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Introduction: The functions and mechanisms of prion proteins (PrPC) are currently unknown, but most experts believe that deformed or pathogenic prion proteins (PrPSc) originate from PrPC, and that there may be plural main sites for the conversion of ...
Liu Xi-Lin +9 more
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Cellular Prion Protein (PrPC): Identification and Characterization of Novel Interacting Partners [PDF]
The cellular prion protein (PrPC) is highly conserved throughout the evolution of mammals. (What does this sentence mean? What do you mean by ``conserved´´? This protein was higly conserved during the evolution
Zafar, Saima
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PrPC has nucleic acid chaperoning properties similar to the nucleocapsid protein of HIV-1.
International audienceThe function of the cellular prion protein (PrPC) remains obscure. Studies suggest that PrPC functions in several processes including signal transduction and Cu2+ metabolism.
Gabus, Caroline +10 more
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Amyloid-based neurodegenerative diseases such as prion, Alzheimer's, and Parkinson's diseases have distinct etiologies and clinical manifestations, but they share common pathological events.
Benoit Schneider +17 more
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Cellular prion protein (PrPC) in the development of Merlin-deficient tumours [PDF]
Loss of function mutations in the neurofibromatosis Type 2 (NF2) gene, coding for a tumour suppressor, Merlin, cause multiple tumours of the nervous system such as schwannomas, meningiomas and ependymomas. These tumours may occur sporadically or as part of the hereditary condition neurofibromatosis Type 2 (NF2). Current treatment is confined to (radio)
Provenzano, L +9 more
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Cellular Prion Protein (PrPc): Putative Interacting Partners and Consequences of the Interaction [PDF]
Cellular prion protein (PrPc) is a small glycosylphosphatidylinositol (GPI) anchored protein most abundantly found in the outer leaflet of the plasma membrane (PM) in the central nervous system (CNS). PrPc misfolding causes neurodegenerative prion diseases in the CNS.
Hajar Miranzadeh Mahabadi +1 more
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Prion protein PrPc interacts with molecular chaperones of the Hsp60 family [PDF]
Prions mediate the pathogenesis of certain neurodegenerative diseases, including bovine spongiform encephalopathy in cattle and Creutzfeldt-Jakob disease in humans. The prion particle consists mainly, if not entirely, of PrPSc, a posttranslationally modified isoform of the cellular host-encoded prion protein (PrPc).
F, Edenhofer +5 more
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The Multifaceted Functions of Prion Protein (PrPC) in Cancer
The cellular prion protein (PrPC) is a glycoprotein anchored to the cell surface by glycosylphosphatidylinositol (GPI). PrPC is expressed both in the brain and in peripheral tissues. Investigations on PrPC’s functions revealed its direct involvement in neurodegenerative and prion diseases, as well as in various physiological processes such as anti ...
Roland Abi Nahed +9 more
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Cross-Linking Cellular Prion Protein Induces Neuronal Type 2-Like Hypersensitivity
BackgroundPrevious reports identified proteins associated with ‘apoptosis’ following cross-linking PrPC with motif-specific anti-PrP antibodies in vivo and in vitro.
Utpal Kumar Adhikari +18 more
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Cells from glioblastoma multiforme (GBM) feature up-regulation of the mechanistic Target of Rapamycin (mTOR), which brings deleterious effects on malignancy and disease course.
Paola Lenzi +11 more
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