Abstract Prions represent an unusual structural form of a protein that is 'infectious'. In mammals, prions are associated with fatal neurodegenerative diseases such as CJD (Creutzfeldt-Jakob disease), while in fungi they act as novel epigenetic regulators of phenotype. Even though most of the human prion diseases arise spontaneously, we still know remarkably little about how infectious prions form de novo
Prion diseases in humans and animals are due to conformational conversion of PrPC, a cellular glycop...
International audienceTwo infectious proteins (prions) of Saccharomyces cerevisiae have been identif...
Although prions were first discovered through their link to severe brain degenerative diseases in an...
Prions are ‘‘infectious’ ’ misfolded protein states that can template their self-perpetuating confor...
Prions are not uniquely associated with rare fatal neurodegenerative diseases in the animal kingdom;...
The term prion, proteinaceus infectious particle, was first used to describe the causative agent of ...
International audienceProteins with prion properties are closely associated to a class of fatal neur...
Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encode...
Prions constitute a rare class of protein, which can switch to a robust amyloid form and then propag...
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
AbstractThe discovery of prion disease transmission in mammals, as well as a non-Mendelian type of i...
AbstractInfectious, self-propagating protein aggregates (prions) as well as structurally related amy...
International audienceIt was believed that only proteins could carry out enzymatic reactions, and on...
According to the Koch postulates an infectious organism is the one that can be isolated from an host...
In 1982, the term “prions” (proteinaceous infectious particles) was coined to specify a new principl...
Prion diseases in humans and animals are due to conformational conversion of PrPC, a cellular glycop...
International audienceTwo infectious proteins (prions) of Saccharomyces cerevisiae have been identif...
Although prions were first discovered through their link to severe brain degenerative diseases in an...
Prions are ‘‘infectious’ ’ misfolded protein states that can template their self-perpetuating confor...
Prions are not uniquely associated with rare fatal neurodegenerative diseases in the animal kingdom;...
The term prion, proteinaceus infectious particle, was first used to describe the causative agent of ...
International audienceProteins with prion properties are closely associated to a class of fatal neur...
Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encode...
Prions constitute a rare class of protein, which can switch to a robust amyloid form and then propag...
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
AbstractThe discovery of prion disease transmission in mammals, as well as a non-Mendelian type of i...
AbstractInfectious, self-propagating protein aggregates (prions) as well as structurally related amy...
International audienceIt was believed that only proteins could carry out enzymatic reactions, and on...
According to the Koch postulates an infectious organism is the one that can be isolated from an host...
In 1982, the term “prions” (proteinaceous infectious particles) was coined to specify a new principl...
Prion diseases in humans and animals are due to conformational conversion of PrPC, a cellular glycop...
International audienceTwo infectious proteins (prions) of Saccharomyces cerevisiae have been identif...
Although prions were first discovered through their link to severe brain degenerative diseases in an...