Related references
Note: Only part of the references are listed.A Drug-Based Cellular Assay (DBCA) for studying cytotoxic and cytoprotective activities of the prion protein: A practical guide
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The hydrophobic core region governs mutant prion protein aggregation and intracellular retention
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A deleted prion protein that is neurotoxic in vivo is localized normally in cultured cells
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PLOS ONE (2009)
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PLOS ONE (2009)
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Prion protein attenuates excitotoxicity by inhibiting NMDA receptors
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JOURNAL OF CELL BIOLOGY (2008)
Pathologic Prion Protein Infects Cells by Lipid-Raft Dependent Macropinocytosis
Jehangir S. Wadia et al.
PLOS ONE (2008)
Cellular prion protein interaction with vitronectin supports axonal growth and is compensated by integrins
Glaucia N. M. Hajj et al.
JOURNAL OF CELL SCIENCE (2007)
Toward molecular dissection of PrPC-PrPSc interactions
Laura Solforosi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Lethal recessive myelin toxicity of prion protein lacking its central domain
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EMBO JOURNAL (2007)
Neonatal lethality in transgenic mice expressing prion protein with a deletion of residues 105-125
Aimin Li et al.
EMBO JOURNAL (2007)
Loss of the cellular prion protein affects the Ca2+ homeostasis in hippocampal CA1 neurons
Martin Fuhrmann et al.
JOURNAL OF NEUROCHEMISTRY (2006)
Gap junctions and connexon hemichannels in human embryonic stem cells
James E. Huettner et al.
STEM CELLS (2006)
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
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Q/R site editing controls kainate receptor inhibition by membrane fatty acids
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JOURNAL OF NEUROSCIENCE (2005)
The aminoglycoside antibiotic dihydrostreptomycin rapidly enters mouse outer hair cells through the mechano-electrical transducer channels
W Marcotti et al.
JOURNAL OF PHYSIOLOGY-LONDON (2005)
The AGAAAAGA palindrome in PrP is required to generate a productive PrPSc-PrPC complex that leads to prion propagation
EM Norstrom et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Anchorless prion protein results in infectious amyloid disease without clinical scrapie
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SCIENCE (2005)
Cytoplasmic and intra-nuclear binding of gentamicin does not require endocytosis
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HEARING RESEARCH (2005)
TRPV1 regulators mediate gentamicin penetration of cultured kidney cells
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HEARING RESEARCH (2005)
A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease
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Treatment of transmissible spongiform encephalopathy by intraventricular drug infusion in animal models
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JOURNAL OF VIROLOGY (2004)
The effect of disease-associated mutations on the folding pathway of human prion protein
AC Apetri et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Hippocampal synaptic plasticity in mice devoid of cellular prion protein
LE Maglio et al.
MOLECULAR BRAIN RESEARCH (2004)
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
B Drisaldi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Copper modulation of ion channels of PrP[106-126] mutant prion peptide fragments
JI Kourie et al.
JOURNAL OF MEMBRANE BIOLOGY (2003)
Monoclonal antibodies inhibit prion replication and delay the development of prion disease
AR White et al.
NATURE (2003)
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol
JY Ma et al.
SCIENCE (2002)
Prion channel proteins and their role in vacuolation and neurodegenerative diseases
JI Kourie
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS (2002)
Differential sorting and fate of endocytosed GPI-anchored proteins
M Fivaz et al.
EMBO JOURNAL (2002)
Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection
SM Zanata et al.
EMBO JOURNAL (2002)
Identification of the heparan sulfate binding sites in the cellular prion protein
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JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases
H Lorenz et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Mutant prion proteins axe partially retained in the endoplasmic reticulum
L Ivanova et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Crystal structure of the human prion protein reveals a mechanism for oligomerization
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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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JOURNAL OF BIOLOGICAL CHEMISTRY (2000)