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1 n of Official Analytical Chemists) and HPLC (High Performance Liquid Chromatography).
2 thod applied for mycotoxin analyses included high performance liquid chromatography.
3 phase extraction followed by reversed phase high performance liquid chromatography.
4 piked milk samples for further estimation by high performance liquid chromatography.
5 olid-phase extraction, and analyzed by ultra-high performance liquid chromatography.
6 plates and the results were validated using high-performance liquid chromatography.
7 e and in the plasma of a rhesus monkey using high-performance liquid chromatography.
8 ults for the sample analysis validated using high-performance liquid chromatography.
9 of (18)F-FNDP in baboons was assessed using high-performance liquid chromatography.
10 ate, glutamine, and GABA were measured using high-performance liquid chromatography.
11 min by instant thin-layer chromatography and high-performance liquid chromatography.
12 ase in the dorsal hippocampus as revealed by high-performance liquid chromatography.
13 dly radiolabeled with (123)I and purified by high-performance liquid chromatography.
14 al TCBD unit, which were separated by chiral high-performance liquid chromatography.
15 ample is directly coupled to its analysis by high-performance liquid chromatography.
16 bolites were measured in monkey plasma using high-performance liquid chromatography.
17 e were measured as dansylated derivatives by high-performance liquid chromatography.
18 uffer with microwave heating and purified by high-performance liquid chromatography.
19 Precursors were quantitated by high-performance liquid chromatography.
20 breath condensate samples by means of ultra high-performance liquid chromatography.
21 osine and inosine) levels were quantified by high-performance liquid chromatography.
22 linical Chemistry [IFCC]) were determined by high-performance liquid chromatography.
23 ully evaluated using SERS and confirmed with high-performance liquid chromatography.
24 to characterize Mn-PyC3A metabolism by using high-performance liquid chromatography.
25 1 age- and sex-matched healthy volunteers by high-performance liquid chromatography.
26 he stability of (18)F-FCP was verified using high-performance liquid chromatography.
27 using polyacrylamide gel electrophoresis and high-performance liquid chromatography.
28 This increase was validated using high-performance liquid chromatography.
29 s); levels of tryptophan were measured using high-performance liquid chromatography.
30 and the limit of detection was comparable to high performance liquid chromatography (0.03% versus 0.0
31 unoblotting; NOS activity was evaluated with high-performance liquid chromatography; action potential
32 ition to being nearly four times faster than high-performance liquid chromatography, allowing for gre
35 in peripheral mouse blood was determined by high-performance liquid chromatography analysis of blood
37 OTATOC and (68)Ga-PSMA-HBED-CC determined by high-performance liquid chromatography analysis was grea
41 introduce an approach for the integration of high performance liquid chromatography and droplet micro
42 d total phenolic contents were quantified by high performance liquid chromatography and spectrophotom
43 e alpha,beta-unsaturated carbonyls employing high performance liquid chromatography and tandem mass s
44 ng on-line solid phase extraction coupled to high performance liquid chromatography and tandem mass s
45 ns generated were analyzed by reversed phase-high performance liquid chromatography and the identity
46 Finally, the technique in combination with high-performance liquid chromatography and capillary ele
47 ropofol concentrations in hospitals comprise high-performance liquid chromatography and ion mobility
49 istry and characterized using reversed-phase high-performance liquid chromatography and matrix-assist
51 4-nonylphenol, and 4-tert-octylphenol using high-performance liquid chromatography and tandem mass s
52 and 16 weeks; bile acids were profiled using high-performance liquid chromatography and the compositi
53 e products were analyzed with reversed-phase high performance liquid chromatography, and the kinetic
54 d with polymerase chain reaction, denaturing high-performance liquid chromatography, and DNA sequenci
55 somer mixture by preparative peak-recycling, high-performance liquid chromatography, and is employed
57 aditional quality control methods, including high performance liquid chromatography, are cumbersome a
58 t milk samples agreed with those obtained by high performance liquid chromatography at the 95% confid
59 itamin E, being comparable to reversed-phase high performance liquid chromatography chosen as referen
