Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.
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Branched polyamines cure prion-infected neuroblastoma cellsChronic wasting disease and potential transmission to humansSpecific genetic modifications of domestic animals by gene targeting and animal cloningThe Potential for Microalgae as Bioreactors to Produce PharmaceuticalsAll clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJDEvidence that bank vole PrP is a universal acceptor for prionsNMR structure of the bovine prion proteinChanging 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.Protein folding pathology in domestic animals.Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathyCorrelation analysis for the incubation period of prion diseaseRationale for diagnosing human prion disease.Potent inhibition of scrapie prion replication in cultured cells by bis-acridines.Population-level retrospective study of neurologically expressed disorders in ruminants before the onset of bovine spongiform encephalopathy (BSE) in Belgium, a BSE risk III country.Prion replication without host adaptation during interspecies transmissions.Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002.Conversion of the BASE prion strain into the BSE strain: the origin of BSE?Resistance of bovine spongiform encephalopathy (BSE) prions to inactivationMultiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.Transmission and detection of prions in fecesTransmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein.Intraspecies prion transmission results in selection of sheep scrapie strains.Transmission barriers for bovine, ovine, and human prions in transgenic mice.Dietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.Prion and water: tight and dynamical hydration sites have a key role in structural stability.Markedly increased susceptibility to natural sheep scrapie of transgenic mice expressing ovine prp.Coinfecting prion strains compete for a limiting cellular resource.Acridine and phenothiazine derivatives as pharmacotherapeutics for prion diseaseVariant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthPrions in skeletal muscle.Detection and analysis of animal materials in food and feed.Human prion strain selection in transgenic mice.Our dwindling national blood supplyDistinct molecular phenotypes in bovine prion diseasesPrions in the urine of patients with variant Creutzfeldt-Jakob disease.Simulations of oligomeric intermediates in prion diseases.Molecular analysis of the protease-resistant prion protein in scrapie and bovine spongiform encephalopathy transmitted to ovine transgenic and wild-type mice.Conformation-dependent high-affinity monoclonal antibodies to prion proteins.Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potential
P2860
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P2860
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Compelling transgenetic eviden ...... cephalopathy prions to humans.
@en
type
label
Compelling transgenetic eviden ...... cephalopathy prions to humans.
@en
prefLabel
Compelling transgenetic eviden ...... cephalopathy prions to humans.
@en
P2093
P2860
P356
P1476
Compelling transgenetic eviden ...... cephalopathy prions to humans.
@en
P2093
P2860
P304
15137-15142
P356
10.1073/PNAS.96.26.15137
P407
P577
1999-12-01T00:00:00Z