Proteolysis targeting chimeras (PROTACs) represent powerful tools to modulate the activity of classically “undruggable” proteins, but their application has been limited to known ligands and a few sele
Datasets of all the 319 targets from the Cytokine Receptors Human on-target siRNA library screen on MDDC-to-SupT1 cells monitored through HIV-1 p24+ staining
