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© 1991 Nature Publishing Group
© 1991 Nature Publishing Group
© 1991 Nature Publishing Group
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Progress on low susceptibility mechanisms of transmissible spongiform encephalopathies.
Spongiform encephalopathies. PrP and the scrapie agent.
The transmissible spongiform encephalopathies of livestock.
The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome.
From slow virus to prion: a review of transmissible spongiform encephalopathies.
Public health issues related to animal and human spongiform encephalopathies: memorandum from a WHO meeting.
Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy.
Could intracrine biology play a role in the pathogenesis of transmissable spongiform encephalopathies, Alzheimer's disease and other neurodegenerative diseases?
Relationship of protease-resistant protein, scrapie-associated fibrils and tubulofilamentous particles to the agent of spongiform encephalopathies.
Abnormalities in Brainstem Auditory Evoked Potentials in Sheep with Transmissible Spongiform Encephalopathies and Lack of a Clear Pathological Relationship.
Protecting effect of PrP codons M142 and K222 in goats orally challenged with bovine spongiform encephalopathy prions.
Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.
Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potential.
Autoimmune encephalopathies.
The age-dependent epileptic encephalopathies.
Paraneoplastic and autoimmune encephalopathies.
Subcritical Water Hydrolysis Effectively Reduces the In Vitro Seeding Activity of PrPSc but Fails to Inactivate the Infectivity of Bovine Spongiform Encephalopathy Prions.
Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay.
Bovine spongiform encephalopathy.
Toxic and metabolic encephalopathies: iconographic essay.
Delusional bovine spongiform encephalopathy.
Bovine spongiform encephalopathy.
Prions and prion proteins.
Bovine spongiform encephalopathy.
Spongiform encephalopathies. The prion's progress.
© 1991 Nature Publishing Group © 1991 Nature Publishing Group © 1991 Nature Publishing Group...
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Recommend Documents
Progress on low susceptibility mechanisms of transmissible spongiform encephalopathies.
Spongiform encephalopathies. PrP and the scrapie agent.
The transmissible spongiform encephalopathies of livestock.
The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome.
From slow virus to prion: a review of transmissible spongiform encephalopathies.
Public health issues related to animal and human spongiform encephalopathies: memorandum from a WHO meeting.
Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy.
Could intracrine biology play a role in the pathogenesis of transmissable spongiform encephalopathies, Alzheimer's disease and other neurodegenerative diseases?
Relationship of protease-resistant protein, scrapie-associated fibrils and tubulofilamentous particles to the agent of spongiform encephalopathies.
Abnormalities in Brainstem Auditory Evoked Potentials in Sheep with Transmissible Spongiform Encephalopathies and Lack of a Clear Pathological Relationship.
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