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1 is of well-defined thioether-functional poly(ethylene glycol).
2 olyhedral oligomeric silsesquioxane and poly(ethylene glycol).
3 stabilization for glucose, dextran, and poly(ethylene glycol).
4 tabilization of reactive intermediates using ethylene glycol.
5 nd exfoliation of functionalized graphite in ethylene glycol.
6 rations at times due to this interference by ethylene glycol.
7 were reduced together with a reducing agent, ethylene glycol.
8 xture of choline chloride and either urea or ethylene glycol.
9 the wax moth Galleria mellonella, producing ethylene glycol.
10 relatively neutral solutes: methanol, +3.12, ethylene glycol +1.66, glucose +1.19, glycerol [< 5 M] +
11 with thiolated macromolecules, such as poly(ethylene glycol) (1 kDa), exhibit ligand exchange effici
12 een alpha-truxillic acid and diols including ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pe
13 adecanoic acid (16-MHA), 11-mercaptoundecane(ethylene glycol)3-COOH (PEG), 3-MPA-LHDLHD-OH, and 3-MPA
14 products (ethanol, glyoxal, glycolaldehyde, ethylene glycol, acetaldehyde, ethane, and methanol).
15 pylacrylamide), N,N-dimethylacrylamide, poly(ethylene glycol) acrylate, 2-hydroxyethyl acrylate (HEA)
16 n: alginate alone (Alg), alginate-graft-poly(ethylene glycol) (Alg-g-PEG) and alginate-graft-poly(eth
18 e hydrogenation of dimethyl oxalate (DMO) to ethylene glycol, an important reaction well known for de
21 atible step-index optical fiber made of poly(ethylene glycol) and alginate hydrogels is demonstrated.
23 ough hydrogel is developed by combining poly(ethylene glycol) and sodium alginate, which synergize to
24 hydrogel by combining dopamine-modified poly(ethylene glycol) and the nanosilicate Laponite, without
25 particle surface functionalization with poly(ethylene glycol) and/or immunological modulators, preven
27 mounts of organic precursors (fructose, poly(ethylene glycol), and ethanol) and can be accomplished w
28 branched polyamines, glucose, arginine, tri(ethylene glycol), and Tyr-D-Arg-Phe-beta-Ala (YRFA) pept
31 vitrification solution containing glycerol, ethylene glycol, and DMSO at concentrations that approxi
32 dechlorination of all 209 PCBs congeners by ethylene glycol anion has been studied theoretically at
33 thylene glycol) ethyl methyl ether, and poly(ethylene glycol) are found on the surface simultaneously
35 composed of a 3-helix coiled coil with poly(ethylene glycol) attached to the exterior of the helix b
36 ated in biocompatible and biodegradable poly(ethylene glycol)-b-poly(D,L-lactic acid) (PEG-b-PLA) mic
37 ndrimers (~5nm in diameter) into larger poly(ethylene glycol)-b-poly(D,L-lactide) (PEG-PLA) NPs (~70n
38 comprising the biodegradable copolymer poly(ethylene glycol)-b-poly(d,l-lactide) into well-defined n
39 hexahistidine tagged OPH (His6-OPH) and poly(ethylene glycol)-b-poly(l-glutamic acid) diblock copolym
40 oped from amphiphilic block copolymers, poly(ethylene glycol)-b-poly(L-glutamic acid)-b-poly(L-phenyl
41 e pH-sensitive block copolymer, methoxy poly(ethylene glycol)-b-poly(l-histidine-co-l-phenylalanine)
42 ion with a conventional block copolymer poly(ethylene glycol)-b-poly(L-lysine) (PEG-PLL) followed by
43 rogels (poly(lactic-co-glycolic acid)-b-poly(ethylene glycol)-b-poly(lactic-co-glycolic acid); PLGA-P
44 from the fragments of cutting wire mixed in ethylene glycol based cutting fluid during Si wafer slic
46 ell as conventional carboxy-terminated oligo(ethylene glycol)-based alkanethiolate self-assembled mon
47 isolated from porcine aortic valves on poly(ethylene glycol)-based hydrogels with physiologically re
49 t was further passivated by a thiolated poly(ethylene glycol)-biotin to improve its cancer targeting
51 thoxysilyl)-1-propanethiol and modified with ethylene glycol bis-mercaptoacetate as a new adsorbent.
