Publicaciones anteriores

Otero A, Duque Velásquez C, Johnson C, Herbst A, Bolea R, Badiola JJ, Aiken J, McKenzie D. Prion protein polymorphisms associated with reduced CWD susceptibility limit peripheral PrPCWD deposition in orally infected white-tailed deer. BMC Vet Res. 15(1):50.(2019). doi: 10.1186/s12917-019-1794-z Pirisinu L, Andreoletti O, Lantier 1, Acutis PL, Acin C, Goldmann W, Sklaviadis T,Ekateriniadou L, Fast C, Papasavva – Stylianou P, Simon S, Spiropoulos J, Agrimi U,Jacobs JG, Bossers A, van Keulen LM, Mazza M, Nonno R,Langeveld JPM. TSEs in European goats discriminated by Western blotting into five types based on five robust molecular parameters. Prion, 13:sup1, 1-141, doi: 10.1080/19336896.2019.1615197

Nonno R, Marín-Moreno A, Espinosa JC, Fast C, Van Keulen L, Spiropoulos J, Lantier F, Andreoletti O, Pirisinu L, Di Bari MA, Aguilar-Calvo P, Sklaviadis T, Papasavva Stylianou P, Acutis PL, Acin C, Bossers A, Jacobs JG, Vaccari G, D’Agostino C,Chiappini B, Lantier F, Groschup M, Agrimi U, Torres JM, Langeveld JPM. Rodent models allow BSE discrimination of goat prions and reveal geographical differences in the biological properties of scrapie. Prion,13:sup1, 1-141. doi:10.1080/19336896.2019.1615197

Llorens F, Barrio T, Correia Â, Villar-Piqué A, Thüne K, Lange P, Badiola JJ, Schmitz M, Lachmann I, Bolea R, Zerr I. Cerebrospinal fluid prion disease biomarkers in pre-clinical and clinical naturally occurrings. Mol Neurobiol 55, 8586-8591 (2018). doi: 10.1007/s12035-018-1014-z

Hedman C, Otero A, Douet JY, Lacroux C, Lugan S, Filali H, Corbière F, Aron, N, Badiola JJ, Andréoletti O, Bolea R. Detection of PrPres in peripheral tissue in pigs with clinical disease induced by intracerebral challenge with sheep-passaged bovine spongiform encephalopathy agent. PLoS One 5, 13-27. e0199914 (2018). doi: 10.1371/journal.pone.0199914. eCollection 2018

Otero A, Bolea R, Hedman C, Fernández-Borges N, Marín B, López-Pérez O, Barrio T, Eraña H, Sánchez-Martín, MA, Monzón M, Badiola JJ, Castilla J. An amino acid substitution found in animals with low susceptibility to prion diseases confers a protective dominant-negative effect in prion-infected transgenic mice. Mol Neurobiol 55,6182-6192 (2018). doi: 10.1007/s12035-017-0832-8

Monzón M, Hernández RS, Garcés M, Sarasa R, Badiola JJ. Glial alterations in human prion diseases: A correlative study of astroglia, reactive microglia, protein deposition, and neuropathological lesions. Medicine (Baltimore), 97(15):e0320. (2018) doi: 10.1097/MD.0000000000010320

Pitarch JL, Raksa HC, Arnal MC, Revilla M, Martínez D, Fernández de Luco D, Badiola JJ, Goldmann W, Acín C. Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain. Vet Res 49, 33-39. (2018). doi: 10.1186/s13567-018-0528-8

Silva CJ, Erickson-Beltran ML, Martín-Burriel I, Badiola JJ, Requena JR, Bolea R. Determining the relative susceptibility of four protein genotypes to atypical scrapie. Anal Chem 90, 1255-1262. (2018) . doi: 10.1021/acs.analchem.7b03985

Bolea R, Hedman C, López-Pérez Ó, Marín B, Vidal E, Pumarola M, Corbière F, Romero A, Moreno B, Martín-Burriel I, Andréoletti O, Badiola JJ. Experimental transmission to a calf of an isolate of Spanish classical scrapie. J Gen Virol 98, 2628-2634 (2017). doi: 10.1099/jgv.0.000906