Transmission and adaptation of chronic wasting disease to hamsters and transgenic mice: evidence for strains. - Wikidata - wikimedia - TriplyDB

Transmission and adaptation of chronic wasting disease to hamsters and transgenic mice: evidence for strains.

Transmission and adaptation of chronic wasting disease to hamsters and transgenic mice: evidence for strains.

http://www.wikidata.org/entity/Q35785409

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Chronic wasting disease prions in elk antler velvet Transmission of chronic wasting disease identifies a prion strain causing cachexia and heart infection in hamsters Transgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion Isolates Evidence that bank vole PrP is a universal acceptor for prions Presence and seeding activity of pathological prion protein (PrP(TSE)) in skeletal muscles of white-tailed deer infected with chronic wasting disease Human prion protein sequence elements impede cross-species chronic wasting disease transmission.Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases.Chronic wasting disease (CWD) susceptibility of several North American rodents that are sympatric with cervid CWD epidemics Susceptibilities of nonhuman primates to chronic wasting disease.Coinfecting prion strains compete for a limiting cellular resource.Prion strain mutation determined by prion protein conformational compatibility and primary structure.A molecular switch controls interspecies prion disease transmission in mice.First case of chronic wasting disease in Europe in a Norwegian free-ranging reindeer Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein.Rapid antemortem detection of CWD prions in deer saliva.Detection of chronic wasting disease in the lymph nodes of free-ranging cervids by real-time quaking-induced conversion.Alteration of the chronic wasting disease species barrier by in vitro prion amplification.In vivo comparison of chronic wasting disease infectivity from deer with variation at prion protein residue 96.Mouse-adapted scrapie strains 139A and ME7 overcome species barrier to induce experimental scrapie in hamsters and changed their pathogenic features.Host Determinants of Prion Strain Diversity Independent of Prion Protein Genotype.Polymorphisms and variants in the prion protein sequence of European moose (Alces alces), reindeer (Rangifer tarandus), roe deer (Capreolus capreolus) and fallow deer (Dama dama) in Scandinavia.Pathological characterization of TgElk mice injected with brain homogenate from elk with chronic wasting disease.Detection and control of prion diseases in food animals.Mucosal transmission and pathogenesis of chronic wasting disease in ferrets.Prions in the environment: occurrence, fate and mitigation Infectious prions accumulate to high levels in non proliferative C2C12 myotubes.Prion transmission prevented by modifying the β2-α2 loop structure of host PrPC Nucleic acid-free mutation of prion strains.Chronic wasting disease: fingerprinting the culprit in risk assessments.The role of genetics in chronic wasting disease of North American cervids.Methods for Differentiating Prion Types in Food-Producing Animals.Cross-species transmission of CWD prions.PrioNet Canada: a network of centres of excellence for research on prion diseases--ongoing and future research directions.Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.Chronic Wasting Disease Prion Strain Emergence and Host Range Expansion.Evidence for distinct chronic wasting disease (CWD) strains in experimental CWD in ferrets.Joint Scientific Opinion on any possible epidemiological or molecular association between TSEs in animals and humans Chronic wasting disease (CWD) in cervids Estimating chronic wasting disease susceptibility in cervids using real-time quaking-induced conversion.Lack of Transmission of Chronic Wasting Disease to Cynomolgus Macaques.

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P2860

Transmission and adaptation of chronic wasting disease to hamsters and transgenic mice: evidence for strains.

http://www.wikidata.org/entity/Q35785409

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Andrew G Hughson

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Cynthia Favara

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Donald Gardner

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Elizabeth S Williams

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Gregory J Raymond

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Kimberly D Meade-White

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Lynne D Raymond

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Michael W Miller

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Richard E Race

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P2860

Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

Entry versus blockade of brain infection following oral or intraperitoneal scrapie administration: role of prion protein expression in peripheral nerves and spleen.

Comparison of abnormal prion protein glycoform patterns from transmissible spongiform encephalopathy agent-infected deer, elk, sheep, and cattle

Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

Transmission of elk and deer prions to transgenic mice

Differences in scrapie-induced pathology of the retina and brain in transgenic mice that express hamster prion protein in neurons, astrocytes, or multiple cell types

Prion protein and the molecular features of transmissible spongiform encephalopathy agents.

Chronic wasting disease of cervids.

Spongiform encephalopathies in Cervidae.

N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state.

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4305-4314

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10.1128/JVI.02474-06

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