PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
12572863-11	2002	An [3H]thymidine incorporation study demonstrated that platelet-derived growth factor (PDGF)-BB, basic fibroblast growth factor (bFGF), and insulin-like growth factor (IGF)-I significantly increased the uptake of [3H]thymidine into isolated SEMFs.	3h]thymidine	4-16	fibroblast growth factor 2	Homo sapiens	97-127
19010836-3	2008	Proliferation, viability, and apoptosis were analyzed on cells exposed to EPO, prednisone, or inhibitors of EPOR pathways by [3H]thymidine incorporation, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and Annexin V/propidium iodide staining.	3h]thymidine	126-138	erythropoietin receptor	Homo sapiens	108-112
15878397-5	2005	DNA synthesis was also inhibited by BIC, as evidenced by a decrease in the cellular incorporation of [3H]thymidine.	3h]thymidine	102-114	Mir155 host gene (non-protein coding)	Mus musculus	36-39
15511088-3	2004	In this study, we demonstrate that overexpression of both dominant negative Rab5 (Rab5:S34N) and full-length Rin1 selectively block EGF activation of the Raf-Erk1/2 kinase pathway and EGF-stimulated incorporation of [3H]thymidine into DNA without affecting the activity of JN and p38 kinase pathways.	3h]thymidine	217-229	RAB5A, member RAS oncogene family	Homo sapiens	76-80
15511088-3	2004	In this study, we demonstrate that overexpression of both dominant negative Rab5 (Rab5:S34N) and full-length Rin1 selectively block EGF activation of the Raf-Erk1/2 kinase pathway and EGF-stimulated incorporation of [3H]thymidine into DNA without affecting the activity of JN and p38 kinase pathways.	3h]thymidine	217-229	RAB5A, member RAS oncogene family	Homo sapiens	82-86
15511088-3	2004	In this study, we demonstrate that overexpression of both dominant negative Rab5 (Rab5:S34N) and full-length Rin1 selectively block EGF activation of the Raf-Erk1/2 kinase pathway and EGF-stimulated incorporation of [3H]thymidine into DNA without affecting the activity of JN and p38 kinase pathways.	3h]thymidine	217-229	Ras and Rab interactor 1	Homo sapiens	109-113
15511088-3	2004	In this study, we demonstrate that overexpression of both dominant negative Rab5 (Rab5:S34N) and full-length Rin1 selectively block EGF activation of the Raf-Erk1/2 kinase pathway and EGF-stimulated incorporation of [3H]thymidine into DNA without affecting the activity of JN and p38 kinase pathways.	3h]thymidine	217-229	zinc fingers and homeoboxes 2	Homo sapiens	154-157
12417265-10	2002	This ET-1 (1-31)-induced increase in [3H]thymidine incorporation was also inhibited by NAC and DPI, but not by ascorbic acid.	3h]thymidine	38-50	endothelin 1	Homo sapiens	5-9
12417265-10	2002	This ET-1 (1-31)-induced increase in [3H]thymidine incorporation was also inhibited by NAC and DPI, but not by ascorbic acid.	3h]thymidine	38-50	X-linked Kx blood group	Homo sapiens	87-90
19386602-12	2009	Furthermore, IL-32-specific small interfering RNA significantly decreased the uptake of [3H]thymidine and increased the annexin V-positive population (apoptotic cells) in PANC-1 cells.	3h]thymidine	89-101	interleukin 32	Homo sapiens	13-18
12572863-11	2002	An [3H]thymidine incorporation study demonstrated that platelet-derived growth factor (PDGF)-BB, basic fibroblast growth factor (bFGF), and insulin-like growth factor (IGF)-I significantly increased the uptake of [3H]thymidine into isolated SEMFs.	3h]thymidine	4-16	fibroblast growth factor 2	Homo sapiens	129-133
12572863-11	2002	An [3H]thymidine incorporation study demonstrated that platelet-derived growth factor (PDGF)-BB, basic fibroblast growth factor (bFGF), and insulin-like growth factor (IGF)-I significantly increased the uptake of [3H]thymidine into isolated SEMFs.	3h]thymidine	4-16	insulin like growth factor 1	Homo sapiens	140-174
11861424-12	2002	In parallel, blockade of Tcf-4 resulted in inhibition of [3H]thymidine incorporation and partial blockade of the G1-S phase transition.	3h]thymidine	58-70	transcription factor 4	Rattus norvegicus	25-30
11924572-4	2002	Both strain-related and 17beta-estradiol-related increases in [3H]thymidine incorporation were abolished by the estrogen receptor (ER) modulator ICI 182,780 (10-8 M).	3h]thymidine	63-75	estrogen receptor 1	Homo sapiens	112-129
11924572-4	2002	Both strain-related and 17beta-estradiol-related increases in [3H]thymidine incorporation were abolished by the estrogen receptor (ER) modulator ICI 182,780 (10-8 M).	3h]thymidine	63-75	estrogen receptor 1	Homo sapiens	131-133
11394655-10	2001	H-35 cells treated with cross-linked anti-CD44 antibodies or HA show an increased rate of incorporation of [3H]thymidine (30 and 25%, respectively) with respect to the control.	3h]thymidine	108-120	CD44 molecule (Indian blood group)	Rattus norvegicus	42-46
10579644-3	1999	When the granulosa cells were cultured with TGF alpha, the cell number as well as the incorporation of [3H]thymidine was increased.	3h]thymidine	104-116	protransforming growth factor alpha	Coturnix japonica	44-53
10880954-4	2000	TNF-alpha (10 ng.mL-1) and C8-ceramide (20 microM) inhibited the incorporation of [3H]thymidine into DNA and led to an accumulation of cells in the G1 phase of the cell cycle.	3h]thymidine	83-95	tumor necrosis factor	Homo sapiens	0-9
9700129-3	1998	The results show that SP-A and SP-D were able to reduce the incorporation of [3H]thymidine into PBMC in a dose-dependent manner.	3h]thymidine	78-90	surfactant protein A1	Homo sapiens	22-26
9951833-4	1999	UVC treatment during G0/G1 phase resulted in decreased incorporation of [3H]thymidine, an effect that was enhanced by pretreatment with TGF-beta1.	3h]thymidine	73-85	transforming growth factor beta 1	Homo sapiens	136-145
9733212-3	1998	When VSMC proliferation was stimulated by fetal bovine serum, the addition of TGF-beta1 (20 ng/ml) or ascorbate (1 mM) to the cell culture medium inhibited the cellular incorporation of [3H]thymidine by 19 and 59%, respectively, and by 85% when added together.	3h]thymidine	187-199	transforming growth factor beta 1	Homo sapiens	78-87
