PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 35179400-14 2022 Moreover, luzindole, a non-selective MT1/MT2 antagonist, but not 4-P-PDOT, a selective MT2 antagonist, blocked the protective effect of Mel-Mic. luzindole 10-19 metallothionein 2 Mus musculus 41-44 2506842-2 1989 Although in two groups treated with different concentrations of hCG the value of 3H-thymidine incorporation into testicular tissue showed no significant difference compared with the untreated control group, treatment with both hCG and hMG induced significant changes in the value of 3H-thymidine incorporation compared with the untreated control group. 3h-thymidine 81-93 hypertrichosis 2 (generalised, congenital) Homo sapiens 227-230 2506842-2 1989 Although in two groups treated with different concentrations of hCG the value of 3H-thymidine incorporation into testicular tissue showed no significant difference compared with the untreated control group, treatment with both hCG and hMG induced significant changes in the value of 3H-thymidine incorporation compared with the untreated control group. 3h-thymidine 283-295 hypertrichosis 2 (generalised, congenital) Homo sapiens 64-67 2506842-2 1989 Although in two groups treated with different concentrations of hCG the value of 3H-thymidine incorporation into testicular tissue showed no significant difference compared with the untreated control group, treatment with both hCG and hMG induced significant changes in the value of 3H-thymidine incorporation compared with the untreated control group. 3h-thymidine 283-295 hypertrichosis 2 (generalised, congenital) Homo sapiens 227-230 2475470-6 1989 Combined light microscopic immunoperoxidase study and autoradiography with 3H-thymidine revealed a higher cumulative labeling index in AFP-positive hepatoma cells than in non-tumorous areas. 3h-thymidine 75-87 alpha fetoprotein Homo sapiens 135-138 2807633-5 1989 The TNF activity in a serum sample could be titrated using the fluorometric method in addition to a method using 3H-thymidine. 3h-thymidine 113-125 tumor necrosis factor Homo sapiens 4-7 2910884-7 1989 bFGF in the presence of heparin is as active as bFGF alone in inducing 3H-thymidine incorporation into Swiss 3T3 fibroblast DNA. 3h-thymidine 71-83 fibroblast growth factor 2 Homo sapiens 48-52 3216421-7 1988 Analysis of the effects of IGF-I on O4-positive, GC-negative intermediate precursor cells revealed a two to fivefold increase in the number of cells that incorporated 3H-thymidine into their DNA during a 5-h pulse. 3h-thymidine 167-179 insulin-like growth factor 1 Rattus norvegicus 27-32 2787441-6 1989 The responsiveness of alveolar lymphocytes to recombinant IL-2 was evaluated by 3H-thymidine uptake in the presence and absence of P. acnes. 3h-thymidine 80-92 interleukin 2 Homo sapiens 58-62 2467365-4 1989 In the present study, we investigated by a combined 3H-Thymidine autoradiography/immunocytochemistry technique whether the mitogenic effect that MBP exerts upon astrocytes in vitro can be prevented by DHEA and DHEA-S. 3h-thymidine 52-64 myelin basic protein Homo sapiens 145-148 2854816-4 1988 Insulin, known to cause redistribution of Tf-R to the cell surface, potentiated the inhibition of 3H-thymidine uptake induced by cis-platin and apotransferrin in the concentrations less than 50 nM. 3h-thymidine 98-110 insulin Homo sapiens 0-7 2798235-6 1989 Exogenous EGF stimulated 3H-thymidine incorporation when cells were plated at low density in serum-free culture medium, while at higher cell density neither cell division nor 3H-thymidine incorporation was significantly altered. 3h-thymidine 25-37 epidermal growth factor Homo sapiens 10-13 3273477-2 1988 Acid-exposed asialo ACT significantly reduced 3H-thymidine incorporation into human peripheral lymphocytes stimulated by phytohemagglutinin (PHA) though native ACT could not inhibit the mitogen-induced lymphoproliferation and asialo ACT moderately inhibited it. 3h-thymidine 46-58 serpin family A member 3 Homo sapiens 20-23 2461376-2 1988 A six-to-nine fold increase in 3H-thymidine (3H-dT) incorporation into the acid insoluble pool and a similar increase of the labeling index can be measured when bFGF, at a concentration between 1 and 10 ng/ml, is added to keratinocytes arrested in serum-free and growth factor-free medium with a Ca++-concentration below 0.1 mM. 3h-thymidine 31-43 fibroblast growth factor 2 Mus musculus 161-165 3166806-2 1988 It was found that a half of 3H-thymidine was degraded to 3H-thymine during 24 hours in PHA stimulation of blood lymphocytes. 3h-thymidine 28-40 lamin B receptor Homo sapiens 87-90 3166644-5 1988 The degree of PHA-induced lymphocyte proliferation was measured by 3H-thymidine incorporation. 3h-thymidine 67-79 lamin B receptor Homo sapiens 14-17 3166905-3 1988 Addition of insulin, transferrin and selenium (ITS) stimulated DNA synthesis, as measured by 3H-thymidine incorporation, in a dose-dependent manner. 3h-thymidine 93-105 insulin Homo sapiens 12-19 3166905-3 1988 Addition of insulin, transferrin and selenium (ITS) stimulated DNA synthesis, as measured by 3H-thymidine incorporation, in a dose-dependent manner. 3h-thymidine 93-105 transferrin Homo sapiens 21-32 3046880-5 1988 Addition of growth hormone caused a significant increase in 3H-thymidine incorporation into both the adult and the fetal islets, but only the adult islets experienced an increase in DNA content. 3h-thymidine 60-72 gonadotropin releasing hormone receptor Rattus norvegicus 12-26 3046880-7 1988 The dynamics of 3H-thymidine incorporation after growth hormone administration were different in the adult and the fetal pancreas. 3h-thymidine 16-28 gonadotropin releasing hormone receptor Rattus norvegicus 49-63 2844457-2 1988 A significantly impaired uptake of 3H-thymidine by CD4 cells was found in BD, as compared with healthy HSV1 sero-positive subjects. 3h-thymidine 35-47 CD4 molecule Homo sapiens 51-54 2844457-7 1988 CD8 cells showed generally rather a low uptake of 3H-thymidine, nevertheless, the values in BD and recurrent herpetic infection were again lower than those in sero-positive controls or rheumatoid arthritis. 3h-thymidine 50-62 CD8a molecule Homo sapiens 0-3 3294304-1 1988 Keratinocyte derived T-cell growth factor was initially described as a product of cultured neonatal keratinocytes and keratinocyte cell lines that induced the proliferation of HT-2 cells, a murine T-cell line that responds to IL-2 and IL-4 by incorporating 3H-Thymidine. 3h-thymidine 257-269 interleukin 2 Mus musculus 21-41 3395331-3 1988 Among growth promoting factors only epidermal growth factor, insulin and transferrin were associated with increased 3H-thymidine incorporation, and none of these agents induced PK-C activation as measured by its translocation from cytosol to membrane fraction. 