Results 11 to 20 of about 1,553,593 (211)

Exploration of the main sites for the transformation of normal prion protein (PrPC) into pathogenic prion protein (PrPsc)

open access: yesJournal of Veterinary Research, 2017
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
doaj   +2 more sources

Cellular Prion Protein (PrPC): Identification and Characterization of Novel Interacting Partners [PDF]

open access: yes, 2011
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
core   +4 more sources

PrPC has nucleic acid chaperoning properties similar to the nucleocapsid protein of HIV-1.

open access: yes, 2002
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
core   +8 more sources

The Cellular Prion Protein—ROCK Connection: Contribution to Neuronal Homeostasis and Neurodegenerative Diseases

open access: yesFrontiers in Cellular Neuroscience, 2021
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
doaj   +1 more source

Cellular prion protein (PrPC) in the development of Merlin-deficient tumours [PDF]

open access: yesOncogene, 2017
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
openaire   +3 more sources

Cellular Prion Protein (PrPc): Putative Interacting Partners and Consequences of the Interaction [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
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
openaire   +2 more sources

Prion protein PrPc interacts with molecular chaperones of the Hsp60 family [PDF]

open access: yesJournal of Virology, 1996
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
openaire   +2 more sources

The Multifaceted Functions of Prion Protein (PrPC) in Cancer

open access: yesCancers, 2023
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
openaire   +4 more sources

Cross-Linking Cellular Prion Protein Induces Neuronal Type 2-Like Hypersensitivity

open access: yesFrontiers in Immunology, 2021
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
doaj   +1 more source

Autophagy Activation Associates with Suppression of Prion Protein and Improved Mitochondrial Status in Glioblastoma Cells

open access: yesCells, 2023
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
doaj   +1 more source

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