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1 ar templates immobilised on glass beads (the solid-phase).
2 iquid phase; and (iii) higher amounts in the solid phase.
3 erts native-fold proteins to an amyloid-like solid phase.
4 till the major form of U associated with the solid phase.
5 s a function of the P resupply from the soil solid phase.
6 d in phosphate buffer in the presence of the solid-phase.
7 n developed utilizing protein conjugation on solid-phase.
8 d to greater extents relative to Cr from all solid phases.
9 be preferentially retained by environmental solid phases.
10 modeling metal ions in the gas, aqueous, and solid phases.
11 increased solubility relative to the initial solid phases.
12 ms and determine thermodynamically favorable solid phases.
13 d the release of Cr, but not of Fe, from all solid phases.
14 ised of a linear fluid phase and a thrombus (solid) phase.
17 of 42 sources were tested with the ImmunoCAP Solid-Phase Allergen Chip (ISAC; TFS, Uppsala, Sweden).
19 for 8 grass pollen molecules by using Immuno Solid-phase Allergy Chip (ISAC) before treatment and aft
20 Membranes are gaining increasing interest in solid-phase analytical assay and biosensors applications
22 However, the complexity of the data from solid phase and crossmatch assays has led to potential c
23 the immobilization of the template onto the solid phase and including the purification and character
24 nt extraction methods such as liquid-liquid, solid phase and membrane extraction has also been presen
26 n MMC conjugate (MMC-TOC) was synthesized on solid-phase and compared with an analog prepared using c
27 2'-phosphoramidites or 3'-triphosphates for solid-phase and polymerase-mediated synthesis, respectiv
29 nanoparticles (nanoMIPs) using an innovative solid-phase approach, which relies on the covalent immob
30 nd shape of the interface between liquid and solid phases are monitored in real-time, concurrently wi
31 by microbial activity led to a reduction of solid phase As species (X-ray absorption fine structure
32 S) data imply that 62-100% (average: 82%) of solid-phase As (Astot: 9-92 mg/kg) was present as organi
37 dation state analysis of the final magnetite solid phase by XANES shows that the majority of Tc is Tc
39 e potential of various fatty acids to induce solid phase can be predicted by the transition temperatu
40 ble 3D structures by utilising the liquid to solid phase change of a composite hydrogel (CH) ink.
45 us, 17 cyclized peptides were synthesized by solid phase click chemistry to develop novel, potent, se
46 ial reduction and alkylation of a peptide on solid phase combined with sequencing of the fully alkyla
48 ive pathway abnormalities from patients with solid-phase complement activation (cluster 4) who had no
50 e functionalities into peptide oligomers via solid-phase copper-catalysed azide-alkyne cycloaddition
54 from fish samples by vortex-assisted matrix solid phase dispersion (VA-MSPD) with detection by liqui
55 rdunculus L.), a modified QuEChERS, a matrix solid phase dispersion and a dispersive ethyl acetate ex
56 thod was developed, which is based on matrix solid phase dispersion and subsequent separation and det
57 e extraction procedure was based on a matrix solid phase dispersion approach, the optimization of whi
58 The determination was performed by matrix solid-phase dispersion (MSPD) coupled on-line to solid p
64 irated and subjected to two-stage dispersive solid phase extraction (dSPE) cleanup and the residues w
65 ultural area was sampled with a large volume solid phase extraction (LVSPE) device using three cartri
67 ntegrates a molecular imprinting polymer for solid phase extraction (MISPE) technique with a sensitiv
68 was used as a clean-up adsorbent in magnetic solid phase extraction (MSPE) for direct determination o
70 lized octadecylsilyl-silica (C18) film micro-solid phase extraction (muSPE) was developed and applied
71 d-phase dispersion (MSPD) coupled on-line to solid phase extraction (SPE) and high performance liquid
74 this study, we developed a simple and rapid solid phase extraction (SPE) method for the separation/p
