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The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone development

Splenic marginal zone lymphoma (SMZL) is a B cell malignancy of unknown pathogenesis, and thus an orphan of targeted therapies. By integrating whole-exome sequencing and copy-number analysis, we show that the SMZL exome carries at least 30 nonsilent gene alterations. Mutations in NOTCH2, a gene requ...

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Autors principals: Rossi, Davide, Trifonov, Vladimir, Fangazio, Marco, Bruscaggin, Alessio, Rasi, Silvia, Spina, Valeria, Monti, Sara, Vaisitti, Tiziana, Arruga, Francesca, Famà, Rosella, Ciardullo, Carmela, Greco, Mariangela, Cresta, Stefania, Piranda, Daniela, Holmes, Antony, Fabbri, Giulia, Messina, Monica, Rinaldi, Andrea, Wang, Jiguang, Agostinelli, Claudio, Piccaluga, Pier Paolo, Lucioni, Marco, Tabbò, Fabrizio, Serra, Roberto, Franceschetti, Silvia, Deambrogi, Clara, Daniele, Giulia, Gattei, Valter, Marasca, Roberto, Facchetti, Fabio, Arcaini, Luca, Inghirami, Giorgio, Bertoni, Francesco, Pileri, Stefano A., Deaglio, Silvia, Foà, Robin, Dalla-Favera, Riccardo, Pasqualucci, Laura, Rabadan, Raul, Gaidano, Gianluca
Format: Artigo
Idioma:Inglês
Publicat: The Rockefeller University Press 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3428941/
https://ncbi.nlm.nih.gov/pubmed/22891273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1084/jem.20120904
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