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1                                              PMMA exists in three different isomeric forms, namely, i
2                                   Nearly 100 PMMA chips were replicated using a single silicon master
3 hen coated with fibronectin: silicone (n=6), PMMA (n=6), and acrylic (n=6).
4                                            A PMMA chip was employed as the microarray device, where z
5                                            A PMMA sheet with an imprinted microchannel was clamped to
6 epared for optical measurements by bonding a PMMA ring to the sclera in the region of the ciliary bod
7 dance one-bond (1)H-(13)C RDCs measured in a PMMA gel and a (3)J coupling constant analysis.
8 ge mapping of polyamine charge carriers in a PMMA matrix is reported.
9 electrophoretic separations of proteins in a PMMA-based microchip.
10              Additionally, the presence of a PMMA or PHEMA overlayer significantly decreased the sput
11 .5, 0.4, 0.6, and 0.1 ppm were obtained on a PMMA film containing 25% w/w di(2-ethylhexyl) phthalate
12 2+), and Pd(2+) were reduced and plated on a PMMA surface and Fe(CN)(6)(3-) was reduced to Fe(CN)(6)(
13 sed hairpin configuration when strapped to a PMMA surface as opposed to glass.
14  guiding layer and a sensing layer or with a PMMA waveguide and a chemically sensitive polymer.
15 s covalently attached onto this UV-activated PMMA surface were evaluated and compared with the same M
16 reaches Ca's bulk heat of sublimation on all PMMA surfaces, where pure, bulk-like Ca thin films form.
17 photocurable resin modified with anisole and PMMA-filled microcapsules.
18 was determined that both silanized glass and PMMA gave working optodes, but the ones on PMMA did not
19 and 688 +/- 54 microm on silanized glass and PMMA, respectively, and the 0.50-mm tips produced diamet
20  microm were obtained on silanized glass and PMMA, respectively, using the polypropylene tips for spo
21 s, ceramics, and polymers, Ni, Si, HfO2, and PMMA, respectively.
22                      A STEP OD-2 monitor and PMMA was used in a simulated environment to estimate the
23 rradiation, the junction between d(8)-PS and PMMA blocks is photocoupled through the anthracene photo
24 iency in the mixed 10/15 mum diameter PS and PMMA particle solutions tested.
25                             Even when PS and PMMA particles have the same diameters, they exhibit str
26 rate these predictions by translating PS and PMMA particles simultaneously in a stationary flow.
27                          Well defined PS and PMMA supramolecular polymers with molecular weights up t
28 homogeneity for the sputter yields of PS and PMMA.
29 S ((13)C-PS) and unlabeled PS ((12)C-PS) and PMMA were synthesized using atom-transfer radical polyme
30 ectra are presented for both bare silver and PMMA-coated silver gratings at a range of angles and pol
31  performance is observed only in toluene and PMMA film.
32 the PMMA resin at 0.1, 0.2, and 0.3 wt%, and PMMA resin without AgBr/NPVP served as the control.
33                             Slow kinetics at PMMA-transferred graphene is attributed to the presence
34 2-3 orders of magnitude higher than those at PMMA-transferred graphene, which demonstrates an anomalo
35 bution of the isomeric content in an atactic PMMA sample is determined quantitatively by fractionatin
36 l acrylate-block-methyl methacrylate) (PBA-b-PMMA).
37 rrently, anthracene-functionalized d(8)-PS-b-PMMA BCP is one of the most promising candidates for the
38 -type phase behavior of its parent d(8)-PS-b-PMMA di-BCPs.
39 ual detection in SEC are evaluated with PS-b-PMMA diblock copolymers to determine the comonomer compo
40         The cation exchange capacity of bare PMMA capillaries was on the order of 1 pequiv/mm(2) with
41    Bonding of the embossed layer and a blank PMMA layer to generate the microchip was achieved by sol
42 mprinted microchannel was clamped to a blank PMMA sheet, and then 80 +/- 5 muL of acetone (bonding so
43 2-(dimethylamino)-ethyl methacrylate) block (PMMA-b-PDMAEMA), was synthesized.