75 ent desorption of the entire spot and online solid phase extraction (SPE) procedure were unaffected b
76 from wine was simplified to a single step of solid phase extraction (SPE) using size exclusion chroma
77 dissolved organic matter (DOM) isolation by solid phase extraction (SPE) with a styrene-divinylbenze
78 SPW) was performed using silver-ion (Ag-ion) solid phase extraction (SPE) without the requirement of
79 chieves selectivity of 1:4500 as compared to solid phase extraction (SPE)(1:3500) and limit of detect
80 ion (LLCE), the FFAs extract was purified by Solid Phase Extraction (SPE), methylated by boron triflu
85 esults revealed the applicability of MMIP in solid phase extraction and determination of melamine fro
87 esticides were extracted from the samples by solid phase extraction and liquid-liquid extraction befo
88 id extraction, clean-up using immunoaffinity solid phase extraction chromatography, and FMOC-derivati
89 ing with acetonitrile followed by dispersive solid phase extraction clean-up using primary secondary
90 S concentrations were measured using on-line solid phase extraction coupled to high performance liqui
92 paration and purification of beer a combined solid phase extraction for trichothecenes, enniatins, be
96 ) was synthesized and applied for dispersive solid phase extraction of copper in water and cereal sam
97 time as an adsorbent for the vortex assisted-solid phase extraction of Pb(II) from cereal, beverage a
99 applied as a sorbent for selective magnetic solid phase extraction of zinc followed by its determina
100 sorbance at 280 nm (SUVA280) between the two solid phase extraction resins, suggesting they capture s
101 ibility of these materials for being used as solid phase extraction sorbent for the selective preconc
102 In this paper, we report a simple and rapid solid phase extraction system for the separation/preconc
103 itrate-buffered salts followed by dispersive solid phase extraction using a primary secondary amine a
105 ing with acetonitrile followed by dispersive solid phase extraction using zirconia-coated silica part
107 An efficient sample treatment involving a solid phase extraction with a C18 sorbent was proposed (
109 nillic acids was carried out by an off-line, solid phase extraction, capillary zone, electrophoresis
114 r laboratory have been applied as dispersive solid-phase extraction (dSPE) sorbent for the extraction
115 he validated method of molecularly imprinted solid-phase extraction (MISPE) cartridge was successfull
116 ich provides automated molecularly imprinted solid-phase extraction (MISPE) followed by liquid chroma
117 ariables affecting the molecularly imprinted solid-phase extraction (MISPE) procedure were optimized.
120 multi-residue pesticides was developed using solid-phase extraction (SPE) coupled with dispersive liq
128 ance liquid chromatography-mass spectrometry-solid-phase extraction (UHPLC-MS-SPE) followed by de nov
130 have been intensively employed in classical solid-phase extraction and solid-phase microextraction.
131 derivatives) were washed and enriched with a solid-phase extraction cartridge prior to analysis by ES
133 nucleosides, enrichment by a reversed-phase solid-phase extraction column, and nanoLC-NSI/MS/MS anal
134 s based on microwave-assisted extraction and solid-phase extraction coupled to ultra-high-performance
137 Different parameters were optimized for the solid-phase extraction procedure and instrumental analys
139 this analysis can extract with the automated solid-phase extraction system and analyze a single sampl
140 hodology was then compared to a conventional solid-phase extraction technique for the analysis of the
141 Herein is a method that utilizes automated solid-phase extraction that is directly coupled to a mas
144 alytical procedure based on dispersive micro solid-phase extraction with the use of oxidized multiwal
145 ted to liquid-liquid extraction, followed by solid-phase extraction, and analyzed by ultra-high perfo
146 olves sample preparation by liquid-liquid or solid-phase extraction, followed by analysis using liqui
147 uent experiments (e.g., 2D-NMR spectroscopy, solid-phase extraction, liquid chromatography prefaced m
