Synthesis and investigation of novel benzimidazole derivatives as antifungal agents von Chandrika, Nishad Thamban, Shrestha, Sanjib K., Ngo, Huy X., Garneau-Tsodikova, Sylvie

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Deorphaning a solute carrier 22 family member, SLC22A15, through functional genomic studies von Yee, Sook Wah, Buitrago, Dina, Stecula, Adrian, Ngo, Huy X., Chien, Huan‐Chieh, Zou, Ling, Koleske, Megan L., Giacomini, Kathleen M.

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Flipping the Switch “On” for Aminoglycoside-Resistance Enzymes: The Mechanism Is Finally Revealed von Ngo, Huy X., Garneau-Tsodikova, Sylvie

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What are the drugs of the future? von Ngo, Huy X, Garneau-Tsodikova, Sylvie

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A Comparative Clinical Pharmacology Analysis of FDA‐Approved Targeted Covalent Inhibitors vs. Reversible Inhibitors in Oncology von Ngo, Huy X., Wen, Yue Winnie, Pisupati, Swathi, Huang, Weize, Mandlekar, Sandhya

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Oncology Dose Selection in Subsequent Indications: What Can We Learn From FDA-approved Oncology Drugs? von Ngo, Huy X, Oh, Elise, Li, Chunze, Yu, Jiajie

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Alkylated Piperazines and Piperazine-Azole Hybrids as Antifungal Agents von Thamban Chandrika, Nishad, Shrestha, Sanjib K, Ngo, Huy X, Tsodikov, Oleg V, Howard, Kaitlind C, Garneau-Tsodikova, Sylvie

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Interfering With DNA Decondensation as a Strategy Against Mycobacteria von Scutigliani, Enzo M, Scholl, Edwin R, Grootemaat, Anita E, Khanal, Sadhana, Kochan, Jakub A, Krawczyk, Przemek M, Reits, Eric A, Garzan, Atefeh, Ngo, Huy X, Green, Keith D, Garneau-Tsodikova, Sylvie, Ruijter, Jan M, van Veen, Henk A, van der Wel, Nicole N

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Drug Metabolites Potently Inhibit Renal Organic Anion Transporters, OAT1 and OAT3 von Zou, Ling, Matsson, Pär, Stecula, Adrian, Ngo, Huy X., Zur, Arik A., Giacomini, Kathleen M.

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Novel fluconazole derivatives with promising antifungal activity von Thamban Chandrika, Nishad, Shrestha, Sanjib K., Ngo, Huy X., Howard, Kaitlind C., Garneau-Tsodikova, Sylvie

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A complex game of hide and seek: the search for new antifungals von Ngo, Huy X, Garneau-Tsodikova, Sylvie, Green, Keith D

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Interactions of Oral Molecular Excipients with Breast Cancer Resistance Protein, BCRP von Zou, Ling, Pottel, Joshua, Khuri, Natalia, Ngo, Huy X, Ni, Zhanglin, Tsakalozou, Eleftheria, Warren, Mark S, Huang, Yong, Shoichet, Brian K, Giacomini, Kathleen M

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Pharmacokinetic-Pharmacodynamic Evidence From a Phase 3 Trial to Support Flat-Dosing of Rifampicin for Tuberculosis von Ngo, Huy X, Xu, Ava Y, Velásquez, Gustavo E, Zhang, Nan, Chang, Vincent K, Kurbatova, Ekaterina V, Whitworth, William C, Sizemore, Erin, Bryant, Kia, Carr, Wendy, Weiner, Marc, Dooley, Kelly E, Engle, Melissa, Dorman, Susan E, Nahid, Payam, Swindells, Susan, Chaisson, Richard E, Nsubuga, Pheona, Lourens, Madeleine, Dawson, Rodney, Savic, Radojka M

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Identification of Ebsulfur Analogues with Broad-Spectrum Antifungal Activity von Ngo, Huy X., Shrestha, Sanjib K., Garneau-Tsodikova, Sylvie

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Development of ebsulfur analogues as potent antibacterials against methicillin-resistant Staphylococcus aureus von Ngo, Huy X., Shrestha, Sanjib K., Green, Keith D., Garneau-Tsodikova, Sylvie

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Structure-Guided Optimization of Inhibitors of Acetyltransferase Eis from Mycobacterium tuberculosis von Punetha, Ankita, Ngo, Huy X., Holbrook, Selina Y. L., Green, Keith D., Willby, Melisa J., Bonnett, Shilah A., Krieger, Kyle, Dennis, Emily K., Posey, James E., Parish, Tanya, Tsodikov, Oleg, Garneau-Tsodikova, Sylvie

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Developing antineoplastic agents that target peroxisomal enzymes: cytisine-linked isoflavonoids as inhibitors of hydroxysteroid 17-beta-dehydrogenase-4 (HSD17B4) von Frasinyuk, Mykhaylo S, Zhang, Wen, Wyrebek, Przemyslaw, Yu, Tianxin, Xu, Xuehe, Sviripa, Vitaliy M, Bondarenko, Svitlana P, Xie, Yanqi, Ngo, Huy X, Morris, Andrew J, Mohler, James L, Fiandalo, Michael V, Watt, David S, Liu, Chunming

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N,N′-diaryl-bishydrazones in a biphenyl platform: Broad spectrum antifungal agents von Thamban Chandrika, Nishad, Dennis, Emily K., Shrestha, Sanjib K., Ngo, Huy X., Green, Keith D., Kwiatkowski, Stefan, Deaciuc, Agripina Gabriela, Dwoskin, Linda P., Watt, David S., Garneau-Tsodikova, Sylvie

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The Effects of Prodrug Size and a Carbonyl Linker on l‐Type Amino Acid Transporter 1‐Targeted Cellular and Brain Uptake von Venteicher, Brooklynn, Merklin, Kasey, Ngo, Huy X., Chien, Huan‐Chieh, Hutchinson, Keino, Campbell, Jerome, Way, Hannah, Griffith, Joseph, Alvarado, Cesar, Chandra, Surabhi, Hill, Evan, Schlessinger, Avner, Thomas, Allen A.

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Inhibition of Pseudomonas aeruginosa Alginate Synthesis by Ebselen Oxide and Its Analogues von Kim, Soo-Kyoung, Ngo, Huy X, Dennis, Emily K, Thamban Chandrika, Nishad, DeShong, Philip, Garneau-Tsodikova, Sylvie, Lee, Vincent T

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