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Titolo Data di pubblicazione Autore(i) File
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy 1-gen-2002 Duga, S; Asselta, R; Bonati, Mt; Malcovati, M; Dalpra, L; Oldani, A; Zucconi, M; Ferinistrambi, L; Tenchini, Ml
Mutational analysis of PRKAR1A and Gs alpha in sporadic adrenocortical tumors 1-gen-2005 Libe, R; Mantovani, G; Bondioni, S; Lania, A; Pedroni, C; Beck-Peccoz, P; Spada, A
A mutational chip to detect TP53, CDKN2A and FAT1 mutations in circulating cell free-DNA of head and neck squamous cell carcinoma patients:a pilot study 1-gen-2019 Ganci, F.; Spinella, F.; Cottone, G.; Cotroneo, E.; Nuccitelli, A.; Biroccio, A.; Sacconi, A.; Manciocco, V.; Pallocca, M.; Rollo, F.; Covello, R.; Benevolo, M.; Spriano, G; Fiorentino, F.; Blandino, G.
Mutational Diversity of Lung Cancer and Associated Lymph Nodes. An Exploratory Prospective Study of 4 Resected cIIIA-N2 1-gen-2019 Legras, Antoine; Roussel, Hélène; Mangiameli, Giuseppe; Arame, Alex; Grand, Bertrand; Pricopi, Ciprian; Badia, Alain; Gibault, Laure; Badoual, Cécile; Fabre, Elizabeth; Laurent-Puig, Pierre; Blons, Hélène; Le Pimpec-Barthes, Françoise
Mutational profile of epithelial, non-glandular sinonasal cancers into 2 prospective clinical trials 1-gen-2019 De, Cecco; Serafini, ; M., S.; Canevari, ; Penso, ; Nicolai, ; Castelnuovo, ; Benazzo, ; Sponghini, ; Orlandi, ; Vischioni, ; Piazza, ; Resteghini, C; Licitra, ; Bossi,
Mutational Profile of Malignant Pleural Mesothelioma (MPM) in the Phase II RAMES Study 1-gen-2020 Pagano, Maria; Ceresoli, Luca Giovanni; Zucali, Paolo Andrea; Pasello, Giulia; Garassino, Marina; Grosso, Federica; Tiseo, Marcello; Soto Parra, Hector; Zanelli, Francesca; Cappuzzo, Federico; Grossi, Francesco; De Marinis, Filippo; Pedrazzoli, Paolo; Gnoni, Roberta; Bonelli, Candida; Torricelli, Federica; Ciarrocchi, Alessia; Normanno, Nicola; Pinto, Carmine
Mutational profile of ZBTB16-RARA-positive acute myeloid leukemia 1-gen-2021 Fabiani, Emiliano; Cicconi, Laura; Nardozza, Anna Maria; Cristiano, Antonio; Rossi, Marianna; Ottone, Tiziana; Falconi, Giulia; Divona, Mariadomenica; Testi, Anna Maria; Annibali, Ombretta; Castelli, Roberto; Lazarevic, Vladimir; Rego, Eduardo; Montesinos, Pau; Esteve, Jordi; Venditti, Adriano; Della Porta, Matteo; Arcese, William; Lo-Coco, Francesco; Voso, Maria Teresa
Mutational screening and functional analyses in the zebrafish model of GIGYF2 as a candidate gene for Parkinson disease 1-gen-2011 Guella, I; Pistocchi, A; Asselta, R; Rimoldi, V; Ghilardi, A; Sironi, F; Trotta, L; Primignani, P; Zini, M; Zecchinelli, A; Coviello, D; Pezzoli, G; Del Giacco, L; Duga, S; Goldwurm, S.
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene 1-gen-2009 Guella, I; Pistocchi, A; Asselta, R; Rimoldi, V; Ghilardi, A; Sironi, F; Trotta, L; Primignani, P; Zini, M; Zecchinelli, A; Coviello, D; Pezzoli, G; Del Giacco, L; Duga, S; Goldwurm, S
Mutational screening of 25 unrelated FV-deficient patients from six countries 1-gen-2009 Guella, I.; Paraboschi, E.; Duga, S.; Peyvandi, F.; Gemmati, D.; Ciavarella, N.; Mannucci, P. M.; Asselta, R.
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects 1-gen-2007 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml
Mutations causing premature termination codons in the Von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay 1-gen-2009 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mutations in disguise 1-gen-2011 Duga, S; Asselta, R
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis 1-gen-2017 Smith, Bn; Topp, Sd; Fallini, C; Shibata, H; Chen, Hj; Troakes, C; King, A; Ticozzi, N; Kenna, Kp; Soragia-Gkazi, A; Miller, Jw; Sato, A; Dias, Dm; Jeon, M; Vance, C; Wong, Ch; de Majo, M; Kattuah, W; Mitchell, Jc; Scotter, El; Parkin, Nw; Sapp, Pc; Nolan, M; Nestor, Pj; Simpson, M; Weale, M; Lek, M; Baas, F; de Jong, Jmv; ten Asbroek, Alma; Redondo, Ag; Esteban-Perez, J; Tiloca, C; Verde, F; Duga, S; Leigh, N; Pall, H; Morrison, Ke; Al-Chalabi, A; Shaw, Pj; Kirby, J; Turner, Mr; Talbot, K; Hardiman, O; Glass, Jd; de Belleroche, J; Maki, M; Moss, Se; Miller, C; Gellera, C; Ratti, A; Al-Sarraj, S; Brown, Rh; Silani, V; Landers, Je; Shaw, Ce
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with allele-specific mRNAs decay 1-gen-2008 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with the decay of the mutant mRNAs 1-gen-2008 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mutations targeting the coagulation pathway are enriched in brain metastases 1-gen-2017 Richichi, C.; Fornasari, L.; Melloni, G. E. M.; Brescia, P.; Patanã, M.; DEL BENE, M.; Mustafa, D. A. M.; Kros, J. M.; Pollo, B.; Pruneri, G.; Sciandivasci, A.; Munzone, E.; Di Meco, F.; Pelicci, P. G.; Riva, L.; Pelicci, G.
Mutual epithelium-macrophage dependency in liver carcinogenesis mediated by ST18 1-gen-2017 Ravà, Micol; D'Andrea, Aleco; Doni, Mirko; Kress, Theresia R.; Ostuni, Renato; Bianchi, Valerio; Morelli, Marco J.; Collino, Agnese; Ghisletti, Serena; Nicoli, Paola; Recordati, Camilla; Iascone, Maria; Sonzogni, Aurelio; D'Antiga, Lorenzo; Shukla, Ruchi; Faulkner, Geoffrey J.; Natoli, Gioacchino; Campaner, Stefano; Amati, Bruno
Mutually exclusive redox forms of HMGB1 promote cell recruitment or proinflammatory cytokine release 1-gen-2012 Venereau, E; Casalgrandi, M; Schiraldi, M; Antoine, Dj; Cattaneo, A; De Marchis, F; Liu, J; Antonelli, A; Preti, A; Raeli, L; Shams, Ss; Yang, H; Varani, L; Andersson, U; Tracey, Kj; Bachi, A; Uguccioni, M; Bianchi, Me
Myasthenia gravis and thymectomy: Many doubts and few certainties 1-gen-2015 Marulli, Giuseppe; Rea, Federico
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