To define the FGFR3 network in multiple myeloma, mass spectrometry was used to recognize and quantify phosphotyrosine (pY) sites modulated simply by FGFR3 activation and inhibition in myeloma-derived KMS11 cells. filled with the tandem pY theme in its activation loop was targeted by PD173074. 40 from the drug-sensitive pY sites, […]