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Aerosols transmit prions to immunocompetent and immunodeficient micePossible case of maternal transmission of feline spongiform encephalopathy in a captive cheetahPrion hypothesis: the end of the controversy?Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyPrionsA clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New GuineaElimination of prions by branched polyamines and implications for therapeuticsKuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceChronic wasting disease prions in elk antler velvetThe role of the cellular prion protein in the immune systemA short purification process for quantitative isolation of PrPSc from naturally occurring and experimental transmissible spongiform encephalopathies.The mechanism of prion strain propagationvCJD risk in the Republic of IrelandAnalysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.Prion diseases: immunotargets and therapyInsights into Mechanisms of Chronic NeurodegenerationGenetics of Prion Disease in CattleAssessing the causes and consequences of co-polymerization in amyloid formationProgress on low susceptibility mechanisms of transmissible spongiform encephalopathiesPRNP haplotype associated with classical BSE incidence in European Holstein cattleNMR structure of the bovine prion proteinPrion disease susceptibility is affected by -structure folding propensity and local side-chain interactions in PrPAtomic Structures Suggest Determinants of Transmission Barriers in Mammalian Prion DiseaseChanging a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers.Florid plaques in ovine PrP transgenic mice infected with an experimental ovine BSE.Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.Protein folding pathology in domestic animals.Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathyMolecular, biochemical and genetic characteristics of BSE in CanadaHistopathological studies of "CH1641-like" scrapie sources versus classical scrapie and BSE transmitted to ovine transgenic mice (TgOvPrP4)Elements modulating the prion species barrier and its passage consequencesTransmissibility of H-Type Bovine Spongiform Encephalopathy to Hamster PrP Transgenic Mice.Scrapie-infected mice and PrP knockout mice share abnormal localization and activity of neuronal nitric oxide synthaseGeneric amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prionsGenetic diversity in the prion protein gene (PRNP) of domestic cattle and water buffaloes in Vietnam, Indonesia and ThailandGenome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPImplications for Creutzfeldt-Jakob disease (CJD) in dentistry: a review of current knowledge.Human prion diseases: surgical lessons learned from iatrogenic prion transmissionInsights into Chronic Wasting Disease and Bovine Spongiform Encephalopathy Species Barriers by Use of Real-Time Conversion
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P2860
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature в жовтні 1997
@uk
name
The same prion strain causes vCJD and BSE
@en
The same prion strain causes vCJD and BSE
@nl
type
label
The same prion strain causes vCJD and BSE
@en
The same prion strain causes vCJD and BSE
@nl
prefLabel
The same prion strain causes vCJD and BSE
@en
The same prion strain causes vCJD and BSE
@nl
P2093
P356
P1433
P1476
The same prion strain causes vCJD and BSE
@en
P2093
Collinge J
Desbruslais M
P2888
P304
448-50, 526
P356
10.1038/38925
P407
P577
1997-10-01T00:00:00Z
P6179
1013318654