Discovery of Small-Molecule Inhibitors of the ATPase Activity of Human Papillomavirus E1 Helicase von Faucher, Anne-Marie, White, Peter W, Brochu, Christian, Grand-Maître, Chantal, Rancourt, Jean, Fazal, Gulrez

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Biphenylsulfonacetic Acid Inhibitors of the Human Papillomavirus Type 6 E1 Helicase Inhibit ATP Hydrolysis by an Allosteric Mechanism Involving Tyrosine 486 von WHITE, Peter W, FAUCHER, Anne-Marie, MASSARIOL, Marie-Josée, WELCHNER, Ewald, RANCOURT, Jean, CARTIER, Mireille, ARCHAMBAULT, Jacques

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A randomized controlled trial of nonpharmacologic approaches for relief of low back pain during labor von Labrecque, M, Nouwen, A, Bergeron, M, Rancourt, J F

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Conformation-Based Restrictions and Scaffold Replacements in the Design of Hepatitis C Virus Polymerase Inhibitors: Discovery of Deleobuvir (BI 207127) von LaPlante, Steven R., Bös, Michael, Brochu, Christian, Chabot, Catherine, Coulombe, René, Gillard, James R., Jakalian, Araz, Poirier, Martin, Rancourt, Jean, Stammers, Timothy, Thavonekham, Bounkham, Beaulieu, Pierre L., Kukolj, George, Tsantrizos, Youla S.

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Les Rohingyas : portrait d’une minorité persécutée von Rancourt, Jean-François

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A Systematic Approach to the Optimization of Substrate-Based Inhibitors of the Hepatitis C Virus NS3 Protease:  Discovery of Potent and Specific Tripeptide Inhibitors von Llinàs-Brunet, Montse, Bailey, Murray D, Ghiro, Elise, Gorys, Vida, Halmos, Ted, Poirier, Martin, Rancourt, Jean, Goudreau, Nathalie

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Optimization of a 1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione series of HIV capsid assembly inhibitors 2: Structure–activity relationships (SAR) of the C3-phenyl moiety von Fader, Lee D., Landry, Serge, Goulet, Sylvie, Morin, Sébastien, Kawai, Stephen H., Bousquet, Yves, Dion, Isabelle, Hucke, Oliver, Goudreau, Nathalie, Lemke, Christopher T., Rancourt, Jean, Bonneau, Pierre, Titolo, Steve, Amad, Ma’an, Garneau, Michel, Duan, Jianmin, Mason, Stephen, Simoneau, Bruno

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Peptide-Based Inhibitors of the Hepatitis C Virus NS3 Protease:  Structure−Activity Relationship at the C-Terminal Position von Rancourt, Jean, Cameron, Dale R, Gorys, Vida, Lamarre, Daniel, Poirier, Martin, Thibeault, Diane, Llinàs-Brunet, Montse

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Highly potent and selective peptide-based inhibitors of the hepatitis C virus serine protease: towards smaller inhibitors von Llinàs-Brunet, Montse, Bailey, Murray, Fazal, Gulrez, Ghiro, Elise, Gorys, Vida, Goulet, Sylvie, Halmos, Ted, Maurice, Roger, Poirier, Martin, Poupart, Marc-André, Rancourt, Jean, Thibeault, Diane, Wernic, Dominik, Lamarre, Daniel

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Allosteric N-acetamide-indole-6-carboxylic acid thumb pocket 1 inhibitors of hepatitis C virus NS5B polymerase — Acylsulfonamides and acylsulfamides as carboxylic acid replacements... von Beaulieu, Pierre L, Coulombe, Rene, Gillard, James, Brochu, Christian, Duan, Jianmin, Garneau, Michel, Jolicoeur, Eric, Kuhn, Peter, Poupart, Marc-Andre, Rancourt, Jean, Stammers, Timothy A, Thavonekham, Bounkham, Kukolj, George

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Studies on the C-terminal of hexapeptide inhibitors of the hepatitis C virus serine protease von Llinàs-Brunet, Montse, Bailey, Murray, Déziel, Robert, Fazal, Gulrez, Gorys, Vida, Goulet, Sylvie, Halmos, Ted, Maurice, Roger, Poirier, Martin, Poupart, Marc-André, Rancourt, Jean, Thibeault, Diane, Wernic, Dominik, Lamarre, Daniel

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Corrigendum: An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus von Lamarre, Daniel, Anderson, Paul C, Bailey, Murray, Beaulieu, Pierre, Bolger, Gordon, Bonneau, Pierre, Bös, Michael, Cameron, Dale R, Cartier, Mireille, Cordingley, Michael G, Faucher, Anne-Marie, Goudreau, Nathalie, Kawai, Stephen H, Kukolj, George, Lagacé, Lisette, Laplante, Steven R, Narjes, Hans, Poupart, Marc-André, Rancourt, Jean, Sentjens, Roel E, St George, Roger, Simoneau, Bruno, Steinmann, Gerhard, Thibeault, Diane, Tsantrizos, Youla S, Weldon, Steven M, Yong, Chan-Loi, Llinàs-Brunet, Montse

