J. Espinosa

发表

Characterization of wine yeasts by temperature gradient gel electrophoresis (TGGE).

S. Hernán-Gómez, J. Espinosa, J. Úbeda, 2000, FEMS microbiology letters.

Cellular prion protein modulates β-amyloid deposition in aged APP/PS1 transgenic mice

F. Wandosell, J. Torres, J. Espinosa, 2013, Neurobiology of Aging.

Distribution of the cellular prion protein (PrPC) in brains of livestock and domesticated species

J. Torres, A. Brun, F. Salguero, 2006, Acta Neuropathologica.

Adenosine A1 Receptor Protein Levels and Activity Is Increased in the Cerebral Cortex in Creutzfeldt-Jakob Disease and in Bovine Spongiform Encephalopathy-Infected Bovine-PrP Mice

I. Ferrer, M. Barrachina, J. Torres, 2006, Journal of neuropathology and experimental neurology.

An assessment of the long-term persistence of prion infectivity in aquatic environments.

R. Girones, O. Andréoletti, J. Torres, 2016, Environmental research.

Persistence of the bovine spongiform encephalopathy infectious agent in sewage.

R. Girones, C. Maluquer de Motes, J. Torres, 2012, Environmental research.

Transmission of bovine spongiform encephalopathy

J. Torres, M. Morales, J. Espinosa, 2006 .

Transgenic mouse models for the study of prion diseases.

J. Torres, J. Espinosa, A. Marín-Moreno, 2020, Progress in molecular biology and translational science.

Protective Effect of Val 129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease

E. Asante, O. Andréoletti, S. Mohri, 2019 .

Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease

E. Asante, O. Andréoletti, S. Mohri, 2017, Emerging infectious diseases.

Sheep and Goat BSE Propagate More Efficiently than Cattle BSE in Human PrP Transgenic Mice

A. Gutiérrez-Adán, B. Pintado, O. Andréoletti, 2011, PLoS pathogens.

Reduced susceptibility to bovine spongiform encephalopathy prions in transgenic mice expressing a bovine PrP with five octapeptide repeats.

J. Castilla, A. Gutiérrez-Adán, B. Pintado, 2007, The Journal of general virology.

Validation of Plasma and CSF Neurofilament Light Chain as an Early Marker for Sporadic Creutzfeldt-Jakob Disease

D. Varges, I. Zerr, F. Llorens, 2022, Molecular Neurobiology.

PMCA-generated prions from the olfactory mucosa of patients with Fatal Familial Insomnia cause prion disease in mice

G. Legname, J. Torres, C. D. De Luca, 2021, eLife.

Transmission Characteristics of Variably Protease-Sensitive Prionopathy

J. Torres, P. Gambetti, Qingzhong Kong, 2014, Emerging infectious diseases.

The emergence of classical BSE from atypical/Nor98 scrapie

R. Bolea, J. Badiola, O. Andréoletti, 2019, Proceedings of the National Academy of Sciences.

Evidence for zoonotic potential of ovine scrapie prions

O. Andréoletti, C. Lacroux, S. Lugan, 2014, Nature Communications.

Classical scrapie in small ruminants is caused by at least four different prion strains

R. Nonno, O. Andréoletti, L. Orge, 2021, Veterinary Research.

Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures

P. Péran, O. Andréoletti, S. Lugan, 2020, mBio.

MicroRNA Alterations in a Tg501 Mouse Model of Prion Disease

J. Toivonen, R. Bolea, J. Badiola, 2020, Biomolecules.

Classical Bovine Spongiform Encephalopathy by Transmission of H-Type Prion in Homologous Prion Protein Context

O. Andréoletti, C. Lacroux, J. Torres, 2011, Emerging infectious diseases.

Allelic Interference in Prion Replication Is Modulated by the Convertibility of the Interfering PrPC and Other Host-Specific Factors

O. Andréoletti, S. Lugan, Alvina Huor, 2021, mBio.

Allelic Interference in Prion Replication Is Modulated by the Convertibility of the Interfering PrP^C and Other Host-Specific Factors

O. Andréoletti, S. Lugan, Alvina Huor, 2021 .

Prion Diseases in Animals and Zoonotic Potential.

