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http://purl.uniprot.org/citations/29444903http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29444903http://www.w3.org/2000/01/rdf-schema#comment"CYP2C11 is involved in the metabolism of many drugs in rats. To assess the roles of CYP2C11 in physiology and drug metabolism, a CYP2C11-null rat model was generated using the clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9method. A 2-base pair insertion was added to exon 6 of CYP2C11 in Sprague-Dawley rats. CYP2C11 was not detected by western blotting in liver microsomes of CYP2C11-null rats. No off-target effects were found at 11 predicted sites of the knockout model. The CYP2C11-null rats were viable and had no obvious abnormalities, with the exception of reduced fertility. Puberty in CYP2C11-null rats appeared to be delayed by ∼20 days, and the average litter size fell by 43%. Tolbutamide was used as a probe in this drug metabolism study. In the liver microsomes of CYP2C11-null rats, the Vmax and intrinsicclearance values decreased by 22% and 47%, respectively, compared with those of wild-type rats. The Km values increased by 47% compared with that of wild types. However, our pharmacokinetics study showed no major differences in any parameters between the two strains, in both males and females. In conclusion, a CYP2C11-null rat model was successfully generated and is a valuable tool to study the in vivo function of CYP2C11."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.org/dc/terms/identifier"doi:10.1124/dmd.117.078444"xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Wang C."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Wei Y."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Zhang X."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Yang L."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Wang H."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Wang K."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Guo D."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Sui D."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/author"Shan M."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/name"Drug Metab Dispos"xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/pages"525-531"xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/title"Generation and Characterization of a CYP2C11-Null Rat Model by Using the CRISPR/Cas9 Method."xsd:string
http://purl.uniprot.org/citations/29444903http://purl.uniprot.org/core/volume"46"xsd:string
http://purl.uniprot.org/citations/29444903http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/29444903
http://purl.uniprot.org/citations/29444903http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/29444903
http://purl.uniprot.org/uniprot/#_A0A0G2K879-mappedCitation-29444903http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29444903
http://purl.uniprot.org/uniprot/#_P08683-mappedCitation-29444903http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29444903
http://purl.uniprot.org/uniprot/A0A0G2K879http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/29444903
http://purl.uniprot.org/uniprot/P08683http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/29444903