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1 racking the surface flow of apically applied microbeads).
2 plysia cell adhesion molecule (apCAM)-coated microbead.
3 n or direct force application using magnetic microbeads.
4 gle-cell genomic DNA onto the coencapsulated microbeads.
5  not compromised by the low concentration of microbeads.
6 d by magnetic bead sorting via EPCAM labeled microbeads.
7 d in solution or immobilized on paramagnetic microbeads.
8 s into multivalent complexes using protein A microbeads.
9 ices (cGMP)-grade anti-biotin immunomagnetic microbeads.
10 forces transmitted via spot-labeled magnetic microbeads.
11  trapping and mixing of solid-phase affinity microbeads.
12 ort, and detect individual superparamagnetic microbeads.
13 cture for supporting antibody-functionalized microbeads.
14 polyacrylamide gel embedded with fluorescent microbeads.
15  obtained through viscous sintering of glass microbeads.
16 rticles, polymer capsules and semiconducting microbeads.
17 were isolated using antibody-linked magnetic microbeads.
18 d optical access to the chemically sensitive microbeads.
19 , viability, or ability to phagocytize latex microbeads.
20 mall (100-200 microm) polymeric methacrylate microbeads.
21 sulted in rolling behavior similar to PSGL-1 microbeads.
22 acrylamide substrates containing fluorescent microbeads.
23  many personal care products contain plastic microbeads.
24 o form a hairpin structure and conjugated on microbeads.
25 tination of aptamer coated magnetic nano- or microbeads.
26 boflavin, amino acids and peptides from whey microbeads.
27 fic oligonucleotide probes bound to magnetic microbeads.
28   This paper focuses on encoding polystyrene microbeads, 10-100 microm in diameter, with a luminescen
29 ting process has been characterized by using microbeads (10microm diameter) resulting in a single bea
30 ed for single-cell analysis using Wnt-coated microbeads (12-18 h of live imaging) and to create a Wnt
31 ions of riboflavin were obtained in 'loaded' microbeads (361 mg/L) compared to riboflavin added to th
32                         We have bonded glass microbeads (425-600 microm diameter) to the inner walls
33 FM probes with an attached N-cadherin-coated microbead (5 mum) induced a progressive clustering of N-
34                                     TentaGel microbeads (90 mum) were spatially segregated into outer
35                                     TentaGel microbeads (90 mum) were spatially segregated into outer
36                             As the volume of microbeads added to the solution was increased, the upta
37                                      Passive microbead affinity for WT and SPARC-null ECM did not dif
38                                          The microbeads allowed mapping of flow patterns and velociti
39 ric (FC) XM, and seven had DSA detectable by microbead analysis only.
40 nd reproducible functionalization of encoded microbeads and a high stability of DNA probes in cell-fr
41 e-coded mixture of multiple affinity-capture microbeads and an inertial microfluidic particle sorter
42 al tracking of collisions between insulating microbeads and an ultramicroelectrode surface are correl
43                            Using fluorescent microbeads and antihepsin treatment, we demonstrated tha
44  innate immunity by clearance of fluorescent microbeads and bacterial particles.
45 n and encapsulation of primer functionalized microbeads and cells.
46 el pad array units for the immobilization of microbeads and each gel pad array is surrounded with a P
47 tro in response to anti-CD3-anti-CD28-coated microbeads and IL-2.
48 haracterizing the antibacterial copper-doped microbeads and monoliths (CuBs and CuMs), their antibact
49 o reconcile dissociation constants of PSGL-1 microbeads and neutrophils on P-selectin was 0.21 microm
50  evaluate PSGL-1/P-selectin bond kinetics of microbeads and neutrophils, rolling and tethering on P-s
51  The device was used to separate polystyrene microbeads and PC-3 human prostate cancer cells with 94.
52 ded in different density solutions, CsCl for microbeads and Percoll for cells.
