PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 12628440-4 2003 Treatment of CHO-IR cells with a cell-permeable calcium chelator, BAPTA-AM, abolished the insulin-induced activation of SGK1. CAV protocol 13-16 insulin Cricetulus griseus 90-97 8617284-3 1996 Exposure of CHO.T cells to insulin, phorbol ester or serum resulted in a rapid increase (up to twofold) in eIF-4E phosphorylation. CAV protocol 12-15 insulin Cricetulus griseus 27-34 9632753-7 1998 Insulin activation of p70 S6 kinase was inhibited by approximately 75% in CHO cells and approximately 30% in 3T3-L1 adipocytes, whereas insulin-induced activation of endogenous Akt was inhibited by 80 to 95%, by expression of Akt-AA. CAV protocol 74-77 insulin Cricetulus griseus 0-7 9632753-9 1998 However, insulin-stimulated glucose uptake in both CHO cells and 3T3-L1 adipocytes was not affected by overexpression of Akt-AA, suggesting that Akt is not required for this effect of insulin. CAV protocol 51-54 insulin Cricetulus griseus 9-16 12556481-2 2003 In this study, we show that SKIP inhibits phosphoinositide 3-kinase signaling in insulin-stimulated CHO cells. CAV protocol 100-103 insulin Cricetulus griseus 81-88 8943212-6 1996 Co-transfection of CHO.T cells with dominant-negative mitogen-activated protein (MAP) kinase-kinase (MKK1) abrogated both insulin- and TZD-mediated activation of PPARgamma; transactivation was markedly increased in cells co-transfected with constitutively active MKK1. CAV protocol 19-22 insulin Cricetulus griseus 122-138 8039498-6 1994 After insulin treatment of CHO-IR cells, anti-dynamin antibodies co-immunoprecipitated the IR beta-subunit and IRS-1, as tyrosine-phosphorylated proteins and PI 3-kinase activity. CAV protocol 27-30 insulin Cricetulus griseus 6-13 7929278-4 1994 In contrast, treatment of CHO.T cells with the compounds resulted in significant increases in insulin-stimulated phosphatidylinositol (PI) 3-kinase activity. CAV protocol 26-29 insulin Cricetulus griseus 94-101 3305910-6 1987 In these cells half maximum stimulation of glucose uptake occurs at 5 X 10(-10)M insulin, whereas normal CHO cells require 5 X 10(-12)M insulin. CAV protocol 105-108 insulin Cricetulus griseus 136-143 8003510-8 1994 Insulin (1 microM) and FCS (9%) stimulate [3H]thymidine incorporation in parental CHO cells to a similar high level whereas in insulin receptor overexpressing CHO cells the maximum of insulin-stimulated [3H]thymidine incorporation is only 55% of the level reached by 9% FCS. CAV protocol 82-85 insulin Cricetulus griseus 0-7 8003510-8 1994 Insulin (1 microM) and FCS (9%) stimulate [3H]thymidine incorporation in parental CHO cells to a similar high level whereas in insulin receptor overexpressing CHO cells the maximum of insulin-stimulated [3H]thymidine incorporation is only 55% of the level reached by 9% FCS. CAV protocol 159-162 insulin Cricetulus griseus 0-7 8003510-8 1994 Insulin (1 microM) and FCS (9%) stimulate [3H]thymidine incorporation in parental CHO cells to a similar high level whereas in insulin receptor overexpressing CHO cells the maximum of insulin-stimulated [3H]thymidine incorporation is only 55% of the level reached by 9% FCS. CAV protocol 159-162 insulin Cricetulus griseus 127-134 8266574-0 1993 [Synergism in the stimulating effect of transforming growth factor beta and insulin on the substrate-independent proliferation of the CHO-719 cell line]. CAV protocol 134-137 insulin Cricetulus griseus 76-83 1329727-2 1992 (1) Insulin treatment of CHO cells over-expressing wild-type insulin receptors resulted in the rapid and substantial (5-10-fold) activation of cytosolic protein kinases which phosphorylated myelin basic protein, Kemptide and two peptide substrates based on sites phosphorylated on ribosomal protein S6 in vivo. CAV protocol 25-28 insulin Cricetulus griseus 61-68 7765921-0 1994 Extracellular insulin degrading activity creates instability in a CHO-based batch-refeed continuous process. CAV protocol 66-69 insulin Cricetulus griseus 14-21 1647198-0 1991 Cytoplasmic juxtamembrane region of the insulin receptor: a critical role in ATP binding, endogenous substrate phosphorylation, and insulin-stimulated bioeffects in CHO cells. CAV protocol 165-168 insulin Cricetulus griseus 40-47 2154747-4 1990 Here we report that PI 3-kinase activity is immunoprecipitated from insulin-stimulated CHO cells by antiphosphotyrosine and anti-insulin receptor antibodies. CAV protocol 87-90 insulin Cricetulus griseus 68-75