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1 ere subsequently identified by reverse phase high pressure liquid chromatography.
2 into its enantiomeric constituents by chiral high pressure liquid chromatography.
3 ity chromatography followed by reverse phase high pressure liquid chromatography.
4 nd analyzed quantitatively by reversed phase high pressure liquid chromatography.
5 chromatography and purified by reverse phase high pressure liquid chromatography.
6 bilateral cortical windows, were analyzed by high pressure liquid chromatography.
7 nicum using size exclusion and reverse-phase high pressure liquid chromatography.
8 as purified to homogeneity by reversed-phase high pressure liquid chromatography.
9 10% of the total radioactivity recovered by high pressure liquid chromatography.
10 two peptides following trypsin digestion and high pressure liquid chromatography.
11 clusion chromatography, and C4 reverse phase high pressure liquid chromatography.
12 ormed a complex detectable by size exclusion high pressure liquid chromatography.
13 romide cleavage and separation by gel and/or high pressure liquid chromatography.
14 nd purified by adsorption chromatography and high pressure liquid chromatography.
15 hat might correlate with mobility changes on high pressure liquid chromatography.
16 ulose/rhamnose ratio (L/R ratio) measured by High Pressure Liquid Chromatography.
17 , and the tryptic peptides were separated by high pressure liquid chromatography.
18 ser desorption ionization time-of-flight and high pressure liquid chromatography.
19 asured every 12 hours over a 7-day period by high-pressure liquid chromatography.
20 etinol, carotenoids, and alpha-tocopherol by high-pressure liquid chromatography.
21 ing the complexation level by size-exclusion high-pressure liquid chromatography.
22 om bovine lung was purified by reverse-phase high-pressure liquid chromatography.
23 denosine concentration was measured by using high-pressure liquid chromatography.
24 amate concentration previously quantified by high-pressure liquid chromatography.
25 n the collected molecules were measured with high-pressure liquid chromatography.
26 orescent derivatives, which were analyzed by high-pressure liquid chromatography.
27 Plasma concentrations were analyzed by high-pressure liquid chromatography.
28 was eluted as a single peak by reverse-phase high-pressure liquid chromatography.
29 duction of C(60) and isolated by preparative high-pressure liquid chromatography.
30 sine and purine metabolites were measured by high-pressure liquid chromatography.
31 Trp and Kyn concentrations were analyzed by high-pressure liquid chromatography.
32 hydroxysuccimidyl carbamate and submitted to high-pressure liquid chromatography.
33 oresis, capillary electrochromatography, and high-pressure liquid chromatography.
34 every 30 min were assayed in a single run by high-pressure liquid chromatography.
35 and the eluates were pooled and submitted to high-pressure liquid chromatography.
36 analyzed by a combination of thin-layer and high-pressure liquid chromatography.
37 antiomers in the presence of NADPH by chiral high-pressure liquid chromatography.
38 yeast culture supernatant by reversed-phase high-pressure liquid chromatography.
39 chromatography and purified by reverse-phase high-pressure liquid chromatography.
40 extracted and quantitated by reverse-phased high-pressure liquid chromatography.
41 s allowed their separation by reversed-phase high-pressure liquid chromatography.
42 the extract were separated by reverse-phase high-pressure liquid chromatography.
43 bile duct walls were quantified by means of high-pressure liquid chromatography.
44 rom NMR spectroscopy, mass spectrometry, and high-pressure liquid chromatography.
45 itrectomy assessed via mass spectrometry and high-pressure liquid chromatography.
