Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
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Whole Blood Gene Expression Profiling in Preclinical and Clinical Cattle Infected with Atypical Bovine Spongiform EncephalopathyPhenotype shift from atypical scrapie to CH1641 following experimental transmission in sheepIntraspecies transmission of BASE induces clinical dullness and amyotrophic changesIdiopathic Brainstem Neuronal Chromatolysis (IBNC): a novel prion protein related disorder of cattle?Atypical 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 BSEIs the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic?Conformational switching within individual amyloid fibrils.Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great BritainPrevalence of the prion protein gene E211K variant in U.S. cattle.No major change in vCJD agent strain after secondary transmission via blood transfusionIdentification of a heritable polymorphism in bovine PRNP associated with genetic transmissible spongiform encephalopathy: evidence of heritable BSE.A C-terminal protease-resistant prion fragment distinguishes ovine "CH1641-like" scrapie from bovine classical and L-Type BSE in ovine transgenic miceTime trends in exposure of cattle to bovine spongiform encephalopathy and cohort effect in France and Italy: value of the classical Age-Period-Cohort approachPrions of ruminants show distinct splenotropisms in an ovine transgenic mouse model.No H- and L-type cases in Belgium in cattle diagnosed with bovine spongiform encephalopathy (1999-2008) aging seven years and older.Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathyMouse neuronal cells expressing exogenous bovine PRNP and simultaneous downregulation of endogenous mouse PRNP using siRNAs.Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice.Phenotypic similarity of transmissible mink encephalopathy in cattle and L-type bovine spongiform encephalopathy in a mouse modelDefining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathy.Experimental H-type and L-type bovine spongiform encephalopathy in cattle: observation of two clinical syndromes and diagnostic challenges.Experimental interspecies transmission studies of the transmissible spongiform encephalopathies to cattle: comparison to bovine spongiform encephalopathy in cattle.Individual factors associated with L- and H-type Bovine Spongiform encephalopathy in France.The pathological and molecular but not clinical phenotypes are maintained after second passage of experimental atypical bovine spongiform encephalopathy in cattleClinical and pathologic features of H-type bovine spongiform encephalopathy associated with E211K prion protein polymorphismMolecular modeling of prion transmission to humansEvaluation of the zoonotic potential of transmissible mink encephalopathy.Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits.Detection and discrimination of classical and atypical L-type bovine spongiform encephalopathy by real-time quaking-induced conversionCharacterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathiesAn overview of animal prion diseases.Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type miceClassical bovine spongiform encephalopathy by transmission of H-type prion in homologous prion protein context.Comparative analysis of Japanese and foreign L-type BSE prions.Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay.Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains.Atypical bovine spongiform encephalopathies, France, 2001-2007.
P2860
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P2860
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
description
2007 nî lūn-bûn
@nan
2007 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մարտին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@ast
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@en
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@nl
type
label
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@ast
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@en
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@nl
prefLabel
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@ast
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@en
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@nl
P2093
P2860
P50
P1433
P1476
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
@en
P2093
Anne Buschmann
Claudia Miccolo
Cristiano Corona
Daniela Gelmetti
Giacomina Rossi
Giorgio Giaccone
Guerino Lombardi
Lucia Limido
Marcella Catania
Maria Caramelli
P2860
P356
10.1371/JOURNAL.PPAT.0030031
P50
P577
2007-03-01T00:00:00Z