Border-independent multi-functional, multi-hazard exposure modelling in Alpine regions
Pittore, M., Campalani, P., Renner, K., Plörer, M., Tagliavini, F.
Published in Natural hazards (Dordrecht) (01.11.2023)
Published in Natural hazards (Dordrecht) (01.11.2023)
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Differential overexpression of SERPINA3 in human prion diseases
Vanni, S., Moda, F., Zattoni, M., Bistaffa, E., De Cecco, E., Rossi, M., Giaccone, G., Tagliavini, F., Haïk, S., Deslys, J. P., Zanusso, G., Ironside, J. W., Ferrer, I., Kovacs, G. G., Legname, G.
Published in Scientific reports (15.11.2017)
Published in Scientific reports (15.11.2017)
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NIM811, a cyclophilin inhibitor without immunosuppressive activity, is beneficial in collagen VI congenital muscular dystrophy models
Zulian, Alessandra, Rizzo, Erika, Schiavone, Marco, Palma, Elena, Tagliavini, Francesca, Blaauw, Bert, Merlini, Luciano, Maraldi, Nadir Mario, Sabatelli, Patrizia, Braghetta, Paola, Bonaldo, Paolo, Argenton, Francesco, Bernardi, Paolo
Published in Human molecular genetics (15.10.2014)
Published in Human molecular genetics (15.10.2014)
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Defective collagen VI alpha 6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies
Tagliavini, F, Pellegrini, C, Sardone, F, Squarzoni, S, Paulsson, M, Wagener, R, Gualandi, F, Trabanelli, C, Ferlini, A, Merlini, L, Santi, S, Maraldi, N M, Faldini, C, Sabatelli, P
Published in Biochimica et biophysica acta (01.09.2014)
Published in Biochimica et biophysica acta (01.09.2014)
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Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies
Tagliavini, F., Pellegrini, C., Sardone, F., Squarzoni, S., Paulsson, M., Wagener, R., Gualandi, F., Trabanelli, C., Ferlini, A., Merlini, L., Santi, S., Maraldi, N.M., Faldini, C., Sabatelli, P.
Published in Biochimica et biophysica acta (01.09.2014)
Published in Biochimica et biophysica acta (01.09.2014)
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Evaluation of Quinacrine Treatment for Prion Diseases
Barret, A, Tagliavini, F, Forloni, G, Bate, C, Salmona, M, Colombo, L, De Luigi, A, Limido, L, Suardi, S, Rossi, G, Auvré, F, Adjou, K T, Salès, N, Williams, A, Lasmézas, C, Deslys, J P
Published in Journal of Virology (01.08.2003)
Published in Journal of Virology (01.08.2003)
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Multiple forms of PKR present in the nuclei of acute leukemia cells represent an active kinase that is responsive to stress
Blalock, W L, Bavelloni, A, Piazzi, M, Tagliavini, F, Faenza, I, Martelli, A M, Follo, M Y, Cocco, L
Published in Leukemia (01.02.2011)
Published in Leukemia (01.02.2011)
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Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein
DE GIOIA, L, SELVAGGINI, C, GHIBAUDI, E, DIOMEDE, L, BUGIANI, O, FORLONI, G, TAGLIAVINI, F, SALMONA, M
Published in The Journal of biological chemistry (18.03.1994)
Published in The Journal of biological chemistry (18.03.1994)
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Abandoned children and population genetics: the cases of Iggio and Tiola
Mazzoni, S., Nicolini, L., Tagliavini, F., Manfredini, M.
