Prion diseases of humans and animals: their causes and molecular basis
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Regulation of embryonic cell adhesion by the prion proteinEvidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyConformational diversity in prion protein variants influences intermolecular beta-sheet formationThe novel sorting nexin SNX33 interferes with cellular PrP formation by modulation of PrP sheddingPrion hypothesis: the end of the controversy?A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New GuineaGenetic susceptibility, evolution and the kuru epidemicKuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceSafety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trialThe role of the cellular prion protein in the immune systemEpidemiological characteristics of human prion diseasesNonruminant Nutrition Symposium: Involvement of gut neural and endocrine systems in pathological disorders of the digestive tractAssessing the causes and consequences of co-polymerization in amyloid formationSelf-propagation of pathogenic protein aggregates in neurodegenerative diseasesMolecular mechanisms of disease-causing missense mutationsTreatment of Prion Disease with Heterologous Prion ProteinsCalcineurin inhibition at the clinical phase of prion disease reduces neurodegeneration, improves behavioral alterations and increases animal survivalThe physical relationship between infectivity and prion protein aggregates is strain-dependentTrans-dominant inhibition of prion propagation in vitro is not mediated by an accessory cofactorDe novo generation of infectious prions in vitro produces a new disease phenotypeTransgenic Rabbits Expressing Ovine PrP Are Susceptible to ScrapieMutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patientsCrystal structure of human prion protein bound to a therapeutic antibodyThermodynamic Stabilization of the Folded Domain of Prion Protein Inhibits Prion Infection in VivoMolecular Structure of β-Amyloid Fibrils in Alzheimer’s Disease Brain TissueA general model of prion strains and their pathogenicityIsolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathyExpression of mutant or cytosolic PrP in transgenic mice and cells is not associated with endoplasmic reticulum stress or proteasome dysfunctionIntroducing a rigid loop structure from deer into mouse prion protein increases its propensity for misfolding in vitroCritical significance of the region between Helix 1 and 2 for efficient dominant-negative inhibition by conversion-incompetent prion proteinAggregate-depleted brain fails to induce Aβ deposition in a mouse model of Alzheimer's diseasePorcine prion protein amyloidIsolation of proteinase K-sensitive prions using pronase E and phosphotungstic acidLoss of Octarepeats in two processed prion pseudogenes in the red squirrel, Sciurus vulgarisPhysical, chemical and kinetic factors affecting prion infectivityGenome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPIs the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic?Heterologous cross-seeding mimics cross-species prion conversion in a yeast model.Nanopore analysis of wild-type and mutant prion protein (PrP(C)): single molecule discrimination and PrP(C) kinetics.Identification of a gene regulatory network associated with prion replication.
P2860
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P2860
Prion diseases of humans and animals: their causes and molecular basis
description
2001 nî lūn-bûn
@nan
2001 թուականին հրատարակուած գիտական յօդուած
@hyw
2001 թվականին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Prion diseases of humans and animals: their causes and molecular basis
@ast
Prion diseases of humans and animals: their causes and molecular basis
@en
Prion diseases of humans and animals: their causes and molecular basis
@nl
type
label
Prion diseases of humans and animals: their causes and molecular basis
@ast
Prion diseases of humans and animals: their causes and molecular basis
@en
Prion diseases of humans and animals: their causes and molecular basis
@nl
prefLabel
Prion diseases of humans and animals: their causes and molecular basis
@ast
Prion diseases of humans and animals: their causes and molecular basis
@en
Prion diseases of humans and animals: their causes and molecular basis
@nl
P3181
P1476
Prion diseases of humans and animals: their causes and molecular basis
@en
P2093
J Collinge
P304
P3181
P356
10.1146/ANNUREV.NEURO.24.1.519
P407
P577
2001-01-01T00:00:00Z