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Duffel M W
Duffel M. W.
Duffel Michael W.
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Michael W.
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http://hub.abes.fr/acs/periodical/jnprdf/1987/volume_50/issue_3/101021np50051a025/authorship/2
http://hub.abes.fr/acs/periodical/crtoec/1988/volume_1/issue_4/101021tx00004a009/authorship/4
http://hub.abes.fr/acs/periodical/jnprdf/1992/volume_55/issue_3/101021np50081a001/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1986/volume_29/issue_8/101021jm00158a028/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_8/101021jo00384a022/authorship/3
http://hub.abes.fr/acs/periodical/crtoec/1996/volume_9/issue_1/101021tx950065t/authorship/3
http://hub.abes.fr/oup/periodical/carcin/1997/volume_18/issue_4/101093carcin184843/authorship/2
http://hub.abes.fr/acs/periodical/jnprdf/1997/volume_60/issue_11/101021np970226o/authorship/2
http://hub.abes.fr/acs/periodical/crtoec/2000/volume_13/issue_12/101021tx990184z/authorship/6
http://hub.abes.fr/oup/periodical/carcin/1998/volume_19/issue_11/101093carcin19112007/authorship/5
http://hub.abes.fr/acs/periodical/crtoec/2006/volume_19/issue_11/101021tx060160/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_21/101021jm990406q/authorship/1
http://hub.abes.fr/acs/periodical/crtoec/2008/volume_21/issue_8/101021tx800133d/authorship/3
http://hub.abes.fr/acs/periodical/crtoec/1999/volume_12/issue_3/101021tx980219f/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_10/101021jm040043g/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_25/101021jm010481c/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_14/101021jm980269h/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32/issue_9/101021jm00129a023/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1985/volume_28/issue_5/101021jm50001a016/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33/issue_7/101021jm00169a002/authorship/3
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Vinblastine and vincristine are inhibitors of monoamine oxidase B
Enzymic and chemical oxidations of leurosine to 5'-hydroxyleurosine
In vitro metabolic transformations of vinblastine: oxidations catalyzed by human ceruloplasmin
Affinity Separations. A Practical Approach Edited by Paul Matejtschuk. Oxford University Press, NewYork. 1997. xix + 253 pp. 15.5 x 23.5 cm. ISBN 0-19-963550-1. $55.00.
Influence of Substrate Structure on the CatalyticEfficiency of Hydroxysteroid Sulfotransferase STa in theSulfation of Alcohols
Oxidation-dependent inactivation of aryl sulfotransferase IV by primary N-hydroxy arylamines during in vitro assays.
Sulfation of alpha-hydroxytamoxifen catalyzed by human hydroxysteroid sulfotransferase results in tamoxifen-DNA adducts.
Importance of peri-Interactions on the Stereospecificityof Rat Hydroxysteroid Sulfotransferase STa with1-Arylethanols
Handbook of Drug Metabolism Edited by ThomasF. Woolf. Marcel Dekker, New York. 1999. xi + 596 pp.18 × 26 cm. ISBN 0-8247-0229-8. $225.00.
Hydroxylated Polychlorinated Biphenyls Are Substrates andInhibitors of Human Hydroxysteroid Sulfotransferase SULT2A1
Oxidations of Vincristine Catalyzed by Peroxidase and Ceruloplasmin
Comparative Molecular Field Analysis of Substrates for an ArylSulfotransferase Based on Catalytic Mechanism and Protein HomologyModeling
Hydrolysis in Drug and Prodrug Metabolism.Chemistry, Biochemistry, and Enzymology ByBernard Testa and Joachim M. Mayer. Wiley-VCH,Zürich, Switzerland. 2003. xx + 780 pp. 18 × 24.5 cm.ISBN 3-906390-25-X. $215.00
Structure−Function Modeling of the Interactions ofN-Alkyl-N-hydroxyanilines with Rat Hepatic ArylSulfotransferase IV
Pentachlorophenol and Other Chlorinated Phenols Are Substrates for Human Hydroxysteroid Sulfotransferase hSULT2A1
Leurosine biotransformations: an unusual ring-fission reaction catalyzed by peroxidase
Metabolism of the Catharanthus Alkaloids: from Streptomyces griseus to Monoamine Oxidase B
One-Electron Oxidation of Vindoline and 16-O-Acetylvindoline Catalyzed by Peroxidase
Transformations of MPTP by Ceruloplasmin and Peroxidase: Comparison with Vinca Alkaloid Biotransformations
N-Substituted sulfonamide carbonic anhydrase inhibitors with topical effects on intraocular pressure
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