MLL-AF4 Spreading Identifies Binding Sites that Are Distinct from Super-Enhancers and that Govern Sensitivity to DOT1L Inhibition in Leukemia.
Understanding the underlying molecular mechanisms of defined cancers is crucial for effective personalized therapies. Translocations of the mixed-lineage leukemia (MLL) gene produce fusion proteins such as MLL-AF4 that disrupt epigenetic pathways and cause poor-prognosis leukemias. Here, we find tha...
المؤلفون الرئيسيون: | Kerry, J, Godfrey, L, Repapi, E, Tapia, M, Blackledge, N, Ma, H, Ballabio, E, O'Byrne, S, Ponthan, F, Heidenreich, O, Roy, A, Roberts, I, Konopleva, M, Klose, R, Geng, H, Milne, T |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
Cell Press
2017
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مواد مشابهة
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MLL-AF4 Spreading Identifies Binding Sites that Are Distinct from Super-Enhancers and that Govern Sensitivity to DOT1L Inhibition in Leukemia
حسب: Jon Kerry, وآخرون
منشور في: (2017-01-01) -
MLL-AF4 binds directly to a BCL-2 specific enhancer and modulates H3K27 acetylation.
حسب: Godfrey, L, وآخرون
منشور في: (2016) -
The role of DOT1L in MLL-AF4 leukaemia
حسب: Godfrey, L
منشور في: (2018) -
Molecular and Epigenetic Mechanisms of MLL in Human Leukemogenesis.
حسب: Ballabio, E, وآخرون
منشور في: (2012) -
P314: THERAPEUTICALLY TARGETING THE UNIQUE BARCODE OF MLL/AF4
حسب: R. Cameron, وآخرون
منشور في: (2022-06-01)