9745442-3	1998	IL-13 dose-dependently (1-100 pmol/L) reduced the incorporation rate of [3H]thymidine in hOB cells by more than 50%.	3h]thymidine	73-85	interleukin 13	Homo sapiens	0-5
9700129-3	1998	The results show that SP-A and SP-D were able to reduce the incorporation of [3H]thymidine into PBMC in a dose-dependent manner.	3h]thymidine	78-90	surfactant protein D	Homo sapiens	31-35
9637698-6	1998	IL-1beta and platelet-derived growth factor together produced an increase in [3H]thymidine greater than either agonist alone; this effect was not, however, seen when we examined changes in cell numbers.	3h]thymidine	78-90	interleukin 1 beta	Homo sapiens	0-8
9582514-4	1998	IGF-I binding to cell surface receptors stimulated phosphorylation of 97 kDa and 93 kDa subunits of the IGF-I receptor and incorporation of [3H]thymidine into RINm5F cells.	3h]thymidine	141-153	insulin-like growth factor 1	Rattus norvegicus	0-5
9585351-7	1998	In addition, cortical cultures derived from two brains generated microtubule-associated protein-2+ neurons, which incorporated [3H]thymidine and exhibited significant calcium increments to depolarization.	3h]thymidine	128-140	microtubule associated protein 2	Homo sapiens	65-97
9682250-5	1998	The cell growth was suppressed in media with higher and lower BCAA concentrations than Dulbecco"s modified Eagle"s medium, and this was grossly correlated with the incorporation of [3H]thymidine into DNA and incorporation of [3H]leucine into intracellular protein.	3h]thymidine	182-194	AT-rich interaction domain 4B	Homo sapiens	62-66
9417122-6	1998	Incubation with sPLA2 of quiescent 1321N1 cells elicited a mitogenic response as judged from an increased incorporation of [3H]thymidine.	3h]thymidine	124-136	phospholipase A2 group IIA	Homo sapiens	16-21
9426155-1	1997	Treatment of reaggregate pituitary cell cultures of 14-day-old female rats with nerve growth factor (NGF) augmented the number of [3H]thymidine ([3H]T)-incorporating lactotrophs in a dose-dependent manner (0.03-3 nM).	3h]thymidine	131-143	nerve growth factor	Rattus norvegicus	80-99
9453004-7	1998	Angiotensin II (10(-6) M) induced an increase in [3H]thymidine incorporation, mediated through the AT1 receptor subtype.	3h]thymidine	50-62	angiotensinogen	Homo sapiens	0-14
9453004-7	1998	Angiotensin II (10(-6) M) induced an increase in [3H]thymidine incorporation, mediated through the AT1 receptor subtype.	3h]thymidine	50-62	angiotensin II receptor type 1	Homo sapiens	99-102
9426155-1	1997	Treatment of reaggregate pituitary cell cultures of 14-day-old female rats with nerve growth factor (NGF) augmented the number of [3H]thymidine ([3H]T)-incorporating lactotrophs in a dose-dependent manner (0.03-3 nM).	3h]thymidine	131-143	nerve growth factor	Rattus norvegicus	101-104
8943310-6	1996	The AII stimulation of [3H]thymidine incorporation was inhibited by PD 098059 with an IC50 of 17.8 +/- 3.1 microM.	3h]thymidine	24-36	angiotensinogen	Rattus norvegicus	4-7
9210398-2	1997	In proliferating cultures, recombinant human (rh)IGF-I was found to increase the incorporation of [3H]thymidine in a dose- and age-dependent manner.	3h]thymidine	99-111	insulin like growth factor 1	Homo sapiens	49-54
9199291-9	1997	Inhibition of the p38 SAP kinase also dramatically reduced basal [3H]thymidine incorporation.	3h]thymidine	66-78	mitogen activated protein kinase 14	Rattus norvegicus	18-21
9029369-3	1996	While PAF (0.1 microM to 1 nM) stimulates the incorporation of [3H]thymidine by freshly isolated adherent human bone marrow cells, PAF has no effect on non adherent cells.	3h]thymidine	64-76	PCNA clamp associated factor	Homo sapiens	6-9
8892315-4	1996	Incorporation of [3H]thymidine and increase in cell number was slightly inhibited by TSH in TSHR-expressing cells in vitro.	3h]thymidine	18-30	thyroid stimulating hormone receptor	Homo sapiens	92-96
8566173-2	1995	We now report that the 5-HT1A receptor agonist R(+)-8-hydroxy-2-(di-n- propylamino)tetralin (8-OH-DPAT) is also capable of stimulating [3H]thymidine incorporation into SCLC GLC-8 cells, although with lower efficacy than 5-HT.	3h]thymidine	136-148	5-hydroxytryptamine receptor 1A	Homo sapiens	23-38
8638734-8	1996	In parallel studies, uptake of [3H]thymidine stimulated by PDGF-AA, but not PDGF-AB or -BB, was inhibited by PDGFR-alpha immobilization.	3h]thymidine	32-44	platelet derived growth factor receptor alpha	Homo sapiens	109-120
8647950-5	1996	As compared to wild-type IRS-1, insulin stimulation of cells transfected with mutant IRS-1 exhibited a 32% decrease in incorporation of [3H]thymidine into DNA (P = 0.002), a 36% decrease in IRS-1 associated phosphatidylinositol (PI) 3-kinase activity (P = 0.004) and a 25% decrease in binding of the p85 regulatory subunit of PI 3-kinase to IRS-1 (P = 0.002).	3h]thymidine	137-149	insulin	Homo sapiens	32-39
8647950-5	1996	As compared to wild-type IRS-1, insulin stimulation of cells transfected with mutant IRS-1 exhibited a 32% decrease in incorporation of [3H]thymidine into DNA (P = 0.002), a 36% decrease in IRS-1 associated phosphatidylinositol (PI) 3-kinase activity (P = 0.004) and a 25% decrease in binding of the p85 regulatory subunit of PI 3-kinase to IRS-1 (P = 0.002).	3h]thymidine	137-149	insulin receptor substrate 1	Homo sapiens	85-90
8647950-5	1996	As compared to wild-type IRS-1, insulin stimulation of cells transfected with mutant IRS-1 exhibited a 32% decrease in incorporation of [3H]thymidine into DNA (P = 0.002), a 36% decrease in IRS-1 associated phosphatidylinositol (PI) 3-kinase activity (P = 0.004) and a 25% decrease in binding of the p85 regulatory subunit of PI 3-kinase to IRS-1 (P = 0.002).	3h]thymidine	137-149	insulin receptor substrate 1	Homo sapiens	85-90