44                           Surface binding by PMMA overlayers results in stable surface binding even a
45 e lower autofluorescence levels exhibited by PMMA at the detection wavelengths used and the improved
46 ponse, yet the negative impact on T(REGS) by PMMA remains persistent.
47 ies confirmed a higher hydrocarbon uptake by PMMA in the presence of plasticizer.
48                          Cylinders of coated PMMA were implanted in porcine corneas ex vivo for 2 wee
49  prepared on gold substrates by spin coating PMMA dissolved in toluene.
50    The sensor was fabricated by spin coating PMMA onto a quartz crystal, and the influence of plastic
51 nally, we examine the fabrication compatible PMMA coating as a viable passivation layer.
52 ponents of molecules dissolved in compressed PMMA gels, allowing a rapid and direct one-shot determin
53                               In conclusion, PMMA-modified AFM probes have shown to be a reliable tec
54                 We also show that contacting PMMA with Teflon depletes this electronic surface charge
55 e graphene films obtained using conventional PMMA-assisted transfer technique exhibits PMMA residues,
56      Fluorescent and positively charged core PMMA-NPs of nearly 60nm, obtained through an emulsion co
57  computations performed on analogue coronene/PMMA oligomers and a reasonable agreement was obtained.
58 o 48.2 cP and suspensions of 10-mum-diameter PMMA particles with particle volume fractions phi = 0.16
59 ermore, it is found that blends of different PMMA isomers with similar molecular weights can be fract
60              ThFFF analysis of the different PMMA isomers in tetrahydrofuran, acetonitrile (ACN), and
61 in the crystalline state and in highly doped PMMA films which are indicative of aggregation induced e
62  the CRP assay, neutravidin-coated PQQ-doped PMMA nanospheres are used to bind with a biotinylated re
63 ole, and efficiencies comparable to embossed PMMA and laser ablated glass chips were obtained.
64  then used as a secondary mold for embossing PMMA, a polymeric substrate with a lower Tg ( approximat
65 al PMMA-assisted transfer technique exhibits PMMA residues, which degrade the sensing performance of
66                          Anti-TNF-alpha/FNAB/PMMA matrix was then integrated over comb structured gol
67 in undiluted serum using Anti-TNF-alpha/FNAB/PMMA/Au reveal that system can detect TNF-alpha in 100pg
68 sion) and highly isospecific ([mm] > 95% for PMMA; [mm] > 99% for PBMA) via enantiomorphic-site contr
69 a from the same buffer are also obtained for PMMA (M = 49 kDa).
70 se, while measurable change was not seen for PMMA.
71                                         Four PMMA lenses received an excimer laser ablation of -6 D w
72  hydrocarbon sensitivity of plasticizer-free PMMA is negligible, while the sensitivity of plasticized
73 e polymers in the negative ion mode and from PMMA and PLA in the positive ion mode.
74 ) coupling to carboxylic acid functionalized PMMA micropillars.
75 ercially available polymer substrates (e.g., PMMA), rendering them suitable for fabricating flexible
76 th methyl methacrylate (MMA) yields PE-graft-PMMA with narrow polydispersities and increasing PMMA co
77 ides were demonstrated using the PEG-grafted PMMA muCE chips.
78 ively a physical mixture of homo-PE and homo-PMMA is obtained.
79                       Porphyrin-doped hybrid PMMA [poly(methyl methacrylate)] polymer films demonstra
80 let excited states in the solid state and in PMMA films with lambda(em)(max) = 621-784 nm.
81 ip capillary electrophoresis (CE) devices in PMMA were created and tested.
82 strate that there are available electrons in PMMA that can participate in redox reactions at a rather
83                 Laser engraving and holes in PMMA along with spacing from surface provide fluidic cha
84      The MSF architecture is manufactured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)]
85 lated magnetic gamma-FeO(x) nanoparticles in PMMA matrix upon applying a magnetic field from 0 to 300
86 on and emission spectroscopy in solution, in PMMA and neat thin films.
87 for decreased IT band energies and widths in PMMA and provides important insight into electron transf
88  with narrow polydispersities and increasing PMMA content at longer reaction times.