48 ndly microextraction by packed sorbent ultra-high pressure liquid chromatography analysis (MEPS/UHPLC
49 dependent, Mn(2+)-mediated reaction based on high pressure liquid chromatography analysis and absorpt
61 No significant difference was detected by high-pressure liquid chromatography analysis of stem pep
65 lactone (BHL) by thin-layer chromatography, high-pressure liquid chromatography analysis, and mass s
66 luding enzymatic deactivation, reverse-phase high-pressure liquid chromatography analysis, sodium dod
70 tity of which was confirmed by reverse phase high pressure liquid chromatography and amino-terminal m
71 of soluble oligomers based on size exclusion high pressure liquid chromatography and atomic force mic
72 pediatric liver recipients by reversed phase high pressure liquid chromatography and correlated our r
75 ic peptides into cells was verified by using high pressure liquid chromatography and matrix-assisted
76 (at Thr(184), Thr(189), and Thr(202)) using high pressure liquid chromatography and matrix-assisted
77 and the resulting peptides were separated by high pressure liquid chromatography and monitored with a
79 se fractions eluted from a molecular sieving high pressure liquid chromatography and the apyrase acti
81 ithout the expensive requirement of an ultra-high pressure liquid chromatography and/or mass spectrom
83 40 mg/kg, subcutaneously) were determined by high-pressure liquid chromatography and electrochemical
84 lial cell line (RTMGL1) using reversed phase high-pressure liquid chromatography and liquid chromatog
86 we screened urine from XT2-knockout mice by high-pressure liquid chromatography and mass spectrometr
87 e and fluorescence spectroscopies as well as high-pressure liquid chromatography and mass spectrometr
89 h its TAF subunits, as shown by ion exchange high-pressure liquid chromatography and sedimentation ve
91 The 1,N6-ethenoadenosine was separated by high-pressure liquid chromatography and then measured by
92 e ligands were first fractionated by high-pH high-pressure liquid chromatography and then subjected t
93 re by conventional column chromatography and high-pressure liquid chromatography and used mass spectr
94 e separation and detection were performed by high-pressure liquid-chromatography and tandem mass-spec
95 tyrosine, and nitrodityrosine as measured by high pressure liquid chromatography, and (iii) oxidation
96 parative SDS-PAGE, in-gel tryptic digestion, high pressure liquid chromatography, and mass spectromet
98 on exchange chromatography, on reverse phase high pressure liquid chromatography, and on thin layer c
99 igested and then separated by size exclusion high pressure liquid chromatography, and the activity to
103 on (DMB) was isolated by using reverse-phase high-pressure liquid chromatography, and its identity wa
106 ted by the immunoadsorbent were submitted to high-pressure liquid chromatography, and their respectiv
107 enase activity was analyzed by reverse-phase high-pressure liquid chromatography; and the results sho
108 for KIT mutations we have adapted denaturing high-pressure liquid chromatography as a method for scre
109 xide in plasma membranes was demonstrated by high pressure liquid chromatography assay for conjugated
113 uctural analysis by analytic and preparative high pressure liquid chromatography, by multidimensional
115 IC(50) values below 600 nm were purified by high pressure liquid chromatography, characterized by ma
119 oteins were identified with multidimensional high pressure liquid chromatography coupled with electro
122 oducts in purine pathway were measured using high-pressure liquid chromatography coupled with a coulo
123 age in the form of 80 HdG was measured using high-pressure liquid chromatography coupled with electro
125 rrant simple sugar profile was determined by high-pressure liquid chromatography coupled with refract
126 and its lysostaphin degradation products by high pressure liquid chromatography, Edman degradation,
127 actone is further purified and quantified by high-pressure liquid chromatography either on a reverse
128 wed that the levels of damage measured using high-pressure liquid chromatography/electrochemical dete
129 52-kDa CGase activity from T. denticola, and high pressure liquid chromatography electrospray ionizat
130 0-kDa protein that, upon characterization by high-pressure liquid chromatography electrospray tandem
131 rides are confirmed by strong anion exchange high-pressure liquid chromatography, electrospray ioniza
134 ching, acid hydrolysis, and isotope dilution high pressure liquid chromatography-electrospray ionizat
136 from two corneas with FSCA were purified by high-pressure liquid chromatography followed by protein
137 the perfusion, and samples were analyzed by high-pressure liquid chromatography for doxorubicin and
138 acid chromatography, CPS-500 was isolated by high-pressure liquid chromatography for glycosyl analysi
139 l lines were treated with DMF and assayed by high-pressure liquid chromatography for intracellular an
140 a tryptic digest of the main reversed phase-high pressure liquid chromatography fraction revealed tw
142 in BAL fluid was confirmed by reverse-phase high-pressure liquid chromatography fractionation follow
144 ce active and lowered the surface tension of high-pressure liquid chromatography-grade water from 72.
