PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 2835972-8 1988 We, therefore, conclude that cAMP mediates the inhibition of growth-related transformation-specific properties either by acting at steps subsequent to the expression of p21v-Ki-ras or on a pathway independent of p21ras function. Cyclic AMP 29-33 Harvey rat sarcoma virus oncogene Mus musculus 212-218 7525612-0 1994 Ornithine decarboxylase gene expression is aberrantly regulated via the cAMP signal transduction pathway in malignant H-ras transformed cell lines. Cyclic AMP 72-76 Harvey rat sarcoma virus oncogene Mus musculus 118-123 1647646-0 1991 Effect of vitamin E succinate and a cAMP-stimulating agent on the expression of c-myc and N-myc and H-ras in murine neuroblastoma cells. Cyclic AMP 36-40 Harvey rat sarcoma virus oncogene Mus musculus 100-105 19167486-5 2009 BCR signaling to ERK1/2 and Akt requires cyclic AMP-regulated Epac, the latter acting as a guanine nucleotide exchange factor for Rap1 and H-Ras independent of protein kinase A. Cyclic AMP 41-51 Harvey rat sarcoma virus oncogene Mus musculus 139-144 19167486-7 2009 Our data indicate that cyclic AMP-dependent Epac signals to ERK1/2 and Akt upon activation of Rap1 and H-Ras, and is involved in BCR-induced growth arrest and apoptosis in WEHI-231 cells. Cyclic AMP 23-33 Harvey rat sarcoma virus oncogene Mus musculus 103-108 9393768-1 1997 The interplay between cyclic AMP (cAMP)-dependent protein kinase A (PKA)- and p21ras-mediated signaling pathways is expected to determine further loss, maintenance, or modulation of differentiation and proliferation of a particular cell. Cyclic AMP 34-38 Harvey rat sarcoma virus oncogene Mus musculus 78-84 9078246-0 1997 cAMP suppresses p21ras and Raf-1 responses but not the Erk-1 response to granulocyte-colony-stimulating factor: possible Raf-1-independent activation of Erk-1. Cyclic AMP 0-4 Harvey rat sarcoma virus oncogene Mus musculus 16-22 7505277-0 1994 Alterations in the cyclic AMP signal transduction pathway regulating ribonucleotide reductase gene expression in malignant H-ras transformed cell lines. Cyclic AMP 19-29 Harvey rat sarcoma virus oncogene Mus musculus 123-128 7693388-0 1993 Cyclic AMP decreases chemotaxis, invasiveness and lung colonization of H-ras transformed mouse fibroblasts. Cyclic AMP 0-10 Harvey rat sarcoma virus oncogene Mus musculus 71-76 2992503-0 1985 Two classes of cAMP analogs synergistically inhibit p21 ras protein synthesis and phenotypic transformation of NIH/3T3 cells transfected with Ha-MuSV DNA. Cyclic AMP 15-19 Harvey rat sarcoma virus oncogene Mus musculus 52-59 3767986-1 1986 cAMP-dependent protein kinase activity in the soluble fraction was decreased in both v-H-ras-transformed and activated-c-H-ras-transformed NIH3T3 cells as compared with that in NIH3T3 cells. Cyclic AMP 0-4 Harvey rat sarcoma virus oncogene Mus musculus 87-92 3767986-1 1986 cAMP-dependent protein kinase activity in the soluble fraction was decreased in both v-H-ras-transformed and activated-c-H-ras-transformed NIH3T3 cells as compared with that in NIH3T3 cells. Cyclic AMP 0-4 Harvey rat sarcoma virus oncogene Mus musculus 121-126 3767986-2 1986 Both of the elution profile of type II cAMP-dependent protein kinase from DEAE-cellulose and the electrophoretic behavior of its regulatory subunits in the particulate fraction of H-ras-transformed cells are different from those of control NIH3T3 cells. Cyclic AMP 39-43 Harvey rat sarcoma virus oncogene Mus musculus 180-185 2992503-3 1985 Treatment of cells with two classes of cAMP analogs which are selective for the two different cAMP-binding sites of type II protein kinase, in combination, synergistically inhibited both p21 ras protein synthesis and phenotypic transformation. Cyclic AMP 39-43 Harvey rat sarcoma virus oncogene Mus musculus 187-194 2992503-3 1985 Treatment of cells with two classes of cAMP analogs which are selective for the two different cAMP-binding sites of type II protein kinase, in combination, synergistically inhibited both p21 ras protein synthesis and phenotypic transformation. Cyclic AMP 94-98 Harvey rat sarcoma virus oncogene Mus musculus 187-194 29054855-7 2018 Genetic modulation studies in cardiomyocytes and cardiac and embryonic fibroblasts revealed that the lack of H-Ras down-regulates the B-RAF/MEK/ERK pathway, which induces the glycogen synthase kinase-3beta-dependent activation of the transcription factor, cAMP response element-binding protein, which is responsible for PKG-Ibeta overexpression in H -ras-/- mouse embryonic fibroblasts. Cyclic AMP 256-260 Harvey rat sarcoma virus oncogene Mus musculus 109-114