PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23564080-11	2013	Administration with simvastatin in ApoE(-/-) mice markedly attenuated the vascular inflammation and atherosclerotic lesion area, and decreased the aortic expression of HMGB1, RAGE, VCAM-1, and MCP-1.	Simvastatin	20-31	vascular cell adhesion molecule 1	Mus musculus	181-187	
32617140-12	2020	Simvastatin-affected parameters that differed between the healthy structure of the aorta and aneurysmal tissue included immune cell infiltration of the aortic wall, VCAM1 mRNA and protein level, extracellular matrix degradation, TGF-beta1 mRNA level, and ERK phosphorylation, but neither oxidative stress nor the level of Angiotensin II Type 1 Receptor (AT1R).	Simvastatin	0-11	vascular cell adhesion molecule 1	Mus musculus	165-170	
23564080-13	2013	Exposure of HUVECs to HMGB1 (100 ng/mL) markedly increased the expression of HMGB1, RAGE and VCAM-1, whereas pretreatment of the cells with simvastatin (10 mumol/L) blocked the HMGB1-caused changes.	Simvastatin	140-151	vascular cell adhesion molecule 1	Mus musculus	93-99	
22038096-7	2012	In addition, simvastatin down-regulated the expression of vascular cell adhesion molecule-1 (VCAM-1) by both inhibition of nuclear factor kappa B (NF-kB) activation and suppression of the expression of the receptor for advanced glycation end products (RAGE).	Simvastatin	13-24	vascular cell adhesion molecule 1	Mus musculus	58-91	
22038096-7	2012	In addition, simvastatin down-regulated the expression of vascular cell adhesion molecule-1 (VCAM-1) by both inhibition of nuclear factor kappa B (NF-kB) activation and suppression of the expression of the receptor for advanced glycation end products (RAGE).	Simvastatin	13-24	vascular cell adhesion molecule 1	Mus musculus	93-99	
16305803-2	2006	The aim of this study was to detect and quantify the changes of endothelial expression of VCAM-1, and ICAM-1 in the vessel wall after the short-term administration of simvastatin, atorvastatin, and micro dispersed derivatives of oxidised cellulose (MDOC) in apolipoprotein-E-deficient (apoE(-/-)) mice atherosclerotic model.	Simvastatin	167-178	vascular cell adhesion molecule 1	Mus musculus	90-96