Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate - Wikidata - awgldk - TriplyDB

Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

http://www.wikidata.org/entity/Q28473442

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Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease Molecular, biochemical and genetic characteristics of BSE in Canada Preclinical deposition of pathological prion protein in muscle of experimentally infected primates Human prion diseases in the United States.No H- and L-type cases in Belgium in cattle diagnosed with bovine spongiform encephalopathy (1999-2008) aging seven years and older.Agent-specific Shadoo responses in transmissible encephalopathies.Can mortality data provide reliable indicators for Creutzfeldt-Jakob disease surveillance? A study in France from 2000 to 2008.Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathy.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.Molecular modeling of prion transmission to humans Evaluation of the zoonotic potential of transmissible mink encephalopathy.Mother to offspring transmission of chronic wasting disease in reeves' muntjac deer.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).Squirrel monkeys (Saimiri sciureus) infected with the agent of bovine spongiform encephalopathy develop tau pathology Transmission of scrapie prions to primate after an extended silent incubation period.Oral transmission of L-type bovine spongiform encephalopathy in primate model.Could immunomodulation be used to prevent prion diseases?Accumulation of L-type bovine prions in peripheral nerve tissues A new mechanism for transmissible prion diseases EU-approved rapid tests for bovine spongiform encephalopathy detect atypical forms: a study for their sensitivities Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay.Differentiation of prions from L-type BSE versus sporadic Creutzfeldt-Jakob disease Asynchronous onset of clinical disease in BSE-infected macaques.Prion diseases as transmissible zoonotic diseases.Atypical and classical forms of the disease-associated state of the prion protein exhibit distinct neuronal tropism, deposition patterns, and lesion profiles.Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice Molecular barriers to zoonotic transmission of prions.Therapy for prion diseases: Insights from the use of RNA interference.Atypical transmissible spongiform encephalopathies in ruminants: a challenge for disease surveillance and control.Biochemical and strain properties of CJD prions: complexity versus simplicity.Creutzfeldt-Jakob disease cluster in the health area of Meixoeiro Hospital.6th International Conference on Emerging Zoonoses.Species-barrier phenomenon in prion transmissibility from a viewpoint of protein science.Molecular diagnosis of human prion disease.Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches.Evaluation of the protection of primates transfused with variant Creutzfeldt-Jakob disease-infected blood products filtered with prion removal devices: a 5-year update.Mathematical Models for Estimating the Risks of Bovine Spongiform Encephalopathy (BSE).

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

http://www.wikidata.org/entity/Q28473442

description

2008 nî lūn-bûn

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2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի օգոստոսին 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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name

Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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prefLabel

Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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JOURNAL.PONE.0003017

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Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate

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Corinne I Lasmézas

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Dominique Marcé

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Emmanuel E Comoy

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Frédéric Auvré

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Jean-Philippe Deslys

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Maria Caramelli

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Marie-Magdeleine Ruchoux

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Nathalie Lescoutra-Etchegaray

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Nicole Salès

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Paul Brown

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P2860

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

Kuru in the 21st century--an acquired human prion disease with very long incubation periods.

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

PrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob disease.

Distinct molecular phenotypes in bovine prion diseases

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

Sporadic and familial CJD: classification and characterisation.

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

Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-- Jakob disease: implications for human health

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

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8

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Gianluigi Zanusso

Salvatore Monaco

Philippe Leboulch

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2008-08-20T00:00:00Z

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23181618

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