149 matography-high-resolution mass spectrometry-solid-phase extraction-nuclear magnetic resonance spectr
155 nanotube (cMWCNT) were used for the magnetic solid phase extractions and determination of Sudan I, II
156 are the direct injection of the samples with solid-phase extractions: reversed-phase (C18) and strong
157 ion spectroscopic (XAS) techniques to assess solid-phase Fe speciation along the vertical redox gradi
158 extensive Fe atom exchange can occur between solid-phase Fe(3+) and aqueous Fe(2+) in a process refer
161 gents with robust preclinical evidence, have solid phase II dosing and timing data, and recruit patie
164 s to incorporate into them a high density of solid-phase interfaces capable of absorbing and annihila
166 ur results provide field-based evidence that solid-phase ligands in oxic sediment, most notably Fe ox
167 ccessible N-mercaptoethoxyglycinamide (MEGA) solid-phase linker for the facile synthesis of latent pe
169 as alternative to conventional headspace and solid phase micro extraction methods and allows users to
171 nd subsequent packing stage were explored by solid phase micro-extraction (SPME) and gas chromatograp
172 oth parameters are commonly quantified using Solid Phase Micro-Extraction (SPME) based on a sorptive
174 In vitro aroma release was monitored by solid phase micro-extraction gas chromatography using an
175 an in vivo sampling mode of direct immersion-solid phase microextraction (DI-SPME) was employed to ca
176 ity Headspace techniques (HCC-HS), Headspace Solid Phase Microextraction (HS-SPME) and Headspace Sorp
177 lidated method based on the use of headspace solid phase microextraction (HS-SPME) coupled with the c
178 ra) berries was investigated using headspace-solid phase microextraction (HS-SPME) followed by gas ch
180 In recent years, the direct coupling of solid phase microextraction (SPME) and mass spectrometry
181 describe a new process for preparing porous solid phase microextraction (SPME) coatings by the sputt
185 ) of honey samples were extracted, using the solid phase microextraction (SPME) technique, and HMF wa
186 verage (TWA) passive sampling with thin film solid phase microextraction (TF-SPME) and liquid chromat
187 In the current study, we introduce magnetic solid phase microextraction coupled with electrochemical
188 ly, quantification of bioactive compounds by solid phase microextraction coupled with liquid chromato
191 novel, simple and efficient pseudo-stir bar solid phase microextraction method for separation and pr
193 on Nuclear Magnetic Resonance ((1)H NMR) and Solid Phase Microextraction-Gas Chromatography/Mass Spec
195 by multiple techniques, including headspace solid phase microextraction-GC-MS (HS-SPME-GC-MS), heads
196 -liquid microextraction (LLME) and headspace solid-phase microextraction (HS-SPME) combined with gas
198 olia) was investigated by applying Headspace Solid-Phase MicroExtraction (HS-SPME), combined with GC-
199 and Chitra were extracted in raw state using solid-phase microextraction (SPME) and cooked state usin
200 re analysed by solid-phase extraction (SPE), solid-phase microextraction (SPME) and gas chromatograph
203 is (SIDA) in conjunction with headspace (HS) solid-phase microextraction (SPME) coupled with gas-chro
204 the current study is to develop a sensitive solid-phase microextraction (SPME) device for direct and
206 aldehydes and alkanes) was carried out using solid-phase microextraction (SPME) followed by a compreh
207 ars, different geometrical configurations of solid-phase microextraction (SPME) have been directly co
208 ese data and previous work we reported, this solid-phase microextraction (SPME) method delivered a ro
210 stigated in batch-equilibrium experiments by solid-phase microextraction (SPME) resulting in partitio
212 olatile organic compounds (VOCs) obtained by solid-phase microextraction and gas chromatograph-mass s
213 four Costa Rican cultivars were analysed by solid-phase microextraction and gas chromatography-mass
215 d volatile compounds has been examined using solid-phase microextraction and gas-chromatography.
