Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains
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Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial InsomniaAdvanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Inactivation of Prions and Amyloid Seeds with Hypochlorous Acid.Early and Non-Invasive Detection of Chronic Wasting Disease Prions in Elk Feces by Real-Time Quaking Induced Conversion.Use of bovine recombinant prion protein and real-time quaking-induced conversion to detect cattle transmissible mink encephalopathy prions and discriminate classical and atypical L- and H-Type bovine spongiform encephalopathy.Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay.Detection of Atypical H-Type Bovine Spongiform Encephalopathy and Discrimination of Bovine Prion Strains by Real-Time Quaking-Induced Conversion.Application of an in vitro-amplification assay as a novel pre-screening test for compounds inhibiting the aggregation of prion protein scrapiePrions: Beyond a Single Protein.Extended and direct evaluation of RT-QuIC assays for Creutzfeldt-Jakob disease diagnosisIntegrated Organotypic Slice Cultures and RT-QuIC (OSCAR) Assay: Implications for Translational Discovery in Protein Misfolding Diseases.Methods for Differentiating Prion Types in Food-Producing Animals.Experimental Models of Inherited PrP Prion Diseases.Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers.Role of the central lysine cluster and scrapie templating in the transmissibility of synthetic prion protein aggregates.RT-QuIC Assays for Prion Disease Detection and Diagnostics.Evolution of Diagnostic Tests for Chronic Wasting Disease, a Naturally Occurring Prion Disease of Cervids.Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity.The real-time quaking-induced conversion assay for detection of human prion disease and study of other protein misfolding diseases.Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine.Sensitive and specific detection of classical scrapie prions in the brains of goats by real-time quaking-induced conversion.Goat K222-PrP(C) polymorphic variant does not provide resistance to atypical scrapie in transgenic mice.Towards authentic transgenic mouse models of heritable PrP prion diseases.High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions.In vitro amplification of H-type atypical bovine spongiform encephalopathy by protein misfolding cyclic amplification.Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.Soluble polymorphic bank vole prion proteins induced by co-expression of quiescin sulfhydryl oxidase in E. coli and their aggregation behaviorsAsparagine and glutamine ladders promote cross-species prion conversion.Correction: Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains.Prion Diagnosis: Application of Real-Time Quaking-Induced Conversion.Real-time Quaking-induced Conversion Assay for Detection of CWD Prions in Fecal Material.Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease.Prion Strains and Transmission Barrier Phenomena.Recombinant PrP and Its Contribution to Research on Transmissible Spongiform Encephalopathies.Ante-mortem detection of chronic wasting disease in recto-anal mucosa-associated lymphoid tissues from elk (Cervus elaphus nelsoni) using real-time quaking-induced conversion (RT-QuIC) assay: A blinded collaborative study.Applications of the real-time quaking-induced conversion assay in diagnosis, prion strain-typing, drug pre-screening and other amyloidopathies.Ultrasensitive and selective detection of 3-repeat tau seeding activity in Pick disease brain and cerebrospinal fluid.Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein.Rapid and ultra-sensitive quantitation of disease-associated α-synuclein seeds in brain and cerebrospinal fluid by αSyn RT-QuIC.Lack of Transmission of Chronic Wasting Disease to Cynomolgus Macaques.
P2860
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P2860
Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains
description
2015 nî lūn-bûn
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2015 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
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2015年論文
@zh-mo
2015年論文
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2015年论文
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name
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@ast
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@en
type
label
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@ast
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@en
prefLabel
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@ast
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@en
P2093
P2860
P1433
P1476
Bank Vole Prion Protein As an ...... iscrimination of Prion Strains
@en
P2093
Andrew G Hughson
Bernardino Ghetti
Bradley R Groveman
Christina D Orrú
Lynne D Raymond
Pierluigi Gambetti
Wenquan Zou
P2860
P304
P356
10.1371/JOURNAL.PPAT.1004983
P407
P577
2015-06-18T00:00:00Z