about
Neurodegeneration in humans caused by prionsA simple, versatile and sensitive cell-based assay for prions from various speciesAllelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation.Recovery of small infectious PrP(res) aggregates from prion-infected cultured cells.Prion diseases: pathogenesis and public health concerns.Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.A model for beta-amyloid aggregation and neurotoxicity based on free radical generation by the peptide: relevance to Alzheimer disease.Mammalian prions: tracking the infectious entitiesAttempts to restore scrapie prion infectivity after exposure to protein denaturantsSolid-state NMR studies of the prion protein H1 fragment.Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoformSynthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.Prion protein fragment 106-126 induces apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in the GH3 cell line.A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits.Effect of scrapie infection on the activity of neuronal nitric-oxide synthase in brain and neuroblastoma cells.Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes.Joint Scientific Opinion on any possible epidemiological or molecular association between TSEs in animals and humansDetection of prion protein in formalin-fixed brain by hydrated autoclaving immunohistochemistry for the diagnosis of scrapie in sheep.A nonfibrillar form of the fusogenic prion protein fragment [118-135] induces apoptotic cell death in rat cortical neurons.
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Chemistry and biology of prions.
@ast
Chemistry and biology of prions.
@en
type
label
Chemistry and biology of prions.
@ast
Chemistry and biology of prions.
@en
prefLabel
Chemistry and biology of prions.
@ast
Chemistry and biology of prions.
@en
P356
P1433
P1476
Chemistry and biology of prions.
@en
P304
12277-12288
P356
10.1021/BI00164A001
P407
P577
1992-12-01T00:00:00Z