Cargando…

Elements Modulating the Prion Species Barrier and Its Passage Consequences

The specific characteristics of Transmissible Spongiform Encephalopathy (TSE) strains may be altered during passage across a species barrier. In this study we investigated the biochemical and biological characteristics of Bovine Spongiform Encephalopathy (BSE) after transmission in both natural host...

Descripción completa

Detalles Bibliográficos
Autores principales:	Torres, Juan-Maria, Espinosa, Juan-Carlos, Aguilar-Calvo, Patricia, Herva, María-Eugenia, Relaño-Ginés, Aroa, Villa-Diaz, Ana, Morales, Mónica, Parra, Beatriz, Alamillo, Elia, Brun, Alejandro, Castilla, Joaquín, Molina, Susana, Hawkins, Steve A. C., Andreoletti, Olivier
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946430/ https://www.ncbi.nlm.nih.gov/pubmed/24608126 http://dx.doi.org/10.1371/journal.pone.0089722

Ejemplares similares

Transgenic Mice Expressing Porcine Prion Protein Resistant to Classical Scrapie but Susceptible to Sheep Bovine Spongiform Encephalopathy and Atypical Scrapie
por: Espinosa, Juan-Carlos, et al.
Publicado: (2009)

Spontaneous Generation of Infectious Prion Disease in Transgenic Mice
por: Torres, Juan-María, et al.
Publicado: (2013)

Porcine Prion Protein as a Paradigm of Limited Susceptibility to Prion Strain Propagation
por: Espinosa, Juan Carlos, et al.
Publicado: (2020)

Erratum to: Porcine Prion Protein as a Paradigm of Limited Susceptibility to Prion Strain Propagation
por: Espinosa, Juan Carlos, et al.
Publicado: (2020)

Prion Replication Occurs in Endogenous Adult Neural Stem Cells and Alters Their Neuronal Fate: Involvement of Endogenous Neural Stem Cells in Prion Diseases
por: Relaño-Ginès, Aroa, et al.
Publicado: (2013)

Classical Bovine Spongiform Encephalopathy by Transmission of H-Type Prion in Homologous Prion Protein Context
por: Torres, Juan-María, et al.
Publicado: (2011)

Systemic Delivery of siRNA Down Regulates Brain Prion Protein and Ameliorates Neuropathology in Prion Disorder
por: Lehmann, Sylvain, et al.
Publicado: (2014)

Propagation of RML Prions in Mice Expressing PrP Devoid of GPI Anchor Leads to Formation of a Novel, Stable Prion Strain
por: Mahal, Sukhvir Paul, et al.
Publicado: (2012)

The proximal promoter region of mTert is sufficient to regulate telomerase activity in ES cells and transgenic animals
por: Pericuesta, Eva, et al.
Publicado: (2006)

Classical scrapie in small ruminants is caused by at least four different prion strains
por: Marín-Moreno, Alba, et al.
Publicado: (2021)

Allelic Interference in Prion Replication Is Modulated by the Convertibility of the Interfering PrP(C) and Other Host-Specific Factors
por: Espinosa, Juan Carlos, et al.
Publicado: (2021)

Thermostability as a highly dependent prion strain feature
por: Marín-Moreno, Alba, et al.
Publicado: (2019)

Radical Change in Zoonotic Abilities of Atypical BSE Prion Strains as Evidenced by Crossing of Sheep Species Barrier in Transgenic Mice
por: Marín-Moreno, Alba, et al.
Publicado: (2020)

Lithium as a disease-modifying agent for prion diseases
por: Relaño-Ginés, A., et al.
Publicado: (2018)

Classic Scrapie in Sheep with the ARR/ARR Prion Genotype in Germany and France
por: Groschup, Martin H., et al.
Publicado: (2007)

Cerebrospinal Fluid and Plasma Small Extracellular Vesicles and miRNAs as Biomarkers for Prion Diseases
por: López-Pérez, Óscar, et al.
Publicado: (2021)

Classical BSE prions emerge from asymptomatic pigs challenged with atypical/Nor98 scrapie
por: Marín, Belén, et al.
Publicado: (2021)

Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner
por: Espinosa, Juan Carlos, et al.
Publicado: (2019)

RNA editing alterations define manifestation of prion diseases
por: Kanata, Eirini, et al.
Publicado: (2019)

Prion-resistant or prion-susceptible species, this is the question
por: Chianini, Francesca, et al.
Publicado: (2013)

Characterization of goat prions demonstrates geographical variation of scrapie strains in Europe and reveals the composite nature of prion strains
por: Nonno, Romolo, et al.
Publicado: (2020)

Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures
por: Cassard, Hervé, et al.
Publicado: (2020)

Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease
por: Ximelis, Teresa, et al.
Publicado: (2021)

Met(166)‐Glu(168) residues in human PrP β2‐α2 loop account for evolutionary resistance to prion infection
por: Espinosa, Juan Carlos, et al.
Publicado: (2020)

Transgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion Isolates
por: Vidal, Enric, et al.
Publicado: (2015)

Molecular Modeling of Prion Transmission to Humans
por: Levavasseur, Etienne, et al.
Publicado: (2014)

Prion disease modelled in Drosophila
por: Bujdoso, Raymond, et al.
Publicado: (2022)

Unraveling the key to the resistance of canids to prion diseases
por: Fernández-Borges, Natalia, et al.
Publicado: (2017)

Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein
por: Joiner, Susan, et al.
Publicado: (2018)

Accelerated High Fidelity Prion Amplification Within and Across Prion Species Barriers
por: Green, Kristi M., et al.
Publicado: (2008)

Mammalian prion propagation in PrP transgenic Drosophila
por: Thackray, Alana M, et al.
Publicado: (2018)

Mixtures of prion substrains in natural scrapie cases revealed by ovinised murine models
por: Barrio, Tomás, et al.
Publicado: (2020)

PMCA-generated prions from the olfactory mucosa of patients with Fatal Familial Insomnia cause prion disease in mice
por: Bistaffa, Edoardo, et al.
Publicado: (2021)

Structural Consequences of Copper Binding to the Prion Protein
por: Salzano, Giulia, et al.
Publicado: (2019)

Prion Remains Infectious after Passage through Digestive System of American Crows (Corvus brachyrhynchos)
por: VerCauteren, Kurt C., et al.
Publicado: (2012)

CWD prions remain infectious after passage through the digestive system of coyotes (Canis latrans)
por: Nichols, Tracy A, et al.
Publicado: (2015)

Second passage experiments of chronic wasting disease in transgenic mice overexpressing human prion protein
por: Race, Brent, et al.
Publicado: (2022)

Generation of a new infectious recombinant prion: a model to understand Gerstmann–Sträussler–Scheinker syndrome
por: Elezgarai, Saioa R., et al.
Publicado: (2017)

Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
por: Miyazawa, Kohtaro, et al.
Publicado: (2017)

Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patients
por: Douet, Jean-Yves, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_hsg3lgkj426h1l1flunkij92od