Mechanism of Nicotinamide Inhibition and Transglycosidation by Sir2 Histone/Protein Deacetylases von Jackson, Michael D., Schmidt, Manning T., Oppenheimer, Norman J., Denu, John M.

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Insights into the mechanism of bovine CD38/NAD+glycohydrolase from the X-ray structures of its Michaelis complex and covalently-trapped intermediates von Egea, Pascal F, Muller-Steffner, Hélène, Kuhn, Isabelle, Cakir-Kiefer, Céline, Oppenheimer, Norman J, Stroud, Robert M, Kellenberger, Esther, Schuber, Francis

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CD38 induces apoptosis of a murine pro-B leukemic cell line by a tyrosine kinase-dependent but ADP-ribosyl cyclase- and NAD glycohydrolase-independent mechanism von Lund, Frances E., Muller-Steffner, Hélène, Romero-Ramirez, Héctor, Moreno-García, Miguel E., Partida-Sánchez, Santiago, Makris, Melissa, Oppenheimer, Norman J., Santos-Argumedo, Leopoldo, Schuber, Francis

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Extracellular NAD+ regulates intracellular free calcium concentration in human monocytes von Gerth, Anja, Nieber, Karen, Oppenheimer, Norman J, Hauschildt, Sunna

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Alteration in substrate specificity of horse liver alcohol dehydrogenase by an acyclic nicotinamide analog of NAD von Malver, Olaf, Sebastian, Mina J., Oppenheimer, Norman J.

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Reactions of Charged Substrates. 2. Gas-Phase Dissociation of 2'-Substituted Nicotinamide Arabinosides von Buckley, Neil, Handlon, Anthony L, Maltby, David, Burlingame, Alma L, Oppenheimer, Norman J

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Reactions of Charged Substrates. 7. The Methoxymethyl Carbenium Ion Problem. 2. A Semiempirical Study of the Kinetic and Thermodynamic Stabilities of Linear and Cyclic Oxo- and Thi... von Buckley, Neil, Oppenheimer, Norman J

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Reactions of Charged Substrates. 5. The Solvolysis and Sodium Azide Substitution Reactions of Benzylpyridinium Ions in Deuterium Oxide von Buckley, Neil, Oppenheimer, Norman J

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Secondary deuterium and nitrogen-15 isotope effects in enzyme-catalyzed reactions. Chemical mechanism of liver alcohol dehydrogenase von Cook, Paul F, Oppenheimer, Norman J, Cleland, W. W

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Reactions of Charged Substrates. 6. The Methoxymethyl Carbenium Ion Problem. 1. A Semiempirical Study of the Kinetic and Thermodynamic Stabilities of Linear and Cyclic Oxo- and Thi... von Buckley, Neil, Oppenheimer, Norman J

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Reactions of Charged Substrates. 8. The Nucleophilic Substitution Reactions of (4-Methoxybenzyl)dimethylsulfonium Chloride von Buckley, Neil, Oppenheimer, Norman J

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Amino acid-specific ADP-ribosylation: structural characterization and chemical differentiation of ADP-ribose-cysteine adducts formed nonenzymically and in a pertussis toxin-catalyz... von McDonald, Lee J, Wainschel, Larry A, Oppenheimer, Norman J, Moss, Joel

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Stereoselectivity of enzymic transfer of hydrogen from nicotinamide coenzymes: a stereochemical imperative? von Oppenheimer, Norman J

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Aldehyde dehydrogenase activity of Drosophila melanogaster alcohol dehydrogenase: burst kinetics at high pH and aldehyde dismutase activity at physiological pH von Henehan, Gary T. M, Chang, Simon H, Oppenheimer, Norman J

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2'-Ribose Substituent Effects on the Chemical and Enzymic Hydrolysis of NAD von Handlon, Anthony L, Xu, Cheng, Muller-Steffner, Helene M, Schuber, Francis, Oppenheimer, Norman J

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Reactions of Charged Substrates. 3. The Hydrolysis of (4-Methoxybenzyl)dimethylsulfonium Chloride von Buckley, Neil, Oppenheimer, Norman J

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Reactions of Charged Substrates. 4. The Gas-Phase Dissociation of (4-Substituted benzyl)dimethylsulfoniums and -pyridiniums von Buckley, Neil, Maltby, David, Burlingame, Alma L, Oppenheimer, Norman J

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Copper-dependent cleavage of DNA by bleomycin von Ehrenfeld, Guy M, Shipley, Joshua B, Heimbrook, David C, Sugiyama, Hiroshi, Long, Eric C, Van Boom, Jacques H, Van der Marel, Gijs A, Oppenheimer, Norman J, Hecht, Sidney M

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Reactions of charged substrates. 1. The effect of product isomerization on kinetics in the reaction of thiocyanate with (4-methoxybenzyl)dimethylsulfonium chloride von Buckley, Neil, Oppenheimer, Norman J

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Stereospecificity of the intramolecular association of reduced pyridine coenzymes von Oppenheimer, Norman J, Arnold, Lyle J, Kaplan, Nathan O

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