Prof. Giorgio Sartor

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HOME Anthropology Biochemistry of marine organisms Biomolecules Enzymes Membranes PROTEINS Biochemistry of pollutants Energy Lipids Metabolism Signal transduction Antifreeze proteins Bioluminescence Heat Shock Proteins Oxygen Transport Proteins p53 Protein Structure Protein Turnover PRIONS A closer look at prion strains - Characterization and important implications A naturally occurring variant of the human prion protein completely prevents prion disease An overview of human prion diseases Atomic structures of amyloid cross-beta spines reveal varied steric zippers Biology and Genetics of Prions Causing Neurodegeneration Competition between crystal and fibril formation in molecular mutations of amyloidogenic peptides Conformational conversion of prion protein in prion diseases Deadly Conformations - Protein Misfolding in Prion Disease Electron crystallography of the scrapie prion protein complexed with heavy metals Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism Evolutionary Implications of Metal Binding Features in Different Species’ Prion Protein: An Inorganic Point of View Fundamentals of prion biology and diseases From Kuru to Alzheimer: A personal outlook In Vitro Generation of Infectious Scrapie Prions Life cycle of cytosolic prions Mammalian Prion Biology: One Century of Evolving Concepts Molecular biology and pathogenesis of prion diseases Molecular Biology and Transgenetics of Prion Diseases On safari with PrP: prion diseases of animals Prion Diseases and the BSE Crisis Prion-Like Propagation of Protein Misfolding and Aggregation in Amyotrophic Lateral Sclerosis Prion diseases Prion protein and cancers Prion Protein Biology Prion protein oligomer and its neurotoxicity Prions (PNAS) Prions and Prion-like Proteins Prions: A model of conformational disease? Prions: so many fibers, so little infectivity Prions Protein aggregation as a paradigm of aging Protein aggregation kinetics, mechanism, and curve-fitting: A review of the literature Protein aggregation: Mechanisms and functional consequences Protein Misfolding and Prion Diseases Shattuck Lecture - Neurodegenrative Disease and Prions Structural and Dynamic Properties of the Human Prion Protein Structure-function aspects of prion proteins The changing face of kuru: a personal perspective The origin of the prion agent of kuru: molecular and biological strain typing The pathogenic mechanisms of prion diseases The prion protein family - Looking outside the central nervous system The Supramolecular Chemistry of β Sheets Transmissible Spongiform Enchephalithies in Humas Update on human prion disease Yeast Prions: Structure, Biology, and Prion-Handling Systems Archeology BIOCHEMISTRY Biology Chemistry Earth Sciences Medicine Physics Political Sciences Space Sciences Tools for sciences Books
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