53 y photobleaching of the dyes attached to the microbeads and presents one of the biggest drawbacks of
54 ty) of previously well-characterized polymer microbeads and subsequently applied to determine the den
55 tly, the frequency of collisions between the microbeads and the electrode is not compromised by the l
56 e nature of the interactions between flowing microbeads and their influence on electrochemical proces
57 containing PDMS in the form of both precured microbeads and uncured liquid precursor, dispersed in wa
58 reptavidin-coated polyvinyltoluene (PVT) SPA microbeads and using [(125)I]IGF-1 as the endogenous lig
59        Finally, using anti-TCR-Vbeta8-coated microbeads and Vbeta8(-) Tregs, we show that TCR stimula
60 sition delivered approximately 16 times more microbeads and yielded approximately 20% more bacteria k
61  fluorescent microspheres, quantum dot-based microbeads, and fluorescent nano rods, some of which cur
62 rmed cylindrical plugs, preformed injectable microbeads, and hydrogel precursor, injected and polymer
63 eating with chemical lysis buffer and silica microbeads are employed for DNA extraction from clinical
64                                          The microbeads are fabricated by adsorbing fluoresceinamine
65                                     The PDMS microbeads are held together in thixotropic granular pas
66 c powder-containing enzyme-carrying alginate microbeads are immobilized on the surface of an electrol
67                  To select for catalysis the microbeads are re-emulsified in a reaction buffer of cho
68             The DNA capture probe containing microbeads are selectively arranged in micromachined cav
69                                     When the microbeads are subjected to DCP vapor, the conversion of
70 No significant response is observed when the microbeads are subjected to other nerve agent simulants,
71                        Fluorescently encoded microbeads are subsequently functionalized by lesion-con
72                                    When whey microbeads are used as sorbents, they show excellent pot
73                                              Microbeads are used to track fluid flow over microband e
74                                         Whey microbeads are well suited to act as sorbents for encaps
75                                     Magnetic microbeads are widely used in biotechnology and biomedic
76 ngle cells, along with primer-functionalized microbeads, are randomly compartmentalized in the drople
77 ment of single human leukocyte antigen (HLA) microbead array assays allows characterization of host a
78                The power and utility of this microbead array DNA detection methodology is demonstrate
79 ol for common biolabs to customize their own microbead array for multi-analyte immunoassays.
80 ely 10(-13) M are obtained readily with this microbead array system.
81 development of more versatile and economical microbead array-based multiplex serological test panels
82  compared with that of a trapped polystyrene microbead as a function of the applied acoustic pressure
83 we describe the use of colloidal polystyrene microbeads as a sacrificial template to create a nanofib
84 ling circle amplification (RCA) and magnetic microbeads as a signal enhancement method.
85 monstrate that the autoassembly of alternate microbeads as well as their directed assembly, by using
86 oth PCV2 and PRRSV were used to validate the microbead assay (MBA) in comparison with the "gold stand
87 -specific antibody responses measured by the microbead assay were comparable to those of the standard
88 posttransplant DSA peaking at MFI >2000 U on microbead assay, rejection did not occur.
89 c antibody (DSA) level of more than 500 in a microbead assay.
90 tokines by immunohistochemistry, RT-PCR, and microbead assays.
91 lant, DSA levels were monitored closely with microbead assays.
92 n the cell monolayer produced by forcing one microbead attached atop a single cell or cell monolayer
93 uction of gold nanoparticles coated magnetic microbeads (Au NPs-MBs), which were prepared through a n
94 netics of blood flow recovery that resembled microbead-based blood flowmetry and laser Doppler blood
95 abeling sequences, and finally detected with microbead-based FFD assays.
96 infection status and a multiplex fluorescent microbead-based immunoassay and/or enzyme-linked immunoa
97 e and miniaturized immunoassay by coupling a microbead-based immunoassay with an interdigitated array
98 ere quantified using comprehensive multiplex microbead-based immunoassays for 46 immune mediators.
99 ne mediators were quantified using multiplex microbead-based immunoassays.
100  brain cells were measured simultaneously in microbead-based immunoassays.
101 y chip for high-throughput and multi-analyte microbead-based immunoassays.
102                       The approach employs a microbead-based protocol for the processes of affinity s
103                           Stringent magnetic microbead-based purification was required for potent sup
104 ust and inexpensive electrochemical magnetic microbeads-based biosensor (EMBIA) platform for PoC sero
105 ffects, and limited diffusion lengths in the microbead bed.
106 er cells with 94.7 and 1.2% of the cells and microbeads being deflected, respectively.
