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1 tween alkyne-containing polymeric backbones (PHEMA-alkyne) and azido-terminated polymeric SCs were co
3 growth of poly(hydroxyl-ethyl methacrylate) (PHEMA) brush, contributing to marked SPR signal enhancem
5 e growth of poly(hydroxyethyl methacrylate) (PHEMA) at the end of immobilized DNA molecules and forme
6 ated with poly(2-hydroxyethyl methacrylate) (PHEMA) brushes that are derivatized with Fe(III)-nitrilo
8 ) (PMMA), poly(2-hydroxyethyl methacrylate) (PHEMA), and trifluoroacetic anhydride-derivatized poly(2
9 omposite of PMMA (poly-methyl-methacrylate), PHEMA (poly-hydroxyl-ethyl-methacrylate), and calcium hy
10 block of poly(2-hydroxyethyl methacrylates) (PHEMA) that is randomly functionalized by anthracene.
12 ptic digests of beta-casein, the Fe(III)-NTA-PHEMA brushes allow detection of as little as 15 fmol of
13 ontaining samples enriched using Fe(III)-NTA-PHEMA-modified plates also demonstrate higher recoveries
16 at takes advantage of the hydroxyl groups of PHEMA brushes from the first step to form hyperbranched
19 ificantly decreased the sputter rate of TFAA-PHEMA underlayers due to ion-induced damage accumulation
21 EO-N3 with Mn = 775 g/mol, were reacted with PHEMA-alkyne (degree of polymerization = 210) at a high
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