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Erratum: Corrigendum: An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus von Lamarre, Daniel, Anderson, Paul C., Bailey, Murray, Beaulieu, Pierre, Bolger, Gordon, Bonneau, Pierre, Bös, Michael, Cameron, Dale R., Cartier, Mireille, Cordingley, Michael G., Faucher, Anne-Marie, Goudreau, Nathalie, Kawai, Stephen H., Kukolj, George, Lagacé, Lisette, Laplante, Steven R., Narjes, Hans, Poupart, Marc-André, Rancourt, Jean, Sentjens, Roel E., St George, Roger, Simoneau, Bruno, Steinmann, Gerhard, Thibeault, Diane, Tsantrizos, Youla S., Weldon, Steven M., Yong, Chan-Loi, Llinàs-Brunet, Montse

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Nonpeptidic, monocharged, cell permeable ligands for the p561ck SH2 domain von PROUDFOOT, John R, BETAGERI, Rajashehar, LUKAS, Susan, PATEL, Usha R, SHARMA, Rajiv, YAZDANIAN, Mehran, MOSS, Neil, BEAULIEU, Pierre L, CAMERON, Dale R, FERLAND, Jean-Marie, GAUTHIER, Jean, GILLARD, James, CARDOZO, Mario, GORYS, Vida, POIRIER, Martin, RANCOURT, Jean, WERNIC, Dominik, LLINAS-BRUNET, Montse, GILMORE, Thomas A, GLYNN, Susan, HICKEY, Eugene R, JAKES, Scott, KABCENELL, Alisa, KIRRANE, Thomas M, TIBOLLA, Annette K

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Ligands for the Tyrosine Kinase p56lck SH2 Domain:  Discovery of Potent Dipeptide Derivatives with Monocharged, Nonhydrolyzable Phosphate Replacements von BEAULIEU, Pierre L., CAMERON, Dale R., FERLAND, Jean-Marie, GAUTHIER, Jean, GHIRO, Elise, GILLARD, James, GORYS, Vida, POIRIER, Martin, RANCOURT, Jean, WERNIC, Dominik, LLINAS-BRUNET, Montse, BETAGERI, Raj, CARDOZO, Mario, HICKEY, Eugene R., INGRAHAM, Richard, JAKES, Scott, KABCENELL, Alisa, KIRRANE, Tom, LUKAS, Susan, PATEL, Usha, PROUDFOOT, John, SHARMA, Rajiv, TONG, Liang, MOSS, Neil

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Ligands for the Tyrosine Kinase p56 lck SH2 Domain:  Discovery of Potent Dipeptide Derivatives with Monocharged, Nonhydrolyzable Phosphate Replacements von Beaulieu, Pierre L, Cameron, Dale R, Ferland, Jean-Marie, Gauthier, Jean, Ghiro, Elise, Gillard, James, Gorys, Vida, Poirier, Martin, Rancourt, Jean, Wernic, Dominik, Llinas-Brunet, Montse, Betageri, Raj, Cardozo, Mario, Hickey, Eugene R, Ingraham, Richard, Jakes, Scott, Kabcenell, Alisa, Kirrane, Tom, Lukas, Susan, Patel, Usha, Proudfoot, John, Sharma, Rajiv, Tong, Liang, Moss, Neil

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Hepatitis c unhibitor tri-peptides von RANCOURT Jean, FAUCHER Anne-Marie, GOUDREAU Nathalie, LLINAS-BRUNET Montse, GHIRO Elise, TSANTRIZOS Youla S, Wernic Dominik M, HALMOS Teddy, POUPART Marc-Andre, CAMERON Dale, SIMONEAU Bruno, BAILEY Murray D

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tripeptídeos inibidores da hepatite c, composição farmacêutica compreendendo os mesmos, seu isômero óptico, uso e processo para sua preparação von MARC-ANDRE POUPART, TEDDY HALMOS, ANNE-MARIE FAUCHER, ELISE GHIRO, DOMINIK M. WERNIC, MONTSE LINNAS-BRUNET, MURRAY D. BAILEY, JEAN RANCOURT, NATHALIE GOUDREAU, DALE CAMERON, YOULA S. TSANTRIZOS

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compostos inibidores de hepatite c, composição farmacêutica, uso dos mesmos, bem como artigo de fabricação von Montse Llinas-Brunet, Elise Ghiro, Murray D. Bailey, Teddy Halmos, Pasquale Forgione, Punit Bhardwaj, Vida J. Gorys, Sylvie Goulet, Jean Rancourt, Nathalie Goudreau, Josée Bordeleau

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Inhibitors of cytomegalovirus von Villemure Elisia, Hucke Oliver, Rancourt Jean, Surprenant Simon, Jolicoeur Eric, Thibeault Carl, Kuhn Cyrille, Leblanc Melissa, Beaulieu Pierre L, Grand-Maitre Chantal, Moreau Benoit, Décor Anne, Lacoste Jean-Eric

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