Results 91 to 100 of about 461,407 (167)

Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits

open access: yesVeterinary Research, 2011
Atypical bovine spongiform encephalopathy (BSE) has recently been identified in Europe, North America, and Japan. It is classified as H-type and L-type BSE according to the molecular mass of the disease-associated prion protein (PrPSc).
Okada Hiroyuki   +9 more
doaj   +1 more source

Bovine Spongiform Encephalopathy in the UK: An Update

open access: yes, 1991
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

The European Union summary report on surveillance for the presence of transmissible spongiform encephalopathies (TSE) in 2018

open access: yesEFSA Journal, 2019
This report presents the results of surveillance on transmissible spongiform encephalopathies (TSE) in bovine animals, sheep, goats, cervids and other species, and genotyping in sheep, carried out in 2018 by 28 Member States (MS) according to legislation,
European Food Safety Authority (EFSA)
doaj   +1 more source

Prevalence of the prion protein gene E211K variant in U.S. cattle

open access: yesBMC Veterinary Research, 2008
Background In 2006, an atypical U.S. case of bovine spongiform encephalopathy (BSE) was discovered in Alabama and later reported to be polymorphic for glutamate (E) and lysine (K) codons at position 211 in the bovine prion protein gene (Prnp) coding ...
Chase Chad C   +16 more
doaj   +1 more source

Overview of BSE in the United Kingdom: U.S. Response: Questions and Answers Regarding Bovine Spongiform Encephalopathy

open access: yes, 1998
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

Characterisation of European Field Goat Prion Isolates in Ovine PrP Overexpressing Transgenic Mice (Tgshp IX) Reveals Distinct Prion Strains

open access: yesPathogens
After the detection of bovine spongiform encephalopathy (BSE), and a zoonotic transmissible spongiform encephalopathy (TSE) caused by the pathological prion protein (PrPSc) in two goats, the investigation of goat prions became of greater interest ...
Sonja Ernst   +12 more
doaj   +1 more source

The Molecular Pathology of Prion Diseases [PDF]

open access: yes, 2004
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
core  

Epidemiology of bovine spongiform encephalopathy in Northern Ireland 1988 to 1995

open access: yes, 1997
Epidemiology of bovine spongiform encephalopathy in Northern Ireland 1988 to 1995.
Hueston, W. D., Denny, G. O.
core   +1 more source

The European Union summary report on data of the surveillance of ruminants for the presence of transmissible spongiform encephalopathies (TSEs) in 2015

open access: yesEFSA Journal, 2016
This report of EFSA presents the results of surveillance activities on transmissible spongiform encephalopathies (TSEs) in bovine animals, sheep and goats as well as genotyping data in sheep, carried out in 2015 in the EU and in three non‐Member States ...
European Food Safety Authority (EFSA)   +6 more
doaj   +1 more source

Atypical and classic bovine spongiform encephalopathy

open access: yes, 2018
This chapter describes the prion diseases of cattle, or bovine transmissible spongiform encephalopathies (BoTSEs). “Classic” bovine spongiform encephalopathy (C-BSE), the major prion protein disorder of Bovidae, was first described in 1986.
Casalone, Cristina   +3 more
core   +1 more source

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