A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V
Open Access
- 1 February 2001
- journal article
- case report
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 276 (8), 6009-6015
- https://doi.org/10.1074/jbc.m007062200
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Neuropathology of Gerstmann‐Sträussler‐Scheinker diseaseMicroscopy Research and Technique, 2000
- A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic miceJournal of Molecular Biology, 2000
- Prion Protein AmyloidosisBrain Pathology, 1996
- Conformational Transformations in Peptides Containing Two Putative α-Helices of the Prion ProteinJournal of Molecular Biology, 1995
- Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein geneNature Genetics, 1992
- Unusual Topogenic Sequence Directs Prion Protein BiogenesisScience, 1990
- Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndromeBiochemical and Biophysical Research Communications, 1989
- Gerstmann‐Sträussler‐Scheinker disease: Immunohistological and experimental studiesAnnals of Neurology, 1988
- Evidence for a secretory form of the cellular prion proteinBiochemistry, 1987
- Über eine eigenartige hereditär- familiäre Erkrankung des ZentralnervensystemsZeitschrift für die gesamte Neurologie und Psychiatrie, 1954