Prion protein expression in different species: analysis with a panel of new mAbs - Wikidata - awgldk - TriplyDB

Prion protein expression in different species: analysis with a panel of new mAbs

Prion protein expression in different species: analysis with a panel of new mAbs

http://www.wikidata.org/entity/Q36222036

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Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity Changing 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 neurons In 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 milk The 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 aggregates A 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 blunder Structural 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 species Effect 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 glycosaminoglycans Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein Doppel induces degeneration of cerebellar Purkinje cells independently of Bax Molecular 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 strain Glycosylphosphatidylinositol 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 mice The Role of Prion Protein Expression in Predicting Gastric Cancer Prognosis Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.Ligand binding promotes prion protein aggregation--role of the octapeptide repeats Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection Association of prion protein expression with pancreatic adenocarcinoma survival in the SEER residual tissue repository Calpain-mediated signaling mechanisms in neuronal injury and neurodegeneration Anti-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

http://www.wikidata.org/entity/Q36222036

description

1998 nî lūn-bûn

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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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

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Prion protein expression in different species: analysis with a panel of new mAbs

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type

label

Prion protein expression in different species: analysis with a panel of new mAbs

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Prion protein expression in different species: analysis with a panel of new mAbs

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prefLabel

Prion protein expression in different species: analysis with a panel of new mAbs

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Prion protein expression in different species: analysis with a panel of new mAbs

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Prion protein expression in different species: analysis with a panel of new mAbs

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P2093

D Liu

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I Hegyi

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J C Manson

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P2860

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

Mice devoid of PrP are resistant to scrapie

Prion protein gene variation among primates

Novel proteinaceous infectious particles cause scrapie

Molecular mass, biochemical composition, and physicochemical behavior of the infectious form of the scrapie precursor protein monomer

Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population.

A new variant of Creutzfeldt-Jakob disease in the UK.

Separation and properties of cellular and scrapie prion proteins.

Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity.

Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells.

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8812-8816

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15

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95

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Gianluigi Zanusso

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1998-07-01T00:00:00Z

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24452081

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9671761

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Prion protein family

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21159

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