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Journal of Medicinal Chemistry|July 9, 2004
A ligand-based approach to identify quantitative structure-activity relationships for the androgen receptorCasey E Bohl, Cheng Chang, Michael L Mohler, et al.
BMC Medical Imaging|October 19, 2023
Weakly supervised video-based cardiac detection for hypertensive cardiomyopathyJiyun Chen, Xijun Zhang, Jianjun Yuan, et al.
Nature Communications|June 26, 2026
Potential role of a CRISPR-Cas-activated toxin-antitoxin system in bacterial immunityJiyun Chen, Linglong Huang, Hong Chen, et al.
Molecules (Basel, Switzerland)|November 11, 2022
One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and SupercapacitorsYuting Lei, Ludmila Dos Santos Madalena, Benjamin D Ossonon, et al.
Nucleic Acids Research|February 25, 2025
Structural basis of ssDNA-guided NADase activation of prokaryotic SPARTA systemRong Hu, Chenmin Guo, Xiaotian Liu, et al.
Scientific Reports|February 3, 2017
Facile Synthesis of Nanoporous Pt-Y alloy with Enhanced Electrocatalytic Activity and DurabilityRongjing Cui, Ling Mei, Guangjie Han, et al.
Bioorganic & Medicinal Chemistry Letters|September 23, 2008
Effect of B-ring substitution pattern on binding mode of propionamide selective androgen receptor modulatorsCasey E Bohl, Zengru Wu, Jiyun Chen, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 15, 2018
FOXO1 inhibition potentiates endothelial angiogenic functions in diabetes via suppression of ROCK1/Drp1-mediated mitochondrial fissionYundi Shi, Shengjun Fan, Di Wang, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 7, 2005
Efflux of depsipeptide FK228 (FR901228, NSC-630176) is mediated by P-glycoprotein and multidrug resistance-associated protein 1Jim J Xiao, Amy B Foraker, Peter W Swaan, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 19, 2005
Chemoresistance to depsipeptide FK228 [(E)-(1S,4S,10S,21R)-7-[(Z)-ethylidene]-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8,7,6]-tricos-16-ene-3,6,9,22-pentanone] is mediated by reversible MDR1 induction in human cancer cell linesJim J Xiao, Ying Huang, Zunyan Dai, et al.
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