Preclinical profile of a novel metabotropic glutamate receptor 5 positive allosteric modulator by Spear, Nathan, Gadient, Reto A., Wilkins, Deidre E., Do, MyLinh, Smith, Jeffrey S., Zeller, Kim L., Schroeder, Patricia, Zhang, Minli, Arora, Jalaj, Chhajlani, Vijay

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4-Aryl piperazine and piperidine amides as novel mGluR5 positive allosteric modulators by Xiong, Hui, Brugel, Todd A., Balestra, Michael, Brown, Dean G., Brush, Kelly A., Hightower, Caprice, Hinkley, Lindsay, Hoesch, Valerie, Kang, James, Koether, Gerard M., McCauley, John P., McLaren, Francis M., Panko, Laura M., Simpson, Thomas R., Smith, Reed W., Woods, James M., Brockel, Becky, Chhajlani, Vijay, Gadient, Reto A., Spear, Nathan, Sygowski, Linda A., Zhang, Minli, Arora, Jalaj, Breysse, Nathalie, Wilson, Julie M., Isaac, Methvin, Slassi, Abdelmalik, King, Megan M.

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N-[(3S)-1-benzylpyrrolidin-3-yl]-(2-thienyl )benzamides : Human dopamine D4 ligands with high affinity for the 5-HT2A receptor by ARORA, Jalaj, BORDELEAU, Michel, DUBE, Laurence, JARVIE, Keith, MAZZOCCO, Lucy, PERAGINE, Jack, TEHIM, Ashok, EGLE, Ian

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N-[(3 S)-1-Benzylpyrrolidin-3-yl]-(2-thienyl)benzamides: Human dopamine D 4 ligands with high affinity for the 5-HT 2A receptor by Arora, Jalaj, Bordeleau, Michel, Dube, Laurence, Jarvie, Keith, Mazzocco, Lucy, Peragine, Jack, Tehim, Ashok, Egle, Ian

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N-(1-Benzylpyrrolidin-3-yl)arylbenzamides as potent and selective human dopamine D 4 antagonists by Egle, Ian, Barriault, Nancy, Bordeleau, Michel, Drage, Jillian, Dube, Laurence, Peragine, Jack, Mazzocco, Lucy, Arora, Jalaj, Jarvie, Keith, Tehim, Ashok

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N-(1-Benzylpyrrolidin-3-yl)arylbenzamides as potent and selective human dopamine D4 antagonists by EGLE, Ian, BARRIAULT, Nancy, BORDELEAU, Michel, DRAGE, Jillian, DUBE, Laurence, PERAGINE, Jack, MAZZOCCO, Lucy, ARORA, Jalaj, JARVIE, Keith, TEHIM, Ashok

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5,5-Diaryl-2-amino-4-pentenoates as novel, potent, and selective glycine transporter type-2 reuptake inhibitors by Isaac, Methvin, Slassi, Abdelmalik, Silva, Kathleen Da, Arora, Jalaj, MacLean, Neil, Hung, Bill, McCallum, Kirk

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Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-bioavailable 5-HT1D agonists by ISAAC, Methvin, SLASSI, Malik, NAISMITH, Angela, MADDAFORD, Shawn, PAPAC, Damon, HARRISON, Shuree, HUA WANG, DRANER, Stan, TEHIM, Ashok, TAO XIN, ARORA, Jalaj, O'BRIEN, Anne, EDWARDS, Louise, MACLEAN, Neil, WILSON, Julie, DEMSCHYSHYN, Lidia, LABRIE, Phillipe

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Design, synthesis and biological activity of novel dimethyl-[2-[6-substituted-indol-1-yl]-ethyl]-amine as potent, selective, and orally-bioavailable 5-HT(1D) agonists by Isaac, Methvin, Slassi, Malik, Xin, Tao, Arora, Jalaj, O'Brien, Anne, Edwards, Louise, MacLean, Neil, Wilson, Julie, Demschyshyn, Lidia, Labrie, Phillipe, Naismith, Angela, Maddaford, Shawn, Papac, Damon, Harrison, Shuree, Wang, Hua, Draper, Stan, Tehim, Ashok

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Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-Bioavailable 5-HT 1D agonists by Isaac, Methvin, Slassi, Malik, Xin, Tao, Arora, Jalaj, O'Brien, Anne, Edwards, Louise, MacLean, Neil, Wilson, Julie, Demschyshyn, Lidia, Labrie, Phillipe, Naismith, Angela, Maddaford, Shawn, Papac, Damon, Harrison, Shuree, Wang, Hua, Draper, Stan, Tehim, Ashok

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Variability in Fatigue Life of Near-α Titanium Alloy IMI 834 by Bhandari, Litton, Kumar, Jalaj, Balasundar, I., Arora, Amit

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