PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10428980-0	1999	Vimentin-dependent utilization of LDL-cholesterol in human adrenal tumor cells is not associated with the level of expression of apoE, sterol carrier protein-2, or caveolin.	Cholesterol	38-49	vimentin	Homo sapiens	0-8	
11802775-11	2002	Cells overexpressing ORP4-S had a 40% reduction in the esterification of low-density-lipoprotein-derived cholesterol, demonstrating that ORP4 interaction with intermediate filaments inhibits an intracellular cholesterol-transport pathway mediated by vimentin.	Cholesterol	105-116	vimentin	Homo sapiens	250-258	
11802775-11	2002	Cells overexpressing ORP4-S had a 40% reduction in the esterification of low-density-lipoprotein-derived cholesterol, demonstrating that ORP4 interaction with intermediate filaments inhibits an intracellular cholesterol-transport pathway mediated by vimentin.	Cholesterol	208-219	vimentin	Homo sapiens	250-258	
9142693-13	1997	The Ca2+/calmodulin kinase promotes transport of cholesterol to mitochondria and does so under conditions in which phosphorylation of vimentin and myosin light chain occurs.	Cholesterol	49-60	vimentin	Homo sapiens	134-142	
3569305-2	1987	Employing gel permeation chromatography of the complexes on Sephacryl S-300, cholesterol, cholesteryl fatty acid esters and mono-, di- and triglycerides were found to efficiently associate with vimentin.	Cholesterol	77-88	vimentin	Homo sapiens	194-202	
9029735-3	1997	Electron microscopy and immunofluorescence reveal that lipid droplets in which steroidogenic cholesterol is stored in the cytoplasm are tightly attached to vimentin intermediate filaments.	Cholesterol	93-104	vimentin	Homo sapiens	156-164	
8547187-5	1995	It has been shown that the two structures involved in cholesterol transport (droplets and mitochondria) are both bound to vimentin intermediate filaments in adrenal and Leydig cells.	Cholesterol	54-65	vimentin	Homo sapiens	122-130	
14731640-3	1994	Recent studies have suggested that vimentin-type intermediate filaments may have a role in cholesterol transport.	Cholesterol	91-102	vimentin	Homo sapiens	35-43	
14731640-4	1994	The mechanism by which vimentin filaments affect this process is not known, but future studies promise to provide new insights into both the post-lysosomal transport of cholesterol and the intracellular functions of intermediate filaments.	Cholesterol	169-180	vimentin	Homo sapiens	23-31	
1527066-0	1992	A functional role for vimentin intermediate filaments in the metabolism of lipoprotein-derived cholesterol in human SW-13 cells.	Cholesterol	95-106	vimentin	Homo sapiens	22-30	
1527066-7	1992	These studies indicate that in SW-13 cells, the intracellular movement of LDL-derived cholesterol from the lysosome to the site of esterification is a vimentin-dependent process.	Cholesterol	86-97	vimentin	Homo sapiens	151-159	
3569305-5	1987	When cholesterol or 1,2-dioleoyl-glycerol was incorporated into phospholipid vesicles, the affinity of the liposomes for vimentin filaments was considerably increased.	Cholesterol	5-16	vimentin	Homo sapiens	121-129	
30625181-9	2019	Similarly, cholesterol treatment inverted metformin-reduced several gene expressions (e.g., Bcl-xL, BCL2, Zeb1, vimentin, and BMI-1).	Cholesterol	11-22	vimentin	Homo sapiens	112-120	
23674515-14	2013	Its presence in areas of artery wall inflammation and O2- production suggests that vimentin activates Dectin-1 and contributes to the oxidation of lipids and cholesterol accumulation in atherosclerosis.	Cholesterol	158-169	vimentin	Homo sapiens	83-91	
28978905-5	2017	Physiologically, the process of LDL-derived cholesterol transport from lysosomes to the sites of its esterification is dependent on vimentin, which is a molecule comprising the cytoskeleton in mesenchymal cells.	Cholesterol	44-55	vimentin	Homo sapiens	132-140