identified daunorubicin, pyrvinium, and pararosaniline as active planar aromatic moieties able to disrupt the RNA‐dependent recruitment of the ALS‐associated TDP‐34, FUS, and hnRNPA2B1 into stress granules, reducing progression to pathological protein aggregates (Fang et al., 2019). The gene discussed is FUS; the disease is amyotrophic lateral sclerosis.