AbstractThe physiological functions of cellular prion protein (PrPC) remain unclear. It has been demonstrated that PrPC is a copper binding protein and proposed that its functions could be strictly linked to copper metabolism and neuroprotection. The aim of this study was to clarify how extracellular copper modifies PrPC expression and metabolism in cultured neurones. We reported here that copper delivered at physiological concentrations significantly decreases PrPC mRNA expression in GN11 neurones. Moreover, copper increases the release of PrPC into the culture medium. These results indicate that extracellular copper strongly affects the amount of cellular PrP and might represent an interesting strategy to decrease the expression of PrPC i...
The cellular form of prion protein (PrPC) is a ubiquitous component of both the central and periphe...
Transmissible spongiform encephalopathy (TSE) or prion diseases are fatal neurodegenerative disorder...
AbstractThe neurodegenerative spongiform encephalopathies, or prion diseases, are characterized by t...
AbstractThe physiological functions of cellular prion protein (PrPC) remain unclear. It has been dem...
none6noneTONI M; MASSIMINO ML; GRIFFONI C; SALVATO B; TOMASI V; SPISNI E.TONI M; MASSIMINO ML; GRIFF...
International audienceThe N-terminal region of the prion protein PrPC contains a series of octapepti...
CTR1 (Copper Transporter 1), PrPC (Cellular Prion Protein), NRAMP2 (Natural Resistance - Associated ...
Prions have been extensively studied since they represent a new class of infectious agents in which ...
ABSTRACTIn mammals the cellular form of the prion protein (PrPC) is a ubiquitous protein involved in...
AbstractCellular prion (PrPc) is a plasma membrane glycosyphosphatidylinositol-anchored protein pres...
Copper dyshomeostasis is responsible for the neurological symptoms observed in the genetically inher...
Over the last decade, a piece of the research studying copper role in biological systems was devoted...
Prion, or PrPSc, is the pathological isoform of the cellular prion protein (PrPC) and it is the etio...
The Prion Protein (PrP) is mostly known for its role in prion diseases, where its misfolding and agg...
Copper dyshomeostasis is responsible for the neurological symptoms observed in the genetically inher...
The cellular form of prion protein (PrPC) is a ubiquitous component of both the central and periphe...
Transmissible spongiform encephalopathy (TSE) or prion diseases are fatal neurodegenerative disorder...
AbstractThe neurodegenerative spongiform encephalopathies, or prion diseases, are characterized by t...
AbstractThe physiological functions of cellular prion protein (PrPC) remain unclear. It has been dem...
none6noneTONI M; MASSIMINO ML; GRIFFONI C; SALVATO B; TOMASI V; SPISNI E.TONI M; MASSIMINO ML; GRIFF...
International audienceThe N-terminal region of the prion protein PrPC contains a series of octapepti...
CTR1 (Copper Transporter 1), PrPC (Cellular Prion Protein), NRAMP2 (Natural Resistance - Associated ...
Prions have been extensively studied since they represent a new class of infectious agents in which ...
ABSTRACTIn mammals the cellular form of the prion protein (PrPC) is a ubiquitous protein involved in...
AbstractCellular prion (PrPc) is a plasma membrane glycosyphosphatidylinositol-anchored protein pres...
Copper dyshomeostasis is responsible for the neurological symptoms observed in the genetically inher...
Over the last decade, a piece of the research studying copper role in biological systems was devoted...
Prion, or PrPSc, is the pathological isoform of the cellular prion protein (PrPC) and it is the etio...
The Prion Protein (PrP) is mostly known for its role in prion diseases, where its misfolding and agg...
Copper dyshomeostasis is responsible for the neurological symptoms observed in the genetically inher...
The cellular form of prion protein (PrPC) is a ubiquitous component of both the central and periphe...
Transmissible spongiform encephalopathy (TSE) or prion diseases are fatal neurodegenerative disorder...
AbstractThe neurodegenerative spongiform encephalopathies, or prion diseases, are characterized by t...