PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28688989-7	2017	The basal intracellular calcium ion level [Ca2+]i was also increased after 4h-exposure to PM2.5 and a pre-treatment with superoxide dismutase and catalase significantly reduced this response.	Calcium	24-31	catalase	Homo sapiens	146-154	
427145-4	1979	Catalase (EC 1.11.1.6) and band 8 were adsorbed to the membranes from the supernatant cytosol with calcium.	Calcium	99-106	catalase	Homo sapiens	0-8	
29970475-2	2018	The membrane potential (Vm) and intracellular calcium (Ca2+) transient (CaT) are usually investigated separately, because incorporating different techniques to acquire both aspects concurrently is challenging.	Calcium	46-53	catalase	Homo sapiens	72-75	
2840397-4	1988	Calcium ionophore-mediated degranulation under aerobic conditions was reduced by the addition of the degradative enzymes catalase and superoxide dismutase, suggesting that active oxygen products enhance degranulation.	Calcium	0-7	catalase	Homo sapiens	121-129	
830369-4	1977	Of these, catalase and lactate dehydrogenase were increased in membranes from HS RBC and from normal cells exposed to calcium.	Calcium	118-125	catalase	Homo sapiens	10-18	
830369-5	1977	Only catalase, however, was present in sufficient quantity and had the correct subunit molecular weight on PAGE SDS and calcium-dependent membrane binding to account for an appreciable portion of 4.5.	Calcium	120-127	catalase	Homo sapiens	5-13	
33022540-5	2021	CPO loaded PLLA microspheres-graft-catalase could provide dissolved oxygen and calcium ions in release media up to 15 days.	Calcium	79-86	catalase	Homo sapiens	35-43	
33022540-9	2021	Based on these results, CPO loaded PLLA microspheres-graft-catalase, with the ability of cell carrying and controlled release of oxygen and calcium ions, can be a promising injectable cell microcarrier system for regeneration of bone tissue defects.	Calcium	140-147	catalase	Homo sapiens	59-67	
22322977-7	2012	Catalase also prevented ANG II from increasing localized subplasmalemmal sites of increased oxidation previously associated with colocalized calcium influx through L-type channels.	Calcium	141-148	catalase	Homo sapiens	0-8	
24796855-0	2014	Catalase mimic property of Co3O4 nanomaterials with different morphology and its application as a calcium sensor.	Calcium	98-105	catalase	Homo sapiens	0-8	
8731015-8	1996	Catalase (though neither bovine serum albumin nor superoxide dismutase) protected LADH against the Cu(II)/H2O2/CAs systems.	Calcium	111-114	catalase	Homo sapiens	0-8	
21359407-0	2011	betagamma-CAT, a non-lens betagamma-crystallin and trefoil factor complex, induces calcium-dependent platelet apoptosis.	Calcium	83-90	catalase	Homo sapiens	10-13	
19766381-6	2009	Catalase, an extracellular H(2)O(2) scavenger, significantly blocked the influx of calcium ions.	Calcium	83-90	catalase	Homo sapiens	0-8	
19084995-3	2009	Similarly, catalase (H(2)O(2) scavenger) or DPI [NAD(P)H oxidase inhibitor] and BAPTA-AM or BAPTA (calcium chelators) prevented chitosan induced stomatal closure, suggesting that reactive oxygen species (ROS) and calcium were involved during such response.	Calcium	99-106	catalase	Homo sapiens	11-19	
9427701-5	1998	In aspirin-treated platelets stimulated with high concentrations of collagen, catalase inhibited platelet aggregation, calcium mobilization, and IP3 production.	Calcium	119-126	catalase	Homo sapiens	78-86	
9227480-11	1997	Catalase and superoxide dismutase blunted or completely abolished the changes in calcium concentration elicited by H2O2 and X/XO.	Calcium	81-88	catalase	Homo sapiens	0-8	
19649279-6	2009	Similarly, contractile and calcium responses to 5-HT were decreased by superoxide dismutase and catalase which, catabolise superoxide anion and H(2)O(2), respectively.	Calcium	27-34	catalase	Homo sapiens	96-104	
11891305-5	2002	Here we report that calmodulin (CaM), a ubiquitous calcium-binding protein, binds to and activates some plant catalases in the presence of calcium, but calcium/CaM does not have any effect on bacterial, fungal, bovine, or human catalase.	Calcium	139-146	catalase	Homo sapiens	110-118	
11891305-6	2002	These results document that calcium/CaM can down-regulate H(2)O(2) levels in plants by stimulating the catalytic activity of plant catalase.	Calcium	28-35	catalase	Homo sapiens	131-139	
11797939-6	1999	The results of the enzymatic, erythrocyitc activities of GST, GGT, catalase and LDH can also be correlated with the parameters of erythrocyitc membrane permeability and with the thiolic groups, fibrinogen and ionic calcium concentration.	Calcium	215-222	catalase	Homo sapiens	67-75	
9840740-3	1998	Attempts to characterize this quasi-lipoxygenase activity revealed that calcium potentiated the quasi-lipoxygenase activities of hemoproteins (hemoglobin, myoglobin, myeloperoxidase, catalase, cytochrome c) and hemin at the physiological pH of 7.5.	Calcium	72-79	catalase	Homo sapiens	183-191	
34290105-5	2021	betagamma-CAT targeted acidic glycosphingolipids on the HSV type 1 (HSV-1) envelope to induce pore formation, as indicated by the oligomer formation of protein and potassium and calcium ion efflux.	Calcium	178-185	catalase	Homo sapiens	10-13	
7599386-10	1995	The substitution for insufficient catalase by a pseudocatalase together with calcium and UVB exposure lead to effective repigmentation.	Calcium	77-84	catalase	Homo sapiens	34-42	
7744509-4	1994	The addition of catalase, a specific H2O2 scavenger, at the beginning of the capacitation process decreased the levels of both hyperactivation and induced-acrosome reaction whereas catalase added 15 min before the induction of the acrosome reaction by the calcium ionophore had no effect.	Calcium	256-263	catalase	Homo sapiens	16-24