PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 28334053-12 2017 An inverse relationship was observed between total cholesterol and aberrant behaviour as determined by ABC-C total score. Cholesterol 51-62 ATP binding cassette subfamily C member 1 Homo sapiens 103-108 28383515-4 2017 Subsequently, further ABC transporters, i.e., ABCG1, ABCG4, ABCB6, ABCC1, ABCC6 or ABCC9, have been shown to directly or indirectly affect cellular cholesterol efflux, the inflammatory response in macrophages, megakaryocyte proliferation and thrombus formation, as well as vascular function and blood pressure, and may thereby contribute to the pathogenesis of CVD and its complications. Cholesterol 148-159 ATP binding cassette subfamily C member 1 Homo sapiens 67-72 22982209-6 2012 The mRNA levels of cholesterol transport regulators ABCA1 and ABCG1 were markedly downregulated by UVB, parallel to the lamellar ichthyosis related glucosylceramide transporter ABCA12 and the suspected sphingosine-1-phosphate and cholesterol sulfate transporter ABCC1. Cholesterol 19-30 ATP binding cassette subfamily C member 1 Homo sapiens 262-267 24225025-1 2013 BACKGROUND: The activity of P-glycoprotein (Pgp) and multidrug resistance related protein 1 (MRP1), two membrane transporters involved in multidrug resistance of colon cancer, is increased by high amounts of cholesterol in plasma membrane and detergent resistant membranes (DRMs). Cholesterol 208-219 ATP binding cassette subfamily C member 1 Homo sapiens 53-91 24225025-1 2013 BACKGROUND: The activity of P-glycoprotein (Pgp) and multidrug resistance related protein 1 (MRP1), two membrane transporters involved in multidrug resistance of colon cancer, is increased by high amounts of cholesterol in plasma membrane and detergent resistant membranes (DRMs). Cholesterol 208-219 ATP binding cassette subfamily C member 1 Homo sapiens 93-97 24225025-4 2013 RESULTS: MDR cells, which overexpressed Pgp and MRP1, had a dysregulated cholesterol metabolism, due to the lower expression of ubiquitin E3 ligase Trc8: this produced lower ubiquitination rate of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCoAR), higher cholesterol synthesis, higher cholesterol content in MDR cells. Cholesterol 73-84 ATP binding cassette subfamily C member 1 Homo sapiens 48-52 24225025-4 2013 RESULTS: MDR cells, which overexpressed Pgp and MRP1, had a dysregulated cholesterol metabolism, due to the lower expression of ubiquitin E3 ligase Trc8: this produced lower ubiquitination rate of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCoAR), higher cholesterol synthesis, higher cholesterol content in MDR cells. Cholesterol 263-274 ATP binding cassette subfamily C member 1 Homo sapiens 48-52 18851956-10 2009 In conclusion, ABCB1 and ABCC1 mRNA levels in PBMC are modulated by atorvastatin and ABCB1 G2677T/A polymorphism and ABCB1 baseline expression is related to differences in serum LDL cholesterol and apoB in response to atorvastatin. Cholesterol 182-193 ATP binding cassette subfamily C member 1 Homo sapiens 25-30 19651114-5 2009 Two of these transporters are relevant to multidrug resistance in tumor cells (Pgp/ABCB1 and MRP1/ABCC1), while the third (ABCA1) is extensively studied in relation to the reverse cholesterol pathway and cellular cholesterol homeostasis. Cholesterol 180-191 ATP binding cassette subfamily C member 1 Homo sapiens 93-97 19651114-5 2009 Two of these transporters are relevant to multidrug resistance in tumor cells (Pgp/ABCB1 and MRP1/ABCC1), while the third (ABCA1) is extensively studied in relation to the reverse cholesterol pathway and cellular cholesterol homeostasis. Cholesterol 180-191 ATP binding cassette subfamily C member 1 Homo sapiens 98-103 19651114-5 2009 Two of these transporters are relevant to multidrug resistance in tumor cells (Pgp/ABCB1 and MRP1/ABCC1), while the third (ABCA1) is extensively studied in relation to the reverse cholesterol pathway and cellular cholesterol homeostasis. Cholesterol 213-224 ATP binding cassette subfamily C member 1 Homo sapiens 98-103 17489102-8 2007 Further cholesterol depletion below 40% yielded both a partial shift of MRP1 to the high-density fraction and a decrease of its functionality. Cholesterol 8-19 ATP binding cassette subfamily C member 1 Homo sapiens 72-76 17489102-9 2007 Taken together, these data suggest that MRP1 functionality depends on its localization in cholesterol-rich membrane microdomains. Cholesterol 90-101 ATP binding cassette subfamily C member 1 Homo sapiens 40-44 17213331-8 2007 Similar but less pronounced alterations in intracellular cholesterol distribution are observed on expression of a temperature-rescued mutant variant of the related ATP-binding cassette (ABC) protein multidrug resistance-associated protein 1 (MRP1). Cholesterol 57-68 ATP binding cassette subfamily C member 1 Homo sapiens 199-240 17213331-8 2007 Similar but less pronounced alterations in intracellular cholesterol distribution are observed on expression of a temperature-rescued mutant variant of the related ATP-binding cassette (ABC) protein multidrug resistance-associated protein 1 (MRP1). Cholesterol 57-68 ATP binding cassette subfamily C member 1 Homo sapiens 242-246 11118294-1 2000 The aim of the present paper is to reinvestigate the role of multidrug resistance P-glycoprotein MDR1 and MDR-associated protein (MRP1) in cholesterol esterification using well-characterized inhibitors. Cholesterol 139-150 ATP binding cassette subfamily C member 1 Homo sapiens 130-134 34822764-5 2021 MRP demonstrates an ability to recover signals such as associations between PCSK9 and LDL cholesterol levels. Cholesterol 90-101 ATP binding cassette subfamily C member 1 Homo sapiens 0-3