Published in Journal of Biological Research (15.11.2012)
Published in Journal of Biological Research (15.11.2012)
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Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP
Ghetti, Bernardino, Piccardo, Pedro, Spillantini, Maria Grazia, Ichimiya, Yousuke, Porro, Monica, Perini, Francesco, Kitamoto, Tetsuyuki, Tateishi, Jun, Seiler, Charles, Frangione, Blas, Bugiani, Orso, Giaccone, Giorgio, Prelli, Frances, Goedert, Michel, Dlouhy, Stephen R., Tagliavini, Fabrizio
Published in Proceedings of the National Academy of Sciences - PNAS (23.01.1996)
Published in Proceedings of the National Academy of Sciences - PNAS (23.01.1996)
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Abandoned children and population genetics: the cases of Iggio and Tiola
S. Mazzoni, L. Nicolini, F. Tagliavini, M. Manfredini
Published in Journal of Biological Research (01.01.2012)
Published in Journal of Biological Research (01.01.2012)
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Synthetic Peptides Homologous to Prion Protein Residues 106-147 Form Amyloid-Like Fibrils in vitro
Tagliavini, Fabrizio, Prelli, Frances, Verga, Laura, Giaccone, Giorgio, Sarma, Ragupathy, Gorevic, Peter, Ghetti, Bernardino, Passerini, Flavio, Ghibaudi, Elena, Forloni, Gianluigi, Salmona, Mario, Bugiani, Orso, Frangione, Blas
Published in Proceedings of the National Academy of Sciences - PNAS (15.10.1993)
Published in Proceedings of the National Academy of Sciences - PNAS (15.10.1993)
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Neurotoxicity of the Putative Transmembrane Domain of the Prion Protein
Haı̈k, S., Peyrin, J.M., Lins, L., Rosseneu, M.Y., Brasseur, R., Langeveld, J.P., Tagliavini, F., Deslys, J.P., Lasmézas, C., Dormont, D.
Published in Neurobiology of disease (01.12.2000)
Published in Neurobiology of disease (01.12.2000)
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Site investigation and modelling at "La Maina" landslide (Carnian Alps, Italy)
Marcato, G., Mantovani, M., Pasuto, A., Silvano, S., Tagliavini, F., Zabuski, L., Zannoni, A.
Published in Natural hazards and earth system sciences (01.01.2006)
Published in Natural hazards and earth system sciences (01.01.2006)
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Evaluation of seismic effects on the landslide deposits of Monte Salta (Eastern Italian Alps) using distinct element method
Marcato, G., Fujisawa, K., Mantovani, M., Pasuto, A., Silvano, S., Tagliavini, F., Zabuski, L.
Published in Natural hazards and earth system sciences (01.01.2007)
Published in Natural hazards and earth system sciences (01.01.2007)
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A novel phenotype of sporadic Creutzfeldt–Jakob disease
Giaccone, G, Di Fede, G, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2007)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2007)
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Amyloid protein of Gerstmann‐Sträussler‐Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N‐terminal glycine at codon 58
Tagliavini, F., Prelli, F., Ghiso, J., Bugiani, O., Serban, D., Prusiner, S. B., Farlow, M. R., Ghetti, B., Frangione, B.
Published in The EMBO journal (01.03.1991)
Published in The EMBO journal (01.03.1991)
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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
Del Dotto, Valentina, Ullah, Farid, Di Meo, Ivano, Magini, Pamela, Gusic, Mirjana, Maresca, Alessandra, Caporali, Leonardo, Palombo, Flavia, Tagliavini, Francesca, Baugh, Evan Harris, Macao, Bertil, Szilagyi, Zsolt, Peron, Camille, Gustafson, Margaret A, Khan, Kamal, La Morgia, Chiara, Barboni, Piero, Carbonelli, Michele, Valentino, Maria Lucia, Liguori, Rocco, Shashi, Vandana, Sullivan, Jennifer, Nagaraj, Shashi, El-Dairi, Mays, Iannaccone, Alessandro, Cutcutache, Ioana, Bertini, Enrico, Carrozzo, Rosalba, Emma, Francesco, Diomedi-Camassei, Francesca, Zanna, Claudia, Armstrong, Martin, Page, Matthew, Stong, Nicholas, Boesch, Sylvia, Kopajtich, Robert, Wortmann, Saskia, Sperl, Wolfgang, Davis, Erica E, Copeland, William C, Seri, Marco, Falkenberg, Maria, Prokisch, Holger, Katsanis, Nicholas, Tiranti, Valeria, Pippucci, Tommaso, Carelli, Valerio
Published in The Journal of clinical investigation (01.01.2020)
Published in The Journal of clinical investigation (01.01.2020)
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