52 ilamellar and tubular polymersomes from poly(ethylene glycol)-bl-poly(propylene sulfide) block copoly
53 icles (NPs) made of poly (lactic acid) poly (ethylene glycol) block copolymer (PLA-PEG), and that gra
54 nd its polymer-drug conjugate, methoxy-poly (ethylene glycol)-block-poly (2-methyl-2-carboxyl-propyle
55 -NH2 to the pendant carboxyl groups of poly (ethylene glycol)-block-poly(2-methyl-2-carboxyl-propylen
59 poly(d,l-lactic-co-glycolic acid)-block-poly(ethylene glycol)-block-poly(d,l-lactic-co-glycolic acid)
62 straight access to indoles from anilines and ethylene glycol by heterogeneous catalysis, based on an
63 amination with heterobifunctional amine-poly(ethylene glycol)-carboxyl allowed covalent attachment of
64 the adamantane cores is constituted of short ethylene glycol chains, and the periphery consists of am
66 ve a critical value of approximately 20 poly(ethylene glycol) chains (MW 5 kDa) per 100 nm(2) prolong
67 ta that follow the dynamics of isolated poly(ethylene glycol) chains adsorbed at a hydrophobic solid-
68 were used to attach water solubilizing poly(ethylene glycol) chains through a click reaction after s
71 MD, forming carboxymethyl-dextran-block-poly(ethylene glycol) (CMD-b-PEG), the PEG block was hypothes
72 141-loaded IgG Fc-conjugated maleimidyl-poly(ethylene glycol)-co-poly(epsilon-caprolactone) (Mal-PEG-
73 veloped a cyclic RGD peptide-conjugated poly(ethylene glycol)-co-poly(lactic acid) polymeric micelle
74 ow that ultrasmall (<10 nm in diameter) poly(ethylene glycol)-coated silica nanoparticles, functional
78 ps were used to bind a layer of diamino-poly(ethylene glycol) (DAPEG) with terminal amino groups.
81 novel effects of the amyloid-binding tetra (ethylene glycol) derivative of benzothiazole aniline, BT
83 le microspheres composed of chitosan or poly(ethylene glycol) derivatives, in situ gelling liquid emb
84 intramolecular anhydride formation of oligo(ethylene glycol) diacids gives macrocycles analogous to
85 The second photopolymerization uses (poly)ethylene glycol diacrylate to encapsulate undesired cell
86 er chip composed of photo-polymerizable poly(ethylene) glycol diacrylate (PEGDA) hydrogel for drug sc
87 ng capture antibody immobilized porous poly (ethylene) glycol diacrylate (PEGDA) hydrogel microsphere
88 pture-antibody immobilized macro-porous poly(ethylene) glycol diacrylate (PEGDA) hydrogel microsphere
90 was dissolved in different mixtures of poly(ethylene glycol) diacrylate (PEGDA) and poly(ethylene gl
91 composed of micro-sized VEGF-releasing poly(ethylene glycol) diacrylate (PEGDA) hydrogel cylinders u
92 al peptide, melittin, to the surface of poly(ethylene glycol) diacrylate (PEGDA) hydrogel microsphere
93 Raman and Brillouin spectra of a molded poly(ethylene glycol) diacrylate (PEGDA) hydrogel sample in c
94 three-component pesticide mixture on a poly(ethylene glycol) diacrylate (PEGDA) monolithic column.
97 el fibers consist of poly(acrylamide-co-poly(ethylene glycol) diacrylate) cores functionalized with p
99 mal stem cells (hMSCs) in a 3D printed poly-(ethylene glycol)-diacrylate (PEG-DA) hydrogel scaffold.
