Prion protein expression in different species: analysis with a panel of new mAbs
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Prion protein-specific antibodies that detect multiple TSE agents with high sensitivityChanging a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers.Induction of cellular prion protein gene expression by copper in neuronsIn vivo conversion of cellular prion protein to pathogenic isoforms, as monitored by conformation-specific antibodies.Immunoaffinity reactors for prion protein qualitative analysis.Clearance and prevention of prion infection in cell culture by anti-PrP antibodies.Prion protein in milkThe POM monoclonals: a comprehensive set of antibodies to non-overlapping prion protein epitopes.Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata)Immunopurification of pathological prion protein aggregatesA novel, drug-based, cellular assay for the activity of neurotoxic mutants of the prion protein.Novel antibody-lectin enzyme-linked immunosorbent assay that distinguishes prion proteins in sporadic and variant cases of Creutzfeldt-Jakob disease.PrP(Sc)-specific antibodies with the ability to immunodetect prion oligomers.Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Characterization of the prion protein in human urine.Generation of antibodies against bovine recombinant prion protein in various strains of mice.Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C).Selective re-routing of prion protein to proteasomes and alteration of its vesicular secretion prevent PrP(Sc) formation.High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo.Binding of pro-prion to filamin A: by design or an unfortunate blunderStructural determinants of phenotypic diversity and replication rate of human prions.The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between speciesEffect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain.Human prion proteins with pathogenic mutations share common conformational changes resulting in enhanced binding to glycosaminoglycansChronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion proteinDoppel induces degeneration of cerebellar Purkinje cells independently of BaxMolecular pathogenesis of sporadic prion diseases in man.Prion Infectivity Plateaus and Conversion to Symptomatic Disease Originate from Falling Precursor Levels and Increased Levels of Oligomeric PrPSc Species.Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strainGlycosylphosphatidylinositol Anchor Modification Machinery Deficiency Is Responsible for the Formation of Pro-Prion Protein (PrP) in BxPC-3 Protein and Increases Cancer Cell Motility.Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties.Potential of active and passive immunizations for the prevention and therapy of transmissible spongiform encephalopathies.GFP-tagged mutant prion protein forms intra-axonal aggregates in transgenic miceThe Role of Prion Protein Expression in Predicting Gastric Cancer PrognosisAggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.Ligand binding promotes prion protein aggregation--role of the octapeptide repeatsCo-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selectionAssociation of prion protein expression with pancreatic adenocarcinoma survival in the SEER residual tissue repositoryCalpain-mediated signaling mechanisms in neuronal injury and neurodegenerationAnti-PrP Mab 6D11 suppresses PrP(Sc) replication in prion infected myeloid precursor line FDC-P1/22L and in the lymphoreticular system in vivo
P2860
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P2860
Prion protein expression in different species: analysis with a panel of new mAbs
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Prion protein expression in different species: analysis with a panel of new mAbs
@ast
Prion protein expression in different species: analysis with a panel of new mAbs
@en
type
label
Prion protein expression in different species: analysis with a panel of new mAbs
@ast
Prion protein expression in different species: analysis with a panel of new mAbs
@en
prefLabel
Prion protein expression in different species: analysis with a panel of new mAbs
@ast
Prion protein expression in different species: analysis with a panel of new mAbs
@en
P2093
P2860
P356
P1476
Prion protein expression in different species: analysis with a panel of new mAbs
@en
P2093
J C Manson
P Gambetti
R B Petersen
R Glockshuber
S Hornemann
P2860
P304
P356
10.1073/PNAS.95.15.8812
P407
P577
1998-07-01T00:00:00Z