Published in J Virol on January 19, 2011
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The membrane environment of endogenous cellular prion protein in primary rat cerebellar neurons. J Neurochem (2005) 0.85
Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding. J Alzheimers Dis (2005) 0.84
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Distance of sequons to the C-terminus influences the cellular N-glycosylation of the prion protein. Biochem J (2003) 0.81
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Cells release prions in association with exosomes. Proc Natl Acad Sci U S A (2004) 5.17
Prions hijack tunnelling nanotubes for intercellular spread. Nat Cell Biol (2009) 3.55
A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes. Proc Natl Acad Sci U S A (2005) 2.47
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Facilitated cross-species transmission of prions in extraneural tissue. Science (2012) 2.26
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Identification of the epitope region capable of inducing neutralizing antibodies against the porcine epidemic diarrhea virus. Mol Cells (2002) 1.77
A bovine prion acquires an epidemic bovine spongiform encephalopathy strain-like phenotype on interspecies transmission. J Neurosci (2007) 1.75
The physical relationship between infectivity and prion protein aggregates is strain-dependent. PLoS Pathog (2010) 1.59
Generation of a replication-competent, propagation-deficient virus vector based on the transmissible gastroenteritis coronavirus genome. J Virol (2002) 1.57
Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathy. PLoS Pathog (2006) 1.55
Transmission of atypical bovine prions to mice transgenic for human prion protein. Emerg Infect Dis (2008) 1.38
Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice. PLoS Pathog (2011) 1.38
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Prions can infect primary cultured neurons and astrocytes and promote neuronal cell death. Proc Natl Acad Sci U S A (2004) 1.27
Atypical/Nor98 scrapie infectivity in sheep peripheral tissues. PLoS Pathog (2011) 1.26
Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD. PLoS One (2008) 1.24
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Genetic evidence for a link between glycolysis and DNA replication. PLoS One (2007) 1.20
Cultured peripheral neuroglial cells are highly permissive to sheep prion infection. J Virol (2004) 1.19
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Expression of prion protein increases cellular copper binding and antioxidant enzyme activities but not copper delivery. J Biol Chem (2002) 1.15
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Antihypertensive drug guanabenz is active in vivo against both yeast and mammalian prions. PLoS One (2008) 1.13
Marked influence of the route of infection on prion strain apparent phenotype in a scrapie transgenic mouse model. Neurobiol Dis (2010) 1.04
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PrPSc binding antibodies are potent inhibitors of prion replication in cell lines. J Biol Chem (2004) 0.99
PrP polymorphisms tightly control sheep prion replication in cultured cells. J Virol (2003) 0.99
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Characterization of atypical scrapie cases from Great Britain in transgenic ovine PrP mice. J Gen Virol (2010) 0.95
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Highly infectious prions generated by a single round of microplate-based protein misfolding cyclic amplification. MBio (2013) 0.89
Transcriptomic analysis brings new insight into the biological role of the prion protein during mouse embryogenesis. PLoS One (2011) 0.88
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Endogenous prion protein conversion is required for prion-induced neuritic alterations and neuronal death. FASEB J (2012) 0.87
Proteasome inhibitors promote the sequestration of PrPSc into aggresomes within the cytosol of prion-infected CAD neuronal cells. J Gen Virol (2009) 0.87
Prion protein and Shadoo are involved in overlapping embryonic pathways and trophoblastic development. PLoS One (2012) 0.87
Atypical scrapie isolates involve a uniform prion species with a complex molecular signature. PLoS One (2011) 0.87
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Scrg1 is induced in TSE and brain injuries, and associated with autophagy. Eur J Neurosci (2005) 0.84
Brain transcriptional stability upon prion protein-encoding gene invalidation in zygotic or adult mouse. BMC Genomics (2010) 0.84
Prion infection of epithelial Rov cells is a polarized event. J Virol (2004) 0.84
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Prions impair bioaminergic functions through serotonin- or catecholamine-derived neurotoxins in neuronal cells. J Biol Chem (2008) 0.82
Identification of atypical scrapie in Canadian sheep. J Vet Diagn Invest (2010) 0.82
Generation of Sprn-regulated reporter mice reveals gonadic spatial expression of the prion-like protein Shadoo in mice. Biochem Biophys Res Commun (2011) 0.82
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Plasminogen-based capture combined with amplification technology for the detection of PrP(TSE) in the pre-clinical phase of infection. PLoS One (2013) 0.80
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Prnp knockdown in transgenic mice using RNA interference. Transgenic Res (2008) 0.80
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Targeted knock-down of cellular prion protein expression in myelinating Schwann cells does not alter mouse prion pathogenesis. J Gen Virol (2013) 0.78
Expression of the prion-like protein Shadoo in the developing mouse embryo. Biochem Biophys Res Commun (2011) 0.78
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The prion protein family: looking outside the central nervous system. Prion (2012) 0.77
Prion proteins from susceptible and resistant sheep exhibit some distinct cell biological features. Biochem Biophys Res Commun (2005) 0.77
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Decontamination of prions in a plasma product manufacturing environment. Transfusion (2013) 0.77
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Variation in Chst8 gene expression level affects PrPC to PrPSc conversion efficiency in prion-infected Mov cells. Biochem Biophys Res Commun (2011) 0.75
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