Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice. - Wikidata - awgldk - TriplyDB

Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice.

Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice.

http://www.wikidata.org/entity/Q37523079

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Involvement of PrP(C) in kainate-induced excitotoxicity in several mouse strains.Functions of the cellular prion protein, the end of Moore's law, and Ockham's razor theory Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Early Generation of New PrPSc on Blood Vessels after Brain Microinjection of Scrapie in Mice Physiological Functions of the Cellular Prion Protein.Mechanisms of prion-induced neurodegeneration.Altered Monoaminergic Systems and Depressive-like Behavior in Congenic Prion Protein Knock-out Mice.Protein Misfolding in Prion and Prion-Like Diseases: Reconsidering a Required Role for Protein Loss-of-Function.

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Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice.

http://www.wikidata.org/entity/Q37523079

description

article científic

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article scientifique

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artigo científico

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bilimsel makale

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scientific article published on 12 July 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Prion protein and susceptibili ...... the use of PrP knockout mice.

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Brent Race

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Bruce Chesebro

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James F Striebel

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Creative Commons Attribution-NonCommercial 3.0 Unported

P2860

Mice devoid of PrP are resistant to scrapie

The prion's elusive reason for being

In vivo conversion of cellular prion protein to pathogenic isoforms, as monitored by conformation-specific antibodies.

Identification of two immunogenic domains of the prion protein--PrP--which activate class II-restricted T cells and elicit antibody responses against the native molecule.

Fishing for prion protein function

Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring

Standards for the publication of mouse mutant studies.

Axonal prion protein is required for peripheral myelin maintenance.

Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.

Differences in scrapie-induced pathology of the retina and brain in transgenic mice that express hamster prion protein in neurons, astrocytes, or multiple cell types

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280-285

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10.4161/PRI.25738

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2013-07-12T00:00:00Z

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249320062

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23851597

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Prion protein family

epileptic seizure

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3904312

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