About: Andrew P. Dove

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

British polymer chemistry professor

Attributes	Values
rdf:type	Item
field of work	wds:Q88221091-210DF4E0-6BA8-495E-BC6C-C91E46BBF671
field of work	polymer science
description	研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) British polymer chemistry professor (en)
rdfs:label	Andrew P Dove (nl) Andrew P. Dove (en)
skos:prefLabel	Andrew P Dove (nl) Andrew P. Dove (en)
name	Andrew P Dove (nl) Andrew P. Dove (en)
Scopus author ID	wds:Q88221091-23175BE3-19BC-40D5-B5C1-4BE09F2BD748
Scopus author ID	8905793200
given name	wds:Q88221091-27FF2978-EAE7-4D3B-9696-5FEBCDCFE4B2 wds:Q88221091-56133aba-4de5-dd86-4018-5121125ebcd1
given name	Andrew Peter
instance of	wds:Q88221091-9A74459C-B065-4695-BAAE-9709254C538F
instance of	Homo sapiens
award received	wds:Q88221091-a04d3f8a-443c-7d31-e4bc-fcda14cd578c
award received	Corday-Morgan Prize
skos:altLabel	Andrew Dove (en) Andrew Peter Dove (en)
occupation	wds:Q88221091-1FB35A0A-9078-405B-9A3E-88A693BEF8A1 wds:Q88221091-80ebc273-4ad6-1e1d-6936-abc95b6a162e
employer	wds:Q88221091-fb34a6d7-4893-b360-0858-e9f461a9167d
NUKAT ID	wds:Q88221091-7ca0ae17-4166-05b8-d19e-0f206e07a158
sex or gender	wds:Q88221091-E7B03DE9-BA7F-49EA-A567-579DB27110ED
VIAF ID	wds:Q88221091-3013aa14-4f04-70b5-3e12-0aa4126f7a70
Library of Congress authority ID	wds:Q88221091-c7d43d9b-47ad-b8a3-7e7c-a79fb54cf2a1
country of citizenship	wds:Q88221091-c683179e-4b2c-4e69-0316-ca5f5c0b1d35
educated at	wds:Q88221091-65928f27-4330-4473-361b-b6e092d18ec9 wds:Q88221091-c15430fd-4328-ab98-7e57-fa5d1d8a5aa6
family name	wds:Q88221091-47A89C45-E2F0-4C97-9067-5AA865AE4B32
VIAF ID	http://viaf.org/viaf/57156131053458312699
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2019085388
occupation	researcher polymer chemist
employer	University of Birmingham
NUKAT ID	n2019149474
sex or gender	male
VIAF ID	57156131053458312699
Library of Congress authority ID	no2019085388
country of citizenship	United Kingdom
educated at	University of York Imperial College London
family name	Dove
ORCID iD	wds:Q88221091-1B3FE315-6E69-4C2F-89DD-FC52E5B65DF3
ORCID iD	https://orcid.org/0000-0001-8208-9309
ORCID iD	0000-0001-8208-9309
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q88221091
is author of	Independent Control of Elastomer Properties through Stereocontrolled Synthesis Postpolymerization Modifications of Alkene-Functional Polycarbonates for the Development of Advanced Materials Biomaterials Synthesis, properties and biomedical applications of hydrolytically degradable materials based on aliphatic polyesters and polycarbonates Shape Effect of Glyco-Nanoparticles on Macrophage Cellular Uptake and Immune Response Unlocking the Potential of Poly(Ortho Ester)s: A General Catalytic Approach to the Synthesis of Surface-Erodible Materials. Hydrogel scaffolds for differentiation of adipose-derived stem cells. Precious metal carborane polymer nanoparticles: characterisation of micellar formulations and anticancer activity Exploiting topology-directed nanoparticle disassembly for triggered drug delivery 1D vs. 2D shape selectivity in the crystallization-driven self-assembly of polylactide block copolymers Self-healing, stretchable and robust interpenetrating network