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1 PEI (-s-s-) derivative (16 kDa) showed excellent transfe
2 PEI (-s-s-) polyplexes showed higher transfection effici
3 PEI adjuvanticity required release of host double-strand
4 PEI controls the release rate, dependent on the charge c
5 PEI formed nanoscale complexes with antigen, which were
6 PEI increased the particle porosity, drug entrapment, an
7 PEI is suggested and discussed to act in several manners
8 PEI therefore merits further investigation as a mucosal
9 PEI-C(60) (CO2 absorption of 0.14 g/g at 0.1 bar/90 degr
10 PEI-CNT fiber microelectrodes were resistant to surface
11 PEI-CNT fibers have lower overpotentials and higher sens
12 PEI-microbubbles coupled to a luciferase bioluminescence
15 Furthermore, compared to perphenazine alone, PEI-P conjugates exhibit an enhanced inhibitory effect d
17 Strikingly, as predicted by the HLCA and PEI models, the first-step decision dynamics were initia
19 Using this spinal nerve injection approach, PEI/DNA polyplexes were delivered to DRG neurons without
21 s for dopamine were adsorption controlled at PEI-CNT fiber microelectrodes, independent of scan repet
23 predicted a strong attractive force between PEI-coated MNPs and algae, which supported the improved
24 nce resonance energy transfer (FRET) between PEI shielded AuNPs (AuNPEI) and DOX was achieved upto 10
25 acid treatment, the first covalently bonded PEI layer and some realigned PAA remained on the membran
26 Systematic studies on the impact of both PEI content and relative humidity on the CO2 capture cap
28 n efficiency: 3.6 times higher than branched PEI 25 kDa in HeLa cells and 7.4 times higher than Lipof
31 ts sites are external and another one, bulky PEI, capable of low CO2 adsorption due to the internal p
37 ine)s with modified surface characteristics, PEI-based copolymers as well as conjugates with bioactiv
41 after I.Vag immunisations, while in contrast PEI and Chitosan were able to induce TT-specific systemi
44 gher transfection efficiency for each cyclic PEI sample when compared to its linear PEI analogue in a
45 iency and cell cytotoxicity, a set of cyclic PEIs were prepared for the first time and compared to a
46 ion has been paid on synthesis of degradable PEI derivatives using low MW one because low MW PEI is m
47 trated the efficacy and safety of delivering PEI/DNA polyplexes to DRG neurons via spinal nerve injec
50 nasal, sublingual or vaginal delivery of DNA-PEI polyplexes to prime immune responses prior to mucosa
55 V structure and function at baseline, during PEI and following administration of 5 mg bisoprolol (bet
57 nd biodegradable CaCO3- poly(ethyleneimine) (PEI) nanostructured microparticles (MPs) to detect and r
58 developed a bioreducible poly(ethylenimine) (PEI (-s-s-)) derived from low molecular weight PEI (1.8
62 conducted by first dissembling the existing PEI-PAA bilayers using strong acid and then reassembling
63 PEI are present in the sorbent, one exposed PEI layer that is responsible for higher CO2 adsorption
66 tch-1 shRNA in this report, Fe3O4@SiO2(FITC)/PEI-FA can be exploited as a novel, non-viral, and concu
67 c targeting capabilities of Fe3O4@SiO2(FITC)/PEI-FA, our results show that by complexing with a secon
68 cant preferential uptake of Fe3O4@SiO2(FITC)/PEI-FA/Notch-1 shRNA nanocomplex by MDA-MB-231 cells.
