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Mutant knock-in mice display enhanced susceptibility to pure prion protein fibrils. [PDF]
J Gen VirolWalsh DJ +4 more
europepmc +1 more source
Control of Prion Uptake by Bone Morphogenetic Protein Signaling
De Cecco E +14 more
europepmc +1 more source
Prions, prionoids and protein misfolding disorders
Nature Reviews Genetics, 2018 Adriano Aguzzi +2 more
exaly +2 more sources
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Cell Biology of Prions and Prionoids: A Status Report
Trends in Cell Biology, 2016Asvin Lakkaraju, Adriano Aguzzi
exaly +2 more sources
Prions and the prion disorders
Mammalian Genome, 1998One of us remembers sitting in a high school biology class in 1977 being taught about scrapie, a naturally occurring disorder of sheep. The teacher had no particular interest in agriculture, but was pointing out some peculiar characteristics of this disease as a biological curiosity on a wet Friday afternoon.
E, Fisher, G, Telling, J, Collinge
openaire +2 more sources
Biochemistry (Moscow), 2007
Prions were originally defined as infectious agents of protein nature, which caused neurodegenerative diseases in animals and humans. The prion concept implies that the infectious agent is a protein in special conformation that can be transmitted to the normal molecules of the same protein through protein-protein interactions.
I S, Shkundina, M D, Ter-Avanesyan
openaire +2 more sources
Prions were originally defined as infectious agents of protein nature, which caused neurodegenerative diseases in animals and humans. The prion concept implies that the infectious agent is a protein in special conformation that can be transmitted to the normal molecules of the same protein through protein-protein interactions.
I S, Shkundina, M D, Ter-Avanesyan
openaire +2 more sources
The Prion Concept and Synthetic Prions
2017Transmissible spongiform encephalopathies or prion diseases are a group of fatal neurodegenerative diseases caused by unconventional infectious agents, known as prions (PrPSc). Prions derive from a conformational conversion of the normally folded prion protein (PrPC), which acquires pathological and infectious features.
Legname, Giuseppe, Moda, Fabio
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Current Biology, 1992
There have been remarkably rapid advances in the understanding of prion diseases over the past year. The controversial notion that the transmissible agent may be an abnormal isoform of a host-encoded protein, the prion protein, is now gaining wide acceptance.
J, Collinge, M S, Palmer
openaire +2 more sources
There have been remarkably rapid advances in the understanding of prion diseases over the past year. The controversial notion that the transmissible agent may be an abnormal isoform of a host-encoded protein, the prion protein, is now gaining wide acceptance.
J, Collinge, M S, Palmer
openaire +2 more sources