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1 y, QW-296 was encapsulated into methoxy poly(ethyleneglycol)-b-poly(carbonate-co-lactide) [mPEG-b-P(C
3 acetic acid to chelate intracellular Ca2+ or ethyleneglycol-bis (beta-aminoethyl ether)- N,N,N',N' -t
5 pretreating leaves with the calcium chelator ethyleneglycol-bis(aminoethyl ether)-N,N'-tetraacetic ac
7 ly, before increasing again in a Gd3+, La3+, ethyleneglycol-bis(beta-aminoethyl ether)-N,N'-tetraacet
8 ic fields; however, addition of the chelator ethyleneglycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetr
10 rylation experiments, the effect of calcium, ethyleneglycol-bis-(beta-aminoethyl ether)-N-N' -tetraac
11 of intracellular calcium stores release, and ethyleneglycol-bis-(beta-aminoethyl)- N,N,N',N'-tetra-ac
12 O and subsequently treated with 1 millimolar ethyleneglycol-bis-[beta-aminoethylether]-N,N,N',N'-tetr
13 he condensation of benzimidazoles with oligo(ethyleneglycol) dichlorides and oligo(ethyleneglycol) di
14 )propionic acid (HFA), as template molecule, ethyleneglycol dimethacrylate (EDMA) as cross-linker, an
15 stals were filled with divinylbenzene (DVB), ethyleneglycol dimethacrylate (EDMA), or a mixture of th
16 oxyethyl methacrylate (HEMA) as monomers and ethyleneglycol dimethacrylate (EGDMA) as crosslinker und
19 r stabilized by 1-mercapto-undecane-11-tetra(ethyleneglycol) has been demonstrated by cyclic voltamme
21 ated different poly(methacrylic acid)-g-poly(ethyleneglycol methacrylate) polymers as in situ coating
22 l methacrylate-co-methylmethacrylate-co-poly(ethyleneglycol)methacrylate) with a low redox potential
23 2008) that contains the amphoteric group di(ethyleneglycol)-methyl ether at position 5 (compound 500
25 racellular Ca(2+) chelator bis(2-aminophenyl)ethyleneglycol-N,N,N',N'-tetraacetic acid significantly
26 f PEDOT and the composite of PEDOT with poly(ethyleneglycol) (PEDOT(PTS):PEG) in the presence of IL m
27 then their effects on the kinetics of poly (ethyleneglycol) (PEG)-mediated fusion of small unilamell
28 a simple model cytoplasm composed of a poly(ethyleneglycol) (PEG)/dextran aqueous two-phase system (
29 muscle transfection through the use of poly(ethyleneglycol) (PEG)/polyethylenimine (PEI) nanocomplex
31 neglycol (ppEG), polystyrene (ppST) and poly(ethyleneglycol-styrene) (ppST-EG) thin-layers have been
32 diameter and coated with a phospholipid/poly(ethyleneglycol) surfactant shell were triply labeled wit