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1 te), and poly(butyl methacrylate), poly(tert-butyl methacrylate).
2 branes at high levels of a key intermediate, butyl methacrylate.
3 meric chip by UV-initiated polymerization of butyl methacrylate and ethylene dimethacrylate, was test
4 er based on dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate, E) to enhanc
5 copolymerization of tert-butyl methacrylate, butyl methacrylate, and ethylene glycol dimethacrylate.
6 ymerized or copolymerized (50mol% each) with butyl methacrylate (BMA) from a reversible addition - fr
7 erization of methyl methacrylate (MMA) and n-butyl methacrylate (BMA) has been investigated using com
9 all concentrations of a hydrophobic monomer (butyl methacrylate, BMA) into the particle shell produce
10 apsules prepared by copolymerization of tert-butyl methacrylate, butyl methacrylate, and ethylene gly
13 were performed on a generic hydrophobic poly(butyl methacrylate-co-ethylene dimethacrylate) layer wit
15 ere fabricated from a 25-mm-long porous poly(butyl methacrylate-co-ethylene dimethacrylate) monolith
16 itions on the performance of monolithic poly(butyl methacrylate-co-ethylene dimethacrylate-co-2-acryl
19 methylamino)ethyl methacrylate)-block-poly(n-butyl methacrylate) (DB) and poly(ethylene glycol)-block
20 by a simple copolymerization of mixtures of butyl methacrylate, ethylene dimethacrylate, and 2-acryl
21 free-radical polymerization of a mixture of butyl methacrylate, ethylene dimethacrylate, and porogen
22 turation in 18-carbon chain phospholipids on butyl methacrylate-induced phase conversion and polymorp
23 as backbones were synthesized by grafting n-butyl methacrylate (nBMA) from the ends and sidewalls of
24 methylamino)ethyl methacrylate)-block-poly(n-butyl methacrylate) (ODB), self-assemble into micelles,
25 y(2-methacryloyloxyethylphosphorylcholine-co-butyl methacrylate), or poly(MPC-co-BMA), was used as a
26 ), poly(trimethylsilylmethyl methacrylate-co-butyl methacrylate), or poly(trimethylsilylmethyl methac
27 sting of a pair of immiscible polymers, poly(butyl)methacrylate (PBMA) and polystyrene (PS), is descr
29 rate how the facile depolymerization of poly(butyl methacrylate) (PBMA) can be leveraged to selective
30 the coating constituents: sirolimus, poly(n-butyl methacrylate) [PBMA], and poly(ethylene-co-vinyl a
31 how that the molecular weight of free poly(n-butyl methacrylate) (PnBMA) increased linearly with nBMA
33 oly(trimethylsilylmethyl methacrylate), poly(butyl methacrylate), poly(trimethylsilylmethyl methacryl
34 ide) monomethyl ether methacrylate)-b-poly(n-butyl methacrylate), prepared by atom-transfer radical p
35 the block copolymer polystyrene-block-poly(n-butyl methacrylate) (PS-b-PBMA), and this behaviour has
36 ubic phases form in trans-chain phospholipid/butyl methacrylate systems, which slowly convert to bila
37 lipid/solvent (cis-chain phospholipid lipid/butyl methacrylate) systems at a 1:6 molar ratio entirel
38 es is easily achieved by copolymerization of butyl methacrylate with ethylene dimethacrylate, or 2-hy