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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 is using a combination of gel filtration and high pressure liquid chromatography.
17 ulose/rhamnose ratio (L/R ratio) measured by High Pressure Liquid Chromatography.
18 , and the tryptic peptides were separated by high pressure liquid chromatography.
19 ser desorption ionization time-of-flight and high pressure liquid chromatography.
20 asured every 12 hours over a 7-day period by high-pressure liquid chromatography.
21 Trp and Kyn concentrations were analyzed by high-pressure liquid chromatography.
22 ing the complexation level by size-exclusion high-pressure liquid chromatography.
23 om bovine lung was purified by reverse-phase high-pressure liquid chromatography.
24 denosine concentration was measured by using high-pressure liquid chromatography.
25 amate concentration previously quantified by high-pressure liquid chromatography.
26 n the collected molecules were measured with high-pressure liquid chromatography.
27 orescent derivatives, which were analyzed by high-pressure liquid chromatography.
28 Plasma concentrations were analyzed by high-pressure liquid chromatography.
29 was eluted as a single peak by reverse-phase high-pressure liquid chromatography.
30 duction of C(60) and isolated by preparative high-pressure liquid chromatography.
31 sine and purine metabolites were measured 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.
46 etinol, carotenoids, and alpha-tocopherol by high-pressure liquid chromatography.
49 ndly microextraction by packed sorbent ultra-high pressure liquid chromatography analysis (MEPS/UHPLC
50 dependent, Mn(2+)-mediated reaction based on high pressure liquid chromatography analysis and absorpt
63 No significant difference was detected by high-pressure liquid chromatography analysis of stem pep
67 lactone (BHL) by thin-layer chromatography, high-pressure liquid chromatography analysis, and mass s
68 luding enzymatic deactivation, reverse-phase high-pressure liquid chromatography analysis, sodium dod
72 tity of which was confirmed by reverse phase high pressure liquid chromatography and amino-terminal m
73 of soluble oligomers based on size exclusion high pressure liquid chromatography and atomic force mic
74 pediatric liver recipients by reversed phase high pressure liquid chromatography and correlated our r
77 ic peptides into cells was verified by using high pressure liquid chromatography and matrix-assisted
78 (at Thr(184), Thr(189), and Thr(202)) using high pressure liquid chromatography and matrix-assisted
79 and the resulting peptides were separated by high pressure liquid chromatography and monitored with a
81 se fractions eluted from a molecular sieving high pressure liquid chromatography and the apyrase acti
84 40 mg/kg, subcutaneously) were determined by high-pressure liquid chromatography and electrochemical
85 lial cell line (RTMGL1) using reversed phase high-pressure liquid chromatography and liquid chromatog
87 we screened urine from XT2-knockout mice by high-pressure liquid chromatography and mass spectrometr
88 e and fluorescence spectroscopies as well as high-pressure liquid chromatography and mass spectrometr
90 h its TAF subunits, as shown by ion exchange high-pressure liquid chromatography and sedimentation ve
92 The 1,N6-ethenoadenosine was separated by high-pressure liquid chromatography and then measured by
93 e ligands were first fractionated by high-pH high-pressure liquid chromatography and then subjected t
94 re by conventional column chromatography and high-pressure liquid chromatography and used mass spectr
95 e separation and detection were performed by high-pressure liquid-chromatography and tandem mass-spec
96 tyrosine, and nitrodityrosine as measured by high pressure liquid chromatography, and (iii) oxidation
97 parative SDS-PAGE, in-gel tryptic digestion, high pressure liquid chromatography, and mass spectromet
99 on exchange chromatography, on reverse phase high pressure liquid chromatography, and on thin layer c
100 igested and then separated by size exclusion high pressure liquid chromatography, and the activity to
104 on (DMB) was isolated by using reverse-phase high-pressure liquid chromatography, and its identity wa
107 ted by the immunoadsorbent were submitted to high-pressure liquid chromatography, and their respectiv
108 enase activity was analyzed by reverse-phase high-pressure liquid chromatography; and the results sho
109 for KIT mutations we have adapted denaturing high-pressure liquid chromatography as a method for scre
110 xide in plasma membranes was demonstrated by high pressure liquid chromatography assay for conjugated
114 uctural analysis by analytic and preparative high pressure liquid chromatography, by multidimensional
116 IC(50) values below 600 nm were purified by high pressure liquid chromatography, characterized by ma
120 oteins were identified with multidimensional high pressure liquid chromatography coupled with electro
123 oducts in purine pathway were measured using high-pressure liquid chromatography coupled with a coulo
124 age in the form of 80 HdG was measured using high-pressure liquid chromatography coupled with electro
126 rrant simple sugar profile was determined by high-pressure liquid chromatography coupled with refract
127 and its lysostaphin degradation products by high pressure liquid chromatography, Edman degradation,
128 actone is further purified and quantified by high-pressure liquid chromatography either on a reverse
129 wed that the levels of damage measured using high-pressure liquid chromatography/electrochemical dete
130 52-kDa CGase activity from T. denticola, and high pressure liquid chromatography electrospray ionizat
131 0-kDa protein that, upon characterization by high-pressure liquid chromatography electrospray tandem
132 rides are confirmed by strong anion exchange high-pressure liquid chromatography, electrospray ioniza
135 ching, acid hydrolysis, and isotope dilution high pressure liquid chromatography-electrospray ionizat
137 from two corneas with FSCA were purified by high-pressure liquid chromatography followed by protein
138 the perfusion, and samples were analyzed by high-pressure liquid chromatography for doxorubicin and
139 acid chromatography, CPS-500 was isolated by high-pressure liquid chromatography for glycosyl analysi
140 l lines were treated with DMF and assayed by high-pressure liquid chromatography for intracellular an
141 a tryptic digest of the main reversed phase-high pressure liquid chromatography fraction revealed tw
143 in BAL fluid was confirmed by reverse-phase high-pressure liquid chromatography fractionation follow
145 ce active and lowered the surface tension of high-pressure liquid chromatography-grade water from 72.
