Báo cáo khoa học: Binding of N- and C-terminal anti-prion protein antibodies generates distinct phenotypes of cellular prion proteins (PrPC) obtained from human, sheep, cattle and mouse
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Prion diseases are neurodegenerative disorders which cause Creutzfeldt–Jakob disease in humans, scrapie in sheep and bovine spongiformencephalopathy in cattle. The infectious agent is a protease resistant iso-form (PrPSc) of a host encoded prion protein (PrPC). PrPScproteins arecharacterized according to size and glycoform pattern.
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Báo cáo khoa học: Binding of N- and C-terminal anti-prion protein antibodies generates distinct phenotypes of cellular prion proteins (PrPC) obtained from human, sheep, cattle and mouse
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Báo cáo khoa học: Binding of N- and C-terminal anti-prion protein antibodies generates distinct phenotypes of cellular prion proteins (PrPC) obtained from human, sheep, cattle and mouse
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