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1 5-20 nmol of NO2- (1-20 micromol/L in 1-5 mL aliquots).
2  to be over 4500 from a single 20 muL plasma aliquot.
3 iglycerides were measured in the same tissue aliquot.
4 yses of NO2- and NO3- separately in the same aliquot.
5 sms from 10 mL of whole blood into a 200 muL aliquot.
6 d volume with a 10-min recovery between each aliquot.
7  expression as anticipated from the same RNA aliquot.
8     Each dust sample was subdivided into six aliquots.
9 serving as the sequencing primer in separate aliquots.
10 ucible and consistent among individual fecal aliquots.
11  STRs (P=.01) in irradiated versus untreated aliquots.
12  beta-globin targets were amplified from all aliquots.
13  donors and divided equally into eight 60-mL aliquots.
14 raditional loss of sensitivity due to sample aliquoting.
15                                           An aliquot (1.5 mL) of the acetonitrile layer was aspirated
16                         Five sequential TAML aliquots (2 muM overall) effected a 31% removal over 60
17                                Serial plasma aliquots (50 mL) obtained from 10 commercial donors who
18 ly negative in USP compared to NALC specimen aliquots (58% versus 43%; P < 0.001).
19  and 3% for no amplification) than untreated aliquots (7% for weak amplification and 0% for no amplif
20 A yields (3.7 microg/aliquot) than untreated aliquots (7.6 microg/aliquot) (P<.0005) and were more li
21 t analysis without the need of measuring and aliquoting a fixed sample volume prior to the on-line SP
22 ration of precious metals for the analytical aliquot, allowing for an empirical estimate of a minimum
23        This thermostabilized, pre-mixed, pre-aliquoted and ready-to-use magnetogenosensing assay simp
24                               Baseline urine aliquots and 24-hr urine collections were collected on d
25 NA expression are assayed in separate lysate aliquots and a dual analyte assay which can measure aP2
26    DNA was extracted from these 6 time point aliquots and analyzed by PCR and pyrosequencing for bact
27  Each laboratory was supplied with identical aliquots and common reagents and culture protocols.
28       The pancreatic digest was divided into aliquots and purified either by Ficoll or by filtration.
29 preparations, however, involve precise serum aliquots and require some skill and training of field pe
30 nriched marrow cells were divided into equal aliquots and transduced with vectors produced by the RD1
31 etermined after UV irradiation of a separate aliquot, and the sum of the fractions retained on the tw
32 oximately 15 g) of homogenized stool sample, aliquoted, and stored at <-20 degrees C, avoiding furthe
33 lecules in a single trap can be divided into aliquots, and the aliquots can be directed along multipl
34         Each sample was divided into 2 equal aliquots, and the SNO-RAC/Ox-RAC procedure was performed
35                      Serum samples in 10 muL aliquots are enzymatically treated to cleave the N-glyca
36                                        These aliquots are mixed at a temperature above the T(m) for a
37                                      The two aliquots are then incubated at equal concentrations, dig
38 r 7 years (2007-2013) by culture of platelet aliquots at time of transfusion and review of reported t
39            Yolks of 80 eggs were analysed as aliquots by the three methods in parallel.
40 ecause of its reversibility, the same enzyme aliquot can be used for performing the whole calibration
41 e trap can be divided into aliquots, and the aliquots can be directed along multiple routes simultane
42  derived from chromatographic methods, since aliquots can be transferred directly from the fraction c
43    The S. agalactiae detection rate by early-aliquot carrot broth-enhanced PCR (66.1%) exceeded that
44                                        Early-aliquot carrot broth-enhanced PCR detection rate differe
45  of these samples (51.8%; P<0.0002) or early-aliquot carrot broth-enhanced PCR of 144 carrot broth al
46                Enhanced sensitivity of early-aliquot carrot broth-enhanced PCR versus direct swab PCR
47 ubjected to carrot broth-enhanced PCR (early-aliquot carrot broth-enhanced PCR) in instances of subse
48  statistics across staining panels, subject, aliquots, channels, or other experimental variables.
49  pronounced in aliquots from 83 carrot broth aliquots collected after 6 h (84.3%) compared to detecti
50 arrot broth-enhanced PCR of 144 carrot broth aliquots collected after fewer than 6 h of incubation (5
51 tion experiments were conducted with aptamer aliquots collected after short-, mid-, and long-term rel
52                                              Aliquots collected along the beginning of the fractional
53 inical vaginal/anorectal swabs, with 500-mul aliquots collected.
54 within 96-well plates such that each culture aliquot contained an average of two unique genotypes.
