Add to ORKGInteraction of the neurotoxic prion peptide PrP180-193 with model membranes: a DSC stud
SIGLEAvailable from British Library Document Supply Centre- DSC:DXN054653 / BLDSC - British Library ...
A key molecular event in prion diseases is the conversion of the normal cellular form of the prion p...
A synthetic peptide corresponding to the 106-126 amyloidogenic region of the cellular human prion pr...
Interaction of neurotoxic Prion peptides PrP106-126 and Prp180-193 with model membranes: a thermodyn...
DSC studies of the interaction of prion peptide Prp 180-193 with DPPC model membranes: effect of the...
The interaction of prion peptide PrP 180-193 with model membranes is modulated by copper: a DSC stud
© 2008 by the Biophysical SocietyTransmissible spongiform encephalopathies are neurodegenerative dis...
Prion diseases are fatal neurodegenerative disorders characterized by the accumulation in the brain ...
Free to read at publisher's site. Transmissible spongiform encephalopathies are neurodegenerative di...
AbstractTransmissible spongiform encephalopathies are neurodegenerative diseases characterized by th...
It has been shown recently that the generation of an abnormal transmembrane form of the prio...
This thesis focuses on peptides derived from the Prion, Doppel and Influenza haemagglutinin proteins...
The Cellular Prion Protein (PrPC), discovered by Nobel Laureate Dr. Stanley Prusiner, represents the...
International audienceSoluble oligomers of prion proteins (PrP), produced during amyloid aggregation...
Prions are an unconventional form of infectious agents composed only of protein and involved in tran...
SIGLEAvailable from British Library Document Supply Centre- DSC:DXN054653 / BLDSC - British Library ...
A key molecular event in prion diseases is the conversion of the normal cellular form of the prion p...
A synthetic peptide corresponding to the 106-126 amyloidogenic region of the cellular human prion pr...
Interaction of neurotoxic Prion peptides PrP106-126 and Prp180-193 with model membranes: a thermodyn...
DSC studies of the interaction of prion peptide Prp 180-193 with DPPC model membranes: effect of the...
The interaction of prion peptide PrP 180-193 with model membranes is modulated by copper: a DSC stud
© 2008 by the Biophysical SocietyTransmissible spongiform encephalopathies are neurodegenerative dis...
Prion diseases are fatal neurodegenerative disorders characterized by the accumulation in the brain ...
Free to read at publisher's site. Transmissible spongiform encephalopathies are neurodegenerative di...
AbstractTransmissible spongiform encephalopathies are neurodegenerative diseases characterized by th...
It has been shown recently that the generation of an abnormal transmembrane form of the prio...
This thesis focuses on peptides derived from the Prion, Doppel and Influenza haemagglutinin proteins...
The Cellular Prion Protein (PrPC), discovered by Nobel Laureate Dr. Stanley Prusiner, represents the...
International audienceSoluble oligomers of prion proteins (PrP), produced during amyloid aggregation...
Prions are an unconventional form of infectious agents composed only of protein and involved in tran...
SIGLEAvailable from British Library Document Supply Centre- DSC:DXN054653 / BLDSC - British Library ...
A key molecular event in prion diseases is the conversion of the normal cellular form of the prion p...
A synthetic peptide corresponding to the 106-126 amyloidogenic region of the cellular human prion pr...