Skip to search formSkip to main contentSkip to account menu

Prion Proteins

Known as: Fatal Familial Insomnia Protein, Major Prion Protein, PrP Proteins 
Membrane glycosylphosphatidylinositol-anchored glycoproteins that may aggregate into rod-like structures. The prion protein (PRNP) gene is… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Vaccines based on peptide epitopes of self-proteins require carrier proteins with T cell epitopes to support B cell responses. We… 
2014
2014
Transmissible spongiform encephalopathies (TSEs), otherwise known as prion disorders, are fatal diseases causing… 
2012
2012
The b site APP cleaving enzyme 1 (BACE1) is the rate-limiting b-secretase enzyme in the amyloidogenic processing of APP and Ab… 
2011
2011
Prion diseases are devastating neurological conditions of the central nervous system that affect animals and human beings. They… 
2009
2009
Keywords: CIBM-AIT Reference EPFL-CONF-178163 Record created on 2012-06-13, modified on 2017-05-12 
2009
2009
The Entropic Landscape Analysis was applied to the prion protein sequences of various mammals in order to detect potential sites… 
2008
2008
Prion diseases are fatal neurodegenerative disorders of humans and animals. The prion hypothesis states that PrP, a misfolded… 
2003
2003
The deposition of abnormal protein fibrils is a prominent pathological feature of many different ‘protein conformational… 
2002
2002
The cellular prion protein (PrP') is encoded by a chromosomal gene, and its scrapie isoform (PrP") features in all aspects of the… 
1993
1993
Transmissible spongiform encephalopathies are fatal neurodegenerative disorders which are linked to abnormal isoforms of the…