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Publications by Jean-Marie Warter
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
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Β-Amyloid 42; Prion Protein (PRNP; PrP; CD230)
Science-Business eXchange
Transmissibility of Gerstmann–Sträussler–Scheinker Syndrome in Rodent Models: New Insights Into the Molecular Underpinnings of Prion Infectivity
Prion
Biochemistry
Molecular Neuroscience
Infectious Diseases
Cell Biology
Cellular
Molecular Origin of Gerstmann-Sträussler-Scheinker Syndrome: Insight From Computer Simulation of an Amyloidogenic Prion Peptide
Biophysical Journal
Biophysics
Prion Protein (PrP) Synthetic Peptides Induce Cellular PrP to Acquire Properties of the Scrapie Isoform.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Deletion of N-Terminal Residues 23–88 From Prion Protein (PrP) Abrogates the Potential to Rescue PrP-deficient Mice From PrP-like Protein/Doppel-Induced Neurodegeneration
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Site-Specific Conformational Studies of Prion Protein (PrP) Amyloid Fibrils Revealed Two Cooperative Folding Domains Within Amyloid Structure
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Elucidation of the Molecular Basis of Abnormal Prion Protein (PrP) Formation in a Cell-Free System Using Baculovirus and Insect Cell-Derived Recombinant PrP
Yakugaku Zasshi
Pharmacology
Pharmaceutical Science
Knockdown of Prion Protein (PrP) by RNA Interference Weakens the Protective Activity of Wild-Type PrP Against Copper Ion and Antagonizes the Cytotoxicity of fCJD-associated PrP Mutants in Cultured Cells
International Journal of Molecular Medicine
Medicine
Genetics
The PrP-like Protein Doppel Binds Copper
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
