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By Charles L. Schmidt

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Additional resources for Mantle Cell Lymphoma: Clinical Characteristics, Prevalence and Treatment Options

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Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. 1182/blood-2011-11-391474 (2012). Bea, S. et al. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma. 1314608110 (2013). Bernard, M. et al. Blastic variant of mantle cell lymphoma: a rare but highly aggressive subtype. Leukemia 15, 1785-1791 (2001). , Colomer, D. & Campo, E. Mantle cell lymphoma: from pathology and molecular pathogenesis to new therapeutic perspectives. Haematologica 91, 11-16 (2006).

Cytogenetic analysis in mantle cell lymphoma: a review of 214 cases. 1080/10428190290016890 (2002). Espinet, B. et al. Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma. 20754 (2010). Royo, C. et al. The complex landscape of genetic alterations in mantle cell lymphoma. 007 (2011). Bea, S. et al. Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

1038/nrc2230 (2007). , Dreyling, M. & Wiestner, A. Mantle cell lymphoma: biology, pathogenesis, and the molecular basis of treatment in the genomic era. 1182/blood-2010-04-189977 (2011). [120] Komatsu, H. et al. A variant chromosome translocation at 11q13 identifying PRAD1/cyclin D1 as the BCL-1 gene. Blood 84, 1226-1231 (1994). , Campo, E. & Rosenwald, A. Pathogenesis of mantle-cell lymphoma: all oncogenic roads lead to dysregulation of cell cycle and DNA damage response pathways. 019 (2005). [122] Slotta-Huspenina, J.

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