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© 1992 Nature Publishing Group
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Relationship of protease-resistant protein, scrapie-associated fibrils and tubulofilamentous particles to the agent of spongiform encephalopathies.
Spongiform encephalopathies. The prion's progress.
The transmissible spongiform encephalopathies of livestock.
Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation.
Progress on low susceptibility mechanisms of transmissible spongiform encephalopathies.
Controlling scrapie and bovine spongiform encephalopathy in goats.
Recently described scrapie-like encephalopathies of animals: case definitions.
The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome.
Public health issues related to animal and human spongiform encephalopathies: memorandum from a WHO meeting.
Sedimentation properties of the scrapie agent.
The search for scrapie agent nucleic acid.
Transgenic Rabbits Expressing Ovine PrP Are Susceptible to Scrapie.
Potent inhibition of scrapie-associated PrP accumulation by congo red.
From slow virus to prion: a review of transmissible spongiform encephalopathies.
Assessment of western immunoblotting for the confirmatory diagnosis of ovine scrapie and bovine spongiform encephalopathy (BSE).
In vitro amplification of scrapie and chronic wasting disease PrP(res) using baculovirus-expressed recombinant PrP as substrate.
Properties of the scrapie agent-endomembrane complex from hamster brain.
Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy.
Resistance of the ME7 scrapie agent to peracetic acid.
Could intracrine biology play a role in the pathogenesis of transmissable spongiform encephalopathies, Alzheimer's disease and other neurodegenerative diseases?
Scrapie in vitro: agent replication and reduced cell yield.
Detection of water-soluble disease-associated PrP species in blood and brain of scrapie-infected hamster.
N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state.
Transmissable spongiform encephalopathy (TSE) agents as crystalline forms of the prion protein (PrP) that multiply by allowing normal metabolic forms of PrP to join the crystal.
Spongiform encephalopathies. PrP and the scrapie agent.
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Relationship of protease-resistant protein, scrapie-associated fibrils and tubulofilamentous particles to the agent of spongiform encephalopathies.
Spongiform encephalopathies. The prion's progress.
The transmissible spongiform encephalopathies of livestock.
Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation.
Progress on low susceptibility mechanisms of transmissible spongiform encephalopathies.
Controlling scrapie and bovine spongiform encephalopathy in goats.
Recently described scrapie-like encephalopathies of animals: case definitions.
The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome.
Public health issues related to animal and human spongiform encephalopathies: memorandum from a WHO meeting.
Sedimentation properties of the scrapie agent.
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