107 ectrophoresis, we used silica or polystyrene microbeads between 3-6 mum in diameter and packed them i
108                                       Silica microbead bioreactors (0.5 microm diameter) coated with
109 ges to the cytoskeleton by applying force to microbeads bound to integrin using magnetic pulling cyto
110  nN) were applied to magnetic laminin-coated microbeads bound to NIH 3T3 cells.
111 lavin loss, a second approach to 'load' whey microbeads by soaking in riboflavin was assessed.
112 ndependently released and recovered from the microbeads by treatment with 0.1 N NaOH; (4) multiple an
113 tte technique, spherical, glassified protein microbeads can be made that allow determination of prote
114 ranching networks in which superparamagnetic microbeads can be routed along dynamically-selected path
115          We propose that MAM7-functionalized microbeads can be used as a topical treatment, to reduce
116                                        These microbeads can then be selected for catalysis or binding
117 uorescence-activated cell sorting (FACS) for microbead+,CD45(low) cells.
118 eads followed by FACS for specifically bound microbead+,CD45(low) cells.
119                                   Binding of microbeads coated with a function-blocking antibody to N
120 ed at controlled densities on the surface of microbeads coated with a phospholipid mixture resembling
121 l-free flow-based adhesion experiments using microbeads coated with CD44 immunoprecipitated from carc
122  assays and flow-based adhesion assays using microbeads coated with CEA immunopurified from LS174T co
123 FLA) onto carboxylate-functionalized polymer microbeads coated with poly(2-vinylpyridine) (PVP).
124 re identified in sera of healthy males using microbeads coated with recombinant denatured HLA-E or a
125                           In our experiment, microbeads coated with streptavidin were driven to the s
126 es labeled with biotin were immobilized onto microbeads coated with streptavidin.
127                   Fluorescence images of the microbead column revealed captured bacteria as bright sp
128                                              Microbeads conjugated directly to antibody specific to L
129 evice, and a suspension of superparamagnetic microbeads conjugated to DNA molecules is introduced int
130 ule ends can be reconstituted in vitro using microbeads conjugated to the budding yeast kinetochore p
131                    Injections of fluorescent microbeads conjugated with a light-sensitive chromophore
132                      Furthermore, FST-loaded microbeads decreased bone ossification in developing chi
133 spray was able to deliver significantly more microbeads deeper in the biofilm compared with diffusion
134 d hydrogels were fully degraded within 2 wk; microbead degradation was more moderate, and plugs degra
135              These results indicate that the microbead device is a low-cost tool that enhances sample
136 n techniques, enzyme-based immunoassays, and microbead diagnostics.
137  acquired videos of single beating cells, of microbead displacement during contractions, and of fluor
138  microwells filled with ion-exchange polymer microbeads doped with various organic dyes.
139 ional element for selective antibody-coated, microbead-driven, large-scale expansion.
140 d with commercially available immunomagnetic microbeads (Dynabeads((R)) anti-Salmonella), polystyrene
141                                       First, microbeads, each displaying a single gene and multiple c
142 used to prepare epoxide-functionalized glass microbeads (EGBs, 500 mum in size and manipulated by twe
143     For mice, a single 1-microL injection of microbeads elicited a highly regular 30% elevation in IO
144 hnique is first applied to match the pair of microbead embedded images before and after deformation,
145     Here we report the development of silica microbeads embedded with both semiconductor quantum dots
146         A proof-of-concept superparamagnetic microbead-enzyme complex was integrated with microfluidi
147                                     Magnetic microbeads exhibit rapid separation characteristics and
148  rate of 2 muL/min, as characterized through microbead experiments, while maintaining measurement acc
149 than 24,000 images of 0.5 microm fluorescent microbeads flowing within mildly inflamed postcapillary
150 o create reaction geometries that confined a microbead flux to within 200 nm of the surface under flo
151 ve the outcome by using biodegradable fibrin microbeads (FMBs) to isolate a population of mesenchymal
152 ed by acoustic streaming (h >> lambdaf), the microbeads follow vortical streamlines in a pattern char
153 tion with D7-FIB-conjugated (antifibroblast) microbeads followed by FACS for specifically bound micro
154 61 mg/L) compared to riboflavin added to the microbead forming solution (48 mg/L).
