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Functional mechanisms of the cellular prion protein (PrPC) associated anti-HI...
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The protein side of the Central Dogma: Permanence and change
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Mechanism of spreading of prion and polyglutamine aggregates and role of the ...
The pathogenesis of most neurodegenerative diseases, including transmissible diseases like prion encephalopathies, inherited disorders like Huntington’s disease, and... -
Alzheimer's disease: analysis of a mathematical model incorporating the role ...
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Alpha-synuclein molecular pathology : potential relationship with prion diseases
The overlap of neurotoxic mecanisms involved in prion diseases and synucleinopathies, and the concomitant detection of pathological forms of prion and α-synuclein in a... -
Rodent models for prion diseases
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A prion disease of cervids: Chronic wasting disease
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Prion agent diversity and species barrier
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TSE pathogenesis in cattle and sheep
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Physiological role of the cellular prion protein
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Cellular pathogenesis in prion diseases
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Degradation of scrapie associated prion protein (PrP$^{Sc}$) by the gastroint...
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Faecal shedding, alimentary clearance and intestinal spread of prions in hams...
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Distinct spatial activation of intrinsic and extrinsic apoptosis pathways in ...
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PrP assemblies: spotting the responsible regions in prion propagation.
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Decrypting Prion Protein Conversion into a β-Rich Conformer by Molecular Dyna...
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Binding of methylene blue to a surface cleft inhibits the oligomerization and...
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The oligomerization properties of prion protein are restricted to the H2H3 do...
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Ploidy controls [URE3] prion propagation in yeast.
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Study of the transmission of bovine spongiform encephalopathy agent to sheep
To characterise in sheep the bovine spongiform encephalopathy agent (BSE) responsible for variant Creutzfeldt-Jakob disease in human beings, three ewes, presenting...