O. Andréoletti, V. Béringue, J. Torres, 2016, Food safety.

Transgenic Mice Expressing Porcine Prion Protein Resistant to Classical Scrapie but Susceptible to Sheep Bovine Spongiform Encephalopathy and Atypical Scrapie

J. Castilla, O. Andréoletti, C. Lacroux, 2009, Emerging infectious diseases.

Radical Change in Zoonotic Abilities of Atypical BSE Prion Strains as Evidenced by Crossing of Sheep Species Barrier in Transgenic Mice

O. Andréoletti, S. Lugan, Alvina Huor, 2020, Emerging infectious diseases.

Classical BSE prions emerge from asymptomatic pigs challenged with atypical/Nor98 scrapie

R. Bolea, J. Badiola, O. Andréoletti, 2021, Scientific Reports.

Presumptive BSE cases with an aberrant prion protein phenotype in Switzerland, 2011: Lack of prion disease in experimentally inoculated cattle and bovine prion protein transgenic mice

J. Torres, A. Oevermann, J. Espinosa, 2018, Transboundary and emerging diseases.

Bovine Spongiform Encephalopathy (BSE)

T. Konold, J. Torres, J. Espinosa, 2016 .

Progression of prion infectivity in asymptomatic cattle after oral bovine spongiform encephalopathy challenge.

J. Castilla, J. Torres, M. Morales, 2007, The Journal of general virology.

Bovine spongiform encephalopathy agent in spleen from an ARR/ARR orally exposed sheep.

P. Sarradin, O. Andréoletti, C. Lacroux, 2006, The Journal of general virology.

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.

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

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

Thermostability as a highly dependent prion strain feature

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

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

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

Identification of a set of genes involved in the biosynthesis of the aminonucleoside moiety of antibiotic A201A from Streptomyces capreolus.

E. Sanz, A. Jimenez, Irene Saugar, 2002, European journal of biochemistry.

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.

Prion protein interaction with glycosaminoglycan occurs with the formation of oligomeric complexes stabilized by Cu(II) bridges.

M. Gasset, M. Pajares, B. Oesch, 2002, Journal of molecular biology.

Yeasts present during wine fermentation: comparative analysis of conventional plating and PCR-TTGE.

J. Espinosa, J. Úbeda, M. Fernández-González, 2001, Systematic and applied microbiology.

Beta-glucosidase activity in a Saccharomyces cerevisiae wine strain.

J. Espinosa, M. Fernández-González, A. Briones, 2003, International journal of food microbiology.

Prion and prion-like diseases in animals.

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

The pur7 Gene from the Puromycin Biosynthetic pur Cluster of Streptomyces alboniger Encodes a Nudix Hydrolase

A. Jimenez, J. Espinosa, J. A. Tercero, 1999, Journal of bacteriology.

The Biosynthetic Pathway of the Aminonucleoside Antibiotic Puromycin, as Deduced from the Molecular Analysis of the pur Cluster of Streptomyces alboniger(*)

A. Jimenez, J. Espinosa, J. A. Tercero, 1996, The Journal of Biological Chemistry.

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.

Identification of Wine Yeasts by PCR-RFLP without Previous Isolation on Plate

J. Espinosa, J. Úbeda, M. Fernández-González, 2002 .

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

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

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.

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.

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.

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

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

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.

Transmission and Replication of Prions.

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

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.

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.

Expression of the Streptomyces alboniger pur cluster in Streptomyces lividans is dependent on the bldA‐encoded tRNALeu

A. Jimenez, J. Espinosa, J. A. Tercero, 1998, FEBS letters.

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.

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.

StgR, a new Streptomyces alboniger member of the LysR family of transcriptional regulators

A. Jimenez, J. Espinosa, J. A. Tercero, 1998, Molecular and General Genetics MGG.

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.

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.

Discrimination of sheep susceptible and resistant to transmissible spongiform encephalopathies by an haplotype specific monoclonal antibody.

O. Andréoletti, N. Morel, J. Grassi, 2007, Journal of virological methods.

Classical BSE dismissed as the cause of CWD in Norwegian red deer despite strain similarities between both prion agents

M. D. Di Bari, R. Nonno, O. Andréoletti, 2024, Veterinary research.