55                                          One aliquot contained the same amount of solvent vehicle use
56 uot up to 40 replicates within seconds, each aliquot containing just 10 nL.
57         Fluorescence intensities of reaction aliquots correlated linearly with reaction yield after d
58 FU S. agalactiae, with the majority of these aliquots demonstrating detection after 2 h of carrot bro
59 bility to signal average spectra of the same aliquot (depending on its size) thereby improving the si
60 Two-color microarray experiments in which an aliquot derived from a common RNA sample is placed on ea
61                           As small as 0.001% aliquot displayed seeding activity.
62 ected from each patient was divided into two aliquots, each of which was assigned a random identifica
63 osphatase to nucleotidyltransferase reaction aliquots enabled the conversion of remaining sugar-1-pho
64                                              Aliquots equivalent to the maximum drop volume of plasma
65 bsequently identified by analyzing a solvent aliquot evaporated to 1% residual volume, while the othe
66 atories should consider providing a specimen aliquot for HPV DNA detection prior to GAA treatment.
67                                              Aliquots for each sample, identified only by study numbe
68 ion of the sperm nuclei, which are stored as aliquots for future use.
69 tain AMBF3-TATE, which was stored in 50-nmol aliquots for radiolabeling.
70 formation about eyeGENE participants and DNA aliquots for their research studies.
71 e the entire process, e.g. by increasing the aliquot forwarded to PCR, the improvement expected to a
72 increased or PCR can be repeated by using an aliquot from a previous PCR as the template.
73 ll subsequent carboplatin courses, a 0.02-mL aliquot from the solution prepared for treatment is inje
74                                           An aliquot from this mixture was spotted on a stainless ste
75 class correlation coefficient (ICC) in serum aliquots from 10 subjects and urine aliquots from 20 sub
76 in serum aliquots from 10 subjects and urine aliquots from 20 subjects across multiple analytic runs.
77                                        Early aliquots from 227 specimens were subjected to carrot bro
78                     In separate experiments, aliquots from 236 ThinPrep vials were forwarded for tand
79                                 We evaluated aliquots from 244 clinical blood culture bottles that de
80                              For this study, aliquots from 405 positive blood cultures were tested ag
81 ion rate differences were most pronounced in aliquots from 83 carrot broth aliquots collected after 6
82 urgdorferi-specific PCR for up to 56 days in aliquots from both ceftriaxone-treated and untreated cul
83                                    Duplicate aliquots from different tissues and samples were solubil
84                              The remaining 6 aliquots from each of the 3 subjects were divided equall
85                                          Two aliquots from each of the 3 subjects were used as a cont
86                  Specimen pools consisted of aliquots from five consecutively processed FCUs combined
87                                              Aliquots from multiple time points are treated with fluo
88 ed by performance of the Aptima HPV assay on aliquots from reprocessed ThinPrep vials.
89      Fourteen aliquots of pooled CSF and two aliquots from six cognitively normal individuals were ra
90 ping, length of the random region and taking aliquots from the original pool on the exploration of se
91 hose of RSV plaque assays performed on fresh aliquots from the same children.
92  in two separate pools (0-6 and 7-24 h), and aliquots from these urine collections were analyzed usin
93                                  We obtained aliquots from two different sources (here we refer to th
94                                   Irradiated aliquots had lower median DNA yields (3.7 microg/aliquot
95 ve variable efficacy associated with product aliquoting, handling, and distribution.
96 ecimen was compared with growth from an STGG aliquot immediately cultured or stored at -70 degrees C
97 e given the difficulty of preparing multiple aliquots in known ratios.
98 e loaded on different chromatographic resins aliquotted in membrane-bottomed microtiter plates.
99 e Trima apheresis platelet unit (n = 12) was aliquoted into five CLX storage bags.
100 Ohm MRSA assay master mix was reconstituted, aliquoted into SmartCycler tubes in 25-microl volumes, a
101 aphSR assay master mix was reconstituted and aliquoted into SmartCycler tubes in 25-mul volumes (fres
102 ic fibrosis (CF) patients were collected and aliquoted into sterile Bijou bottles.
103          Sample is rapidly and automatically aliquoted into the sample spots due to the interplay of
104               Further, normoxic samples were aliquoted into two sub-groups for in vitro nitration wit
105 n (from finger-prick of blood), metering and aliquoting into separate reaction chambers for paralleli
106 and were split into equal aliquots, with one aliquot irradiated by electron-beam (E-beam) irradiation
107                     The DNA template in each aliquot is amplified by multiple displacement amplificat
108 lable only in widely-dispersed, insect-sized aliquots - it was originally intended for insect pollina
109        The ability to cryopreserve alteplase aliquots makes it an economically reasonable alternative
110 s system performs sample and enzyme cocktail aliquotting, mixing of reagents, data acquisition, and d
111              Frozen master mix and overnight aliquot modifications of the BD GeneOhm Cdiff assay fail
112  removing N-glycans from the original sample aliquot, O-glycans were chemically released from urinary
113 otease sequencing using cryopreserved plasma aliquots obtained from 46 heavily treated HIV-1-infected
114 om each time point was hybridized against an aliquot of 0 time point RNA from the same prostate.
