R. Barron

发表

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

Declan King, R. Williamson, J. Manson, 2007, Journal of Biological Chemistry.

The transmissible spongiform encephalopathies: emerging and declining epidemics.

M. Bishop, J. Manson, E. Cancellotti, 2006, Biochemical Society transactions.

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

Richard C. Moore, D. Melton, Declan King, 2005, The Journal of general virology.

Transmission of murine scrapie to P101L transgenic mice.

D. Melton, Declan King, J. Manson, 2003, The Journal of general virology.

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

G. Telling, Declan King, J. Manson, 2013, Journal of Virology.

The Human Urinary Proteome Fingerprint Database UPdb

H. Husi, J. Ross, C. Greig, 2013, International journal of proteomics.

Short Communication 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

N. Hunter, F. Tagliavini, M. Simmons, 2012 .

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

N. Hunter, R. Barron, T. Baron, 2013, The Journal of general virology.

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

N. Hunter, W. Goldmann, Declan King, 2013, The Journal of general virology.

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

N. Hunter, R. Barron, T. Baron, 2012, The Journal of general virology.

Host PrP Glycosylation: A Major Factor Determining the Outcome of Prion Infection

J. Manson, E. Cancellotti, R. Barron, 2008, PLoS biology.

The role of host PrP in control of incubation time

M. Bishop, J. Manson, R. Barron, 2005 .

A single amino acid alteration in murine PrP dramatically alters TSE incubation time.

I. Mcconnell, D. Melton, J. Manson, 2000, Archives of virology. Supplementum.

Molecular Barriers to Zoonotic Transmission of Prions

J. Ironside, J. Manson, M. Head, 2014, Emerging infectious diseases.

Quantitative imaging of tissue sections using infrared scanning technology

S. Eaton, Declan King, J. Del-Pozo, 2015, Journal of anatomy.

Explorer Molecular barriers to zoonotic transmission of prions

J. Ironside, A. Barria, J. Manson, 2022 .

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

Declan King, M. Jeffrey, R. Barron, 2016, Acta Neuropathologica.

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

N. Hunter, J. Manson, R. Barron, 2014, The Journal of general virology.

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

N. Hunter, J. Manson, R. Barron, 2014 .

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

N. Hunter, A. Chong, J. Foster, 2010, Journal of Virology.

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

K. Brown, J. Manson, E. Cancellotti, 2010, Journal of Virology.

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

J. Manson, R. Barron, 2003, Clinics in laboratory medicine.

Infectious prions and proteinopathies

R. Barron, 2017, Prion.

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

R. Barron, K. Dobie, Karen Dobie, 2013, Journal of Virology.

The role of host PrP in Transmissible Spongiform Encephalopathies.

M. Bishop, J. Manson, E. Cancellotti, 2007, Biochimica et biophysica acta.

Assessing the risk of Sheep BSE transmission to humans

N. Hunter, J. Foster, J. Manson, 2010 .

Membrane pathology and microglial activation of mice expressing membrane anchored or membrane released forms of Aβ and mutated human Alzheimer's precursor protein (APP)

F. Baumann, M. Jeffrey, R. Barron, 2015, Neuropathology and applied neurobiology.

Edinburgh Research Explorer Membrane pathology and microglial activation of mice expressing membrane anchored or membrane released forms of A and mutated human APP

F. Baumann, M. Jeffrey, R. Barron, 2014 .

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

Emily V. Chambers, B. Ghetti, Declan King, 2012, Brain pathology.

Insights into Mechanisms of Chronic Neurodegeneration

J. Manson, R. Barron, P. Piccardo, 2016, International journal of molecular sciences.

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.

Marco Sbriccoli, Maurizio Pocchiari, Cristina Casalone, 2012, The Journal of general virology.

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

D. Melton, J. Ironside, J. Manson, 2001, The EMBO journal.

A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy

I. Mcconnell, D. Melton, J. Hope, 1999, The EMBO journal.

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

B. Ghetti, Declan King, J. Manson, 2007, Proceedings of the National Academy of Sciences.

Prion Seeding Activities of Mouse Scrapie Strains with Divergent PrPSc Protease Sensitivities and Amyloid Plaque Content Using RT-QuIC and eQuIC

B. Caughey, G. Baron, Declan King, 2012, PloS one.

Variable tau accumulation in murine models with abnormal prion protein deposits

Declan King, R. Barron, P. Piccardo, 2017, Journal of the Neurological Sciences.

Molecular Model of Prion Transmission to Humans

C. Prowse, J. Ironside, J. Manson, 2009, Emerging infectious diseases.

Microarray profiling emphasizes transcriptomic differences between hippocampal in vivo tissue and in vitro cultures

Declan King, P. Skehel, T. Wishart, 2021, Brain communications.

Differential protein expression profiling in BSE disease

D. Waddington, R. Barron, J. Barr, 2010, Archives of physiology and biochemistry.

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

M. Watson, J. Ironside, M. Head, 2009, BMC infectious diseases.