Search Results - "Di Bari, Michele"

Novel Type of Chronic Wasting Disease Detected in Moose (Alces alces), Norway by Pirisinu, Laura, Tran, Linh, Chiappini, Barbara, Vanni, Ilaria, Di Bari, Michele A, Vaccari, Gabriele, Vikøren, Turid, Madslien, Knut Ivar, Våge, Jørn, Spraker, Terry, Mitchell, Gordon, Balachandran, Aru, Baron, Thierry, Casalone, Cristina, Rolandsen, Christer M, Røed, Knut H, Agrimi, Umberto, Nonno, Romolo, Benestad, Sylvie L

“…Chronic wasting disease (CWD) persists in cervid populations of North America and in 2016 was detected for the first time in Europe in a wild reindeer in…”
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Cofactor and glycosylation preferences for in vitro prion conversion are predominantly determined by strain conformation by Burke, Cassandra M, Walsh, Daniel J, Mark, Kenneth M K, Deleault, Nathan R, Nishina, Koren A, Agrimi, Umberto, Di Bari, Michele A, Supattapone, Surachai

“…Prion diseases are caused by the misfolding of a host-encoded glycoprotein, PrPC, into a pathogenic conformer, PrPSc. Infectious prions can exist as different…”
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Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt–Jakob disease prions is strongly seed and substrate dependent by Bélondrade, Maxime, Nicot, Simon, Mayran, Charly, Bruyere-Ostells, Lilian, Almela, Florian, Di Bari, Michele A., Levavasseur, Etienne, Watts, Joel C., Fournier-Wirth, Chantal, Lehmann, Sylvain, Haïk, Stéphane, Nonno, Romolo, Bougard, Daisy

“…Unlike variant Creutzfeldt–Jakob disease prions, sporadic Creutzfeldt–Jakob disease prions have been shown to be difficult to amplify in vitro by protein…”
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Full restoration of specific infectivity and strain properties from pure mammalian prion protein by Burke, Cassandra M, Walsh, Daniel J, Steele, Alexander D, Agrimi, Umberto, Di Bari, Michele Angelo, Watts, Joel C, Supattapone, Surachai

“…The protein-only hypothesis predicts that infectious mammalian prions are composed solely of PrPSc, a misfolded conformer of the normal prion protein, PrPC…”
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Characterization of goat prions demonstrates geographical variation of scrapie strains in Europe and reveals the composite nature of prion strains by Nonno, Romolo, Marin-Moreno, Alba, Carlos Espinosa, Juan, Fast, Christine, Van Keulen, Lucien, Spiropoulos, John, Lantier, Isabelle, Andreoletti, Olivier, Pirisinu, Laura, Di Bari, Michele A., Aguilar-Calvo, Patricia, Sklaviadis, Theodoros, Papasavva-Stylianou, Penelope, Acutis, Pier Luigi, Acin, Cristina, Bossers, Alex, Jacobs, Jorge G., Vaccari, Gabriele, D’Agostino, Claudia, Chiappini, Barbara, Lantier, Frederic, Groschup, Martin H., Agrimi, Umberto, Maria Torres, Juan, Langeveld, Jan P. M.

“…Bovine Spongiform Encephalopathy (BSE) is the only animal prion which has been recognized as a zoonotic agent so far. The identification of BSE in two goats…”
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Prion Disease in Dromedary Camels, Algeria by Babelhadj, Baaissa, Di Bari, Michele Angelo, Pirisinu, Laura, Chiappini, Barbara, Gaouar, Semir Bechir Suheil, Riccardi, Geraldina, Marcon, Stefano, Agrimi, Umberto, Nonno, Romolo, Vaccari, Gabriele