217 l as an example compound, this protocol uses solid-phase microextraction and scintillation detection
222 nal applications were identified by means of solid-phase microextraction followed by gas chromatograp
223 and volatile organic compounds determined by solid-phase microextraction gas chromatography-mass spec
226 , and the release of limonene as assessed by solid-phase microextraction using gas chromatography mas
229 The volatile compounds were analyzed using solid-phase microextraction-gas chromatography-mass spec
232 Odorous volatile compounds were analysed by solid-phase microextraction/gas chromatography-mass spec
233 hering has depleted over 40% of the original solid-phase Mn from the near-surface, and hydrologic gra
234 II/IV) oxides is inhibited by the buildup of solid-phase Mn(II/III), specifically in interlayer sites
236 consists of micro-pipette tips and embedded solid phase nucleic acid extraction membranes, and fully
237 nzymatic amplification reactor that combines solid-phase nucleic acid extraction, concentration, and
239 alled precision glycomacromolecules based on solid phase oligomer synthesis and the Staudinger ligati
241 at the calcite surface can sequester Sb as a solid phase on calcite, which has environmental implicat
247 beled ADM analogues synthesized by Fmoc/t-Bu solid phase peptide synthesis were used to analyze their
249 ted to linear thiopeptide cores prepared via solid-phase peptide synthesis (SPPS), giving an efficien
250 ically to KTag, available via semi-automated solid-phase peptide synthesis (SPPS), while equipping th
251 The protein is synthesized using Fmoc-based solid-phase peptide synthesis and assembled using combin
256 lid-phase extraction (SPE) with TELOS ENV as solid phase performed superior compared to ten other sor
257 ome these limitations we have introduced the solid-phase polymerase chain reaction (SP-PCR) to form t
259 n solution but have been recently adapted to solid-phase providing unique advantages such as simplifi
264 hibiting similar Fe(II)/Fe(III) ratio in the solid phase showed similar adsorption properties for NA
265 time, we systematically display gradation of solid phase soil-arsenic speciation across defined redox
266 thereby speeding up sample flow through the solid phase sorbent during phenol extraction and, furthe
269 e cells occurs by phase separation, and that solid-phase stores provide a major ion reservoir that ca
272 nanoparticles, prepared in aqueous media by solid phase synthesis with immobilised L-thyroxine, gluc
273 beled antimicrobial peptide BODIPY-cPAF26 by solid-phase synthesis (6-7 d) and its spectral and biolo
276 e issues, in the present study we report the solid-phase synthesis of lanthionine-bridged analogues o
277 methylcytidine (hm(5)rC) phosphoramidite for solid-phase synthesis of modified RNA oligonucleotides.
278 amino acids and demonstrate their use in the solid-phase synthesis of N-amino peptide derivatives.
279 ion of several of these phosphoramidites for solid-phase synthesis of oligoribonucleotides containing
280 l can be divided into three major parts: (i) solid-phase synthesis of the fluorescence-labeled HyCoSu
281 ynthesis of IGF-1 analogs, which entails the solid-phase synthesis of two IGF-1 precursor chains that
282 d conjugates were constructed stepwise using solid-phase synthesis starting from immobilized primary
284 The ease of preparation, high affinity of solid-phase synthesised imprinted nanoparticles and the
285 However, it has so far been restricted to solid-phase synthesized seleno-peptides and thus constra
287 l role of nanoporosity (3% by volume) on the solid phase transformation through a dissolution-recryst
288 pressure range includes the well-known solid-solid phase transition from Ga-I to Ga-II at low tempera
289 met by mechanistically designing a liquid-to-solid phase transition of oxidized catholyte (or reduced
291 of minimal model systems that exhibits solid-solid phase transitions that are driven by changes in th
292 hange that occurs indirectly in atomic solid-solid phase transitions via changes in temperature, pres
293 f a series of isochoric, diffusionless solid-solid phase transitions within a single shape family and
294 e analysis of analytes in vapor, liquid, and solid phases using a single carbon fiber (length : appro
297 observed that the structure of the reduced U solid phases was time dependent and largely influenced b
299 ified thio-As species in solution and AsS in solid phase, which suggests that the As(V) was reduced t
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