Results 131 to 140 of about 6,019 (214)

Transmissible subacute spongiform encephalopathies

Biomedicine & Pharmacotherapy, 1999
openaire   +2 more sources

Laboratory activities involving transmissible spongiform encephalopathy causing agents: risk assessment and biosafety recommendations in Belgium. [PDF]

Prion, 2013
Leunda A, Van Vaerenbergh B, Baldo A, Roels S, Herman P.   +4 more
europepmc   +1 more source

State of the art in biosafety at the European National Reference Laboratories for Transmissible Spongiform Encephalopathies. [PDF]

Front Public Health
Begovoeva M, Nonno R, Mazza M, Bozzetta E, Ru G, Colleagues of the European Network of National Reference Laboratories for Transmissible Spongiform Encephalopathies.   +5 more
europepmc   +1 more source

Mechanism of PrP-amyloid formation in mice without transmissible spongiform encephalopathy. [PDF]

Brain Pathol, 2012
Jeffrey M, McGovern G, Chambers EV, King D, González L, Manson JC, Ghetti B, Piccardo P, Barron RM.   +8 more
europepmc   +1 more source

Folding and fibril formation of prions [PDF]

Prions diseases are a group of fatal neurodegenerative disorders called the transmissible spongiform encephalopathies (TSEs), which include bovine spongiform encephalopathy in cattle, scrapie in sheep and Creutzfeldt-Jakob disease (CJD) in humans ...
Gierusz, Leszek A.
core  

Oral Transmission of Classical Bovine Spongiform Encephalopathy in ARR/ARR Sheep. [PDF]

Emerg Infect Dis
Huor A, Lantier F, Douet JY, Lugan S, Aron N, Mesic C, Cassard H, Barrio T, Simmons H, Lantier I, Andreoletti O.   +10 more
europepmc   +1 more source

Variant Creutzfeldt-Jakob disease surveillance in Spain, 1993-2021. [PDF]

Front Public Health
De Pedro-Cuesta J, García López FJ, Calero M, Ruiz-Tovar M, Almazán-Isla J.   +4 more
europepmc   +1 more source

Transmissible spongiform encephalopathies or prion diseases – update 2007

, 2007
Prion diseases or transmissible spongiform encephalopathies are a group of neurodegenerative disorders characterized by a widespread deposition in the central nervous system, and some other tissues, of the pathological isoform of the prion protein (PrPd;
Sikorska, Beata, Liberski, Paweł P., Budka, Hubert, Bratosiewicz-Wąsik, Jolanta, Ironside, James W.   +4 more
core  

Strain Traits of Intracranially Administered L-Type Bovine Spongiform Encephalopathy Prions Are not Significantly Modified During Intraspecies Transmission in Cynomolgus Monkeys. [PDF]

Microbiol Immunol
Hagiwara K, Shibata H, Tobiume M, Sato Y, Ohto K, Okabayashi S, Nakano N, Horiuchi M, Ono F.   +8 more
europepmc   +1 more source

Prion Protein Codon Implicated in Resistance in Dogs Detected in Non-Domesticated Members of Mammalia. [PDF]

Animals (Basel)
Wright EA, Lacy VA, Brugette GG, Roberts SM, Brookover EK, Hardy DM, Bradley RD.   +6 more
europepmc   +1 more source