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Potential approaches for heterologous prion protein treatment of prion diseases

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Pages 18-24 | Received 21 Oct 2015, Accepted 17 Nov 2015, Published online: 04 Apr 2016

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Laurence K. Jennings, Ishtiaq Ahmed, Alan L. Munn & Anthony R. Carroll. (2018) Yeast-based screening of natural product extracts results in the identification of prion inhibitors from a marine sponge. Prion 12:3-4, pages 234-244.
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Chandrasekaran Murugesan, Paramasivan Manivannan & Muralitharan Gangatharan. (2020) Pros and cons in prion diseases abatement: Insights from nanomedicine and transmissibility patterns. International Journal of Biological Macromolecules 145, pages 21-27.
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Alicia Otero, Carlos Hedman, Natalia Fernández-Borges, Hasier Eraña, Belén Marín, Marta Monzón, Manuel A. Sánchez-Martín, Romolo Nonno, Juan José Badiola, Rosa Bolea & Joaquín Castilla. (2019) A Single Amino Acid Substitution, Found in Mammals with Low Susceptibility to Prion Diseases, Delays Propagation of Two Prion Strains in Highly Susceptible Transgenic Mouse Models. Molecular Neurobiology 56:9, pages 6501-6511.
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Jorge Charco, Hasier Eraña, Vanessa Venegas, Sandra García-Martínez, Rafael López-Moreno, Ezequiel González-Miranda, Miguel Pérez-Castro & Joaquín Castilla. (2017) Recombinant PrP and Its Contribution to Research on Transmissible Spongiform Encephalopathies. Pathogens 6:4, pages 67.
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W. Allison, Michèle DuVal, Kim Nguyen-Phuoc & Patricia Leighton. (2017) Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology. International Journal of Molecular Sciences 18:10, pages 2223.
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