Yeast Prions: Discovery, Nature, Cellular Manipulation and Implication. [PDF]
Son M.
europepmc +1 more source
Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo. [PDF]
Hill E +22 more
europepmc +1 more source
Beyond prion-like spreading in neurodegenerative disease. [PDF]
Meisl G, Rowe JB, Klenerman D.
europepmc +1 more source
Characterization of the prion protein in relation to normal cellular function and in disease
Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, are a group of rare and fatal neurodegenerative disorders that can affect both human and animals. Evidence indicates that the key event in prion disease pathogenesis is the conformational conversion of the normal cellular prion protein (PrPC) into an aggregated isoform ...
openaire +1 more source
Infecting human brain organoids with FFI or sCJD preserves prion traits regardless of host genotype. [PDF]
Groveman BR +6 more
europepmc +1 more source
Parkinson\u27s disease and multiple system atrophy have distinct α-synuclein seed characteristics [PDF]
Cairns, Nigel J. +8 more
core +1 more source
The Strain Properties of Korean and North American Chronic Wasting Disease Prions Are Indistinguishable. [PDF]
Sohn HJ +9 more
europepmc +1 more source
NMR structure of the human prion protein with the pathological Q212P mutation reveals unique structural features. [PDF]
Giachin, G +3 more
core +1 more source
Prions and protein aggregates as pathogens, self-propagating structures, biomarkers, and therapeutic targets. [PDF]
Caughey B +9 more
europepmc +1 more source
Prion 2024 conference: from two decades of growth to a new journey forward. [PDF]
Kong Y +8 more
europepmc +1 more source

