AbstractAutocatalytic changes in the conformation and aggregation state of prion protein appear to be fundamental to transmissible spongiform encephalopathies or prion diseases. Here we review the considerable progress that has been made in describing the normal properties of prion protein and the changes that occur during these devastating neurodegenerative diseases
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
Transmissible spongiform encephalopathies (TSE) are a heterogeneous group of neurodegenerative disor...
Prion diseases, or transmissible spongiform encephalopathies (TSEs) are typically characterised by C...
AbstractAutocatalytic changes in the conformation and aggregation state of prion protein appear to b...
Recent findings strongly support the hypothesis that diverse human disorders, including the most com...
Transmissible spongiform encephalopathies (TSEs) or prion diseases are unique disorders that are not...
none3noPrion diseases, also known as transmissible spongiform encephalopathies (TSEs), are a group o...
Prion diseases are a group of neurodegenerative diseases that can arise spontaneously, be inherited...
Prion diseases are a group of neurodegenerative diseases that can arise spontaneously, be inherited,...
According to the Koch postulates an infectious organism is the one that can be isolated from an host...
Protein aggregation causes malfunction in several biochemical processes. Genetic and spontaneous for...
Prions are responsible for a heterogeneous group of fatal neurodegenerative diseases, involving post...
Prion diseases are transmissible neurodegenerative disorders which affect a range of mammalian speci...
Prion diseases are neurodegenerative disorders caused by conformational conversion of the cellular p...
The cellular prion protein, PrPC, is a small, cell-surface glycoprotein with a function that is curr...
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
Transmissible spongiform encephalopathies (TSE) are a heterogeneous group of neurodegenerative disor...
Prion diseases, or transmissible spongiform encephalopathies (TSEs) are typically characterised by C...
AbstractAutocatalytic changes in the conformation and aggregation state of prion protein appear to b...
Recent findings strongly support the hypothesis that diverse human disorders, including the most com...
Transmissible spongiform encephalopathies (TSEs) or prion diseases are unique disorders that are not...
none3noPrion diseases, also known as transmissible spongiform encephalopathies (TSEs), are a group o...
Prion diseases are a group of neurodegenerative diseases that can arise spontaneously, be inherited...
Prion diseases are a group of neurodegenerative diseases that can arise spontaneously, be inherited,...
According to the Koch postulates an infectious organism is the one that can be isolated from an host...
Protein aggregation causes malfunction in several biochemical processes. Genetic and spontaneous for...
Prions are responsible for a heterogeneous group of fatal neurodegenerative diseases, involving post...
Prion diseases are transmissible neurodegenerative disorders which affect a range of mammalian speci...
Prion diseases are neurodegenerative disorders caused by conformational conversion of the cellular p...
The cellular prion protein, PrPC, is a small, cell-surface glycoprotein with a function that is curr...
Prions are proteins that acquire alternative conformations that become self-propagating. Transformat...
Transmissible spongiform encephalopathies (TSE) are a heterogeneous group of neurodegenerative disor...
Prion diseases, or transmissible spongiform encephalopathies (TSEs) are typically characterised by C...
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