60 btained with concentrations determined using high-performance liquid chromatography (correlation coef
61 w chromatographic method using reverse-phase high performance liquid chromatography coupled to diode
62 gated for their phenolic profile by means of high performance liquid chromatography coupled to diode
64 in and subsequently quercetin, identified by high performance liquid chromatography coupled to mass s
66 sugars, organic acids and tocopherols (using high performance liquid chromatography coupled to refrac
68 sing a QuEChERS extraction followed by ultra-high performance liquid chromatography coupled to tandem
69 ation of pesticides in orange juice by ultra high performance liquid chromatography coupled to tandem
70 e, sensitive and specific method using ultra-high performance liquid chromatography coupled to tandem
71 powdered milk using QuEChERS extraction and high performance liquid chromatography coupled to tandem
73 cides determination was achieved using ultra high performance liquid chromatography coupled to triple
74 X) and nitarsone (NIT) in livestock feeds by high performance liquid chromatography coupled to ultrav
75 ents of respective extracts were analyzed by high performance liquid chromatography coupled with DAD
76 hout further clean-up, and analysis by ultra-high performance liquid chromatography coupled with fluo
78 antified using the Folin-Ciocalteu assay and high performance liquid chromatography coupled with phot
79 been developed and characterised using ultra-high performance liquid chromatography coupled with tand
80 Individual phenolics were characterized by high-performance liquid chromatography coupled to a diod
81 odology and were separated and identified by high-performance liquid chromatography coupled to a mass
82 ultiplexed relative quantification and ultra-high-performance liquid chromatography coupled to accura
83 phenolic profile by means of reversed phase high-performance liquid chromatography coupled to diode
84 ime-of-flight mass spectrometry and by ultra-high-performance liquid chromatography coupled to electr
86 seeds, a target analysis was performed using high-performance liquid chromatography coupled to photod
88 phenols were identified and quantified using high-performance liquid chromatography coupled with diod
89 d (n = 2,866) for 3HPMA and CEMA using ultra-high-performance liquid chromatography coupled with elec
90 EDTA, and rapid analysis via anion-exchange high-performance liquid chromatography coupled with elec
92 atisfactory agreement with those obtained by high-performance liquid chromatography coupled with fluo
93 An unbiased scanning methodology using ultra high-performance liquid chromatography coupled with high
94 yanins and phenolic compounds) determined by high-performance liquid chromatography coupled with phot
95 IS patients and 31 healthy controls by ultra high-performance liquid chromatography coupled with quad
96 nalysis with discriminant analysis and ultra-high-performance liquid chromatography coupled with tand
98 acid extraction followed by determination by high-performance liquid chromatography coupled with tand
100 were validated using commercially available high performance liquid chromatography diode array detec
102 sequent detection by Ion-Pair-Reversed Phase-High Performance Liquid Chromatography-Diode Array Detec
104 ueberry were identified and quantified using high-performance liquid chromatography-diode array detec
106 d TLC spots were chemically identified using high-performance liquid chromatography-diode array detec
107 column chromatography, and preparative-scale high performance liquid chromatography, each sample prov
108 led gas chromatography/mass spectrometry and high-performance liquid chromatography electrospray ioni
109 coli, bottom-up proteomic characterization, high-performance liquid chromatography-electrospray ioni
110 ponents, mass spectrometric screens based on high-performance liquid chromatography-electrospray ioni
111 yphenols from caper berries was developed on high-performance liquid chromatography/electrospray ioni
113 S) with o-phthalaldehyde (OPA) reagent using high-performance liquid chromatography-fluorescence dete
114 copherol and gamma-tocopherol, reverse phase high performance liquid chromatography for the quantific
115 ve liquid-liquid microextraction followed by high-performance liquid chromatography for the determina
116 he French Atlantic coast was investigated by high performance liquid chromatography-high resolution m
117 ucosidase inhibition profiling combined with high-performance liquid chromatography-high-resolution m
122 after 4 months storage at 10 degrees C using high performance liquid chromatography (HPLC) and abilit
123 ssava starch wastewater using reversed-phase high performance liquid chromatography (HPLC) and capill
