ASSELTA, ROSANNA

ASSELTA, ROSANNA  

Dipartimento Scienze Biomediche  

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A functional variant in ERAP1 predisposes to multiple sclerosis 1-gen-2012 Guerini, Fr; Cagliani, R; Forni, D; Agliardi, C; Caputo, D; Cassinotti, A; Galimberti, D; Fenoglio, C; Biasin, M; Asselta, R; Scarpini, E; Comi, Gp; Bresolin, N; Clerici, M; Sironi, M
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 in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family 1-gen-2009 Song, J; Guella, I; KWON K., Y; Cho, H; Park, R; Asselta, R; CHOI J., R
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
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 1-gen-2020 Benetti, Elisa; Tita, Rossella; Spiga, Ottavia; Ciolfi, Andrea; Birolo, Giovanni; Bruselles, Alessandro; Doddato, Gabriella; Giliberti, Annarita; Marconi, Caterina; Musacchia, Francesco; Pippucci, Tommaso; Torella, Annalaura; Trezza, Alfonso; Valentino, Floriana; Baldassarri, Margherita; Brusco, Alfredo; Asselta, Rosanna; Bruttini, Mirella; Furini, Simone; Seri, Marco; Nigro, Vincenzo; Matullo, Giuseppe; Tartaglia, Marco; Mari, Francesca; Renieri, Alessandra; Pinto, Anna Maria
Activation of NF-kappaB by IL-1beta blocks IL-6-induced sustained STAT3 activation and STAT3-dependent gene expression of the human gamma-fibrinogen gene 1-gen-2007 Albrecht, U; Yang, X; Asselta, R; Keitel, V; Tenchini, Ml; Ludwig, S; Heinrich, Pc; Haussinger, D; Schaper, F; Bode, Jg
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
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
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate 1-gen-2015 Quadri, M; Yang, X; Cossu, G; Olgiati, S; Saddi, Vm; Breedveld, Gj; Ouyang, L; Hu, J; Xu, N; Graafland, J; Ricchi, V; Murgia, D; Guedes, Lc; Mariani, C; Marti, Mj; Tarantino, P; Asselta, R; Valldeoriola, F; Gagliardi, M; Pezzoli, G; Ezquerra, M; Quattrone, A; Ferreira, J; Annesi, G; Goldwurm, S; Tolosa, E; Oostra, Ba; Melis, M; Wang, J; Bonifati, V
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