作者: Federico Innocenti , Wanqing Liu , Peixian Chen , Apurva A. Desai , Soma Das
DOI: 10.1097/01213011-200505000-00004
关键词:
摘要: ObjectivesNine different functional UGT1A enzymes are generated from a single gene by alternative splicing, with each enzyme having unique exon 1. SN-38, the active metabolite of anticancer agent irinotecan, is metabolized both UGT1A1 and UGT1A9. We aim to characterize UGT1A9–UGT1