69 Our results showed that Fe3O4@SiO2(FITC)/PEI-FA/Notch-1 shRNA nanoparticles are 64 nm in diameter
71 ting higher CO2 capacity and uptake rate for PEI supported in a hydrophobically modified silica, whic
76 ults demonstrate that mRNA delivery using GO-PEI-RNA complexes can efficiently generate "footprint-fr
80 e)/hyaluronic acid-poly(ethylene glycol) (HA-PEI/HA-PEG) self-assembling nanoparticle-based non-viral
87 R received four cycles of PE and ifosfamide (PEI) at total doses of platinum 420 mg/m(2), etoposide 1
88 of particular plating additives (SPS, Imep, PEI, and PAG) used in the semiconductor industry for the
89 antibody cetuximab to poly(ethylene imine) (PEI) via a PEG-spacer and subsequent DNA or siRNA comple
90 polymers, specifically poly(ethylene imine) (PEI), are promising gene delivery vectors due to their i
92 however, 8-fold more cadmium accumulated in PEI QD-treated leaves than in those exposed to PAA-EG QD
99 oreflex activation (post-exercise ischaemia; PEI) following leg cycling exercise, (3) isometric handg
100 n New York, Maine, and Prince Edward Island (PEI), Canada, all have nearly identical genotypes that d
102 n this work, we present a crosslinked linear PEI (xLPEI) system in which either disulfide-responsive
103 alled dPEI (a nearly fully hydrolysed linear PEI with 11% additional free protonatable nitrogen atoms
104 yclic PEI sample when compared to its linear PEI analogue in addition to reduced toxicity relative to
107 lyzes these techniques applied to liposomal, PEI, dendrimer, stem cell and viral gene delivery system
109 Improvements in the synthesis of tailor-made PEIs in combination with new in-depth analytical techniq
110 agarose particles were modified with MANAE, PEI and glyoxyl groups and evaluated to stabilize polyga
111 following exercise with a large muscle mass (PEI following leg cycling) is there a contribution from
113 structure complexed with galactose-modified PEI could generate effective RNAi-mediated gene silencin
114 2/N2 at 23 degrees C, the uptake of modified PEI, G2, and G3 supported on SBA-15PL was 2.07, 2.35, an
115 dsorption capacity of PME-supported modified PEI and G3 was significantly higher, reaching 4.68 and 4
119 mmetry (CV) and UV-vis methods on the MWCNT-(PEI/DNA)2/OPH/AChE biosensor, showing great potential in
120 terization of PEI-coated gold nanoparticles (PEI-AuNP), which were applied as a new platform in the i
121 elevated temperatures when compared to neat PEI films and other high-temperature polymer and nanocom
123 ative humidity increased CO2 capacity of NFC/PEI foams at the expense of a high H2O uptake in the ran
127 t the critical role that the architecture of PEI can play in both optimizing transfection and reducin
128 cribes the synthesis and characterization of PEI-coated gold nanoparticles (PEI-AuNP), which were app
130 odel it was demonstrated that co-delivery of PEI-(pBMP-2+pFGF-2) embedded in collagen scaffolds resul
131 suggest that these less toxic derivatives of PEI could be utilised for topical plasmid DNA vaccine de
133 NA vaccine complexed to a less toxic form of PEI called dPEI (a nearly fully hydrolysed linear PEI wi
134 results demonstrate that less toxic forms of PEI can be effective delivery vehicles for plasmid DNAs
140 e in vivo ultrasound contrast persistence of PEI-microbubbles was measured in the healthy mouse kidne
141 e characterized and revealed the presence of PEI as well as its interaction with CO2 at low temperatu
143 Transfection efficiency and toxicity of PEI are highly dependent upon their molecular weight and
145 d non-degradability although the toxicity of PEI depends on its molecular weight (MW) and structure.
148 and positively charged (zeta = +40 mV), PEG-PEI (MSNPs modified with exposed polyamines), but not PE
149 ggests that, in addition to facilitating PEG/PEI nanocomplex delivery from the bloodstream to tissue,
150 -fold increase in luciferase activity in PEG/PEI nanocomplex-treated muscles over muscles treated wit
154 n polyethylene glycol-polyethyleneimine (PEG/PEI) nanoparticles and loaded into ESTA-MSV microparticl
157 onsistently greater after treatment with PEG/PEI nanocomplexes at 0.6 MPa as compared to 0.8 MPa.
