Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain.
about
Continuous quinacrine treatment results in the formation of drug-resistant prionsAnalysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob diseaseAtypical BSE (BASE) transmitted from asymptomatic aging cattle to a primatePost-translational modifications in PrP expand the conformational diversity of prions in vivoHuman prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.Rationale for diagnosing human prion disease.Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.Experimental verification of a traceback phenomenon in prion infection.Molecular analysis of the abnormal prion protein during coinfection of mice by bovine spongiform encephalopathy and a scrapie agent.Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.Prion strain interactions are highly selective.Molecular pathology of human prion disease.Review: contribution of transgenic models to understanding human prion disease.Heterogeneity of the Abnormal Prion Protein (PrPSc) of the Chandler Scrapie Strain.Pathological diagnosis of variant Creutzfeldt-Jakob disease.Molecular biology and pathology of prion strains in sporadic human prion diseases.Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease.Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study.Different prion disease phenotypes result from inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain.Tracking protein aggregate interactions.White-tailed deer are susceptible to the agent of sheep scrapie by intracerebral inoculation.Diversity in prion protein oligomerization pathways results from domain expansion as revealed by hydrogen/deuterium exchange and disulfide linkageSquirrel monkeys (Saimiri sciureus) infected with the agent of bovine spongiform encephalopathy develop tau pathologyPrion subcellular fractionation reveals infectivity spectrum, with a high titre-low PrPres level disparity.Molecular pathogenesis of sporadic prion diseases in man.Prion protein glycosylation.Overlap between neurodegenerative disorders.Phenotypic variability in human prion diseases.Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions.Bovine spongiform encephalopathy in Japan: history and recent studies on oxidative stress in prion diseases.The prion strain phenomenon: molecular basis and unprecedented features.Insights into prion strains and neurotoxicity.Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USAPrions: Beyond a Single Protein.Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristicsIncidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classificationAbsence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic MiceIsolation of two distinct prion strains from a scrapie-affected sheep.
P2860
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P2860
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP
@nl
Sporadic Creutzfeldt-Jakob dis ...... of PrP(Sc) in the same brain.
@en
type
label
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP
@nl
Sporadic Creutzfeldt-Jakob dis ...... of PrP(Sc) in the same brain.
@en
prefLabel
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP
@nl
Sporadic Creutzfeldt-Jakob dis ...... of PrP(Sc) in the same brain.
@en
P2093
P356
P1433
P1476
Sporadic Creutzfeldt-Jakob dis ...... of PrP(Sc) in the same brain.
@en
P2093
P304
P356
10.1212/WNL.53.9.2173
P407
P577
1999-12-01T00:00:00Z