The discovery of rofecoxib, [MK 966, VIOXX ®, 4-(4′-methylsulfonylphenyl)-3-phenyl-2(5 H)-furanone], an orally active cyclooxygenase-2 inhibitor von Prasit, P, Wang, Z, Brideau, C, Chan, C.-C, Charleson, S, Cromlish, W, Ethier, D, Evans, J.F, Ford-Hutchinson, A.W, Gauthier, J.Y, Gordon, R, Guay, J, Gresser, M, Kargman, S, Kennedy, B, Leblanc, Y, Léger, S, Mancini, J, O'Neill, G.P, Ouellet, M, Percival, M.D, Perrier, H, Riendeau, D, Rodger, I, Tagari, P, Thérien, M, Vickers, P, Wong, E, Xu, L.-J, Young, R.N, Zamboni, R, Boyce, S, Rupniak, N, Forrest, M, Visco, D, Patrick, D

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Ni-Mn-Ga single crystal Shape Memory Alloy magneto-thermomechanical modeling von Brémand, Fabrice, Gauthier, J.Y., Lexcellent, C., Hubert, A., Abadie, J., Chaillet, N.

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Fluid mechanical response of a pulse tube cryocooler: modelling and experimental validation von Lauzier, K, Bribiesca-Argomedo, F, Gauthier, J-Y, Sesmat, S, Lin-Shi, X, Carvalho Lopes, D

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From indomethacin to a selective COX-2 inhibitor: Development of indolalkanoic acids as potent and selective cyclooxygenase-2 inhibitors von Black, W.C., Bayly, C., Belley, M., Chan, C.-C., Charleson, S., Denis, D., Gauthier, J.Y., Gordon, R., Guay, D., Kargman, S., Lau, C.K., Leblanc, Y., Mancini, J., Ouellet, M., Percival, D., Roy, P., Skorey, K., Tagari, P., Vickers, P., Wong, E., Xu, L., Prasit, P.

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Discovery of MK-0476, a potent and orally active leukotriene D4 receptor antagonist devoid of peroxisomal enxyme induction von Labelle, M., Belley, M., Gareau, Y., Gauthier, J.Y., Guay, D., Gordon, R., Grossman, S.G., Jones, T.R., Leblanc, Y., McAuliffe, M., McFarlane, C., Masson, P., Metters, K.M., Ouimet, N., Patrick, D.H., Piechuta, H., Rochette, C., Sawyer, N., Xiang, Y.B., Pickett, C.B., Ford-Hutchinson, A.W., Zamboni, R.J., Young, R.N.

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A new series of selective COX-2 inhibitors: 5,6-diarylthiazolo[3,2-b][1,2,4]triazoles von Roy, P., Leblanc, Y., Ball, R.G., Brideau, C., Chan, C.C., Chauret, N., Cromlish, W., Ethier, D., Gauthier, J.Y., Gordon, R., Greig, G., Guay, J., Kargman, S., Lau, C.K., O'Neill, G., Silva, J., Thérien, M., van Staden, C., Wong, E., Xu, L., Prasit, P.

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Synthesis and biological evaluation of both enantiomers of L-761,000 as inhibitors of cyclooxygenase 1 and 2 von Leblanc, Y., Black, W.C., Chan, C.C., Charleson, S., Delorme, D., Denis, D., Gauthier, J.Y., Grimm, E.L., Gordon, R., Guay, D., Hamel, P., Kargman, S., Lau, C.K., Mancini, J., Ouellet, M., Percival, D., Roy, P., Skorey, K., Tagari, P., Vickers, P., Wong, E., Xu, L., Prasit, P.

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Sensorless Position Control for Surface Permanent Magnet Synchronous Motors at Zero Speed and Acceleration von Zgorski, A., Lin-Shi, X., Gauthier, J.Y.

