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Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood

PloS one, 2023-11, Vol.18 (11), p.e0293845-e0293845

2023

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Preclinical transmission of prions by blood transfusion is influenced by donor genotype and route of infection

PLoS pathogens, 2021-02, Vol.17 (2), p.e1009276

2021

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Spermine increases acetylation of tubulins and facilitates autophagic degradation of prion aggregates

Scientific reports, 2018-07, Vol.8 (1), p.10004-17, Article 10004

2018

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Subclinical infection occurs frequently following low dose exposure to prions by blood transfusion

Scientific reports, 2022-06, Vol.12 (1), p.10923-10923, Article 10923

2022

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Oral Prion Neuroinvasion Occurs Independently of PrPC Expression in the Gut Epithelium

Journal of virology, 2018-10, Vol.92 (19)

2018

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Dramatic Reduction of PrPC Level and Glycosylation in Peripheral Nerves following PrP Knock-Out from Schwann Cells Does Not Prevent Transmissible Spongiform Encephalopathy Neuroinvasion

The Journal of neuroscience, 2009-12, Vol.29 (49), p.15445-15454

2009

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Human Prion Diseases

1, 2018

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A novel, resistance-linked ovine PrP variant and its equivalent mouse variant modulate the in vitro cell-free conversion of rPrP to PrPres

Journal of general virology, 2006-12, Vol.87 (12), p.3747-3751

2006

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Evaluating the Species Barrier

Food Safety, 2016, Vol.4(4), pp.135-141

2016

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Development of a sensitive real-time quaking-induced conversion

PloS one, 2023-11, Vol.18 (11), p.e0293845

2023

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Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes

Brain (London, England : 1878), 2019-05, Vol.142 (5), p.e22-e22

2019

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Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood

PloS one, 2023-01, Vol.18 (11), p.e0293845

2023

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Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid-[beta] or Pathologic Phenotype

PloS one, 2016-07, Vol.11 (7), p.e0159119

2016

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The Glycosylation Status of PrP C Is a Key Factor in Determining Transmissible Spongiform Encephalopathy Transmission between Species

Journal of virology, 2015-05, Vol.89 (9), p.4738-4747

2015

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Transgenic models of the transmissible spongiform encephalopathies

Expert reviews in molecular medicine, 2001-05, Vol.3 (12), p.1-15

2001

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Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid- square or Pathologic Phenotype

PloS one, 2016-07, Vol.11 (7)

2016

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Glycosylation of PrP C Determines Timing of Neuroinvasion and Targeting in the Brain following Transmissible Spongiform Encephalopathy Infection by a Peripheral Route

Journal of virology, 2010-04, Vol.84 (7), p.3464-3475

2010

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Mice with gene targetted prion protein alterations show that Prnp, Sine and Prni are congruent

Nature genetics, 1998-02, Vol.18 (2), p.118-125

1998

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High Titers of Transmissible Spongiform Encephalopathy Infectivity Associated with Extremely Low Levels of PrP super(Sc) in Vivo

The Journal of biological chemistry, 2007-12, Vol.282 (49), p.35878-35886

2007

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High Titers of Transmissible Spongiform Encephalopathy Infectivity Associated with Extremely Low Levels of PrPScin Vivo

The Journal of biological chemistry, 2007-12, Vol.282 (49), p.35878-35886

2007

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A polymorphism in the regulatory region of PRNPis associated with increased risk of sporadic Creutzfeldt-Jakob disease

BMC medical genetics, 2011-05, Vol.12 (1), Article 73

2011

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A novel, resistance-linked ovine PrP variant and its equivalent mouse variant modulate the in vitro cell-free conversion of rPrP to PrP super(res)

Journal of general virology, 2006-12, Vol.87 (12), p.3747-3751

2006

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DEVELOPMENT OF A QUANTITATIVE IMMUNOASSAY FOR THE CYSTIC FIBROSIS GENE

The Lancet (British edition), 1980-02, Vol.315 (8164), p.330-331

1980

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A protein specific to mitochondria from S‐type male‐sterile cytoplasm of maize is encoded by an episomal DNA

The EMBO journal, 1986-11, Vol.5 (11), p.2775-2780

1986

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Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood

Preclinical transmission of prions by blood transfusion is influenced by donor genotype and route of infection

Spermine increases acetylation of tubulins and facilitates autophagic degradation of prion aggregates

Subclinical infection occurs frequently following low dose exposure to prions by blood transfusion

Oral Prion Neuroinvasion Occurs Independently of PrPC Expression in the Gut Epithelium

Dramatic Reduction of PrPC Level and Glycosylation in Peripheral Nerves following PrP Knock-Out from Schwann Cells Does Not Prevent Transmissible Spongiform Encephalopathy Neuroinvasion

Human Prion Diseases

A novel, resistance-linked ovine PrP variant and its equivalent mouse variant modulate the in vitro cell-free conversion of rPrP to PrPres

Evaluating the Species Barrier

Development of a sensitive real-time quaking-induced conversion

Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes

Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood

Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid-[beta] or Pathologic Phenotype

The Glycosylation Status of PrP C Is a Key Factor in Determining Transmissible Spongiform Encephalopathy Transmission between Species

Transgenic models of the transmissible spongiform encephalopathies

Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid- square or Pathologic Phenotype

Glycosylation of PrP C Determines Timing of Neuroinvasion and Targeting in the Brain following Transmissible Spongiform Encephalopathy Infection by a Peripheral Route

Mice with gene targetted prion protein alterations show that Prnp, Sine and Prni are congruent

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

High Titers of Transmissible Spongiform Encephalopathy Infectivity Associated with Extremely Low Levels of PrP super(Sc) in Vivo

High Titers of Transmissible Spongiform Encephalopathy Infectivity Associated with Extremely Low Levels of PrPScin Vivo

A polymorphism in the regulatory region of PRNPis associated with increased risk of sporadic Creutzfeldt-Jakob disease

A novel, resistance-linked ovine PrP variant and its equivalent mouse variant modulate the in vitro cell-free conversion of rPrP to PrP super(res)

DEVELOPMENT OF A QUANTITATIVE IMMUNOASSAY FOR THE CYSTIC FIBROSIS GENE

A protein specific to mitochondria from S‐type male‐sterile cytoplasm of maize is encoded by an episomal DNA

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