89 omparison study suggests that an inexpensive PMMA IOL design modification-a squared optic edge-could
90  nanoparticle self-assembly from inexpensive PMMA-based materials present an attractive alternative t
91 microchip was prepared by hot embossing into PMMA from a brass mold master fabricated via high-precis
92  reduced beta (beta)-relaxation of isotactic PMMA most efficiently suppresses vibrational triplet dec
93  Nanoparticles with complementary st- and it-PMMA ligands could then be spontaneously assembled upon
94 nated syndiotactic (st-) and isotactic (it-) PMMA polymers were prepared and subsequently functionali
95 sion electron microscopy (TEM) measurements, PMMA oligomers conformally coat the metal-oxide nanopart
96                             Mechanistically, PMMA particles induce T(REG) instability evident by redu
97 oven cytotoxicity, poly-methyl methacrylate (PMMA) resin is one of the most frequently and extensivel
98                    Poly-methyl methacrylate (PMMA)-based dental resins with strong and long-lasting a
99 ulfate (CaSO4) and poly methyl methacrylate (PMMA).
100 wth substrate using polymethyl methacrylate (PMMA) and a wet etch to allow the user to transfer the f
101 (polystyrene (PS)-b-polymethyl methacrylate (PMMA) block copolymers (BCP)) using either ultralow ener
102 ridge integrating a polymethyl methacrylate (PMMA) micro-reactor with a polycarbonate (PC)-based pris
103 raphy at 100 kV and polymethyl methacrylate (PMMA) resist at different thicknesses.
104  laser engraving of polymethyl methacrylate (PMMA) sheet as off surface matrix was integrated in very
105 ointegration, using polymethyl methacrylate (PMMA)--the principal component of the Boston KPro--as a
106          Ultrathin poly(methyl methacrylate) PMMA films were prepared on gold substrates by spin coat
107 line coated with poly (methyl methacrylate) (PMMA) and a sensing line coated with a chemically sensit
108 lysorbate 80, and poly(methyl methacrylate) (PMMA) as analytes.
109  sensitivity of a poly(methyl methacrylate) (PMMA) based QCM sensor can be significantly enhanced for
110 and a hydrophobic poly(methyl methacrylate) (PMMA) block was developed to similarly reduce the minera
111 ene (d(8)-PS) and poly(methyl methacrylate) (PMMA) blocks, as well as a short middle block of poly(2-
112 n (LDR) and (2) a poly(methyl methacrylate) (PMMA) chip for the detection of the LDR products using a
113 ly used spherical poly(methyl methacrylate) (PMMA) colloids, suspended in an apolar organic medium.
114 c" hydroxyapatite/poly(methyl methacrylate) (PMMA) composites are developed by processing large-scale
115     We describe a poly(methyl methacrylate) (PMMA) dip-coating procedure, which results in surface st
116 iated with a thin poly(methyl methacrylate) (PMMA) film that is coupled to a silver-coated diffractio
117 uene, chloroform, poly(methyl methacrylate) (PMMA) film, and powder state, while its analogue CDB2 (o
118  the conventional poly(methyl methacrylate) (PMMA) for graphene transfer from a growth substrate.
119                   Poly(methyl methacrylate) (PMMA) gels prepared by copolymerizing methyl methacrylat
120 micromachining on poly(methyl methacrylate) (PMMA) has the potential for flexible, low cost, rapid pr
121 470 nm) both in a poly(methyl methacrylate) (PMMA) matrix and in solution at 77 K.
122               The poly(methyl methacrylate) (PMMA) microchips feature integral in-plane contactless c
123 sis separation in poly(methyl methacrylate) (PMMA) microchips.
124 hemistries within poly(methyl methacrylate) (PMMA) microfluidic channels that enabled specific and se
125  respectively, on poly(methyl methacrylate) (PMMA) micropillar surfaces, as well as assessing ligand-
126 ive silver-coated Poly(methyl methacrylate) (PMMA) microspheres (50 mum diameter) into tailored patte
127 ystyrene (PS) and poly(methyl methacrylate) (PMMA) microspheres based entirely on their difference in
128 ), is loaded into poly(methyl methacrylate) (PMMA) nanospheres in the presence of methanol.
