, Karen L, Bradford, Barry M, Hopkins, John, Bailey, Mick, Rajewsky, Klaus, Manson, Jean C, Mabbott, Neil A

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Highly efficient prion transmission by blood transfusion von Andréoletti, Olivier, Litaise, Claire, Simmons, Hugh, Corbière, Fabien, Lugan, Séverine, Costes, Pierrette, Schelcher, François, Vilette, Didier, Grassi, Jacques, Lacroux, Caroline

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Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC von Vascellari, Sarah, Orrù, Christina D, Hughson, Andrew G, King, Declan, Barron, Rona, Wilham, Jason M, Baron, Gerald S, Race, Brent, Pani, Alessandra, Caughey, Byron

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Aggregate-depleted brain fails to induce Aβ deposition in a mouse model of Alzheimer's disease von Duran-Aniotz, Claudia, Morales, Rodrigo, Moreno-Gonzalez, Ines, Hu, Ping Ping, Fedynyshyn, Joseph, Soto, Claudio

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Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS von Asante, Emmanuel A, Grimshaw, Andrew, Smidak, Michelle, Jakubcova, Tatiana, Tomlinson, Andrew, Jeelani, Asif, Hamdan, Shyma, Powell, Caroline, Joiner, Susan, Linehan, Jacqueline M, Brandner, Sebastian, Wadsworth, Jonathan D F, Collinge, John

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Disease phenotype of classical sheep scrapie is changed upon experimental passage through white-tailed deer von Kokemuller, Robyn D, Moore, S Jo, Bian, Jifeng, West Greenlee, M Heather, Greenlee, Justin J

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Cofactor and glycosylation preferences for in vitro prion conversion are predominantly determined by strain conformation von Burke, Cassandra M, Walsh, Daniel J, Mark, Kenneth M K, Deleault, Nathan R, Nishina, Koren A, Agrimi, Umberto, Di Bari, Michele A, Supattapone, Surachai

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Preclinical transmission of prions by blood transfusion is influenced by donor genotype and route of infection von Salamat, M Khalid F, Blanco, A Richard Alejo, McCutcheon, Sandra, Tan, Kyle B C, Stewart, Paula, Brown, Helen, Smith, Allister, de Wolf, Christopher, Groschup, Martin H, Becher, Dietmar, Andréoletti, Olivier, Turner, Marc, Manson, Jean C, Houston, E Fiona

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Kinetics of α-synuclein prions preceding neuropathological inclusions in multiple system atrophy von Woerman, Amanda L, Patel, Smita, Kazmi, Sabeen A, Oehler, Abby, Lee, Jisoo, Mordes, Daniel A, Olson, Steven H, Prusiner, Stanley B

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A single amino acid residue in bank vole prion protein drives permissiveness to Nor98/atypical scrapie and the emergence of multiple strain variants von Pirisinu, Laura, Di Bari, Michele Angelo, D’Agostino, Claudia, Vanni, Ilaria, Riccardi, Geraldina, Marcon, Stefano, Vaccari, Gabriele, Chiappini, Barbara, Benestad, Sylvie L., Agrimi, Umberto, Nonno, Romolo

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Neuronal Ndst1 depletion accelerates prion protein clearance and slows neurodegeneration in prion infection von Aguilar-Calvo, Patricia, Malik, Adela, Sandoval, Daniel R, Barback, Christopher, Orrù, Christina D, Standke, Heidi G, Thomas, Olivia R, Dwyer, Chrissa A, Pizzo, Donald P, Bapat, Jaidev, Soldau, Katrin, Ogawa, Ryotaro, Riley, Mckenzie B, Nilsson, K Peter R, Kraus, Allison, Caughey, Byron, Iliff, Jeffrey J, Vera, David R, Esko, Jeffrey D, Sigurdson, Christina J

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The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients von Moore, Roger A, Head, Mark W, Ironside, James W, Ritchie, Diane L, Zanusso, Gianluigi, Choi, Young Pyo, Pyo Choi, Young, Priola, Suzette A

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Soil humic acids degrade CWD prions and reduce infectivity von Kuznetsova, Alsu, Cullingham, Catherine, McKenzie, Debbie, Aiken, Judd M

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Emergence of prions selectively resistant to combination drug therapy von Burke, Cassandra M, Mark, Kenneth M K, Kun, Judit, Beauchemin, Kathryn S, Supattapone, Surachai

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Unraveling the key to the resistance of canids to prion diseases von Fernández-Borges, Natalia, Parra, Beatriz, Vidal, Enric, Eraña, Hasier, Sánchez-Martín, Manuel A, de Castro, Jorge, Elezgarai, Saioa R, Pumarola, Martí, Mayoral, Tomás, Castilla, Joaquín

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