8647950-5	1996	As compared to wild-type IRS-1, insulin stimulation of cells transfected with mutant IRS-1 exhibited a 32% decrease in incorporation of [3H]thymidine into DNA (P = 0.002), a 36% decrease in IRS-1 associated phosphatidylinositol (PI) 3-kinase activity (P = 0.004) and a 25% decrease in binding of the p85 regulatory subunit of PI 3-kinase to IRS-1 (P = 0.002).	3h]thymidine	137-149	insulin receptor substrate 1	Homo sapiens	85-90
7599071-8	1995	The detection of receptor transcripts was complemented by [3H]thymidine and bromodeoxyuridine incorporation studies, in which mitogenic responses to PTH and PTHrP were observed in MCF-7 cells but not in Hs578T cells.	3h]thymidine	59-71	parathyroid hormone	Homo sapiens	149-152
7649376-8	1995	The addition of bFGF to the pulp cultures suppressed the increases in ALPase activity, SPARC synthesis, and their mRNA levels, although it increased the incorporation of [3H]thymidine into DNA > 10-fold.	3h]thymidine	171-183	fibroblast growth factor 2	Homo sapiens	16-20
7877996-8	1995	A polyclonal antibody raised against HRG beta 1 reduced human and rat Schwann cell incorporation of [3H]thymidine by nearly 80% and up to 49%, respectively, relative to controls.	3h]thymidine	101-113	histidine rich glycoprotein	Homo sapiens	37-40
7757997-3	1995	LNCaP is an androgen-sensitive, human prostatic cancer cell line that responds to TNF in culture by undergoing programmed cell death, as determined by the loss of cell number, failure to exclude trypan blue, detection of DNA fragmentation, and increased release of previously incorporated [3H]thymidine.	3h]thymidine	290-302	tumor necrosis factor	Homo sapiens	82-85
7782537-5	1995	Incorporation of [3H]thymidine (TdR) was increased in 3 Den-Fb and 3 Nor-Fb lines in the presence of interleukin-1-beta (IL-1 beta) (10 U/mL) and tumor necrosis factor-alpha (TNF-alpha) (from 10 to 100 U/mL).	3h]thymidine	18-30	interleukin 1 beta	Homo sapiens	101-119
7782537-5	1995	Incorporation of [3H]thymidine (TdR) was increased in 3 Den-Fb and 3 Nor-Fb lines in the presence of interleukin-1-beta (IL-1 beta) (10 U/mL) and tumor necrosis factor-alpha (TNF-alpha) (from 10 to 100 U/mL).	3h]thymidine	18-30	interleukin 1 beta	Homo sapiens	121-130
7782537-5	1995	Incorporation of [3H]thymidine (TdR) was increased in 3 Den-Fb and 3 Nor-Fb lines in the presence of interleukin-1-beta (IL-1 beta) (10 U/mL) and tumor necrosis factor-alpha (TNF-alpha) (from 10 to 100 U/mL).	3h]thymidine	18-30	tumor necrosis factor	Homo sapiens	146-173
7900856-3	1995	In Northern blot analysis, MCP-1/JE transcripts were not observed in unstimulated VSMC, but its expression was clearly observed by exposure to lipopolysaccharide (1 micrograms/ml) for 6 h. Human recombinant MCP-1 inhibited the uptake of [3H]thymidine by VSMC cultured in 0.5% fetal bovine serum (FBS) containing Dulbecco"s modified Eagle"s medium (DMEM) in a dose-dependent manner.	3h]thymidine	238-250	C-C motif chemokine ligand 2	Rattus norvegicus	27-32
7572276-5	1995	A possible role for this glial-derived IL-1 beta as an astroglial growth factor was substantiated by experiments showing that the lymphokine increased the incorporation of [3H]thymidine into astroglial, but not microglial cultures.	3h]thymidine	173-185	interleukin 1 beta	Homo sapiens	39-48
7744858-7	1995	Antisense ODNs against TR alpha significantly inhibited [3H]thymidine incorporation, whereas antisense TR beta had no significant effect.	3h]thymidine	57-69	T cell receptor delta constant	Gallus gallus	23-31
7636797-6	1995	However, ICI 182,780 potently inhibited the incorporation of [3H]thymidine stimulated by EGF in endometrial stromal cells, suggesting interdependence between oestradiol and EGF in the control of endometrial stromal proliferation.	3h]thymidine	62-74	epidermal growth factor	Homo sapiens	89-92
7538368-2	1995	Basic bFGF stimulated incorporation of [3H]thymidine into DNA with a half-maximum concentration (ED50) of 3.23 +/- 0.33 pmol/l, more than 500-fold more potent than acidic FGF (ED50 = 2.13 +/- 0.5 nmol/l).	3h]thymidine	40-52	fibroblast growth factor 2	Gallus gallus	6-10
7538368-2	1995	Basic bFGF stimulated incorporation of [3H]thymidine into DNA with a half-maximum concentration (ED50) of 3.23 +/- 0.33 pmol/l, more than 500-fold more potent than acidic FGF (ED50 = 2.13 +/- 0.5 nmol/l).	3h]thymidine	40-52	fibroblast growth factor 2	Gallus gallus	7-10
7529135-7	1995	Incorporation of [3H]thymidine by mesenteric blood vessels was negligible in control animals but came to involve 20 and 40% of endothelial cells lining mesenteric vessels in MOT and TA3/St ascites tumor-bearing mice, respectively.	3h]thymidine	18-30	RIKEN cDNA 2700049A03 gene	Mus musculus	182-185
7923629-5	1994	PKC activation with 100 nmol/L PMA stimulated VSMC mitogenesis measured as incorporation of [3H]leucine and [3H]thymidine and increased cell number.	3h]thymidine	109-121	protein kinase C alpha	Homo sapiens	0-3
8587388-6	1995	Both phosphoramidon and anti-ET-1 antibody inhibited basal [3H]thymidine incorporation.	3h]thymidine	60-72	endothelin 1	Bos taurus	29-33
7977752-6	1994	Even though apical EGF receptors were demonstrated, only basolateral membrane stimulation with EGF increased tyrosine kinase activity and enhanced uptake of [3H]thymidine.	3h]thymidine	158-170	epidermal growth factor	Homo sapiens	95-98
8045917-14	1994	In cell cultures, bombesin significantly stimulated the growth of Hs746T cells in vitro as shown by an increase in the uptake of [3H]thymidine.	3h]thymidine	130-142	gastrin releasing peptide	Homo sapiens	18-26
8040268-7	1994	Purified PF 4 also inhibited the basal incorporation of [3H]thymidine into 3T3 fibroblasts and the increased [3H]thymidine incorporation occurring after wounding of a cell monolayer.	3h]thymidine	57-69	platelet factor 4	Homo sapiens	9-13
8175024-5	1994	Similarly, the stimulation of [3H]thymidine incorporation by IL-1 but not by TNF-alpha was blocked by TNF-alpha antisense transfection.	3h]thymidine	31-43	interleukin 1 alpha	Homo sapiens	61-65
8175024-5	1994	Similarly, the stimulation of [3H]thymidine incorporation by IL-1 but not by TNF-alpha was blocked by TNF-alpha antisense transfection.	3h]thymidine	31-43	tumor necrosis factor	Homo sapiens	102-111