3h-thymidine 116-128 epidermal growth factor like 1 Rattus norvegicus 36-59 3395331-3 1988 Among growth promoting factors only epidermal growth factor, insulin and transferrin were associated with increased 3H-thymidine incorporation, and none of these agents induced PK-C activation as measured by its translocation from cytosol to membrane fraction. 3h-thymidine 116-128 transferrin Rattus norvegicus 73-84 3216494-0 1988 [In vitro erythropoietin bioassay based on 3H-thymidine incorporation into spleen cells from phenylhydrazine-treated mice]. 3h-thymidine 43-55 erythropoietin Mus musculus 10-24 3356754-4 1988 Purified MGSA-stimulated melanoma cell growth in both 3H-thymidine and cell number assays over a concentration range of 0.06 to 6 ng/ml. 3h-thymidine 54-66 C-X-C motif chemokine ligand 1 Homo sapiens 9-13 2967213-10 1988 Both IGF-I and II stimulated 3H-thymidine incorporation into K562 cells whereas insulin was without effect. 3h-thymidine 29-41 insulin like growth factor 1 Homo sapiens 5-10 2891388-5 1988 In all three ATL samples tested, stimulation of 3H-thymidine uptake by purified TGF-beta from platelets was apparent. 3h-thymidine 48-60 transforming growth factor beta 1 Homo sapiens 80-88 3261121-5 1988 Lyt-2- cells which were negatively selected by monoclonal antibody and complement effected the Con A stimulated 3H-thymidine incorporation of a spleen cell culture in a different way depending on their state of differentiation. 3h-thymidine 112-124 CD8 antigen, alpha chain Mus musculus 0-5 3046234-6 1988 Incubation of cultures with insulin caused a time and dose-dependent stimulation of DNA, RNA and protein synthesis in C6 glioma cells (measured by 3H-thymidine, 3H-uridine or 3H-leucine incorporation into DNA, RNA, or protein respectively). 3h-thymidine 147-159 insulin Bos taurus 28-35 2828627-2 1987 IL-2 was able to significantly increase 3H-thymidine uptake and Tac antigen expression in unstimulated and anti-T3 activated lymphocytes. 3h-thymidine 40-52 interleukin 2 Homo sapiens 0-4 3500659-6 1987 IL-2 activity was bioassayed in recovered bronchoalveolar lavage fluid (BAL) using 3H-thymidine uptake by IL-2-dependent T-cells. 3h-thymidine 83-95 interleukin 2 Homo sapiens 0-4 3500659-6 1987 IL-2 activity was bioassayed in recovered bronchoalveolar lavage fluid (BAL) using 3H-thymidine uptake by IL-2-dependent T-cells. 3h-thymidine 83-95 interleukin 2 Homo sapiens 106-110 2460238-3 1988 Cellular responsiveness to graded levels of phytohemagglutinin (PHA), concanavalin A (Con A), and recombinant interleukin-2(r IL-2) was monitored by 3H-thymidine (3H-TdRO) uptake, production, and release of interleukin-2 (IL-2) and interleukin-2 receptor (IL-2R) and cytotoxic activities against K-562 and breast carcinoma (BCa) short-term cell lines. 3h-thymidine 149-161 interleukin 2 Homo sapiens 126-130 2907753-2 1988 The mixed D1/D2 dopaminergic antagonists chlorpromazine, haloperidol and flupentixol inhibited 3H-Thymidine incorporation into adult BALB/c mouse spleen cells stimulated by concanavalin A, lipopolysaccharide from Escherichia coli, and allogenic cells in a mixed lymphocyte reaction. 3h-thymidine 95-107 deiodinase, iodothyronine, type I Mus musculus 10-15 2960684-7 1987 IGF-I and insulin increased HL60 cell proliferation, as assessed by 3H-thymidine uptake, IGF-I greater than insulin. 3h-thymidine 68-80 insulin like growth factor 1 Homo sapiens 0-5 2960684-7 1987 IGF-I and insulin increased HL60 cell proliferation, as assessed by 3H-thymidine uptake, IGF-I greater than insulin. 3h-thymidine 68-80 insulin Homo sapiens 10-17 3121222-2 1987 B lymphocytes from patients tested showed a direct response to recombinant interleukin (rIL-2) during culture in vitro as shown by: (a) a ligand-mediated upregulation in the level of IL-2 receptor (IL-2R) expression (12 of 12 patients), (b) an increase in cell size (eight of nine patients), (c) an increase in 3H-thymidine uptake (four of six patients). 3h-thymidine 311-323 interleukin 2 Rattus norvegicus 88-93 2448891-2 1987 Addition of urokinase type plasminogen activator (1.35 x 10(-9) M) or thrombin (10(-7) M) to the culture medium caused a two-fold increase of 3H-thymidine incorporation, regardless of the origin of the prostatic cells. 3h-thymidine 142-154 plasminogen activator, urokinase Homo sapiens 12-48 2448891-2 1987 Addition of urokinase type plasminogen activator (1.35 x 10(-9) M) or thrombin (10(-7) M) to the culture medium caused a two-fold increase of 3H-thymidine incorporation, regardless of the origin of the prostatic cells. 3h-thymidine 142-154 coagulation factor II, thrombin Homo sapiens 70-78 3121222-2 1987 B lymphocytes from patients tested showed a direct response to recombinant interleukin (rIL-2) during culture in vitro as shown by: (a) a ligand-mediated upregulation in the level of IL-2 receptor (IL-2R) expression (12 of 12 patients), (b) an increase in cell size (eight of nine patients), (c) an increase in 3H-thymidine uptake (four of six patients). 3h-thymidine 311-323 interleukin 2 receptor subunit beta Homo sapiens 183-196 3121222-2 1987 B lymphocytes from patients tested showed a direct response to recombinant interleukin (rIL-2) during culture in vitro as shown by: (a) a ligand-mediated upregulation in the level of IL-2 receptor (IL-2R) expression (12 of 12 patients), (b) an increase in cell size (eight of nine patients), (c) an increase in 3H-thymidine uptake (four of six patients). 3h-thymidine 311-323 interleukin 2 receptor subunit alpha Homo sapiens 198-203 3114550-9 1987 In a short-term in vitro test we studied the effect of IFN-alpha 2 on the incorporation of 3H-thymidine and 3H-uridine into hairy cells of five patients. 3h-thymidine 91-103 interferon alpha 2 Homo sapiens 55-66 3594481-6 1987 3H-thymidine and 3H-uridine uptake per cell of clone A exposed to rH-TNF was not decreased. 3h-thymidine 0-12 tumor necrosis factor Rattus norvegicus 69-72 3611870-3 1987 In those three cell lines, VP16-213 suppressed cellular 3H-thymidine uptake by 70% as compared with the control. 3h-thymidine 56-68 host cell factor C1 Homo sapiens 27-31 3473988-2 1987 Continuous exposure to TGF beta inhibited DNA synthesis of cultured hepatocytes to a similar degree in both groups when labelled with 3H thymidine from 24-48 h or 48-72 h. At 20 pM TGF beta, 3H-thymidine incorporation was reduced by 64-78% in hepatocytes from normal liver and by 60-73% in cells from 18 h regenerating liver. 3h-thymidine 191-203 transforming growth factor, beta 1 Rattus norvegicus 23-31 3552073-0 1987 [Determination of lymphokine-induced cytolytic activity of macrophages by measuring the 3H-thymidine residue in prelabeled tumor cells]. 