Molecular pathogenesis of sporadic prion diseases in man.
about
Wrecked regulation of intrinsically disordered proteins in diseases: pathogenicity of deregulated regulatorsProteotoxicity: an underappreciated pathology in cardiac diseaseSpontaneous variants of the [RNQ+] prion in yeast demonstrate the extensive conformational diversity possible with prion proteinsIntrinsically disordered proteins and their (disordered) proteomes in neurodegenerative disordersMagnetic microparticle-based multimer detection system for the detection of prion oligomers in sheep.Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer's disease.Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selectionRapidly progressive Alzheimer's disease features distinct structures of amyloid-β.Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases.From Neurodegeneration to Brain Health: An Integrated Approach.Extensive diversity of prion strains is defined by differential chaperone interactions and distinct amyloidogenic regions.Extracellular environment modulates the formation and propagation of particular amyloid structures.Methods for Molecular Diagnosis of Human Prion Disease.
P2860
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P2860
Molecular pathogenesis of sporadic prion diseases in man.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Molecular pathogenesis of sporadic prion diseases in man.
@ast
Molecular pathogenesis of sporadic prion diseases in man.
@en
type
label
Molecular pathogenesis of sporadic prion diseases in man.
@ast
Molecular pathogenesis of sporadic prion diseases in man.
@en
prefLabel
Molecular pathogenesis of sporadic prion diseases in man.
@ast
Molecular pathogenesis of sporadic prion diseases in man.
@en
P2860
P921
P356
P1433
P1476
Molecular pathogenesis of sporadic prion diseases in man.
@en
P2093
Jiri G Safar
P2860
P304
P356
10.4161/PRI.18666
P5008
P577
2012-04-01T00:00:00Z