Slow-Dissociation and Slow-Recombination Assumptions in Nonequilibrium Capillary Electrophoresis of Equilibrium Mixtures von Krylova, Svetlana M, Dove, Peter M, Kanoatov, Mirzo, Krylov, Sergey N

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Synthesis and Protection of Aryl Sulfates Using the 2,2,2-Trichloroethyl Moiety von Liu, Yong, Lien, I-Feh Felicia, Ruttgaizer, Scott, Dove, Peter, Taylor, Scott D

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Le patrimoine culturel arabe dans les nouvelles de Zakariyyā Tāmir: Une esthétique du grotesque von Dové, Peter

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Abstract 3854: Preclinical characterization of a novel non-cyclic dinucleotide small molecule STING agonist with potent antitumor activity in mice von Wang, Zezhou, Dove, Peter, Rosa, David, Bossen, Bolette, Helke, Simone, Charbonneau, Marilyse, Brinen, Laura, Dodge, Karen, Lin, Gloria H., Galligan, Carole, Viller, Natasja N., Wong, Mark, Lee, Vivian, Catalano, Tina, Uger, Robert A., Slassi, Malik, Winston, Jeff

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TTI-281, an Orally Bioavailable Bromodomain and Extraterminal Domain (BET) Inhibitor, Is a Promising Candidate for the Treatment of Multiple Myeloma von Wang, Zezhou, Choi, Jaehyun, Dove, Peter, Wang, Chunlei, Schimmer, Aaron D., Petrova, Penka S., Uger, Robert A., Slassi, Malik

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Genomic Characterization of the Istrian Shorthaired Hound von Kusec, Ivona Djurkin, Boskovic, Ivica, Zorc, Minja, Gvozdanovic, Kristina, Skorput, Dubravko, Dove, Peter, Kusec, Goran

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DDIS-11. TTI-2341: A NOVEL, ORALLY BIOAVAILABLE, BRAIN-PENETRANT, COVALENT EPIDERMAL GROWTH FACTOR RECEPTOR (EGFR) INHIBITOR FOR TREATMENT OF GLIOBLASTOMA MULTIFORME (GBM) AND BRAI... von Wang, Zezhou, Dove, Peter, Rosa, David, Marshall, Andrew, Catalano, Tina, Bossen, Bolette, Choi, Jaehyun, Wang, Chunlei, Wong, Mark, Winston, Jeff, Slassi, Malik, Petrova, Penka S, Uger, Robert A

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Discovery of cis-N-(1-(4-(Methylamino)cyclohexyl)indolin-6-yl)thiophene-2-carboximidamide: A 1,6-Disubstituted Indoline Derivative as a Highly Selective Inhibitor of Human Neuronal... von Annedi, Subhash C, Ramnauth, Jailall, Maddaford, Shawn P, Renton, Paul, Rakhit, Suman, Mladenova, Gabriela, Dove, Peter, Silverman, Sarah, Andrews, John S, Felice, Milena D, Porreca, Frank

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The Highly Potent Bromodomain (BRD) Inhibitor FV-281 Displays Preclinical Efficacy in Acute Myeloid Leukemia (AML) von Wang, Zezhou, Dove, Peter, Shamas-Din, Aisha, Hurren, Rose, Wang, Xiaoming, MacLean, Neil, Gronda, Marcela, Bo, Feng, Li, Janessa, Skorupski, Clarissa, Hadri, Wissam, O'Neill, David, Aman, Ahmed, Al-awar, Rima, Minden, Mark D., Slassi, Malik, Schimmer, Aaron D.