100 from poly(glyceric acid carbonate) and poly(ethylene glycol) diaziridine show significant degradatio
102 odegradable poly(lactide-coglycolide)-b-poly(ethylene glycol) diblock copolymer and a self-synthesize
103 ehyde, a conventional cross-linker, and poly(ethylene glycol) diglycidyl ether (PEGDE), a milder immo
105 isation of methyl methacrylate (monomer) and ethylene glycol dimethacrylate (cross-linker) in the pre
106 ate), methacrylic acid (functional monomer), ethylene glycol dimethacrylate (cross-linking agent) and
107 methacrylamide (MAM) as functional monomers, ethylene glycol dimethacrylate (EDMA) as cross-linker an
108 hacrylic acid (MAA) as a functional monomer, ethylene glycol dimethacrylate (EGDMA) as a cross-linker
109 nm RAFT-modified silica core particles using ethylene glycol dimethacrylate (EGDMA) as cross-linker r
110 ns of methacrylic acid (MAA) as the monomer, ethylene glycol dimethacrylate (EGDMA) as the cross link
111 mate (APDC) using styrene as the monomer and ethylene glycol dimethacrylate (EGDMA) as the cross link
112 VPP; a resin of N-vinyl-2-pyrrolidinone with ethylene glycol dimethacrylate and triallyl isocyanurate
113 ed polymersomes (prepared by the addition of ethylene glycol dimethacrylate as a third comonomer) als
114 c acid or methyl methacrylate as monomer and ethylene glycol dimethacrylate as cross-linker at differ
115 ing 2-vinylpyridine as a functional monomer, ethylene glycol dimethacrylate as the cross-linker, 2,2'
118 corbic acid and dopamine), and cross-linker (ethylene glycol dimethacrylate), in the presence of mult
119 ve molecularly imprinted poly[acrylamide-co-(ethylene glycol dimethacrylate)] polymer particles (MIPs
120 P) hydrogel microparticles with 3 mol% tetra(ethylene glycol) dimethacrylate crosslinker, a small pol
121 rate, PVP-DEGMA-TAIC; and poly(acrylamide-co-ethylene glycol-dimethacrylate), PA-EGDMA) to remove fum
123 ired with ethyl methyl carbonate (EMC), poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) e
125 hyl acetate, acetone, acetaldehyde, ethanol, ethylene glycol, dimethylsilanediol, formaldehyde, isopr
126 onding increase in the amount of glycerol or ethylene glycol diminishes further its damaging effect d
128 ide range of common explosives such as EGDN (ethylene glycol dinitrate), urea nitrate, PETN (pentaery
131 tally benign solvents namely water, ethanol, ethylene glycol (EG), ethyl acetate (EA), isopropanol (I
132 his new method relies on the substitution of ethylene glycol (EG)--the solvent most commonly used in
134 anediol, 2,2,4-trimethyl-1,3-pentanediol, or ethylene glycol (EGH2) react with silica sources, such a
136 , poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether, and poly(ethylene g
140 new class of nanoparticle antioxidants, poly(ethylene glycol)-functionalized hydrophilic carbon clust
142 ZnO have been found to slowly dehydrogenate ethylene glycol generating, after condensation with the
143 Triblock copolymers containing the blocks of ethylene glycol, glutamic acid and phenylalanine (PEG-PG
145 id-poly(ethylene imine)/hyaluronic acid-poly(ethylene glycol) (HA-PEI/HA-PEG) self-assembling nanopar
146 (HS(CH2)nH) demonstrates that SAMs of oligo(ethylene glycol) have values of beta (beta(EG)n = 0.29 +
148 Ms) of thiol-terminated derivatives of oligo(ethylene glycol) (HS(CH2CH2O)nCH3; HS(EG)nCH3); these SA
149 re, by means of a model system of 4-arm poly(ethylene glycol) hydrogels crosslinked with multiple, ki
151 ologous PMN-conditioned medium (PCM) on poly(ethylene glycol) hydrogels, poly(dimethyl siloxane), and
152 Herein, the polymer conformation of poly(ethylene glycol) is detailed and compared with those of
153 of Al in protonic solvents (e.g., water and ethylene glycol), is validated as the actual reducing ag
156 , were prepared by a short sequence from the ethylene glycol ketal of hydrocodone; a carbocyclic anal
157 n, the N-terminal leptin conjugate with poly(ethylene glycol) (LepNPEG5K), and two conjugates of lept
158 ith low and high molecular weight additives (ethylene glycol, linear polyacrylamide and poly(ethylene
163 we examine the different mechanisms of poly(ethylene glycol)-mediated fusion of small unilamellar ve
164 hetic, injectable hydrogels based upon oligo(ethylene glycol) methacrylate (OEGMA) monomers has been
