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ACS Infectious Diseases|December 15, 2020
Two-Way Regulation of MmpL3 Expression Identifies and Validates Inhibitors of MmpL3 Function in Mycobacterium tuberculosisShipra Grover, Curtis A Engelhart, Esther Pérez-Herrán, et al.Journal of Medicinal Chemistry|August 25, 2015
Targeting Mycobacterium tuberculosis Biotin Protein Ligase (MtBPL) with Nucleoside-Based Bisubstrate Adenylation InhibitorsMatthew R Bockman, Alvin S Kalinda, Riccardo Petrelli, et al.The Journal of Experimental Medicine|November 2, 2005
Protection from Alzheimer's-like disease in the mouse by genetic ablation of inducible nitric oxide synthaseCarl Nathan, Noel Calingasan, Jon Nezezon, et al.Plos Pathogens|September 25, 2023
Differentiating the roles of Mycobacterium tuberculosis substrate binding proteins, FecB and FecB2, in iron uptakeRodger de Miranda, Bonnie J Cuthbert, Thaís Klevorn, et al.Molecular Microbiology|May 11, 2005
A glutamate-alanine-leucine (EAL) domain protein of Salmonella controls bacterial survival in mice, antioxidant defence and killing of macrophages: role of cyclic diGMPKatherine B Hisert, Michael MacCoss, Michael U Shiloh, et al.Mbio|April 20, 2026
Utilization of a CRISPRi-based ex vivo challenge model to reveal temporally dependent gene essentiality in intracellular Mycobacterium tuberculosisMonique E Theriault, Andrew I Wong, Michael A DeJesus, et al.Nature Microbiology|February 7, 2017
Programmable transcriptional repression in mycobacteria using an orthogonal CRISPR interference platformJeremy M Rock, Forrest F Hopkins, Alejandro Chavez, et al.Chemistry & Biology|January 6, 2015
Target-based identification of whole-cell active inhibitors of biotin biosynthesis in Mycobacterium tuberculosisSae Woong Park, Dominick E Casalena, Daniel J Wilson, et al.Antimicrobial Agents and Chemotherapy|August 19, 2025
Microbiological evidence for the trisubstituted benzimidazoles targeting MmpL3 in Mycobacterium tuberculosisMengyun Zhang, Renee Allen, Lauren Ames, et al.Journal of Medicinal Chemistry|November 24, 2025
Design, Synthesis, and Biological Evaluation of Mono- and Diamino-Substituted Squaramide Derivatives as Potent Inhibitors of Mycobacterial Adenosine Triphosphate (ATP) SynthasePaul R Palme, Shipra Grover, Rana Abdelaziz, et al.Pageof 19