CPI-0610, a potent and selective BET bromodomain inhibitor optimized for clinical development
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE71758
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SUDHL5 cells were treated with DMSO or 2.5 μM CPI203 for 4 hours, then processed for ChIP-Seq to obtain genome-wide binding changes for BRD4 upon treatment with a BET inhibitor. Examination of BRD4 binding in the absence or presence of a BET inhibitor in SUDHL5 DLBCL cell line using ChIP-Seq
创建时间：
2023-01-07
