Truncated Forms of the Human Prion Protein in Normal Brain and in Prion Diseases
Open Access
- 1 August 1995
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 270 (32), 19173-19180
- https://doi.org/10.1074/jbc.270.32.19173
Abstract
No abstract availableKeywords
This publication has 63 references indexed in Scilit:
- Soluble Amyloid β-Protein Is a Marker of Alzheimer Amyloid in Brain But Not in Cerebrospinal FluidBiochemical and Biophysical Research Communications, 1994
- Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencingBiochemistry, 1993
- Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchorGlycobiology, 1993
- Identification of glycoinositol phospholipid-linked and truncated forms of the scrapie prion proteinBiochemistry, 1990
- Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells.The Journal of cell biology, 1990
- Molecular pathology of scrapie‐associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapieEuropean Journal of Biochemistry, 1988
- Immunoreactivity of a Synthetic Pentadecapeptide Corresponding to the N-Terminal Region of the Scrapie Prion ProteinJournal of General Virology, 1986
- Human Prion Protein cDNA: Molecular Cloning, Chromosomal Mapping, and Biological ImplicationsScience, 1986
- High resolution two-dimensional electrophoresis of basic as well as acidic proteinsCell, 1977
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970