Synthetically tractable click hydrogels for three-dimensional cell culture formed using tetrazine-norbornene chemistry - Wikidata - wikimedia - TriplyDB

Synthetically tractable click hydrogels for three-dimensional cell culture formed using tetrazine-norbornene chemistry

Synthetically tractable click hydrogels for three-dimensional cell culture formed using tetrazine-norbornene chemistry

http://www.wikidata.org/entity/Q36757961

about

Modular and orthogonal synthesis of hybrid polymers and networks Click-Crosslinked Injectable Gelatin Hydrogels.Design of thiol-ene photoclick hydrogels using facile techniques for cell culture applications†Electronic supplementary information (ESI) available. See DOI: 10.1039/c4bm00187gClick here for additional data file.Microscale Bioadhesive Hydrogel Arrays for Cell Engineering Applications Thiol-norbornene photo-click hydrogels for tissue engineering applications Recent advances in crosslinking chemistry of biomimetic poly(ethylene glycol) hydrogels An efficient and mild oxidant for the synthesis of s-tetrazines.Design of Thiol- and Light-sensitive Degradable Hydrogels using Michael-type Addition Reactions.Thiol-ene and photo-cleavage chemistry for controlled presentation of biomolecules in hydrogels Bio-Orthogonally Crosslinked, Engineered Protein Hydrogels with Tunable Mechanics and Biochemistry for Cell Encapsulation.Synthesis and orthogonal photopatterning of hyaluronic acid hydrogels with thiol-norbornene chemistry.Facile and efficient Lewis acid catalyzed synthesis of an asymmetric tetrazine useful for bio-orthogonal click chemistry applications.Visible light cured thiol-vinyl hydrogels with tunable degradation for 3D cell culture.Thiol-ene click hydrogels for therapeutic delivery Bioorthogonal chemistry: implications for pretargeted nuclear (PET/SPECT) imaging and therapy."Click" reactions: a versatile toolbox for the synthesis of peptide-conjugates.Multi-Functional Macromers for Hydrogel Design in Biomedical Engineering and Regenerative Medicine.Functional protein micropatterning for drug design and discovery.Injectable hydrogels for cartilage and bone tissue engineering.Nitrile Oxide-Norbornene Cycloaddition as a Bioorthogonal Crosslinking Reaction for the Preparation of Hydrogels.Degradable thiol-acrylate hydrogels as tunable matrices for three-dimensional hepatic culture.Bioorthogonal Radiopaque Hydrogel for Endoscopic Delivery and Universal Tissue Marking Meter-long multiblock copolymer microfibers via interfacial bioorthogonal polymerization.An injectable and fast-degradable poly(ethylene glycol) hydrogel fabricated via bioorthogonal strain-promoted azide-alkyne cycloaddition click chemistry.Biodegradable hydrogels composed of oxime crosslinked poly(ethylene glycol), hyaluronic acid and collagen: a tunable platform for soft tissue engineering.Interfacial Bioorthogonal Cross-Linking.Peptide-functionalized oxime hydrogels with tunable mechanical properties and gelation behavior.Kinetic studies of inverse electron demand Diels-Alder reactions (iEDDA) of norbornenes and 3,6-dipyridin-2-yl-1,2,4,5-tetrazine.Soft PEG-Hydrogels with Independently Tunable Stiffness and RGDS-Content for Cell Adhesion Studies.Bioactive hydrogels: Lighting the way."Bio"-macromolecules: polymer-protein conjugates as emerging scaffolds for therapeutics.Liquid crystal elastomer foams with elastic properties specifically engineered as biodegradable brain tissue scaffolds.Spatially and Temporally Controlled Hydrogels for Tissue Engineering.Injectable nanocomposite cryogels for versatile protein drug delivery.Spatiotemporal hydrogel biomaterials for regenerative medicine.Hydrogel scaffolds for differentiation of adipose-derived stem cells.A microfluidic-based cell encapsulation platform to achieve high long-term cell viability in photopolymerized PEGNB hydrogel microspheres.Combinatorial hydrogels with biochemical gradients for screening 3D cellular microenvironments.A fast and activatable cross-linking strategy for hydrogel formation.PEG-based hydrogels prepared by catalyst-free thiol-yne addition and their post-antibacterial modification.

