PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 2439563-2 1986 Superoxide dismutase (SOD) and catalase were modified with PEG and used to immunize mice. Polyethylene Glycols 59-62 catalase Mus musculus 31-39 9895216-2 1999 This in vivo study in pregnant CD-1 mice evaluated whether maternal administration of the antioxidative enzymes superoxide dismutase (SOD) and/or catalase conjugated with polyethylene glycol (PEG) could reduce phenytoin teratogenicity. Polyethylene Glycols 171-190 catalase Mus musculus 146-154 8150225-6 1994 The treatment with catalase-polyethylene glycol showed a similar tendency which did not reach significance. Polyethylene Glycols 28-47 catalase Mus musculus 19-27 35098641-7 2022 Moreover, PEG upregulated the activities of CAT, GSH-Px, SOD and decreased MDA level, and suppressed the production of IL-1beta, IL-6, PGE 2 , TNF-alpha, and COX-2 in UV-irradiated mice. Polyethylene Glycols 10-13 catalase Mus musculus 44-47 2439563-9 1986 Modification with PEG resulted in a decrease in immunogenicity of both SOD and catalase. Polyethylene Glycols 18-21 catalase Mus musculus 79-87 27554969-8 2016 Pre-treatment of wild type (WT) and KO MEFs with polyethylene glycol-conjugated Cu-Zn superoxide dismutase (PEG-SOD) and catalase (PEG-CAT) combination prior to irradiation showed a partial rescue of clonogenic survival, thus demonstrating a role for increased intracellular oxidants in promoting IR-induced cell death. Polyethylene Glycols 49-68 catalase Mus musculus 108-129 29870994-7 2018 Arteriolar O2 - was increased further by ET-1 and contractions to ET-1 reduced by PEG-SOD in both groups whereas H2O2 unchanged by ET-1 and contractions were reduced by PEG-catalase selectively in diabetic mice. Polyethylene Glycols 82-85 catalase Mus musculus 173-181 31698794-3 2019 In this study, we successfully conjugated folate to polyethylene glycol 100 monostearate as film-forming material and further prepared methotrexate (MTX) and catalase (CAT) co-encapsulated liposomes, herein, shortened to FOL-MTX&CAT-L, that could actively target to activated macrophages. Polyethylene Glycols 52-71 catalase Mus musculus 158-166 31698794-3 2019 In this study, we successfully conjugated folate to polyethylene glycol 100 monostearate as film-forming material and further prepared methotrexate (MTX) and catalase (CAT) co-encapsulated liposomes, herein, shortened to FOL-MTX&CAT-L, that could actively target to activated macrophages. Polyethylene Glycols 52-71 catalase Mus musculus 168-171 24412573-3 2014 In this study, we devised a novel translational antioxidant intervention targeted to the vascular endothelium using PEG-liposomes loaded with EUK-134 (EUK), a potent superoxide dismutase/catalase mimetic. Polyethylene Glycols 116-119 catalase Mus musculus 187-195 18155117-1 2008 The carcinogenic mycotoxin aflatoxin B(1) (AFB(1)) induces 8-hydroxy-2"-deoxyguanosine (8-OHdG) formation in mouse lung, an effect that can be prevented by treatment with polyethylene glycol-conjugated catalase (PEG-CAT). Polyethylene Glycols 171-190 catalase Mus musculus 202-210 21953593-2 2012 To inhibit bone metastasis, catalase was conjugated with 3,5-di(ethylamino-2,2-bisphosphono)benzoic acid (Bip), a derivative of bone-seeking bisphosphonates, polyethylene glycol (PEG), or both. Polyethylene Glycols 158-177 catalase Mus musculus 28-36 21953593-2 2012 To inhibit bone metastasis, catalase was conjugated with 3,5-di(ethylamino-2,2-bisphosphono)benzoic acid (Bip), a derivative of bone-seeking bisphosphonates, polyethylene glycol (PEG), or both. Polyethylene Glycols 179-182 catalase Mus musculus 28-36 21953593-4 2012 The tissue distribution of (111) In-labeled catalase derivatives indicated that the accumulation of radioactivity in bones was increased by conjugation of either Bip or PEG with catalase. Polyethylene Glycols 169-172 catalase Mus musculus 44-52 21953593-4 2012 The tissue distribution of (111) In-labeled catalase derivatives indicated that the accumulation of radioactivity in bones was increased by conjugation of either Bip or PEG with catalase. Polyethylene Glycols 169-172 catalase Mus musculus 178-186 21953593-7 2012 These results indicate that targeted delivery of catalase to the bones can be achieved by conjugating the enzyme with either Bip or PEG, and this delivery is effective in inhibiting the bone metastasis of tumor cells. Polyethylene Glycols 132-135 catalase Mus musculus 49-57 12954382-1 2003 In the present study antileukemic enzyme L-asparaginase (ASNase) and catalase (as a model enzyme) were modified in solid-phase with activated polyethylene glycol (PEG(2)) by using ligand-immobilized affinity column systems L-asparagine-Sepharose CL-4B and Procion red-Sepharose CL-4B, respectively. Polyethylene Glycols 142-161 catalase Mus musculus 69-77