PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 33033903-7 2020 The impact of UGT2B15 polymorphisms on the pharmacokinetics of oxazepam and lorazepam was simulated and glucuronide metabolites were also simulated for all four drugs. Lorazepam 76-85 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 14-21 30921829-5 2019 Furthermore, we found some drug models within the SimCYP library can be improved, e.g., the minor allele frequency of ABCG2 and the fraction metabolized by UGT2B15 should be incorporated for rosuvastatin and lorazepam, respectively. Lorazepam 209-218 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 157-164 30443442-0 2018 The Relationship of UGT2B15 Pharmacogenetics and Lorazepam for Anxiety. Lorazepam 49-58 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 20-27 27622723-0 2016 Implication of UGT2B15 Genotype Polymorphism on Postoperative Anxiety Levels in Patients Receiving Lorazepam Premedication. Lorazepam 99-108 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 15-22 27622723-2 2016 The UGT2B15 genotype is of importance for the metabolism of lorazepam. Lorazepam 60-69 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 4-11 27622723-3 2016 The clinical effect of genetic polymorphisms in UGT2B15 genotype on the treatment of anxiety levels in same-day surgery patients receiving lorazepam, however, is unknown. Lorazepam 139-148 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 48-55 27622723-10 2016 Striking was that females with high preoperative anxiety scores and genetically reduced lorazepam glucuronidation (UGT2B15*2 homozygotes) showed more postoperative anxiety reduction than males with the same genotype. Lorazepam 88-97 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 115-122 27622723-11 2016 CONCLUSIONS: UGT2B15 genotype contributes to postoperative anxiety reduction after lorazepam premedication. Lorazepam 83-92 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 13-20 15961980-0 2005 Effect of the UGT2B15 genotype on the pharmacokinetics, pharmacodynamics, and drug interactions of intravenous lorazepam in healthy volunteers. Lorazepam 111-120 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 14-21 17687269-6 2008 Our study suggests that the UGT2B7 genotype probably affects lorazepam-valproate pharmacodynamic interaction, especially in subjects who have homovariant genotypes of UGT2B7 and UGT2B15, although the effects on the pharmacokinetics are less significant. Lorazepam 61-70 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 178-185 15961980-9 2005 CONCLUSIONS: Our results suggest that the UGT2B15*2 polymorphism is a major determinant of interindividual variability with respect to the pharmacokinetics and pharmacodynamics of lorazepam. Lorazepam 180-189 UDP glucuronosyltransferase family 2 member B15 Homo sapiens 42-49