PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 9841495-7 1998 Accordingly, although IGF-I was not proliferative in NG, it increased [3H]thymidine incorporation and cell number in HG to an extent proportional to the decrease in IGFBP-2. Thymidine 74-83 insulin-like growth factor 1 Mus musculus 22-27 11340640-6 2001 IGF1 null dentate cell proliferation, assessed by thymidine analogue incorporation, was actually increased at P10 (33%, P < 0.05) and P50 (167%, P = 0.001). Thymidine 50-59 insulin-like growth factor 1 Mus musculus 0-4 10383152-7 1999 Parallel binding experiments using IGF-I missing the first 3 amino acids revealed a 47% increase in binding sites for IGF-I and an increase of at least 335% in DNA synthesis, as measured by labeled thymidine incorporation into DNA. Thymidine 198-207 insulin-like growth factor 1 Mus musculus 35-40 11564700-8 2001 GHRH antagonist JV-1-38 inhibited the autonomous growth of MXT cells and the proliferation induced by IGF-I or GH and diminished (3)H-thymidine-incorporation stimulated by IGF-I and GH. Thymidine 134-143 insulin-like growth factor 1 Mus musculus 172-177 11090910-5 2000 Combined treatment of TGF-beta and IGF-1 resulted in elevated 3H-thymidine incorporation and DNA and protein contents, reduction of 35S-sulfate incorporation and alkaline phosphatase activity, with no significant change in the activity of acid phosphatase. Thymidine 65-74 insulin-like growth factor 1 Mus musculus 35-40 11090910-9 2000 It is concluded that although 3H-thymidine incorporation and alkaline phosphatase activity appeared to be induced by TGF-beta and IGF-1, the overall responsiveness of cartilage from aged mice to these growth factors appeared to be inhibitory. Thymidine 33-42 insulin-like growth factor 1 Mus musculus 130-135 9741830-2 1998 Bioactivity of recombinant IGF-1 in transgenic mouse milk extracts was demonstrated by a concentration-dependent increase in [3H]thymidine incorporation in clonal bovine mammary epithelial cells (MAC-T) compared with control mouse milk extracts; moreover, addition of excess recombinant human insulin-like growth factor binding protein-3 (rhlGFBP-3) abolished the increase in [3H]thymidine incorporation attributed to recombinant IGF-1 in transgenic mouse milk. Thymidine 129-138 insulin-like growth factor 1 Mus musculus 27-32 9600271-3 1998 IGF-1 was able to stimulate glucose uptake, glucose incorporation into glycogen and thymidine incorporation in such cells. Thymidine 84-93 insulin-like growth factor 1 Mus musculus 0-5 7686165-4 1993 Overexpression of IGF-I receptors in NIH-3T3 cells resulted in increased sensitivity and maximal responsiveness of thymidine incorporation, 2-deoxyglucose uptake, and phosphatidylinositol-3 (PI3) kinase activation to IGF-I stimulation. Thymidine 115-124 insulin-like growth factor 1 Mus musculus 18-23 8621590-10 1996 Overexpression of Crk also enhanced IGF-I-induced mitogenesis of NIH-3T3 cells, as measured by [3H]thymidine incorporation. Thymidine 99-108 insulin-like growth factor 1 Mus musculus 36-41 7693688-4 1993 A mutant IGF-I receptor, in which 3 tyrosines (Tyr1131, Tyr1135, and Tyr1136) analogous to the three major autophosphorylation sites in the insulin receptor kinase were replaced by phenylalanines, was devoid of kinase activity in vivo and in vitro and inactive with respect to IGF-I internalization and stimulation of thymidine incorporation. Thymidine 318-327 insulin-like growth factor 1 Mus musculus 9-14 8708541-11 1996 In studies on IGFBP-6 actions, IGFBP-6 completely inhibited IGF-II-induced [3H]thymidine incorporation in MC3T3-E1 mouse osteoblast cells while it had only minimal inhibitory effects on IGF-I-induced [3H]thymidine incorporation. Thymidine 79-88 insulin-like growth factor 1 Mus musculus 60-65 7588225-6 1995 Despite the reduction in autophosphorylation and receptor internalization, IGF-I-induced thymidine incorporation and cellular proliferation were unaffected. Thymidine 89-98 insulin-like growth factor 1 Mus musculus 75-80 8440329-8 1993 CDGF together with small concentrations of bFGF (3.5 pM), higher concentrations of PDGF (300 pM), or IGF-I (1 nM) increased synergistically thymidine incorporation in the 2-h pulse, exceeding in the case of PDGF and bFGF the values obtained with 10% serum. Thymidine 140-149 insulin-like growth factor 1 Mus musculus 101-106 8492073-6 1993 Immunoinhibition of IGF-I resulted in an almost complete inhibition (-91%) of thymidine incorporation into DNA, as well as in marked degenerative changes in the morphological appearance of the condyle. Thymidine 78-87 insulin-like growth factor 1 Mus musculus 20-25 8492081-2 1993 When activin A was added together with IGF-I to competent cells primed with epidermal growth factor (primed competent cells), both [3H]thymidine incorporation and nuclear labelling induced by IGF-I were inhibited. Thymidine 135-144 insulin-like growth factor 1 Mus musculus 39-44 8492081-2 1993 When activin A was added together with IGF-I to competent cells primed with epidermal growth factor (primed competent cells), both [3H]thymidine incorporation and nuclear labelling induced by IGF-I were inhibited. Thymidine 135-144 insulin-like