Area of research
Organic Chemistry · Biomaterials
Research interest
Research interests include Supramolecular Self-Assembly in Materials, Catalytic C–H Functionalization Methods, Catalytic Cross-Coupling Reactions, and Axial and Atropisomeric Chirality Synthesis.
Assembling Ruthenium Complexes to Form Ruthenosome Unleashing Ferritinophagy-Mediated Tumor Suppression.
Fluorogenic Crystallization via Enzyme-Instructed Excited-State Intramolecular Proton Transfer for Dynamic Microenvironment Profiling.
Optimization of a Dissolvable Lipid Nanoparticle Microneedle Formulation for mRNA Delivery Using Design of Experiments.
Enzyme-Responsive Assembly of Cysteine-Terminated Heparan Sulfate Proteoglycan Ligands for Osteoinductive Biphasic Scaffold Formation
Engineering Apical Integrin-binding Cellular Patches to Directed Cell Reprogramming via Mechanical Remodeling
Influence of polyethylene glycol on the mucus penetration and stability of lipid nanoparticles in cryopreservation and lyophilization.
Engineering Heparan Sulfate-Guided Peptide Self-Assembly to Restore Endothelial Angiogenesis under Hyperglycemia.
Engineering a Viscosity-Gated Dual-Rotor Probe for Comprehensive Mapping of Lipid Droplet Heterogeneity.
Electrochemical Oxidative Difunctionalization of Diazo Compounds with Diselenides and Nucleophiles
Chinmedomics strategy for elucidating the effects and effective constituents of Danggui Buxue Decoction in treating blood deficiency syndrome
Dual-targeted halofuginone hydrobromide nanocomplexes for promotion of macrophage repolarization and apoptosis of rheumatoid arthritis fibroblast-like synoviocytes in adjuvant-induced arthritis in rats
Transcription factors Pbr3RAV2 and PbrTTG1 regulate pear resistance to <i>Botryosphaeria dothidea</i> via the autophagy pathway
Formulate Adaptive Biphasic Scaffold via Sequential Protein-Instructed Peptide Co-Assembly.
Physiological and autophagy evaluation of different pear varieties (<i>Pyrus</i> spp.) in response to <i>Botryosphaeria dothidea</i> infection
Control cell migration by engineering integrin ligand assembly.
Constructing ECM-like Structure on the Plasma Membrane via Peptide Assembly to Regulate the Cellular Response.
Capture Phosphates via Peptide Self‐assembly to Construct Templates Assisting Mineralization
Enhancing the Cellular Uptake of Macromolecules via Enzyme-Instructed Self-Assembly.
The Ubiquitin E3 Ligase TRIM21 Promotes Hepatocarcinogenesis by Suppressing the p62-Keap1-Nrf2 Antioxidant Pathway
Robust Packing of a Self‐Assembling Iridium Complex via Endocytic Trafficking for Long‐Term Lysosome Tracking
Robust Packing of a Self-Assembling Iridium Complex via Endocytic Trafficking for Long-Term Lysosome Tracking.
Lipid-Raft-Targeted Molecular Self-Assembly Inactivates YAP to Treat Ovarian Cancer.
Heparan Sulfate-Instructed Self-Assembly Selectively Inhibits Cancer Cell Migration.
Microtubule-Targeted Self-Assembly Triggers Prometaphase-Metaphase Oscillations Suppressing Tumor Growth.
Developing biomaterials to mediate the spatial distribution of integrins.
Robust Packing of a Self‐Assembling Iridium Complex via Endocytic Trafficking for Long‐Term Lysosome Tracking
Control Cell Migration by Engineering Integrin Ligand Assembly
Proinflammatory macrophage-derived microvesicles exhibit tumor tropism dependent on CCL2/CCR2 signaling axis and promote drug delivery <i>via</i> SNARE-mediated membrane fusion
Integrin and Heparan Sulfate Dual-Targeting Peptide Assembly Suppresses Cancer Metastasis.
Self-Assembly of Integrin Ligands on the Apical Membrane Inhibits the Migration of Glioma Cells.