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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1038/leu.2014.184</dc:identifier><dc:language>eng</dc:language><dc:creator>Fernández-Rodríguez, C</dc:creator><dc:creator>Bellosillo, B</dc:creator><dc:creator>García-García, M</dc:creator><dc:creator>Sánchez-González, B</dc:creator><dc:creator>Gimeno, E</dc:creator><dc:creator>Vela, M C</dc:creator><dc:creator>Serrano, S</dc:creator><dc:creator>Besses, C</dc:creator><dc:creator>Salar, A</dc:creator><dc:title>MYD88 (L265P) mutation is an independent prognostic factor for outcome in patients with diffuse large B-cell lymphoma</dc:title><dc:identifier>ART-2014-129720</dc:identifier><dc:description>Diffuse large B-cell lymphoma (DLBCL) encompasses an aggressive and heterogeneous group of malignancies. Gene expression profiling (GEP) unraveled two main subtypes based on their putative cell of origin named germinal center B-cell-like (GCB) and activated B-cell-like (ABC), with specific genetic alterations and different clinical outcome. Recent studies have reported several somatic mutations in the myeloid differentiation primary response gene 88 (MYD88) affecting B-cell lymphomas. Among them, the leucine to proline exchange at position 265 (L265P) is the most recurrent and biologically potent MYD88 variation, being found in about 30% of ABC-DLBCL but uncommon in GCB-DLBCL. Here, we have investigated the occurrence of MYD88 L265P mutation in adult patients with DLBCL and its relation to clinical and biological characteristics, including patients’ outcome.</dc:description><dc:date>2014</dc:date><dc:source>http://zaguan.unizar.es/record/147841</dc:source><dc:doi>10.1038/leu.2014.184</dc:doi><dc:identifier>http://zaguan.unizar.es/record/147841</dc:identifier><dc:identifier>oai:zaguan.unizar.es:147841</dc:identifier><dc:identifier.citation>Leukemia 28, 10 (2014), 2104-2106</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights></dc:dc>

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