Published in Prion on October 30, 2009
Rabbits are not resistant to prion infection. Proc Natl Acad Sci U S A (2012) 1.63
Assessment of the genetic susceptibility of sheep to scrapie by protein misfolding cyclic amplification and comparison with experimental scrapie transmission studies. J Virol (2011) 0.90
Naturally prion resistant mammals: a utopia? Prion (2012) 0.85
Enhanced virulence of sheep-passaged bovine spongiform encephalopathy agent is revealed by decreased polymorphism barriers in prion protein conversion studies. J Virol (2013) 0.82
Transgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion Isolates. PLoS Pathog (2015) 0.78
In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies. BMC Vet Res (2013) 0.77
Exploring the risks of a putative transmission of BSE to new species. Prion (2013) 0.76
Assessing transmissible spongiform encephalopathy species barriers with an in vitro prion protein conversion assay. J Vis Exp (2015) 0.75
Prions: Beyond a Single Protein. Clin Microbiol Rev (2016) 0.75
An in vitro approach to identify the key amino acids in the low susceptibility of rabbit PrP to misfolding. J Virol (2017) 0.75
In vitro generation of infectious scrapie prions. Cell (2005) 6.86
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature (2001) 6.20
Cell-free formation of protease-resistant prion protein. Nature (1994) 6.07
Predicting susceptibility and incubation time of human-to-human transmission of vCJD. Lancet Neurol (2006) 3.29
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein. EMBO J (2002) 2.98
Scrapie infectivity found in resistant species. Nature (1998) 2.28
Cell-free propagation of prion strains. EMBO J (2008) 2.20
Crossing the species barrier by PrP(Sc) replication in vitro generates unique infectious prions. Cell (2008) 2.09
Protein misfolding cyclic amplification for diagnosis and prion propagation studies. Methods Enzymol (2006) 2.04
The host range of chronic wasting disease is altered on passage in ferrets. Virology (1998) 1.95
Spongiform encephalopathies in Cervidae. Rev Sci Tech (1992) 1.92
Accelerated high fidelity prion amplification within and across prion species barriers. PLoS Pathog (2008) 1.89
Markedly increased susceptibility to natural sheep scrapie of transgenic mice expressing ovine prp. J Virol (2001) 1.86
Experimental subacute spongiform virus encephalopathies in primates and other laboratory animals. Science (1973) 1.71
Susceptibility of sheep for scrapie as assessed by in vitro conversion of nine naturally occurring variants of PrP. J Virol (2000) 1.52
Cyclic amplification of protein misfolding and aggregation. Methods Mol Biol (2005) 1.48
Strain fidelity of chronic wasting disease upon murine adaptation. J Virol (2006) 1.40
Sheep-passaged bovine spongiform encephalopathy agent exhibits altered pathobiological properties in bovine-PrP transgenic mice. J Virol (2006) 1.25
Prion protein alleles showing a protective effect on the susceptibility of sheep to scrapie and bovine spongiform encephalopathy. J Virol (2007) 1.10
The fate of ME7 scrapie infection in rats, guinea-pigs and rabbits. Res Vet Sci (1976) 1.09
The potential for transmissible spongiform encephalopathies in non-ruminant livestock and fish. Rev Sci Tech (2003) 1.01
PrP polymorphisms tightly control sheep prion replication in cultured cells. J Virol (2003) 0.99
Protective effect of the AT137RQ and ARQK176 PrP allele against classical scrapie in Sarda breed sheep. Vet Res (2009) 0.95
Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification. J Biol Chem (2006) 2.98
Prion strain mutation determined by prion protein conformational compatibility and primary structure. Science (2010) 2.71
Presymptomatic detection of prions in blood. Science (2006) 2.14
Accelerated high fidelity prion amplification within and across prion species barriers. PLoS Pathog (2008) 1.89
Isolation and characterization of a proteinase K-sensitive PrPSc fraction. Biochemistry (2006) 1.86
Amyloids, prions and the inherent infectious nature of misfolded protein aggregates. Trends Biochem Sci (2006) 1.77
The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity. J Neurosci (2005) 1.74
Rabbits are not resistant to prion infection. Proc Natl Acad Sci U S A (2012) 1.63
Unfolded protein response transcription factor XBP-1 does not influence prion replication or pathogenesis. Proc Natl Acad Sci U S A (2008) 1.60
Cyclic amplification of protein misfolding and aggregation. Methods Mol Biol (2005) 1.48
A molecular switch controls interspecies prion disease transmission in mice. J Clin Invest (2010) 1.41
In vivo generation of neurotoxic prion protein: role for hsp70 in accumulation of misfolded isoforms. PLoS Genet (2009) 1.29
Amyloid formation modulates the biological activity of a bacterial protein. J Biol Chem (2005) 1.27
Sheep-passaged bovine spongiform encephalopathy agent exhibits altered pathobiological properties in bovine-PrP transgenic mice. J Virol (2006) 1.25
Perturbation of endoplasmic reticulum homeostasis facilitates prion replication. J Biol Chem (2007) 1.13
Progression of prion infectivity in asymptomatic cattle after oral bovine spongiform encephalopathy challenge. J Gen Virol (2007) 1.07
Genome comparison of a nonpathogenic myxoma virus field strain with its ancestor, the virulent Lausanne strain. J Virol (2008) 1.02
Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases. PLoS Pathog (2013) 1.00
Bovine spongiform encephalopathy induces misfolding of alleged prion-resistant species cellular prion protein without altering its pathobiological features. J Neurosci (2013) 0.98
Structure of the β2-α2 loop and interspecies prion transmission. FASEB J (2012) 0.91
Prion transmission prevented by modifying the β2-α2 loop structure of host PrPC. J Neurosci (2014) 0.90
Detection of PrPres in genetically susceptible fetuses from sheep with natural scrapie. PLoS One (2011) 0.87
Proteinase K enhanced immunoreactivity of the prion protein-specific monoclonal antibody 2A11. Neurosci Res (2004) 0.86
Naturally prion resistant mammals: a utopia? Prion (2012) 0.85
Human prion protein sequence elements impede cross-species chronic wasting disease transmission. J Clin Invest (2015) 0.83
Recombinant human prion protein inhibits prion propagation in vitro. Sci Rep (2013) 0.82
Spontaneous generation of infectious prion disease in transgenic mice. Emerg Infect Dis (2013) 0.79
Infectivity versus Seeding in Neurodegenerative Diseases Sharing a Prion-Like Mechanism. Int J Cell Biol (2013) 0.79
Human prion protein sequence elements impede cross-species chronic wasting disease transmission. J Clin Invest (2015) 0.79
Coenzyme Q and protein/lipid oxidation in a BSE-infected transgenic mouse model. Free Radic Biol Med (2007) 0.78
Reduced susceptibility to bovine spongiform encephalopathy prions in transgenic mice expressing a bovine PrP with five octapeptide repeats. J Gen Virol (2007) 0.78
Cell expression of a four extra octarepeat mutated PrPC modifies cell structure and cell cycle regulation. FEBS Lett (2006) 0.78
Prion-resistant or prion-susceptible species, this is the question. Virulence (2013) 0.76
Exploring the risks of a putative transmission of BSE to new species. Prion (2013) 0.76
Animal models for testing anti-prion drugs. Curr Top Med Chem (2013) 0.75