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RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features
Gaidzik, V. I. et al. (2016)
Wissenschaftlicher Artikel
Frequent evolution of copy number alterations in CLL following first-line treatment with FC(R) is enriched with TP53 alterations: results from the CLL8 trial
Edelmann, J. et al. (2017)
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The clathrin-binding domain of CALM and the OM-LZ domain of AF10 are sufficient to induce acute myeloid leukemia in mice
Deshpande, A. J. et al. (2011)
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Integrative nucleophosmin mutation-associated microRNA and gene expression pattern analysis identifies novel microRNA - target gene interactions in acute myeloid leukemia
Russ, Annika C. et al. (2011)
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Differences in expression and function of LEF1 isoforms in normal versus leukemic hematopoiesis
Feder, Kristin et al. (2020)
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MicroRNA-708 is a novel regulator of the Hoxa9 program in myeloid cells
Schneider, Edith et al. (2020)
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Genomic alterations in high-risk chronic lymphocytic leukemia frequently affect cell cycle key regulators and NOTCH1-regulated transcription
Edelmann, Jennifer et al. (2020)
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The ParaHox gene Cdx4 induces acute erythroid leukemia in mice
Thoene, Silvia et al. (2019)
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IGF1R as druggable target mediating PI3K-delta inhibitor resistance in a murine model of chronic lymphocytic leukemia
Scheffold, Annika et al. (2019)
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Rituximab and obinutuzumab differentially hijack the B cell receptor and NOTCH1 signaling pathways
Edelmann, Jennifer et al. (2021)
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