Diagnosis of transmissible spongiform encephalopathies in animals: a review. - Wikidata - awgldk - TriplyDB

Diagnosis of transmissible spongiform encephalopathies in animals: a review.

Diagnosis of transmissible spongiform encephalopathies in animals: a review.

http://www.wikidata.org/entity/Q36395418

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Molecular, biochemical and genetic characteristics of BSE in Canada Prion protein gene variability in Spanish goats. Inference through susceptibility to classical scrapie strains and pathogenic distribution of peripheral PrP(sc.)The Priority position paper: Protecting Europe's food chain from prions Review: A review on classical and atypical scrapie in caprine: Prion protein gene polymorphisms and their role in the disease.Clinical findings in two cases of atypical scrapie in sheep: a case report.Surveillance and simulation of bovine spongiform encephalopathy and scrapie in small ruminants in Switzerland Relationship between clinical signs and postmortem test status in cattle experimentally infected with the bovine spongiform encephalopathy agent The expanding universe of prion diseases.No temporal trends in the prevalence of atypical scrapie in British sheep, 2002-2006 Experimental oral transmission of chronic wasting disease to red deer (Cervus elaphus elaphus): early detection and late stage distribution of protease-resistant prion protein.Archival search for historical atypical scrapie in sheep reveals evidence for mixed infections.Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathy Time and frequency domain analysis of heart rate variability in cattle affected by bovine spongiform encephalopathy.Genotyping and surveillance for scrapie in Finnish sheep Susceptibility of European red deer (Cervus elaphus elaphus) to alimentary challenge with bovine spongiform encephalopathy.A comparative study of modified confirmatory techniques and additional immuno-based methods for non-conclusive autolytic bovine spongiform encephalopathy cases Molecular typing of protease-resistant prion protein in transmissible spongiform encephalopathies of small ruminants, France, 2002-2009 Early and Non-Invasive Detection of Chronic Wasting Disease Prions in Elk Feces by Real-Time Quaking Induced Conversion.Experimental transmission of bovine spongiform encephalopathy to European red deer (Cervus elaphus elaphus).Prion diseases as transmissible zoonotic diseases.Infectivity-associated PrP(Sc) and disease duration-associated PrP(Sc) of mouse BSE prions.Biochemical typing of pathological prion protein in aging cattle with BSE.The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease.Methods for Differentiating Prion Types in Food-Producing Animals.Discontools: Identifying gaps in controlling bovine spongiform encephalopathy.Evaluation of removal of prion infectivity from red blood cells with prion reduction filters using a new rapid and highly sensitive cell culture-based infectivity assay.Investigation of the effects of experimental autolysis on the detection of abnormal prion protein in lymphoid and central nervous system tissues from elk and sheep using the Western blotting method.Transcriptional changes in the brains of cattle orally infected with the bovine spongiform encephalopathy agent precede detection of infectivity.Disease characteristics of bovine spongiform encephalopathy following inoculation into mice via three different routes.Sensitive, preclinical detection of prions in brain by nanospray liquid chromatography/tandem mass spectrometry.High-resolution differentiation of transmissible spongiform encephalopathy strains by quantitative N-terminal amino acid profiling (N-TAAP) of PK-digested abnormal prion protein.PRNP variants in goats reduce sensitivity of detection of PrP(Sc) by immunoassay.Experimental transmission of chronic wasting disease (CWD) of elk (Cervus elaphus nelsoni), white-tailed deer (Odocoileus virginianus), and mule deer (Odocoileus hemionus hemionus) to white-tailed deer by intracerebral route.Modelling BSE trend over time in Europe, a risk assessment perspective

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P2860

Diagnosis of transmissible spongiform encephalopathies in animals: a review.

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2005 nî lūn-bûn

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Journal of Veterinary Diagnostic Investigation

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Diagnosis of transmissible spongiform encephalopathies in animals: a review.

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Aru Balachandran

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Dolores Gavier-Widén

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Marion Simmons

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Michael J Stack

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Thierry Baron

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P2860

Novel proteinaceous infectious particles cause scrapie

Eight prion strains have PrP(Sc) molecules with different conformations

Inactivation of transmissible degenerative encephalopathy agents: A review.

Clinical signs, histopathology and genetics of experimental transmission of BSE and natural scrapie to sheep and goats.

A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseases.

Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding.

Distinct molecular phenotypes in bovine prion diseases

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

Epidemiological observations on spongiform encephalopathies in captive wild animals in the British Isles.

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