115                                Maximum lioAW aliquot of 0.03mug seemed to effectively contrast the in
116 n, only dilution with 0.1 M formic acid, one aliquot of 100 microL of serum was injected into a comme
117 rcial HPLC system and injected with a 10 muL aliquot of 10000 ppm caffeine DI-water solution, the mic
118                                           An aliquot of a crude Escherichia coli extract containing t
119 asurement of chemical exchange from a single aliquot of a ligand hyperpolarized by dissolution dynami
120 (2) the ability to interrogate a nearly pure aliquot of analyte, and (3) the ability to signal averag
121        Sample treatment involved diluting an aliquot of baby food with ultra-high quality water and a
122       We conclude that discarding an initial aliquot of blood when obtaining blood cultures from IVCs
123 an be monitored in real-time by measuring an aliquot of conditioned medium in culture or a few microl
124                   Nineteen patients drank an aliquot of deuterated water (2H2O) daily for 84 days, an
125     Intravenous (i.v.) inoculation of a 1-ml aliquot of diluted ramp-up-stage plasma containing 20 vR
126                                           An aliquot of freshly reconstituted Abeta(1-42) in sterile
127  degradation demonstrated that a significant aliquot of GPR17 is recycled to the cell surface.
128 permethylated glycans derived from a 0.1-muL aliquot of HBS.
129 sis, corresponding to the analysis of a 2 ng aliquot of homogenate from the 6 ng cell lysate.
130                                     A single aliquot of one enzyme was found to be sufficient for bot
131     After the collection disc filled with an aliquot of plasma the upper membranes were stripped from
132 xtraction technology that collects a 2.5 muL aliquot of plasma within three minutes from a finger-sti
133 ix has a 3-nL reactor, and a single 2-microL aliquot of polymerase is amortized over all 400 independ
134                                           An aliquot of positive-blood-culture broth was incubated wi
135                           The (1)H NMR of an aliquot of reaction mixture and in situ trapping with 2-
136                                  A 25-microL aliquot of sample is placed on the tungsten filament rem
137 spersed in application buffer, and a 100 muL aliquot of sample was applied to the sample chamber.
138 ed the detection of the drug (to 1 ng) in an aliquot of serum (30 microL) with a 5-order magnitude of
139                                     A 0.5-ml aliquot of stool was heated to 80 degrees C for 10 min,
140               Repeated screening of the DMSO aliquot of synthesized 1 revealed increasing APOBEC3G in
141                Under optimum conditions, one aliquot of TAML 1a (400 nM) catalyzed 5% degradation ove
142                                           An aliquot of the blood culture was centrifuged, and the re
143                                           An aliquot of the library is added to bacterial S30 extract
144 he lenses were then placed into a fresh 1-mL aliquot of the lipid being tested, and the procedure was
145  the depleted limiting primers to a separate aliquot of the multiplex reaction.
146                                Then, a 0.5mL aliquot of the partitioned supernatant was cleaned-up us
147   Replicate PCR/ESI-MS testing from a second aliquot of the PCR/ESI-MS-positive/culture-negative spec
148                                           An aliquot of the protein complex is then exposed to a stim
149              Lp(a) was removed from a second aliquot of the same serum sample by carbohydrate affinit
150                                           An aliquot of the supernatant was mixed with an equal volum
151         The consecutive loading, mixing, and aliquoting of the LAMP primers/reagents and DNA sample s
152 d measurement of fat absorption by analyzing aliquots of <1% of total feces.
153 state shivering response, at which point two aliquots of 1.5 ml kg(-1) (SML) and 3.0 ml kg(-1) (LRG),
154                                       Frozen aliquots of 145 (for HPeV, n = 70; for EV, n = 75) previ
155                                        Fresh aliquots of 161 BM and 147 PB stem-cell allografts from
156             Group 1 (n = 25) ingested 150-mL aliquots of 2% barium sulfate suspension with meals and
157 e were inoculated into their right eyes with aliquots of 5 x 10(5)/2.5 muL B16LS9 melanoma cells and
158                       Test panels, including aliquots of 50 patient samples (40 positive samples and
159 ar and rotary molecular motors are driven by aliquots of a chemical fuel, trichloroacetic acid.
