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1   Affinity monoliths based on a copolymer of glycidyl methacrylate and ethylene dimethacrylate were d
2 These monoliths were based on a copolymer of glycidyl methacrylate and ethylene dimethacrylate.
3 red by direct in situ photopolymerization of glycidyl methacrylate and ethylene glycol dimethacrylate
4 crofluidic channel by photopolymerization of glycidyl methacrylate and trimethylolpropane trimethacry
5 ting frits by in situ photopolymerization of glycidyl methacrylate and trimethylolpropane trimethacry
6  the UV photopolymerization of a solution of glycidyl methacrylate and trimethylolpropane trimethacry
7  the UV photopolymerization of a solution of glycidyl methacrylate and trimethylopropane trimethacryl
8 ic cationic PGEA (ethanolamine-aminated poly(glycidyl methacrylate)) and type IV collagen targeted pe
9 l F diglycidyl ether (BFDGE) and Bisphenol A glycidyl methacrylate (BISGMA) after their exposure to l
10 The monomer mixture consisted of bisphenol A glycidyl methacrylate (BisGMA), hexanediol dimethacrylat
11 chemical degradation products of bisphenol A glycidyl methacrylate (BisGMA), oligomers of bisphenol-A
12 t bisphenol A (BPA) leaches from bisphenol A-glycidyl methacrylate (bisGMA)-based dental materials.
13 hydroxyethymethacrylate, laurylmethacrylate, glycidyl methacrylate, bisphenol diacrylate, benzylmetha
14 actor was fabricated in a fused silica using glycidyl methacrylate-co-ethylene dimethacrylate polymer
15 onolithic capillary prepared using GMA-EDMA (glycidyl methacrylate-co-ethylene dimethacrylate) as pol
16 ties of uniformly sized 3-microm porous poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads
17 tionary phase obtained by hydrolysis of poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads
18           The column is prepared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoli
19       These columns are prepared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoli
20 alities originating from the hydrolyzed poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoli
21 ionalization of our affinity substrate, poly(glycidyl methacrylate-co-ethylene dimethacrylate) porous
22 his paper, we present the obtainment of poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate)
23 ced a surface-reactive acrylic polymer, poly(glycidyl methacrylate-co-methyl methacrylate) (PGMAMMA),
24     A surface-reactive acrylic polymer, poly(glycidyl methacrylate-co-methyl methacrylate) (PGMAMMA),
25 ng a buffer ion-permeable membrane in a poly(glycidyl methacrylate-co-methyl methacrylate) micro elec
26 ox polymer, namely neutral-red-modified poly(glycidyl methacrylate-co-methylmethacrylate-co-poly(ethy
27 rticularly notable for a hydrophobic monomer glycidyl methacrylate combined with a nonionic surfactan
28       2-Hydroxyethyl methacrylate (HEMA) and glycidyl methacrylate (GMA) are examined to provide exce
29            An ethylenediamine functionalized glycidyl methacrylate (GMA) based terpolymeric chelating
30 ified sequentially with silica (Fe3O4@SiO2), glycidyl methacrylate (GMA) by surface initiated atom tr
31                                              Glycidyl methacrylate (GMA) was examined to provide exce
32 ylate (MMA) statistically copolymerized with glycidyl methacrylate (GMA), resulting in p(MMA-stat-GMA
33 ed carbon nanotube (MWCNT) was grafted using glycidyl methacrylate (GMA).
34 ion using La2O3, (ii) La2O3 embedded in poly(glycidyl methacrylate (GMA)/divinylbenzene (DVB)) tip, a
35                   A maleic anhydride-styrene-glycidyl methacrylate (MA-St-GMA) terpolymer was synthes
36 WNSYY was immobilized to the surface of poly(glycidyl methacrylate) nanoparticles (PGMA NPs).
37 ydroquinidine , ethylene dimethacrylate, and glycidyl methacrylate or 2-hydroxyethyl methacrylate in
38 cess: poly(Ethylene glycol Dimethacrylate-co-Glycidyl methacrylate) or poly(EDMA-co-GMA) [196.0 degre
39 macroporous poly(hydroxylmethyl methacrylate/glycidyl methacrylate [p(HEMA-GMA)] cryogels with large
40 ethoxy-poly(ethylene glycol) methacrylate-co-glycidyl methacrylate) [P(MALC)-b-P(PEGMA-co-GM)] block
41 ds were prepared by chemical modification of glycidyl methacrylate particles.
42 olymeric matrix composed of poly(ethylene-co-glycidyl methacrylate) (PEGM) has been prepared.
43 phores located at the interface between poly(glycidyl methacrylate) (PGMA) polymer brushes and Si waf
44 nd toughening agent, ethylene-ethyl acrylate-glycidyl methacrylate terpolymer (E-EA-GMA), a functiona
45  of a trimethacrylate monomer or bisphenol A glycidyl methacrylate, which is a monomer standard in de
46 rylate with the sodium salt of N-reaction of glycidyl methacrylate with the sodium salt of N-(3,5-dim
47 ) was synthesized by an addition reaction of glycidyl methacrylate with the sodium salt of N-reaction