Novel HDAC6 isoform selective chiral small molecule histone deacetylase inhibitors von Smil, David V., Manku, Sukhdev, Chantigny, Yves A., Leit, Silvana, Wahhab, Amal, Yan, Theresa P., Fournel, Marielle, Maroun, Christiane, Li, Zuomei, Lemieux, Anne-Marie, Nicolescu, Alina, Rahil, Jubrail, Lefebvre, Sylvain, Panetta, Anthony, Besterman, Jeffrey M., Déziel, Robert

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An efficient synthesis of base-substituted analogues of S-adenosyl- dl-homocysteine von Llewellyn, David B., Wahhab, Amal

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A solid phase procedure for the synthesis of 6-methyl-1,3-disubstituted uracils von Wahhab, Amal, Leban, Johann

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Discovery of bicyclic pyrazoles as class III histone deacetylase SIRT1 and SIRT2 inhibitors von Therrien, Eric, Larouche, Guillaume, Nguyen, Natalie, Rahil, Jubrail, Lemieux, Anne-Marie, Li, Zuomei, Fournel, Marielle, Yan, Theresa P., Landry, Anne-Julie, Lefebvre, Sylvain, Wang, James J., MacBeth, Kyle, Heise, Carla, Nguyen, Aaron, Besterman, Jeffrey M., Déziel, Robert, Wahhab, Amal

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N-Benzyl-1-heteroaryl-3-(trifluoromethyl)-1H-pyrazole-5-carboxamides as inhibitors of co-activator associated arginine methyltransferase 1 (CARM1) von Allan, Martin, Manku, Sukhdev, Therrien, Eric, Nguyen, Natalie, Styhler, Sylvia, Robert, Marie-France, Goulet, Anne-Christine, Petschner, Andrea J, Rahil, Gabi, Robert Macleod, A, Déziel, Robert, Besterman, Jeffrey M, Nguyen, Hannah, Wahhab, Amal

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Diphenylmethylene hydroxamic acids as selective class IIa histone deacetylase inhibitors von Tessier, Pierre, Smil, David V., Wahhab, Amal, Leit, Silvana, Rahil, Jubrail, Li, Zuomei, Déziel, Robert, Besterman, Jeffrey M.

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1,2-Diamines as inhibitors of co-activator associated arginine methyltransferase 1 (CARM1) von Therrien, Eric, Larouche, Guillaume, Manku, Sukhdev, Allan, Martin, Nguyen, Natalie, Styhler, Sylvia, Robert, Marie-France, Goulet, Anne-Christine, Besterman, Jeffrey M., Nguyen, Hannah, Wahhab, Amal

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Discovery of a novel and potent series of thieno[3,2- b]pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases von Claridge, Stephen, Raeppel, Franck, Granger, Marie-Claude, Bernstein, Naomy, Saavedra, Oscar, Zhan, Lijie, Llewellyn, David, Wahhab, Amal, Deziel, Robert, Rahil, Jubrail, Beaulieu, Normand, Nguyen, Hannah, Dupont, Isabelle, Barsalou, Annie, Beaulieu, Carole, Chute, Ian, Gravel, Serge, Robert, Marie-France, Lefebvre, Sylvain, Dubay, Marja, Pascal, Roussen, Gillespie, Jeff, Jin, Zhiyun, Wang, James, Besterman, Jeffrey M., MacLeod, A. Robert, Vaisburg, Arkadii

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Constrained ( l-)- S-adenosyl- l-homocysteine (SAH) analogues as DNA methyltransferase inhibitors von Isakovic, Ljubomir, Saavedra, Oscar M., Llewellyn, David B., Claridge, Stephen, Zhan, Lijie, Bernstein, Naomy, Vaisburg, Arkadii, Elowe, Nadine, Petschner, Andrea J., Rahil, Jubrail, Beaulieu, Norman, Gauthier, France, MacLeod, A. Robert, Delorme, Daniel, Besterman, Jeffrey M., Wahhab, Amal