124 mers and polymers, involved separation using high performance liquid chromatography (HPLC) and detect
125 o chromatographic separation techniques like high performance liquid chromatography (HPLC) and gas ch
126 taric acid) were separated and quantified by high performance liquid chromatography (HPLC) and the da
127 By combining high volume injection with high performance liquid chromatography (HPLC) and ultrah
130 paration was accomplished with reverse phase-high performance liquid chromatography (HPLC) hyphenated
135 ort the development and validation of a fast high performance liquid chromatography (HPLC) multiplexi
136 f BrC chromophores were investigated using a high performance liquid chromatography (HPLC) platform c
138 s were evaluated by electroanalysis, whereas high performance liquid chromatography (HPLC) was used f
140 on-line to solid phase extraction (SPE) and high performance liquid chromatography (HPLC) with fluor
141 milk and powdered infant formula samples by high performance liquid chromatography (HPLC) with visib
142 ion is focused on the on-line combination of high performance liquid chromatography (HPLC), cryogenic
143 immunosorbent assays (ELISA), Western blot, high performance liquid chromatography (HPLC), spectroph
149 onstituents were determined by using on-line high-performance liquid chromatography (HPLC) analysis c
151 nic glycosides were analyzed with the aid of high-performance liquid chromatography (HPLC) and mass s
152 oglycosidase sequencing, in conjunction with high-performance liquid chromatography (HPLC) and matrix
153 itol mixture was preseparated on an off-line high-performance liquid chromatography (HPLC) column, an
155 ogenic amines is described and compared with high-performance liquid chromatography (HPLC) method cou
156 performance liquid chromatography (UPLC) and high-performance liquid chromatography (HPLC) methods fo
157 de detection involves conventional multistep high-performance liquid chromatography (HPLC) methods, r
158 as a vapor generation (VG) device to couple high-performance liquid chromatography (HPLC) separation
161 quid microextraction (MAE-DLLME) followed by high-performance liquid chromatography (HPLC) was develo
163 ssisted liquid-liquid extraction (SALLE) and high-performance liquid chromatography (HPLC) with diode
164 , flavones and flavanones were determined by high-performance liquid chromatography (HPLC) with diode
165 y of the jaboticaba peel were analyzed using high-performance liquid chromatography (HPLC) with photo
166 e profiling, i.e., radiolabeling followed by high-performance liquid chromatography (HPLC) with radio
168 egy, based on bioassay-guided fractionation, high-performance liquid chromatography (HPLC), and high-
169 c2C2@Cs(hept)-C88 was purified by multistage high-performance liquid chromatography (HPLC), cocrystal
170 caffeine and chlorogenic acid content using high-performance liquid chromatography (HPLC), sucrose c
171 t species, Piper kelleyi (Piperaceae), using high-performance liquid chromatography (HPLC), to unders
172 BaP-treated rodents, and indirectly through high-performance liquid chromatography (HPLC)-fluorescen
178 tu by ethylenediaminetetraacetate (EDTA) and high performance liquid chromatography hyphenated to ind
179 ometry (ICP-MS) and urinary As speciation by high performance liquid chromatography ICP-MS (HPLC-ICP-
180 e disulphide) aminothiols were quantified by high performance liquid chromatography in 1411 patients
183 d and were compared to the reference method (high-performance liquid chromatography-inductively coupl
184 ts were separated by ion-pair reversed-phase high-performance liquid chromatography (IP-RP-HPLC) and
186 ght regions in Nigeria was carried out using high performance liquid chromatography (LC) coupled with
187 Extensive isomerism was revealed by ultra-high-performance liquid chromatography, leading to evide
188 e solid phase extraction (dSPE) material and high performance liquid chromatography-linear trap quadr
189 nization of the sample prior to analysis via high-performance liquid chromatography mass spectrometry
192 ment of M. truncatula macrosclereid cells, a high performance liquid chromatography-mass spectrometry
193 as a model protein for developing a top-down high-performance liquid chromatography-mass spectrometry
194 rations, which were measured with the use of high-performance liquid chromatography-mass spectrometry
195 5-hydroxyvitamin D [25(OH)D] with the use of high-performance liquid chromatography-mass spectrometry
198 ytometry with highly efficient 3-dimensional high performance liquid chromatography/mass spectrometry
199 by bioinformatics analyses and confirmed by high-performance liquid chromatography measurements.
