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  • Prion proteins are cellular membrane-bound glycoproteins. In the prevalent α-helix conformation called PrPC, they are common proteinaceous constituents of mammalian cells. However, if misfolded into the β-sheet conformation called PrPSc, they cause incurable and lethal neurodegenerative diseases (transmissible spongiform encephalopaties), referred to as scrapie, Creutzfeldt-Jakob disease, bovine spongiform encephalopathy etc. In general, prions are higly resistant to proteases and common sterilization procedures.
  • Prion proteins are cellular membrane-bound glycoproteins. In the prevalent α-helix conformation called PrPC, they are common proteinaceous constituents of mammalian cells. However, if misfolded into the β-sheet conformation called PrPSc, they cause incurable and lethal neurodegenerative diseases (transmissible spongiform encephalopaties), referred to as scrapie, Creutzfeldt-Jakob disease, bovine spongiform encephalopathy etc. In general, prions are higly resistant to proteases and common sterilization procedures. (en)
Title
  • Inactivation of prions using electrical DC discharges at atmospheric pressure and ambient temperature
  • Inactivation of prions using electrical DC discharges at atmospheric pressure and ambient temperature (en)
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  • Inactivation of prions using electrical DC discharges at atmospheric pressure and ambient temperature
  • Inactivation of prions using electrical DC discharges at atmospheric pressure and ambient temperature (en)
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  • RIV/68407700:21230/10:00176471!RIV13-MSM-21230___
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  • Scholtz, Vladimír
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  • RIV/68407700:21230/10:00176471
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  • discharge; prion (en)
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  • Scholtz, Vladimír
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  • 21230
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