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Rs28898617 (UGT1A6, A > G) variation was associated with an increase in NCVPA.
Oxidative stress and histone modifications may promote transcriptional activation of Ugt1a6 and Ugt1a7 (show UGT1A7 ELISA Kits) genes.
Identified coding variants on UGT1A1 (show UGT1A1 ELISA Kits) and UGT1A6 genes in association with serum bilirubin level and hyperbilirubinemia risk in elderly subjects.
Results suggest that CYP3A4 (show CYP3A4 ELISA Kits) changes the catalytic function of the UGT1A (show UGT1A1 ELISA Kits) subfamily in a UGT (show SLC35A2 ELISA Kits) isoform-specific manner.
Evaluating the association of UGT1A6 2 Ser7Ala polymorphism with drug response, there was no significant difference in the genotypic distribution between responders and non-responders.
Validation of variants in SLC28A3 (show SLC28A3 ELISA Kits) and UGT1A6 as genetic markers predictive of anthracycline-induced cardiotoxicity in children.
Lower adjusted plasma VPA concentrations were also observed in patients with UGT1A6 double heterozygosities than those with single heterozygosity.
UGT1A6 polymorphisms may be used to identify people with increased risk of developing lung cancer
Polymorphism in UDP-glucuronosyltransferase 1A6 is associated with colorectal cancer.
Dual polymorphisms of UDP glucuronosyl-transferases 1A6 and 1A1 (show SLC45A2 ELISA Kits) in a patient with Gilbert's syndrome who had persistent hyperserotoninemia that responded to octreotide are reported.
the difference in expression levels between Ugt1a6a and Ugt1a6b in the hippocampus led us to speculate that Ugt1a6a is likely the predominant catalyst of serotonin glucuronidation in the mouse brain.
This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene is active on phenolic and planar compounds. Alternative splicing in the unique 5' end of this gene results in two transcript variants.
UDP glycosyltransferase 1 family, polypeptide A6
, UDP-glucuronosyltransferase 1-6
, UDP glucuronosyltransferase 1 family, polypeptide A5
, UDP glycosyl transferase 1A6
, UDP glucuronosyltransferase 1 family, polypeptide A6
, UDP-glucuronosyltransferase 1-6-like
, UDP-glucuronosyltransferase 1A6
, UDP glucuronosyltransferase 1 family, polypeptide A10
, UDP glucuronosyltransferase 1 family, polypeptide A7
, UDP glucuronosyltransferase 1 family, polypeptide A8
, UDP glucuronosyltransferase 1 family, polypeptide A9
, UDP-glucuronosyltransferase 1 family polypeptide A6s
, UDP-glucuronosyltransferase 1-F
, phenol-metabolizing UDP-glucuronosyltransferase
, P-nitrophenol specific
, P-nitrophenol-specific UDPGT
, UDP glucuronosyltransferase 1A6
, phenol UDP-glucuronosyltransferase