Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.
about
Cells infected with scrapie and Creutzfeldt-Jakob disease agents produce intracellular 25-nm virus-like particlesA brief history of prionsTwo Creutzfeldt-Jakob disease agents reproduce prion protein-independent identities in cell cultures.Investigating the conformational stability of prion strains through a kinetic replication model.Evidence that DNA is present in abnormal tubulofilamentous structures found in scrapieImmunoaffinity purification and neutralization of scrapie prion infectivityConservation of infectivity in purified fibrillary extracts of scrapie-infected hamster brain after sequential enzymatic digestion or polyacrylamide gel electrophoresisNeuroinvasion by a Creutzfeldt-Jakob disease agent in the absence of B cells and follicular dendritic cellsQuantitative recovery of scrapie agent with minimal protein from highly infectious cultures.Viral particles are required for infection in neurodegenerative Creutzfeldt-Jakob disease.Astrocyte gene expression in Creutzfeldt-Jakob disease.Tubulofilaments in negatively stained scrapie-infected brains: relationship to scrapie-associated fibrils.Vaccination with an attenuated Creutzfeldt-Jakob disease strain prevents expression of a virulent agent.Nucleic acid binding proteins in highly purified Creutzfeldt-Jakob disease preparations.A transmissible Creutzfeldt-Jakob disease-like agent is prevalent in the human populationProtease sensitivity and nuclease resistance of the scrapie agent propagated in vitro in neuroblastoma cellsPhysical properties of the Creutzfeldt-Jakob disease agentEvidence of mitochondrial involvement in scrapie infection.Potential retroviral RNAs in Creutzfeldt-Jakob diseaseGrowth factor production by Creutzfeldt-Jakob disease cell lines.Immunological analysis of host and agent effects on Creutzfeldt-Jakob disease and scrapie prion proteins.The search for scrapie agent nucleic acidA versatile prion replication assay in organotypic brain slices.Prion liposomes.Cross currents in protein misfolding disorders: interactions and therapy.Microglia from Creutzfeldt-Jakob disease-infected brains are infectious and show specific mRNA activation profiles.A rapid accurate culture assay for infectivity in Transmissible Encephalopathies.Presence of mitochondrial D-loop DNA in scrapie-infected brain preparations enriched for the prion protein.Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.
P2860
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P2860
Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.
@en
type
label
Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.
@en
prefLabel
Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.
@en
P2860
P1433
P1476
Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease
@en
P2093
E E Manuelidis
L Manuelidis
P2860
P304
P356
10.1002/J.1460-2075.1987.TB04760.X
P407
P577
1987-02-01T00:00:00Z