PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9767522-3	1998	METHODS: LPS- or BK-induced increments of intracellular Ca2+ were assessed by microspectrofluorimetry with fura-2 in passaged bovine aortic endothelial cells.	Fura-2	107-113	kininogen 1	Bos taurus	17-19	
3136667-2	1988	In the present study, measurement of BK-induced changes in fura-2 fluorescence and 86Rb+ efflux were used to monitor changes in cytosolic Ca2+ and K+ permeability in cultured bovine aortic endothelial cells.	Fura-2	59-65	kininogen 1	Bos taurus	37-39	
2294097-1	1990	The effects of oxidant stress and inhibition of glutathione reductase on the bradykinin-stimulated changes in cytosolic free Ca2+ concentration ([Ca2+]i) of calf pulmonary artery endothelial cells were determined using the intracellular fluorescent probe, fura-2.	Fura-2	256-262	kininogen 1	Bos taurus	77-87	
2782436-4	1989	The effect of membrane depolarization with high K+ buffer on the bradykinin-stimulated changes in cytosolic Ca2+ was determined using the fluorescent Ca2+ indicator, fura-2.	Fura-2	166-172	kininogen 1	Bos taurus	65-75	
2909543-1	1989	Bradykinin-evoked rises in [Ca2+]i were measured in fura-2-loaded bovine pulmonary artery endothelial cell monolayers by dual wavelength excitation fluorimetry.	Fura-2	52-58	kininogen 1	Bos taurus	0-10	
9582501-7	1998	In fura-2 loaded BAG cells, BK (100 nM) induced a typical biphasic Ca2+ response composed of a rapid and transient increase of intracellular Ca2+ concentration [Ca2+]i which slowly declined to a level that remained above basal level for about 5 min.	Fura-2	3-9	kininogen 1	Bos taurus	28-30	
8712453-4	1996	METHODS: The effect of halothane and isoflurane on the Ca2+ response to bradykinin of bovine aortic endothelial (BAE) cells was investigated using the fluorescent Ca2+ indicator fura-2.	Fura-2	178-184	kininogen 1	Bos taurus	72-82	
7729011-4	1995	In cultured bovine aortic endothelial cells, extracellular application of bradykinin (BK, 10 to 20 mumol/L) caused transient (sometimes oscillatory) increase in [Ca2+]i, which was measured with the fluorescent Ca2+ indicator fura 2 and fluorescence imaging microscopy.	Fura-2	225-231	kininogen 1	Bos taurus	74-84	
7729011-4	1995	In cultured bovine aortic endothelial cells, extracellular application of bradykinin (BK, 10 to 20 mumol/L) caused transient (sometimes oscillatory) increase in [Ca2+]i, which was measured with the fluorescent Ca2+ indicator fura 2 and fluorescence imaging microscopy.	Fura-2	225-231	kininogen 1	Bos taurus	86-88	
1996698-8	1991	These findings, together with our previously described results using fura-2, suggest that oxidant stress initially inhibits bradykinin-stimulated Ca2+ influx and later inhibits stimulated Ca2+ efflux.	Fura-2	69-75	kininogen 1	Bos taurus	124-134	
2154452-1	1990	The effects of membrane potential on resting and bradykinin-stimulated changes in [Ca2+]i were measured in fura-2 loaded cultured endothelial cells from bovine atria by spectrofluorimetry.	Fura-2	107-113	kininogen 1	Bos taurus	49-59	
3263034-5	1988	In addition, bradykinin and melittin stimulated an increase in intracellular calcium concentration in fura-2 loaded endothelial cells and an increase in inositol 1,4,5-trisphosphate (Ins[1,4,5]P3) in cells prelabeled with 3H-myoinositol.	Fura-2	102-108	kininogen 1	Bos taurus	13-23	
3263034-6	1988	Bradykinin stimulation produced transient increases in Ins(1,4,5)P3, fura-2 fluorescence and transient EDRF release.	Fura-2	69-75	kininogen 1	Bos taurus	0-10	
2444358-2	1987	After bradykinin (100 nM) exposure, endothelial cell associated fura-2 fluorescence peaked within 10-20 seconds and then declined to a steady level 2- to 3-fold above resting values.	Fura-2	64-70	kininogen 1	Bos taurus	6-16	
2444358-4	1987	Chelation of extracellular calcium with EGTA before addition of bradykinin resulted in a substantial decrease in the fura-2 transient and elimination of the long-lasting component.	Fura-2	117-123	kininogen 1	Bos taurus	64-74