Long-term subclinical carrier state precedes scrapie replication and adaptation in a resistant species: analogies to bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease in humans.
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Silent Prions and Covert Prion TransmissionGenesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion diseaseBeyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob diseaseElements modulating the prion species barrier and its passage consequencesTransmissibility of H-Type Bovine Spongiform Encephalopathy to Hamster PrP Transgenic Mice.Prion replication without host adaptation during interspecies transmissions.Conversion of the BASE prion strain into the BSE strain: the origin of BSE?Molecular distinction between pathogenic and infectious properties of the prion protein.Prions in milk from ewes incubating natural scrapie.Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases.Dietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.Atypical/Nor98 scrapie infectivity in sheep peripheral tissues.Redox control of prion and disease pathogenesis.Iron content of ferritin modulates its uptake by intestinal epithelium: implications for co-transport of prions.Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked.Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171.Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study.Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potentialComparison of abnormal prion protein glycoform patterns from transmissible spongiform encephalopathy agent-infected deer, elk, sheep, and cattlePrP polymorphisms tightly control sheep prion replication in cultured cellsTransmission characteristics of variably protease-sensitive prionopathy.Species-barrier-independent prion replication in apparently resistant species.Rapid assessment of bovine spongiform encephalopathy prion inactivation by heat treatment in yellow grease produced in the industrial manufacturing process of meat and bone mealsMother to offspring transmission of chronic wasting disease in reeves' muntjac deer.Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.In vivo comparison of chronic wasting disease infectivity from deer with variation at prion protein residue 96.Insights into prion biology: integrating a protein misfolding pathway with its cellular environment.Increased infectivity of anchorless mouse scrapie prions in transgenic mice overexpressing human prion proteinAccumulation of prion protein in the brain that is not associated with transmissible disease.Subcritical Water Hydrolysis Effectively Reduces the In Vitro Seeding Activity of PrPSc but Fails to Inactivate the Infectivity of Bovine Spongiform Encephalopathy PrionsIon channels induced by the prion protein: mediators of neurotoxicity.Magnetic microparticle-based multimer detection system for the detection of prion oligomers in sheep.Stabilization of a prion strain of synthetic origin requires multiple serial passagesSpiroplasma as a candidate agent for the transmissible spongiform encephalopathies.[PSI(+) ] prion variant establishment in yeastInvestigation of a possible iatrogenic case of Creutzfeldt-Jakob disease after a neurosurgical procedure.Prion neurotoxicity: insights from prion protein mutantsDetection and control of prion diseases in food animals.Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfaces.Prions are secreted in milk from clinically normal scrapie-exposed sheep.
P2860
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P2860
Long-term subclinical carrier state precedes scrapie replication and adaptation in a resistant species: analogies to bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease in humans.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@en
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@nl
type
label
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@en
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@nl
prefLabel
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@en
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@nl
P2093
P2860
P1433
P1476
Long-term subclinical carrier ...... feldt-Jakob disease in humans.
@en
P2093
P2860
P304
10106-10112
P356
10.1128/JVI.75.21.10106-10112.2001
P407
P577
2001-11-01T00:00:00Z