155                  Riboflavin was added to the microbead forming solution however diffusional losses of
156                            The United States Microbead-Free Waters Act was signed into law in Decembe
157  was created for the capture of solid silica microbeads functionalized with enzyme.
158                              In this method, microbeads functionalized with multiple forward primers
159 e show that topical application of polymeric microbeads functionalized with the adhesin MAM7 to a bur
160 loped an in vitro actin assembly assay using microbeads functionalized with the nucleation promoting
161 arker) and anti-CD34 (EPC marker) conjugated-microbeads had the highest sensitivity and specificity f
162    RBCs were trapped directly (i.e., without microbead handles) in the dual optical tweezers where th
163 composed of individually addressable agarose microbeads has been demonstrated for the rapid detection
164 taneously pack multiple channels with silica microbeads having different sizes and surface properties
165                             On both RBCs and microbeads, human CD47 potently inhibits phagocytosis as
166 cking velocimetry (PTV) or by processing the microbead images by particle image velocimetry (PIV) sof
167 of four automated immunoassays (BioPlex 2200 microbead immunoassay [MBIA], Liaison chemiluminescence
168  serum samples of H7N9 patients by multiplex-microbead immunoassays.
169 ed stored sera with HLA bound to polystyrene microbeads in a retrospective analysis of heart recipien
170       Velocities were determined by tracking microbeads in a solution containing electroactive potass
171 e microplastics, the bill banned all plastic microbeads in selected cosmetic products.
172 nts revealed fractionation of nanobeads from microbeads in the optimized device with high sorting eff
173 y to image cultured cells and membrane-bound microbeads in twelve independently-focusing channels sim
174 or cells together with primer functionalized microbeads in uniform PCR mix droplets.
175 nzymatic mineralization occur on polystyrene microbeads in water-in-oil emulsions, yielding synthetic
176 ered and microencapsulated human stem cells (MicroBeads) in the mouse eye, and to study the impact of
177                  Estimates using fluorescent microbeads indicated approximately 7,000 C1C2-binding si
178        The authors used tonometry to measure microbead-induced IOP elevations.
179 he same mice appears to be normal based on a microbeads-induced glaucoma model.
180                                              Microbead-injected eyes showed reduced optokinetic track
181                                      Using a microbead injection technique to chronically raise IOP f
182      The AC loss began 4 weeks after initial microbead injection, corresponding to the time course of
183 d retrograde tracer (Fluorogold, Fluororuby, microbeads) injections in the IC to study the morphology
184 lizing the enzyme on microbeads, packing the microbeads into a chip-based microreactor (volume approx
185 ted unilaterally by injection of polystyrene microbeads into the anterior chamber to occlude aqueous
186 the final protein concentration of the solid microbead is controlled, and ranges from 700 to 1150 mg/
187     The use of flow cytometry and HLA-coated microbeads is recommended for detection of HLA antibodie
188                     Light focusing through a microbead leads to the formation of a photonic nanojet f
189 r transplantation, in 8 of 10 cases when the microbead level of DSA had median fluorescence intensity
190 dissociated hippocampal neurons we show that microbeads loaded with CASPR2, but not with a deletion m
191 sensitivity, and subsecond response of these microbeads make them suitable for nerve agent vapor dete
192                                         Whey microbeads manufactured using a cold-set gelation proces
193 gen evolution reaction and superparamagnetic microbeads (MBs) as pre-concentration/purification platf
194 rsible capacity than conventional mesocarbon microbead (MCMB) powder.
195 sing ion selectivity of hydrogel-infiltrated microbead membranes.
196 ntibody (TPA) levels were measured using the microbead method in 44 presensitized patients who had re
197 intensity (MFI) >2000 U, in 6 of 10 when the microbead MFI >4000 U.
198                        In 8 of 10 cases, the microbead MFI at the time of resolution was greater than
199  Here we demonstrate for the first time that microbeads (microBs) can be used as contrast agents to t
200 he detection of single molecules in magnetic microbead microwell array formats revolutionized the dev
201 s (MNBs); (2) optical imaging using magnetic microbeads (MMBs).
202 s has mainly been characterized by following microbead motion by optical microscopy either by particl
203 splacement field obtained is associated with microbead movements; (2) it considers the finite thickne
204 was measured continuously by positioning the microbeads near the electrode surface with a magnet.
