Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice. - Wikidata - awgldk - TriplyDB

Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice.

Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice.

http://www.wikidata.org/entity/Q33893587

about

Prion hypothesis: the end of the controversy?Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cells Spontaneous generation of prion infectivity in fatal familial insomnia knockin mice Intraperitoneal Infection of Wild-Type Mice with Synthetically Generated Mammalian Prion Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotype Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis Cytoplasmic prion protein induces forebrain neurotoxicity A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome.Spontaneous generation of rapidly transmissible prions in transgenic mice expressing wild-type bank vole prion protein.Immunopurification of pathological prion protein aggregates Biology and genetics of prions causing neurodegeneration Prion diseases and their biochemical mechanisms.A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases High-resolution structure of infectious prion protein: the final frontier Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins Mouse models for studying the formation and propagation of prions.Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171.Protease-resistant prions selectively decrease Shadoo protein.De novo prions.The importance of prions.Prions.Molecular pathology of human prion disease.Review: contribution of transgenic models to understanding human prion disease.Motor behavioral and neuropathological deficits in mice deficient for normal prion protein expression The N-terminal sequence of prion protein consists an epitope specific to the abnormal isoform of prion protein (PrP(Sc))High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo.Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.Prions on the move.Abrogation of complex glycosylation by swainsonine results in strain- and cell-specific inhibition of prion replication.Accumulation of prion protein in the brain that is not associated with transmissible disease.A simplified recipe for prions.Prion infection of muscle cells in vitro Molecular pathogenesis of sporadic prion diseases in man.Characterization of conformation-dependent prion protein epitopes.Cellular prion protein: from physiology to pathology.Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation

P2860

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P2860

Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice.

http://www.wikidata.org/entity/Q33893587

description

2005 nî lūn-bûn

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2005 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2005 թվականի հունիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Immunodetection of disease-ass ...... isease in GSS transgenic mice.

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Immunodetection of disease-ass ...... isease in GSS transgenic mice.

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type

label

Immunodetection of disease-ass ...... isease in GSS transgenic mice.

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Immunodetection of disease-ass ...... isease in GSS transgenic mice.

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Immunodetection of disease-ass ...... isease in GSS transgenic mice.

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Immunodetection of disease-ass ...... isease in GSS transgenic mice.

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SJ.EMBOJ.7600717

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The EMBO Journal

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Immunodetection of disease-ass ...... isease in GSS transgenic mice.

@en

P2093

Aisling M Power

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Alex J Raeber

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Bruno Oesch

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Daniel Zwald

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Franziska Kuhn

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Glenn C Telling

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Jaqueline Schmid

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Karah E Nazor

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Karin Biffiger

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Mario Pürro

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P2860

The binding of prion proteins to serum components is affected by detergent extraction conditions

Novel proteinaceous infectious particles cause scrapie

Eight prion strains have PrP(Sc) molecules with different conformations

Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

Characterization of 2'-fluoro-RNA aptamers that bind preferentially to disease-associated conformations of prion protein and inhibit conversion.

Molecular distinction between pathogenic and infectious properties of the prion protein.

Prion protein conformation in a patient with sporadic fatal insomnia.

Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent.

A prion protein epitope selective for the pathologically misfolded conformation.

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein.

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2472-2480

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10.1038/SJ.EMBOJ.7600717

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13

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24

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2005-06-16T00:00:00Z

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7781347

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15962001

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1173157

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