BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 19150343)

  • 1. Topological aspects of oligomeric UDP-glucuronosyltransferases in endoplasmic reticulum membranes: advances and open questions.
    Bock KW; Köhle C
    Biochem Pharmacol; 2009 May; 77(9):1458-65. PubMed ID: 19150343
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Determinants of UDP glucuronosyltransferase membrane association and residency in the endoplasmic reticulum.
    Meech R; Mackenzie PI
    Arch Biochem Biophys; 1998 Aug; 356(1):77-85. PubMed ID: 9681994
    [TBL] [Abstract][Full Text] [Related]  

  • 3. In vitro-in vivo correlation for drugs and other compounds eliminated by glucuronidation in humans: pitfalls and promises.
    Miners JO; Knights KM; Houston JB; Mackenzie PI
    Biochem Pharmacol; 2006 May; 71(11):1531-9. PubMed ID: 16455060
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kinetic properties of UDP-glucuronosyltransferase(S) in different membranes of rat liver cells.
    Antoine B; Magdalou J; Siest G
    Xenobiotica; 1984 Jul; 14(7):575-9. PubMed ID: 6438924
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The prediction of drug-glucuronidation parameters in humans: UDP-glucuronosyltransferase enzyme-selective substrate and inhibitor probes for reaction phenotyping and in vitro-in vivo extrapolation of drug clearance and drug-drug interaction potential.
    Miners JO; Mackenzie PI; Knights KM
    Drug Metab Rev; 2010 Feb; 42(1):196-208. PubMed ID: 19795925
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A functional role for histidyl residues of the UDP-glucuronic acid carrier in rat liver endoplasmic reticulum membranes.
    Battaglia E; Radominska-Pandya A
    Biochemistry; 1998 Jan; 37(1):258-63. PubMed ID: 9425046
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios.
    Williams JA; Hyland R; Jones BC; Smith DA; Hurst S; Goosen TC; Peterkin V; Koup JR; Ball SE
    Drug Metab Dispos; 2004 Nov; 32(11):1201-8. PubMed ID: 15304429
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular mechanism of phase I and phase II drug-metabolizing enzymes: implications for detoxification.
    Iyanagi T
    Int Rev Cytol; 2007; 260():35-112. PubMed ID: 17482904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Posttranscriptional regulation of uridine diphosphate glucuronosyltransferases.
    Riches Z; Collier AC
    Expert Opin Drug Metab Toxicol; 2015 Jun; 11(6):949-65. PubMed ID: 25797307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structure of UDP-glucuronosyltransferases in membranes.
    Radominska-Pandya A; Ouzzine M; Fournel-Gigleux S; Magdalou J
    Methods Enzymol; 2005; 400():116-47. PubMed ID: 16399347
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Renal UDP-glucuronosyltransferases and the glucuronidation of xenobiotics and endogenous mediators.
    Knights KM; Miners JO
    Drug Metab Rev; 2010 Feb; 42(1):63-73. PubMed ID: 19780654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. UDP-glucuronosyltransferases and clinical drug-drug interactions.
    Kiang TK; Ensom MH; Chang TK
    Pharmacol Ther; 2005 Apr; 106(1):97-132. PubMed ID: 15781124
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Glucuronate, the precursor of vitamin C, is directly formed from UDP-glucuronate in liver.
    Linster CL; Van Schaftingen E
    FEBS J; 2006 Apr; 273(7):1516-27. PubMed ID: 16689937
    [TBL] [Abstract][Full Text] [Related]  

  • 14. N-glucuronidation of drugs and other xenobiotics by human and animal UDP-glucuronosyltransferases.
    Kaivosaari S; Finel M; Koskinen M
    Xenobiotica; 2011 Aug; 41(8):652-69. PubMed ID: 21434773
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Recent data on the metabolism of drugs by UDP-glucuronosyltransferases and sulfotransferases (author's transl)].
    Batt AM; Magdalou J; Martin N; Lepage C; Kiffel L; Siest G
    Ann Biol Clin (Paris); 1980; 38(1):35-47. PubMed ID: 6769373
    [TBL] [Abstract][Full Text] [Related]  

  • 16. In vitro glucuronidation of thyroxine and triiodothyronine by liver microsomes and recombinant human UDP-glucuronosyltransferases.
    Tong Z; Li H; Goljer I; McConnell O; Chandrasekaran A
    Drug Metab Dispos; 2007 Dec; 35(12):2203-10. PubMed ID: 17875670
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The role of xenobiotic glucuronidating enzymes in drug resistance of tumour tissues and cells.
    Burchell B; Baird S; Coughtrie MW
    Princess Takamatsu Symp; 1990; 21():263-75. PubMed ID: 1966888
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Product inhibition of UDP-glucuronosyltransferase (UGT) enzymes by UDP obfuscates the inhibitory effects of UGT substrates.
    Fujiwara R; Nakajima M; Yamanaka H; Katoh M; Yokoi T
    Drug Metab Dispos; 2008 Feb; 36(2):361-7. PubMed ID: 17998297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Substrate selectivity of human intestinal UDP-glucuronosyltransferases (UGTs): in silico and in vitro insights.
    Tripathi SP; Bhadauriya A; Patil A; Sangamwar AT
    Drug Metab Rev; 2013 May; 45(2):231-52. PubMed ID: 23461702
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Glucuronidation of amine substrates by purified and expressed UDP-glucuronosyltransferase proteins.
    Green MD; Tephly TR
    Drug Metab Dispos; 1998 Sep; 26(9):860-7. PubMed ID: 9733664
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.