129                   Poly(methyl methacrylate) (PMMA) optical fibers in a series of different diameters
130 system utilizes a poly(methyl methacrylate) (PMMA) or glass substrates sputtered by 40-nm-thick gold
131 ls in an embossed poly(methyl methacrylate) (PMMA) piece are filled with a heated liquid (paraffin wa
132               As poly (methyl methacrylate) (PMMA) remains the main material employed in the fabricat
133 by using a porous poly(methyl methacrylate) (PMMA) sacrificial layer, which creates a space between t
134 wn on electrospun poly(methyl methacrylate) (PMMA) scaffolds with a diameter of 0.938 +/- 0.304 um an
135 d for fabricating poly(methyl methacrylate) (PMMA) separation microchips is introduced.
136 netically coupled poly(methyl methacrylate) (PMMA) spheres with wavelength-scale diameters were recor
137 proximately 3 mm) poly(methyl methacrylate) (PMMA) spherical beads, threaded on a flexible string.
138 nnel assembled in poly(methyl methacrylate) (PMMA) substrate connected to an amperometric detector.
139 ss-transferred on poly(methyl methacrylate) (PMMA) substrates and are easily coupled to microfluidic
140  system exploited poly(methyl methacrylate) (PMMA) substrates of high optical quality to fabricate a
141 ite directly on a poly(methyl methacrylate) (PMMA) surface (also known as plexiglass or acrylic).
142 ectron-irradiated poly(methyl methacrylate) (PMMA) surfaces at 300 K has been studied by adsorption m
143 rts consisting of poly(methyl methacrylate) (PMMA) that provide enhanced performance levels for molec
144  the formation of poly(methyl methacrylate) (PMMA) triple-helices.
145 through tuning of poly(methyl methacrylate) (PMMA) triple-helix stereocomplexes.
146 terfaced with a poly- (methyl methacrylate) (PMMA) well-containing holders resulting in a low cost mu
147 the separation of poly(methyl methacrylate) (PMMA) with regard to molecular microstructure.
148 st multilayers of poly(methyl methacrylate) (PMMA), poly(2-hydroxyethyl methacrylate) (PHEMA), and tr
149 fferent polymers, poly(methyl methacrylate) (PMMA), poly(ethylene terephthalate) (PET), poly(lactic a
150 droplets(13) with poly(methyl methacrylate) (PMMA), poly(n-butyl acrylate) (PBMA), poly(2-dimethylami
151  Silanized glass, poly(methyl methacrylate) (PMMA), polycarbonate, and poly(dimethylsiloxane) were te
152 asily accessible poly (methyl methacrylate) (PMMA), polyethylene terephthalate (polyester, PET), and
153 he thermoplastics poly(methyl methacrylate) (PMMA), polystyrene (PS), polycarbonate (PC), and cyclic
154 erimide (PEI) and poly(methyl methacrylate) (PMMA), were used to make the reusable secondary master a
155 zole) (TPBi), and poly(methyl methacrylate) (PMMA), without any exciplex formation, and its OLPL dura
156 laser-writing and poly(methyl methacrylate) (PMMA)-assisted lithographic processes, leading to unprec
157 es of interest on poly(methyl methacrylate) (PMMA)-covered monolayer MoS2 triangles.
158 al ligand loss in poly(methyl methacrylate) (PMMA).
159 ystyrene (PS) and poly(methyl methacrylate) (PMMA).
160 mally responsive poly (methyl methacrylate) (PMMA)/paper hybrid disk (PT-Disk) was developed as a nov
161 yrene (PS) and poly(methylene methacrylate) (PMMA).
162 nnels poised on a poly(methyl methacrylate), PMMA, chip.
163 ere replicated in poly(methyl methacrylate), PMMA, from a metal mold master.
164 was fabricated in poly(methyl methacrylate), PMMA, using a single-step, double-sided hot-embossing ap
165 e, stereoregular poly(methyl methacrylates) (PMMAs) were separated according to tacticity on a carbon
166 a-exonuclease onto poly(methylmethacrylate) (PMMA) micropillars populated within a microfluidic devic
167                The poly(methylmethacrylate), PMMA, chip contained 8 devices, each equipped with 16 cu
168  polymer nano-composite (AgBr/NPVP)-modified PMMA-based dental resin.