P2860

Q28087551-0CE71030-123D-4F5E-B20C-67374F8F0F4F Q30749482-CBAD1AA7-EF89-4236-9C87-71123B7B8EB6 Q30900316-C429A403-9B8A-47C1-9F6B-77D4F153F6BD Q34334970-4A00A7D0-C3F8-4003-A6BB-846B2DE9B50C Q34792325-0B137A1D-9A7A-4644-B493-A8F4A4169D91 Q35653922-AF015814-05D1-4574-9666-B6D3FA2498B6 Q35801746-25FAB8E9-FD44-4A58-BE75-516C68EFB3E2 Q35955111-157E6235-9CD2-4320-AA40-26555F95C450 Q36307667-BF9F80AE-7DA9-44E0-91D9-8571B0EBB93E Q37249337-627D7116-724A-4273-9F9F-52CF7B3CD4B6 Q37316557-B2D4F185-D3F0-46E6-B8E3-0F37F6C4F86B Q37326794-74611ED5-888B-47E2-B223-69D628204F63 Q37341460-1BEDCB4B-AD9C-48E4-86CC-0406851B84F6 Q37724937-DA23C25E-0AD4-4381-9978-06DF71E65C4B Q38206206-D545B4B4-0A6D-4CC0-83BF-AFD186AC62B4 Q38226023-CC696A73-35AA-4EBD-93C4-1D78614B155D Q38648779-F64936FB-9E22-417D-8440-9D4AE0BC5180 Q38654896-27B5A477-6CFC-4FAA-8D77-D15995F7289A Q38674409-8374BF4B-5639-4880-A695-31C27F2240A3 Q38845741-2D332080-8EC8-4153-A2DC-095C29A1BA42 Q39052236-024F012F-9982-4B34-BC93-877343A7E48D Q39629946-B2359F53-7DA7-47FE-8150-9E89BA406F69 Q40405903-6C9745C7-DB34-4084-8F11-FD4741CADDAA Q40778293-5C9EB458-B4DE-43D5-8879-6B1734CB73F4 Q41631238-A331E68E-15CB-4A39-BBF4-D3D1EE0B5F0B Q42095958-91163190-9E95-4420-AF1E-26D9BF459AB3 Q42222672-EB301BB2-6603-4165-96AB-68B8B68C829C Q42776933-E000CAE3-532A-45E8-946D-3719C63E6F2D Q42826012-63557A78-F3D3-4088-9991-8320A2798305 Q45048221-53437D8F-C267-486C-B544-EC1BED668DE1 Q46335892-A504EEF6-7D7A-4749-B545-D29958ADA542 Q47253724-CA2B4757-EBF9-408C-9107-AD3FAF601CC7 Q47287984-CD21D617-710B-4C0B-BFBD-21D525AC810B Q47358123-0230DC7A-8B72-4454-A59D-F980EDFCD92F Q47780338-60B35B82-DA34-4FC9-8DC8-9C63E0C9C1E4 Q47785789-83AFC92D-2B39-49DD-8BC2-1D789A60E8F0 Q48876017-6859E418-873C-40DB-877B-63D136EDCF0F Q50091505-3B621B1E-ABD0-41BD-B3FF-28F51EFD7BE6 Q51022891-B7889D60-D398-420D-810C-EB7AB411F9A7 Q51135627-036DE44A-DE54-44A4-87A6-64622337C702

P2860

Synthetically tractable click hydrogels for three-dimensional cell culture formed using tetrazine-norbornene chemistry

http://www.wikidata.org/entity/Q36757961

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Synthetically tractable click ...... tetrazine-norbornene chemistry