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A series of non-quinoline cysLT1 receptor antagonists : Sar study on pyridyl analogs of singulair von GUAY, D, GAUTHIER, J. Y, SAWYER, N, ZAMBONI, R, DUFRESNE, C, JONES, T. R, MCAULIFFE, M, MCFARLANE, C, METTERS, K. M, PRASIT, P, ROCHETTE, C, ROY, P

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A series of non-quinoline cysLT 1 receptor antagonists: Sar study on pyridyl analogs of singulair von Guay, Daniel, Gauthier, J.Y., Dufresne, C., Jones, T.R., McAuliffe, M., McFarlane, C., Metters, K.M., Prasit, P., Rochette, C., Roy, P., Sawyer, N., Zamboni, R.

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A new series of potent LTD 4 antagonists in the styrylquinoline class von Guay, D., Gauthier, J.Y., Metters, K.M., Roy, P., Zamboni, R.J.

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A new series of potent LTD4 antagonists in the styrylquinoline class von Guay, D., Gauthier, J.Y., Metters, K.M., Roy, P., Zamboni, R.J.

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(Methylsulfonyl) phenyl-2-(5H)-furanones as cos-2 inhibitors von M. BELLEY, E. GRIMM, J.Y. GAUTHIER

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The discovery of a new structural class of potent orally active leukotriene D4 antagonists von Labelle, M., Prasit, P., Belley, M., Blouin, M., Champion, E., Charette, L., DeLuca, J.G., Dufresne, C., Frenette, R., Gauthier, J.Y., Grimm, E., Grossman, S.J., Guay, D., Herold, E.G., Jones, T.R., Lau, C.K., Leblanc, Y., Léger, S., Lord, A., McAuliffe, M., McFarlane, C., Masson, P., Metters, K.M., Ouimet, N., Patrick, D.H., Perrier, H., Pickett, C.B., Piechuta, H., Roy, P., Williams, H., Wang, Z., Xiang, Y.B., Zamboni, R.J., Ford-Hutchinson, A.W., Young, R.N.

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Asymmetric dithioacetals II: A novel and versatile method for the preparation of chiral dithioacetals von Thérien, M, Gauthier, J.Y, Young, R.N

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Discovery of MK-0476, a potent and orally active leukotriene D 4 receptor antagonist devoid of peroxisomal enxyme induction von Labelle, M., Belley, M., Gareau, Y., Gauthier, J.Y., Guay, D., Gordon, R., Grossman, S.G., Jones, T.R., Leblanc, Y., McAuliffe, M., McFarlane, C., Masson, P., Metters, K.M., Ouimet, N., Patrick, D.H., Piechuta, H., Rochette, C., Sawyer, N., Xiang, Y.B., Pickett, C.B., Ford-Hutchinson, A.W., Zamboni, R.J., Young, R.N.

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A novel and efficient method for the preparation of asymmetric dithioacetals von Gauthier, J.Y., Henien, T., Lo, L., Thérien, M., Young, R.N.

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A new class of leukotriene biosynthesis inhibitors: The development of ((4-(4-chlorophenyl)-1-(4-(2-quinolinylmethoxy)phenyl)butyl)thio)acetic acid, L-674,636 von Prasit, P., Belley, M., Evans, J.F., Gauthier, J.Y., Léveillé, C., McFarlane, C.S., MacIntyre, E., Peterson, L., Piechuta, H., Thérien, M., Young, R.N., Zamboni, R.

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Estimating snow cover at the sub-pixel level over the French Alps from VEGETATION images von Fortin, J.P., Savary, S., Dedieu, J.P., Bernier, M., Gauthier, J.Y.

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The discovery of a new structural class of potent orally active leukotriene D 4 antagonists von Labelle, M., Prasit, P., Belley, M., Blouin, M., Champion, E., Charette, L., DeLuca, J.G., Dufresne, C., Frenette, R., Gauthier, J.Y., Grimm, E., Grossman, S.J., Guay, D., Herold, E.G., Jones, T.R., Lau, C.K., Leblanc, Y., Léger, S., Lord, A., McAuliffe, M., McFarlane, C., Masson, P., Metters, K.M., Ouimet, N., Patrick, D.H., Perrier, H., Pickett, C.B., Piechuta, H., Roy, P., Williams, H., Wang, Z., Xiang, Y.B., Zamboni, R.J., Ford-Hutchinson, A.W., Young, R.N.

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