Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein
Open Access
- 1 May 1996
- journal article
- Published by Elsevier
- Vol. 271 (21), 12661-12668
- https://doi.org/10.1074/jbc.271.21.12661
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Truncated Forms of the Human Prion Protein in Normal Brain and in Prion DiseasesJournal of Biological Chemistry, 1995
- Fatal Familial Insomnia and Familial Creutzfeldt‐Jakob Disease: Clinical, Pathological and Molecular FeaturesBrain Pathology, 1995
- Processing of a cellular prion protein: identification of N- and C-terminal cleavage sitesBiochemistry, 1993
- The Endoplasmic Reticulum as a Site of Protein DegradationPublished by Springer Nature ,1993
- Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA PolymorphismScience, 1992
- A PrP gene codon 178 base substitution and a 24‐bp interstitial deletion in familial Creutzfeldt‐Jakob diseaseNeurology, 1992
- Alteration in molecular structure which results in disease: the Met-30 variant of human plasma transthyretinBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1992
- In vitro expression in eukaryotic cells of a prion protein gene cloned from scrapie-infected mouse brain.Proceedings of the National Academy of Sciences, 1988
- Use of an Epstein-Barr virus episomal replicon for anti-sense RNA-mediated gene inhibition in a human cytotoxic T-cell clone.Proceedings of the National Academy of Sciences, 1988
- INHIBITORS OF THE BIOSYNTHESIS AND PROCESSING OF N-LINKED OLIGOSACCHARIDE CHAINSAnnual Review of Biochemistry, 1987