PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 9722539-6 1998 UTP, ionomycin, and phorbol ester (phorbol 12-myristate 13-acetate) increased MAP kinase activity and also promoted the tyrosine phosphorylation of RAFTK, the epidermal growth factor (EGF) receptor, SHC, and p120(cbl). Phorbol Esters 20-33 epidermal growth factor receptor Rattus norvegicus 159-197 15284022-5 2004 RIE-1 cells express TACE, and treatment with phorbol ester, an established TACE stimulus, triggered the extracellular release of an EGFR ligand, transforming growth factor-alpha. Phorbol Esters 45-58 epidermal growth factor receptor Rattus norvegicus 132-136 1729394-6 1992 This latter activity was relatively resistant to staurosporine inhibition and phorbol ester treatment, but it phosphorylated the exogenous PKC substrates, histone 1 and the epidermal growth factor receptor peptide KTRLRR. Phorbol Esters 78-91 epidermal growth factor receptor Rattus norvegicus 173-205 17307332-1 2007 While a great deal of attention has been focused on G-protein-coupled receptor (GPCR)-induced epidermal growth factor receptor (EGFR) transactivation, it has been known for many years that the tyrosine kinase activity of the EGFR is inhibited in cells treated with tumor-promoting phorbol esters, a process termed EGFR transmodulation. Phorbol Esters 281-295 epidermal growth factor receptor Rattus norvegicus 94-126 17307332-1 2007 While a great deal of attention has been focused on G-protein-coupled receptor (GPCR)-induced epidermal growth factor receptor (EGFR) transactivation, it has been known for many years that the tyrosine kinase activity of the EGFR is inhibited in cells treated with tumor-promoting phorbol esters, a process termed EGFR transmodulation. Phorbol Esters 281-295 epidermal growth factor receptor Rattus norvegicus 128-132 17307332-1 2007 While a great deal of attention has been focused on G-protein-coupled receptor (GPCR)-induced epidermal growth factor receptor (EGFR) transactivation, it has been known for many years that the tyrosine kinase activity of the EGFR is inhibited in cells treated with tumor-promoting phorbol esters, a process termed EGFR transmodulation. Phorbol Esters 281-295 epidermal growth factor receptor Rattus norvegicus 225-229 17307332-1 2007 While a great deal of attention has been focused on G-protein-coupled receptor (GPCR)-induced epidermal growth factor receptor (EGFR) transactivation, it has been known for many years that the tyrosine kinase activity of the EGFR is inhibited in cells treated with tumor-promoting phorbol esters, a process termed EGFR transmodulation. Phorbol Esters 281-295 epidermal growth factor receptor Rattus norvegicus 225-229