Evidence that bank vole PrP is a universal acceptor for prions
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Changes in retinal function and morphology are early clinical signs of disease in cattle with bovine spongiform encephalopathyHuman prion protein sequence elements impede cross-species chronic wasting disease transmission.Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial InsomniaPrion replication without host adaptation during interspecies transmissions.Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion StrainsGerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.Bank voles accrue scientific interest.PrPC Governs Susceptibility to Prion Strains in Bank Vole, While Other Host Factors Modulate Strain Features.Secondary-structure prediction revisited: Theoretical β-sheet propensity and coil propensity represent structures of amyloids and aid in elucidating phenomena involved in interspecies transmission of prions.Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutationGuinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.Prion disease: experimental models and reality.G-quadruplexes within prion mRNA: the missing link in prion disease?Cross-species transmission of CWD prions.Experimental Models of Inherited PrP Prion Diseases.Goat K222-PrP(C) polymorphic variant does not provide resistance to atypical scrapie in transgenic mice.Towards authentic transgenic mouse models of heritable PrP prion diseases.Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.Soluble polymorphic bank vole prion proteins induced by co-expression of quiescin sulfhydryl oxidase in E. coli and their aggregation behaviorsAsparagine and glutamine ladders promote cross-species prion conversion.Shedding light on prion disease.Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner.Prion Strains and Transmission Barrier Phenomena.A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles.Sub-ångström cryo-EM structure of a prion protofibril reveals a polar clasp.Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties.Seeding and Cross-seeding Fibrillation of N-terminal Prion Protein Peptides PrP(120-144).Detection of amyloid fibrils in Parkinson's disease using plasmonic chirality.Evolutionary biology and the risk of scrapie disease in sheep
P2860
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P2860
Evidence that bank vole PrP is a universal acceptor for prions
description
2014 nî lūn-bûn
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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2014 թվականի ապրիլին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
@zh-hk
2014年論文
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2014年論文
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2014年论文
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name
Evidence that bank vole PrP is a universal acceptor for prions
@ast
Evidence that bank vole PrP is a universal acceptor for prions
@en
Evidence that bank vole PrP is a universal acceptor for prions
@nl
type
label
Evidence that bank vole PrP is a universal acceptor for prions
@ast
Evidence that bank vole PrP is a universal acceptor for prions
@en
Evidence that bank vole PrP is a universal acceptor for prions
@nl
prefLabel
Evidence that bank vole PrP is a universal acceptor for prions
@ast
Evidence that bank vole PrP is a universal acceptor for prions
@en
Evidence that bank vole PrP is a universal acceptor for prions
@nl
P2860
P50
P3181
P1433
P1476
Evidence that bank vole PrP is a universal acceptor for prions
@en
P2093
Joel C Watts
Smita Patel
P2860
P304
P3181
P356
10.1371/JOURNAL.PPAT.1003990
P407
P577
2014-04-01T00:00:00Z