Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes - Wikidata - awgldk - TriplyDB

Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

http://www.wikidata.org/entity/Q27318658

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Whole Blood Gene Expression Profiling in Preclinical and Clinical Cattle Infected with Atypical Bovine Spongiform Encephalopathy Transgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion Isolates Biochemical Characteristics and PrP(Sc) Distribution Pattern in the Brains of Cattle Experimentally Challenged with H-type and L-type Atypical BSE Resistance to classical scrapie in experimentally challenged goats carrying mutation K222 of the prion protein gene.Enhanced neuroinvasion by smaller, soluble prions.Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice.Evaluation of two sets of immunohistochemical and Western blot confirmatory methods in the detection of typical and atypical BSE cases.Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathy.Experimental H-type and L-type bovine spongiform encephalopathy in cattle: observation of two clinical syndromes and diagnostic challenges.Experimental interspecies transmission studies of the transmissible spongiform encephalopathies to cattle: comparison to bovine spongiform encephalopathy in cattle.Individual factors associated with L- and H-type Bovine Spongiform encephalopathy in France.The pathological and molecular but not clinical phenotypes are maintained after second passage of experimental atypical bovine spongiform encephalopathy in cattle Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits.Detection and discrimination of classical and atypical L-type bovine spongiform encephalopathy by real-time quaking-induced conversion Characterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathies Expression of genes involved in the T cell signalling pathway in circulating immune cells of cattle 24 months following oral challenge with Bovine Amyloidotic Spongiform Encephalopathy (BASE).Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice Accumulation of L-type bovine prions in peripheral nerve tissues Detergents modify proteinase K resistance of PrP Sc in different transmissible spongiform encephalopathies (TSEs).Detection of Atypical H-Type Bovine Spongiform Encephalopathy and Discrimination of Bovine Prion Strains by Real-Time Quaking-Induced Conversion.Prion diseases as transmissible zoonotic diseases.Biochemical typing of pathological prion protein in aging cattle with BSE.Ultramicroscopy reveals axonal transport impairments in cortical motor neurons at prion disease Similarities between forms of sheep scrapie and Creutzfeldt-Jakob disease are encoded by distinct prion types.Oral Transmission of L-Type Bovine Spongiform Encephalopathy Agent among Cattle.Atypical transmissible spongiform encephalopathies in ruminants: a challenge for disease surveillance and control.Discontools: Identifying gaps in controlling bovine spongiform encephalopathy.L-BSE experimentally transmitted to sheep presents as a unique disease phenotype.Experimental challenge of cattle with German atypical bovine spongiform encephalopathy (BSE) isolates.Scientific Opinion on a second update on the risk for human and animal health related to the revision of the BSE monitoring regime in some Member States Joint Scientific Opinion on any possible epidemiological or molecular association between TSEs in animals and humans Scientific Opinion on the revision of the quantitative risk assessment (QRA) of the BSE risk posed by processed animal proteins (PAPs)Scientific Opinion on a review of the BSE-related risk in bovine intestines Scientific and technical assistance on the minimum sample size to test should an annual BSE statistical testing regime be authorised in healthy slaughtered cattle Protocol for further laboratory investigations into the distribution of infectivity of Atypical BSE Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats.Experimental classical bovine spongiform encephalopathy: definition and progression of neural PrP immunolabeling in relation to diagnosis and disease controls

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

http://www.wikidata.org/entity/Q27318658

description

2008 nî lūn-bûn

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2008 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2008 թվականի մայիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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JOURNAL.PPAT.1000075

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Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

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Alessia Farinazzo

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Antonio D' Angelo

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Barbara Iulini

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Daniela Gelmetti

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Elisa Fasoli

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Ilaria Barbieri

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Maria Caramelli

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P2860

Transmission dynamics and epidemiology of BSE in British cattle

Loss of prion protein in a transgenic model of amyotrophic lateral sclerosis.

The expanding universe of prion diseases.

A major genetic component of BSE susceptibility.

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

Variant Creutzfeldt-Jakob disease.

Distinct molecular phenotypes in bovine prion diseases

A new variant of Creutzfeldt-Jakob disease in the UK.

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

Different prion disease phenotypes result from inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain.

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Gianluigi Zanusso

Salvatore Monaco

Lorenzo Capucci

Michele Fiorini

Fabrizio Tagliavini

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5351993

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