PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9048591-8	1997	PAE during the last 5 days of gestation blunted the PRL-induced increase in [3H]thymidine incorporation and TNF alpha levels in cells grown in the absence of ethanol in the culture medium.	Thymidine	80-89	prolactin	Rattus norvegicus	52-55	
12099388-3	2002	The effect of prolactin on thymidine incorporation and tissue alkaline phosphatase, maltase and lactase activity was studied on jejunal explants from fetal, newborn and 2 week-old rats.	Thymidine	27-36	prolactin	Rattus norvegicus	14-23	
8845300-9	1995	The addition of PRL, IL-2, and TPA significantly stimulated[3H] thymidine incorporation, while only the polypeptide growth factors augmented cell density.	Thymidine	64-73	prolactin	Rattus norvegicus	16-19	
18638761-6	1994	IL-1 inhibition of PRL production occurred in parallel with IL-1 inhibition of DNA synthesis in GH3 as measured by [(3)H] thymidine incorporation.	Thymidine	122-131	prolactin	Rattus norvegicus	19-22	
1830268-11	1991	The rate of DNA labeling with [3H]thymidine was activated in the cultured explants, but it was higher in those grown with T, E, or PRL than in those grown in the basal medium.	Thymidine	34-43	prolactin	Rattus norvegicus	131-134	
2222430-4	1990	The effects of various concentrations of prolactin and metoclopramide on [3H]thymidine uptake by DNA of spleen lymphocytes was also studied in vitro.	Thymidine	77-86	prolactin	Rattus norvegicus	41-50	
3097147-6	1987	However, A23187 significantly elevated PRL-stimulated ODC activity with a subsequent inhibition of [3H]thymidine incorporation, suggesting a block of entry into S phase.	Thymidine	103-112	prolactin	Rattus norvegicus	39-42	
2676483-5	1989	Both rPRL and rGH increased islet insulin content and [3H]thymidine incorporation.	Thymidine	58-67	prolactin	Rattus norvegicus	5-9	
2917354-3	1989	E17 beta (10(-7) M) caused a significant increase in PRL cell proliferation in normal pituitary [3.9 +/- 0.4 versus 7.7 +/- 0.9% (SEM) of immunostained PRL cells with thymidine incorporation] [P less than 0.01] but produced a significant decrease in PRL cell proliferation in MtT/W15 primary cell cultures [6.7 +/- 1.0 versus 3.7 +/- 0.8%] [P less than 0.05].	Thymidine	167-176	prolactin	Rattus norvegicus	53-56	
6641474-1	1983	The thymidine analog, 5-bromodeoxyuridine (BrdUrd), induces prolactin (Prl) synthesis and Prl gene amplification in a subclone of GH cells (rat pituitary tumor cells in culture).	Thymidine	4-13	prolactin	Rattus norvegicus	60-69	
4092669-7	1985	Although the percentage of immunoreactive PRL cells which took up thymidine in their nuclei increased to more than double after estrogen treatment, the increase in the total number of immunoreactive PRL cells was small.	Thymidine	66-75	prolactin	Rattus norvegicus	42-45	
6641474-1	1983	The thymidine analog, 5-bromodeoxyuridine (BrdUrd), induces prolactin (Prl) synthesis and Prl gene amplification in a subclone of GH cells (rat pituitary tumor cells in culture).	Thymidine	4-13	prolactin	Rattus norvegicus	71-74	
6641474-1	1983	The thymidine analog, 5-bromodeoxyuridine (BrdUrd), induces prolactin (Prl) synthesis and Prl gene amplification in a subclone of GH cells (rat pituitary tumor cells in culture).	Thymidine	4-13	prolactin	Rattus norvegicus	90-93	
172358-1	1975	Effect of prolactin on [3H]thymidine incorporation.	Thymidine	27-36	prolactin	Rattus norvegicus	10-19	
1144425-3	1975	Prolactin alone stimulated some [3-H] thymidine uptake in ductal and alveolar epithelium, but when combined with either estradiol or progesterone synergistic effects were observed.	Thymidine	38-47	prolactin	Rattus norvegicus	0-9