169 owth was inhibited on the AgBr/NPVP-modified PMMA resin compared to the control (P < 0.05), and the a
170 ber of fungal cells attached to the modified PMMA resin was considerably lower than in the control.
171 -bound nanospheres (ca. 20,000 PQQ molecules/PMMA particle).
172 ity of polymethylmethacrylate nanoparticles (PMMA-NPs) to promote survivin MB uptake in human A549 ce
173 ate measurement of IR absorption of nanothin PMMA films on glass and Silicon validates the robust cap
174                       The carrier ability of PMMA-NPs in A549 was examined by confocal microscopy.
175 3)(2+) and S(2)O(8)(2-) with the addition of PMMA powder.
176 ith two esters to form the Ca carboxylate of PMMA, because this reaction's heat would be close to tha
177 r dose for the breast simulated by 4.5 cm of PMMA was calculated with methods described in the "Europ
178              By varying the concentration of PMMA, spin coating speed and curing condition, we obtain
179                    Combining the low cost of PMMA manufacture and flexible designs of TADF molecules,
180 nal to the PTFE surface area; the effects of PMMA and glass balls were negligible by comparison.
181 the vertebral body, followed by injection of PMMA cement.
182       Importantly, intra-tibial injection of PMMA initiates an acute innate immune and inflammatory r
183 o the proposal of an adsorption mechanism of PMMA on aluminum oxide, which shows the formation of met
184 25 to 0.94, and the molecular weight (Mn) of PMMA-b-PAA was controlled from 10 kDa to 90 kDa.
185      This unprecedentedly high reactivity of PMMA-free CVD-grown graphene electrodes is fundamentally
186                               This series of PMMA-b-PAA block copolymers was synthesized by reversibl
187 kyl catalysts: a constant syndiotacticity of PMMA produced over a wide polymerization temperature ran
188 with a PS M(n) slightly smaller than that of PMMA underwent self-reorganization, exhibiting a differe
189 faces, is believed to be superior to that of PMMA-mediated samples.
190                           The versatility of PMMA stereocomplexation was highlighted by assembling hy
191 I) can be controlled by changing the wt % of PMMA in the dipcoating solution.
192                 HAp coatings were induced on PMMA discs after treatment with concentrated NaOH and co
193  on silanized glass and 839 +/- 28 microm on PMMA.
194 d PMMA gave working optodes, but the ones on PMMA did not fit the theoretical model.
195 h B) and fluorescein (FL), were performed on PMMA microchips to demonstrate the feasibility of the fa
196  the adhesion of Candida albicans cells onto PMMA surfaces by employing an atomic force microscopy (A
197  complement to the MBs when immobilized onto PMMA, and this was attributed to both the lower autofluo
198 ached to the acrylic than to the silicone or PMMA lenses (P<0.001).
199 n, we developed a simple, miniaturized paper/PMMA (poly(methyl methacrylate)) hybrid microfluidic mic
200 butadiene)-b-poly(methylmethacrylate), PS-PB-PMMA, triblock terpolymers, assemble into a monolayer at
201 riven by a microbial fuel cell (see picture; PMMA = poly(methyl methacrylate), E = electrode).
202 igible, while the sensitivity of plasticized PMMA was similar to or in some cases greater relative to
203 served trend in sensitivity for the polymers PMMA, poly(isobutylene), poly(epichlorohydrin), and poly
204   It was applied to a blend of two polymers, PMMA and PS.
205  to silicone (n=18), polymethylmethacrylate (PMMA; n=18), and acrylic (n=18) intraocular lenses in vi
206 t particles, such as polymethylmethacrylate (PMMA), which are persistently released following implant
207  to a 16-20 mum bore polymethylmethacrylate (PMMA) capillary.
208  used to apply dense polymethylmethacrylate (PMMA) microneedles to the skin models in a controlled an
209 of a suspended Au NP/polymethylmethacrylate (PMMA) polymer close packed monolayer results in one-dime
210 uoroethylene (PTFE), polymethylmethacrylate (PMMA), and borosilicate glass with no headspace.
