Orally active, nonpeptide oxytocin antagonists von Evans, Ben E, Leighton, James L, Rittle, Kenneth E, Gilbert, Kevin F, Lundell, George F, Gould, Norman P, Hobbs, Doug W, DiPardo, Robert M, Veber, Daniel F, Pettibone, Douglas J, Clineschmidt, Bradley V, Anderson, Paul S, Freidinger, Roger M

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Design of nonpeptidal ligands for a peptide receptor: cholecystokinin antagonists von Evans, B. E, Rittle, K. E, Bock, M. G, DiPardo, R. M, Freidinger, R. M, Whitter, W. L, Gould, N. P, Lundell, G. F, Homnick, C. F

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Development of a novel class of cyclic hexapeptide oxytocin antagonists based on a natural product von Williams, Peter D, Bock, Mark G, Tung, Roger D, Garsky, Victor M, Perlow, Debra S, Erb, Jill M, Lundell, G. F, Gould, Norman P, Whitter, Willie L

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Novel glutamic acid-derived cholecystokinin receptor ligands von Freidinger, R. M, Whitter, W. L, Gould, N. P, Holloway, M. K, Chang, R. S. L, Lotti, V. J

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3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 2. Structural modification of 7-(substituted aryl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives von Hoffman, William F, Alberts, A. W, Cragoe, E. J, Deana, A. A, Evans, B. E, Gilfillan, J. L, Gould, N. P, Huff, J. W, Novello, F. C

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Agents for the treatment of brain edema. 2. [(2,3,9,9a-Tetrahydro-3-oxo-9a-substituted-1H-fluoren-7-yl)oxy]alkanoic acids and some of their analogs von Cragoe, E. J, Woltersdorf, O. W, Gould, N. P, Pietruszkiewicz, A. M, Ziegler, C, Sakurai, Y, Stokker, G. E, Anderson, P. S, Bourke, R. S

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Agents for the treatment of brain injury. 1. (Aryloxy)alkanoic acids von Cragoe, E. J, Gould, N. P, Woltersdorf, O. W, Ziegler, C, Bourke, R. S, Nelson, L. R, Kimelberg, H. K, Waldman, J. B, Popp, A. J, Sedransk, N

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Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptid... von Perlow, Debra S, Erb, Jill M, Gould, Norman P, Tung, Roger D, Freidinger, Roger M, Williams, Peter D, Veber, Daniel F

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Cyclic hexapeptide oxytocin antagonists. Potency-, selectivity-, and solubility-enhancing modifications von Freidinger, Roger M, Williams, P. D, Tung, R. D, Bock, M. G, Pettibone, D. J, Clineschmidt, B. V, DiPardo, R. M, Erb, J. M, Garsky, V. M

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Prostaglandin isosteres. 2. Chain-modified thiazolidinone prostaglandin analogs as renal vasodilators von Bicking, John B, Bock, Mark G, Cragoe, Edward J, DiPardo, Robert M, Gould, Norman, Holtz, Wilbur J, Lee, T. J, Robb, Charles M, Smith, Robert L

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11,12-Secoprostaglandins. 3. 8-Alkylthio(sulfinyl and sulfonyl)-12-hydroxyalkanoic acids and related compounds von Smith, Robert L, Bicking, John B, Gould, Norman P, Lee, Ta-Jyh, Robb, Charles M, Kuehl, Frederick A, Mandel, Lewis R, Cragoe, Edward J

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The printing of backbone titles on thin books and magazines von Gould, P. N., Raines, L. C., Ruckmick, C. A.

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Nanomolar-affinity, non-peptide oxytocin receptor antagonists von Evans, Ben E, Lundell, George F, Gilbert, Kevin F, Bock, Mark G, Rittle, Kenneth E, Carroll, Leigh Anne, Williams, Peter D, Pawluczyk, Joseph M, Leighton, James L

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Inhibitors of gastric acid secretion: antisecretory 2-pyridylurea derivatives von Bolhofer, William A, Deana, Albert A, Habecker, Charles N, Hoffman, Jacob M, Gould, Norman P, Pietruszkiewicz, Adolph M, Prugh, John D, Torchiana, Mary Lou, Cragoe, Edward J, Hirschmann, Ralph

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Agents for the treatment of brain edema. 2. [(2,3,9,9a-Tetrahydro-3-oxo-9a-substituted-1H-fluoren-7-yl)oxy]+ ++alkanoi c acids and some of their analogues von Cragoe, Jr, E J, Woltersdorf, Jr, O W, Gould, N P, Pietruszkiewicz, A M, Ziegler, C, Sakurai, Y, Stokker, G E, Anderson, P S, Bourke, R S, Kimelberg, H K

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Prostaglandin isosteres. 1. (8-Aza-, 8,10-diaza-, and 8-aza-11-thia)-9-oxoprostanoic acids and their derivatives von Smith, Robert L, Lee, Ta-Jyh, Gould, Norman P, Cragoe, Edward J, Oien, Helen G, Kuehl, Frederick A

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Dianions of methylated thiophene-2-carboxylic acids: their formation and reactivity von Gould, Norman P, Lee, Ta-Jyh

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Agents for the treatment of brain edema. II: [(2,3,9,9a-tetrahydro-3-oxo-9a-substituted-1H-fluoren-7-yl)oxy[alkanoic acids and some of their analogues von CRAGOE, E. J. JR, WOLTERSDORF, O. W. JR, NELSON, L. R, BARRON, K. D, ROSE, J. R, SZAROWSKI, D, POPP, A. J, WALDMAN, J. B, GOULD, N. P, PIETRUSZKIEWICZ, A. M, ZIEGLER, C, SAKURAI, Y, STOKKER, G. E, ANDERSON, P. S, BOURKE, R. S, KIMELBERG, H. K

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3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. II: Structural modification of 7-(substituted aryl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives von HOFFMAN, W. F, ALBERTS, A. W, RITTLE, K. E, SMITH, R. L, STOKKER, G. E, WILLARD, A. K, CRAGOE, E. J. JR, DEANA, A. A, EVANS, B. E, GILFILLAN, J. L, GOULD, N. P, HUFF, J. W, NOVELLO, F. C, PRUGH, J. D

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Early Childhood Administrators: Are They Using Planned Communication To Reach Key Publics? von Gould, Nora Palmer

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