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Design, Synthesis, and Biological Evaluation of 3,4-Dihydroquinolin-2(1H)-one and 1,2,3,4-Tetrahydroquinoline-Based Selective Human Neuronal Nitric Oxide Synthase (nNOS) Inhibitors von Ramnauth, Jailall, Speed, Joanne, Maddaford, Shawn P, Dove, Peter, Annedi, Subhash C, Renton, Paul, Rakhit, Suman, Andrews, John, Silverman, Sarah, Mladenova, Gabriela, Zinghini, Salvatore, Nair, Sheela, Catalano, Concettina, Lee, David K.H, De Felice, Milena, Porreca, Frank

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Developing citizen leadership in Myanmar: the DeBoer fellowship von Steffensmeier, Timothy, McBride, Julia Fabris, Dove, Peter

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Discovery of a potent, orally bioavailable and highly selective human neuronal nitric oxide synthase (nNOS) inhibitor, N-(1-(piperidin-4-yl)indolin-5-yl)thiophene-2-carboximidamide... von Annedi, Subhash C., Maddaford, Shawn P., Ramnauth, Jailall, Renton, Paul, Rybak, Taras, Silverman, Sarah, Rakhit, Suman, Mladenova, Gabriela, Dove, Peter, Andrews, John S., Zhang, Dongqin, Porreca, Frank

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Novel, druglike 1,7-disubstituted 2,3,4,5-tetrahydro-1H-benzo[b]azepine-based selective inhibitors of human neuronal nitric oxide synthase (nNOS) von Annedi, Subhash C., Ramnauth, Jailall, Cossette, Michele, Maddaford, Shawn P., Dove, Peter, Rakhit, Suman, Andrews, John S., Porreca, Frank

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1,2,3,4-Tetrahydroquinoline-Based Selective Human Neuronal Nitric Oxide Synthase (nNOS) Inhibitors: Lead Optimization Studies Resulting in the Identification of N-(1-(2-(Methylamin... von Ramnauth, Jailall, Renton, Paul, Dove, Peter, Annedi, Subhash C, Speed, Joanne, Silverman, Sarah, Mladenova, Gabriela, Maddaford, Shawn P, Zinghini, Salvatore, Rakhit, Suman, Andrews, John, Lee, David K. H, Zhang, Dongqin, Porreca, Frank

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Le patrimoine culturel arabe dans les nouvelles de Zakariyyā Tāmir: Une esthétique du grotesque von Dové, Peter

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FV-009 candidate drug: Novel and selective P/Q-type Ca2 + and voltage-gated Na+ ion channel modulation for epilepsy and pain von Slassi, Malik, Dove, Peter, Climie, Shane, O'Neill, David, Wang, Zezhou, Lee, David K.H., de Lannoy, Ines, Chen, Tracy, Stables, Jim, Saldivia, Victor, Pan, Sophie, Lau, Winnie, Silenieks, Leo B., Higgins, Guy A.

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FV-137 candidate drug: Novel and selective ion channel modulation for epilepsy and pain von Slassi, Malik, Dove, Peter, Climie, Shane, O'Neill, David, Wang, Zezhou, Tsirulnikov, Lilly, Henrianna, Lee, David K.H, de Lannoy, Ines, Chen, Tracy, Stables, Jim, Lau, Winnie, Silenieks, Leo B, Higgins, Guy A

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FV-082: A safer orally active broad-spectrum antiepileptic drug candidate von Slassi, Malik, Dove, Peter, Climie, Shane, O'Neill, David, Wang, Zezhou, Tsirulnikov, Lilly, Henrianna, Lee, David K.H, de Lannoy, Ines, Chen, Tracy, Stables, Jim, Lau, Winnie, Silenieks, Leo B, Higgins, Guy A

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Le patrimoine culturel arabe dans les nouvelles de Zakariyyā Tāmir : une esthétique du grotesque von Dové, Peter

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FV-009 candidate drug: Novel and selective P/Q-type Ca 2 + and voltage-gated Na+ ion channel modulation for epilepsy and pain von Slassi, Malik, Dove, Peter, Climie, Shane, O'Neill, David, Wang, Zezhou, Lee, David K.H, de Lannoy, Ines, Chen, Tracy, Stables, Jim, Saldivia, Victor, Pan, Sophie, Lau, Winnie, Silenieks, Leo B, Higgins, Guy A

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