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Biochemistry|October 13, 2004
Mutational analysis of the nuclease domain of Escherichia coli ribonuclease III. Identification of conserved acidic residues that are important for catalytic function in vitroWeimei Sun, Gang Li, Allen W Nicholson
Nucleic Acids Research|February 9, 2005
Catalytic mechanism of Escherichia coli ribonuclease III: kinetic and inhibitor evidence for the involvement of two magnesium ions in RNA phosphodiester hydrolysisWeimei Sun, Alexandre Pertzev, Allen W Nicholson
Frontiers in Medicine|July 3, 2026
Concordant ETV6::RUNX1-positive acute lymphoblastic leukemia in monozygotic twins: a case report and review of the literatureXiaohua Li, Cuicui Wang, Jianchang Li, et al.
The Journal of Organic Chemistry|November 16, 2020
Synthesis and Reactivity of Spirocarbocycles as Scaffolds for Nucleoside AnaloguesJonas Verhoeven, Xavier Deraet, Vineet Pande, et al.
Plos One|January 3, 2009
Incomplete inhibition of sphingosine 1-phosphate lyase modulates immune system function yet prevents early lethality and non-lymphoid lesionsPeter Vogel, Michael S Donoviel, Robert Read, et al.
Bioorganic & Medicinal Chemistry Letters|July 20, 2011
Optimization of a pyrazole hit from FBDD into a novel series of indazoles as ketohexokinase inhibitorsXuqing Zhang, Fengbing Song, Gee-Hong Kuo, et al.
Bioorganic & Medicinal Chemistry Letters|March 13, 2021
Discovery of a novel series of guanidinebenzoates as gut-restricted enteropeptidase and trypsin dual inhibitors for the treatment of metabolic syndromeXuqing Zhang, Bin Zhu, Weimei Sun, et al.
Journal of Medicinal Chemistry|November 2, 2010
Electron density guided fragment-based lead discovery of ketohexokinase inhibitorsAlan C Gibbs, Marta C Abad, Xuqing Zhang, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 9, 2020
Targeting Enteropeptidase with Reversible Covalent Inhibitors To Achieve Metabolic BenefitsWeimei Sun, Xuqing Zhang, Maxwell D Cummings, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 15, 2019
Preparation of 4'-Spirocyclobutyl Nucleoside Analogues as Novel and Versatile Adenosine ScaffoldsJonas Verhoeven, Freija De Vleeschouwer, Hanchu Kong, et al.
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