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注意：仅列出部分参考文献，下载原文获取全部文献信息。A Drug-Based Cellular Assay (DBCA) for studying cytotoxic and cytoprotective activities of the prion protein: A practical guide
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Cellular prion protein mediates impairment of synaptic plasticity by amyloid-β oligomers
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Prion protein attenuates excitotoxicity by inhibiting NMDA receptors
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Pathologic Prion Protein Infects Cells by Lipid-Raft Dependent Macropinocytosis
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Cellular prion protein interaction with vitronectin supports axonal growth and is compensated by integrins
Glaucia N. M. Hajj et al.
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Toward molecular dissection of PrPC-PrPSc interactions
Laura Solforosi et al.
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Lethal recessive myelin toxicity of prion protein lacking its central domain
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Aimin Li et al.
EMBO JOURNAL (2007)
Loss of the cellular prion protein affects the Ca2+ homeostasis in hippocampal CA1 neurons
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Clearance and prevention of prion infection in cell culture by anti-PrP antibodies
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EUROPEAN JOURNAL OF NEUROSCIENCE (2006)
Prion disease genetics
S Mead
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Q/R site editing controls kainate receptor inhibition by membrane fatty acids
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The aminoglycoside antibiotic dihydrostreptomycin rapidly enters mouse outer hair cells through the mechano-electrical transducer channels
W Marcotti et al.
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The AGAAAAGA palindrome in PrP is required to generate a productive PrPSc-PrPC complex that leads to prion propagation
EM Norstrom et al.
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Anchorless prion protein results in infectious amyloid disease without clinical scrapie
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Cytoplasmic and intra-nuclear binding of gentamicin does not require endocytosis
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A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease
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AC Apetri et al.
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Hippocampal synaptic plasticity in mice devoid of cellular prion protein
LE Maglio et al.
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Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis
G Mallucci et al.
SCIENCE (2003)
The mechanism of internalization of glycosylphosphatidylinositol-anchored prion protein
C Sunyach et al.
EMBO JOURNAL (2003)
Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Copper modulation of ion channels of PrP[106-126] mutant prion peptide fragments
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Monoclonal antibodies inhibit prion replication and delay the development of prion disease
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Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol
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Prion channel proteins and their role in vacuolation and neurodegenerative diseases
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Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection
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EMBO JOURNAL (2002)
Identification of the heparan sulfate binding sites in the cellular prion protein
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Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases
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Mutant prion proteins axe partially retained in the endoplasmic reticulum
L Ivanova et al.
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Prion protein affects Ca2+-activated K+ currents in cerebellar Purkinje cells
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Solution structure of the E200K variant of human prion protein -: Implications for the mechanism of pathogenesis in familial prion diseases
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