165 ox-insensitive), which consist of poly(oligo(ethylene glycol) methacrylate) (POEG) hydrophilic blocks
166 uling layer of a polymer brush of poly[oligo(ethylene glycol) methacrylate] grown by surface-initiate
167 nmodified gold nanoparticles into poly(oligo(ethylene glycol)methacrylate) (POEGMA) brushes grown on
168 k copolymerization by sequential addition of ethylene glycol methyl ether acrylate and PEGA480 to a p
169 introducing an acetic acid terminated poly (ethylene glycol) methyl ether (aaPEG) onto the Thr resid
170 es (SPE) through a blend formation with poly(ethylene glycol) methyl ether (mPEG) to prevent its leac
171 rylate monomers, including macromonomer poly(ethylene glycol) methyl ether acrylate (PEGA480), tert-b
172 eous precipitation polymerization (PP) of di(ethylene glycol) methyl ether methacrylate (MEO2MA), a t
173 black nanoparticles functionalised with poly(ethylene glycol) methyl ether of mean molecular weight 5
174 es by functionalizing the nanorods with poly(ethylene glycol) methyl ether thiol (PEG-thiol) prior to
176 ricate ligand-conjugated alginate-graft-poly(ethylene glycol) microspheres for intracellular delivery
177 oxidation variants of pegfilgrastim, a poly(ethylene glycol) modified recombinant human granulocyte-
179 odification is the attachment of methoxypoly(ethylene glycol) (mPEG), termed PEGylation, which has le
181 ly used low-fouling carboxy-functional oligo(ethylene glycol) (OEG)-based alkanethiolate self-assembl
182 ition, observed well below the LCST of oligo(ethylene glycol) (OEG)-based dendrons, where the host-gu
183 ethylenimine (PEI) (35.3 +/- 6.6 nm) or poly(ethylene glycol) of anionic poly(acrylic acid) (PAA-EG)
184 nhibitor pharmacophores, coupled with either ethylene glycol oligomeric or polymeric diamines to yiel
185 s are varied to include, for instance, oligo(ethylene glycol) or chains containing 1,2,3-triazole uni
186 three different coatings: Poly(acrylic acid-ethylene glycol) (PAA-EG), polyethylenimine (PEI) and po
187 ditives based on palmitic acid-modified poly(ethylene glycol) (Pal-PEG) are combined with a tailored
189 xploiting the phase-separating polymers poly(ethylene) glycol (PEG) and dextran (DEX) have been used
192 antification of the pharmacokinetics of poly(ethylene glycol) (PEG) and PEGylated molecules is critic
194 ug delivery vehicles, are conjugated to poly(ethylene glycol) (PEG) as this improves their bioavailab
195 e synthesis of 12 variations of the PLA-poly(ethylene glycol) (PEG) based precision-polyester (P2s) p
196 ore-photocleavable, poly(norbornene)-co-poly(ethylene glycol) (PEG) brush-arm star polymers (BASPs) v
197 he reversible attachment of lysozyme to poly(ethylene glycol) (PEG) by degradable carbamate linkers.
203 des of increasing chain length and with poly(ethylene glycol) (PEG) changing certain physicochemical
206 the thresholds for NP size and surface poly(ethylene glycol) (PEG) density for penetration within tu
208 arrays were further micropatterned with poly(ethylene glycol) (PEG) gel to define annular cell adhesi
211 mal stem cells (hMSCs) cultured on soft poly(ethylene glycol) (PEG) hydrogels (Young's modulus E ~ 2
212 e flexibility of peptide-functionalized poly(ethylene glycol) (PEG) hydrogels for modeling tumor prog
213 lls were cultured on chemically-defined poly(ethylene glycol) (PEG) hydrogels formed by "thiol-ene" p
214 ar remodeling of peptide-functionalized poly(ethylene glycol) (PEG) hydrogels that degrade in respons
215 we have shown that the introduction of poly(ethylene glycol) (PEG) improves pharmacokinetics, includ
219 an engineered calmodulin (CaM) within a poly(ethylene glycol) (PEG) matrix that involves the reversib
223 oparticles coated with either non-ionic poly(ethylene glycol) (PEG) or zwitterionic poly(carboxybetai
224 bed on a biocompatible amine-terminated poly(ethylene glycol) (PEG) polymer brush and further functio
225 cent signal as a hydrogel consisting of poly(ethylene glycol) (PEG) polymerizes on top of the cellulo
226 The DSPEI is further grafted with a poly(ethylene glycol) (PEG) section to afford high carrier st
227 ed mucic acid segment and a hydrophilic poly(ethylene glycol) (PEG) tail were non-covalently complexe
228 ethylene glycol) diacrylate (PEGDA) and poly(ethylene glycol) (PEG) that were solidified by the actio
