DUGA, STEFANO

DUGA, STEFANO  

Dipartimento Scienze Biomediche  

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Titolo Data di pubblicazione Autore(i) File
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity Relationships 1-gen-2017 Straniero, V; Zanotto, C; Straniero, L; Casiraghi, A; Duga, S; Radaelli, A; De Giuli Morghen, C; Valoti, E
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 1-gen-2017 de Filippis, T; Gelmini, G; Paraboschi, E; Vigone, Mc; Di Frenna, M; Marelli, F; Bonomi, M; Cassio, A; Larizza, D; Moro, M; Radetti, G; Salerno, M; Ardissino, D; Weber, G; Gentilini, D; Guizzardi, F; Duga, S; Persani, L.
A new genetic mechanism for congenital afibrinogenemia: maternal uniparental isodisomy for chromosome 4 containing a 15-kb deletion in fibrinogen Aalpha-chain gene 1-gen-2004 Duga, S; Spena, S; Asselta, R; Peyandi, F; Mahasandana, C; Malcovati, M; Mannucci, Pm; Tenchini, Ml
A novel 15-kb deletion involving fibrinogen Aalpha-chain gene causes congenital afibrinogenemia as a consequence of uniparental isodisomy of chromosome 4 1-gen-2004 Spena, S; Asselta, R; Duga, S; Monaldini, L; Malcovati, M; Mannucci, Pm; Tenchini, Ml
A novel mechanism for congenital afibrinogenemia based on pseudoexon activation in the fibrinogen gamma-chain gene 1-gen-2007 Spena, S; Asselta, R; Platè, M; Castaman, G; Duga, S; Tenchini, Ml
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 1-gen-2020 Asselta, Rosanna; Paraboschi, Elvezia Maria; Mantovani, Alberto; Duga, Stefano
Afibrinogenemia congenita: l’identificazione di una mutazione missense nell’esone 7 del gene per il beta fibrinogeno suggerisce un ruolo del D-domain nell’assemblaggio della proteina 1-gen-1999 Asselta, R; Duga, S; Simonic, T; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml
Afibrinogenemia congenita: nuova mutazione nel gene per la catena Bbeta del fibrinogeno che causa ritenzione intracellulare della molecola 1-gen-2002 Spena, S; Duga, Stefano; Asselta, Rosanna; Malcovati, M; Tenchini, Ml
Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation 1-gen-2000 Asselta, R; Duga, S; Simonic, T; Malcovati, M; Santagostino, E; Giangrande, Pl; Mannucci, Pm; Tenchini, Ml
Afibrinogenemia: identificazione di cinque nuove mutazioni nel gene FGB 1-gen-2001 Spena, S; Duga, Stefano; Asselta, Rosanna; Malcovati, M; Tenchini, Ml
Afibrinogenemia: un possibile modello per lo studio dei meccanismi responsabili del controllo della sintesi, dell'assemblaggio e della secrezione del fibrinogeno nella specie umana 1-gen-1999 Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality 1-gen-2021 Nakanishi, Tomoko; Pigazzini, Sara; Degenhardt, Frauke; Cordioli, Mattia; Butler-Laporte, Guillaume; Maya-Miles, Douglas; Bujanda, Luis; Bouysran, Youssef; Niemi, Mari Ek; Palom, Adriana; Ellinghaus, David; Khan, Atlas; Martínez-Bueno, Manuel; Rolker, Selina; Amitrano, Sara; Roade Tato, Luisa; Fava, Francesca; Spinner, Christoph D; Prati, Daniele; Bernardo, David; Garcia, Federico; Darcis, Gilles; Fernández-Cadenas, Israel; Holter, Jan Cato; Banales, Jesus M; Frithiof, Robert; Kiryluk, Krzysztof; Duga, Stefano; Asselta, Rosanna; Pereira, Alexandre C; Romero-Gómez, Manuel; Nafría-Jiménez, Beatriz; Hov, Johannes R; Migeotte, Isabelle; Renieri, Alessandra; Planas, Anna M; Ludwig, Kerstin U; Buti, Maria; Rahmouni, Souad; Alarcón-Riquelme, Marta E; Schulte, Eva C; Franke, Andre; Karlsen, Tom H; Valenti, Luca; Zeberg, Hugo; Richards, J Brent; Ganna, Andrea
Allelic heterogeneity of severe factor V deficiency 1-gen-2001 Montefusco, Mc; Duga, S; Asselta, R; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Allelic heterogeneity of severe factor V deficiency: doubling of the mutational spectrum of the factor V gene, and expression of the identified mutations 1-gen-2003 Asselta, R; Montefusco, Mc; Duga, S; Peyvandi, F; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 1-gen-2017 Chiereghin, C; Robusto, M; Mastrangelo, A; Castorina, P; Montini, G; Giani, M; Duga, S; Asselta, R; Solda, G
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function 1-gen-2018 de Majo, M; Topp, Sd; Smith, Bn; Nishimura, Al; Chen, Hj; Gkazi, As; Miller, J; Wong, Ch; Vance, C; Baas, F; Ten Asbroek, Alma; Kenna, Kp; Ticozzi, N; Redondo, Ag; Esteban-Pérez, J; Tiloca, C; Verde, F; Duga, S; Morrison, Ke; Shaw, Pj; Kirby, J; Turner, Mr; Talbot, K; Hardiman, O; Glass, Jd; de Belleroche, J; Gellera, C; Ratti, A; Al-Chalabi, A; Brown, Rh; Silani, V; Landers, Je; Shaw, Ce
Alterations of mRNA processing and stability as pathogenic mechanism in von willebrand factor quantitative deficiencies 1-gen-2010 Castaman, G; Plate', M; Giacomelli, Sh; Rodeghiero, F; Duga, S
Alternative splicing and nonsense-mediated decay in the F5 gene 1-gen-2007 Dall’Osso, C; Duga, S; Locatelli, N; Peyvandi, F; Tenchini, Ml; Asselta, R
Analisi dei siti di risposta all’interleuchina 6 nel promotore del gene della catena gamma del fibrinogeno umano 1-gen-1998 Asselta, R; Duga, S; Malcovati, M; Tenchini, Ml
Analisi genetico-molecolare della carenza grave di fattore XI della coagulazione in pazienti italiani 1-gen-2003 Zadra, G; Duga, Stefano; Asselta, Rosanna; Malcovati, M; Tenchini, Ml