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SAR around ( l)- S-adenosyl- l-homocysteine, an inhibitor of human DNA methyltransferase (DNMT) enzymes von Saavedra, Oscar M., Isakovic, Ljubomir, Llewellyn, David B., Zhan, Lijie, Bernstein, Naomy, Claridge, Stephen, Raeppel, Franck, Vaisburg, Arkadii, Elowe, Nadine, Petschner, Andrea J., Rahil, Jubrail, Beaulieu, Norman, MacLeod, A. Robert, Delorme, Daniel, Besterman, Jeffrey M., Wahhab, Amal

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Differences in Backbone Structure between Angiotensin II Agonists and Type I Antagonists von Matsoukas, John M, Agelis, George, Wahhab, Amal, Hondrelis, John, Panagiotopoulos, Dimitris, Yamdagni, Raghav, Wu, Qiao, Mavromoustakos, Thomas, Maia, Hernani L. S

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Sulfamides as novel histone deacetylase inhibitors von Wahhab, Amal, Smil, David, Ajamian, Alain, Allan, Martin, Chantigny, Yves, Therrien, Eric, Nguyen, Natalie, Manku, Sukhdev, Leit, Silvana, Rahil, Jubrail, Petschner, Andrea J., Lu, Ai-Hua, Nicolescu, Alina, Lefebvre, Sylvain, Montcalm, Samuel, Fournel, Marielle, Yan, Theresa P., Li, Zuomei, Besterman, Jeffrey M., Déziel, Robert

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Synthesis and evaluation of lysine derived sulfamides as histone deacetylase inhibitors von Manku, Sukhdev, Allan, Martin, Nguyen, Natalie, Ajamian, Alain, Rodrigue, Jacques, Therrien, Eric, Wang, James, Guo, Tim, Rahil, Jubrail, Petschner, Andrea J., Nicolescu, Alina, Lefebvre, Sylvain, Li, Zuomei, Fournel, Marielle, Besterman, Jeffrey M., Déziel, Robert, Wahhab, Amal

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N-Benzyl-1-heteroaryl-3-(trifluoromethyl)-1H-pyrazole-5-carboxamid es as inhibitors of co-activator associated arginine methyltransferase 1 (CARM1) von Allan, Martin, Manku, Sukhdev, Therrien, Eric, Nguyen, Natalie, Styhler, Sylvia, Robert, Marie-France, Goulet, Anne-Christine, Petschner, Andrea J, Rahil, Gabi, MacLeod, A Robert, Deziel, Robert, Besterman, Jeffrey M, Nguyen, Hannah, Wahhab, Amal

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N-Benzyl-1-heteroaryl-3-(trifluoromethyl)-1 H-pyrazole-5-carboxamides as inhibitors of co-activator associated arginine methyltransferase 1 (CARM1) von Allan, Martin, Manku, Sukhdev, Therrien, Eric, Nguyen, Natalie, Styhler, Sylvia, Robert, Marie-France, Goulet, Anne-Christine, Petschner, Andrea J., Rahil, Gabi, Robert MacLeod, A., Déziel, Robert, Besterman, Jeffrey M., Nguyen, Hannah, Wahhab, Amal

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درجة ممارسة القيادة الخادمة لرؤساء الأقسام العلمية وعلاقتها بالتعلم المهني لفريق العمل من وجهة نظر المعلمين في مدارس التعليم العام في دولة الكويت... von الصالح, أمل عبد الوهاب

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Optically pure (S)-cyclopent-2-en-1-ol and (S)-3-methoxycyclopentene von Wahhab, Amal, Tavares, Donald F, Rauk, Arvi

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LIBRARIES OF DIVERSE MACROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING THE SAME von MACDONALD, DWIGHT, WAHHAB, AMAL, RICHARD, LUC, DUBE, DANIEL, THOMAS, HELMUT, PETERSON, MARK L

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A simple procedure for the solid phase synthesis of unsymmetrically functionalised diamides from symmetric diacids von Wahhab, Amal, Leban, Johann

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Peptide macrocycles against Acinetobacter baumannii von Kroll, Carsten, Bleicher, Konrad, Hu, Taishan, Kolczewski, Sabine, Hilpert, Hans, Beignet, Julien, Fasching, Bernhard, Zampaloni, Claudia, Alanine, Alexander, Stoll, Theodor, Thomas, Helmut, MacDonald, Dwight, Shen, Hong, Wahhab, Amal, Jackson, Stephen, Schaeublin, Adrian

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