PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 23401258-7 2013 However, under supraphysiological conditions, upon infusion with increasing amounts of the bile salt tauroursodeoxycholic acid, Abcg5 became fully rate-limiting for biliary cholesterol secretion. Bile Acids and Salts 91-100 ATP binding cassette subfamily G member 5 Mus musculus 128-133 21241519-9 2011 We confirmed here for the first time simvastatin increased the expression of hepatic ABCB4 and ABCG5, which involved in secretion of cholesterol and bile acids into the bile, besides upregulated ABCA1 and apoA-I. Bile Acids and Salts 149-159 ATP binding cassette subfamily G member 5 Mus musculus 95-100 22981383-11 2012 In addition, genes involved in cholesterol uptake (Ldlr) and bile acid excretion (Abcg5 and Abcg8) were increased in the livers of fat-1 mice. Bile Acids and Salts 61-70 ATP binding cassette subfamily G member 5 Mus musculus 82-87 21319191-10 2011 Study of tissue-specific Fxr knockout mice demonstrated that loss of the Fxr gene in the liver attenuated bile acid induction of hepatic Abcg5/g8 and gallbladder cholesterol content, suggesting a role of FXR in the regulation of cholesterol transport. Bile Acids and Salts 106-115 ATP binding cassette subfamily G member 5 Mus musculus 137-142 22665165-6 2012 The hepatic levels of mRNA encoding transporters Abcb11, Abcb4, Abca1, Abcg5, and Abcg8 were diminished in Ppara-null mice, leading to the accumulation of bile acids in the liver during the CA challenge. Bile Acids and Salts 155-165 ATP binding cassette subfamily G member 5 Mus musculus 71-76 21118090-5 2011 MDR3/Mdr2 and ABCG5/G8 secrete phosphatidylcholine and cholesterol, respectively, in coordination with BSEP-mediated bile acid secretion to mask the detergent/toxic effects of bile acids in the bile ductular space. Bile Acids and Salts 117-126 ATP binding cassette subfamily G member 5 Mus musculus 14-19 21118090-5 2011 MDR3/Mdr2 and ABCG5/G8 secrete phosphatidylcholine and cholesterol, respectively, in coordination with BSEP-mediated bile acid secretion to mask the detergent/toxic effects of bile acids in the bile ductular space. Bile Acids and Salts 176-186 ATP binding cassette subfamily G member 5 Mus musculus 14-19 17825296-0 2007 The sterol transporting heterodimer ABCG5/ABCG8 requires bile salts to mediate cholesterol efflux. Bile Acids and Salts 57-67 ATP binding cassette subfamily G member 5 Mus musculus 36-41 32382260-6 2020 Real-time PCR and western blot results demonstrated that the expression levels of two enzymes (cholesterol 7alpha-hydroxylase (CYP7a1) and sterol 12alpha-hydroxylase (CYP8b1)) to catalyze the synthesis of bile acid from cholesterol were decreased and that two cholesterol transporters (ATP-binding cassette transporter G5/G8 (ABCG5/8)) were increased in the liver of lithogenic diet-fed mice. Bile Acids and Salts 205-214 ATP binding cassette subfamily G member 5 Mus musculus 326-331 16606610-5 2006 Upon EE2 treatment, estrogen receptor alpha (ERalpha) repressed the expression of bile acid and cholesterol transporters (bile salt export pump (BSEP), Na(+)/taurocholate cotransporting polypeptide (NTCP), OATP1, OATP2, ABCG5, and ABCG8) in the liver. Bile Acids and Salts 82-91 ATP binding cassette subfamily G member 5 Mus musculus 220-225 30611276-5 2019 Here, we found a significant increase of mRNA expression levels of phospholipid, bile salt and cholesterol/sterol transporters Abcb1b, Abcb11, Abcg1, Abcg5 and Abcg8. Bile Acids and Salts 81-90 ATP binding cassette subfamily G member 5 Mus musculus 150-155 28065787-15 2017 The altered bile salt pool stimulated robust secretion of cholesterol into the intestinal lumen via the sterol-exporting heterodimer adenosine triphosphate binding cassette subfamily G member 5/8 (ABCG5/G8). Bile Acids and Salts 12-21 ATP binding cassette subfamily G member 5 Mus musculus 197-202 29286073-6 2018 Notably, the expression of genes associated with cholesterol synthesis (sterol regulatory element-binding protein-2 and 3-hydroxy-3-methylglutaryl-CoA reductase), cholesterol secretion [ATP-binding cassette subfamily G member 5 (ABCG5) and ABCG8] and bile acid synthesis [cytochrome P450 family 7 subfamily A member 1 (Cyp7a1), Cyp7b1, Cyp27a1 and Cyp8b1] was reduced in the livers of mice injected with BT or CF. Bile Acids and Salts 251-260 ATP binding cassette subfamily G member 5 Mus musculus 186-227 25582706-10 2015 Thus in conclusion, CA and DCA are more potent FXR activators than CDCA and LCA when fed to mice, and thus they are more effective in decreasing the expression of the rate limiting gene in BA synthesis Cyp7a1 and the 12-hydroxylation of BAs Cyp8b1, and are also more effective in increasing the expression of Abcg5/Abcg8, which is responsible for biliary cholesterol excretion. Bile Acids and Salts 189-191 ATP binding cassette subfamily G member 5 Mus musculus 309-314