A versatile approach to high-throughput microarrays using thiol-ene chemistry. - Wikidata - awgldk - TriplyDB

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

http://www.wikidata.org/entity/Q42788150

about

Small molecule microarrays: the first decade and beyond.Direct fabrication of functional and biofunctional nanostructures through reactive imprinting Spatial and Temporal Control of Thiol-Michael Addition via Photocaged Superbase in Photopatterning and Two-Stage Polymer Networks Formation The use of elemental sulfur as an alternative feedstock for polymeric materials.Synthetically simple, highly resilient hydrogels.Synthetic mimics of the extracellular matrix: how simple is complex enough?Synthesis of non-linear protein dimers through a genetically encoded Thiol-ene reaction.Ester-free Thiol-X Resins: New Materials with Enhanced Mechanical Behavior and Solvent Resistance Non-cell-adhesive substrates for printing of arrayed biomaterials.Cytocompatible click-based hydrogels with dynamically tunable properties through orthogonal photoconjugation and photocleavage reactions.A robust platform for functional microgels via thiol-ene achemistry with reactive polyether-based nanoparticles Controlled proliferation and screening of mammalian cells on a hydrogel-functionalized small molecule microarray.Photogenerated lectin sensors produced by thiol-ene/yne photo-click chemistry in aqueous solution Development of peptide-functionalized synthetic hydrogel microarrays for stem cell and tissue engineering applications.Bioorthogonal Click Chemistry: An Indispensable Tool to Create Multifaceted Cell Culture Scaffolds.Ester-free thiol-ene dental restoratives--Part A: Resin development.A combinatorial cell-laden gel microarray for inducing osteogenic differentiation of human mesenchymal stem cells.Recent advancements in optical DNA biosensors: exploiting the plasmonic effects of metal nanoparticles.Deciphering enzyme function using peptide arrays."Clicking" on/with polymers: a rapidly expanding field for the straightforward preparation of novel macromolecular architectures.Fabrication and functionalization of hydrogels through "click" chemistry.Nitrile Oxide-Norbornene Cycloaddition as a Bioorthogonal Crosslinking Reaction for the Preparation of Hydrogels.Towards scanning probe lithography-based 4D nanoprinting by advancing surface chemistry, nanopatterning strategies, and characterization protocols.An extremely simple method for fabricating 3D protein microarrays with an anti-fouling background and high protein capacity.Reactivity mapping with electrochemical gradients for monitoring reactivity at surfaces in space and time.Chemoselective Strategies to Peptide and Protein Bioprobes Immobilization on Microarray Surfaces.Peptide-functionalized oxime hydrogels with tunable mechanical properties and gelation behavior.Gel-based microarrays in clinical diagnostics in Russia.Designing functionalizable hydrogels through thiol-epoxy coupling chemistry.Tunable, high modulus hydrogels driven by ionic coacervation.High-throughput approaches for screening and analysis of cell behaviors.A fast and activatable cross-linking strategy for hydrogel formation.Screening Mammalian Cells on a Hydrogel: Functionalized Small Molecule Microarray.Beyond PDMS: off-stoichiometry thiol-ene (OSTE) based soft lithography for rapid prototyping of microfluidic devices.Capture of 2D Microparticle Arrays via a UV-Triggered Thiol-yne "Click" Reaction.Synthesis and modification of thermoresponsive poly(oligo(ethylene glycol) methacrylate) via catalytic chain transfer polymerization and thiol–ene Michael addition ‘Clickable’ hydrogels for all: facile fabrication and functionalization Thiol–epoxy/maleimide ternary networks as softening substrates for flexible electronics Chemically orthogonal trifunctional Janus beads by photochemical “sandwich” microcontact printing Revisiting thiol-yne chemistry: Selective and efficient monoaddition for block and graft copolymer formation

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A versatile approach to high-throughput microarrays using thiol-ene chemistry.

http://www.wikidata.org/entity/Q42788150

description

2009 nî lūn-bûn

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2009年の論文

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2009年论文

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name

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

@en

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

@nl

type

label

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

@en

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

@nl

prefLabel

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

@en

A versatile approach to high-throughput microarrays using thiol-ene chemistry.

@nl

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Nature Chemistry

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A versatile approach to high-throughput microarrays using thiol-ene chemistry.

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P2093

Brian F Lin

http://www.w3.org/2001/XMLSchema#string

Dennis O Clegg

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Edward J Kramer

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Luis M Campos

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Matthew V Tirrell

http://www.w3.org/2001/XMLSchema#string

Michael D Dimitriou

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Nalini Gupta

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Neil D Treat

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Sherry T Hikita

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P2860

Click Chemistry: Diverse Chemical Function from a Few Good Reactions

RGD and other recognition sequences for integrins

Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule

Peptide and small molecule microarray for high throughput cell adhesion and functional assays.

Peptide chips for the quantitative evaluation of protein kinase activity.

Semi-automated synthesis and screening of a large library of degradable cationic polymers for gene delivery.

Polymer microarrays for cellular adhesion.

Combinatorial synthesis of peptide arrays with a laser printer.

Navigating gene expression using microarrays--a technology review.

Photo- and electropatterning of hydrogel-encapsulated living cell arrays.

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138-145

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10.1038/NCHEM.478

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2

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2

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49651514

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21124405

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