Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
about
Assignment of the human and mouse prion protein genes to homologous chromosomesRadiation metabolomics and its potential in biodosimetryRisk assessment of bovine spongiform encephalopathy transmission through bone graft material derived from bovine bone used for dental applications.Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthAbsence of Spiroplasma or other bacterial 16s rRNA genes in brain tissue of hamsters with scrapieTubulofilaments in negatively stained scrapie-infected brains: relationship to scrapie-associated fibrils.Scrapie: Report of an outbreak and brief reviewA 54-kDa normal cellular protein may be the precursor of the scrapie agent protease-resistant protein.Scrapie prion proteins are synthesized in neuronsSpiroplasma as a candidate agent for the transmissible spongiform encephalopathies.Molecular biology and transgenetics of prion diseases.Branched chain mechanism of polymerization and ultrastructure of prion protein amyloid fibrils.Analyses of frequency of infection, specific infectivity, and prion protein biosynthesis in scrapie-infected neuroblastoma cell clones.Scrapie PrP 27-30 is a sialoglycoprotein.Purified scrapie prions resist inactivation by UV irradiationThe search for scrapie agent nucleic acidInactivation of RNA Viruses by Gamma Irradiation: A Study on Mitigating Factors.Kuru: memories of the NIH years.Isolation of a cDNA clone encoding the leader peptide of prion protein and expression of the homologous gene in various tissues.Prion liposomes.Transmissible spongiform encephalopathy in the gray tremor mutant mouse.The nature of the scrapie agent. Biological characteristics of scrapie in different scrapie strain-host combinations.The nature of the scrapie agent: the virus theory.General aspects of transmissible spongiform encephalopathies and hypotheses about the agents.Unconventional viruses or prions?Evidence that homologous ssDNA is present in scrapie, Creutzfeldt-Jakob disease, and bovine spongiform encephalopathy.Spongiform encephalopathy: a neurocytologist's viewpoint with a note on Alzheimer's disease.Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein.Decontamination of prions in a plasma product manufacturing environment.Some physico-chemical parameters that influence proteinase K resistance and the infectivity of PrPSc after high pressure treatment.Straining the prion hypothesis
P2860
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P2860
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年学术文章
@wuu
1984年学术文章
@zh
1984年学术文章
@zh-cn
1984年学术文章
@zh-hans
1984年学术文章
@zh-my
1984年学术文章
@zh-sg
1984年學術文章
@yue
1984年學術文章
@zh-hant
name
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@en
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@nl
type
label
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@en
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@nl
prefLabel
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@en
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@nl
P2860
P356
P1433
P1476
Scrapie infectious agent is virus-like in size and susceptibility to inactivation.
@en
P2093
P2860
P2888
P304
P356
10.1038/308658A0
P407
P577
1984-04-01T00:00:00Z
P6179
1049362883