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Medicinal Chemistry Research : an International Journal for Rapid Communications on Design and Mechanisms of Action of Biologically Active Agents|November 4, 2024
Structure-activity relationships and pharmacokinetic evaluation of L-cystine diamides as L-cystine crystallization inhibitors for cystinuriaLongqin Hu, Haifa Albanyan, Jeffrey Yang, et al.
Biochemical Pharmacology|August 12, 2009
Testing double mutants of the enzyme nitroreductase for enhanced cell sensitisation to prodrugs: effects of combining beneficial single mutationsMansooreh Jaberipour, Simon O Vass, Christopher P Guise, et al.
Journal of Medicinal Chemistry|October 31, 2003
Nitroaryl phosphoramides as novel prodrugs for E. coli nitroreductase activation in enzyme prodrug therapyLongqin Hu, Chengzhi Yu, Yongying Jiang, et al.
ACS Medicinal Chemistry Letters|November 20, 2024
Discovery of l-Lysine Dioxalate (LH1513) as a Novel Inhibitor of Calcium Oxalate Crystallization for HyperoxaluriaLongqin Hu, Akash Taneja, Husam Zahid, et al.
ACS Medicinal Chemistry Letters|March 19, 2025
Correction to "Discovery of l-Lysine Dioxalate (LH1513) as a Novel Inhibitor of Calcium Oxalate Crystallization for Hyperoxaluria"Longqin Hu, Akash Taneja, Husam Zahid, et al.
Crystal Growth & Design|December 14, 2017
Role of Molecular Recognition in l-Cystine Crystal Growth InhibitionLaura N Poloni, Zina Zhu, Nelson Garcia-Vázquez, et al.
Molecular Microbiology|February 18, 2015
Unravelling the role of SNM1 in the DNA repair system of Trypanosoma bruceiJames A Sullivan, Jie Lun Tong, Martin Wong, et al.
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