Recurrent mutations in NF-κB pathway components, KMT2D, and NOTCH1/2 in ocular adnexal MALT-type marginal zone lymphomas
Authors:
Open Access
- 23 August 2016
- journal article
- Published by Impact Journals, LLC in Oncotarget
- Vol. 7 (38) , 62627-62639
Abstract
Recurrent mutations in NF-B pathway components, KMT2D, and NOTCH1/2 in ocular adnexal MALT-type marginal zone lymphomasKeywords
This publication has 55 references indexed in Scilit:
- Landscape of somatic mutations and clonal evolution in mantle cell lymphomaProceedings of the National Academy of Sciences, 2013
- Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphomaJournal of Experimental Medicine, 2012
- The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone developmentJournal of Experimental Medicine, 2012
- Integrative Genomics Viewer (IGV): high-performance genomics data visualization and explorationBriefings in Bioinformatics, 2012
- Fast gapped-read alignment with Bowtie 2Nature Methods, 2012
- Frequent mutation of histone-modifying genes in non-Hodgkin lymphomaNature, 2011
- Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activationJournal of Experimental Medicine, 2011
- Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemiaNature, 2011
- Identification of deleterious mutations within three human genomesGenome Research, 2009
- TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphomaJournal of Experimental Medicine, 2009