PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 17557286-8 2007 Furthermore, we could show that antiangiogenic effects of thalidomide are related to tumor-cell derived factors including vascular endothelial growth factor, basic fibroblast growth factor, hepatocyte growth factor and Il-8 some known and with, granulocyte colony stimulating growth factor and granulocyte macrophage colony stimulating growth factor, some new target molecules of thalidomide. Thalidomide 58-69 fibroblast growth factor 2 Mus musculus 158-188 9301478-1 1997 Thalidomide, when administered orally, is an inhibitor of angiogenesis in the basic fibroblast growth factor (bFGF)-induced rabbit cornea micropocket assay. Thalidomide 0-11 fibroblast growth factor 2 Mus musculus 110-114 9301478-2 1997 We now show in the mouse that thalidomide given intraperitoneally but not orally significantly inhibits bFGF-induced and vascular endothelial growth factor (VEGF)-induced corneal neovascularization. Thalidomide 30-41 fibroblast growth factor 2 Mus musculus 104-108 9301478-4 1997 Experiments examining thalidomide"s enantiomers reveal-that the S(-)-enantiomer has the strongest antiangiogenic activity in VEGF-induced and bFGF-induced corneal neovascularization. Thalidomide 22-33 fibroblast growth factor 2 Mus musculus 142-146