Pages that link to "Q36200377"
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The following pages link to Attempts to restore scrapie prion infectivity after exposure to protein denaturants (Q36200377):
Displaying 50 items.
- Transmission of prions (Q24540228) (← links)
- Prions (Q24633319) (← links)
- Elimination of prions by branched polyamines and implications for therapeutics (Q24646752) (← links)
- The strain-encoded relationship between PrP replication, stability and processing in neurons is predictive of the incubation period of disease (Q27312083) (← links)
- PK-sensitive PrP is infectious and shares basic structural features with PK-resistant PrP (Q27347266) (← links)
- Strain-specified relative conformational stability of the scrapie prion protein (Q28361583) (← links)
- Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform (Q33761104) (← links)
- Prion protein interconversions and the transmissible spongiform encephalopathies (Q33764321) (← links)
- Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoform (Q33847297) (← links)
- Quantitative detection and biological propagation of scrapie seeding activity in vitro facilitate use of prions as model pathogens for disinfection (Q33925227) (← links)
- The role of dimerization in prion replication (Q34177517) (← links)
- Inactivation of prions by acidic sodium dodecyl sulfate (Q34232938) (← links)
- Viral particles are required for infection in neurodegenerative Creutzfeldt-Jakob disease. (Q34291443) (← links)
- Non-equilibrium proteins (Q34311409) (← links)
- Structural clues to prion replication (Q34322278) (← links)
- Prion protein interactions with nucleic acid: possible models for prion disease and prion function (Q35115973) (← links)
- Structure and polymorphism of the mouse prion protein gene (Q35573850) (← links)
- Mimicking dominant negative inhibition of prion replication through structure-based drug design (Q35759964) (← links)
- Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity (Q35856829) (← links)
- Using small molecule reagents to selectively modify epitopes based on their conformation. (Q36005166) (← links)
- Thermal stability and conformational transitions of scrapie amyloid (prion) protein correlate with infectivity (Q36277843) (← links)
- Sporadic Creutzfeldt-Jakob disease subtype-specific alterations of the brain proteome: impact on Rab3a recycling (Q36590404) (← links)
- Copper and the prion protein: methods, structures, function, and disease (Q36640347) (← links)
- Novel aspects of prions, their receptor molecules, and innovative approaches for TSE therapy (Q36676179) (← links)
- Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus (Q37693769) (← links)
- The role of RNA in mammalian prion protein conversion (Q37957794) (← links)
- Proteinase K and the structure of PrPSc: The good, the bad and the ugly (Q38393679) (← links)
- Rapid chemical decontamination of infectious CJD and scrapie particles parallels treatments known to disrupt microbes and biofilms (Q38820338) (← links)
- Detection of bovine spongiform encephalopathy-specific PrP(Sc) by treatment with heat and guanidine thiocyanate (Q39596556) (← links)
- Prion Protein Isoforms, a Convergence of Biological and Structural Investigations (Q40464138) (← links)
- Transgenetics of prion diseases. (Q40975176) (← links)
- The anti-prion activity of Congo red. Putative mechanism (Q41062006) (← links)
- A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice (Q41717349) (← links)
- Infectivity of scrapie prions (Q43010608) (← links)
- Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease (Q43057853) (← links)
- Antigenic characterization of an abnormal isoform of prion protein using a new diverse panel of monoclonal antibodies (Q44788460) (← links)
- A change in the conformation of prions accompanies the emergence of a new prion strain. (Q45939477) (← links)
- Assembly of natural and recombinant prion protein into fibrils (Q46591995) (← links)
- Scrapie prions: a three-dimensional model of an infectious fragment (Q46879245) (← links)
- Pathologic conformations of prion proteins (Q46894080) (← links)
- Dehydration of prions on environmentally relevant surfaces protects them from inactivation by freezing and thawing (Q47693858) (← links)
- Protease-resistant and detergent-insoluble prion protein is not necessarily associated with prion infectivity (Q48190062) (← links)
- Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease (Q48343268) (← links)
- Reversibility of scrapie inactivation is enhanced by copper (Q48390188) (← links)
- Photo-induced crosslinking of prion protein oligomers and prions (Q48446343) (← links)
- Persistence of Aβ seeds in APP null mouse brain. (Q52149660) (← links)
- [Natural history of human transmissible subacute spongiform encephalopathies]. (Q54222189) (← links)
- Closely similar values obtained when the ME7 strain of scrapie agent was titrated in parallel by two individuals in separate laboratories using two sublines of C57BL mice (Q73539385) (← links)
- Domain-specific Quantification of Prion Protein in Cerebrospinal Fluid by Targeted Mass Spectrometry (Q90316130) (← links)
- Cryo-EM structure of a human prion fibril with a hydrophobic, protease-resistant core (Q91875083) (← links)