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Article

Generation of monoclonal antibodies against human prion proteins in PrP0/0 mice.

Molecular medicine (Cambridge, Mass.) - 1 Nov 1996

Krasemann S, Groschup M H, Harmeyer S, Hunsmann G, Bodemer W

Abstract excerpt

BACKGROUND: Prion diseases belong to a group of neurodegenerative disorders affecting humans and animals. The human diseases include kuru, Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker syndrome (GSS), and fatal familial insomnia (FFI). The pathogenic mechanisms of the prion diseases are not yet understood. Monoclonal antibodies provide valuable tools in the diagnosis, as well as in the basic...

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Topics

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Share to Antibodies, Monoclonal
Share to Blotting, Western
Share to Cells, Cultured

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cloning, Molecular

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Source

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Identifiers

PMID: 8972487
PMCID: PMC2230140

Genes

GSS
PRNP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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