J. Torres

J. Torres, A. Brun, F. Salguero, 2006, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

Correlation between Bioassay and Protein Misfolding Cyclic Amplification for Variant Creutzfeldt-Jakob Disease Decontamination Studies

V. Béringue, J. Torres, S. Lehmann, 2020, mSphere.

Aquaporin 1 and aquaporin 4 overexpression in bovine spongiform encephalopathy in a transgenic murine model and in cattle field cases

A. Bassols, I. Ferrer, J. Torres, 2007, Brain Research.

Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain

M. D. Di Bari, R. Nonno, U. Agrimi, 2015, BMC Research Notes.

Vertical Transmission of Bovine Spongiform Encephalopathy Prions Evaluated in a Transgenic Mouse Model

J. Castilla, A. Gutiérrez-Adán, B. Pintado, 2005, Journal of Virology.

Involvement of PrPC in kainate-induced excitotoxicity in several mouse strains

J. D. del Río, G. Legname, F. Llorens, 2015, Scientific Reports.

Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy

J. Castilla, R. Bolea, J. Badiola, 2022, PLoS pathogens.

Development of Protection against Coronavirus Induced Diseases

J. Castilla, B. Pintado, I. Sola, 1995 .

Induction of an immune response to transmissible gastroenteritis coronavirus using vectors with enteric tropism.

J. Castilla, F. Graham, C. Sánchez, 1993, Advances in experimental medicine and biology.

Role of the Cellular Prion Protein in Oligodendrocyte Precursor Cell Proliferation and Differentiation in the Developing and Adult Mouse CNS

J. García-Verdugo, J. D. del Río, F. Llorens, 2012, PloS one.

Detection of Infectivity in Blood of Persons with Variant and Sporadic Creutzfeldt-Jakob Disease

I. Zerr, O. Andréoletti, C. Lacroux, 2014, Emerging infectious diseases.

Thermostability as a highly dependent prion strain feature

M. Moudjou, V. Béringue, J. Torres, 2019, Scientific Reports.

recombinant adenoviruses expressing virus antigens porcine transmissible gastroenteritis (TGEV) and their use in the formation of vaccines.

C. Sánchez, L. Enjuanes, J. Torres, 1995 .

Reelin Expression in Creutzfeldt-Jakob Disease and Experimental Models of Transmissible Spongiform Encephalopathies

I. Ferrer, I. Zerr, F. Llorens, 2017, Molecular Neurobiology.

RNA editing alterations define manifestation of prion diseases

I. Zerr, D. Dafou, S. Bonn, 2019, Proceedings of the National Academy of Sciences.

Homozygous R136S mutation in PRNP gene causes recessive inherited early onset prion disease

J. Castilla, R. Sánchez-Valle, H. Eraña, 2021 .

Nonpathogenic Heterologous Prions Can Interfere with Prion Infection in a Strain-Dependent Manner

J. Torres, J. Pitarch, J. Espinosa, 2018, Journal of Virology.

Development of protection against coronavirus induced diseases. A review.

J. Castilla, B. Pintado, I. Sola, 1995, Advances in experimental medicine and biology.

[Transmissible spongiform encephalopathies in animals].

J. Castilla, J. Torres, A. Brun, 2000, Revista de neurologia.

Bona fide atypical scrapie faithfully reproduced for the first time in a rodent model

M. D. Di Bari, R. Nonno, J. Castilla, 2022, Acta neuropathologica communications.

An optimized Western blot assay provides a comprehensive assessment of the physiological endoproteolytic processing of the prion protein

R. Nonno, U. Agrimi, J. Castilla, 2022, The Journal of biological chemistry.

Epigenetic Control of the Notch and Eph Signaling Pathways by the Prion Protein: Implications for Prion Diseases

O. Andréoletti, C. Lacroux, V. Béringue, 2018, Molecular Neurobiology.

Prion and prion-like diseases in animals.

