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The glucuronidation of exogenous and endogenous compounds by stably expressed rat and human UDP-glucuronosyltransferase 1.1
1996
King, C.D.; Green, M.D.; Rios, G.R.; Coffman, B.L.; Owens, I.S.; Bishop, W.P.; Tephly, T.R.
Arch. Biochem. Biophys.
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Glucuronidation of opioids, carboxylic acid-containing drugs, and hydroxylated xenobiotics catalyzed by expressed monkey UDP-glucuronosyltransferase 2B9 protein
1997
Green, M.D.; Belanger, G.; Hum, D.W.; Belanger, A.; Tephly, T.R.
Drug Metab. Dispos.
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The effect of incubation conditions on the enzyme kinetics of UDP-glucuronosyltransferases
2003
Soars, M.G.; Ring, B.J.; Wrighton, S.A.
Drug Metab. Dispos.
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Molecular cloning of the baboon UDP-glucuronosyltransferase 1A gene family: evolution of the primate UGT1 locus and relevance for models of human drug metabolism
2007
Caspersen, C.S.; Reznik, B.; Weldy, P.L.; Abildskov, K.M.; Stark, R.I.; Garland, M.
Pharmacogenet. Genomics
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Endogenous regulators of G protein signaling differentially modulate full and partial mu-opioid agonists at adenylyl cyclase as predicted by a collision coupling model
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Clark, M.J.; Linderman, J.J.; Traynor, J.R.
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Opiates inhibit paclitaxel uptake by P-glycoprotein in preparations of human placental inside-out vesicles
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Hemauer, S.J.; Patrikeeva, S.L.; Nanovskaya, T.N.; Hankins, G.D.; Ahmed, M.S.
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