200 helping regulatory authorities, a sensitive high performance liquid chromatography method was valida
204 sured MMC concentration determined using the high-performance liquid chromatography method for all sa
210 c approach based on a core-shell column with high-performance liquid chromatography multi-wavelength
211 activity were fractionated with normal phase high-performance liquid chromatography (NP-HPLC) and eac
212 ic 4,4'-bipyridines were enantioseparated by high performance liquid chromatography on chiral station
213 by costly, large-scale instruments (such as high-performance liquid chromatography) or reagent insta
215 amino acid hydroxyproline, using preparative high-performance liquid chromatography (Prep-HPLC).
216 of protein concentrations by reversed-phase high-performance liquid chromatography provided independ
217 (11)C-methyltriflate with 4-HBZA followed by high-performance liquid chromatography purification.
218 eld 49.8% +/- 5.9% within 20-25 min) without high-performance liquid chromatography purification.
219 (11)C-methyltriflate with 4-HBZA followed by high-performance liquid chromatography purification.
221 ic components were analyzed by reverse phase high performance liquid chromatography (RP-HPLC) to dete
223 tion of phenolic compounds by reversed-phase high-performance liquid chromatography (RP-HPLC), using
224 roteins were characterized by size exclusion high-performance liquid chromatography (SE-HPLC) and sod
225 borne fractions determined by reversed-phase high-performance liquid chromatography, showed that the
226 x followed by semi-preparative reverse phase-high performance liquid chromatography (SP RP-HPLC).
227 elected ethylene-bridged hybrid phenyl ultra-high-performance liquid chromatography stationary phase
228 t and highly sensitive method based on ultra-high performance liquid chromatography tandem mass spect
229 biological activities and developed an ultra-high performance liquid chromatography tandem mass spect
230 ty, we performed metabolomic profiling using high performance liquid chromatography tandem mass spect
231 iquid extraction (SALLE) combined with ultra-high performance liquid chromatography tandem mass spect
232 and solid-phase extraction coupled to ultra-high-performance liquid chromatography tandem mass spect
233 action cleanup step) followed by analysis by high-performance liquid chromatography tandem mass spect
234 t, a matrix-specific procedure for the ultra-high performance liquid chromatography-tandem mass spect
237 ipeptides in authentic water, we developed a high-performance liquid chromatography-tandem mass spect
238 es and their metabolites were analyzed using high-performance liquid chromatography-tandem mass spect
239 e then measured for 13 case-control pairs by high-performance liquid chromatography-tandem mass spect
240 ography (GC) approaches, a simple and unique high-performance liquid chromatography-tandem mass spect
241 gle solid-phase extraction (SPE) method with high-performance liquid chromatography-tandem mass spect
242 e were measured over 12 h postprandially via high-performance liquid chromatography-tandem mass spect
243 g using glutathione (GSH) and analysis using high-performance liquid chromatography-tandem mass spect
244 ling for antiretroviral concentrations using high-performance liquid chromatography-tandem mass spect
245 bolites, parabens, triclosan, and BP-3 using high-performance liquid chromatography/tandem mass spect
247 ure, showing a single radioactive species by high-performance liquid chromatography that was stable i
248 ional cohorts and analyzed for HMOs by using high-performance liquid chromatography.There was an effe
249 extraction cartridges and detection by ultra-high-performance liquid chromatography/time-of-flight ma
250 uide strands was coupled with anion exchange high performance liquid chromatography to quantitate gui
251 involving ion mobility mass spectrometry and high-performance liquid chromatography to comprehensivel
252 online electrochemical mass spectrometry and high-performance liquid chromatography to determine the
