NBS1 Heterozygosity and Cancer Risk

Por di Masi, Alessandra, Antoccia, Antonio
Publicado em 2008

NBN Gene Polymorphisms and Cancer Susceptibility: A Systemic Review

Por Berardinelli, Francesco, di Masi, Alessandra, Antoccia, Antonio
Publicado em 2013

Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report

Por Folgori, Laura, Scarselli, Alessia, Angelino, Giulia, Ferrari, Francesca, Antoccia, Antonio, Chessa, Luciana, Finocchi, Andrea
Publicado em 2010

Genotoxicity Induced by Foetal and Infant Exposure to Magnetic Fields and Modulation of Ionising Radiation Effects

Por Udroiu, Ion, Antoccia, Antonio, Tanzarella, Caterina, Giuliani, Livio, Pacchierotti, Francesca, Cordelli, Eugenia, Eleuteri, Patrizia, Villani, Paola, Sgura, Antonella
Publicado no PLoS One (2015)

Identification of the Interactors of Human Nibrin (NBN) and of Its 26 kDa and 70 kDa Fragments Arising from the NBN 657del5 Founder Mutation

Por Cilli, Domenica, Mirasole, Cristiana, Pennisi, Rosa, Pallotta, Valeria, D'Alessandro, Angelo, Antoccia, Antonio, Zolla, Lello, Ascenzi, Paolo, di Masi, Alessandra
Publicado no PLoS One (2014)

Altered microRNA Expression Patterns in Hepatoblastoma Patients

Por Magrelli, Armando, Azzalin, Gianluca, Salvatore, Marco, Viganotti, Mara, Tosto, Fabrizio, Colombo, Teresa, Devito, Rita, Di Masi, Alessandra, Antoccia, Antonio, Lorenzetti, Stefano, Maranghi, Francesca, Mantovani, Alberto, Tanzarella, Caterina, Macino, Giuseppe, Taruscio, Domenica
Publicado em 2009

Selective killing of p53-deficient cancer cells by SP600125

Por Jemaà, Mohamed, Vitale, Ilio, Kepp, Oliver, Berardinelli, Francesco, Galluzzi, Lorenzo, Senovilla, Laura, Mariño, Guillermo, Malik, Shoaib Ahmad, Rello-Varona, Santiago, Lissa, Delphine, Antoccia, Antonio, Tailler, Maximilien, Schlemmer, Frederic, Harper, Francis, Pierron, Gérard, Castedo, Maria, Kroemer, Guido
Publicado em 2012

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

Por D’Apice, Maria Rosaria, Novelli, Antonio, di Masi, Alessandra, Biancolella, Michela, Antoccia, Antonio, Gullotta, Francesca, Licata, Norma, Minella, Daniela, Testa, Barbara, Nardone, Anna Maria, Palmieri, Giampiero, Calabrese, Emma, Biancone, Livia, Tanzarella, Caterina, Frontali, Marina, Sangiuolo, Federica, Novelli, Giuseppe, Pallone, Francesco
Publicado no BMC Med Genet (2015)