O. Andréoletti, J. Torres, J. Espinosa, 2015, Virus research.

Tropism of human adenovirus type 5-based vectors in swine and their ability to protect against transmissible gastroenteritis coronavirus

F. Graham, L. Enjuanes, J. Torres, 1996, Journal of virology.

Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice

I. Ferrer, J. Torres, M. Pumarola, 2006, Acta Neuropathologica.

TREM2 expression in the brain and biological fluids in prion diseases

K. Blennow, B. Mollenhauer, J. D. del Río, 2021, Acta Neuropathologica.

Regulation of GABAA and Glutamate Receptor Expression, Synaptic Facilitation and Long-Term Potentiation in the Hippocampus of Prion Mutant Mice

José María Delgado-García, Lauro Sumoy, Rosalina Gavín, 2009, PloS one.

YKL-40 in the brain and cerebrospinal fluid of neurodegenerative dementias

I. Ferrer, I. Zerr, R. Sánchez-Valle, 2017, Molecular Neurodegeneration.

The Cellular Prion Protein Controls Notch Signaling in Neural Stem/Progenitor Cells

J. Launay, V. Béringue, J. Torres, 2017, Stem cells.

Molecular Alterations in the Cerebellum of Sporadic Creutzfeldt–Jakob Disease Subtypes with DJ-1 as a Key Regulator of Oxidative Stress

B. Mollenhauer, I. Zerr, F. Llorens, 2016, Molecular Neurobiology.

Regional and subtype-dependent miRNA signatures in sporadic Creutzfeldt-Jakob disease are accompanied by alterations in miRNA silencing machinery and biogenesis

J. Díez, J. D. del Río, I. Zerr, 2018, PLoS pathogens.

Stem cell therapy extends incubation and survival time in prion-infected mice in a time window-dependant manner.

J. Torres, S. Lehmann, C. Crozet, 2011, The Journal of infectious diseases.

Comparison of mRNA expression levels of selected genes in the brain stem of cattle naturally infected with classical and atypical BSE

J. Torres, J. Żmudziński, M. Larska, 2010, Brain Research.

Classic Scrapie in Sheep with the ARR/ARR Prion Genotype in Germany and France

O. Andréoletti, C. Lacroux, S. Lugan, 2007, Emerging infectious diseases.

Variably protease‐sensitive prionopathy: A new sporadic disease of the prion protein

B. Crain, D. Dickson, N. Cairns, 2010, Annals of neurology.

Met166‐Glu168 residues in human PrP β2‐α2 loop account for evolutionary resistance to prion infection

J. Torres, J. Espinosa, A. Marín-Moreno, 2020, Neuropathology and applied neurobiology.

Porcine Prion Protein as a Paradigm of Limited Susceptibility to Prion Strain Propagation

O. Andréoletti, S. Benestad, J. Torres, 2020, The Journal of infectious diseases.

Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner

J. Torres, M. Birling, J. Deslys, 2019, Scientific Reports.

DNA Vaccination Can Break Immunological Tolerance to PrP in Wild-Type Mice and Attenuates Prion Disease after Intracerebral Challenge

F. Rodríguez, J. Torres, J. Whitton, 2006, Journal of Virology.

Synthesis in Vitro of Rabbit Hemorrhagic Disease Virus Subgenomic RNA by Internal Initiation on (–)Sense Genomic RNA

J. Torres, J. Bárcena, M. Morales, 2004, Journal of Biological Chemistry.

Altered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob disease

P. Liberski, I. Zerr, S. Bonn, 2017, Acta Neuropathologica Communications.

The Priority position paper: Protecting Europe's food chain from prions

A. Aguzzi, K. Kristensson, J. D. del Río, 2016, Prion.

Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease

J. Castilla, R. Sánchez-Valle, H. Eraña, 2021, Alzheimer's research & therapy.

PrPC Governs Susceptibility to Prion Strains in Bank Vole, While Other Host Factors Modulate Strain Features

M. D. Di Bari, R. Nonno, U. Agrimi, 2016, Journal of Virology.

Crossing Species Barriers Relies on Structurally Distinct Prion Assemblies and Their Complementation