7919154-3	1994	A 2-h infusion of 0.2 microgram/250 g body wt per minute of ANP suppressed the subsequent uptake of [3H]thymidine into the renal DNA of uninephrectomized but not intact rats.	3h]thymidine	101-113	natriuretic peptide A	Rattus norvegicus	60-63
7682481-4	1993	DNA synthetic activity in response to addition of HGF, aFGF or EGF to the cultures was assayed by incorporation of [3H]thymidine.	3h]thymidine	116-128	hepatocyte growth factor	Rattus norvegicus	50-53
8284045-5	1993	The labelling index (percentage of F4/80+ cells labelled by [3H]thymidine) 1 h after injection the isotope rose to 17% from a control value of less than 1%.	3h]thymidine	61-73	adhesion G protein-coupled receptor E1	Mus musculus	35-40
8149696-4	1993	Arginine-vasopressin-induced [3H]thymidine incorporation was used to determine the peptide mitogenicity.	3h]thymidine	30-42	arginine vasopressin	Rattus norvegicus	9-20
7682481-4	1993	DNA synthetic activity in response to addition of HGF, aFGF or EGF to the cultures was assayed by incorporation of [3H]thymidine.	3h]thymidine	116-128	fibroblast growth factor 1	Rattus norvegicus	55-59
7682481-4	1993	DNA synthetic activity in response to addition of HGF, aFGF or EGF to the cultures was assayed by incorporation of [3H]thymidine.	3h]thymidine	116-128	epidermal growth factor	Rattus norvegicus	63-66
8458401-1	1993	We examined the mechanisms by which Ca2+ channel antagonists inhibit the growth of smooth muscle cells by determining their effect on epidermal growth factor (EGF)-stimulated (i) induction of the early signalling gene, c-fos, (ii) incorporation of [3H]thymidine into cells as a measure of DNA synthesis, and (iii) increase in cell number.	3h]thymidine	249-261	epidermal growth factor	Homo sapiens	134-157
8452936-5	1993	After 4 days of treatment with FSH alone, the number of preantral follicles (stages 1-3) increased significantly compared to that in HX controls and reached cyclic numbers; however, incorporation of [3H]thymidine into these preantral follicles as compared to HX controls did not increase.	3h]thymidine	200-212	follicle stimulating hormone beta	Mus musculus	31-34
8458401-1	1993	We examined the mechanisms by which Ca2+ channel antagonists inhibit the growth of smooth muscle cells by determining their effect on epidermal growth factor (EGF)-stimulated (i) induction of the early signalling gene, c-fos, (ii) incorporation of [3H]thymidine into cells as a measure of DNA synthesis, and (iii) increase in cell number.	3h]thymidine	249-261	epidermal growth factor	Homo sapiens	159-162
8430092-2	1993	We investigated the effects of oncostatin M on cultured rabbit aorta smooth muscle cells (SMCs) and found that the peptide stimulated an increase in the incorporation of [3H]thymidine into DNA.	3h]thymidine	171-183	oncostatin-M	Oryctolagus cuniculus	31-43
1330669-7	1992	The interaction of EGF and C-AMP is further demonstrated in experiments where the incorporation of [3H]thymidine into RPE cells was studied, as an index for proliferation.	3h]thymidine	100-112	epidermal growth factor	Homo sapiens	19-22
1618924-9	1992	LIF/D-factor dose-dependently suppressed incorporation of [3H]thymidine into MC3T3-E1 cells.	3h]thymidine	59-71	leukemia inhibitory factor	Mus musculus	0-3
1618924-9	1992	LIF/D-factor dose-dependently suppressed incorporation of [3H]thymidine into MC3T3-E1 cells.	3h]thymidine	59-71	leukemia inhibitory factor	Mus musculus	4-12
1537057-5	1992	The uptake of [3H]thymidine by treated effector cells was dependent on time and rIL-2 concentration and was not increased in the cells treated with low-dose rIL-2/mismatched dsRNA, compared to those treated with low-dose rIL-2 or mismatched dsRNA alone.	3h]thymidine	15-27	interleukin 2	Rattus norvegicus	80-85
1341235-4	1992	H322a, H226b, H460a, and H596b cells showed stimulated [3H]thymidine (Thd) uptake in response to TGF-alpha.	3h]thymidine	56-68	transforming growth factor alpha	Homo sapiens	97-106
1594582-4	1992	However, at 10(-5)-10(-7) M, linoleic acid, which is an essential fatty acid, a ligand of L-FABP, and the precursor of many eicosanoids and related lipids, stimulated the incorporation of [3H]thymidine in three randomly isolated and stably transfected cell clones that expressed L-FABP, but virtually did not stimulate the incorporation of [3H]thymidine in three L-FABP-nonexpressing clones transfected with the antisense DNA.	3h]thymidine	189-201	fatty acid binding protein 1	Rattus norvegicus	90-96
1594582-4	1992	However, at 10(-5)-10(-7) M, linoleic acid, which is an essential fatty acid, a ligand of L-FABP, and the precursor of many eicosanoids and related lipids, stimulated the incorporation of [3H]thymidine in three randomly isolated and stably transfected cell clones that expressed L-FABP, but virtually did not stimulate the incorporation of [3H]thymidine in three L-FABP-nonexpressing clones transfected with the antisense DNA.	3h]thymidine	189-201	fatty acid binding protein 1	Rattus norvegicus	279-285
1594582-4	1992	However, at 10(-5)-10(-7) M, linoleic acid, which is an essential fatty acid, a ligand of L-FABP, and the precursor of many eicosanoids and related lipids, stimulated the incorporation of [3H]thymidine in three randomly isolated and stably transfected cell clones that expressed L-FABP, but virtually did not stimulate the incorporation of [3H]thymidine in three L-FABP-nonexpressing clones transfected with the antisense DNA.	3h]thymidine	189-201	fatty acid binding protein 1	Rattus norvegicus	279-285
1850332-7	1991	Inhibition of labeling by [3H]thymidine was mimicked by other agents that elevated cellular cAMP (10 microM histamine, 1 microM isoproterenol plus 0.1 mM IBMX, and 10 microM forskolin) and by 1 mM dibutyryl cAMP.	3h]thymidine	27-39	cathelicidin-7	Bos taurus	92-96
1425010-5	1992	Incorporation of [3H]thymidine into DNA was increased by LIF in cells (most probably osteoblasts) of the newborn mouse bones.	3h]thymidine	18-30	leukemia inhibitory factor	Mus musculus	57-60
