The comprehensive native interactome of a fully functional tagged prion protein
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Protein-protein interaction networks: probing disease mechanisms using model systemsNCAM1 Polysialylation: The Prion Protein's Elusive Reason for Being?Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperonesMutant PrP suppresses glutamatergic neurotransmission in cerebellar granule neurons by impairing membrane delivery of VGCC α(2)δ-1 SubunitThe Prion Protein Controls Polysialylation of Neural Cell Adhesion Molecule 1 during Cellular MorphogenesisEffects of FlAsH/tetracysteine (TC) Tag on PrP proteolysis and PrPres formation by TC-scanning.Mammalian prions: tolerance to sequence changes-how far?Unexpected tolerance of alpha-cleavage of the prion protein to sequence variationsImmunohistochemical detection of transgene expression in the brain using small epitope tags.Na+/K+-ATPase is present in scrapie-associated fibrils, modulates PrP misfolding in vitro and links PrP function and dysfunction.Prion protein at the crossroads of physiology and disease.Integrity of helix 2-helix 3 domain of the PrP protein is not mandatory for prion replication.Membrane-enriched proteome changes and prion protein expression during neural differentiation and in neuroblastoma cells.Synaptic dysfunction in prion diseases: a trafficking problem?Tunnelling nanotubes: a highway for prion spreading?The inhibition of functional expression of calcium channels by prion protein demonstrates competition with α2δ for GPI-anchoring pathways.Structural requirements for efficient prion protein conversion: cofactors may promote a conversion-competent structure for PrP(C).Allosteric function and dysfunction of the prion protein.Proteomic analysis of prion diseases: creating clarity or causing confusion?Overcoming barriers and thresholds - signaling of oligomeric Aβ through the prion protein to Fyn.The changing landscape of voltage-gated calcium channels in neurovascular disorders and in neurodegenerative diseasesRoles of the cellular prion protein in the regulation of cell-cell junctions and barrier functionNeuroprotective role of PrPC against kainate-induced epileptic seizures and cell death depends on the modulation of JNK3 activation by GluR6/7-PSD-95 bindingPrion protein "gamma-cleavage": characterizing a novel endoproteolytic processing event.Dual role of cellular prion protein in normal host and Alzheimer's disease.Rapid cell-surface prion protein conversion revealed using a novel cell system.Unraveling the neuroprotective mechanisms of PrP (C) in excitotoxicity.GABAA receptor subunit beta1 is involved in the formation of protease-resistant prion protein in prion-infected neuroblastoma cells.Analysis of Cellular Prion Protein Endoproteolytic Processing.An inter-domain regulatory mechanism controls toxic activities of PrPC.The prion protein is embedded in a molecular environment that modulates transforming growth factor β and integrin signaling.Alterations in the brain interactome of the intrinsically disordered N-terminal domain of the cellular prion protein (PrPC) in Alzheimer's disease.
P2860
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P2860
The comprehensive native interactome of a fully functional tagged prion protein
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
The comprehensive native interactome of a fully functional tagged prion protein
@ast
The comprehensive native interactome of a fully functional tagged prion protein
@en
type
label
The comprehensive native interactome of a fully functional tagged prion protein
@ast
The comprehensive native interactome of a fully functional tagged prion protein
@en
prefLabel
The comprehensive native interactome of a fully functional tagged prion protein
@ast
The comprehensive native interactome of a fully functional tagged prion protein
@en
P2093
P2860
P1433
P1476
The comprehensive native interactome of a fully functional tagged prion protein
@en
P2093
Anna Maria Calella
Dorothea Rutishauser
Erich Brunner
Kirsten D Mertz
Thomas Rülicke
P2860
P356
10.1371/JOURNAL.PONE.0004446
P407
P577
2009-02-11T00:00:00Z