PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 15177893-4 2004 In this study, induction of LMP1 increased the EGFR in both protein and promoter levels in a dose dependent manner using tetracycline-regulated LMP1 expression in nasopharyngeal carcinoma (NPC) cell line. Tetracycline 121-133 PDZ and LIM domain 7 Homo sapiens 28-32 15177893-4 2004 In this study, induction of LMP1 increased the EGFR in both protein and promoter levels in a dose dependent manner using tetracycline-regulated LMP1 expression in nasopharyngeal carcinoma (NPC) cell line. Tetracycline 121-133 PDZ and LIM domain 7 Homo sapiens 144-148 15115657-4 2004 In this study, induction of LMP1 increased the EGFR in both protein and promoter levels in a dose-dependent manner using tetracycline-regulated LMP1 expression in nasopharyngeal carcinoma (NPC) cell line. Tetracycline 121-133 PDZ and LIM domain 7 Homo sapiens 28-32 15115657-4 2004 In this study, induction of LMP1 increased the EGFR in both protein and promoter levels in a dose-dependent manner using tetracycline-regulated LMP1 expression in nasopharyngeal carcinoma (NPC) cell line. Tetracycline 121-133 PDZ and LIM domain 7 Homo sapiens 144-148 12504573-3 2002 Using the epithelial cell line HeLa in which the expression of LMP1 is inducibly regulated by tetracycline, we demonstrate that apoptosis triggered by ligation of the death receptor, Fas, or by the chemotherapeutic agent, etoposide, is potentiated by LMP1. Tetracycline 94-106 PDZ and LIM domain 7 Homo sapiens 63-67 14523478-5 2003 Similarly, induction of LMP1 in the 3A4 cells (exposed to tetracycline) was accompanied by a 13-fold increase in lymphotoxin levels (ELISA) as compared to uninduced (LMP1-negative) cells. Tetracycline 58-70 PDZ and LIM domain 7 Homo sapiens 24-28 12549222-5 2001 We further showed that telomerase activation in infected cells was dependent on the protein level of latent membrane protein 1 (LMP1) encoded by Epstein-Barr virus using a Tetracycline regulatory cell line expressing LMP1, pTet-on-LMP1-HNE2. Tetracycline 172-184 PDZ and LIM domain 7 Homo sapiens 128-132 11780335-2 2001 METHODS: A tetracycline-regulated LMP1-expressing nasopharyngeal carcinoma cell line, Tet-on-LMP1-HNE2, was used as the cell model. Tetracycline 11-23 PDZ and LIM domain 7 Homo sapiens 34-38 11780335-2 2001 METHODS: A tetracycline-regulated LMP1-expressing nasopharyngeal carcinoma cell line, Tet-on-LMP1-HNE2, was used as the cell model. Tetracycline 11-23 PDZ and LIM domain 7 Homo sapiens 93-97 11783085-2 2001 METHODS: A nasopharyngeal carcinoma cell line, Tet-on-LMP1 HNE2, transfected with LMP1, the expression of which was regulated by tetracycline, was used in this study. Tetracycline 129-141 PDZ and LIM domain 7 Homo sapiens 82-86 15995625-4 2005 METHODS: Tet-on LMP1 HNE2, a tetracycline-regulated LMP1-expression nasopharyngeal carcinoma cell line, was used as cell model. Tetracycline 29-41 PDZ and LIM domain 7 Homo sapiens 52-56 9351829-8 1997 Using a tetracycline-regulated LMP-1 allele, we demonstrate that JNK is also an effector of non-cytotoxic LMP-1 signaling in B cells, the physiological target cells of EBV. Tetracycline 8-20 PDZ and LIM domain 7 Homo sapiens 31-36 9351829-8 1997 Using a tetracycline-regulated LMP-1 allele, we demonstrate that JNK is also an effector of non-cytotoxic LMP-1 signaling in B cells, the physiological target cells of EBV. Tetracycline 8-20 PDZ and LIM domain 7 Homo sapiens 106-111