3h-thymidine 88-100 interleukin 2 Homo sapiens 18-28 2439406-4 1987 The combined techniques of immunocytochemistry and ratioautography revealed that AFP-positive foci and nodule had more 3H-thymidine labeling index than did areas without AFP-positive cells in liver with hyperplastic nodules; also one type of AFP-positive foci had a higher labeling index than the other type and in AFP-positive nodules there was active cell proliferation; but AFP-positive foci or nodules had less 3H-thymidine labeling than AFP-positive hepatoma cells. 3h-thymidine 119-131 alpha-fetoprotein Rattus norvegicus 81-84 2950212-10 1987 Concurrent studies of Sm/IGF stimulation of 3H-thymidine incorporation revealed that these cells were most sensitive to Sm-C/IGF I, followed by IGF II and MSA, and insulin. 3h-thymidine 44-56 insulin-like growth factor 1 Rattus norvegicus 125-130 2950212-12 1987 Half-maximal stimulations of 3H-thymidine incorporation corresponded closely with half-maximal binding displacement for Sm-C/IGF I and less so for IGF II and MSA. 3h-thymidine 29-41 insulin-like growth factor 1 Rattus norvegicus 125-130 2950212-12 1987 Half-maximal stimulations of 3H-thymidine incorporation corresponded closely with half-maximal binding displacement for Sm-C/IGF I and less so for IGF II and MSA. 3h-thymidine 29-41 insulin-like growth factor 2 Rattus norvegicus 147-153 3569440-2 1987 The assay, based on 3H-thymidine incorporation into phenylhydrazine-treated mouse spleen cells, showed a dose-response curve from 0.2 to 20 mU of sheep plasma or human urinary erythropoietin, with a 50-100-fold increase in 3H-thymidine incorporation. 3h-thymidine 20-32 erythropoietin Homo sapiens 176-190 3569440-2 1987 The assay, based on 3H-thymidine incorporation into phenylhydrazine-treated mouse spleen cells, showed a dose-response curve from 0.2 to 20 mU of sheep plasma or human urinary erythropoietin, with a 50-100-fold increase in 3H-thymidine incorporation. 3h-thymidine 223-235 erythropoietin Homo sapiens 176-190 8591897-4 1987 By autoradiography with 3H-thymidine, the authors observed that EGF stimulated corneal epithelial cell proliferation; however, fibronectin had no effect on cell proliferation. 3h-thymidine 24-36 pro-epidermal growth factor Oryctolagus cuniculus 64-67 2950245-12 1987 This ECGF retained its mitogenic properties, causing a 1000% to 1200% increase in 3H-thymidine incorporation into newly synthesized DNA in test murine LE-II cells. 3h-thymidine 82-94 fibroblast growth factor 1 Homo sapiens 5-9 3583501-3 1987 Exposure to T-2 toxin (10(-11)-10(-10)M) after 24 h increased 3H-thymidine uptake by splenic cells. 3h-thymidine 62-74 brachyury 2 Mus musculus 12-15 2853271-2 1987 This immunosuppression was observed as a reduced incorporation of 3H-thymidine in the lymphocyte proliferative response to Con A, was highly correlated with reduced secretion of interleukin 2 (IL2), and could not be augmented by addition of exogenous IL2. 3h-thymidine 66-78 interleukin 2 Mus musculus 178-191 3692307-8 1987 Intraperitoneal injection of neurotensin induced an increase of pancreatic DNA content and stimulated 3H-thymidine incorporation into DNA, whereas caerulein only augmented 3H-thymidine incorporation. 3h-thymidine 102-114 neurotensin Rattus norvegicus 29-40 2853271-2 1987 This immunosuppression was observed as a reduced incorporation of 3H-thymidine in the lymphocyte proliferative response to Con A, was highly correlated with reduced secretion of interleukin 2 (IL2), and could not be augmented by addition of exogenous IL2. 3h-thymidine 66-78 interleukin 2 Mus musculus 193-196 2853271-11 1987 By 18 days post-infection, when 3H-thymidine uptake could be induced at control level, Thy 1.2+, L3T4+, and Lyt 2+ (T-cytotoxic/suppressor) cells were each responsive to Con A activation at levels comparable to control but Lyt 1+ and IL2 R+ cells were still substantially suppressed (ca. 3h-thymidine 32-44 thymus cell antigen 1, theta Mus musculus 87-94 2853271-11 1987 By 18 days post-infection, when 3H-thymidine uptake could be induced at control level, Thy 1.2+, L3T4+, and Lyt 2+ (T-cytotoxic/suppressor) cells were each responsive to Con A activation at levels comparable to control but Lyt 1+ and IL2 R+ cells were still substantially suppressed (ca. 3h-thymidine 32-44 CD4 antigen Mus musculus 97-101 2853271-2 1987 This immunosuppression was observed as a reduced incorporation of 3H-thymidine in the lymphocyte proliferative response to Con A, was highly correlated with reduced secretion of interleukin 2 (IL2), and could not be augmented by addition of exogenous IL2. 3h-thymidine 66-78 interleukin 2 Mus musculus 251-254 3091392-3 1986 The maximal incorporation of 3H-thymidine and 14C-alanine into DNA and protein, respectively, was significantly stimulated by EGF (100 ng/ml). 3h-thymidine 29-41 epidermal growth factor like 1 Rattus norvegicus 126-129 2853271-11 1987 By 18 days post-infection, when 3H-thymidine uptake could be induced at control level, Thy 1.2+, L3T4+, and Lyt 2+ (T-cytotoxic/suppressor) cells were each responsive to Con A activation at levels comparable to control but Lyt 1+ and IL2 R+ cells were still substantially suppressed (ca. 3h-thymidine 32-44 CD5 antigen Mus musculus 223-228 2853271-11 1987 By 18 days post-infection, when 3H-thymidine uptake could be induced at control level, Thy 1.2+, L3T4+, and Lyt 2+ (T-cytotoxic/suppressor) cells were each responsive to Con A activation at levels comparable to control but Lyt 1+ and IL2 R+ cells were still substantially suppressed (ca. 3h-thymidine 32-44 interleukin 2 Mus musculus 234-237 2956668-4 1987 DHEA inhibited 3H-thymidine uptake of mitogen-stimulated cells from both G-6-PD+ and G-6-PD- (mediterranean type deficiency) individuals in a dose-dependent and reversible fashion. 3h-thymidine 15-27 glucose-6-phosphate dehydrogenase Homo sapiens 73-79 2956668-4 1987 DHEA inhibited 3H-thymidine uptake of mitogen-stimulated cells from both G-6-PD+ and G-6-PD- (mediterranean type deficiency) individuals in a dose-dependent and reversible fashion. 3h-thymidine 15-27 glucose-6-phosphate dehydrogenase Homo sapiens 85-91 3498694-3 1987 A dose-related stimulatory effect on the spontaneous 3H-thymidine incorporation of human thymocytes was obtained with methionine-enkephalin (met-enk), motilin and neurotensin. 3h-thymidine 53-65 motilin Homo sapiens 151-158 3498694-3 1987 A dose-related stimulatory effect on the spontaneous 3H-thymidine incorporation of human thymocytes was obtained with methionine-enkephalin (met-enk), motilin and neurotensin. 3h-thymidine 53-65 neurotensin Homo sapiens 163-174 3494553-1 1986 We have tested the reliability of a standard IL-2 microassay (3H-thymidine uptake by IL-2-dependent T cell lines) as a measure of the colony promoting activity (CPA) required for PHA-induced T cell colony growth in semi-solid cultures. 