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Molecular Diversity|September 23, 2011
Potent antimicrobial small molecules screened as inhibitors of tyrosine recombinases and Holliday junction-resolving enzymesMarc C Rideout, Jeffrey L Boldt, Gabriel Vahi-Ferguson, et al.
Clinical Chemistry|December 8, 2018
Species Typing of Nontuberculous Mycobacteria by Use of Deoxyribozyme SensorsHillary N Wood, Ashelyn E Sidders, Lauren E Brumsey, et al.
Blood|May 26, 2005
Inhibitors of XIAP sensitize CD40-activated chronic lymphocytic leukemia cells to CD95-mediated apoptosisArnon P Kater, Frank Dicker, Massimo Mangiola, et al.
Bioorganic & Medicinal Chemistry|July 7, 2009
Identification, structure-activity relationships and molecular modeling of potent triamine and piperazine opioid ligandsAustin B Yongye, Jon R Appel, Marc A Giulianotti, et al.
ACS Infectious Diseases|May 8, 2025
Discovery of 2,4,5-Substituted Benzoxazole Derivatives as Pks13 Inhibitors via the Scaffold Hopping StrategyBabatunde Samuel Obadawo, Priscila Cristina Bartolomeu Halicki, Kindra L Becker, et al.
Scientific Reports|December 20, 2019
Growth hormone-mediated reprogramming of macrophage transcriptome and effector functionsAugusto Schneider, Hillary N Wood, Sandra Geden, et al.
International Journal of Molecular Sciences|September 9, 2022
Bis-Cyclic Guanidine Heterocyclic Peptidomimetics as Opioid Ligands with Mixed μ-, κ- and δ-Opioid Receptor Interactions: A Potential Approach to Novel AnalgesicsJay P McLaughlin, Ramanjaneyulu Rayala, Ashley J Bunnell, et al.
Bioorganic & Medicinal Chemistry Letters|March 21, 2020
Discovery of cyclic guanidine-linked sulfonamides as inhibitors of LMTK3 kinaseMaria A Ortiz, Heather Michaels, Brandon Molina, et al.
The Journal of Biological Chemistry|December 16, 2017
The Rv2633c protein of Mycobacterium tuberculosis is a non-heme di-iron catalase with a possible role in defenses against oxidative stressZhongxin Ma, Kyle T Strickland, Michelle D Cherne, et al.
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