158 ar motif, the polyethylenimine-perphenazine (PEI-P) conjugate which has a dual "acceleration-inhibiti
160 hosphorylation of AKT was inhibited by [pIC](PEI) in PDAC, and this event was critical for stimulatin
162 proof-of-concept for the evaluation of [pIC](PEI) as an immunochemotherapy to treat pancreatic cancer
164 mulation of pIC with polyethylenimine ([pIC](PEI)) in PDAC and investigated its mechanism of action.
165 deliver polyethylenimine mixed with plasmid (PEI/DNA polyplexes) containing green fluorescent protein
167 prising polyethylenimine-polyethyleneglycol (PEI-PEG) tethered to the PSMA ligand, 2-[3-(1, 3-dicarbo
171 ed with g-C3N4, TiO2, and polyethyleneimine (PEI) and then the amine terminal aptamerTROP probe was a
172 ion dendrimers as well as polyethyleneimine (PEI) were developed for the selective removal of SO2.
173 eglycol 2000, azobenzene, polyethyleneimine (PEI)(1.8 kDa), and 1,2-dioleyl-sn-glycero-3-phosphoethan
174 of non-covalently coupled polyethyleneimine (PEI) and folic acid (FA) to the magnetic and fluorescent
175 d with CNT dispersions in polyethyleneimine (PEI) provided lower overpotentials, higher sensitivity a
176 c polymers such as linear polyethyleneimine (PEI), tiRNA assembled to form a stable nano-structured c
177 th a final outer layer of polyethyleneimine (PEI), for the local therapeutic treatment of colonic inf
178 rodes with the polycation polyethyleneimine (PEI) prior to adsorption of CDH from Myriococcum thermop
179 es a hydrophilic polymer, polyethyleneimine (PEI), into the thermally responsive hydrogel poly(N-isop
182 Ps were synthesized using polyethyleneimine (PEI) as a capping agent, resulting in particles with an
183 a proof-of-concept where polyethyleneimine (PEI) is converted to a high capacity and highly selectiv
184 thus functionalized with polyethyleneimine (PEI) and the functionalized silica nanoparticles ((f)Si
185 thus functionalized with polyethyleneimine (PEI) and the functionalized silica nanoparticles ((f)Si
186 t evaporation method with polyethyleneimine (PEI) as a porosigen and characterized the formulations f
187 chemically modified with polyethyleneimine (PEI), which showed good effectiveness for the immobiliza
188 ammonium](+) (PDDA), [Polyethyleneimine](+) (PEI), [Polystyrene sulfonate](2-) (PSS) and neutral poly
191 demonstrated with aqueous polyethylenimine (PEI) adsorbed onto mica substrates, which has a large co
192 the commercially available polyethylenimine (PEI), have the ability to deliver genetic material into
193 We show that branched polyethylenimine (PEI) beads obtained from an inverse suspension process c
194 nctionalized with branched polyethylenimine (PEI) molecules for efficient interparticle cross-linking
196 S QDs coated with cationic polyethylenimine (PEI) (35.3 +/- 6.6 nm) or poly(ethylene glycol) of anion
197 (QDs) coated with cationic polyethylenimine (PEI) were more toxic to pure cultures of nitrogen-cyclin
198 ethylene glycol) (PAA-EG), polyethylenimine (PEI) and poly(maleic anhydride-alt-1-octadecene)-poly(et
199 with one of the following: polyethylenimine (PEI)+TSP-2 siRNA, saline, PEI only, or PEI+control siRNA
200 loying graphene oxide (GO)-polyethylenimine (PEI) complexes for the efficient generation of "footprin
201 es with CNT fibers made in polyethylenimine (PEI), which have much higher conductivity than PVA-CNT f