hydrogels Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers Nonswelling Thiol-Yne Cross-Linked Hydrogel Materials as Cytocompatible Soft Tissue Scaffolds. In situ-forming robust chitosan-poly(ethylene glycol) hydrogels prepared by copper-free azide-alkyne click reaction for tissue engineering Recent Advances and Challenges in the Design of Organic Photoacid and Photobase Generators for Polymerizations Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies. Update and Challenges in Carbon Dioxide-Based Polycarbonate Synthesis Additive-Free Green Light-Induced Ligation Using BODIPY Triggers Poly(oligo(ethylene glycol) vinyl acetate)s: A Versatile Class of Thermoresponsive and Biocompatible Polymers. 3D Printing for the Clinic: Examining Contemporary Polymeric Biomaterials and Their Clinical Utility Uniform Biodegradable Fiber-Like Micelles and Block Comicelles via "Living" Crystallization-Driven Self-Assembly of Poly(l-lactide) Block Copolymers: The Importance of Reducing Unimer Self-Nucleation via Hydrogen Bond Disruption Modular Functionalization of Laminarin to Create Value-Added Naturally Derived Macromolecules Synthesis of Rapidly Surface Eroding Polyorthoesters and Polyacetals Using Thiol–ene Click Chemistry Organocatalytic Synthesis of Alkyne-Functional Aliphatic Polycarbonates via Ring-Opening Polymerization of an Eight-Membered-N-Cyclic Carbonate Click Step-Growth Polymerization and <i>E</i>/<i>Z</i> Stereochemistry Using Nucleophilic Thiol–yne/–ene Reactions: Applying Old Concepts for Practical Sustainable (Bio)Materials pH-Responsive, Functionalizable Spyrocyclic Polycarbonate: A Versatile Platform for Biocompatible Nanoparticles Selective Reactivity of Myrcene for Vat Photopolymerization 3D Printing and Postfabrication Surface Modification Elastomeric polyamide biomaterials with stereochemically tuneable mechanical properties and shape memory Harnessing the Chemical Diversity of the Natural Product Magnolol for the Synthesis of Renewable, Degradable Neolignan Thermosets with Tunable Thermomechanical Characteristics and Antioxidant Activity Robust alginate/hyaluronic acid thiol-yne click-hydrogel scaffolds with superior mechanical performance and stability for load-bearing soft tissue engineering A microstereolithography resin based on thiol-ene chemistry: towards biocompatible 3D extracellular constructs for tissue engineering Catalytically Active N-Heterocyclic Carbene Release from Single-Chain Nanoparticles Following a Thermolysis-Driven Unfolding Strategy
is author of	wds:Q28820939-363FB0F4-2BA5-4DD1-BE62-8C364D3FED9D wds:Q37289629-C930D2F2-6714-475A-B20B-948A898387A7 wds:Q47395714-ECD29AA9-275B-4F80-B37C-358134D10A9A wds:Q39007434-07FA3FD7-6635-4044-A674-2AD576C3F36B wds:Q47785789-59329523-D09F-43E8-A860-D2DA788DFAE8 wds:Q90506452-C1D8E1CB-77FF-4E5C-963A-FE0185E037BC wds:Q91701091-10BC0842-A025-40A5-8490-5B434AD1D0BE wds:Q38961127-06EBE0D2-C688-4EF5-ABBC-B8DDEBA46691 wds:Q38951818-9EDDC3D7-7D64-4B43-983B-6FA0F1D6AF42 wds:Q91458303-9662098B-036B-418A-98CC-B34A91ECE00D wds:Q91437974-C12B19A8-D0EC-4068-8B59-B6B28B78D889 wds:Q96119608-93D3AAE6-7A2D-4949-8F2A-155BEC4FB474 wds:Q47361957-DD03D97C-97A0-497E-A829-5C6ED19B6223 wds:Q89715997-A266BE08-55F8-4CD1-8BA9-B3421DED6DCA

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