growth factor 1 Mus musculus 192-197 8472869-4 1993 Thus, the tumor contents of IGF-I and the rate of IGF-I-positive cells were inversely correlated to the tumor growth and the [3H]thymidine-labeled cell rate in this in vivo study, although IGF-I is known to be a mitogen for breast cancer cells in vitro. Thymidine 129-138 insulin-like growth factor 1 Mus musculus 28-33 8472869-4 1993 Thus, the tumor contents of IGF-I and the rate of IGF-I-positive cells were inversely correlated to the tumor growth and the [3H]thymidine-labeled cell rate in this in vivo study, although IGF-I is known to be a mitogen for breast cancer cells in vitro. Thymidine 129-138 insulin-like growth factor 1 Mus musculus 50-55 8472869-4 1993 Thus, the tumor contents of IGF-I and the rate of IGF-I-positive cells were inversely correlated to the tumor growth and the [3H]thymidine-labeled cell rate in this in vivo study, although IGF-I is known to be a mitogen for breast cancer cells in vitro. Thymidine 129-138 insulin-like growth factor 1 Mus musculus 50-55 2205200-4 1990 In contrast, in undifferentiated cells insulin and IGF-I stimulated a large increase of [3H]thymidine incorporation into DNA via IGF-I receptors, indicating that undifferentiated 3T3-L1 cells are equipped with fully functioning hormone (IGF-I) receptors. Thymidine 92-101 insulin-like growth factor 1 Mus musculus 51-56 1321252-5 1992 In vitro proliferative response of MGH-OGS cells to IGF-I and other pituitary-dependent factors was determined by thymidine-incorporation experiments. Thymidine 114-123 insulin-like growth factor 1 Mus musculus 52-57 1310625-5 1992 Both insulin and IGF1 stimulate thymidine incorporation in a dose-dependent manner with similar increases above the basal level. Thymidine 32-41 insulin-like growth factor 1 Mus musculus 17-21 19912810-2 1991 IGF-1 and insulin increased thymidine incorporation and cell number, but Bt(2)cAMP inhibited incorporation and FGF did not change thymidine incorporation after 24 h of treatment. Thymidine 28-37 insulin-like growth factor 1 Mus musculus 0-5 2205200-4 1990 In contrast, in undifferentiated cells insulin and IGF-I stimulated a large increase of [3H]thymidine incorporation into DNA via IGF-I receptors, indicating that undifferentiated 3T3-L1 cells are equipped with fully functioning hormone (IGF-I) receptors. Thymidine 92-101 insulin-like growth factor 1 Mus musculus 129-134 2205200-4 1990 In contrast, in undifferentiated cells insulin and IGF-I stimulated a large increase of [3H]thymidine incorporation into DNA via IGF-I receptors, indicating that undifferentiated 3T3-L1 cells are equipped with fully functioning hormone (IGF-I) receptors. Thymidine 92-101 insulin-like growth factor 1 Mus musculus 129-134 2162851-4 1990 In contrast, IGF-I increased calcium entry, radioactivity in [3H]diacylglycerol, and [3H]thymidine incorporation in primed competent cells while these reactions were not induced by IGF-I in quiescent cells. Thymidine 89-98 insulin-like growth factor 1 Mus musculus 13-18 2785831-5 1989 [3H]Thymidine incorporation into acid insoluble radioactivity was stimulated by IGF-1 in all populations but the greatest increase was in intermediate populations. Thymidine 4-13 insulin-like growth factor 1 Mus musculus 80-85 2720200-2 1989 IGF-I stimulated [3H]thymidine incorporation into the DNA of the cells at concentrations of 1.3-130 X 10(-9) M. The alkaline phosphatase (ALP) activity in cultures was also raised by the hormone at the same concentrations. Thymidine 21-30 insulin-like growth factor 1 Mus musculus 0-5 25356638-9 2015 Consistently, IGF-1 promoted the G2/M progression of thymidine-treated mSSCs, which were arrested at G1/S boundary synchronously; while GDNF and/or FGF2 stimulated their entry into the S phase. Thymidine 53-62 insulin-like growth factor 1 Mus musculus 14-19 2460452-9 1988 In primed competent cells, IGF-I-stimulated [3H]thymidine incorporation was dependent on extracellular calcium and was attenuated by cobalt and tetramethrin. Thymidine 48-57 insulin-like growth factor 1 Mus musculus 27-32 21266309-9 2012 Compared with wild-type control, recovery of pressure development and relaxation indices relative to baseline performance were significantly reduced in transgenic alphaMHC-IGF-1 Ea after 60-min reperfusion (34+-7% vs. 62+-7% recovery of +dP/dt; 35+-11% vs. 57+-8% recovery of -dP/dt). Thymidine 241-243 insulin-like growth factor 1 Mus musculus 172-177 21266309-9 2012 Compared with wild-type control, recovery of pressure development and relaxation indices relative to baseline performance were significantly reduced in transgenic alphaMHC-IGF-1 Ea after 60-min reperfusion (34+-7% vs. 62+-7% recovery of +dP/dt; 35+-11% vs. 57+-8% recovery of -dP/dt). Thymidine 280-282 insulin-like growth factor 1 Mus musculus 172-177 16293644-5 2006 IGF-1-TTC retains IGF-1 activity as indicated by [(3)H]thymidine incorporation into L6 myoblasts. Thymidine 55-64 insulin-like growth factor 1 Mus musculus 0-5 15329054-6 2004 RESULTS: The stimulatory effect of IGF-I on thymidine incorporation seen in WT animals was absent in eNOSKO mice. Thymidine 44-53 insulin-like growth factor 1 Mus musculus 35-40