PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 2699432-0 1989 Receptor downregulation and DNA synthesis are modulated by EGF and TPA in cells expressing an EGFR/neu chimera. Tetradecanoylphorbol Acetate 67-70 epidermal growth factor receptor Rattus norvegicus 94-98 15048868-6 2004 In addition, inhibition of conventional and novel PKC isoforms by chronic (24 h) exposure to phorbol 12-myristate 13-acetate (PMA) inhibited AVP-induced activation of ERK and p70S6 kinase as well as EGF-R phosphorylation. Tetradecanoylphorbol Acetate 93-124 epidermal growth factor receptor Rattus norvegicus 199-204 15048868-6 2004 In addition, inhibition of conventional and novel PKC isoforms by chronic (24 h) exposure to phorbol 12-myristate 13-acetate (PMA) inhibited AVP-induced activation of ERK and p70S6 kinase as well as EGF-R phosphorylation. Tetradecanoylphorbol Acetate 126-129 epidermal growth factor receptor Rattus norvegicus 199-204 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). Tetradecanoylphorbol Acetate 35-66 epidermal growth factor receptor Rattus norvegicus 159-197 9722539-9 1998 The similar effects of UTP, ionomycin, and phorbol 12-myristate 13-acetate (PMA) on these signaling proteins demonstrate that the two signaling molecules from phosphatidylinositol 4,5-bisphosphate hydrolysis ([Ca2+]i, from inositol 1,4,5-trisphosphate production, and diacylglycerol) can individually initiate the activation of MAP kinase in an EGF receptor-dependent manner. Tetradecanoylphorbol Acetate 43-74 epidermal growth factor receptor Rattus norvegicus 345-357 9722539-9 1998 The similar effects of UTP, ionomycin, and phorbol 12-myristate 13-acetate (PMA) on these signaling proteins demonstrate that the two signaling molecules from phosphatidylinositol 4,5-bisphosphate hydrolysis ([Ca2+]i, from inositol 1,4,5-trisphosphate production, and diacylglycerol) can individually initiate the activation of MAP kinase in an EGF receptor-dependent manner. Tetradecanoylphorbol Acetate 76-79 epidermal growth factor receptor Rattus norvegicus 345-357 2288880-8 1990 Since the phorbol ester 12-O-tetradecanoylphorbol-13-acetate also decreases 125I-EGF binding and increases EGF receptor biosynthesis in GP6ac cells, we tested the effect of RA in cells depleted of protein kinase C by prolonged treatment (18 h) with 10 microM 12-O-tetradecanoylphorbol-13-acetate. Tetradecanoylphorbol Acetate 24-60 epidermal growth factor receptor Rattus norvegicus 107-119 2786455-7 1989 TPA also increased epidermal growth factor receptor mRNA in GP6ac cells but the effect was less prolonged; maximal levels were seen at 4 h after TPA exposure and returned to control levels by 12 h. TPA increased TGF-alpha mRNA in GP6ac cells, in part, by increasing transcription of the TGF-alpha gene as measured by run-on transcription rates in isolated nuclei. Tetradecanoylphorbol Acetate 0-3 epidermal growth factor receptor Rattus norvegicus 19-51 2790804-7 1989 These results demonstrate that phenobarbital, like TPA and other tumor promoters, can modulate the EGF receptor system but suggest that it does so without directly competing with EGF for binding to its receptor or by activating protein kinase C. Tetradecanoylphorbol Acetate 51-54 epidermal growth factor receptor Rattus norvegicus 99-111 2699432-8 1989 These results show that the chimeric EGFR/neu receptor undergoes typical downregulation upon ligand binding and TPA pretreatment and is capable of transducing an EGF-induced mitogenic signal. Tetradecanoylphorbol Acetate 112-115 epidermal growth factor receptor Rattus norvegicus 37-41