Add to ORKGSIGLEAvailable from British Library Document Supply Centre- DSC:DXN054653 / BLDSC - British Library Document Supply CentreGBUnited Kingdo
International audienceThe pathological conversion of cellular prion protein (PrP(C)) into the scrapi...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN027638 / BLDSC - British Library D...
A key molecular event in prion diseases is the conversion of the prion protein (PrP) from its normal...
The binding of the Syrian hamster prion protein, SHaPrP(90-231), to model lipid membranes was invest...
The key molecular event underlying prion diseases is the conversion of the monomeric and alpha-helic...
A key molecular event in prion diseases is the conversion of the normal cellular form of the prion p...
A key molecular event in prion diseases is the conversion of PrP (prion protein) from its normal cel...
The conversion of prion protein (PrP) to the pathogenic PrPSc conformation is central to prion disea...
AbstractThe key molecular event underlying prion diseases is the conversion of the monomeric and α-h...
Prion diseases are characterised by the conversion of the normal a-helical prion protein (PrPc), to ...
Prion diseases are a group of fatal neurodegenerative disorders that include Creutzfeldt-Jakob Disea...
The prion protein (PrP) is an endogenous metal binding protein present in the neuronal cells of the ...
Conversion of PrP(C) into PrP(Sc) is the central event in the pathogenesis of transmissible prion di...
Prion diseases are fatal neurodegenerative disorders characterized by the accumulation in the brain ...
Recent studies introduced two experimental protocols for converting full-length recombinant prion pr...
International audienceThe pathological conversion of cellular prion protein (PrP(C)) into the scrapi...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN027638 / BLDSC - British Library D...
A key molecular event in prion diseases is the conversion of the prion protein (PrP) from its normal...
The binding of the Syrian hamster prion protein, SHaPrP(90-231), to model lipid membranes was invest...
The key molecular event underlying prion diseases is the conversion of the monomeric and alpha-helic...
A key molecular event in prion diseases is the conversion of the normal cellular form of the prion p...
A key molecular event in prion diseases is the conversion of PrP (prion protein) from its normal cel...
The conversion of prion protein (PrP) to the pathogenic PrPSc conformation is central to prion disea...
AbstractThe key molecular event underlying prion diseases is the conversion of the monomeric and α-h...
Prion diseases are characterised by the conversion of the normal a-helical prion protein (PrPc), to ...
Prion diseases are a group of fatal neurodegenerative disorders that include Creutzfeldt-Jakob Disea...
The prion protein (PrP) is an endogenous metal binding protein present in the neuronal cells of the ...
Conversion of PrP(C) into PrP(Sc) is the central event in the pathogenesis of transmissible prion di...
Prion diseases are fatal neurodegenerative disorders characterized by the accumulation in the brain ...
Recent studies introduced two experimental protocols for converting full-length recombinant prion pr...
International audienceThe pathological conversion of cellular prion protein (PrP(C)) into the scrapi...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN027638 / BLDSC - British Library D...
A key molecular event in prion diseases is the conversion of the prion protein (PrP) from its normal...