3h-thymidine 62-74 interleukin 2 Homo sapiens 85-89 3546050-0 1986 Epidermal growth factor stimulates (pro-)insulin biosynthesis and 3H-thymidine incorporation in isolated pancreatic rat islets. 3h-thymidine 66-78 epidermal growth factor like 1 Rattus norvegicus 0-23 2945302-4 1986 In cells from patients with chronic GVHD, 3H-thymidine uptake after the addition of FN was enhanced to the level of that in lymphocytes of the corresponding marrow donor without exogenous FN. 3h-thymidine 42-54 fibronectin 1 Homo sapiens 84-86 3528513-5 1986 Pulse-chase experiments with 3H-thymidine (3H-TdR) indicate that vimentin containing SMC possess a higher replicative activity than vimentin plus desmin containing SMC, thus explaining the selection of vimentin containing cells during culture. 3h-thymidine 29-41 vimentin Rattus norvegicus 65-73 3086327-8 1986 Restimulation of these cells with CM or IL-3 resulted in a dramatic rise in 3H-thymidine uptake 20-24 hours after restimulation. 3h-thymidine 76-88 interleukin 3 Mus musculus 40-44 3467533-7 1986 Only in those cells which had been treated with PGD 2, an almost complete blockade of 3H-thymidine incorporation was seen even after the single administration. 3h-thymidine 86-98 prostaglandin D2 synthase Homo sapiens 48-53 3964563-2 1986 When bone marrow from mice depleted of haemoglobin containing cells, was cultured in vitro in the presence of human urinary erythropoietin (Ep) a significant degree of erythroid cell proliferation and maturation occurred as measured directly by 3H-thymidine (3H-TdR) incorporation into DNA (autoradiographical measurement). 3h-thymidine 245-257 erythropoietin Homo sapiens 124-138 2427445-9 1986 IL-2 production or lack of production was established by 3H-uridine and 3H-thymidine incorporation as well as viable cell count using the IL-2 dependent cell line CTLL-2. 3h-thymidine 72-84 interleukin 2 Mus musculus 0-4 3484660-4 1986 IL2 production was measured by the 3H-thymidine-labeled CT6 assay on the supernatants of the PBL of cancer patients and normal controls after 24 hours of stimulation with PHA. 3h-thymidine 35-47 interleukin 2 Homo sapiens 0-3 3003975-7 1986 Similar to the mitogen activation of human peripheral blood lymphocytes, CsA was capable of inhibiting the induction of ODC and 3H-thymidine uptake of T cell tumor lines cultured with either fresh serum or mitogen. 3h-thymidine 128-140 ERCC excision repair 8, CSA ubiquitin ligase complex subunit Homo sapiens 73-76 3003975-11 1986 The suppression of ODC induction and 3H-thymidine incorporation associated with CsA treatment cannot be accounted for with changes in C-kinase and cAMPd PK activation. 3h-thymidine 37-49 ERCC excision repair 8, CSA ubiquitin ligase complex subunit Homo sapiens 80-83 3492089-4 1986 In five cases additional experiments were undertaken to evaluate the biological response of cultured cells to EGF as assessed by 3H-thymidine incorporation. 3h-thymidine 129-141 epidermal growth factor Homo sapiens 110-113 3492089-5 1986 In all cases EGF was a potent stimulus and increased 3H-thymidine incorporation by 2.5 to 6-fold. 3h-thymidine 53-65 epidermal growth factor Homo sapiens 13-16 3455709-3 1986 CRP causes minimal enhancement of proliferation in a mixed lymphocyte culture and a slight increase in 3H-thymidine uptake by unstimulated cells. 3h-thymidine 103-115 C-reactive protein Homo sapiens 0-3 4054251-1 1985 The uptake of 3H-thymidine by a suspension of spleen cells, obtained from mice made anemic by phenylhydrazine injections, is increased above the values obtained with native human or mouse erythropoietin (Ep) if the hormone is enzymatically asialylated. 3h-thymidine 14-26 erythropoietin Mus musculus 188-202 3100885-5 1986 The IL-2-induced 3H-thymidine uptake was completely blocked by a monoclonal antibody to IL-2 receptor, which indicates that IL-2 acted directly through functional IL-2 receptors. 3h-thymidine 17-29 interleukin 2 Homo sapiens 4-8 3100885-5 1986 The IL-2-induced 3H-thymidine uptake was completely blocked by a monoclonal antibody to IL-2 receptor, which indicates that IL-2 acted directly through functional IL-2 receptors. 3h-thymidine 17-29 interleukin 2 receptor subunit beta Homo sapiens 88-101 3100885-5 1986 The IL-2-induced 3H-thymidine uptake was completely blocked by a monoclonal antibody to IL-2 receptor, which indicates that IL-2 acted directly through functional IL-2 receptors. 3h-thymidine 17-29 interleukin 2 Homo sapiens 88-92 3100885-5 1986 The IL-2-induced 3H-thymidine uptake was completely blocked by a monoclonal antibody to IL-2 receptor, which indicates that IL-2 acted directly through functional IL-2 receptors. 3h-thymidine 17-29 interleukin 2 Homo sapiens 88-92 3879566-7 1985 The antimicrobial agent does not seem to have any effect on interleukin 2 (IL-2) production, whereas the uptake of 3H-thymidine by IL-2-dependent T cell blasts was severely reduced. 3h-thymidine 115-127 interleukin 15 Gallus gallus 131-135 4042784-1 1985 Phytohemagglutinin-stimulated human peripheral blood lymphocytes incorporating high concentrations of 3H-thymidine accumulate in G2 and show a consequent reduction in the number of cells entering M (division delay). 3h-thymidine 102-114 proline rich coiled-coil 2A Homo sapiens 129-131 4089532-1 1985 26 of 32 patients with multiple myeloma (MM) were successfully tested in vitro for human leucocyte interferon (IFN) sensitivity by use of the human tumour stem cell assay (HTCA) and/or 3H-thymidine incorporation (LI). 3h-thymidine 185-197 interferon alpha 1 Homo sapiens 89-115 4042784-6 1985 3H-thymidine caused an initial accumulation of lymphocytes in G2A, followed within 3-6 h by a gradual movement of some cells into G2B, with a subsequent accumulation of cells in G2B. 3h-thymidine 0-12 G protein-coupled receptor 132 Homo sapiens 62-65 4042784-6 1985 3H-thymidine caused an initial accumulation of lymphocytes in G2A, followed within 3-6 h by a gradual movement of some cells into G2B, with a subsequent accumulation of cells in G2B. 3h-thymidine 0-12 proline rich coiled-coil 2A Homo sapiens 130-133 4042784-6 1985 3H-thymidine caused an initial accumulation of lymphocytes in G2A, followed within 3-6 h by a gradual movement of some cells into G2B, with a subsequent accumulation of cells in G2B. 3h-thymidine 0-12 proline rich coiled-coil 2A Homo sapiens 178-181 3878884-5 1985 Addition of IL-2 to unstimulated T cells or T cells stimulated in vitro with either tetanus toxoid or PPD sometimes potentiated incorporation of 3H-thymidine into the cells after 6 days of culture. 3h-thymidine 145-157 interleukin 2 Homo sapiens 12-16 3891240-7 1985 Similar quantitative results were obtained to those using 3H-thymidine uptake inhibition, in terms of microgram protein of pure colicin required to affect adversely 50% of the cells. 