Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases. - Wikidata - thesis-toulmin - TriplyDB

Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases.

Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases.

http://www.wikidata.org/entity/Q33455497

about

Evidence that bank vole PrP is a universal acceptor for prions Human prion protein sequence elements impede cross-species chronic wasting disease transmission.Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain Molecular Mechanisms of Chronic Wasting Disease Prion Propagation.Biochemical characterization of prion strains in bank voles Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.PrPC Governs Susceptibility to Prion Strains in Bank Vole, While Other Host Factors Modulate Strain Features.Mouse models for studying the formation and propagation of prions.Infectious particles, stress, and induced prion amyloids: a unifying perspective.Experimental infection of meadow voles (Microtus pennsylvanicus) with sheep scrapie Correlation between infectivity and disease associated prion protein in the nervous system and selected edible tissues of naturally affected scrapie sheep.Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.Prion disease tempo determined by host-dependent substrate reduction.Strain Typing of Prion Diseases Using In Vivo Mouse Models.Methods for Differentiating Prion Types in Food-Producing Animals.Cross-species transmission of CWD prions.Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers.Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy.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 behaviors Asparagine and glutamine ladders promote cross-species prion conversion.Shedding light on prion disease.Chronic wasting disease (CWD) in cervids Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.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.Detection of amyloid fibrils in Parkinson's disease using plasmonic chirality.Prion Disease in Dromedary Camels, Algeria.Prion replication environment defines the fate of prion strain adaptation.

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P2860

Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases.

http://www.wikidata.org/entity/Q33455497

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2013 nî lūn-bûn

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2013 թուականի Մարտին հրատարակուած գիտական յօդուած

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2013 թվականի մարտին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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Chronic wasting disease in ban ...... time model for prion diseases.

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Chronic wasting disease in ban ...... time model for prion diseases.

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Geraldina Riccardi

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Jan Langeveld

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Joaquín Castilla

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Juergen Richt

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Michela Conte

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Michele Angelo Di Bari

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Robert Kunkle

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Umberto Agrimi

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P2860

Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.

A general model of prion strains and their pathogenicity

Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

Ultra-efficient PrP(Sc) amplification highlights potentialities and pitfalls of PMCA technology

Prion protein amino acid determinants of differential susceptibility and molecular feature of prion strains in mice and voles

Accelerated high fidelity prion amplification within and across prion species barriers.

Identification of the pathological prion protein allotypes in scrapie-infected heterozygous bank voles (Clethrionomys glareolus) by high-performance liquid chromatography-mass spectrometry.

Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivo.

Quantitative profiling of the pathological prion protein allotypes in bank voles by liquid chromatography-mass spectrometry.

The bank vole (Myodes glareolus) as a sensitive bioassay for sheep scrapie.

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Gabriele Vaccari

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2013-03-07T00:00:00Z

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236021119

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Prion protein family

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