1653767-4	1991	Endothelin-3 also caused an increase in [3H]thymidine incorporation into cellular DNA and stimulated the production of cyclic guanosine 3",5"-monophosphate, 6-ketoprostaglandin F1 alpha, and immunoreactive endothelin-1 in cultured human endothelial cells.	3h]thymidine	41-53	endothelin 3	Homo sapiens	0-12
1645342-25	1991	Similarly, ganglioside GM3, but not de-N-acetyl ganglioside GM3, inhibited the EGF-dependent incorporation of [3H]thymidine into DNA by transfected fibroblasts.	3h]thymidine	111-123	granulocyte macrophage antigen 3	Mus musculus	23-26
1645342-25	1991	Similarly, ganglioside GM3, but not de-N-acetyl ganglioside GM3, inhibited the EGF-dependent incorporation of [3H]thymidine into DNA by transfected fibroblasts.	3h]thymidine	111-123	epidermal growth factor	Homo sapiens	79-82
1723403-6	1991	Cyclosporin A and ascomycin did not inhibit interleukin 2 dependent proliferation, whereas the dunaimycins and rapamycin blocked the uptake of [3H]thymidine in mixed cultures supplemented with exogenous interleukin 2.	3h]thymidine	144-156	interleukin 2	Mus musculus	203-216
1744575-5	1991	Bombesin, bradykinin and EGF stimulated the incorporation of [3H]thymidine into DNA in quiescent cells.	3h]thymidine	62-74	gastrin releasing peptide	Homo sapiens	0-8
1744575-5	1991	Bombesin, bradykinin and EGF stimulated the incorporation of [3H]thymidine into DNA in quiescent cells.	3h]thymidine	62-74	kininogen 1	Homo sapiens	10-20
1744575-5	1991	Bombesin, bradykinin and EGF stimulated the incorporation of [3H]thymidine into DNA in quiescent cells.	3h]thymidine	62-74	epidermal growth factor	Homo sapiens	25-28
1758971-2	1991	We report the effects of three of these peptides HP-1, HP-1-56 and HP-4 on the incorporation of [3H]thymidine into the DNA of the leukemic cell line HL60.	3h]thymidine	97-109	chromobox 5	Homo sapiens	49-53
1758971-2	1991	We report the effects of three of these peptides HP-1, HP-1-56 and HP-4 on the incorporation of [3H]thymidine into the DNA of the leukemic cell line HL60.	3h]thymidine	97-109	chromobox 5	Homo sapiens	55-59
1758971-2	1991	We report the effects of three of these peptides HP-1, HP-1-56 and HP-4 on the incorporation of [3H]thymidine into the DNA of the leukemic cell line HL60.	3h]thymidine	97-109	defensin alpha 4	Homo sapiens	67-71
1675999-5	1991	DNA synthesis was reduced to about 35% of that measured in control, untreated cells after 48 h of EGF treatment, as measured by the incorporation of [3H]thymidine.	3h]thymidine	150-162	epidermal growth factor	Homo sapiens	98-101
1850332-7	1991	Inhibition of labeling by [3H]thymidine was mimicked by other agents that elevated cellular cAMP (10 microM histamine, 1 microM isoproterenol plus 0.1 mM IBMX, and 10 microM forskolin) and by 1 mM dibutyryl cAMP.	3h]thymidine	27-39	cathelicidin-7	Bos taurus	207-211
1850332-9	1991	However, similar to 5HT, the 5HT1A agonist, (+/-)-8-hydroxy-(+/-)-2-dipropylamino-8-hydroxy-1,2,3, 4-tetrahydronaphthalenehydrobromide, in association with IBMX, produced an elevation in cAMP and inhibition of labeling by [3H]thymidine.	3h]thymidine	223-235	5-hydroxytryptamine receptor 1A	Bos taurus	29-34
1649664-2	1991	In contrast to a labeling index (LI) of 35.8% in control animals, administration of the opioid peptide [Met5]-enkephalin (100 micrograms/kg) significantly reduced (10.6%) the proportion of cells incorporating [3H]thymidine; concomitant injection of 1 mg/kg naloxone blocked the inhibitory effects of [Met5]-enkephalin on cell division.	3h]thymidine	210-222	proenkephalin	Rattus norvegicus	110-120
2005393-6	1991	In vitro physiological concentrations (2.5 ng/ml) of either ovine or rat PRL or GH stimulated the incorporation of [3H]thymidine by thymus and spleen cells.	3h]thymidine	116-128	prolactin	Rattus norvegicus	73-76
2011576-4	1991	At a concentration of 20 micrograms/ml, SPARC inhibited the incorporation of [3H]thymidine into newly synthesized DNA by approximately 70%, as compared to control cultures within 24 hr after the release from G0 phase.	3h]thymidine	78-90	secreted protein acidic and cysteine rich	Bos taurus	40-45
2398084-6	1990	Growth-factor activity was determined by assessing the effect of serum on the incorporation of [3H]thymidine and on cell counts in primary cultures of osteoblastic cells from the calvaria of fetal rats.	3h]thymidine	96-108	myotrophin	Rattus norvegicus	0-13
1702323-3	1990	GM-CSF was identified by its stimulation of [3H]thymidine incorporation into a GM-CSF-responsive line, TALL-101, and the inhibition of its stimulation by a GM-CSF-specific MAB.	3h]thymidine	45-57	colony stimulating factor 2	Homo sapiens	0-6
1702323-3	1990	GM-CSF was identified by its stimulation of [3H]thymidine incorporation into a GM-CSF-responsive line, TALL-101, and the inhibition of its stimulation by a GM-CSF-specific MAB.	3h]thymidine	45-57	colony stimulating factor 2	Homo sapiens	79-85
1702323-3	1990	GM-CSF was identified by its stimulation of [3H]thymidine incorporation into a GM-CSF-responsive line, TALL-101, and the inhibition of its stimulation by a GM-CSF-specific MAB.	3h]thymidine	45-57	colony stimulating factor 2	Homo sapiens	79-85
2003580-5	1991	Reductions in pHi induced by lowering extracellular pH also attenuated the incorporation of [3H]-thymidine into DNA, while increases in pHi were associated with an acceleration in the rate of incorporation of [3H]thymidine into DNA.	3h]thymidine	210-222	glucose-6-phosphate isomerase	Rattus norvegicus	14-17
2003580-5	1991	Reductions in pHi induced by lowering extracellular pH also attenuated the incorporation of [3H]-thymidine into DNA, while increases in pHi were associated with an acceleration in the rate of incorporation of [3H]thymidine into DNA.	3h]thymidine	210-222	glucose-6-phosphate isomerase	Rattus norvegicus	14-16