“…Prions cause fatal and transmissible neurodegenerative diseases, including Creutzfeldt-Jakob disease in humans, scrapie in small ruminants, and bovine…”
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Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles by Nonno, Romolo, Di Bari, Michele A, Cardone, Franco, Vaccari, Gabriele, Fazzi, Paola, Dell'Omo, Giacomo, Cartoni, Claudia, Ingrosso, Loredana, Boyle, Aileen, Galeno, Roberta, Sbriccoli, Marco, Lipp, Hans-Peter, Bruce, Moira, Pocchiari, Maurizio, Agrimi, Umberto

“…Transmission of prions between species is limited by the "species barrier," which hampers a full characterization of human prion strains in the mouse model. We…”
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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 by 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

“…Prions are infectious agents that replicate through the autocatalytic misfolding of the cellular prion protein (PrP C ) into infectious aggregates (PrP Sc )…”
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Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases by Pirisinu, Laura, Di Bari, Michele A., D’Agostino, Claudia, Marcon, Stefano, Riccardi, Geraldina, Poleggi, Anna, Cohen, Mark L., Appleby, Brian S., Gambetti, Pierluigi, Ghetti, Bernardino, Agrimi, Umberto, Nonno, Romolo

“…Gerstmann-Sträussler-Scheinker disease (GSS) is an inherited neurodegenerative disorder associated with mutations in the prion protein gene and accumulation of…”
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Cofactors influence the biological properties of infectious recombinant prions by Fernández-Borges, Natalia, Di Bari, Michele A., Eraña, Hasier, Sánchez-Martín, Manuel, Pirisinu, Laura, Parra, Beatriz, Elezgarai, Saioa R., Vanni, Ilaria, López-Moreno, Rafael, Vaccari, Gabriele, Venegas, Vanessa, Charco, Jorge M., Gil, David, Harrathi, Chafik, D’Agostino, Claudia, Agrimi, Umberto, Mayoral, Tomás, Requena, Jesús R., Nonno, Romolo, Castilla, Joaquín

“…Prion diseases are caused by a misfolding of the cellular prion protein (PrP) to a pathogenic isoform named PrP Sc . Prions exist as strains, which are…”
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Prion disease tempo determined by host-dependent substrate reduction by Mays, Charles E, Kim, Chae, Haldiman, Tracy, van der Merwe, Jacques, Lau, Agnes, Yang, Jing, Grams, Jennifer, Di Bari, Michele A, Nonno, Romolo, Telling, Glenn C, Kong, Qingzhong, Langeveld, Jan, McKenzie, Debbie, Westaway, David, Safar, Jiri G

“…The symptoms of prion infection can take years or decades to manifest following the initial exposure. Molecular markers of prion disease include accumulation…”
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Stability of BSE infectivity towards heat treatment even after proteolytic removal of prion protein by Langeveld, Jan P M, Balkema-Buschmann, Anne, Becher, Dieter, Thomzig, Achim, Nonno, Romolo, Andréoletti, Olivier, Davidse, Aart, Di Bari, Michele A, Pirisinu, Laura, Agrimi, Umberto, Groschup, Martin H, Beekes, Michael, Shih, Jason

“…The unconventional infectious agents of transmissible spongiform encephalopathies (TSEs) are prions. Their infectivity co-appears with PrP , aberrant…”
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Identification of an allelic variant of the goat PrP gene associated with resistance to scrapie by Vaccari, Gabriele, Bari, Michele A. Di, Morelli, Luisella, Nonno, Romolo, Chiappini, Barbara, Antonucci, Giovanni, Marcon, Stefano, Esposito, Elena, Fazzi, Paola, Palazzini, Nadia, Troiano, Pasquale, Petrella, Antonio, Guardo, Giovanni Di, Agrimi, Umberto

