" /> PrPSc proteins - CISMeF





Preferred Label : PrPSc proteins;

MeSH definition : Abnormal isoform of prion proteins (PRIONS) resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).; Abnormal isoform of PRION PROTEINS resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).;

MeSH synonym : scrapie prp 33-35; prp-res; prp res; sp 33-35; scrapie prp; prp 33-35;

MeSH hyponym : PrP (CJD); PrP (GSS); scrapie HaSp33-37 protein; HaSp 33-37;

Related MeSH term : scrapie agent; Scrapie Virus;

MeSH annotation : prion proteins; PrPSc stands for PRion Protein SCrapie; do not confuse with PRPC PROTEINS; /pathogen permitted; DF: PRPSC; PrPSc stands for PRion Protein SCrapie; do not confuse with PRPC PROTEINS;

Is substance : O;

Détails


Position du mot-clé dans l'(les) arborescence(s) : arborescence

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Abnormal isoform of prion proteins (PRIONS) resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).
Abnormal isoform of PRION PROTEINS resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).

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27/07/2025


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