MYB function in normal and cancer cells
By R. Ramsay, T. Gonda. Nature Reviews. Cancer, 2008
621 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/413d1d09d453b796eb562380288634bb66bcbb16
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In Cancer Research
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Citations in the corpus
- Recurrent fusion of MYB and NFIB transcription factor genes in carcinomas of the breast and head and neck (2009, background): “MYB plays an important role in the control of cell proliferation, apoptosis, and differentiation, is highly expressed in immature, proliferating cells, and is down-regulated as cells become more differentiated (10, 11).”
- Topology based data analysis identifies a subgroup of breast cancers with a unique mutational profile and excellent survival (2011, result): “We wanted to find out whether other genes, known to be associated with (or downstream of) c-MYB overexpression (12), also show similar association in the c-MYB tumor group.”
- Tissue-Resident Macrophage Ontogeny and Homeostasis. (2016, background): “…to establish a robust and consistentmodel of immune cell ontogeny from the early embryonic stage right through to the steady-state adult. c-Myb Dependence c-Myb is a transcription factor required for the expansion and differentiation of all hematopoietic cell lineages (Ramsay and Gonda, 2008).”
- Polycomb group proteins: navigators of lineage pathways led astray in cancer (2009, neutral): “Some specific examples include the oncogenes MYB”
- METTL14 Inhibits Hematopoietic Stem/Progenitor Differentiation and Promotes Leukemogenesis via mRNA m6A Modification (2017, background): “MYB and MYC both are master regulators of self-renewal and differentiation of normal HSPCs and AML cells (Ramsay andGonda, 2008;Wall et al., 2008) and are essential for AML initiation andmaintenance (Delgado and León, 2010; Ramsay and Gonda, 2008).”