256 ometry (LC-Q-ToF-MS) and quantified by ultra high performance liquid chromatography-triple quadrupole
257 iridoid oxidative compounds were examined by high-performance liquid chromatography/triple quadrupole
258 quential ion-exchange/reversed-phase (ultra) high-performance liquid chromatography [(U)HPLC] using a
259 The compounds were determined using ultra high performance liquid chromatography (UHPLC) coupled t
260 fication of the phenols was done using ultra-high performance liquid chromatography (UHPLC) coupled w
262 auraptene in some vegetable oils using ultra high performance liquid chromatography (UHPLC) with phot
263 novel strategy that combines a typical ultra high performance liquid chromatography (UHPLC), data-ind
264 ted a simple, specific, sensitive and stable high performance liquid chromatography-ultraviolet detec
265 ene (PYR) in chrysanthemum tea samples using high performance liquid chromatography-ultraviolet detec
267 analyzed for the presence of aldehydes using high-performance liquid chromatography-ultraviolet detec
268 inidase activity is achieved utilizing ultra-high performance liquid chromatography (UPLC) and isotop
269 nary concentrations of TMSe were measured by high-performance liquid chromatography/vapor generation/
272 n exchange chromatography and reversed phase high performance liquid chromatography was used to purif
274 he-art reversed phase (RP) columns for ultra-high performance liquid chromatography were tested for t
275 orescence matrices derived from kinetics and high-performance liquid chromatography, were adapted to
276 of API and counterion release profiles using high-performance liquid chromatography, which had stoich
277 bsequently annotated by reversed-phase ultra-high performance liquid chromatography with a photo diod
278 d chromatographic technique UHPLC-DAD (Ultra High Performance Liquid Chromatography with Diode Array
279 fferent chemical classes were analysed using high performance liquid chromatography with diode-array
280 ification of 30 pesticides was conducted via high performance liquid chromatography with diode-array
281 olites, were evaluated using amperometry and high performance liquid chromatography with electrochemi
282 nd red snapper (Lutjanus campechanus), using high performance liquid chromatography with fluorescence
284 he corresponding extract analyzed with ultra high performance liquid chromatography with photodiode a
286 ontent in the PHWE extracts were analysed on high performance liquid chromatography with ultra violet
287 id-liquid microextraction (DLLME) coupled to high performance liquid chromatography with ultraviolet
288 ication of the acrylamide was carried out by high performance liquid chromatography with UV detection
289 ication of the compounds was developed using high-performance liquid chromatography with diode array
290 a Pieve) and Sardinia, have been analysed by high-performance liquid chromatography with diode array
291 simple, sensitive and selective multiresidue high-performance liquid chromatography with diode array
292 bust analytical method, using reversed phase high-performance liquid chromatography with diode array
293 -2-yl]amino) fluorescein (DTAF), detected by high-performance liquid chromatography with diode-array
294 rmination of maltodextrin in raw milk, using high-performance liquid chromatography with evaporative
295 SO2 was detected in adipose tissue using high-performance liquid chromatography with fluorescence
296 ng inductively coupled mass spectrometry and high-performance liquid chromatography with inductively
297 arotenoids were extracted and analysed using high-performance liquid chromatography with photodiode a
298 e veterinary antibiotics were quantified via high-performance liquid chromatography with tandem mass
299 urenine metabolite analysis, performed using high-performance liquid chromatography with tandem mass
300 es, and an off-line MISPE method followed by high-performance liquid chromatography with UV diode-arr
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