The interaction of prion peptide PrP 180-193 with model membranes is modulated by copper: a DSC stud
International audienceThe N-terminal region of the prion protein PrPC contains a series of octapepti...
Investigating the Cellular Prion Protein’s Metal Driven cis InteractionKathleen A. Markham The ...
ABSTRACTIn mammals the cellular form of the prion protein (PrPC) is a ubiquitous protein involved in...
DSC studies of the interaction of prion peptide Prp 180-193 with DPPC model membranes: effect of the...
Interaction of the neurotoxic prion peptide PrP180-193 with model membranes: a DSC stud
An abnormal interaction between copper and the prion protein is believed to play a pivotal role in t...
The flexible N-terminal domain of the prion protein (PrP(c)) is believed to play a pivotal role in b...
The prion protein is usually pictured as globular structured C-terminal domain that is linked to an ...
The opossum is a peculiar model of immunity to prion diseases. Here we scrutinised the bis-decarepea...
The cellular prion protein (PrPC) is a Cu2+ binding protein connected to the outer cell membrane. Th...
Prion proteins (PrPs) from different species have the enormous ability to anchor copper ions. The N-...
The human prion protein fragment PrP106-126 is a highly fibrillogenic peptide, resistant to proteina...
Transmissible spongiform encephalopathies (TSEs) in mammals are neurodegenerative diseases caused by...
We have shown previously that the protease-resistant and neurotoxic prion peptide fragment PrP[106-1...
The human prion protein fragment PrP106-126 is a highly fibrillogenic peptide, resistant to protein...
International audienceThe N-terminal region of the prion protein PrPC contains a series of octapepti...
Investigating the Cellular Prion Protein’s Metal Driven cis InteractionKathleen A. Markham The ...
ABSTRACTIn mammals the cellular form of the prion protein (PrPC) is a ubiquitous protein involved in...
DSC studies of the interaction of prion peptide Prp 180-193 with DPPC model membranes: effect of the...
Interaction of the neurotoxic prion peptide PrP180-193 with model membranes: a DSC stud
An abnormal interaction between copper and the prion protein is believed to play a pivotal role in t...
The flexible N-terminal domain of the prion protein (PrP(c)) is believed to play a pivotal role in b...
The prion protein is usually pictured as globular structured C-terminal domain that is linked to an ...
The opossum is a peculiar model of immunity to prion diseases. Here we scrutinised the bis-decarepea...
The cellular prion protein (PrPC) is a Cu2+ binding protein connected to the outer cell membrane. Th...
Prion proteins (PrPs) from different species have the enormous ability to anchor copper ions. The N-...
The human prion protein fragment PrP106-126 is a highly fibrillogenic peptide, resistant to proteina...
Transmissible spongiform encephalopathies (TSEs) in mammals are neurodegenerative diseases caused by...
We have shown previously that the protease-resistant and neurotoxic prion peptide fragment PrP[106-1...
The human prion protein fragment PrP106-126 is a highly fibrillogenic peptide, resistant to protein...
International audienceThe N-terminal region of the prion protein PrPC contains a series of octapepti...
Investigating the Cellular Prion Protein’s Metal Driven cis InteractionKathleen A. Markham The ...
ABSTRACTIn mammals the cellular form of the prion protein (PrPC) is a ubiquitous protein involved in...