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Intracellular accumulation of a mild-denatured monomer of the human PrP fragment 90-231, as possible mechanism of its neurotoxic effects.
Chiovitti K, Corsaro A, Thellung S, Villa V, Paludi D, D'Arrigo C, Russo C, Perico A, Ianieri A, Di Cola D, Vergara A, Aceto A, Florio T. Chiovitti K, et al. Among authors: paludi d, d arrigo c. J Neurochem. 2007 Dec;103(6):2597-609. doi: 10.1111/j.1471-4159.2007.04965.x. Epub 2007 Oct 18. J Neurochem. 2007. PMID: 17944873 Free article.
Contribution of two conserved glycine residues to fibrillogenesis of the 106-126 prion protein fragment. Evidence that a soluble variant of the 106-126 peptide is neurotoxic.
Florio T, Paludi D, Villa V, Principe DR, Corsaro A, Millo E, Damonte G, D'Arrigo C, Russo C, Schettini G, Aceto A. Florio T, et al. Among authors: paludi d, d arrigo c. J Neurochem. 2003 Apr;85(1):62-72. doi: 10.1046/j.1471-4159.2003.01664.x. J Neurochem. 2003. PMID: 12641727 Free article.
Identification of a conserved N-capping box important for the structural autonomy of the prion alpha 3-helix: the disease associated D202N mutation destabilizes the helical conformation.
Gallo M, Paludi D, Cicero DO, Chiovitti K, Millo E, Salis A, Damonte G, Corsaro A, Thellung S, Schettini G, Melino S, Florio T, Paci M, Aceto A. Gallo M, et al. Among authors: paludi d. Int J Immunopathol Pharmacol. 2005 Jan-Mar;18(1):95-112. doi: 10.1177/039463200501800111. Int J Immunopathol Pharmacol. 2005. PMID: 15698515 Free article.
33 results