2003580-5	1991	Reductions in pHi induced by lowering extracellular pH also attenuated the incorporation of [3H]-thymidine into DNA, while increases in pHi were associated with an acceleration in the rate of incorporation of [3H]thymidine into DNA.	3h]thymidine	210-222	glucose-6-phosphate isomerase	Rattus norvegicus	136-139
2295801-2	1990	IL-6 alone induced minimal incorporation of [3H]thymidine by unstimulated or Staphylococcus aureus (SA)-stimulated B cells and did not augment proliferation induced by SA and IL-2.	3h]thymidine	45-57	interleukin 6	Homo sapiens	0-4
1974557-1	1990	The postnatal development of neuropeptide Y (NPY)-immunoreactive neurons, previously labeled with [3H]thymidine on embryonic days E14-E21, has been studied in the rat occipital cortex.	3h]thymidine	99-111	neuropeptide Y	Rattus norvegicus	45-48
2114361-6	1990	The addition of antibodies specific for murine interleukin-1 beta to cocultures of Kupffer cells and T lymphocytes eliminated the antigen-stimulated incorporation of [3H]thymidine, indicating a requirement for interleukin-1.	3h]thymidine	167-179	interleukin 1 beta	Mus musculus	47-65
1692923-3	1990	The inhibitory activity of TGF-beta was evaluated by autoradiographic labeling index at 48 hours in hepatocyte cultures exposed to [3H]thymidine between hours 24 and 48 in culture.	3h]thymidine	132-144	transforming growth factor, beta 1	Rattus norvegicus	27-35
2316310-4	1990	It became evident that the fragment hPTH (1-34) enhanced the incorporation of [3H]thymidine, a fact that could be noted only in serum-free medium.	3h]thymidine	79-91	parathyroid hormone	Homo sapiens	36-40
1689692-7	1990	The human CD4 subset of T cells was then examined by stimulating the cells with SA or SP and measuring the uptake of [3H]thymidine [( 3H]TdR).	3h]thymidine	118-130	CD4 molecule	Homo sapiens	10-13
2788497-9	1989	This EGF-like molecule induced a maximal increase (36%) in incorporation of [3H]thymidine into DNA of parental HSG cells as well as low molecular weight human EGF.	3h]thymidine	77-89	epidermal growth factor	Homo sapiens	5-8
2557615-5	1989	In addition, NGF induced a dose-dependent increase in B-cell DNA synthesis as determined by incorporation of [3H]thymidine.	3h]thymidine	110-122	nerve growth factor	Homo sapiens	13-16
1703783-3	1990	Unstimulated CD5+ and CD5- B cells showed a comparable, low level of incorporation of [3H]thymidine into DNA.	3h]thymidine	87-99	CD5 molecule	Homo sapiens	13-16
1703783-3	1990	Unstimulated CD5+ and CD5- B cells showed a comparable, low level of incorporation of [3H]thymidine into DNA.	3h]thymidine	87-99	CD5 molecule	Homo sapiens	22-25
2768555-1	1989	The postnatal development of vasoactive intestinal polypeptide (VIP)-immunoreactive neurons, previously labeled with [3H]thymidine on embryonic days E14-E22, has been studied in the rat occipital cortex.	3h]thymidine	118-130	vasoactive intestinal peptide	Rattus norvegicus	64-67
3259906-8	1988	Incorporation of [3H]thymidine (dThd) increased significantly in all kinds of thyroid cells examined following the addition of 10 nM EGF, and the paired study showed that the size of this increase was not significantly different in neoplastic and adjacent nonneoplastic cells.	3h]thymidine	18-30	epidermal growth factor	Homo sapiens	133-136
2495301-5	1989	IFN-gamma (1,000 U/ml) reduced [3H]thymidine (TdR) incorporation into DNA by SMC stimulated with the well-defined mitogens IL 1 (from 15.3 +/- 0.7 to 6.2 +/- 0.7 dpm X 10(-3)/24 h) or platelet-derived growth factor (PDGF) (from 18.5 +/- 1.0 to 7.3 +/- 0.7 dpm X 10(-3)/24 h).	3h]thymidine	32-44	interferon gamma	Homo sapiens	0-9
2495301-5	1989	IFN-gamma (1,000 U/ml) reduced [3H]thymidine (TdR) incorporation into DNA by SMC stimulated with the well-defined mitogens IL 1 (from 15.3 +/- 0.7 to 6.2 +/- 0.7 dpm X 10(-3)/24 h) or platelet-derived growth factor (PDGF) (from 18.5 +/- 1.0 to 7.3 +/- 0.7 dpm X 10(-3)/24 h).	3h]thymidine	32-44	interleukin 1 beta	Homo sapiens	123-127
3135922-5	1988	Injections of [3H]thymidine into mice and autoradiographic analysis of [3H]thymidine incorporation showed that the increase in c-fos preceded glial cell division following injury.	3h]thymidine	15-27	FBJ osteosarcoma oncogene	Mus musculus	127-132
2656686-9	1989	Likewise, the presence of MA10 caused a 10-fold increase in the concentration of insulin needed to stimulate half-maximal incorporation of [3H]thymidine and also led to diminished IGF-I-stimulated responses.	3h]thymidine	140-152	insulin	Homo sapiens	81-88
3264335-4	1988	The pups fed formula containing EGF for 39 h had a significant increase in hepatic incorporation of [3H]thymidine into DNA compared with pups not fed EGF.	3h]thymidine	101-113	epidermal growth factor like 1	Rattus norvegicus	32-35
2827895-3	1988	BCGF-II augmented incorporation of [3H]thymidine by murine thymocytes in combination with suboptimal doses (0.5 microgram/ml) of concanavalin A (Con A) but not at lower doses (0.1 microgram/ml) of Con A, a concentration usually used for interleukin 1 (IL-1) assays.	3h]thymidine	36-48	interleukin 5	Mus musculus	0-7
3257412-9	1988	The proliferative response of rat spleen or blood lymphocytes to rIL-2 appeared to be primarily associated with LGL/NK cells since depletion of NK cells by anti-asialo-GM1 or anti-laminin antibody plus complement or by L-leucine methyl ester significantly (P less than 0.001) reduced the incorporation of [3H]thymidine into DNA.	3h]thymidine	306-318	interleukin 2	Rattus norvegicus	65-70
3305046-9	1987	Epidermal growth factor does not alter the length of the latency period prior to S phase but appears to stimulate the uptake of [3H]thymidine subsequently.	3h]thymidine	129-141	epidermal growth factor like 1	Rattus norvegicus	0-23
2445427-2	1987	Analysis of temporal changes in synthesis of DNA, RNA, protein, and in activity of ornithine decarboxylase in transected and sham-operated nerves 0-5 days postoperatively indicated that incorporation of [3H]thymidine, a marker of premitotic activity, was the earliest and only specific marker of early Wallerian degeneration.	3h]thymidine	204-216	ornithine decarboxylase, structural 1	Mus musculus	83-106
