Search Results - "Vetrugno, Vito"
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Trapping Prion Protein in the Endoplasmic Reticulum Impairs PrPC Maturation and Prevents PrPSc Accumulation
Published in The Journal of biological chemistry (07-01-2005)“…The conversion of the normal cellular prion protein (PrPC) into the abnormal scrapie isoform (PrPSc) is a key feature of prion diseases. The pathogenic…”
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Accumulation and aberrant composition of cholesteryl esters in Scrapie-infected N2a cells and C57BL/6 mouse brains
Published in Lipids in health and disease (04-08-2011)“…Cholesterol changes have been described in prion-cell models and in experimental rodent scrapie; yet, the pattern of this association is still controversial…”
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Transmission of sporadic Creutzfeldt-Jakob disease by blood transfusion: risk factor or possible biases
Published in Transfusion (Philadelphia, Pa.) (01-07-2011)“…BACKGROUND: The occurrence of transfusion transmissions of variant Creutzfeldt‐Jakob disease (CJD) cases has reawakened attention to the possible similar risk…”
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Scrapie infectivity is quickly cleared in tissues of orally-infected farmed fish
Published in BMC veterinary research (15-06-2006)“…Scrapie and bovine spongiform encephalopathy (BSE) belongs to the group of animal transmissible spongiform encephalopathy (TSE). BSE epidemic in the UK and…”
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Safety of milk and milk derivatives in relation to BSE: the lactoferrin example
Published in Biometals (01-06-2004)“…Bovine Spongiform Encephalopathy (BSE) belongs to Transmissible Spongiform Encephalopathies (TSEs) or Prion diseases. BSE is a feed borne infection of cattle…”
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Management of notifications of donors with Creutzfeldt-Jakob disease (post-donation information)
Published in Blood transfusion = Trasfusione del sangue (01-01-2014)Get full text
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Oral pravastatin prolongs survival time of scrapie-infected mice
Published in Journal of general virology (01-07-2009)“…Statins are potent inhibitors of HMG–CoA (3-hydroxy-3-methylglutaryl coenzyme A) reductase in the cholesterol-biosynthesis pathway. They are either lipophilic…”
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KDEL-tagged anti-prion intrabodies impair PrP lysosomal degradation and inhibit scrapie infectivity
Published in Biochemical and biophysical research communications (30-12-2005)“…Transmissible spongiform encephalopathy or prion diseases are fatal neurodegenerative disorders characterized by the conversion of the cellular prion protein…”
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Regulation of intrinsic prion protein by growth factors and tnf-α: the role of intracellular reactive oxygen species
Published in Free radical biology & medicine (15-09-2003)“…Function and regulation of the intrinsic prion protein (PrP c) are largely unknown. In the present study the regulation of PrP c expression by growth factors…”
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Molecular diagnostics of transmissible spongiform encephalopathies
Published in Trends in Molecular Medicine (01-06-2002)“…Clinical criteria for the diagnosis of sporadic, iatrogenic and variant Creutzfeldt–Jakob diseases are now available and show an excellent sensitivity and…”
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Expression of wild-type and V210I mutant prion protein in human neuroblastoma cells
Published in Neuroscience letters (23-07-1999)“…The conversion of the host-encoded prion protein (PrPc) into the insoluble, protease-resistant isoform (PrPsc) is the main pathogenic mechanism of…”
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