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Accumulation of prion protein in the brain that is not associated with transmissible disease

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (11), p.4712-4717

2007

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Variable tau accumulation in murine models with abnormal prion protein deposits

Journal of the neurological sciences, 2017-12, Vol.383, p.142-150

2017

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Host PrP glycosylation: a major factor determining the outcome of prion infection

PLoS biology, 2008-04, Vol.6 (4), p.e100-e100

2008

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Infectious prions and proteinopathies

Prion, 2017-01, Vol.11 (1), p.40-47

Barron, Rona M.

2017

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PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions

Acta neuropathologica, 2016-10, Vol.132 (4), p.611-624

2016

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

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

2007

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Dissociation between Transmissible Spongiform Encephalopathy (TSE) Infectivity and Proteinase K-Resistant PrPSc Levels in Peripheral Tissue from a Murine Transgenic Model of TSE Disease

Journal of Virology, 2013-05, Vol.87 (10), p.5895-5903

2013

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Dissociation of Prion Protein Amyloid Seeding from Transmission of a Spongiform Encephalopathy

Journal of Virology, 2013-11, Vol.87 (22), p.12349-12356

2013

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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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Presence of subclinical infection in gene-targeted human prion protein transgenic mice exposed to atypical bovine spongiform encephalopathy

Journal of general virology, 2013-12, Vol.94 (Pt 12), p.2819-2827

2013

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Characterization of an unusual transmissible spongiform encephalopathy in goat by transmission in knock-in transgenic mice

Journal of general virology, 2013-08, Vol.94 (Pt 8), p.1922-1932

2013

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Increased Susceptibility of Human-PrP Transgenic Mice to Bovine Spongiform Encephalopathy Infection following Passage in Sheep

Journal of Virology, 2011-02, Vol.85 (3), p.1174-1181

2011

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Molecular barriers to zoonotic transmission of prions

Emerging infectious diseases, 2014-01, Vol.20 (1), p.88-97

2014

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Increased susceptibility of transgenic mice expressing human PrP to experimental sheep bovine spongiform encephalopathy is not due to increased agent titre in sheep brain tissue

Journal of general virology, 2014-08, Vol.95 (Pt 8), p.1855-1859

2014

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Bovine PrP expression levels in transgenic mice influence transmission characteristics of atypical bovine spongiform encephalopathy

Journal of general virology, 2012-05, Vol.93 (Pt 5), p.1132-1140

2012

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Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC

PloS one, 2012-11, Vol.7 (11), p.e48969-e48969

2012

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Insights into Mechanisms of Chronic Neurodegeneration

International Journal of Molecular Sciences, 2016-01, Vol.17 (1), p.82-82

2016

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Glycosylation of PrPC 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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Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers

The EMBO journal, 2001-09, Vol.20 (18), p.5070-5078

2001

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Molecular model of prion transmission to humans

Emerging infectious diseases, 2009-12, Vol.15 (12), p.2013-2016

2009

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Differential protein expression profiling in BSE disease

Archives of physiology and biochemistry, 2010-12, Vol.116 (4-5), p.233-243

2010

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Dissociation between transmissible spongiform encephalopathy (TSE) infectivity and proteinase K-resistant PrP(Sc) levels in peripheral tissue from a murine transgenic model of TSE disease

Journal of virology, 2013-05, Vol.87 (10), p.5895-5903

2013

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The role of host PrP in Transmissible Spongiform Encephalopathies

Biochimica et biophysica acta, 2007-06, Vol.1772 (6), p.673-680

2007

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Dissociation between Transmissible Spongiform Encephalopathy (TSE) Infectivity and Proteinase K-Resistant PrP Sc Levels in Peripheral Tissue from a Murine Transgenic Model of TSE Disease

Journal of virology, 2013-05, Vol.87 (10), p.5895-5903

2013

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Differential protein profiling as a potential multi-marker approach for TSE diagnosis

BMC infectious diseases, 2009-11, Vol.9 (1), p.188-188, Article 188

2009

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Accumulation of prion protein in the brain that is not associated with transmissible disease

Variable tau accumulation in murine models with abnormal prion protein deposits

Host PrP glycosylation: a major factor determining the outcome of prion infection

Infectious prions and proteinopathies

PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions

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

Dissociation between Transmissible Spongiform Encephalopathy (TSE) Infectivity and Proteinase K-Resistant PrPSc Levels in Peripheral Tissue from a Murine Transgenic Model of TSE Disease

Dissociation of Prion Protein Amyloid Seeding from Transmission of a Spongiform Encephalopathy

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

Presence of subclinical infection in gene-targeted human prion protein transgenic mice exposed to atypical bovine spongiform encephalopathy

Characterization of an unusual transmissible spongiform encephalopathy in goat by transmission in knock-in transgenic mice

Increased Susceptibility of Human-PrP Transgenic Mice to Bovine Spongiform Encephalopathy Infection following Passage in Sheep

Molecular barriers to zoonotic transmission of prions

Increased susceptibility of transgenic mice expressing human PrP to experimental sheep bovine spongiform encephalopathy is not due to increased agent titre in sheep brain tissue

Bovine PrP expression levels in transgenic mice influence transmission characteristics of atypical bovine spongiform encephalopathy

Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC

Insights into Mechanisms of Chronic Neurodegeneration

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

Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers

Molecular model of prion transmission to humans

Differential protein expression profiling in BSE disease

Dissociation between transmissible spongiform encephalopathy (TSE) infectivity and proteinase K-resistant PrP(Sc) levels in peripheral tissue from a murine transgenic model of TSE disease

The role of host PrP in Transmissible Spongiform Encephalopathies

Dissociation between Transmissible Spongiform Encephalopathy (TSE) Infectivity and Proteinase K-Resistant PrP Sc Levels in Peripheral Tissue from a Murine Transgenic Model of TSE Disease

Differential protein profiling as a potential multi-marker approach for TSE diagnosis

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