Matches in Nanopublications for { ?s ?p "[Accumulation of an isoform of protease-resistant PrP fragment in FFI distinct from that found in a familial form of Creutzfeldt-Jakob disease with the same D178N mutation, shows the effect of the polymorphism at codon 129 of PRNP on phenotypic expression and the possibility of distinct prion strains with diverse pathological potential.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP401120.RAizsg7sb62xKNKqFmQvgdkLgsw2RkX4UwZhwL0tUXf4U130_assertion description "[Accumulation of an isoform of protease-resistant PrP fragment in FFI distinct from that found in a familial form of Creutzfeldt-Jakob disease with the same D178N mutation, shows the effect of the polymorphism at codon 129 of PRNP on phenotypic expression and the possibility of distinct prion strains with diverse pathological potential.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401120.RAizsg7sb62xKNKqFmQvgdkLgsw2RkX4UwZhwL0tUXf4U130_provenance.
- NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_assertion description "[Accumulation of an isoform of protease-resistant PrP fragment in FFI distinct from that found in a familial form of Creutzfeldt-Jakob disease with the same D178N mutation, shows the effect of the polymorphism at codon 129 of PRNP on phenotypic expression and the possibility of distinct prion strains with diverse pathological potential.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_provenance.