Results 1 to 10 of about 14,159 (251)
Resistance of Bovine Spongiform Encephalopathy (BSE) Prions to Inactivation [PDF]
Distinct prion strains often exhibit different incubation periods and patterns of neuropathological lesions. Strain characteristics are generally retained upon intraspecies transmission, but may change on transmission to another species.
Kurt Giles +2 more
exaly +2 more sources
Protease-Sensitive Synthetic Prions [PDF]
Prions arise when the cellular prion protein (PrP(C)) undergoes a self-propagating conformational change; the resulting infectious conformer is designated PrP(Sc).
David W Colby +2 more
exaly +2 more sources
Artificial strain of human prions created in vitro
Synthetic prions have previously been generated from recombinant rodent PrP. Here the authors generate synthetic human prions, by seeding human PrP with CJD prions, and characterize its infectivity in mice.
Chae Kim, Xiangzhu Xiao, Shugui Chen
exaly +2 more sources
Infectious prions in brains and muscles of domestic pigs experimentally challenged with the BSE, scrapie, and CWD agents [PDF]
Experimental studies suggest that animal species not previously described as naturally infected by prions are susceptible to prion diseases affecting sheep, cattle, and deer.
Francisca Bravo-Risi +9 more
doaj +2 more sources
Distribution of chronic wasting disease (CWD) prions in tissues from experimentally exposed coyotes (Canis latrans). [PDF]
Cervids susceptible to chronic wasting disease (CWD) are sympatric with multiple other animal species that can interact with infectious prions. Several reports have described the susceptibility of other species to CWD prions, or their potential to ...
Nancy Ho +7 more
doaj +2 more sources
Background The microtubule-associated protein tau forms aggregates in different neurodegenerative diseases called tauopathies. Prior work has shown that a single P301L mutation in tau gene, MAPT, can promote alternative tau folding pathways that ...
Sang-Gyun Kang +8 more
doaj +1 more source
Innate Immune Status of Glia Modulates Prion Propagation in Early Stage of Infection
Prion diseases are progressive neurodegenerative disorders affecting humans and various mammals. The prominent neuropathological change in prion-affected brains is neuroinflammation, histopathologically characterized by reactive gliosis surrounding prion
Sang-Gyun Kang +3 more
doaj +1 more source
Conversion of β-amyloid (Aβ) peptides from soluble random-coil to aggregated protein enriched with β-sheet-rich intermediates has been suggested to play a role in the degeneration of neurons and development of Alzheimer’s disease (AD) pathology ...
Pallabi Sil Paul +7 more
doaj +1 more source
Susceptibility of Beavers to Chronic Wasting Disease
Chronic wasting disease (CWD) is a contagious, fatal, neurodegenerative prion disease of cervids. The expanding geographical range and rising prevalence of CWD are increasing the risk of pathogen transfer and spillover of CWD to non-cervid sympatric ...
Allen Herbst +8 more
doaj +1 more source
The accumulation of tau protein in the form of filamentous aggregates is a hallmark of many neurodegenerative diseases such as Alzheimer’s disease (AD) and chronic traumatic encephalopathy (CTE).
Hadeel Alyenbaawi +2 more
doaj +1 more source

