about
Prion-like domains as epigenetic regulators, scaffolds for subcellular organization, and drivers of neurodegenerative diseaseDisease Transmission by Misfolded Prion-Protein Isoforms, Prion-Like Amyloids, Functional Amyloids and the Central DogmaTechniques to elucidate the conformation of prionsDegradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies.The Role of Prion Protein Expression in Predicting Gastric Cancer PrognosisThe role of the unusual threonine string in the conversion of prion protein.Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity.Confined Water in Amyloid-Competent Oligomers of the Prion Protein.Prion infectivity is encoded exclusively within the structure of proteinase K-resistant fragments of synthetically generated recombinant PrPSc.Prion protein modulates glucose homeostasis by altering intracellular iron.
P2860
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P2860
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh
2014年學術文章
@zh-hant
name
Prion disease and the 'protein-only hypothesis'.
@en
type
label
Prion disease and the 'protein-only hypothesis'.
@en
prefLabel
Prion disease and the 'protein-only hypothesis'.
@en
P2860
P356
P1476
Prion disease and the 'protein-only hypothesis'
@en
P2093
P2860
P304
P356
10.1042/BSE0560181
P577
2014-01-01T00:00:00Z