Mammalian prion diseases are a group of neurodegenerative conditions caused by infection of the central nervous system with proteinaceous agents called prions, including sporadic, variant, and iatrogenic Creutzfeldt-Jakob disease; kuru; inherited prion disease; sheep scrapie; bovine spongiform encephalopathy; and chronic wasting disease. Prions are composed of misfolded and multimeric forms of the normal cellular prion protein (PrP). Prion diseases require host expression of the prion protein gene (PRNP) and a range of other cellular functions to support their propagation and toxicity. Inherited forms of prion disease are caused by mutation of PRNP, whereas acquired and sporadically occurring mammalian prion diseases are controlled ...
Prion diseases, or transmissible spongiform encephalopathies (TSE), are a group of neurodegenerative...
Prion is a disease-causing agent that is neither bacterial nor fungal nor viral and contains no gene...
The infectious agents, prions, are composed mainly of conformational isomers of the cellular prion p...
Prion diseases are transmissible neurodegenerative disorders which affect a range of mammalian speci...
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
Introduction: Prion diseases or transmissible spongiform encephalopathies (TSEs) are rare, fatal and...
Prion diseases are enigmatic, neurodegenerative disorders affecting several mammalian species. The ...
Prion diseases or transmissible spongiform encephalopathies (TSEs) are rare, fatal and incurable neu...
Transmissible spongiform encephalopathies (TSEs) or prion diseases are a group of fatal neurodegener...
Prion diseases include a group of either sporadic, inherited or infectious disorders characterized b...
1To whom correspondence should be addressed Prion diseases are fatal transmissible neurological diso...
Abstract Prion diseases are transmissible neurodegenerative conditions affecting human and a wide ra...
Transmissible spongiform encephalopathies (TSE, prion diseases) are invariably fatal, neurodegenerat...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Prions were initially discovered in studies of scrapie, a transmissible neurodegenerative disease (N...
Prion diseases, or transmissible spongiform encephalopathies (TSE), are a group of neurodegenerative...
Prion is a disease-causing agent that is neither bacterial nor fungal nor viral and contains no gene...
The infectious agents, prions, are composed mainly of conformational isomers of the cellular prion p...
Prion diseases are transmissible neurodegenerative disorders which affect a range of mammalian speci...
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
Introduction: Prion diseases or transmissible spongiform encephalopathies (TSEs) are rare, fatal and...
Prion diseases are enigmatic, neurodegenerative disorders affecting several mammalian species. The ...
Prion diseases or transmissible spongiform encephalopathies (TSEs) are rare, fatal and incurable neu...
Transmissible spongiform encephalopathies (TSEs) or prion diseases are a group of fatal neurodegener...
Prion diseases include a group of either sporadic, inherited or infectious disorders characterized b...
1To whom correspondence should be addressed Prion diseases are fatal transmissible neurological diso...
Abstract Prion diseases are transmissible neurodegenerative conditions affecting human and a wide ra...
Transmissible spongiform encephalopathies (TSE, prion diseases) are invariably fatal, neurodegenerat...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Prions were initially discovered in studies of scrapie, a transmissible neurodegenerative disease (N...
Prion diseases, or transmissible spongiform encephalopathies (TSE), are a group of neurodegenerative...
Prion is a disease-causing agent that is neither bacterial nor fungal nor viral and contains no gene...
The infectious agents, prions, are composed mainly of conformational isomers of the cellular prion p...