Targeted design and identification of AC1NOD4Q to block activity of HOTAIR by abrogating the scaffold interaction with EZH2.
Yu RenYun-Fei WangJing ZhangQi-Xue WangLei HanMei MeiChun-Sheng KangPublished in: Clinical epigenetics (2019)
Our findings suggest of a potential new strategy to discover the lead compound for targeted lincRNA therapy and potentially pave the way for exploiting ADQ as a scaffold for more effective small molecule drugs.