Results 81 to 90 of about 302,501 (209)
Bovine Spongiform Encephalopathy in the UK: An Update
Bovine Spongiform Encephalopathy, BSE, was first diagnosed in England in November 1986. It is a slow disease and the incubation period varies between two and five years, and so mainly affects cows.
Edmondson, Peter W.
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It is hypothesised that exposure to bovine spongiform encephalopathy through contaminated food could have resulted in a large proportion of latent variant Creutzfeldt-Jakob disease cases in humans. Here the authors demonstrate that inoculation with blood
Emmanuel E. Comoy +12 more
doaj +1 more source
Transmission of New Bovine Prion to Mice
We previously reported that cattle were affected by a prion disorder that differed from bovine spongiform encephalopathy (BSE) by showing distinct molecular features of disease-associated protease-resistant prion protein (PrPres).
Thierry G.M. Baron +3 more
doaj +1 more source
Modeling localized deer removal strategies for managing chronic wasting disease
We used an agent‐based model developed for chronic wasting disease (CWD) in Midwestern white‐tailed deer to assess localized deer removal strategies and how local conditions affect management outcomes. Parcel‐based and ring culling were most effective at reducing CWD prevalence and persistence, and transmission was always greater at greater deer ...
Noelle E. Thompson +5 more
wiley +1 more source
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD [PDF]
Variant CJD (vCJD) is an incurable, infectious human disease, likely arising from the consumption of BSE-contaminated meat products. Whilst the epidemic appears to be waning, there is much concern that vCJD infection may be perpetuated in humans by the ...
Smith, Antony +58 more
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Transmission of Atypical Bovine Prions to Mice Transgenic for Human Prion Protein
To assess risk for cattle-to-human transmission of prions that cause uncommon forms of bovine spongiform encephalopathy (BSE), we inoculated mice expressing human PrP Met129 with field isolates.
Vincent Béringue +6 more
doaj +1 more source
Below, by the following five topics, are some questions and answers related to this situation:Topics:1. Bovine spongiform encephalopathy (BSE)2. Other human and animal transmissible spongiform encephalopathies (TSEs)3. Creutzfeldt-Jakob disease (CJD) and
Detwiler, Linda A.
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Epidemiology of bovine spongiform encephalopathy in Northern Ireland 1988 to 1995
Epidemiology of bovine spongiform encephalopathy in Northern Ireland 1988 to 1995.
Hueston, W. D., Denny, G. O.
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Prion diseases, blood and the immune system: concerns and reality
There is a great amount of uncertainty about the nature of the agent which causes spongiform encephalopathies. In recent years the occurrence of bovine spongiform encephalopathy and of new variant-Creutzfeldt Jakob disease, has raised concerns that ...
A Aguzzi
doaj
The Molecular Pathology of Prion Diseases [PDF]
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are a group of invariably fatal neurodegenerative disorders. Uniquely, they may present as sporadic, inherited, or infectious forms, all of which involve conversion of the normal ...
Vassallo, Neville +2 more
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