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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
33 FM probes with an attached N-cadherin-coated microbead (5 mum) induced a progressive clustering of N-
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
46 el pad array units for the immobilization of microbeads and each gel pad array is surrounded with a P
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.
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
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
66 c powder-containing enzyme-carrying alginate microbeads are immobilized on the surface of an electrol
70 No significant response is observed when the microbeads are subjected to other nerve agent simulants,
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
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
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
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
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.
104 ust and inexpensive electrochemical magnetic microbeads-based biosensor (EMBIA) platform for PoC sero
107 ectrophoresis, we used silica or polystyrene microbeads between 3-6 mum in diameter and packed them i
109 ges to the cytoskeleton by applying force to microbeads bound to integrin using magnetic pulling cyto
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
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
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
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
137 acquired videos of single beating cells, of microbead displacement during contractions, and of fluor
140 d with commercially available immunomagnetic microbeads (Dynabeads((R)) anti-Salmonella), polystyrene
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
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
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
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
169 ed stored sera with HLA bound to polystyrene microbeads in a retrospective analysis of heart recipien
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
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
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
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
193 gen evolution reaction and superparamagnetic microbeads (MBs) as pre-concentration/purification platf
196 ntibody (TPA) levels were measured using the microbead method in 44 presensitized patients who had re
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
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.
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
211 diffraction intensity and the density of the microbeads on the surface varied as a function of PDGF-B
213 positive cases, and in two of seven (29%) of microbead-only cases at a median of 6.5 days after trans
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
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
228 tinal injections of 1 micro L of fluorescent microbeads, saline, or INS37217 (1-200 micro M) were mad
232 permeability measurements using fluorescent microbeads show that high-risk mucus was more permeable
238 plete evaporation, we infiltrated the porous microbead structure with a positively or negatively char
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.
246 describe the preparation and application of microbeads that exhibit a "turn on" fluorescence respons
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
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
261 latter recombinant protein could also couple microbeads to the ends of shortening microtubules and us
263 s of microscale particles, such as cells and microbeads, to biofunctional surfaces is difficult becau
269 igh-density sensor arrays were prepared with microbead vapor sensors to explore and compare the infor
271 -the-spot packing of antibody-functionalized microbeads was completed in <20 s followed by autonomous
273 ch the binding to rhSHBG-coated paramagnetic microbeads was inhibited by any other binding (designer)
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
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
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
300 he microfluidic chip contained packed silica microbeads zones to filter and enrich the norovirus infe
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