@ast

Synthetically tractable click ...... tetrazine-norbornene chemistry

@en

type

label

Synthetically tractable click ...... tetrazine-norbornene chemistry

@ast

Synthetically tractable click ...... tetrazine-norbornene chemistry

@en

prefLabel

Synthetically tractable click ...... tetrazine-norbornene chemistry

@ast

Synthetically tractable click ...... tetrazine-norbornene chemistry

@en

P1433

Q36757961-3F13429E-16E9-47F2-A9E2-A0D16E8ACC00

P1476

Q36757961-7BADE381-1105-4D41-A099-72129E2B8F3A

P2093

Q36757961-0452F622-86CF-485D-8C08-FE9C5706EB13

Q36757961-1020B04D-1AC3-49B4-9307-9DC7F0E11FAC

Q36757961-124B1B6D-BBF0-43D4-BBB2-8D149ECBE5F3

Q36757961-605669A3-B34A-4FF6-A094-B7477A665AC5

P2860

Q36757961-043632DC-D666-4FA9-B595-A07BAC294654

Q36757961-05FE7FC8-52EC-4621-B5B8-73E631E07C52

Q36757961-1E57D959-3D52-4744-990F-5883E3EE6687

Q36757961-2026570B-C85E-4548-8DBF-E2FCC010CE62

Q36757961-37451DB1-556C-46DB-BC34-5662C497830C

Q36757961-3F824C09-A8EB-4591-BD50-BF8200B2EDCD

Q36757961-48130A06-7727-4339-938D-2743ED1EF86F

Q36757961-48C3124C-F8AB-4FFF-99E4-A6D6BFEA91DA

Q36757961-4CF45DB1-5BE9-4080-B282-20B10D9C62C7

Q36757961-55E81C53-5041-4F2F-9F33-F1F9C8CEFC3D

P304

Q36757961-304647E1-185D-4AB1-B3C1-CA9AE518A68A

P31

Q36757961-057369EC-0C81-4374-AC33-AF3B057A1830

P356

Q36757961-29A39AAD-797B-416B-A66F-F3FB7E470B87

P433

Q36757961-01826788-A07E-4008-91B8-F9E75D5F42BC

P478

Q36757961-733BBEF3-C5C9-4323-BE2A-2668D3444144

P577

Q36757961-F5BDA9FD-0351-4BE1-B79C-FA9FD13993A4

P5875

Q36757961-6BC17935-E517-4FBA-8D84-DB8DAF4E2CE9

P698

Q36757961-E9A54AB7-B68C-47B5-BB72-6F21ACFCB0AD

P921

Q36757961-FF900586-E379-4121-8794-D96A3904FABB

P932

Q36757961-346A9638-4717-4642-A181-EFFEB5BC3F9C

P356

P1433

Biomacromolecules

P1476

Synthetically tractable click ...... tetrazine-norbornene chemistry

@en

P2093

Daniel L Alge

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

Dillon F Donohue

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

Kristi S Anseth

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

Malar A Azagarsamy

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

P2860

Tetrazine-based cycloadditions: application to pretargeted live cell imaging

In vitro and in vivo performance of porcine islets encapsulated in interfacially photopolymerized poly(ethylene glycol) diacrylate membranes.

Genetically encoded tetrazine amino acid directs rapid site-specific in vivo bioorthogonal ligation with trans-cyclooctenes.

Additive-free clicking for polymer functionalization and coupling by tetrazine-norbornene chemistry.

Bioorthogonal reaction pairs enable simultaneous, selective, multi-target imaging.

A Versatile Synthetic Extracellular Matrix Mimic via Thiol-Norbornene Photopolymerization.

Synthetic matrix metalloproteinase-sensitive hydrogels for the conduction of tissue regeneration: engineering cell-invasion characteristics

Hydrogels as extracellular matrix mimics for 3D cell culture.

A Mild, Large-Scale Synthesis of 1,3-Cyclooctanedione: Expanding Access to Difluorinated Cyclooctyne for Copper-Free Click Chemistry.

Cytocompatible click-based hydrogels with dynamically tunable properties through orthogonal photoconjugation and photocleavage reactions.

P304

949-953

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

P31

scholarly article

P356

10.1021/BM4000508

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

P433

4

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

P478

14

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

P577

2013-03-08T00:00:00Z

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

P5875

235755533

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

P698

23448682

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

P921

P932

3623454

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