“…1 Department of Food Safety and Veterinary Public Health, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy 2 Istituto Zooprofilattico…”
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A tetracationic porphyrin with dual anti-prion activity by Masone, Antonio, Zucchelli, Chiara, Caruso, Enrico, Lavigna, Giada, Eraña, Hasier, Giachin, Gabriele, Tapella, Laura, Comerio, Liliana, Restelli, Elena, Raimondi, Ilaria, Elezgarai, Saioa R., De Leo, Federica, Quilici, Giacomo, Taiarol, Lorenzo, Oldrati, Marvin, Lorenzo, Nuria L., García-Martínez, Sandra, Cagnotto, Alfredo, Lucchetti, Jacopo, Gobbi, Marco, Vanni, Ilaria, Nonno, Romolo, Di Bari, Michele A., Tully, Mark D., Cecatiello, Valentina, Ciossani, Giuseppe, Pasqualato, Sebastiano, Van Anken, Eelco, Salmona, Mario, Castilla, Joaquín, Requena, Jesús R., Banfi, Stefano, Musco, Giovanna, Chiesa, Roberto

“…Prions are deadly infectious agents made of PrPSc, a misfolded variant of the cellular prion protein (PrPC) which self-propagates by inducing misfolding of…”
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Correlation between infectivity and disease associated prion protein in the nervous system and selected edible tissues of naturally affected scrapie sheep by Chianini, Francesca, Cosseddu, Gian Mario, Steele, Philip, Hamilton, Scott, Hawthorn, Jeremy, Síso, Sílvia, Pang, Yvonne, Finlayson, Jeanie, Eaton, Samantha L, Reid, Hugh W, Dagleish, Mark P, Di Bari, Michele Angelo, D'Agostino, Claudia, Agrimi, Umberto, Terry, Linda, Nonno, Romolo

“…The transmissible spongiform encephalopathies (TSEs) or prion diseases are a group of fatal neurodegenerative disorders characterised by the accumulation of a…”
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Studies in bank voles reveal strain differences between chronic wasting disease prions from Norway and North America by Nonno, Romolo, Di Bari, Michele A., Pirisinu, Laura, D’Agostino, Claudia, Vanni, Ilaria, Chiappini, Barbara, Marcon, Stefano, Riccardi, Geraldina, Tran, Linh, Vikøren, Turid, Våge, Jørn, Madslien, Knut, Mitchell, Gordon, Telling, Glenn C., Benestad, Sylvie L., Agrimi, Umberto

“…Chronic wasting disease (CWD) is a relentless epidemic disorder caused by infectious prions that threatens the survival of cervid populations and raises…”
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Accumulation and aberrant composition of cholesteryl esters in Scrapie-infected N2a cells and C57BL/6 mouse brains by Vascellari, Sarah, Banni, Sebastiano, Vacca, Claudia, Vetrugno, Vito, Cardone, Franco, Di Bari, Michele A, La Colla, Paolo, Pani, Alessandra

“…Cholesterol changes have been described in prion-cell models and in experimental rodent scrapie; yet, the pattern of this association is still controversial…”
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Molecular discrimination of sheep bovine spongiform encephalopathy from scrapie by Pirisinu, Laura, Migliore, Sergio, Di Bari, Michele Angelo, Esposito, Elena, Baron, Thierry, D'Agostino, Claudia, De Grossi, Luigi, Vaccari, Gabriele, Agrimi, Umberto, Nonno, Romolo

“…Sheep CH1641-like transmissible spongiform encephalopathy isolates have shown molecular similarities to bovine spongiform encephalopathy (BSE) isolates. We…”
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Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity by Nonno, Romolo, Angelo Di Bari, Michele, Agrimi, Umberto, Pirisinu, Laura

“…Prion diseases, or transmissible spongiform encephalopathies, have revealed the bewildering phenomenon of transmissibility in neurodegenerative diseases…”
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Biochemical characterization of prion strains in bank voles by Pirisinu, Laura, Marcon, Stefano, Di Bari, Michele Angelo, D'Agostino, Claudia, Agrimi, Umberto, Nonno, Romolo

“…Prions exist as different strains exhibiting distinct disease phenotypes. Currently, the identification of prion strains is still based on biological strain…”
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