3297308-10	1987	When incorporation of [3H]thymidine was used as an assay of cell growth, saturating levels of basic fibroblast growth factor (20 ng/ml) showed a stimulation 1.35 times greater than EGF (20 ng/ml).	3h]thymidine	23-35	fibroblast growth factor 2	Mus musculus	94-124
3494774-3	1987	The human astrocytoma U373 was found to incorporate [3H]thymidine after exposure to recombinant human IL 1 alpha and IL 1 beta and murine IL 1 alpha.	3h]thymidine	53-65	interleukin 1 alpha	Homo sapiens	102-112
3607463-4	1987	Injection of methionine-enkephalin, an endogenous opioid peptide, also resulted in a decrease in the proportion of cells incorporating [3H]thymidine.	3h]thymidine	136-148	proenkephalin	Rattus norvegicus	24-34
3494774-3	1987	The human astrocytoma U373 was found to incorporate [3H]thymidine after exposure to recombinant human IL 1 alpha and IL 1 beta and murine IL 1 alpha.	3h]thymidine	53-65	interleukin 1 beta	Homo sapiens	117-126
3494774-3	1987	The human astrocytoma U373 was found to incorporate [3H]thymidine after exposure to recombinant human IL 1 alpha and IL 1 beta and murine IL 1 alpha.	3h]thymidine	53-65	interleukin 1 alpha	Mus musculus	138-148
3494774-4	1987	Surprisingly, U373 also incorporated [3H]thymidine after exposure to recombinant TNF.	3h]thymidine	38-50	tumor necrosis factor	Homo sapiens	81-84
3087668-4	1986	Incorporation of [3H]thymidine was also higher in measles patients when exogenous natural or recombinant IL-2 was added to unstimulated cultured cells.	3h]thymidine	18-30	interleukin 2	Homo sapiens	105-109
3493947-3	1986	Mitogenic activity of EGF from both tissues was demonstrated by stimulating the incorporation of [3H]thymidine in two different cell lines of fibroblast culture in a dose-dependent manner.	3h]thymidine	98-110	epidermal growth factor	Mus musculus	22-25
3489285-2	1986	As assessed by uptake of [3H]thymidine, proliferation induced with anti-T3 +/- recombinant IL-2 at 72 h was inhibited by greater than 80% in the presence of nifedipine at 50 microM, and almost completely arrested (greater than 95% inhibition) with the other agents at the same concentration.	3h]thymidine	26-38	interleukin 2	Homo sapiens	91-95
3528935-5	1986	In one case, GalC-positive cells isolated from a biopsy of an 8-year old girl were able to incorporate [3H]thymidine as revealed by autoradiography.	3h]thymidine	104-116	galactosylceramidase	Homo sapiens	13-17
3029154-8	1987	GnRH antagonists rapidly inhibited [3H]thymidine incorporation into DNA (within 3 hr), and this effect was reversible.	3h]thymidine	36-48	gonadotropin releasing hormone 1	Homo sapiens	0-4
2948816-11	1987	All three peptides stimulated the incorporation of [3H]thymidine into the DNA of FRTL-5 cells, IGF-I being the most potent, followed in decreasing order of potency of rIGF-II and insulin.	3h]thymidine	52-64	insulin-like growth factor 1	Rattus norvegicus	95-100
3121922-7	1987	Also, insulin alone was able to stimulate quiescent bovine granulosa cells to incorporate [3H]thymidine into DNA under serum-conditions.	3h]thymidine	91-103	insulin	Bos taurus	6-13
3020992-2	1986	The cholecystokinin (CCK) analogue caerulein and cholecystokinin octapeptide (CCK-8) each led to threefold increases in incorporation of [3H]thymidine into DNA.	3h]thymidine	138-150	cholecystokinin	Mus musculus	4-19
3020992-2	1986	The cholecystokinin (CCK) analogue caerulein and cholecystokinin octapeptide (CCK-8) each led to threefold increases in incorporation of [3H]thymidine into DNA.	3h]thymidine	138-150	cholecystokinin	Mus musculus	21-24
3020992-2	1986	The cholecystokinin (CCK) analogue caerulein and cholecystokinin octapeptide (CCK-8) each led to threefold increases in incorporation of [3H]thymidine into DNA.	3h]thymidine	138-150	cholecystokinin	Mus musculus	49-64
3020992-2	1986	The cholecystokinin (CCK) analogue caerulein and cholecystokinin octapeptide (CCK-8) each led to threefold increases in incorporation of [3H]thymidine into DNA.	3h]thymidine	138-150	cholecystokinin	Mus musculus	78-81
2998905-2	1985	The incorporation of [3H]thymidine into DNA within 72 h was about 25-fold with fetal calf serum (FCS, 1%), 20-fold with epidermal growth factor (EGF, 1 ng/ml) and 3.5-fold with insulin (10 micrograms/ml) as compared to controls.	3h]thymidine	22-34	LOC521832	Bos taurus	120-143
3487617-3	1986	When added to astroglia grown in culture, microglial IL-1 increased the cell number of five- to sevenfold, and increased astroglial incorporation of [3H]thymidine by three- to fivefold.	3h]thymidine	150-162	interleukin 1 complex	Mus musculus	53-57
3486241-1	1986	Subconfluent human thyroid cells in monolayer, isolated from thyrotoxic tissue or non-toxic goitres obtained at surgery, responded to the addition of epidermal growth factor (EGF) with an increase in cell growth as measured by increased incorporation of [3H]thymidine into trichloroacetic acid-precipitable material.	3h]thymidine	255-267	epidermal growth factor	Homo sapiens	150-173
3486241-1	1986	Subconfluent human thyroid cells in monolayer, isolated from thyrotoxic tissue or non-toxic goitres obtained at surgery, responded to the addition of epidermal growth factor (EGF) with an increase in cell growth as measured by increased incorporation of [3H]thymidine into trichloroacetic acid-precipitable material.	3h]thymidine	255-267	epidermal growth factor	Homo sapiens	175-178
3003017-5	1985	Moreover, incorporation of [3H]thymidine into TMK-1 cells was stimulated by gastrin in a dose-dependent manner.	3h]thymidine	28-40	gastrin	Homo sapiens	76-83
6604568-6	1983	Commitment to increased incorporation of [3H]thymidine required a minimum of 6 h continuous incubation with EGF.	3h]thymidine	42-54	epidermal growth factor like 1	Rattus norvegicus	108-111