205                          Here we applied the microbead occlusion model of glaucoma to different trans
206 elevating the intraocular pressure (IOP) via microbead occlusion of ocular fluid outflow in mice.
207  week period of elevated pressure induced by microbead occlusion of ocular fluid, Trpv1(-/-) accelera
208 phic imaging performance is quantified using microbeads of different dimensions, as well as by imagin
209 ed 3D fabrication techniques we integrated a microbead on an AFM cantilever thus realizing a system t
210            The dissociation rates for PSGL-1 microbeads on P-selectin were briefer than those of neut
211 diffraction intensity and the density of the microbeads on the surface varied as a function of PDGF-B
212  cytometric XM, and 23 had DSA detectable by microbead only.
213 positive cases, and in two of seven (29%) of microbead-only cases at a median of 6.5 days after trans
214                    These include multiplexed microbead or kinase activity assays, flow cytometry base
215 d to covalently immobilize Wnt3a proteins on microbeads or a glass surface.
216 ge on ground beef, without using antibodies, microbeads or any other reagents, towards a preliminary
217 ls and mouse tumor cells were isolated using microbeads or flow cytometry and analyzed for sphere-for
218 is carried out by immobilizing the enzyme on microbeads, packing the microbeads into a chip-based mic
219 on of collisions between individual magnetic microbeads, present at subattomolar concentrations, and
220 using a magnetic field to preconcentrate the microbeads prior to detection in a microfluidic electroc
221          Microencapsulated human stem cells (MicroBeads) promise to overcome limitations inherent wit
222                               Therefore, the Microbead Quantum-dots Detection System (MQDS) was devel
223              For rats, a single injection of microbeads raised IOP by 21% to 34%, depending on volume
224  GFP-marked cells encapsulated in subretinal MicroBeads remained viable over a period of up to 4 mont
225 ECL signal, generated by thousands of carbon microbeads remotely addressed via bipolar electrochemist
226 ported in vivo VEGF release profile from the microbeads resulted in highly vascularized s.c. tissue c
227                                The 3% pectin microbeads resulted the best compromise between spherici
228 tinal injections of 1 micro L of fluorescent microbeads, saline, or INS37217 (1-200 micro M) were mad
229                                  Fluorescent microbead sensor arrays were prepared to determine senso
230 rve agent vapor detection and inclusion into microbead sensor arrays.
231 o form a narrow channel with the polystyrene microbeads serving as spacers.
232  permeability measurements using fluorescent microbeads show that high-risk mucus was more permeable
233                           After 52weeks, the microbeads showed a total-astaxanthin retention of 94.1+
234 0 microg/ml) +/- CHC and unmodified alginate microbeads showed low responses.
235           Moreover, by using spatial encoded microbeads, simultaneous detection of both hCG and PSA o
236 rogeneous phase by immobilization on polymer microbead solid supports.
237 ssay evaluating C3d deposition on HLA-coated microbeads spiked with alloantibodies.
238 plete evaporation, we infiltrated the porous microbead structure with a positively or negatively char
239 ly of different tag combinations onto SiO(2) microbead supports via biotin-avidin binding.
240 magnetic field acting on a superparamagnetic microbead suspended in an active medium.
241 sentation of engineered cell-secreted ECM on microbeads suspended in alginate hydrogels would promote
242      25 cytokines were measured by multiplex microbead system (Invitrogen, UK) on a Luminex platform.
243                                A cell-scaled microbead system was used to analyze the force-dependent
244                   To test this hypothesis, a microbead system was utilized to measure relative L-sele
245                                         Such microbeads that can be sequentially deprotected and conv
246  describe the preparation and application of microbeads that exhibit a "turn on" fluorescence respons
247                                The composite microbeads that we describe are likely to find uses in o
248        When either fragment was coupled to a microbead, the force it could transduce from a shortenin
249 uidic channels with silica nanoparticles and microbeads, thereby indirectly producing functional nano
250 the density and compressibility of cells and microbeads; these being the two central material propert
251 eport both forced and spontaneous motions of microbeads tightly bound to the CSK of human muscle cell
252 mplemented with ssDNA aptamer functionalized microbeads to address the specific capturing of thrombin
253  covalently immobilised on superparamagnetic microbeads to allow the isolation of BBI from soy whey m
254 ident retinal detachment and distributed the microbeads to almost all the subretinal space.
