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Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10210

2022

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Detection of exosomal prions in blood by immunochemistry techniques

Journal of general virology, 2015-07, Vol.96 (Pt 7), p.1969-1974

2015

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RT-QuIC detection of pathological prion protein in subclinical goats following experimental oral transmission of L-type BSE

BMC research notes, 2021-12, Vol.14 (1), p.442-442, Article 442

2021

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Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles

PLoS pathogens, 2006-02, Vol.2 (2), p.e12-e12

2006

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Gerstmann-Sträussler-Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles

Biomolecules (Basel, Switzerland), 2022-10, Vol.12 (10), p.1537

2022

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Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD

Annals of clinical and translational neurology, 2020-11, Vol.7 (11), p.2262-2271

2020

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

FEBS letters, 2005-01, Vol.579 (3), p.638-642

2005

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Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt–Jakob Disease

The New England journal of medicine, 2003-02, Vol.348 (8), p.711-719

2003

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Ultra-High-Pressure Inactivation of Prion Infectivity in Processed Meat: A Practical Method to Prevent Human Infection

Proceedings of the National Academy of Sciences - PNAS, 2003-05, Vol.100 (10), p.6093-6097

2003

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The pathological prion protein forms ionic conductance in lipid bilayer

Neurochemistry international, 2011-08, Vol.59 (2), p.168-174

2011

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Accumulation and aberrant composition of cholesteryl esters in Scrapie-infected N2a cells and C57BL/6 mouse brains

Lipids in health and disease, 2011-08, Vol.10 (1), p.132-132, Article 132

2011

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Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease

Electrophoresis, 2002-01, Vol.23 (2), p.347-355

2002

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Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease

Journal of virology, 2017-06, Vol.91 (11)

2017

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Chronic wasting disease and atypical forms of bovine spongiform encephalopathy and scrapie are not transmissible to mice expressing wild-type levels of human prion protein

Journal of general virology, 2012-07, Vol.93 (Pt 7), p.1624-1629

2012

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Concordance of cerebrospinal fluid real‐time quaking‐induced conversion across the European Creutzfeldt–Jakob Disease Surveillance Network

European journal of neurology, 2022-08, Vol.29 (8), p.2431-2438

2022

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Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients

Nature medicine, 1997-05, Vol.3 (5), p.521-525

1997

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Scrapie infectivity is quickly cleared in tissues of orally-infected farmed fish

BMC veterinary research, 2006-06, Vol.2 (1), p.21-21, Article 21

2006

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Role of proteomics in understanding prion infection

Expert review of proteomics, 2012-12, Vol.9 (6), p.649-666

2012

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Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt–Jakob disease patients

Biochemical and biophysical research communications, 2014-11, Vol.454 (2), p.289-294

2014

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Proteomic profiling of PrP27-30-enriched preparations extracted from the brain of hamsters with experimental scrapie

Proteomics (Weinheim), 2009-08, Vol.9 (15), p.3802-3814

2009

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Sporadic Creutzfeldt-Jakob disease subtype-specific alterations of the brain proteome: Impact on Rab3a recycling

Proteomics (Weinheim), 2012-12, Vol.12 (23-24), p.3610-3620

2012

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Assessment of prion reduction filters in decreasing infectivity of ultracentrifuged 263K scrapie-infected brain homogenates in "spiked" human blood and red blood cells

Transfusion (Philadelphia, Pa.), 2014-04, Vol.54 (4), p.990-995

2014

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Choosing Wisely Canada Students and Trainees Advocating for Resource Stewardship (STARS) campaign: a descriptive evaluation

CMAJ open, 2017-12, Vol.5 (4), p.E864-E871

2017

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Assessment of prion reduction filters in decreasing infectivity of ultracentrifuged 263 K scrapie‐infected brain homogenates in “spiked” human blood and red blood cells

Transfusion (Philadelphia, Pa.), 2014-04, Vol.54 (4), p.990-995

2014

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Increased levels of acute-phase inflammatory proteins in plasma of patients with sporadic CJD

Neurology, 2012-09, Vol.79 (10), p.1012-1018

2012

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Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene

Detection of exosomal prions in blood by immunochemistry techniques

RT-QuIC detection of pathological prion protein in subclinical goats following experimental oral transmission of L-type BSE

Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles

Gerstmann-Sträussler-Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles

Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD

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

Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt–Jakob Disease

Ultra-High-Pressure Inactivation of Prion Infectivity in Processed Meat: A Practical Method to Prevent Human Infection

The pathological prion protein forms ionic conductance in lipid bilayer

Accumulation and aberrant composition of cholesteryl esters in Scrapie-infected N2a cells and C57BL/6 mouse brains

Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease

Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease

Chronic wasting disease and atypical forms of bovine spongiform encephalopathy and scrapie are not transmissible to mice expressing wild-type levels of human prion protein

Concordance of cerebrospinal fluid real‐time quaking‐induced conversion across the European Creutzfeldt–Jakob Disease Surveillance Network

Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients

Scrapie infectivity is quickly cleared in tissues of orally-infected farmed fish

Role of proteomics in understanding prion infection

Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt–Jakob disease patients

Proteomic profiling of PrP27-30-enriched preparations extracted from the brain of hamsters with experimental scrapie

Sporadic Creutzfeldt-Jakob disease subtype-specific alterations of the brain proteome: Impact on Rab3a recycling

Assessment of prion reduction filters in decreasing infectivity of ultracentrifuged 263K scrapie-infected brain homogenates in "spiked" human blood and red blood cells

Choosing Wisely Canada Students and Trainees Advocating for Resource Stewardship (STARS) campaign: a descriptive evaluation

Assessment of prion reduction filters in decreasing infectivity of ultracentrifuged 263 K scrapie‐infected brain homogenates in “spiked” human blood and red blood cells

Increased levels of acute-phase inflammatory proteins in plasma of patients with sporadic CJD

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