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Glucuronosyltransferase

Function of UDP-glucuronosyltransferase 2B17 (UGT2B17) is ...

Carcinogenesis vol.31 no.9 pp.1620–1626, 2010 doi:10.1093/carcin/bgq124 Advance Access publication June 16, 2010 Function of UDP-glucuronosyltransferase 2B17 (UGT2B17) is involved in endometrial

Glucuronide Isomers: Synthesis, Structural Characterization ...

of UDP-glucuronosyltransferase activity in human small intestine. J Biol Chem 275 (2000) 36164-36171. 11. Tukey, R.H. and Strassburg, C.P., Human UDP-glucuronosyltransferases:

Curcuminoids inhibit multiple human cytochromes P450 (CYP ...

Basu NK, Kole L and Owens IS (2003) Evidence for phosphorylation requirement for human bilirubin UDP-glucuronosyltransferase (UGT1A1) activity.

STUDY OF BILIRUBIN - URIDINE DIPHOSPHATE ...

bilirubin - uridine diphosphate glucuronosyltransferase (ugt1a1) gene mutations among newborn babies in the malay population in kelantan with hyperbilirubinaemia study of bilirubin - uridine diphosphate glucuronosyltransferase (ugt1a1) gene in neonatal hyperbilirubinaemia among malays

Tissue-specific,Inducible,andHormonalControlofthe HumanUDP ...

Tissue-specific,Inducible,andHormonalControlofthe HumanUDP-Glucuronosyltransferase-1(UGT1)Locus * Receivedforpublication,June20,2005,andinrevisedform,September8,2005 Published,JBCPapersinPress,September9,2005,DOI10.1074/jbc.M506683200

Diabetes Mellitus Reduces Activity of Human UDP ...

Diabetes Mellitus Reduces Activity of Human UDP Glucuronosyltransferase 2B7 in Liver and Kidney Leading to Decreased Formation of Mycophenolic Acid Acyl

UDP-Glucuronosyltransferase (UGT) 2B15 Pharmacogenetics ...

UDP-Glucuronosyltransferase (UGT) 2B15 Pharmacogenetics: UGT2B15 D85Y Genotype and Gender Are Major Determinants of Oxazepam Glucuronidation by Human Liver

DIABETES MELLITUS REDUCE ACTIVITY OF HUMAN UDP ...

Bhasker C, McKinnon W, Stone A, Lo A, Kubota T, Ishizaki T and Miners J (2000) Genetic polymorphism of UDP-glucuronosyltransferase 2B7 (UGT2B7) at amino acid 268: ...

Gilbert's syndrome: High frequency of the (TA)7 TAA allele in ...

The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase defi ciency.

Crigler-Najjar Syndrome

... familial nonhemolytic jaundice associated with high level of unconjugated bilirubin due to deficient uridine diphosphate glucuronosyltransferase (UDPG-T) activity in the liver.