146 tural interface with microbore and capillary high-pressure liquid chromatography, has become the meth
147 and (poly)phenol catabolites with the use of high-pressure liquid chromatography-high resolution mass
150 d analyzed by a combination of reverse-phase-high pressure liquid chromatography (HPLC) and mass spec
151 bound to GPIX and GPIb were also analyzed by high pressure liquid chromatography (HPLC) and scintilla
154 henacyl esters were prepared and analyzed by high pressure liquid chromatography (HPLC) with detectio
155 de digestion, immunoaffinity chromatography, high pressure liquid chromatography (HPLC), and enzyme-l
156 se extraction (SPE) preparation step and two high pressure liquid chromatography (HPLC)-based analyti
157 roblasts, and 3T3-L1 adipocytes) that show a high pressure liquid chromatography (HPLC)-detectable pe
160 A (rRNA) retention using model compounds and high-pressure liquid chromatography (HPLC) analyses, enh
162 enriched by chromatographic separation using high-pressure liquid chromatography (HPLC) and a chiral
163 n conditions in capillary electrophoresis or high-pressure liquid chromatography (HPLC) and can signi
165 ments of real eddy dispersion data in modern high-pressure liquid chromatography (HPLC) columns were
166 tecan plasma concentrations were measured by high-pressure liquid chromatography (HPLC) during infusi
167 d within the first 24 hours were measured by high-pressure liquid chromatography (HPLC) for topotecan
168 try (MS), in combination with reversed-phase high-pressure liquid chromatography (HPLC) fractionation
169 des from 12B1 leukemia-derived CRCL and used high-pressure liquid chromatography (HPLC) fractions to
170 ugh the TOF-SIMS spectra and is supported by high-pressure liquid chromatography (HPLC) measurements
171 sources, magnitudes, and variability) for a high-pressure liquid chromatography (HPLC) method design
173 ographic separation of peptides and the nano-high-pressure liquid chromatography (HPLC) separation of
174 of the PAH were obtained from reversed-phase high-pressure liquid chromatography (HPLC) utilizing an
175 bral ganglia using three sequential modes of high-pressure liquid chromatography (HPLC) was followed
176 better characterize this pathway in humans, high-pressure liquid chromatography (HPLC) was used to d
177 A and 5-HT, as well as major metabolites, by high-pressure liquid chromatography (HPLC) with electroc
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 the presence of a mixture of all four dNTPs, high pressure liquid chromatography-mass spectrometry an