3h-thymidine 58-70 colicin Escherichia coli 128-135 3928979-3 1985 Antibodies directed against the murine interleukin-2 receptor blocked 3H-thymidine incorporation by 32D cl-23 cells grown in interleukin-2, but had no effect on 32D cl-23 in interleukin-3. 3h-thymidine 70-82 interleukin 2 Mus musculus 39-52 3928979-3 1985 Antibodies directed against the murine interleukin-2 receptor blocked 3H-thymidine incorporation by 32D cl-23 cells grown in interleukin-2, but had no effect on 32D cl-23 in interleukin-3. 3h-thymidine 70-82 interleukin 2 Mus musculus 125-138 2985157-1 1985 Spontaneous velocity sedimentation of B lymphocytes activated by intraperitoneal injection of ovalbumin into mice was used to obtain cell cycle synchronized cells, evidenced by differences in the incorporation of labeled precursors of protein and nucleic synthesis (14C-methionine and 3H-thymidine). 3h-thymidine 285-297 serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus 94-103 3919035-5 1985 At 24 hr of culture the increase in cellular Ca2+ correlated well with the proliferative response as measured by 3H-thymidine incorporation. 3h-thymidine 113-125 carbonic anhydrase 2 Homo sapiens 45-48 2582223-1 1985 Systemic administration of Neurotensin, a tridecapeptide, in immature rats treated with estradiol benzoate significantly enhances uterine DNA synthesis as reflected by the incorporation of 3H-thymidine. 3h-thymidine 189-201 neurotensin Rattus norvegicus 27-38 3884636-5 1985 The combination of insulin, epidermal growth factor, and arginine-vasopressin was maximally effective in stimulating both bumetanide-sensitive K+ uptake and 3H-thymidine incorporation in quiescent cells; bumetanide, however, did not interfere with the hormonal stimulation of DNA synthesis. 3h-thymidine 157-169 insulin Homo sapiens 19-26 3884636-5 1985 The combination of insulin, epidermal growth factor, and arginine-vasopressin was maximally effective in stimulating both bumetanide-sensitive K+ uptake and 3H-thymidine incorporation in quiescent cells; bumetanide, however, did not interfere with the hormonal stimulation of DNA synthesis. 3h-thymidine 157-169 epidermal growth factor Homo sapiens 28-51 3884636-5 1985 The combination of insulin, epidermal growth factor, and arginine-vasopressin was maximally effective in stimulating both bumetanide-sensitive K+ uptake and 3H-thymidine incorporation in quiescent cells; bumetanide, however, did not interfere with the hormonal stimulation of DNA synthesis. 3h-thymidine 157-169 arginine vasopressin Homo sapiens 66-77 3888615-4 1985 Factors that stimulated 3H-thymidine incorporation included cholera toxin, epidermal growth factor, and rat serum. 3h-thymidine 24-36 epidermal growth factor like 1 Rattus norvegicus 75-98 6315022-2 1983 A 72-hour exposure of confluent monolayers of rabbit synovial fibroblasts in 10% fetal calf serum to partially purified TGF-beta in the presence of TGF-alpha gave a 2- to 5-fold increase in incorporation of 3H-thymidine, protein content, and cell number. 3h-thymidine 207-219 protransforming growth factor alpha Oryctolagus cuniculus 148-157 4043440-3 1985 The effect of the NSP fraction and its four peptide constituents (A, C2, D and G) on the 3H-thymidine incorporation into REF and R-XC cells in vitro was described. 3h-thymidine 89-101 complement C2 Bos taurus 69-80 6391762-5 1984 (3) Addition of exogenous, purified human interleukin-2 (IL-2) to antigen stimulated PBMC from some lepromatous patients showed the best improvement in terms of overall 3H-thymidine incorporation, indicating that lepromatous patients possess T cells which can differentiate to an IL-2 responsive state. 3h-thymidine 169-181 interleukin 2 Homo sapiens 42-55 6391762-5 1984 (3) Addition of exogenous, purified human interleukin-2 (IL-2) to antigen stimulated PBMC from some lepromatous patients showed the best improvement in terms of overall 3H-thymidine incorporation, indicating that lepromatous patients possess T cells which can differentiate to an IL-2 responsive state. 3h-thymidine 169-181 interleukin 2 Homo sapiens 57-61 6319299-2 1984 The expression of B3/25 antigen was correlated to DNA synthesis as measured by spontaneous 3H-thymidine incorporation (p = 0.0003) and histopathologically high-grade malignancy (p = 0.00003). 3h-thymidine 91-103 immunoglobulin kappa variable 4-1 Homo sapiens 18-23 6376085-4 1984 For in vitro exposures, PRP were incubated with 3H-thymidine (3H-TdR) in the presence of genotoxic agents for 18-22 hr. 3h-thymidine 48-60 proline rich protein 2-like 1 Rattus norvegicus 24-27 6239124-2 1984 Concentrations of Fn less than 30 micrograms/ml enhanced the growth rate of these cells as judged by 3H-thymidine incorporation, whereas higher levels of Fn were inhibitory. 3h-thymidine 101-113 fibronectin 1 Mus musculus 18-20 3880762-5 1985 The effects of SM-C and insulin on 3H-thymidine incorporation were additive. 3h-thymidine 35-47 insulin Homo sapiens 24-31 6735433-3 1984 Experiments suggest that this inhibition is unlikely to be the result of alpha 2HS glycoprotein binding either PHA or 3H-thymidine but is more likely to act at the cellular level. 3h-thymidine 118-130 alpha 2-HS glycoprotein Homo sapiens 73-95 6884443-0 1983 A simple microassay for erythropoietin based on 3H-thymidine incorporation into spleen cells from phenylhydrazine treated mice. 3h-thymidine 48-60 erythropoietin Mus musculus 24-38 6225510-1 1983 Harvest fluid derived from a primary hepatocellular carcinoma cell line (PLC/PRF/5) inhibited the incorporation of 3H-thymidine into PHA-activated human lymphocytes. 3h-thymidine 115-127 heparan sulfate proteoglycan 2 Homo sapiens 73-76 6223096-1 1983 The results presented here show that Fab" antibody fragments directed to complement proteins C5, C6, and C7 inhibit lymphocyte stimulation in mixed lymphocyte culture (MLC) by up to 65%, as determined by decreased incorporation of 3H-thymidine. 3h-thymidine 231-243 FA complementation group B Homo sapiens 37-40 6830705-4 1983 Dexamethasone inhibited the incorporation of 3H-thymidine into DNA in fetal liver cells stimulated with erythropoietin, supporting the hypothesis that dexamethasone inhibits the proliferation but not the differentiation of fetal liver CFU-E and BFU-E. 3h-thymidine 45-57 erythropoietin Homo sapiens 104-118 6573546-2 1983 Thrombin induced a significant increase of 3H-thymidine uptake into cells with a 1,5- to 2-fold increase of cell count. 3h-thymidine 43-55 coagulation factor II, thrombin Homo sapiens 0-8 6571789-2 1983 Thrombin induced a significant increase of 3H-thymidine uptake into cells with a 1,5- to 2-fold increase of cell count. 3h-thymidine 43-55 coagulation factor II, thrombin Homo sapiens 0-8 6196225-8 1983 Only the weak MBP positive cells incorporated 3H-Thymidine. 