Experimental verification of a traceback phenomenon in prion infection.
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Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problemsEvidence that bank vole PrP is a universal acceptor for prionsAnalysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease PrionsAgent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USADeciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein.Prion disease: experimental models and reality.UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approachesBiochemical and strain properties of CJD prions: complexity versus simplicity.Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.Human prion diseases: molecular, cellular and population biology.Prion disease: a tale of folds and strains.The influence of PRNP polymorphisms on human prion disease susceptibility: an update.Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions.Co-occurrence of types 1 and 2 PrP(res) in sporadic Creutzfeldt-Jakob disease MM1.An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification.Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties.Extensive cortical spongiform changes with cerebellar small amyloid plaques: the clinicopathological case of MV2K+C subtype in Creutzfeldt-Jakob disease.
P2860
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P2860
Experimental verification of a traceback phenomenon in prion infection.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Experimental verification of a traceback phenomenon in prion infection.
@ast
Experimental verification of a traceback phenomenon in prion infection.
@en
type
label
Experimental verification of a traceback phenomenon in prion infection.
@ast
Experimental verification of a traceback phenomenon in prion infection.
@en
prefLabel
Experimental verification of a traceback phenomenon in prion infection.
@ast
Experimental verification of a traceback phenomenon in prion infection.
@en
P2093
P2860
P356
P1433
P1476
Experimental verification of a traceback phenomenon in prion infection.
@en
P2093
Atsushi Kobayashi
Nobuyuki Sakuma
Shirou Mohri
Tetsuyuki Kitamoto
P2860
P304
P356
10.1128/JVI.02387-09
P577
2010-01-20T00:00:00Z