Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference41 articles.
1. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease
2. The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive.
3. In vitro expression in eukaryotic cells of a prion protein gene cloned from scrapie-infected mouse brain.
4. Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells
5. Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells
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2. Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt–Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene;International Journal of Molecular Sciences;2022-12-02
3. Proteostasis unbalance in prion diseases: Mechanisms of neurodegeneration and therapeutic targets;Frontiers in Neuroscience;2022-09-06
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