M. Moudjou, H. Laude, V. Béringue, 2020, Molecular Neurobiology.

Complementation between pathological prion protein subassemblies to cross existing species barriers

M. Moudjou, H. Laude, V. Béringue, 2019, bioRxiv.

Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo

J. Torres, P. Gambetti, T. Kitamoto, 2021, Acta neuropathologica communications.

Proteinase K enhanced immunoreactivity of the prion protein-specific monoclonal antibody 2A11

J. Sánchez-Vizcaíno, J. Castilla, J. Torres, 2004, Neuroscience Research.

Mixtures of prion substrains in natural scrapie cases revealed by ovinised murine models

R. Bolea, J. Badiola, O. Andréoletti, 2020, Scientific Reports.

Immunotherapeutic effect of anti-PrP monoclonal antibodies in transmissible spongiform encephalopathy mouse models: pharmacokinetic and pharmacodynamic analysis.

O. Andréoletti, S. Simon, C. Lacroux, 2010, The Journal of general virology.

Role of the Goat K222-PrPC Polymorphic Variant in Prion Infection Resistance

A. Gutiérrez-Adán, B. Pintado, O. Andréoletti, 2013, Journal of Virology.

Genetic Resistance to Scrapie Infection in Experimentally Challenged Goats

O. Andréoletti, C. Lacroux, S. Lugan, 2013, Journal of Virology.

Bovine Spongiform Encephalopathy Induces Misfolding of Alleged Prion-Resistant Species Cellular Prion Protein without Altering Its Pathobiological Features

J. Castilla, B. Pintado, J. Torres, 2013, The Journal of Neuroscience.

Subclinical Bovine Spongiform Encephalopathy Infection in Transgenic Mice Expressing Porcine Prion Protein

J. Sánchez-Vizcaíno, J. Castilla, A. Gutiérrez-Adán, 2004, The Journal of Neuroscience.

Canine D163-PrP polymorphic variant does not provide complete protection against prion infection in small ruminant PrP context

J. Torres, J. Espinosa, J. L. Pitarch, 2021, Scientific Reports.

Elements Modulating the Prion Species Barrier and Its Passage Consequences

J. Castilla, O. Andréoletti, J. Torres, 2014, PloS one.

Molecular Modeling of Prion Transmission to Humans

J. Torres, S. Haïk, N. Privat, 2014, Viruses.

Transmission and Replication of Prions.

O. Andréoletti, J. Torres, J. Espinosa, 2017, Progress in molecular biology and translational science.

PrPC regulates epidermal growth factor receptor function and cell shape dynamics in Neuro2a cells

J. D. del Río, F. Llorens, P. Fortes, 2013, Journal of neurochemistry.

Sheep-Passaged Bovine Spongiform Encephalopathy Agent Exhibits Altered Pathobiological Properties in Bovine-PrP Transgenic Mice

J. Castilla, J. Langeveld, O. Andréoletti, 2006, Journal of Virology.

Induction of Antibodies Protecting against Transmissible Gastroenteritis Coronavirus (TGEV) by Recombinant Adenovirus Expressing TGEV Spike Protein

F. Graham, C. Sánchez, L. Enjuanes, 1995, Virology.

First field trial of a transmissible recombinant vaccine against myxomatosis and rabbit hemorrhagic disease.

J. Sánchez-Vizcaíno, J. Torres, J. Bárcena, 2001, Vaccine.

Cell expression of a four extra octarepeat mutated PrPC modifies cell structure and cell cycle regulation

J. Castilla, J. Torres, A. Brun, 2006, FEBS letters.

Isolation of an attenuated myxoma virus field strain that can confer protection against myxomatosis on contacts of vaccinates

J. Sánchez-Vizcaíno, J. Torres, J. Bárcena, 2000, Archives of Virology.

Central nervous system extracellular matrix changes in a transgenic mouse model of bovine spongiform encephalopathy.