145 tural interface with microbore and capillary high-pressure liquid chromatography, has become the meth
146 and (poly)phenol catabolites with the use of high-pressure liquid chromatography-high resolution mass
149 d analyzed by a combination of reverse-phase-high pressure liquid chromatography (HPLC) and mass spec
150 bound to GPIX and GPIb were also analyzed by high pressure liquid chromatography (HPLC) and scintilla
153 henacyl esters were prepared and analyzed by high pressure liquid chromatography (HPLC) with detectio
154 de digestion, immunoaffinity chromatography, high pressure liquid chromatography (HPLC), and enzyme-l
155 se extraction (SPE) preparation step and two high pressure liquid chromatography (HPLC)-based analyti
156 roblasts, and 3T3-L1 adipocytes) that show a high pressure liquid chromatography (HPLC)-detectable pe
159 A (rRNA) retention using model compounds and high-pressure liquid chromatography (HPLC) analyses, enh
161 enriched by chromatographic separation using high-pressure liquid chromatography (HPLC) and a chiral
162 n conditions in capillary electrophoresis or high-pressure liquid chromatography (HPLC) and can signi
164 ments of real eddy dispersion data in modern high-pressure liquid chromatography (HPLC) columns were
165 tecan plasma concentrations were measured by high-pressure liquid chromatography (HPLC) during infusi
166 d within the first 24 hours were measured by high-pressure liquid chromatography (HPLC) for topotecan
167 try (MS), in combination with reversed-phase high-pressure liquid chromatography (HPLC) fractionation
168 des from 12B1 leukemia-derived CRCL and used high-pressure liquid chromatography (HPLC) fractions to
169 ugh the TOF-SIMS spectra and is supported by high-pressure liquid chromatography (HPLC) measurements
170 sources, magnitudes, and variability) for a high-pressure liquid chromatography (HPLC) method design
172 ographic separation of peptides and the nano-high-pressure liquid chromatography (HPLC) separation of
173 of the PAH were obtained from reversed-phase high-pressure liquid chromatography (HPLC) utilizing an
174 bral ganglia using three sequential modes of high-pressure liquid chromatography (HPLC) was followed
175 better characterize this pathway in humans, high-pressure liquid chromatography (HPLC) was used to d
176 A and 5-HT, as well as major metabolites, by high-pressure liquid chromatography (HPLC) with electroc
177 onodisperse spherical particles for nanoflow high-pressure liquid chromatography (HPLC), current stat
178 ating glycated insulin has been evaluated by high-pressure liquid chromatography (HPLC), electrospray
181 hase extraction (SPE) apparatus intended for high-pressure liquid chromatography (HPLC)-NMR hyphenati
189 by metal (Al3+) chelate chromatography, and high pressure liquid chromatography identified a 32P-pen
190 encing of peptides purified by reverse-phase high-pressure liquid chromatography identified FMSF as a
191 es have been investigated rarely by means of high-pressure liquid chromatography in combination with
193 samples were analyzed in a masked fashion by high-pressure liquid chromatography in two independent l
194 cleavage products separated by reverse-phase high-pressure liquid chromatography indicate that LF see
196 inant non-native monomeric forms isolated by high-pressure liquid chromatography indicated the presen
197 er1105 by direct sequencing of reverse-phase high pressure liquid chromatography-isolated phosphopept
199 ard this end, we used single-dimension ultra-high-pressure liquid chromatography mass spectrometry to
202 ing dynamic light scattering (DLS) and ultra high pressure liquid chromatography-mass spectrometry (U
203 the presence of a mixture of all four dNTPs, high pressure liquid chromatography-mass spectrometry an
205 The identity of the protein was verified by high pressure liquid chromatography-mass spectrometry.
206 e following four products were identified by high pressure liquid chromatography-mass spectrometry: 5
207 uman embryos culture medium were analyzed by high-pressure liquid chromatography-mass spectrometry (H
208 -SSP), whole-body autoradiography (WBA), and high-pressure liquid chromatography-mass spectrometry (H
209 nucleosides from several of these phages by high-pressure liquid chromatography-mass spectrometry co
210 cid mixture was fractionated and analyzed by high-pressure liquid chromatography-mass spectrometry in
213 discrete PtdIns(3,5)P(2) subfraction as the high pressure liquid chromatography-measurable insulin-d
216 mitations, we have developed a reverse-phase high-pressure liquid chromatography method for cytochrom
219 phosphorylation sites in TTP using nanoflow high pressure liquid chromatography microelectrospray io
220 were measured by chemiluminescence; ADMA by high pressure liquid chromatography; monocyte chemotacti
221 , from solution, by a nanoflow reverse phase-high pressure liquid chromatography-mu-electrospray ioni
222 igestion of the cross-linked MTF followed by high pressure liquid chromatography of the digest yielde
223 erythroblasts was analyzed by size-exclusion high-pressure liquid chromatography of band 3 extracts d
226 ion of the primary granules by reverse phase high-pressure liquid chromatography on a C(4) column ove
