erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships von Schnur, R C, Corman, M L, Gallaschun, R J, Cooper, B A, Dee, M F, Doty, J L, Muzzi, M L, DiOrio, C I, Barbacci, E G, Miller, P E

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Potent, orally active aldose reductase inhibitors related to zopolrestat: surrogates for benzothiazole side chain von Mylari, Banavara L, Beyer, Thomas A, Scott, Pamela J, Aldinger, Charles E, Dee, Michael F, Siegel, Todd W, Zembrowski, William J

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Inhibition of the oncogene product p185erbB-2 in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives von Schnur, R. C, Corman, M. L, Gallaschun, R. J, Cooper, B. A, Dee, M. F, Doty, J. L, Muzzi, M. L, Moyer, J. D, DiOrio, C. I

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Novel, potent aldose reductase inhibitors: 3,4-dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazolyl]methyl]-1-phthalazineacetic acid (zopolrestat) and congeners von Mylari, Banavara L, Larson, Eric R, Beyer, Thomas A, Zembrowski, William J, Aldinger, Charles E, Dee, Michael F, Siegel, Todd W, Singleton, David H

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erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships von Schnur, R. C, Corman, M. L, Gallaschun, R. J, Cooper, B. A, Dee, M. F, Doty, J. L, Muzzi, M. L, DiOrio, C I, Barbacci, E. G

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Aminotriazine 5-HT7 antagonists von MATTSON, Ronald J, DENHART, Derek J, PURANDARE, Ashok, TORTOLANI, David, YUFEN ZHAO, HUA YANG, YEOLA, Suresh, PALMER, Jane, TORRENTE, John, STARK, Arlene, JOHNSON, Graham, CATT, John D, DEE, Michael F, DESKUS, Jeffrey A, DITTA, Jonathan L, EPPERSON, James, KING, H. Dalton, AIMING GAO, POSS, Michael A

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Synthesis of α-hydroxy statine through a facially selective osmylation of a chiral α-amido crotonate von Dee, Michael F., Rosati, Robert L.

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Synthesis and stereochemistry of some thiazolidines related to 6-(hydroxyethyl)-penams von Urban, Frank J., Bordner, Jon, DeCosta, Debra, Dee, Michael F., Vincent, Lawrence A.

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Inhibition of the oncogene product p185 super(erbB-2) in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives von Schnur, R C, Corman, M L, Gallaschun, R J, Cooper, BA, Dee, M F, Doty, J L, Muzzi, M L, Moyer, J D, DiOrio, C I, Barbacci, E G, Miller, P E, O'Brien, A T, Morin, MJ, Foster, BA, Pollack, V A

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Novel, potent aldose reductase inhibitors: 3,4-Dihydro-4-oxo-3-((5-(trifluoromethyl)-2-benzothiazolyl)methyl) -1-phthalazine-acetic acid (Zopolrestat) and congeners von Mylari, B L, Larson, E R, Beyer, T A, Zembrowski, W J, Aldinger, CE, Dee, M F, Siegel, T W, Singleton, D H

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Novel, potent aldose reductase inhibitors : 3,4-dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazolyl]methyl]-1-phthalazine-acetic acid (zopolrestat) and congeners von MYLARI, B. L, LARSON, E. R, BEYER, T. A, ZEMBROWSKI, W. J, ALDINGER, C. E, DEE, M. F, SIEGEL, T. W, SINGLETON, D. H

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Bigelow: "Cases on the Law of Property. Volume I. Personal Property" (Book Review) von Dee, M F

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Cases on the Law of Property. Volume I. Personal Property von Dee, M. F.

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Law Library Purchasing in an Interdisciplinary Era von Dee, Mathew F

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The Impact of Computerized Methods on Legal Research Courses: A Survey of LEXIS Experience and Some Probable Effects of WESTLAW von Dee, Mathew F, Kessler, Ruth M

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Law School Libraries: Survey Relating to Autonomy and Faculty Status von Bailey, James F, Dee, Mathew F

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Phase 1 study of safety and tolerability of an oral contraceptive containing low‐dose ethinyl oestradiol combined with glecaprevir/pibrentasvir treatment in healthy premenopausal w... von Shiller, Dee‐Dee, Yao, Betty B., Chen, Mong‐Jen, Orejudos, Amelia, Mostafa, Nael M., Marcinak, John F., Burroughs, Margaret, Boyle, Craig

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Temporal changes in population structure of a marine planktonic diatom von Tesson, Sylvie V M, Montresor, Marina, Procaccini, Gabriele, Kooistra, Wiebe H C F

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Radiocarbon-Based Chronology for Dynastic Egypt von Ramsey, Christopher Bronk, Dee, Michael W, Rowland, Joanne M, Higham, Thomas F.G, Harris, Stephen A, Brock, Fiona, Quiles, Anita, Wild, Eva M, Marcus, Ezra S, Shortland, Andrew J

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The fungal pathogen Moniliophthora perniciosa has genes similar to plant PR-1 that are highly expressed during its interaction with cacao von Teixeira, Paulo J P L, Thomazella, Daniela P T, Vidal, Ramon O, do Prado, Paula F V, Reis, Osvaldo, Baroni, Renata M, Franco, Sulamita F, Mieczkowski, Piotr, Pereira, Gonçalo A G, Mondego, Jorge M C

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