about
Degradation of the disease-associated prion protein by a serine protease from lichensOral transmissibility of prion disease is enhanced by binding to soil particlesNotification and support for people exposed to the risk of Creutzfeldt-Jakob disease (CJD) (or other prion diseases) through medical treatment (iatrogenically)Notification and support for people exposed to the risk of Creutzfeldt-Jakob disease (CJD) through medical treatment (iatrogenically)Genetics of Prion Disease in CattleYeast studies reveal moonlighting functions of the ancient actin cytoskeletonCholesterol balance in prion diseases and Alzheimer's diseaseIntraspecies transmission of BASE induces clinical dullness and amyotrophic changesEvidence that bank vole PrP is a universal acceptor for prionsIsolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathyPrion infected meat-and-bone meal is still infectious after biodiesel productionCritical significance of the region between Helix 1 and 2 for efficient dominant-negative inhibition by conversion-incompetent prion proteinProfoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases.Parallels between pathogens and gluten peptides in celiac spruePathologic prion protein infects cells by lipid-raft dependent macropinocytosisUltraviolet-ozone treatment reduces levels of disease-associated prion protein and prion infectivity.Molecular interactions between prions as seeds and recombinant prion proteins as substrates resemble the biological interspecies barrier in vitroTranscriptome analysis of the medulla tissue from cattle in response to bovine spongiform encephalopathy using digital gene expression tag profiling.Redox control of prion and disease pathogenesis.Chronic wasting disease.Role of the highly conserved middle region of prion protein (PrP) in PrP-lipid interactionDistinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassayDoes the central dogma still stand?In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathiesTranslation of the prion protein mRNA is robust in astrocytes but does not amplify during reactive astrocytosis in the mouse brainMeat and bone meal and mineral feed additives may increase the risk of oral prion disease transmissionTransgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.Early and Non-Invasive Detection of Chronic Wasting Disease Prions in Elk Feces by Real-Time Quaking Induced Conversion.Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cellsThe variant Creutzfeldt-Jakob Disease: Risk, uncertainty or safety in the use of blood and blood derivatives?Structural plasticity of the cellular prion protein and implications in health and disease.CWD prions remain infectious after passage through the digestive system of coyotes (Canis latrans).A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD.Ethics in prion disease.Synaptic dysfunction in prion diseases: a trafficking problem?Could avian scavengers translocate infectious prions to disease-free areas initiating new foci of chronic wasting disease?Procedures for identifying infectious prions after passage through the digestive system of an avian species.The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease.Evidence of a prion-like transmission of p53 amyloid in Saccharomyces cerevisiae.Cellular copper homeostasis: current concepts on its interplay with glutathione homeostasis and its implication in physiology and human diseases.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
The expanding universe of prion diseases.
@ast
The expanding universe of prion diseases.
@en
type
label
The expanding universe of prion diseases.
@ast
The expanding universe of prion diseases.
@en
prefLabel
The expanding universe of prion diseases.
@ast
The expanding universe of prion diseases.
@en
P2093
P2860
P921
P1433
P1476
The expanding universe of prion diseases.
@en
P2093
Aru Balachandran
David Westaway
Joel C Watts
P2860
P356
10.1371/JOURNAL.PPAT.0020026
P5008
P577
2006-03-01T00:00:00Z