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pH-Reversible, High-Capacity Binding of Proteins on a Substrate with Nanostructure |
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Lysine-PEG-modified polyurethane as a fibrinolytic surface: Effect of PEG chain length on protein interactions, platelet interactions and clot lysis |
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A facile approach to modify polyurethane surfaces for biomaterial applications |
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Protein Adsorption on Poly(N-vinylpyrrolidone)-Modified Silicon Surfaces Prepared by Surface-Initiated Atom Transfer Radical Polymerization |
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Biomacromolecular affinity: Interactions between lysozyme and regioselectively sulfated chitosan |
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Concerning the spectral resolution enhancement of dynamic 2D-IR |
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Immobilization of proteins on metal ion chelated polymer surfaces |
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Surfaces having dual fibrinolytic and protein resistantproperties by immobilization of lysine on polyurethanethrough a PEG spacer |
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One-stage fabrication of sub-micron hydrophilic microchannels on PDMS |
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Phenomenon of "contact guidance" on the surface with nano-micro-groove-like pattern and cell physiological effects |
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The effect of surface microtopography of poly(dimethylsiloxane) on protein adsorption, platelet and cell adhesion |
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Effect of chain density and conformation on protein adsorption at PEG-grafted polyurethane surfaces |
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Fibrinolytic poly(dimethyl siloxane) surfaces |
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Biocompatible polymer materials: Role of protein-surface interactions |
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Protein adsorption on materials surfaces with nano-topography |
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Generic bioaffinity silicone surfaces |
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