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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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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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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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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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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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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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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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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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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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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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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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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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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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Mechanism of PrP-Amyloid Formation in Mice Without Transmissible Spongiform Encephalopathy

Brain pathology (Zurich, Switzerland), 2012-01, Vol.22 (1), p.58-66

2012

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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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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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Polymorphisms at codons 108 and 189 in murine PrP play distinct roles in the control of scrapie incubation time

Journal of general virology, 2005-03, Vol.86 (3), p.859-868

2005

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Transmission of murine scrapie to P101L transgenic mice

Journal of general virology, 2003-11, Vol.84 (11), p.3165-3172

2003

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A gene-targeted mouse model of P102L Gerstmann-Sträussler-Scheinker syndrome

Clinics in Laboratory Medicine, 2003-03, Vol.23 (1), p.161-173

2003

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Prion disease zoonosis: assessing risk associated with new and emerging prion agents

CABI Reviews, 2014-09, p.1-10

Barron, R. M.

2014

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Differential protein expression profiling in BSE disease: Biomarker Discovery using SELDI-TOF Protein Chip Technology

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

2010

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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

Journal of general virology, 2012, Vol.93, p.1624-1629

2012

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

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

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

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

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

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

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

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

Variable tau accumulation in murine models with abnormal prion protein deposits

Infectious prions and proteinopathies

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

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

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

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

Mechanism of PrP-Amyloid Formation in Mice Without Transmissible Spongiform Encephalopathy

Differential protein expression profiling in BSE disease

The role of host PrP in Transmissible Spongiform Encephalopathies

Polymorphisms at codons 108 and 189 in murine PrP play distinct roles in the control of scrapie incubation time

Transmission of murine scrapie to P101L transgenic mice

A gene-targeted mouse model of P102L Gerstmann-Sträussler-Scheinker syndrome

Prion disease zoonosis: assessing risk associated with new and emerging prion agents

Differential protein expression profiling in BSE disease: Biomarker Discovery using SELDI-TOF Protein Chip Technology

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

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

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