The role for cellular prion protein PrP(c) in beta-amyloid (Abeta) oligomer-induced synaptic impairment is a topic of great interest and some controversy. In this issue of EMBO Molecular Medicine Aguzzi and co-workers explore the contribution of PrP(c) to deficient long term potentiation (LTP) and soluble Abeta levels in an Alzheimer's disease mouse model and show that the role of prions in Abeta related toxicity is far from 'black and white' suggesting complex interpretations of the data available thus far.status: publishe
Previous studies indicate an important role for the cellular prion Protein (PrPc) in the development...
Introduction: Cellular prion protein (PrPc) is a normal glycosyl phosphatidylinositol-anchored prote...
A pathological hallmark of Alzheimer’s disease (AD) is an accumulation of insoluble plaque containin...
Alzheimer's disease (AD), the most common neurodegenerative disorder, goes along with extracellular ...
Albeit we know much about the pathogenesis of prion disorders, our understanding of the molecular an...
The cellular prion protein (PrPC) is a membrane-bound glycoprotein especially abundant in the centr...
International audienceThe cellular prion protein PrP(C) was identified over twenty-five years ago as...
Prion diseases are very rare, neurodegenerative diseases caused by misfolding of the Prion protein. ...
Prion diseases are neurodegenerative disorders caused by conformational conversion of the cellular p...
Alzheimer's disease (AD) is characterized mainly by the accumulation of Amyloid-β oligomers (Aβo) in...
Specific protein misfolding and aggregation are mechanisms underlying various neurodegenerative dise...
This research was originally published in the Journal of Biological Chemistry. Younan, N. D., et al....
International audienceThe cellular prion protein (PrPC), a cell surface glycoprotein originally iden...
There is increasing evidence of molecular and cellular links between Alzheimer's disease (AD) and pr...
The human cellular prion protein (PrPC) is a glycosylphosphatidylinositol (GPI) anchored membrane gl...
Previous studies indicate an important role for the cellular prion Protein (PrPc) in the development...
Introduction: Cellular prion protein (PrPc) is a normal glycosyl phosphatidylinositol-anchored prote...
A pathological hallmark of Alzheimer’s disease (AD) is an accumulation of insoluble plaque containin...
Alzheimer's disease (AD), the most common neurodegenerative disorder, goes along with extracellular ...
Albeit we know much about the pathogenesis of prion disorders, our understanding of the molecular an...
The cellular prion protein (PrPC) is a membrane-bound glycoprotein especially abundant in the centr...
International audienceThe cellular prion protein PrP(C) was identified over twenty-five years ago as...
Prion diseases are very rare, neurodegenerative diseases caused by misfolding of the Prion protein. ...
Prion diseases are neurodegenerative disorders caused by conformational conversion of the cellular p...
Alzheimer's disease (AD) is characterized mainly by the accumulation of Amyloid-β oligomers (Aβo) in...
Specific protein misfolding and aggregation are mechanisms underlying various neurodegenerative dise...
This research was originally published in the Journal of Biological Chemistry. Younan, N. D., et al....
International audienceThe cellular prion protein (PrPC), a cell surface glycoprotein originally iden...
There is increasing evidence of molecular and cellular links between Alzheimer's disease (AD) and pr...
The human cellular prion protein (PrPC) is a glycosylphosphatidylinositol (GPI) anchored membrane gl...
Previous studies indicate an important role for the cellular prion Protein (PrPc) in the development...
Introduction: Cellular prion protein (PrPc) is a normal glycosyl phosphatidylinositol-anchored prote...
A pathological hallmark of Alzheimer’s disease (AD) is an accumulation of insoluble plaque containin...