204 NFC) and a high molar mass polyethylenimine (PEI) have been prepared via a freeze-drying process.
206 ted by assembling multiple polyethylenimine (PEI) and poly(acrylic acid) (PAA) bilayers on a polydopa
208 strate that disposition of polyethylenimine (PEI)/DNA polyplexes that were microinjected into the ooc
209 , which was immobilized on polyethylenimine (PEI)-functionalized carbon nanotube transducer on glassy
210 poly(ethyleneglycol) (PEG)/polyethylenimine (PEI) nanocomplex gene carriers and adjustments to US and
211 d with a cationic polymer, polyethylenimine (PEI), toward the separation of Scenedesmus dimorphus fro
212 the cells, especially the polyethylenimine (PEI) which has been used as a golden standard polymer ow
213 ding BMP-2) complexed with polyethylenimine (PEI) and made comparisons with PEI complexed with conven
214 es (O: 50 mum) coated with polyethylenimine (PEI) and SWCNTs were aligned to form a 2 x 2 junction ar
215 Condensing RepRNA with polyethylenimine (PEI) gave positive in vitro readouts, but was largely in
219 using the cationic linear polyethylenimines (PEI) as a gene carrier was investigated in adult mouse b
221 which has great doping affinity with polymer PEI to switch-off the fluorescence of P-CNDs, leading to
223 itively charged poly(ethyleneimine) polymer (PEI) was self-assembled onto the Fe3O4@SiO2 by electrost
228 ormulations - [Rep/PEI-4,000 (1:3)] and [Rep/PEI-40,000 (1:2)/(Arg)9] were efficacious in vivo in mic
230 : (i) PEI molecular weight (MW); (ii) RepRNA:PEI (weight:weight) ratio; and (iii) inclusion of cell p
235 ) with multiple disulfide cross-linked short PEIs to harness the advantageous properties of GNR based
236 In this paper, a multifunctional Fe3O4@SiO2@PEI-Au/Ag@PDA nanocomposite catalyst with highly stabili
242 he PEI-decorated silica microparticles (SiO2@PEI MPs) were characterized using scanning electron micr
243 ults of this study show that the use of SiO2@PEI MPs is a promising and practical approach to ensure
244 tigates the selective deposition of the SiO2@PEI MPs on the damage area using confocal laser scanning
247 ntation allowed the analysis of the specific PEI-PEG-cetuximab binding to EGFR and the determination
251 m of siRNA, transferrin-polyethylenimine (Tf-PEI), to selectively deliver siRNA to ATCs in the lung.
252 n a murine asthmatic model confirmed that Tf-PEI polyplexes can efficiently and selectively deliver s
254 more resistant to oxidative degradation than PEI, even while containing secondary amines, as supporte
255 lyplexes was shown to be more effective than PEI/siRNA polyplexes in three cell lines with the follow
258 ysisorption analysis, the data indicate that PEI first forms a thin conformal coating on the pore wal
261 roism, and atomic force microscopy show that PEI-P conjugates accelerate formation of Abeta prefibril
262 bone defect model in rats, it was shown that PEI-cmRNA (encoding BMP-2)-activated matrices promoted s
267 ositive charge of the Cu-NPs imparted by the PEI allowed a simple electrostatic functionalization of
271 arge-discharge efficiency is achieved in the PEI sandwiched with CVD-grown h-BN films at elevated tem
273 livery allows for the direct delivery of the PEI-siRNA nano-complex to the central nervous system, wh
274 Cell viability assays indicate that the PEI-P conjugates reduce the cytotoxicity of Abeta aggreg
281 e terminal aptamerTROP probe was attached to PEI by the use of glutaraldehyde (GA) as cross-linker.
284 t mucosally applied plasmid DNA complexed to PEI followed by a mucosal protein boost generates suffic
289 recise modifications of low molecular weight PEI improve its bio-responsiveness and yield delivery ve
290 rovide optimal DNA delivery activity whereas PEIs with molecular weights below 1.8kDa are ineffective
292 ethylenimine (PEI) and made comparisons with PEI complexed with conventional plasmid DNA (encoding BM
293 lex virus type-2 (HSV-2) glycoprotein D with PEI elicited robust antibody-mediated protection from an
294 ing bystander cells such as fibroblasts with PEI/DNA complexes leads to efficient cross-presentation
296 tudy demonstrated that scaffolds loaded with PEI-(pBMP-2+pFGF-2) could be an effective way of promoti
297 IR-GR group, and escalation of therapy with PEI did not significantly improve OS and EFS in patients
298 vested from mouse liver and transfected with PEI DNA and calcium phosphate DNA nanoparticles in 384-w
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