3h-thymidine 46-58 myelin basic protein Mus musculus 14-17 6642186-5 1983 In cultures supplemented with 200 ng of vasopressin per ml of medium, the amount of the incorporated 3H-thymidine was lower than in the control cultures, whereas in cultures to which higher quantities of the same hormone (10 micrograms/ml) were added a reverse effect was observed and the difference was statistically significant as compared with the control cultures (p less than 0.001). 3h-thymidine 101-113 arginine vasopressin Rattus norvegicus 40-51 6220984-2 1983 PS-K addition to primary alloantigen sensitization cultures (C57B1/6J spleen cells against X-irradiated P815 cells) resulted in augmented 3H-thymidine uptake and cell mediated cytolytic activity. 3h-thymidine 138-150 TAO kinase 2 Mus musculus 0-4 6365577-1 1983 Normal human IMR 90 fibroblasts at population doubling levels (PDL) 28 approximately 33 had an increased incorporation of 3H-thymidine into DNA when the cells were pretreated with physiologic concentrations of insulin (5 approximately 10 ng/ml) prior to re-initiation of the cell cycle. 3h-thymidine 122-134 insulin Homo sapiens 210-217 6984422-6 1982 In addition, iota CGN induced an early peak of 3H-thymidine uptake at day 1, which found out to be cytoplasmic uptake of 3H-thymidine. 3h-thymidine 47-59 cingulin Homo sapiens 18-21 6681829-4 1983 However, in BeWo cells, an inverse relationship between the incorporation of 3H-thymidine and secretion of hCG was not clearly observed. 3h-thymidine 77-89 hypertrichosis 2 (generalised, congenital) Homo sapiens 107-110 6867466-1 1983 In 70 experiments, the existence of a circulating renal growth factor was confirmed by 9.3% stimulation of 3H-thymidine into the DNA of renal fragments incubating for 90 min in the presence of sera from 20-hour unilaterally nephrectomized rats compared to sera from 20-hour sham-operated rats (p less than 0.001). 3h-thymidine 107-119 myotrophin Rattus norvegicus 56-69 6984422-6 1982 In addition, iota CGN induced an early peak of 3H-thymidine uptake at day 1, which found out to be cytoplasmic uptake of 3H-thymidine. 3h-thymidine 121-133 cingulin Homo sapiens 18-21 7108226-4 1982 The HNK-1+ cells exhibited virtually no response to either mitogens (PHA, Con A, and PWM) or allogeneic cells, because the 3H-thymidine uptake for HNK-1+ cells was only 1 to 3% of that for HNK-1- cells. 3h-thymidine 123-135 beta-1,3-glucuronyltransferase 1 Homo sapiens 147-152 7108226-4 1982 The HNK-1+ cells exhibited virtually no response to either mitogens (PHA, Con A, and PWM) or allogeneic cells, because the 3H-thymidine uptake for HNK-1+ cells was only 1 to 3% of that for HNK-1- cells. 3h-thymidine 123-135 beta-1,3-glucuronyltransferase 1 Homo sapiens 147-152 7028591-0 1981 Reduced mitogenic action of insulin evaluated as 3H-thymidine uptake in diabetic cultured fibroblasts. 3h-thymidine 49-61 insulin Homo sapiens 28-35 7097184-2 1982 The technique used for detection of H-2 antigens on the embryos was a highly sensitive, automated, complement-dependent cytotoxicity assay, based on the principle that live embryos will incorporate 3H-thymidine into DNA, but embryos killed with antiserum and complement will not. 3h-thymidine 198-210 histocompatibility-2, MHC Mus musculus 36-39 6218870-5 1982 Mitomycin C-treated LNC and TIL inhibited PHA induced 3H-thymidine incorporation of admixed autologous PBL, suggesting the presence of suppressor cells. 3h-thymidine 54-66 toll like receptor 1 Homo sapiens 28-31 6978603-6 1981 Furthermore alpha 1-AT decreases 3H-thymidine incorporation into lymphocytes stimulated by B or T cell mitogens or by allogeneic cells. 3h-thymidine 33-45 serpin family A member 1 Homo sapiens 12-22 7032623-4 1981 The proliferating and insulin-synthetizing beta-cells were detected by selective 3H-thymidine or 3H-leucine incorporation. 3h-thymidine 81-93 insulin Sus scrofa 22-29 7112553-2 1982 Hemoglobin, transferrin and ferritin enhanced the incorporation of 3H-thymidine into DNA after PHA-stimulation of lymphocytes, while hemin, iron metal powder, ferrous sulfate, chromium powder, and zinc sulfate have little effect. 3h-thymidine 67-79 transferrin Homo sapiens 12-23 6296417-7 1982 EGF was maximally effective in stimulating 3H-thymidine incorporation at concentrations between 1-10 ng/ml. 3h-thymidine 43-55 epidermal growth factor Rattus norvegicus 0-3 7028591-6 1981 However, when lower doses of insulin were used, 2 out 5 cases of JODM and 4 out of 8 cases of AODM showed a similar response to controls, while 3H-thymidine uptake was low or absent in the remaining cases, including all those with CDM. 3h-thymidine 144-156 insulin Homo sapiens 29-36 6977309-1 1981 Purified human alpha 1-antitrypsin (alpha 1-AT) was shown to inhibit 3H-thymidine incorporation into mouse or human lymphocytes stimulated by various mitogens or by allogeneic cells. 3h-thymidine 69-81 serpin family A member 1 Homo sapiens 15-34 6977309-1 1981 Purified human alpha 1-antitrypsin (alpha 1-AT) was shown to inhibit 3H-thymidine incorporation into mouse or human lymphocytes stimulated by various mitogens or by allogeneic cells. 3h-thymidine 69-81 serpin family A member 1 Homo sapiens 36-46 7251692-4 1981 In kinetic pulse experiments TPA enhanced 3H-thymidine incorporation in density-inhibited cells stimulated by fresh serum but only after markedly suppressing incorporation 8-13 hrs after serum stimulation. 3h-thymidine 42-54 promotion susceptibility QTL 1 Mus musculus 29-32 7459282-2 1981 Effects of human transferrin bound iron and of serum on the stimulation of incorporation of 3H-thymidine into DNA. 3h-thymidine 92-104 transferrin Homo sapiens 17-28 7032452-5 1981 Increased numbers of mitoses and elevated incorporation of 3H-thymidine into the nuclear chromatin were observed in both anti-LH beta reactive cells and other pituitary cells after castration. 3h-thymidine 59-71 luteinizing hormone subunit beta Rattus norvegicus 126-133 7459282-3 1981 Iron bound to human transferrin but not apotransferrin, increases the effect of erythropoietin in stimulating incorporation of 3H-thymidine into DNA in fetal mouse liver cells in vitro. 3h-thymidine 127-139 transferrin Homo sapiens 20-31 7459282-3 1981 Iron bound to human transferrin but not apotransferrin, increases the effect of erythropoietin in stimulating incorporation of 3H-thymidine into DNA in fetal mouse liver cells in vitro. 3h-thymidine 127-139 erythropoietin Homo sapiens 80-94 7459282-5 1981 Human sera contain factors in addition to erythropoietin and transferin-iron which may modify the stimulation of incorporation of 3H-thymidine into fetal mouse liver DNA induced by erythropoietin. 