The prion protein knockout mouse: a phenotype under challenge.
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Hijacking PrP(c)-dependent signal transduction: when prions impair Aβ clearanceInvolvement of PrP(C) in kainate-induced excitotoxicity in several mouse strains.NCAM1 Polysialylation: The Prion Protein's Elusive Reason for Being?The Prion Protein Controls Polysialylation of Neural Cell Adhesion Molecule 1 during Cellular MorphogenesisFunctions of the cellular prion protein, the end of Moore's law, and Ockham's razor theoryLoss of Octarepeats in two processed prion pseudogenes in the red squirrel, Sciurus vulgarisPrion protein attenuates excitotoxicity by inhibiting NMDA receptorsFishing for prion protein functionContext dependent neuroprotective properties of prion protein (PrP).LPS-induced systemic inflammation reveals an immunomodulatory role for the prion protein at the blood-brain interface.Loss of prion protein induces a primed state of type I interferon-responsive genes.Axonal prion protein is required for peripheral myelin maintenance.Prion protein and Abeta-related synaptic toxicity impairment.Expression and knockdown of cellular prion protein (PrPC) in differentiating mouse embryonic stem cells.To develop with or without the prion protein.The prion hypothesis: from biological anomaly to basic regulatory mechanism.Conserved roles of the prion protein domains on subcellular localization and cell-cell adhesionThe elusive role of the prion protein and the mechanism of toxicity in prion disease.Prion protein at the crossroads of physiology and disease.Hematological shift in goat kids naturally devoid of prion protein.Disparate Modes of Evolution Shaped Modern Prion (PRNP) and Prion-Related Doppel (PRND) Variation in Domestic CattleMembrane-enriched proteome changes and prion protein expression during neural differentiation and in neuroblastoma cells.Expression of the Prion Protein Family Member Shadoo Causes Drug Hypersensitivity That Is Diminished by the Coexpression of the Wild Type Prion Protein.Strictly co-isogenic C57BL/6J-Prnp-/- mice: A rigorous resource for prion science.Prion neurotoxicity: insights from prion protein mutantsA structural overview of the vertebrate prion proteins.Prion diseases as transmissible zoonotic diseases.Prions: Beyond a Single Protein.Olfactory behavior and physiology are disrupted in prion protein knockout miceSIRPα polymorphisms, but not the prion protein, control phagocytosis of apoptotic cells.The role of calorie restriction and SIRT1 in prion-mediated neurodegeneration.Cells and prions: a license to replicate.Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice.Role of prions in neuroprotection and neurodegeneration: a mechanism involving glutamate receptors?The inhibition of functional expression of calcium channels by prion protein demonstrates competition with α2δ for GPI-anchoring pathways.PrPs: Proteins with a purpose: Lessons from the zebrafishEmergence and natural selection of drug-resistant prions.Physiological Functions of the Cellular Prion Protein.Possible role for Ca2+ in the pathophysiology of the prion protein?Copper-dependent regulation of NMDA receptors by cellular prion protein: implications for neurodegenerative disorders.
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The prion protein knockout mouse: a phenotype under challenge.
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 25 April 2007
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
The prion protein knockout mouse: a phenotype under challenge.
@en
The prion protein knockout mouse: a phenotype under challenge.
@nl
type
label
The prion protein knockout mouse: a phenotype under challenge.
@en
The prion protein knockout mouse: a phenotype under challenge.
@nl
prefLabel
The prion protein knockout mouse: a phenotype under challenge.
@en
The prion protein knockout mouse: a phenotype under challenge.
@nl
P2860
P356
P1433
P1476
The prion protein knockout mouse: a phenotype under challenge.
@en
P2093
Andrew D Steele
P2860
P356
10.4161/PRI.1.2.4346
P577
2007-04-25T00:00:00Z