Results 21 to 30 of about 10,114 (213)

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

open access: yesPLoS Pathogens, 2007
Atypical neuropathological and molecular phenotypes of bovine spongiform encephalopathy (BSE) have recently been identified in different countries.
Raffaella Capobianco   +21 more
doaj   +1 more source

Candidate Cell Substrates, Vaccine Production, and Transmissible Spongiform Encephalopathies

open access: yesEmerging Infectious Diseases, 2011
Transmissible spongiform encephalopathy (TSE) agents have contaminated human tissue–derived medical products, human blood components, and animal vaccines.
Pedro Piccardo   +10 more
doaj   +1 more source

State-of-the-art review of goat TSE in the European Union, with special emphasis on PRNP genetics and epidemiology [PDF]

open access: yes, 2009
Scrapie is a fatal, neurodegenerative disease of sheep and goats. It is also the earliest known member in the family of diseases classified as transmissible spongiform encephalopathies (TSE) or prion diseases, which includes Creutzfeldt-Jakob disease in ...
Olivier Andreéoletti   +54 more
core   +1 more source

Diagnosis of bovine spongiform encephalopathy: A review [PDF]

open access: yesVeterinary Quarterly, 2000
Cows affected with bovine spongiform encephalopathy (BSE) display chronic neurological signs consisting of behavioural changes, abnormalities of posture and movement, and/or hyperaesthesia. At present, there are no laboratory test available to diagnose BSE in the live animal. In this article, we describe the post-mortem diagnostic examination of brains
van Keulen, L.J.M.   +5 more
openaire   +3 more sources

Oral Transmission of L-type Bovine Spongiform Encephalopathy in Primate Model

open access: yesEmerging Infectious Diseases, 2012
We report transmission of atypical L-type bovine spongiform encephalopathy to mouse lemurs after oral or intracerebral inoculation with infected bovine brain tissue.
Nadine Mestre-Francés   +7 more
doaj   +1 more source

BSE case associated with prion protein gene mutation. [PDF]

open access: yesPLoS Pathogens, 2008
Bovine spongiform encephalopathy (BSE) is a transmissible spongiform encephalopathy (TSE) of cattle and was first detected in 1986 in the United Kingdom. It is the most likely cause of variant Creutzfeldt-Jakob disease (CJD) in humans.
Jürgen A Richt, S Mark Hall
doaj   +1 more source

Pruritus is a common feature in sheep infected with the BSE agent. [PDF]

open access: yes, 2008
BACKGROUND: The variability in the clinical or pathological presentation of transmissible spongiform encephalopathies (TSEs) in sheep, such as scrapie and bovine spongiform encephalopathy (BSE), has been attributed to prion protein genotype, strain ...
Vidal-Diez, Alberto   +50 more
core   +1 more source

Kuru: A Journey Back in Time from Papua New Guinea to the Neanderthals’ Extinction

open access: yesPathogens, 2013
Kuru, the first human transmissible spongiform encephalopathy was transmitted to chimpanzees by D. Carleton Gajdusek (1923–2008). In this review, I briefly summarize the history of this seminal discovery along its epidemiology, clinical picture ...
Pawel P. Liberski
doaj   +1 more source

Differentiation of ruminant transmissible spongiform encephalopathy isolate types, including bovine spongiform encephalopathy and CH1641 scrapie

open access: yes, 2010
With increased awareness of the diversity of transmissible spongiform encephalopathy (TSE) strains in the ruminant population, comes an appreciation of the need for improved methods of differential diagnosis. Exposure to bovine spongiform encephalopathy (
Bossers, A.   +12 more
core   +1 more source

Genetics of Prion Disease in Cattle

open access: yesBioinformatics and Biology Insights, 2015
Bovine spongiform encephalopathy (BSE) is a prion disease that is invariably fatal in cattle and has been implicated as a significant human health risk.
Brenda M. Murdoch, Gordon K. Murdoch
doaj   +1 more source

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