231 racterization of proteins modified with poly(ethylene glycol) (PEG), such as recombinant human granul
233 sules were subsequently placed within a poly(ethylene glycol) (PEG)-coated poly(epsilon-caprolactone)
234 ne modified membranes, and conventional poly(ethylene glycol) (PEG)-grafted membranes, the HPG grafte
235 We present unexpected evidence that a poly (ethylene glycol) (PEG)-lipid conjugate enables cholester
236 the efficacy of two stir bar coatings, poly(ethylene glycol) (PEG)-modified silicone (EG-Silicone) a
237 polyion complex of SOD1 with polycation poly(ethylene glycol) (PEG)-polylysine (single-coat (SC) nano
242 on of natural clay mineral particles in poly(ethylene glycol) (PEG)/dextran (Dx) aqueous two-phase sy
243 containing both ammonium bisulfate and poly(ethylene glycol) (PEG-300), likely due to diffusion and
244 nically validated poly(D,L-lactide) and poly(ethylene glycol) (PEG-Dlink(m)-PDLLA) for safe and effec
245 1V, and W14A mutants on the kinetics of poly(ethylene glycol)(PEG)-mediated fusion of small unilamell
246 LC/MS analysis of 5000 molecular weight poly(ethylene glycol) (PEG5000) generated an average charge s
247 ethylene glycol)-poly(propylene glycol)-poly(ethylene glycol) (PEO-PPO-PEO) triblock copolymers (Plur
248 between poly(lactic-coglycolic acid)-b-poly(ethylene glycol) (PLGA-b-PEG) and an endothelial-targete
249 tely 60 nm) (AuNR = gold nanorod; PEG = poly(ethylene glycol); PLGA = poly(lactic-co-glycolic acid))
250 poly(maleic anhydride-alt-1-octadecene)-poly(ethylene glycol) (PMAO-PEG), which are anionic, cationic
251 and doxorubicin (Dox) co-loaded Methoxy poly(ethylene glycol)-poly(epsilon-caprolactone) (MPEG-PCL) n
252 ; the resulting DA-TAT is conjugated to poly(ethylene glycol)-poly(epsilon-caprolactone) (PEG-PCL, PE
254 dium dodecyl sulfate (SDS) and nonionic poly(ethylene glycol)-poly(propylene glycol)-poly(ethylene gl
255 olymers composed of poly(l-lactide) and poly ethylene glycol/poly(-caprolactone), allowing diffusion-
256 ch were obtained by vesicle fusion on a poly(ethylene glycol) polymer brush functionalized with fatty
259 ly, poly(p-phenylene) beta-cyclodextrin poly(ethylene glycol) (PPP-CD-g-PEG) combined with gold nanop
261 hydraulic fracturing compounds (2-propanol, ethylene glycol, propargyl alcohol, 2-butoxyethanol, and
264 lymers that incorporate dimethylsiloxane and ethylene glycol repeat units within the side chains, all
265 or the ESI-MS analysis of several large poly(ethylene glycol)s (PEGs), up to 40 kDa, typical of those
268 dying in-house prepared, low dispersity poly(ethylene glycols)s (PEGs), also known as poly(ethylene o
269 glycol) (Alg-g-PEG) and alginate-graft-poly(ethylene glycol)-S-S-arginine-glycine-aspartic acid (Alg
273 M) containing maleimide end groups and oligo(ethylene glycol) spacer segments was achieved through a
278 n (G protein-coupled receptor inhibitor) and ethylene glycol tetraacetic acid (calcium chelator) sugg
279 and systemically, while the Ca(2+) chelator ethylene glycol tetraacetic acid (EGTA) significantly re
280 lso used other absorption enhancers, such as ethylene glycol tetraacetic acid (EGTA), or inhibitors,
282 ubstantially enhanced in poorly polarized or ethylene glycol tetraacetic acid-treated cells, indicati
283 old nanoparticles capped with thiolated poly(ethylene glycol), the measured grafting densities across
284 anches separately modified with methoxy-poly(ethylene glycol)-thiol (PEG) to improve their stability,
286 side chains, allowing short chains of oligo(ethylene glycol) to be solubilised within silicone oil a
287 organocatalysts for the polyaddition of poly(ethylene glycol) to hexamethylene diisocyanate in soluti
288 f di-stearyl lipid tails linked through poly(ethylene glycol) to the peptide exhibited higher exocyto
290 armycin SA that feature the incorporation of ethylene glycol units (n = 1-5) into the methoxy substit
295 ed from the KCl matrix and transferred in an ethylene glycol-water solution to support materials form
297 lactose, glucose, carboxybetaine, and oligo(ethylene glycol) were installed via postpolymerization t
299 as quantum dot-polymer hybrids, DNA and poly(ethylene glycol)), which still require, for the most par
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