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- W2006427685 abstract "Atypical neuropathological and molecular phenotypes of bovine spongiform encephalopathy (BSE) have recently been identified in different countries. One of these phenotypes, named bovine amyloidotic spongiform encephalopathy (BASE), differs from classical BSE for the occurrence of a distinct type of the disease-associated prion protein (PrP), termed PrP(Sc), and the presence of PrP amyloid plaques. Here, we show that the agents responsible for BSE and BASE possess different biological properties upon transmission to transgenic mice expressing bovine PrP and inbred lines of nontransgenic mice. Strikingly, serial passages of the BASE strain to nontransgenic mice induced a neuropathological and molecular disease phenotype indistinguishable from that of BSE-infected mice. The existence of more than one agent associated with prion disease in cattle and the ability of the BASE strain to convert into the BSE strain may have important implications with respect to the origin of BSE and spongiform encephalopathies in other species, including humans." @default.
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- W2006427685 date "2007-03-09" @default.
- W2006427685 modified "2023-09-23" @default.
- W2006427685 title "Conversion of the BASE Prion Strain into the BSE Strain: The Origin of BSE?" @default.
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- W2006427685 doi "https://doi.org/10.1371/journal.ppat.0030031" @default.
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