Results 81 to 90 of about 302,503 (203)
Differentiation of Prions from L-type BSE versus Sporadic Creutzfeldt-Jakob Disease
We compared transmission characteristics for prions from L-type bovine spongiform encephalopathy and MM2-cortical sporadic Creutzfeldt-Jakob disease in the Syrian golden hamster and an ovine prion protein–transgenic mouse line and isolated distinct prion
Simon Nicot +5 more
doaj +1 more source
Unlocking the Potential of Sea Bass Skin: Characterization of Gelatin and Edible Gelatin Films
Sea bass (Dicentrarchus labrax) skin waste was successfully valorized into high‐purity gelatin. SSG exhibited significantly higher oil binding capacity than commercial bovine and fish gelatins. Edible films developed from sea bass skin displayed a smooth, compact, and ordered matrix morphology.
Mehmet Gokcin +2 more
wiley +1 more source
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.
core +1 more source
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
core +1 more source
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.
core +1 more source
Scrapie is a notifiable transmissible spongiform encephalopathy (TSE) in sheep that relies on clinical examinations for reporting suspects. A short examination protocol was used in 1002 sheep to define clinical markers suggestive of scrapie.
Timm Konold, Laura J. Phelan
doaj +1 more source

