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2010•Unpublished venueRequires access

Altered membrane distribution and increased Fyn activity in scrapie-infected neuronal cells

Hanna Gyllberg, Kajsa Löfgren Söderberg, Ana Carolina de Almeida, Katarina Bedecs

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Abstract

The suggested cause of Prion diseases is conversion of the cellular prion protein (PrPC) into aberrant scrapie prion protein (PrPSc) isoform triggered by the latter. PrPC is localized to membrane r ...

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What this paper is about

The suggested cause of Prion diseases is conversion of the cellular prion protein (PrPC) into aberrant scrapie prion protein (PrPSc) isoform triggered by the latter. PrPC is localized to membrane r ...

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Available abstract

The suggested cause of Prion diseases is conversion of the cellular prion protein (PrPC) into aberrant scrapie prion protein (PrPSc) isoform triggered by the latter. PrPC is localized to membrane r ...

Key concepts: Scrapie, Prion protein, Gene isoform, FYN, Cell biology, Virology, Biology, Chemistry

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