A. Bassols, I. Ferrer, J. Torres, 2009, Veterinary journal.

Ancestor, the Virulent Lausanne Strain Myxoma Virus Field Strain with Its Genome Comparison of a Nonpathogenic Supplemental Material

J. Castilla, J. Torres, J. Bárcena, 2008 .

Safety evaluation of a recombinant myxoma-RHDV virus inducing horizontal transmissible protection against myxomatosis and rabbit haemorrhagic disease

J. Sánchez-Vizcaíno, J. Torres, J. Bárcena, 2000, Vaccine.

Effect of Q211 and K222 PRNP Polymorphic Variants in the Susceptibility of Goats to Oral Infection With Goat Bovine Spongiform Encephalopathy.

J. Langeveld, W. Goldmann, O. Andréoletti, 2015, The Journal of infectious diseases.

Structural and functional analysis of the ovine laminin receptor gene (RPSA): Possible involvement of the LRP/LR protein in scrapie response

I. Martín-Burriel, J. Torres, J. Calvo, 2008, Mammalian Genome.

Altered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob disease

P. Liberski, I. Zerr, S. Bonn, 2017, Acta neuropathologica communications.

Coenzyme Q and protein/lipid oxidation in a BSE-infected transgenic mouse model.

J. Castilla, J. Torres, J. M. Villalba, 2007, Free radical biology & medicine.

Group I mGluR signaling in BSE-infected bovine-PrP transgenic mice

M. Barrachina, I. Ferrer, J. Torres, 2006, Neuroscience Letters.

Goat K222-PrPC polymorphic variant does not provide resistance to atypical scrapie in transgenic mice

O. Andréoletti, L. Orge, J. Torres, 2016, Veterinary Research.

Pre‐symptomatic detection of prions by cyclic amplification of protein misfolding

J. Castilla, P. Saá, C. Soto, 2005, FEBS letters.

Stress response in the central nervous system of a transgenic mouse model of bovine spongiform encephalopathy.

I. Ferrer, J. Torres, M. Pumarola, 2008, Veterinary journal.

Mapping of neurotrophins and their receptors in the adult mouse brain and their role in the pathogenesis of a transgenic murine model of bovine spongiform encephalopathy.

J. Torres, M. Pumarola, E. Vidal, 2014, Journal of comparative pathology.

Dysfunction of the PI3K–Akt–GSK‐3 pathway is a common feature in cell culture and in vivo models of prion disease

A. I. Rojo, A. Cuadrado, F. Wandosell, 2014, Neuropathology and applied neurobiology.

Prion infection of differentiated neurospheres

J. Torres, A. Villa, A. Relaño-Ginés, 2010, Journal of Neuroscience Methods.

Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain

M. D. Di Bari, R. Nonno, U. Agrimi, 2015, BMC Research Notes.

Induction of transmissible gastroenteritis coronavirus specific immune responses using vectors with enteric tropism.

C. Sánchez, L. Enjuanes, J. Torres, 1995, Advances in experimental medicine and biology.

Spontaneous Generation of Infectious Prion Disease in Transgenic Mice

I. Ferrer, J. Manzanares, J. Castilla, 2013, Emerging infectious diseases.

TITLE : Role of the goat K 222-PrPC polymorphic variant in prion 1 infection resistance

B. Pintado, O. Andréoletti, J. Torres, 2013 .

Effect of Q 211 and K 222 PRNP Polymorphic Variants in the Susceptibility of Goats to Oral Infection With Goat Bovine Spongiform Encephalopathy

J. Langeveld, W. Goldmann, O. Andréoletti, 2015 .

Transgenic Mouse Models for the Study of Neurodegenerative Diseases.

J. Torres, J. Espinosa, A. Marín-Moreno, 2023, Frontiers in bioscience.

Genome Comparison of a Nonpathogenic Myxoma Virus Field Strain with Its Ancestor, the Virulent Lausanne Strain

J. Castilla, J. Torres, J. Bárcena, 2008, Journal of Virology.