PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 32345540-4 2020 Mild HHcy was induced in ApoE-/- mice receiving a high-methionine diet. Methionine 55-65 apolipoprotein E Mus musculus 25-29 26606905-0 2015 High-methionine diets accelerate atherosclerosis by HHcy-mediated FABP4 gene demethylation pathway via DNMT1 in ApoE(-/-) mice. Methionine 5-15 apolipoprotein E Mus musculus 112-116 28472596-3 2017 In the aorta of ApoE-/- mice fed a high methionine diet, increased expression of miR-148a/152, with decreased DNMT1 mRNA and protein levels, was detected. Methionine 40-50 apolipoprotein E Mus musculus 16-20 28188730-0 2017 Involvement of histone methylation in macrophage apoptosis and unstable plaque formation in methionine-induced hyperhomocysteinemic ApoE-/- mice. Methionine 92-102 apolipoprotein E Mus musculus 132-136 28188730-12 2017 Histone methylation might be involved in macrophage apoptosis and unstable plaque formation in methionine induced hyperhomocysteinemic ApoE-/- mice. Methionine 95-105 apolipoprotein E Mus musculus 135-139 26956896-4 2016 In the present study, ApoE-/- mice were administrated methionine or atorvastatin, and were sacrificed after 2 months. Methionine 54-64 apolipoprotein E Mus musculus 22-26 27936205-4 2016 The levels of EZH2 and H3K27me3 were increased in the aorta of ApoE-/- mice fed a high-methionine diet for 16 weeks, whereas miR-92a expression was decreased. Methionine 87-97 apolipoprotein E Mus musculus 63-67 19776495-7 2009 RESULTS: Our data demonstrated that ApoE-/- mice fed a high methionine diet generated Hhcy, which subsequently increased the atherosclerotic lesion size significantly, promoted oxidative stress-associated DNA damage and PARP activation, then increased the expression of proinflammatory fac-tors within atherosclerotic plaques. Methionine 60-70 apolipoprotein E Mus musculus 36-40 23593564-5 2013 Compared with the control group, atherosclerotic lesions in ApoE(-/-) mice fed a high methionine diet significantly increased, as did the expression of MCP-1. Methionine 86-96 apolipoprotein E Mus musculus 60-64 23017835-3 2012 ApoE(-/-) mice were fed with high cholesterol and methionine diet for 15 weeks to induce hyperlipidemia and hyperhomocysteinemia. Methionine 50-60 apolipoprotein E Mus musculus 0-4 19298207-0 2009 Methionine-induced hyperhomocysteinemia modulates lipoprotein profile and oxidative stress but not progression of atherosclerosis in aged apolipoprotein E knockout mice. Methionine 0-10 apolipoprotein E Mus musculus 138-154 19261978-12 2008 We also observed increased immunohistochemical staining for N-Hcy-protein in aortic lesions from ApoE-deficient mice with hyperhomocysteinemia induced by a high methionine diet, relative to the mice fed a normal chow diet. Methionine 161-171 apolipoprotein E Mus musculus 97-101 1512507-2 1992 The findings of the present study demonstrate that: a) as determined by density gradient ultracentrifugation and gel filtration chromatography, about 20% of the secreted [35S]methionine-labeled apoE expressed by C127E cells is lipid-associated. Methionine 175-185 apolipoprotein E Mus musculus 194-198 18501553-6 2008 We also observed increased immunohistochemical staining for N-Hcy-proteins in aortic lesions from ApoE-/- mice with hyperhomocysteinemia induced by a high methionine diet, relative to ApoE-/- mice fed a control chow diet. Methionine 155-165 apolipoprotein E Mus musculus 98-102 16876491-10 2006 In this study, post-translationally modified apolipoproteins, involving loss of amino acids from both the N- and C-termini, oxidation of methionine residues and possible acylation, were noted following reverse-phase separation. Methionine 137-147 apolipoprotein E Mus musculus 45-60 16876491-11 2006 Further analyses by tandem mass spectrometry (MSMS) done on the tryptic digests of apolipoproteins separated by reverse phase chromatography enabled us to confirm sequence differences between the two strains, to verify selected apoA-I sequences that had been entered into the GenBank and to identify which methionines in apoA-I, apoC-III and apoE had been converted to methionine sulfoxides. Methionine 306-317 apolipoprotein E Mus musculus 83-98 16910166-3 2006 Herein, we examined the influence of ApoE and folate deficiency on expression and activity of several enzymes of the methionine cycle. Methionine 117-127 apolipoprotein E Mus musculus 37-41 11254667-2 2001 Here we show that induction of HHcy in apoE-null mice by a diet enriched in methionine but depleted in folate and vitamins B6 and B12 increased atherosclerotic lesion area and complexity, and enhanced expression of receptor for advanced glycation end products (RAGE), VCAM-1, tissue factor, and MMP-9 in the vasculature. Methionine 76-86 apolipoprotein E Mus musculus 39-43 1512507-7 1992 c) Expression of apoE by C127E cells was associated with an increased release of [35S]methionine-labeled protein and [3H]glycerol-labeled lipid (3- to 5- and 4- to 8-fold, respectively) compared to nontransfected C127 cells. Methionine 86-96 apolipoprotein E Mus musculus 17-21