2982858-9	1985	151-IgG inhibited the EGF-stimulated incorporation of [3H]thymidine into quiescent bovine corneal endothelial cells, rabbit corneal endothelial cells, epithelial normal rat kidney cells, and SW 3T3 cells while it enhanced the EGF-stimulated [3H]thymidine incorporation into quiescent human foreskin fibroblasts.	3h]thymidine	55-67	epidermal growth factor like 1	Rattus norvegicus	22-25
2982858-9	1985	151-IgG inhibited the EGF-stimulated incorporation of [3H]thymidine into quiescent bovine corneal endothelial cells, rabbit corneal endothelial cells, epithelial normal rat kidney cells, and SW 3T3 cells while it enhanced the EGF-stimulated [3H]thymidine incorporation into quiescent human foreskin fibroblasts.	3h]thymidine	242-254	epidermal growth factor like 1	Rattus norvegicus	22-25
2989031-4	1985	Addition of EGF and insulin to the hepatocyte cultures enhanced the rate of DNA synthesis as measured by the incorporation of [3H]thymidine.	3h]thymidine	127-139	insulin S homeolog	Xenopus laevis	20-27
6097338-3	1984	As much as 50-70% of the cells incorporated [3H]thymidine as visualized by the high labeling index of galactocerebroside (GalC)-positive cells.	3h]thymidine	45-57	galactosylceramidase	Rattus norvegicus	122-126
6757329-4	1982	This method routinely gives a 10-20-fold greater release of [3H]thymidine from cultures containing MAF than from cultures containing macrophages and target cells alone.	3h]thymidine	61-73	avian musculoaponeurotic fibrosarcoma oncogene homolog	Mus musculus	99-102
6132955-1	1983	Hyperprolactinaemia produced in rats by the transplanted prolactin-secreting tumours MtTW15 and 7315a significantly (P less than 0.01) inhibited by 70% the incorporation of [3H]thymidine into the pituitary DNA of the host animals.	3h]thymidine	174-186	prolactin	Rattus norvegicus	5-14
6301860-1	1983	Senescent human diploid fibroblasts, TIG-1, had labelling indices of about 0.5-3% when labelled with [3H]thymidine for 3 days in fresh medium containing 10% fetal bovine serum.	3h]thymidine	102-114	retinoic acid receptor responder 1	Homo sapiens	37-42
6181537-4	1982	Incorporation rates in vivo of [3H]thymidine into DNA, [3H]uridine into RNA and [14C]phenylalanine into total protein were significantly depressed by somatostatin.	3h]thymidine	32-44	somatostatin	Rattus norvegicus	150-162
7047684-5	1982	In vivo, [3H]thymidine retention in CSF and brain after entry from blood was increased when the efflux of [3H]thymidine from CSF and the phosphorylation of [3H]thymidine in brain were depressed by the intraventricular injection of unlabeled thymidine.	3h]thymidine	10-22	colony stimulating factor 2	Rattus norvegicus	36-39
7047684-5	1982	In vivo, [3H]thymidine retention in CSF and brain after entry from blood was increased when the efflux of [3H]thymidine from CSF and the phosphorylation of [3H]thymidine in brain were depressed by the intraventricular injection of unlabeled thymidine.	3h]thymidine	10-22	colony stimulating factor 2	Rattus norvegicus	125-128
7273292-5	1981	Combined immunofluorescent and autoradiographic labeling studies reveal that many of the small cells contain AFP; approximately half of the alpha-fetoprotein-containing cells are labeled with [3H]thymidine (dT).	3h]thymidine	193-205	alpha-fetoprotein	Rattus norvegicus	140-157
6983644-2	1982	The incorporation of [3H]thymidine into cells prepared from bone marrow increased in the presence of LPS, but the addition of anti-Ia serum to the cultures reduced the incorporation.	3h]thymidine	22-34	toll-like receptor 4	Mus musculus	101-104
6953438-7	1982	Repair synthesis was shown to continue during the G2 arrest by using synchronized cells pulse labeled with [3H]thymidine after HN2 treatment and autoradiography.	3h]thymidine	108-120	MT-RNR2 like 2 (pseudogene)	Homo sapiens	127-130
6158364-8	1980	Incubation of cultures with insulin caused a time- and dose-dependent stimulation of [3H]thymidine and [3H]uridine incorporation into TCA-precipitable material.	3h]thymidine	86-98	insulin	Bos taurus	28-35
6252249-5	1980	The IGF I stimulatory effect on the incorporation of [3H]thymidine was seen in both the periosteum and periosteum-free calvarium, whereas that on the labeling of CDP was seen only in the central, osteoblastic-rich, non-periosteal bone.	3h]thymidine	54-66	insulin-like growth factor 1	Rattus norvegicus	4-9
6998827-3	1980	Following pulse labeling after five repeated injections of [3H]thymidine at 6-hr intervals, the labeling index of the gastrin cells showed a linear increase (from 1.2% on the 1st day to 5.2% on the 4th day), and attained a plateau (5.6%) on the 5th day.	3h]thymidine	60-72	gastrin	Homo sapiens	118-125
192752-4	1977	Somatomedin A, NSILA-s, MSA, insulin and proinsulin all stimulated the incorporation of [3H]thymidine into DNA in human fibroblasts.	3h]thymidine	89-101	insulin	Homo sapiens	29-36
527586-3	1979	At low daunomycin concentrations (1 and 2 muM) the rate of [3H]thymidine incorporation decreased progressively with the duration of exposure to the inhibitor.	3h]thymidine	60-72	latexin	Homo sapiens	42-45
192752-4	1977	Somatomedin A, NSILA-s, MSA, insulin and proinsulin all stimulated the incorporation of [3H]thymidine into DNA in human fibroblasts.	3h]thymidine	89-101	insulin	Homo sapiens	41-51
955349-6	1976	Analysis of the labeling index curves obtained during and after the administration of [3H]thymidine confirmed that the majority of the gastrin cells were renewed through replication of other gastrin cells.	3h]thymidine	87-99	gastrin	Mus musculus	135-142
955349-6	1976	Analysis of the labeling index curves obtained during and after the administration of [3H]thymidine confirmed that the majority of the gastrin cells were renewed through replication of other gastrin cells.	3h]thymidine	87-99	gastrin	Mus musculus	191-198
58715-2	1976	The maximum level of serum AFP reached in 4 days after a single dose of CCl4 was much higher than that after partial hepatectomy, although the incorporation of [3H]thymidine into liver DNA increased nearly to the same extent by either of these treatments.	3h]thymidine	161-173	alpha-fetoprotein	Rattus norvegicus	27-30