211 f a square-edge (SE) polymethylmethacrylate (PMMA) intraocular lens (IOL) modification in comparison
212            Suspended polymethylmethacrylate (PMMA) membranes were used as shadow masks for defining o
213 e different particle materials (polystyrene, PMMA, and silica) of the same size (2 mum) led to each b
214       Different combinations of polystyrene, PMMA, and silica particles with a commercially available
215 Cyphochilus, we fabricate ultra-thin, porous PMMA films by foaming with CO2 saturation.
216 hotothermal biosensing principle in portable PMMA/paper-based analytical devices, which offers not on
217                                  On pristine PMMA, the initial sticking probability of Ca is 0.5, inc
218                        We show that pristine PMMA can spontaneously transfer electrons to species in
219 n yield, the observed effects through the PS/PMMA interface can be greatly minimized, thereby signifi
220 nd (13)C secondary ion yields through the PS/PMMA interface; however, it is shown that this behavior
221 ncreased the force and work required to pull PMMA cylinders out of porcine corneas ex vivo.
222  were successfully introduced to obtain as q-PMMA-b-PDMAEMA.
223                                The PVDF/GO/q-PMMA-b-PDMAEMA@PVA nanofibers has superhydrophilic prope
224                                        The q-PMMA-b-PDMAEMA in the nanofiber matrix was confirmed by
225 ication in comparison with a round-edge (RE) PMMA IOL or an SE hydrophobic acrylic IOL (SE-Acrylic).
226                                        An RE-PMMA IOL was implanted in the fellow eye in 46 patients
227  IOL eyes compared with the contralateral RE-PMMA eyes at all follow-up visits (P < 0.05).
228 s were 2% for SE-PMMA IOLs versus 37% for RE-PMMA IOLs in group A (P < 0.001), and 4% for SE-PMMA IOL
229                                       The RE-PMMA PCO rate did not plateau and continued to increase
230 ne is attributed to the presence of residual PMMA.
231                                The resulting PMMA substrate possessed the same features as those of t
232  for bilateral phacoemulsification had an SE-PMMA IOL implanted in 1 eye.
233 A IOLs in group A (P < 0.001), and 4% for SE-PMMA IOLs versus 10% for SE-Acrylic IOLs in group B (P =
234 year Nd:YAG capsulotomy rates were 2% for SE-PMMA IOLs versus 37% for RE-PMMA IOLs in group A (P < 0.
235  PCO score was significantly lower in the SE-PMMA IOL eyes compared with the contralateral RE-PMMA ey
236  PCO score was statistically lower in the SE-PMMA IOL eyes compared with the contralateral SE-Acrylic
237                               Significantly, PMMA strand exchange was demonstrated and utilized to re
238 lon and Teflon beads, but leaves the smaller PMMA beads essentially uncharged; the resulting electros
239  bonding solvent (acetonitrile) and softened PMMA from filling the channels.
240 mined in toluene and acetonitrile solutions, PMMA layers, solid films, and crystal phase.
241 y indistinguishable densities-Nylon spheres, PMMA spheres, and drug spheres-demonstrate the applicabi
242 ss of helical strand exchange, stereoregular PMMA/polyethylene glycol (PEG) block copolymers capable
243     The aligning properties of the stretched PMMA gels were evaluated by monitoring the quadrupolar s
244 te complex 4, however, produces syndiotactic PMMA predominantly via chain-end control.
245 aration of highly isotactic and syndiotactic PMMAs of different molar masses.
246 to ester groups below the CH3/CH2-terminated PMMA surface.
247                                We found that PMMA substrates welded together using this method could
248               Our measurements indicate that PMMA passivated black phosphorus thin film flakes can st
249 microscope (SEM) observations indicated that PMMA-b-PAA polymer treatment protected enamel from acid
250                         We further show that PMMA enhance T(H)17 response at the expense of other T e
251 n intra-tibial injection model, we show that PMMA particles abrogate the osteoclast suppressive funct
252  level, gene expression analysis showed that PMMA particles negatively regulate Nrp-1/Foxo3a axis to
253                                          The PMMA film sputtered in a controlled manner for SF(5)(+)
254                                          The PMMA films were transformed into highly reactive film co
255                                          The PMMA micro-chip was tested under an electric field stren
256                                          The PMMA microdevices were fabricated reproducibly and with
257 e waveguide surface by plasma activating the PMMA and the use of carbodiimide coupling chemistry.
