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Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease

The Journal of biological chemistry, 2008-11, Vol.283 (45), p.30557-30565

2008

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Detection of Type 1 Prion Protein in Variant Creutzfeldt-Jakob Disease

The American journal of pathology, 2006, Vol.168 (1), p.151-157

2006

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Transmission of new bovine prion to mice

Emerging infectious diseases, 2006-07, Vol.12 (7), p.1125-1128

2006

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

Annals of neurology, 2010-08, Vol.68 (2), p.162-172

2010

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Diagnosis of the first cases of scrapie in Poland

The veterinary journal (1997), 2010-10, Vol.186 (1), p.47-52

2010

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Molecular Discrimination of Atypical Bovine Spongiform Encephalopathy Strains from a Geographical Region Spanning a Wide Area in Europe

Journal of Clinical Microbiology, 2007-06, Vol.45 (6), p.1821-1829

2007

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Scrapie incidence and PRNP polymorphisms: rare small ruminant breeds of Sicily with TSE protecting genetic reservoirs

BMC veterinary research, 2016-07, Vol.12 (1), p.141-141, Article 141

2016

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EU-approved rapid tests might underestimate bovine spongiform encephalopathy infection in goats

Journal of veterinary diagnostic investigation, 2017-03, Vol.29 (2), p.232-236

2017

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All major prion types recognised by a multiplex immunofluorometric assay for disease screening and confirmation in sheep

Journal of immunological methods, 2012-06, Vol.380 (1-2), p.30-39

2012

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H-Type Bovine Spongiform Encephalopathy: Complex Molecular Features and Similarities with Human Prion Diseases

Prion, 2007-01, Vol.1 (1), p.61-68

2007

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Bovine spongiform encephalopathy in Sweden: an H-type variant

Journal of veterinary diagnostic investigation, 2008-01, Vol.20 (1), p.2-10

2008

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Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

Brain (London, England : 1878), 2009-10, Vol.132 (10), p.2643-2658

2009

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Effect of different baculovirus inactivation procedures on the integrity and immunogenicity of porcine parvovirus-like particles

Vaccine, 2000-11, Vol.19 (7), p.726-734

2000

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Inactivated recombinant plant virus protects dogs from a lethal challenge with canine parvovirus

Vaccine, 2001-06, Vol.19 (27), p.3661-3670

2001

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Change in the molecular properties of CH1641 prions after transmission to wild‐type mice: Evidence for a single strain

Neuropathology and applied neurobiology, 2024-02, Vol.50 (1), p.e12963-n/a

2024

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Adult human microglia secrete cytokines when exposed to neurotoxic prion protein peptide: no intermediary role for prostaglandin E2

Brain research, 2002-01, Vol.925 (2), p.195-203

2002

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An in vitro screening assay based on synthetic prion protein peptides for identification of fibril-interfering compounds

Analytical biochemistry, 2004-10, Vol.333 (2), p.372-380

2004

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Activation of human microglia by fibrillar prion protein-related peptides is enhanced by amyloid-associated factors SAP and C1q

Neurobiology of disease, 2005-06, Vol.19 (1), p.273-282

2005

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Stability of BSE infectivity towards heat treatment even after proteolytic removal of prion protein

Veterinary research (Paris), 2021-04, Vol.52 (1), p.59-59, Article 59

2021

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Detection of prion protein particles in blood plasma of scrapie infected sheep

PloS one, 2012-05, Vol.7 (5), p.e36620-e36620

2012

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Four types of scrapie in goats differentiated from each other and bovine spongiform encephalopathy by biochemical methods

Veterinary research (Paris), 2019-11, Vol.50 (1), p.97-97, Article 97

2019

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Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity

PloS one, 2014-03, Vol.9 (3), p.e91143-e91143

2014

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Enhanced Virulence of Sheep-Passaged Bovine Spongiform Encephalopathy Agent Is Revealed by Decreased Polymorphism Barriers in Prion Protein Conversion Studies

Journal of Virology, 2014-03, Vol.88 (5), p.2903-2912

2014

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Enzymatic Degradation of Prion Protein in Brain Stem from Infected Cattle and Sheep

The Journal of infectious diseases, 2003-12, Vol.188 (11), p.1782-1789

2003

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Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease

Detection of Type 1 Prion Protein in Variant Creutzfeldt-Jakob Disease

Transmission of new bovine prion to mice

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

Diagnosis of the first cases of scrapie in Poland

Characterization of goat prions demonstrates geographical variation of scrapie strains in Europe and reveals the composite nature of prion strains

Molecular Discrimination of Atypical Bovine Spongiform Encephalopathy Strains from a Geographical Region Spanning a Wide Area in Europe

Scrapie incidence and PRNP polymorphisms: rare small ruminant breeds of Sicily with TSE protecting genetic reservoirs

EU-approved rapid tests might underestimate bovine spongiform encephalopathy infection in goats

All major prion types recognised by a multiplex immunofluorometric assay for disease screening and confirmation in sheep

H-Type Bovine Spongiform Encephalopathy: Complex Molecular Features and Similarities with Human Prion Diseases

Bovine spongiform encephalopathy in Sweden: an H-type variant

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

Effect of different baculovirus inactivation procedures on the integrity and immunogenicity of porcine parvovirus-like particles

Inactivated recombinant plant virus protects dogs from a lethal challenge with canine parvovirus

Change in the molecular properties of CH1641 prions after transmission to wild‐type mice: Evidence for a single strain

Adult human microglia secrete cytokines when exposed to neurotoxic prion protein peptide: no intermediary role for prostaglandin E2

An in vitro screening assay based on synthetic prion protein peptides for identification of fibril-interfering compounds

Activation of human microglia by fibrillar prion protein-related peptides is enhanced by amyloid-associated factors SAP and C1q

Stability of BSE infectivity towards heat treatment even after proteolytic removal of prion protein

Detection of prion protein particles in blood plasma of scrapie infected sheep

Four types of scrapie in goats differentiated from each other and bovine spongiform encephalopathy by biochemical methods

Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity

Enhanced Virulence of Sheep-Passaged Bovine Spongiform Encephalopathy Agent Is Revealed by Decreased Polymorphism Barriers in Prion Protein Conversion Studies

Enzymatic Degradation of Prion Protein in Brain Stem from Infected Cattle and Sheep

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