204 The identity of the protein was verified by high pressure liquid chromatography-mass spectrometry.
205 e following four products were identified by high pressure liquid chromatography-mass spectrometry: 5
206 uman embryos culture medium were analyzed by high-pressure liquid chromatography-mass spectrometry (H
207 -SSP), whole-body autoradiography (WBA), and high-pressure liquid chromatography-mass spectrometry (H
210 discrete PtdIns(3,5)P(2) subfraction as the high pressure liquid chromatography-measurable insulin-d
213 mitations, we have developed a reverse-phase high-pressure liquid chromatography method for cytochrom
216 phosphorylation sites in TTP using nanoflow high pressure liquid chromatography microelectrospray io
217 were measured by chemiluminescence; ADMA by high pressure liquid chromatography; monocyte chemotacti
218 , from solution, by a nanoflow reverse phase-high pressure liquid chromatography-mu-electrospray ioni
219 igestion of the cross-linked MTF followed by high pressure liquid chromatography of the digest yielde
220 erythroblasts was analyzed by size-exclusion high-pressure liquid chromatography of band 3 extracts d
223 ion of the primary granules by reverse phase high-pressure liquid chromatography on a C(4) column ove
224 With one set of purification of histones by high pressure liquid chromatography or SDS-PAGE, nearly
225 mples T1 to T3 were analyzed with the use of high-pressure liquid chromatography/positive ion mode at
226 entify the reactive residue, we compared the high pressure liquid chromatography profile of trypsin-d
227 Examination of CD45-depleted HIV-1(MN) by high-pressure liquid chromatography, protein sequencing,
228 d H9 and CEM(ss) cell lines were analyzed by high-pressure liquid chromatography, protein sequencing,
229 onochloramine and aldehyde were confirmed by high pressure liquid chromatography purification of the
235 , UV visible absorption spectrometry, GC and high pressure liquid chromatography retention times, and
236 cterized by comparison of its mass spectrum, high-pressure liquid chromatography retention time, and
237 s, and pyridoxal-5'-phosphate (PLP) by using high-pressure liquid chromatography, retinol-binding pro
239 ntaining amidated and deamidated forms using high pressure liquid chromatography-reverse phase chroma
242 ic extraction with subsequent reversed-phase-high-pressure liquid chromatography (RP-HPLC) separation
243 ion was performed with either reversed-phase high-pressure liquid chromatography (RP-HPLC), gel elect
245 ligand blotting assay, which, together with high pressure liquid chromatography/SDS-polyacrylamide g
247 mixed disulfides followed by reversed-phase high pressure liquid chromatography separation of phenyl
248 equencing after tryptic in-gel digestion and high pressure liquid chromatography separation of the re
250 arried out in a single step by reverse phase high-pressure liquid chromatography separation followed
251 in eluate was further purified by successive high pressure liquid chromatography separations on hydro
252 by combined ion exchange and reversed phase high pressure liquid chromatography steps and was shown
253 ory-secretory (ES) products by reverse-phase high-pressure liquid chromatography, subjected to amino-
254 ty columns were identified by microcapillary high pressure liquid chromatography tandem mass spectrom
255 rylation sites were mapped by microcapillary high-pressure liquid chromatography tandem mass spectrom
256 We validated a fast and sensitive ultra-high-pressure liquid chromatography tandem mass spectrom
257 mM) and UVA (0.06 J/cm(2)) as quantified by high-pressure liquid chromatography-tandem mass spectrom
260 ion, we used affinity chromatography-coupled high pressure liquid chromatography/tandem mass spectrom
262 ncentration was above 1 mM, as determined by high-pressure liquid chromatography, the serum cytotoxic
263 isolated by lectin binding and reverse phase high pressure liquid chromatography; their molecular mas
265 f the pathway, we used mass spectrometry and high pressure liquid chromatography to quantify oxidatio
266 r blended whiskeys were analysed using ultra high pressure liquid chromatography (UHPLC) coupled with
268 flow capillary-based microreactor with ultra-high-pressure liquid chromatography (UHPLC) for fast onl
269 hic separation of macromolecules in an ultra-high-pressure liquid chromatography (UHPLC) format.
270 costly and time consuming processes such as high pressure liquid chromatography, ultrahigh pressure
271 fluorescence microscopy were validated by an high-pressure liquid chromatography/ultraviolet (HPLC/UV
272 end groups (FTD) were investigated by ultra high pressure liquid chromatography under critical condi
273 ic conditions and identified the products by high pressure liquid chromatography, UV, mass spectromet
275 ssessed by measurement of 3-nitrotyrosine by high-pressure liquid chromatography) was elevated at 16
276 of the mobile phase that take place in very high pressure liquid chromatography were studied based o
277 tical ultracentrifugation and size exclusion high pressure liquid chromatography were used to investi
278 microbiological assay) and 5-MTHF (by using high-pressure liquid chromatography) were measured in fa
279 acetyl lysine was purified by reversed phase high pressure liquid chromatography, which was character
280 flavan-3-ols were analyzed by reverse-phase high-pressure liquid chromatography, while the size and
281 oaffinity column (IAC) tandem reversed-phase high pressure liquid chromatography with fluorescence de
282 (IAC), and identification by reversed-phase high pressure liquid chromatography with fluorescence de
283 revealed by immunocytochemical staining and high pressure liquid chromatography with on-line electro
285 ayed for monoamines and major metabolites by high-pressure liquid chromatography with electrochemical
286 ed serum acetaminophen-protein adducts using high-pressure liquid chromatography with electrochemical
287 acid) in the samples were measured by use of high-pressure liquid chromatography with fluorescence de
290 ically produced from CoM, as demonstrated by high-pressure liquid chromatography with indirect photom
291 Serum carotenoid levels were obtained by high-pressure liquid chromatography with photodiode arra
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