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Neurodegenerative diseases: expanding the prion conceptProteasomes and ubiquitin are involved in the turnover of the wild-type prion proteinMapping the early steps in the pH-induced conformational conversion of the prion protein.Notifying patients exposed to blood products associated with Creutzfeldt-Jakob disease: integrating science, legal duties and ethical mandates.Prion infection of mouse neurospheres.Defined α-synuclein prion-like molecular assemblies spreading in cell culture.Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicityCreutzfeldt-Jakob disease, new variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy - An update.From conversion to aggregation: protofibril formation of the prion protein.Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice.Creutzfeldt-Jakob disease in the United States, 1979-1994: using national mortality data to assess the possible occurrence of variant cases.Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.De Novo Generation of a Unique Cervid Prion Strain Using Protein Misfolding Cyclic Amplification.The Role of Microglia in Prion Diseases: A Paradigm of Functional Diversity.Peroxiredoxin 6 promotes upregulation of the prion protein (PrP) in neuronal cells of prion-infected miceThe failure of Daudi cells to express the cellular prion protein is caused by a lack of glycosyl-phosphatidylinositol anchor formation.Aβ seeds and prions: How close the fit?Molecular modelling indicates that the pathological conformations of prion proteins might be beta-helical.Polymorphisms in the HSP90AA1 5' flanking region are associated with scrapie incubation period in sheep.Prion Diagnosis: Application of Real-Time Quaking-Induced Conversion.
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Etiology and pathogenesis of prion diseases.
@ast
Etiology and pathogenesis of prion diseases.
@en
type
label
Etiology and pathogenesis of prion diseases.
@ast
Etiology and pathogenesis of prion diseases.
@en
prefLabel
Etiology and pathogenesis of prion diseases.
@ast
Etiology and pathogenesis of prion diseases.
@en
P2860
P1476
Etiology and pathogenesis of prion diseases
@en
P2093
S J DeArmond
P2860
P304
P407
P577
1995-04-01T00:00:00Z