Transgenic mice expressing porcine prion protein resistant to classical scrapie but susceptible to sheep bovine spongiform encephalopathy and atypical scrapie - Wikidata - wikimedia - TriplyDB

Transgenic mice expressing porcine prion protein resistant to classical scrapie but susceptible to sheep bovine spongiform encephalopathy and atypical scrapie

Transgenic mice expressing porcine prion protein resistant to classical scrapie but susceptible to sheep bovine spongiform encephalopathy and atypical scrapie

http://www.wikidata.org/entity/Q33628616

about

Dynamics of the natural transmission of bovine spongiform encephalopathy within an intensively managed sheep flock Phenotype shift from atypical scrapie to CH1641 following experimental transmission in sheep Transgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion Isolates Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy Elements modulating the prion species barrier and its passage consequences Porcine prion protein amyloid Preclinical detection of variant CJD and BSE prions in blood.Surveillance and simulation of bovine spongiform encephalopathy and scrapie in small ruminants in Switzerland Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain Prion replication without host adaptation during interspecies transmissions.Atypical/Nor98 scrapie in the Basque Country: a case report of eight outbreaks Atypical/Nor98 scrapie infectivity in sheep peripheral tissues.Increased susceptibility of transgenic mice expressing human PrP to experimental sheep bovine spongiform encephalopathy is not due to increased agent titre in sheep brain tissue.Increased susceptibility of human-PrP transgenic mice to bovine spongiform encephalopathy infection following passage in sheep.Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice Does the Presence of Scrapie Affect the Ability of Current Statutory Discriminatory Tests To Detect the Presence of Bovine Spongiform Encephalopathy?Mouse-adapted scrapie strains 139A and ME7 overcome species barrier to induce experimental scrapie in hamsters and changed their pathogenic features.Minimum Effective Dose of Cattle and Sheep BSE for Oral Sheep Infection.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.Naturally prion resistant mammals: a utopia?Transmission of sheep-bovine spongiform encephalopathy to pigs.Enhanced virulence of sheep-passaged bovine spongiform encephalopathy agent is revealed by decreased polymorphism barriers in prion protein conversion studies.Atypical transmissible spongiform encephalopathies in ruminants: a challenge for disease surveillance and control.Disruption of glycosylation enhances ubiquitin-mediated proteasomal degradation of Shadoo in Scrapie-infected rodents and cultured cells.Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.L-BSE experimentally transmitted to sheep presents as a unique disease phenotype.Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.Experimental oral transmission of atypical scrapie to sheep.Distinct molecular signature of bovine spongiform encephalopathy prion in pigs.Scientific Opinion on BSE/TSE infectivity in small ruminant tissues Joint Scientific Opinion on any possible epidemiological or molecular association between TSEs in animals and humans Chronic wasting disease (CWD) in cervids Evidence for zoonotic potential of ovine scrapie prions.Detection of PrPres in peripheral tissue in pigs with clinical disease induced by intracerebral challenge with sheep-passaged bovine spongiform encephalopathy agent

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P2860

Transgenic mice expressing porcine prion protein resistant to classical scrapie but susceptible to sheep bovine spongiform encephalopathy and atypical scrapie

http://www.wikidata.org/entity/Q33628616

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Transgenic mice expressing por ...... halopathy and atypical scrapie

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Transgenic mice expressing por ...... halopathy and atypical scrapie

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type

label

Transgenic mice expressing por ...... halopathy and atypical scrapie

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Transgenic mice expressing por ...... halopathy and atypical scrapie

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prefLabel

Transgenic mice expressing por ...... halopathy and atypical scrapie

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Transgenic mice expressing por ...... halopathy and atypical scrapie

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P1433

Emerging Infectious Diseases

P1476

Transgenic mice expressing por ...... halopathy and atypical scrapie

@en

P2093

Caroline Lacroux

http://www.w3.org/2001/XMLSchema#string

Danielle Padilla

http://www.w3.org/2001/XMLSchema#string

Hervé Cassard

http://www.w3.org/2001/XMLSchema#string

Isabelle Lantier

http://www.w3.org/2001/XMLSchema#string

Joaquin Castilla

http://www.w3.org/2001/XMLSchema#string

Juan Carlos Espinosa

http://www.w3.org/2001/XMLSchema#string

Juan Maria Torres

http://www.w3.org/2001/XMLSchema#string

María Eugenia Herva

http://www.w3.org/2001/XMLSchema#string

Olivier Andréoletti

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P2860

Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UK.

Classic scrapie in sheep with the ARR/ARR prion genotype in Germany and France.

A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes.

The epidemiology of scrapie.

Cases of scrapie with unusual features in Norway and designation of a new type, Nor98.

TSE strain variation.

A new variant of Creutzfeldt-Jakob disease: neuropathological and clinical features.

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease.

Molecular behaviors of "CH1641-like" sheep scrapie isolates in ovine transgenic mice (TgOvPrP4).

Propagation of prion strains through specific conformers of the prion protein

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1214-1221

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scholarly article

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10.3201/EID1508.081218

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P433

8

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P478

15

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P577

2009-08-01T00:00:00Z

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P5875

26809608

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P698

19751582

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P921

Prion protein family

P932

2815954

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