PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 10447088-4 1999 A [3H]thymidine incorporation study showed that SS significantly and concentration-dependently inhibited HL60 and BALL-1 leukemia cell growth. Tritium 3-5 somatostatin Homo sapiens 48-50 15680393-4 2005 Cell proliferation in response to SST treatment (0.04, 0.2, or 1 ng/ml) was performed by [3H]thymidine incorporation. Tritium 90-92 somatostatin Homo sapiens 34-37 15680393-11 2005 SST-treated cells showed a significant reduction in [3H]thymidine incorporation in a dose-dependent manner. Tritium 53-55 somatostatin Homo sapiens 0-3 10598791-3 1999 Total [3H]phosphoinositide (IPx) accumulation, a measure of phospholipase C (PLC) activity, induced by somatostatin (somatotropin release-inhibiting factor, SRIF) and cortistatin (CST) analogues was studied at human somatostatin receptor subtypes 1-5 (hsst1-5) recombinantly expressed in CCL39 (Chinese hamster lung fibroblast) cells. Tritium 7-9 somatostatin Homo sapiens 103-115 2888257-4 1987 It was shown that SST (10(-7)-10(-5) M) significantly inhibited the [3H]-thymidine incorporation. Tritium 69-71 somatostatin Homo sapiens 18-21 7905785-8 1994 Furthermore, SST and OCT inhibited VIP-induced [3H]thymidine incorporation, cyclic AMP formation, and tyrosine kinase activity with IC50 values < 10 nM. Tritium 48-50 somatostatin Homo sapiens 13-16 1362264-4 1992 A significant (p < 0.02) inhibitory effect of somatostatin (1 nM to 10 microM) on 3H-thymidine DNA incorporation was observed in cultured chondrocytes from fetuses of all gestational ages studied (12-40 wk), with no significant differences among fetal ages. Tritium 85-87 somatostatin Homo sapiens 49-61 6117356-2 1981 Local injection of somatostatin, i.e., without any measurable systemic effect, resulted in a 75% reduction of cell proliferation as measured by [3H]thymidine incorporation and ornithine decarboxylase activities. Tritium 145-147 somatostatin Homo sapiens 19-31 3026563-4 1986 The binding of [3H]somatostatin in both the frontal cortex and cerebellar cortex demonstrated pharmacological specificity, since somatostatin-28, but not somatostatin-28(1-12) or Des AA1,2,4,5,12,13, D-Trp8-somatostatin, competed for the binding sites. Tritium 16-18 somatostatin Homo sapiens 129-144