227 With one set of purification of histones by high pressure liquid chromatography or SDS-PAGE, nearly
228 ere analyzed for stability by size-exclusion high-pressure liquid chromatography, pH measurement, osm
229 mples T1 to T3 were analyzed with the use of high-pressure liquid chromatography/positive ion mode at
230 entify the reactive residue, we compared the high pressure liquid chromatography profile of trypsin-d
231 Examination of CD45-depleted HIV-1(MN) by high-pressure liquid chromatography, protein sequencing,
232 d H9 and CEM(ss) cell lines were analyzed by high-pressure liquid chromatography, protein sequencing,
233 onochloramine and aldehyde were confirmed by high pressure liquid chromatography purification of the
239 , UV visible absorption spectrometry, GC and high pressure liquid chromatography retention times, and
240 cterized by comparison of its mass spectrum, high-pressure liquid chromatography retention time, and
241 s, and pyridoxal-5'-phosphate (PLP) by using high-pressure liquid chromatography, retinol-binding pro
243 ntaining amidated and deamidated forms using high pressure liquid chromatography-reverse phase chroma
246 ic extraction with subsequent reversed-phase-high-pressure liquid chromatography (RP-HPLC) separation
247 ion was performed with either reversed-phase high-pressure liquid chromatography (RP-HPLC), gel elect
249 ligand blotting assay, which, together with high pressure liquid chromatography/SDS-polyacrylamide g
251 mixed disulfides followed by reversed-phase high pressure liquid chromatography separation of phenyl
252 equencing after tryptic in-gel digestion and high pressure liquid chromatography separation of the re
254 arried out in a single step by reverse phase high-pressure liquid chromatography separation followed
255 in eluate was further purified by successive high pressure liquid chromatography separations on hydro
256 by combined ion exchange and reversed phase high pressure liquid chromatography steps and was shown
257 ory-secretory (ES) products by reverse-phase high-pressure liquid chromatography, subjected to amino-
258 ty columns were identified by microcapillary high pressure liquid chromatography tandem mass spectrom
259 rylation sites were mapped by microcapillary high-pressure liquid chromatography tandem mass spectrom
261 We validated a fast and sensitive ultra-high-pressure liquid chromatography tandem mass spectrom
262 mM) and UVA (0.06 J/cm(2)) as quantified by high-pressure liquid chromatography-tandem mass spectrom
265 ion, we used affinity chromatography-coupled high pressure liquid chromatography/tandem mass spectrom
267 ncentration was above 1 mM, as determined by high-pressure liquid chromatography, the serum cytotoxic
268 isolated by lectin binding and reverse phase high pressure liquid chromatography; their molecular mas
270 f the pathway, we used mass spectrometry and high pressure liquid chromatography to quantify oxidatio
271 the optimization of a one dimensional ultra-high-pressure liquid chromatography top-down mass spectr
272 r blended whiskeys were analysed using ultra high pressure liquid chromatography (UHPLC) coupled with
274 for the first time to extract whereas Ultra High pressure liquid chromatography (UHPLC-DAD) was used
275 flow capillary-based microreactor with ultra-high-pressure liquid chromatography (UHPLC) for fast onl
276 hic separation of macromolecules in an ultra-high-pressure liquid chromatography (UHPLC) format.
277 costly and time consuming processes such as high pressure liquid chromatography, ultrahigh pressure
278 fluorescence microscopy were validated by an high-pressure liquid chromatography/ultraviolet (HPLC/UV
279 end groups (FTD) were investigated by ultra high pressure liquid chromatography under critical condi
280 ic conditions and identified the products by high pressure liquid chromatography, UV, mass spectromet
282 ssessed by measurement of 3-nitrotyrosine by high-pressure liquid chromatography) was elevated at 16
283 of the mobile phase that take place in very high pressure liquid chromatography were studied based o
284 tical ultracentrifugation and size exclusion high pressure liquid chromatography were used to investi
285 microbiological assay) and 5-MTHF (by using high-pressure liquid chromatography) were measured in fa
286 acetyl lysine was purified by reversed phase high pressure liquid chromatography, which was character
287 flavan-3-ols were analyzed by reverse-phase high-pressure liquid chromatography, while the size and
288 oaffinity column (IAC) tandem reversed-phase high pressure liquid chromatography with fluorescence de
289 (IAC), and identification by reversed-phase high pressure liquid chromatography with fluorescence de
290 revealed by immunocytochemical staining and high pressure liquid chromatography with on-line electro
291 ed serum acetaminophen-protein adducts using high-pressure liquid chromatography with electrochemical
293 ayed for monoamines and major metabolites by high-pressure liquid chromatography with electrochemical
294 acid) in the samples were measured by use of high-pressure liquid chromatography with fluorescence de
297 ically produced from CoM, as demonstrated by high-pressure liquid chromatography with indirect photom
298 Serum carotenoid levels were obtained by high-pressure liquid chromatography with photodiode arra