New 4-Point Pharmacophore Method for Molecular Similarity and Diversity Applications:  Overview of the Method and Applications, Including a Novel Approach to the Design of Combinat... by Mason, Jonathan S, Morize, Isabelle, Menard, Paul R, Cheney, Daniel L, Hulme, Christopher, Labaudiniere, Richard F

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Chemistry Space Metrics in Diversity Analysis, Library Design, and Compound Selection by Menard, Paul R, Mason, Jonathan S, Morize, Isabelle, Bauerschmidt, Susanne

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Rational Screening Set Design and Compound Selection:  Cascaded Clustering by Menard, Paul R, Lewis, Richard A, Mason, Jonathan S

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Synthesis and diversity analysis of lead discovery piperazine-2-carboxamide libraries by Herpin, T F, Morton, G C, Dunn, A K, Fillon, C, Menard, P R, Tang, S Y, Salvino, J M, Labaudinière, R F

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Angiotensin-converting enzyme inhibitors: new orally active 1,4-thiazepine-2,5-diones, 1,4-thiazine-2,5-diones, and 1,4-benzothiazepine-2,5-diones possessing antihypertensive activ... by Skiles, Jerry W, Suh, John T, Williams, Bruce E, Menard, Paul R, Barton, Jeffrey N, Loev, Bernard, Jones, Howard, Neiss, Edward S, Schwab, Alfred

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Angiotensin converting enzyme inhibitors. 9. Novel [[N-(1-carboxyl-3-phenylpropyl)amino]acyl]glycine derivatives with diuretic activity by Barton, Jeffrey N, Piwinski, John J, Skiles, Jerry W, Regan, John R, Menard, Paul R, Desai, Rohit, Golec, F. S, Reilly, Laurence W, Goetzen, Thomas

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Angiotensin converting enzyme inhibitors. 10. Aryl sulfonamide substituted N-[1-carboxy-3-phenylpropyl]-L-alanyl-L-proline derivatives as novel antihypertensives by Mencel, James J, Regan, John R, Barton, Jeffrey, Menard, Paul R, Bruno, Joseph G, Calvo, Raul R, Kornberg, Brian E, Schwab, Alfred, Neiss, Edward S, Suh, John T

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Angiotensin converting enzyme inhibitors. (Mercaptoaroyl)amino acids by Menard, Paul R, Suh, John T, Jones, Howard, Loev, Bernard, Neiss, Edward S, Wilde, Joyce, Schwab, Alfred, Mann, William S

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Angiotensin-converting enzyme inhibitors. 9. Novel ((N-(-carboxy-3-phenylpropyl)-amino)acyl)glycine derivatives with diuretic activity by Barton, J N, Piwinski, J J, Skiles, J W, Regan, J R, Menard, PR, Desai, R, Golec, F S, Reilly, L W, Suhn, J T

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Angiotensin converting inhibitors. (Mercaptoaroyl)amino acids by Menard, PR, Suh, J T, Jones, H, Leov, B, Neiss, E S, Wilde, J, Schwab, A, Mann, W S

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The EUV Imaging Spectrometer for Hinode by Culhane, J. L., Harra, L. K., James, A. M., Al-Janabi, K., Bradley, L. J., Chaudry, R. A., Rees, K., Tandy, J. A., Thomas, P., Whillock, M. C. R., Winter, B., Doschek, G. A., Korendyke, C. M., Brown, C. M., Myers, S., Mariska, J., Seely, J., Lang, J., Kent, B. J., Shaughnessy, B. M., Young, P. R., Simnett, G. M., Castelli, C. M., Mahmoud, S., Mapson-Menard, H., Probyn, B. J., Thomas, R. J., Davila, J., Dere, K., Windt, D., Shea, J., Hagood, R., Moye, R., Hara, H., Watanabe, T., Matsuzaki, K., Kosugi, T., Hansteen, V., Wikstol, Ø.

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Markedly different acyl papain structures deacylate at similar rates: resonance Raman spectroscopic and kinetic evidence by Tonge, Peter J, Menard, Robert, Storer, Andrew C, Ruzsicska, Bela P, Carey, Paul R

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