258 surface was carried out by UV activating the PMMA to produce surface-confined carboxylate groups, whi
259                          In solution and the PMMA matrix the S1 of BET-B relaxes to a correlated trip
260 reduced the inflammatory response around the PMMA implants in vivo.
261                                 Exposing the PMMA surface to electrons increases Ca's initial stickin
262                                 However, the PMMA used for a redox reaction or contacted with Teflon
263 asured by PALS was significantly less in the PMMA films compared to the PIB, and this result correlat
264 nted into fluidic channels embossed into the PMMA substrate.
265  can be further tuned by complexation of the PMMA chains with lithium ions that are introduced into t
266 mum ion dose limited by the thickness of the PMMA film.
267                         The thickness of the PMMA overlayer on TiO2-Ru(II) can be controlled by chang
268       The erosion-preventing efficacy of the PMMA-b-PAA block copolymer in inhibiting HAP mineral los
269          As an example of the utility of the PMMA-based immobilization strategies developed for MBs,
270 These results demonstrate the ability of the PMMA-NPs to promote the survivin-MB internalization, sug
271  pulp cells were viable when cultured on the PMMA resin for 24 hours, while over 70% of the cells wer
272 (7 mm x 1 mm) positioned and centered on the PMMA substrate (33 mm x 9 mm).
273 nd where the SW bundles were embedded on the PMMA substrate, giving the electrode a high stability.
274 lity were verified after adsorption onto the PMMA-NPs.
275 were evident by using the MB loaded onto the PMMA-NPs.
276 les of SWs that were highly ordered over the PMMA at the background where the SW bundles were embedde
277 y more negative reduction potential than the PMMA bonding electrons.
278              FTIR spectra confirmed that the PMMA-b-PAA block copolymer could bind to HAP via bridgin
279                   AgBr/NPVP was added to the PMMA resin at 0.1, 0.2, and 0.3 wt%, and PMMA resin with
280 ngal effects against Candida albicans to the PMMA resin, and it has low toxicity toward HDPCs, and it
281 ature transfer from the aluminum mold to the PMMA substrate was verified by profilometry.
282 hment of primary amine-containing MBs to the PMMA surface was carried out by UV activating the PMMA t
283 sticizer levels ( approximately 10% w/w) the PMMA film was more sensitive toward ethylbenzene and p-x
284 s showed that the adhesion of C. albicans to PMMA is morphology dependent, as hyphal tubes had increa
285                                  Compared to PMMA, CaSO4 had a more rapid short term rate of elution
286                       The addition of NAC to PMMA resin significantly ameliorated its cytotoxicity to
287 rated the application of the UV/O(3) treated PMMA films for the detection of microRNAs using a label-
288 ition, we obtained very smooth and ultrathin PMMA films.
289        Therefore, the interface of ultrathin PMMA films on native aluminum oxide, deposited by reacti
290 ocyte proliferation compared with unmodified PMMA surfaces.
291 F architecture is manufactured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)], utilizes
292                                Of note, when PMMA spheres occupy a volume greater than 18% of the foc
293          Moreover, protons were reduced when PMMA powder was dropped into a slightly acidic solution,
294 re is manufactured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)], utilizes on-chip valv
295 st compromise for general detection, whereas PMMA:11 mum is better suited for catechol-like polypheno
296                                Compared with PMMA, often used as a standard, ZIF-8 attenuates 7 times
297         This concept of strand exchange with PMMA-based triple-helix stereocomplexes offers new oppor
298 ess AFM cantilevers were functionalized with PMMA microspheres and probed against C. albicans cells i
299 ich involved ball-milling of Cu powders with PMMA as solid carbon source, in-situ growth of graphene
300                     AFM tips terminated with PMMA colloids are used to pattern molecules in both seri

 
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