. However, protease treatment cannot be used to isolate abnormal forms of PrP lacking conventional protease resistance, such as those found in several genetic and atypical sporadic cases. in a protein misfolding cyclic amplification reaction, and mutant PrP aggregates from transgenic mice were toxic to cultured neurons.The immunopurification protocol described here isolates biologically active forms of aggregated PrP. These preparations may be useful for investigating the structural and chemico-physical properties of infectious and neurotoxic PrP aggregates
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prion pathologies are a group of fatal neurodegenerative disorders that afflict mammalian species. I...
. However, protease treatment cannot be used to isolate abnormal forms of PrP lacking conventional p...
Background: Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gen...
BACKGROUND:Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gene...
Background: Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gen...
Background: Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gen...
The conversion of the cellular form of the prion protein (PrPC) to an abnormal, alternatively folded...
Prion diseases are characterized by deposits of abnormal conformers of the PrP protein. Although lar...
Prions arise when the cellular prion protein (PrP(C)) undergoes a self-propagating conformational ch...
<div><p>Prions are infectious proteins that possess multiple self-propagating structures. The inform...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prions arise when the cellular prion protein (PrP(C)) undergoes a self-propagating conformational ch...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prion pathologies are a group of fatal neurodegenerative disorders that afflict mammalian species. I...
. However, protease treatment cannot be used to isolate abnormal forms of PrP lacking conventional p...
Background: Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gen...
BACKGROUND:Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gene...
Background: Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gen...
Background: Prion diseases are fatal neurodegenerative disorders that can arise sporadically, be gen...
The conversion of the cellular form of the prion protein (PrPC) to an abnormal, alternatively folded...
Prion diseases are characterized by deposits of abnormal conformers of the PrP protein. Although lar...
Prions arise when the cellular prion protein (PrP(C)) undergoes a self-propagating conformational ch...
<div><p>Prions are infectious proteins that possess multiple self-propagating structures. The inform...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prions arise when the cellular prion protein (PrP(C)) undergoes a self-propagating conformational ch...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prion pathologies are a group of fatal neurodegenerative disorders that afflict mammalian species. I...