3h-thymidine 130-142 erythropoietin Mus musculus 42-56 7459282-5 1981 Human sera contain factors in addition to erythropoietin and transferin-iron which may modify the stimulation of incorporation of 3H-thymidine into fetal mouse liver DNA induced by erythropoietin. 3h-thymidine 130-142 erythropoietin Mus musculus 181-195 7211212-0 1980 [The effect of human cord plasma on the incorporation of 3H-thymidine by PHA-stimulated peripheral blood lymphocytes of cervical cancer patient (author"s transl)]. 3h-thymidine 57-69 lamin B receptor Homo sapiens 73-76 6259408-2 1981 In contrast fibronectin inhibits the 3H-thymidine uptake of fibroblasts. 3h-thymidine 37-49 fibronectin 1 Homo sapiens 12-23 7286039-4 1981 Because of their increased specific activity of dihydrofolate reductase, the cells were able to maintain normal DNA metabolism, as measured by the ratio of the incorporation rates of 3H-deoxyuridine and 3H-thymidine, as well as normal cell growth at 1 X 10(-6) M, and in some cases at 1 X 10(-5) M triamterene. 3h-thymidine 203-215 dihydrofolate reductase Homo sapiens 48-71 7204643-0 1980 Non-specific esterase activity in reactive cells in injured nervous tissue labeled with 3H-thymidine or 125iododeoxyuridine injected before injury. 3h-thymidine 88-100 enolase 2 Homo sapiens 0-21 519028-3 1979 When 3H-thymidine was injected to the mice at 2 a. m., tG2min was 1h; tG2+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 15.9h. 3h-thymidine 5-17 transglutaminase 2, C polypeptide Mus musculus 55-58 7448388-1 1980 The action of various doses of PHA and Con A on 3H-thymidine incorporation in DNA of blood lymphocytes was studied in health and schizophrenia. 3h-thymidine 48-60 lamin B receptor Homo sapiens 31-34 7388515-1 1980 Human retroplacental blood serum significantly (p less than 0.01) suppresses the in-vitro uptake of 3H-thymidine--that is, synthesis of deoxyribonucleic acid--by spontaneously growing human lymphocytes in the presence of exogenous spermine, but only in concentrations with a higher polyamine oxidase activity than that found in maternal peripheral blood serum during pregnancy. 3h-thymidine 100-112 polyamine oxidase Homo sapiens 282-299 6154115-9 1980 A significant inverse correlation was observed between 3H-thymidine uptake and the areas under the alpha-fetoprotein time curves in the controls (p less than 0.001). 3h-thymidine 55-67 alpha-fetoprotein Rattus norvegicus 99-116 6993072-6 1980 Peripheral blood lymphocyte proliferation was studied with several PPD concentrations, 10 microgram/ml always inducing the maximum 3H-thymidine uptake. 3h-thymidine 131-143 cellular communication network factor 6 Homo sapiens 67-70 6264232-8 1980 Since native and biotinyl EGF have identical abilities to stimulate the uptake of 3H-thymidine into DNA when incubated with cultured murine 3T3 cells, the direct linkage of EGF to its receptor does not appear to play an important role in EGF-stimulated mitogenesis. 3h-thymidine 82-94 epidermal growth factor Mus musculus 26-29 519028-3 1979 When 3H-thymidine was injected to the mice at 2 a. m., tG2min was 1h; tG2+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 15.9h. 3h-thymidine 5-17 triglyceride level 1 Mus musculus 130-133 519028-4 1979 When 3H-thymidine was injected at 2 p. m., tS rose up to 8.2 and tG1+1/2 M up to 14.8h. 3h-thymidine 5-17 triglyceride level 1 Mus musculus 65-68 519028-3 1979 When 3H-thymidine was injected to the mice at 2 a. m., tG2min was 1h; tG2+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 15.9h. 3h-thymidine 5-17 transglutaminase 2, C polypeptide Mus musculus 70-73 519028-3 1979 When 3H-thymidine was injected to the mice at 2 a. m., tG2min was 1h; tG2+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 2h; tS was 7.1; tG1+1/2 M was 15.9h. 3h-thymidine 5-17 triglyceride level 1 Mus musculus 100-103 312867-7 1979 More than 40% of the TdT-positive cells incorporated 3H-thymidine during a 20-min pulse. 3h-thymidine 53-65 deoxynucleotidyltransferase, terminal Mus musculus 21-24 422280-3 1979 The purified PAG inhibited clearly the 3H-thymidine uptake of normal lymphocytes stimulated with phytohemagglutinin and also the spontaneous attachment of sheep erythrocytes to normal lymphocytes. 3h-thymidine 39-51 phosphoprotein membrane anchor with glycosphingolipid microdomains 1 Homo sapiens 13-16 449250-2 1979 Fibrin as well as thrombin showed dose-dependent growth promoting activities as revealed by cell counting and 3H-thymidine uptake. 3h-thymidine 110-122 coagulation factor II, thrombin Homo sapiens 18-26 428519-3 1979 Labelling of the cells with activated charcoal or 3H-thymidine gave evidence of their invasion into the CAM mesoderm, where they induced the formation of new capillaries. 3h-thymidine 50-62 calmodulin 2 Mus musculus 104-107 422280-4 1979 17 of 19 rheumatoid plasmas inhibited the 3H-thymidine uptake of normal lymphocytes and intensity of their inhibitory effects correlated with serum PAG levels. 3h-thymidine 42-54 phosphoprotein membrane anchor with glycosphingolipid microdomains 1 Homo sapiens 148-151 698040-2 1978 The effects of bovine insulin (5.0 microgram/ml) human placental lactogen (10.0 microgram/ml) and human growth hormone (10.0 microgram/ml) on 3H-thymidine incorporation into DNA were determined on the cultured tumour slices. 3h-thymidine 142-154 growth hormone 1 Homo sapiens 104-118 309487-2 1978 The addition of HFIF (100 to 400 IFU/ml) to mixed leukocyte cultures decreased alloantigen-induced lymphocyte proliferative responses as determined by both recovery of responding cells and by 3H-thymidine incorporation into responding cells. 3h-thymidine 192-204 interferon beta 1 Homo sapiens 16-20 310345-3 1978 Bru Pel was also found to cause increases in the incorporation of 3H-thymidine of phytohemagglutinin-sensitive splenic T lymphocytes and lipopolysaccharide-sensitive splenic B lymphocytes over 3H-thymidine-incorporated values for untreated tumor controls. 3h-thymidine 66-78 collagen, type IV, alpha 1 Mus musculus 0-3 310345-3 1978 Bru Pel was also found to cause increases in the incorporation of 3H-thymidine of phytohemagglutinin-sensitive splenic T lymphocytes and lipopolysaccharide-sensitive splenic B lymphocytes over 3H-thymidine-incorporated values for untreated tumor controls. 3h-thymidine 193-205 collagen, type IV, alpha 1 Mus musculus 0-3 212239-3 1978 Comparative growth, determined by measuring 3H-thymidine uptake, showed that the combination of FGF, DME and insulin in medium with 20% foetal calf serum produced the highest growth rate. 3h-thymidine 44-56 insulin Homo sapiens 109-116 206567-2 1978 This work demonstrates (1) that thrombin has to be prensent during most or all of the G1 period to ensure maximal DNA synthesis, (2) that DNA synthesis increases about three hours later after thrombin than after serum treatment, (3) that both thrombin and serum activate transport of uridine, D--2-deoxy-glucose and putrescine, (4) that thrombin is able to increase 3H-thymidine incorporation also in SV40 transformed human fibroblasts, in HeLa cells and in two continuous monkey cell lines. 