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Results: 6

1.

The major chemical-detoxifying system of UDP-glucuronosyltransferases requires regulated phosphorylation supported by protein kinase C.

Basu NK, Kole L, Basu M, Chakraborty K, Mitra PS, Owens IS.

J Biol Chem. 2008 Aug 22;283(34):23048-61. doi: 10.1074/jbc.M800032200. Epub 2008 Jun 13.

PMID:
18556656
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

A historical overview of the heterologous expression of mammalian UDP-glucuronosyltransferase isoforms over the past twenty years.

Radominska-Pandya A, Bratton S, Little JM.

Curr Drug Metab. 2005 Apr;6(2):141-60. Review.

PMID:
15853765
[PubMed - indexed for MEDLINE]
3.

Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.

Bock KW.

Crit Rev Biochem Mol Biol. 1991;26(2):129-50. Review.

PMID:
1914494
[PubMed - indexed for MEDLINE]
4.

UDP-glucuronosyltransferases (UGTs): from purification of Ah-receptor-inducible UGT1A6 to coordinate regulation of subsets of CYPs, UGTs, and ABC transporters by nuclear receptors.

Bock KW, Bock-Hennig BS.

Drug Metab Rev. 2010 Feb;42(1):6-13. doi: 10.3109/03602530903205492. Review.

PMID:
19831498
[PubMed - indexed for MEDLINE]
5.

First-pass metabolism via UDP-glucuronosyltransferase: a barrier to oral bioavailability of phenolics.

Wu B, Kulkarni K, Basu S, Zhang S, Hu M.

J Pharm Sci. 2011 Sep;100(9):3655-81. doi: 10.1002/jps.22568. Epub 2011 Apr 11. Review.

PMID:
21484808
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

The crystal structure of human UDP-glucuronosyltransferase 2B7 C-terminal end is the first mammalian UGT target to be revealed: the significance for human UGTs from both the 1A and 2B families.

Radominska-Pandya A, Bratton SM, Redinbo MR, Miley MJ.

Drug Metab Rev. 2010 Feb;42(1):133-44. doi: 10.3109/03602530903209049. Review.

PMID:
19821783
[PubMed - indexed for MEDLINE]
Free PMC Article

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