Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.
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The Croonian Lecture 2004 risk: food, fact and fantasyEfficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.Genetics of Prion Disease in CattleA Comparison of Classical and H-Type Bovine Spongiform Encephalopathy Associated with E211K Prion Protein Polymorphism in Wild-Type and EK211 Cattle Following Intracranial Inoculation.Whole Blood Gene Expression Profiling in Preclinical and Clinical Cattle Infected with Atypical Bovine Spongiform EncephalopathyIntraspecies transmission of BASE induces clinical dullness and amyotrophic changesTransgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion IsolatesIdiopathic Brainstem Neuronal Chromatolysis (IBNC): a novel prion protein related disorder of cattle?The amyloid-Congo red interface at atomic resolutionIsolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathyAtypical BSE (BASE) transmitted from asymptomatic aging cattle to a primateMolecular, biochemical and genetic characteristics of BSE in CanadaBiochemical Characteristics and PrP(Sc) Distribution Pattern in the Brains of Cattle Experimentally Challenged with H-type and L-type Atypical BSESmall ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathyTransmissibility of H-Type Bovine Spongiform Encephalopathy to Hamster PrP Transgenic Mice.Generic amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prionsThe challenge of emerging and re-emerging infectious diseasesProduction of cattle lacking prion protein.Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great BritainThe expanding universe of prion diseases.Prion gene haplotypes of U.S. cattleConversion of the BASE prion strain into the BSE strain: the origin of BSE?Host PrP glycosylation: a major factor determining the outcome of prion infection.Prevalence of the prion protein gene E211K variant in U.S. cattle.Identification of a heritable polymorphism in bovine PRNP associated with genetic transmissible spongiform encephalopathy: evidence of heritable BSE.A sequencing strategy for identifying variation throughout the prion gene of BSE-affected cattle.A C-terminal protease-resistant prion fragment distinguishes ovine "CH1641-like" scrapie from bovine classical and L-Type BSE in ovine transgenic miceFrequencies of polymorphisms associated with BSE resistance differ significantly between Bos taurus, Bos indicus, and composite cattle.Species and strain glycosylation patterns of PrPScDistinct transmissibility features of TSE sources derived from ruminant prion diseases by the oral route in a transgenic mouse model (TgOvPrP4) overexpressing the ovine prion protein.No H- and L-type cases in Belgium in cattle diagnosed with bovine spongiform encephalopathy (1999-2008) aging seven years and older.Enhanced neuroinvasion by smaller, soluble prions.Differential protein expression profiling in BSE disease.A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.Intraspecies prion transmission results in selection of sheep scrapie strains.Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice.Types and Strains: Their Essential Role in Understanding Protein Aggregation in Neurodegenerative Diseases.Dietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.Phenotypic similarity of transmissible mink encephalopathy in cattle and L-type bovine spongiform encephalopathy in a mouse modelA molecular switch controls interspecies prion disease transmission in mice.
P2860
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P2860
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Identification of a second bov ...... dic Creutzfeldt-Jakob disease.
@en
type
label
Identification of a second bov ...... dic Creutzfeldt-Jakob disease.
@en
prefLabel
Identification of a second bov ...... dic Creutzfeldt-Jakob disease.
@en
P2093
P2860
P50
P356
P1476
Identification of a second bov ...... dic Creutzfeldt-Jakob disease.
@en
P2093
Cristina Casalone
Fabrizio Tagliavini
Maria Caramelli
Pierluigi Acutis
Sergio Ferrari
P2860
P304
P356
10.1073/PNAS.0305777101
P407
P577
2004-02-17T00:00:00Z