3h-thymidine 366-378 coagulation factor II, thrombin Homo sapiens 32-40 1085380-3 1975 Reactivity (3H-thymidine incorporation) of lymphocytes of patients after the therapy, to specific antigen, ie., purified protein derivative (PPD) or Bordetella pertussis organisms in vitro, was markedly depressed. 3h-thymidine 12-24 cellular communication network factor 6 Homo sapiens 141-144 63929-1 1977 Phytohemagglutin (PHA)-induced lymphocyte transformation (PILT) was determined in 217 women taking oral contraceptives and 203 control women by means of the uptake of 3H-thymidine into DNA of lymphocytes cultured in heterologous serum. 3h-thymidine 167-179 tight junction associated protein 1 Homo sapiens 58-62 944704-4 1976 The addition of hEGF to quiescent confluent monolayers of HF cells, maintained in a medium with 1% calf serum for 48 hours, resulted in a 10- to 20-fold increase in the amount of 3H-thymidine incorporation after 20-24 hours. 3h-thymidine 179-191 epidermal growth factor Homo sapiens 16-20 1008504-3 1976 Administration of h CG at pharmacological doses for three days to male rat during puberty increases plasma testosterone levels and 3H-thymidine incorporation into testicular DNA. 3h-thymidine 131-143 hypertrichosis 2 (generalised, congenital) Homo sapiens 20-22 311626-8 1978 At low concentrations, alpha-1-antitrypsin (AAT) had no effect, but at high concentrations it inhibited 3H-thymidine uptake. 3h-thymidine 104-116 serpin family A member 1 Homo sapiens 23-42 62806-3 1976 The data indicate that HLA-D differences and poliferative MLC responses as measured by 3H-thymidine incorporation are not requisite for the in vitro generation of cytotoxic cells and suggest the existence of a CML-S locus (loci) distinct from HLA-A, HLA-B and HLA-D. 3h-thymidine 87-99 modulator of VRAC current 1 Homo sapiens 58-61 51071-10 1975 It should be stressed that the examination of CSF cells by 3H-thymidine autoradiography in cases of brain tumors could be one of the valuable methods indicating the DNA synthesis of the tumor cells, which is an important parameter of malignancy. 3h-thymidine 59-71 colony stimulating factor 2 Homo sapiens 46-49 33317684-8 2021 Using a 3H-thymidine incorporation assay, isolated CD4+CD25+ Tregs induced by the different treatments suppressed the proliferation of CD4+CD25- T cells. 3h-thymidine 8-20 CD4 antigen Mus musculus 51-54 1209610-1 1975 The effect of morphine on lymphocyte blastoid transformation induced by PHA was studied in vitro by observing the uptake of 3H-thymidine into nucleic acid of the lymphocytes. 3h-thymidine 124-136 lamin B receptor Homo sapiens 72-75 1179419-1 1975 The effect of pentazocine on lymphocyte transformation induced by PHA was studied in vitro by observing the incorporation of 3H-thymidine into nucleic acid of the lymphocytes. 3h-thymidine 125-137 lamin B receptor Homo sapiens 66-69 33504617-7 2021 The stimulation of CD8+ T cells by fibrocytes was examined in MLRs with a 3H-thymidine incorporation assay. 3h-thymidine 74-86 CD8a molecule Homo sapiens 19-22 4431051-0 1974 Prolactin-stimulating effect on 3H-thymidine incorporation in 3-methylcholanthrene-induced cervical carcinomas in normal and estrogenized mice. 3h-thymidine 32-44 prolactin Mus musculus 0-9 4280235-0 1974 Correlation between morphological blastformation rate and functional 3H-thymidine uptake in mixed lymphocyte culture in the presence of PHA. 3h-thymidine 69-81 lamin B receptor Homo sapiens 136-139 33317684-8 2021 Using a 3H-thymidine incorporation assay, isolated CD4+CD25+ Tregs induced by the different treatments suppressed the proliferation of CD4+CD25- T cells. 3h-thymidine 8-20 interleukin 2 receptor, alpha chain Mus musculus 55-59 33317684-8 2021 Using a 3H-thymidine incorporation assay, isolated CD4+CD25+ Tregs induced by the different treatments suppressed the proliferation of CD4+CD25- T cells. 3h-thymidine 8-20 CD4 antigen Mus musculus 135-138 33317684-8 2021 Using a 3H-thymidine incorporation assay, isolated CD4+CD25+ Tregs induced by the different treatments suppressed the proliferation of CD4+CD25- T cells. 3h-thymidine 8-20 interleukin 2 receptor, alpha chain Mus musculus 139-143 21245963-15 2011 AREG significantly stimulated 3H-thymidine and 3H-leucine uptake in SRA01/04 cells as did a positive control epidermal growth factor (EGF). 3h-thymidine 30-42 amphiregulin Homo sapiens 0-4 33053110-3 2020 The exposure in vitro of SK-N-SH cells to RU486 revealed a dose-dependent inhibition of 3H-thymidine incorporation due to a rapid but persistent inhibition of MAPKinase activity and ERK phosphorylation. 3h-thymidine 88-100 mitogen-activated protein kinase 1 Homo sapiens 182-185 26676103-7 2016 The proliferation of CD4+ CD25- T cells was determined by 3H-thymidine incorporation. 3h-thymidine 58-70 CD4 molecule Homo sapiens 21-24 26676103-7 2016 The proliferation of CD4+ CD25- T cells was determined by 3H-thymidine incorporation. 3h-thymidine 58-70 interleukin 2 receptor subunit alpha Homo sapiens 26-30 32818904-5 2021 Using 3H-thymidine as a marker, it was also demonstrated that insulin and IGF-1-stimulated cell proliferation in lamellar explants over the same concentration range as each other (1-100 nM), implying that each peptide acts via its own receptor (P < 0.001). 3h-thymidine 6-18 INS Equus caballus 62-69 32818904-5 2021 Using 3H-thymidine as a marker, it was also demonstrated that insulin and IGF-1-stimulated cell proliferation in lamellar explants over the same concentration range as each other (1-100 nM), implying that each peptide acts via its own receptor (P < 0.001). 3h-thymidine 6-18 insulin like growth factor 1 Equus caballus 74-79 22753710-3 2012 MATERIALS AND METHODS: In vitro study: Huh7 proliferation was assayed by 3H-thymidine incorporation and by thiazolyl blue tetrazolium bromide (MTT) assay. 3h-thymidine 73-85 MIR7-3 host gene Homo sapiens 39-43 19957574-4 2009 The direct suppression effect of CD-4+ CD-25+ regulatory T cells on CD-4+ CD-25- T lymphocytes proliferation was performed by the mixed lymphocytes reaction and measured by 3H-thymidine radioactive assay. 3h-thymidine 173-185 CD4 molecule Homo sapiens 33-37 19957574-4 2009 The direct suppression effect of CD-4+ CD-25+ regulatory T cells on CD-4+ CD-25- T lymphocytes proliferation was performed by the mixed lymphocytes reaction and measured by 3H-thymidine radioactive assay. 3h-thymidine 173-185 CD4 molecule Homo sapiens 68-72 21187475-3 2010 MATERIALS AND METHODS: Huh7 proliferation was assayed by 3H-thymidine incorporation and by MTT assay. 3h-thymidine 57-69 MIR7-3 host gene Homo sapiens 23-27