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Cell Engineering with Functional Poly(oxanorbornene) Block Copolymers.
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Engineering live cell surfaces with functional polymers via cytocompatible controlled radical polymerization.
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Precision Synthesis of Alternating Copolymers via Ring-Opening Polymerization of 1-Substituted Cyclobutenes.
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Engineering orthogonality in supramolecular polymers: from simple scaffolds to complex materials.
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Secondary Structure in Nonpeptidic Supramolecular Block Copolymers.
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Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers.
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General synthetic route to cell-permeable block copolymers via ROMP.
J Am Chem Soc. 2009 Jun 3;131(21):7327-33. doi: 10.1021/ja809284s.
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Optimal Hydrophobicity in Ring-Opening Metathesis Polymerization-Based Protein Mimics Required for siRNA Internalization.
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Innovative approaches to boost mesenchymal stem cells efficacy in myocardial infarction therapy.
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Cell-drug conjugates.
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Degradable polymers via olefin metathesis polymerization.
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Site-selected in situ polymerization for living cell surface engineering.
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Polynorbornene-based bioconjugates by aqueous grafting-from ring-opening metathesis polymerization reduce protein immunogenicity.
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Water-Accelerated Decomposition of Olefin Metathesis Catalysts.
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Principles of glycocalyx engineering with hydrophobic-anchored synthetic mucins.
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Surface Engineering for Cell-Based Therapies: Techniques for Manipulating Mammalian Cell Surfaces.
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CAR-T cells secreting BiTEs circumvent antigen escape without detectable toxicity.
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Folate-Decorated Amphiphilic Cyclodextrins as Cell-Targeted Nanophototherapeutics.
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Cell surface engineering and application in cell delivery to heart diseases.
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Programming Cell-Cell Interactions through Non-genetic Membrane Engineering.
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Chimeric Antigen Receptor T Cell Therapy: Challenges to Bench-to-Bedside Efficacy.
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Nanoparticle targeted folate receptor 1-enhanced photodynamic therapy for lung cancer.
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Synthetic Glycopolymers for Highly Efficient Differentiation of Embryonic Stem Cells into Neurons: Lipo- or Not?
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Inducible Caspase-9 Selectively Modulates the Toxicities of CD19-Specific Chimeric Antigen Receptor-Modified T Cells.
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