255 valuate the strategy of using self-assembled microbeads to build a robust and tunable membrane for fr
256 ned by replacing the bacteria by polystyrene microbeads to demonstrate the internalization of the lig
257 video microscopy, we tracked selectin-coated microbeads to detect the formation frequency of adhesive
258 ion of DNA-based fluorescent chemosensors on microbeads to differentiate eight toxic metal ions in wa
259  (digital diffraction diagnosis) system uses microbeads to generate unique diffraction patterns which
260                  Finally, utilizing magnetic microbeads to mechanically stimulate mechanically-inhibi
261 latter recombinant protein could also couple microbeads to the ends of shortening microtubules and us
262           Here we show, by conjugating glass microbeads to tubulin polymers through strong inert link
263 s of microscale particles, such as cells and microbeads, to biofunctional surfaces is difficult becau
264                                              Microbead trajectories show a systematic deviation towar
265                     The dynamics of magnetic microbead transport by domain walls has been well studie
266  of a depolymerizing MT and can couple it to microbead transport in vitro.
267       It consists of monomeric avidin-coated microbeads trapped in a pipette tip and has been used fo
268              The fluidic system used a novel microbead-trapping flow cell to capture antibody-coupled
269 igh-density sensor arrays were prepared with microbead vapor sensors to explore and compare the infor
270                        Detection of a single microbead was successfully demonstrated using a capacita
271 -the-spot packing of antibody-functionalized microbeads was completed in <20 s followed by autonomous
272  peptides of varying hydrophobicities by the microbeads was examined.
273 ch the binding to rhSHBG-coated paramagnetic microbeads was inhibited by any other binding (designer)
274                     Intraocular injection of microbeads was made in mouse eyes to elevate intraocular
275                     Riboflavin uptake by the microbeads was shown to be via a partition process.
276                   Long-term stability of the microbeads was studied for 6 months taking into account
277 em, a positive selection with antifibroblast microbeads was used, combined with fluorescence-activate
278 grade tracer, red (RFB) or green (GFB) latex microbeads, was injected into the gustatory PBN under el
279 tributions of noninteracting and interacting microbeads, we observed that tether bond formation rates
280 ed for Thy-1 expression using immunomagnetic microbeads were enriched from 5.2%-87.2% Thy-1(+).
281  only in the grease that the much publicised microbeads were found.
282                                              MicroBeads were implanted into the subretinal space of S
283 r scale by passive microrheology techniques: microbeads were injected in jellyfish ECM and their Brow
284 esia, up to 2 muL of fluorescent or magnetic microbeads were injected intracamerally into the mouse e
285  green (GFB) and red (RFB) fluorescent latex microbeads were injected iontophoretically or by pressur
286                       The DNA-functionalized microbeads were packed into each of three microchambers
287                                   Blank whey microbeads were placed in solutions of the compounds.
288                                        While microbeads were present in the host sediment matrix, the
289                           In this study whey microbeads were used to encapsulate riboflavin using 2 m
290  multi-use immunosensor, disposable magnetic microbeads were used to immobilize biomarker-recognition
291 of the resolution enhancement induced by the microbead, which sheds light into the many contradictory
292  amplification factor of 250000 and magnetic microbeads, which are mobile solid-phase supports for th
293 ARC-null mice were injected with fluorescent microbeads, which were also passively exposed to freshly
294 ens were coated onto eight different colored microbeads, which were mixed together in one tube for si
295 d particles were performed using polystyrene microbeads with different sizes to demonstrate rapid (<1
296 thelial progenitor cells (EPCs) by combining microbeads with fluorescence quantum dots (Q-dots) coupl
297 approach was used to obtain calcium-alginate microbeads with high polyphenol content and good morphol
298 labeled sandwich immunoassay on paramagnetic microbeads with mouse IgG as the analyte and beta-galact
299                               Porous agarose microbeads, with high surface to volume ratios and high
300 he microfluidic chip contained packed silica microbeads zones to filter and enrich the norovirus infe

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