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PrPC Proteins

Known as: Cp33-35, Scrapie, PrPC Proteins [Chemical/Ingredient], Cp 33-35 
Normal cellular isoform of PRION PROTEINS encoded by a chromosomal gene and found in normal and scrapie-infected brain tissue, and other normal… 
National Institutes of Health

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In BloodProcess of secretionagonistsantagonists & inhibitors

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Copper and Zinc Interactions with Cellular Prion Proteins Change Solubility of Full-Length Glycosylated Isoforms and Induce the Occurrence of Heterogeneous Phenotypes
Prion diseases are characterized biochemically by protein aggregation of infectious prion isoforms (PrPSc), which result from the… 
2008
2008
Effect of different periods of hyperbaric oxygen on ischemia-reperfusion injury of rat small bowel.
PURPOSE To determine whether hyperbaric oxygen (HBO) could effectively protect the small intestine mucosa against an ischemic… 
2006
2006
Cell type‐specific transgene expression of the prion protein in Xenopus intermediate pituitary cells
The cellular form of prion protein (PrPC) is anchored to the plasma membrane of the cell and expressed in most tissues, but… 
2001
2001
Deletion of β-Strand and α-Helix Secondary Structure in Normal Prion Protein Inhibits Formation of Its Protease-Resistant Isoform
ABSTRACT A fundamental event in the pathogenesis of transmissible spongiform encephalopathies (TSE) is the conversion of a normal… 
2001
2001
Factors affecting interactions between prion protein isoforms.
Interactions between normal, protease-sensitive prion protein (PrP-sen or PrP(C)) and its protease-resistant isoform (PrP-res or… 
1999
1999
Assays of protease-resistant prion protein and its formation.
1999
1999
Methods for studying prion protein (PrP) metabolism and the formation of protease-resistant PrP in cell culture and cell-free systems. An update.
Transmissible spongiform encephalopathies (TSE) or prion diseases result in aberrant metabolism of prion protein (PrP) and the… 
1998
1998
Measurement of altered aspartyl residues in the scrapie associated form of prion protein.
In transmissible spongiform encephalopathies (TSE), the endogenous protease-sensitive prion protein (PrP-sen) of the host is… 
1994
1994
Use of single event upsets in dynamic random access memories as the basis for a position sensitive radiation detector.
Heavy charged particle induced soft errors in semiconductor memory devices have been a field failure problem for the… 
1991
1991
Differences in the membrane interaction of scrapie amyloid precursor proteins in normal and scrapie- or Creutzfeldt-Jakob disease-infected brains.
The membrane interaction and hydrophobicity of the normal (PrPC) and infectious isoform (PrPSc/CJD) of scrapie and Creutzfeldt… 
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