160                                         When aliquots of a human urine sample spiked with 1 microg/mL
161  The separation protocol involves taking two aliquots of a mixture of particles that vary in size and
162 of reaction during a series of injections of aliquots of a reactant into a sample cell.
163   Upon mixing Cu(II), Abeta(1-16)(Y10W), and aliquots of Abeta(1-42) taken from samples incubated for
164                        Cryopreserved 1-mg/mL aliquots of alteplase are safe and effective in the clea
165 eated pressure-based injections of nanoliter aliquots of amplicon (along with the DNA sizing standard
166 The microbubbles form explosively when small aliquots of an aqueous suspension of droplets of a water
167 ulated with 2 ml of banked whole blood, 1-ml aliquots of antibiotic suspension, and organisms diluted
168 oma and targeted sequencing on cryopreserved aliquots of autologous stem-cell products from 401 patie
169           Standard curves obtained from 2-ml aliquots of BAL fluid were linear over a wide range of c
170 AA and varying concentrations of TAA to 2-ml aliquots of BAL fluid, the deuterium and protium forms o
171 entrations of TAA from 0.0 to 24,600 pg/2-ml aliquots of BAL fluid.
172 zed primarily by a standardized assay, where aliquots of batch-cultured cells are rapidly pipetted in
173 etabolomics was used to analyze 60 muL serum aliquots of blood collected 4 days post-oral exposure.
174 -based technology that targets EpCAM to rank aliquots of blood for the presence or absence of a CTC.
175 mycobacteremia in adults, we inoculated 5-ml aliquots of blood from patients with suspected mycobacte
176 o the portal vein and as many as four 7.5-mL aliquots of blood were aspirated.
177 cterial (MB) bottles and incubated, and 5-ml aliquots of blood were extracted and tested by real-time
178  Mycobacterium tuberculosis bacteremia, 5-ml aliquots of blood were inoculated into bioMerieux mycoba
179                                              Aliquots of blood, sputum, and bronchoalveolar lavage fl
180 of the peptide biosensor at fmol levels from aliquots of cell lysate equivalent to ~15,000 cells.
181                                              Aliquots of cells were plated and cultured for 24 and 48
182 ected and uninfected hamsters using 2-microl aliquots of cerebral spinal fluid.
183                               After 4 hours, aliquots of culture medium were collected for high-perfo
184 bundance of Burkholderia multivorans between aliquots of DTT-treated sputum samples with and without
185                  After clonal proliferation, aliquots of each clone were cultured in Th1- or Th2-indu
186                                              Aliquots of each clone were then maintained in either th
187                                              Aliquots of each fraction were assayed for sensitizer ac
188 DTT, peptides were separated by RP-HPLC, and aliquots of each fraction were counted for 3H label with
189 racterized by the microinjection of standard aliquots of either ascorbic acid or hydrogen peroxide.
190                                              Aliquots of fresh or pretreated cells were spotted onto
191 e analysed using a microsatellite primer and aliquots of genomic DNA were obtained from single spores
192  cultured human bone marrow stromal cells to aliquots of HA-TCP particles and were placed in subcutan
193                To improve sequence coverage, aliquots of immunoprecipitated TTR samples were digested
194                In this procedure, 200 microL aliquots of isopropyl alcohol were repeatedly dropped on
195                                       First, aliquots of linear phage library displaying 10(10th) 12m
196 0 min for the former experiment, while daily aliquots of medium were sampled for the latter experimen
197 interactions, SPR can rapidly quantify small aliquots of nanoRx formulations for desired and undesire
198              Group 2 (n = 21) ingested 10-mL aliquots of nonionic iodinated contrast material (ioprom
199 tion of possible adulteration by addition of aliquots of oil from whole paste to the most valuable oi
200 rification methods were compared among equal aliquots of oral rinse samples collected from a subset o
201 cent detection of anti-HDV antibody in small aliquots of patient serum.
202                                     Fourteen aliquots of pooled CSF and two aliquots from six cogniti
203 ate tandem mass spectrometry (MS/MS) data on aliquots of pooled serum and plasma from healthy subject
204 sion to the fibrils can be seeded with small aliquots of preformed fibrils.
205                                              Aliquots of serum collected at enrollment in either of t
206                                              Aliquots of soil were sampled for up to 14 days for cult
207                                              Aliquots of solubilized proteins from a lung adenocarcin
208                                              Aliquots of solubilized proteins from a pancreatic cance
209 urface of the sample by applying a series of aliquots of solvent, then analyzing their contents after
210 ted microcolumns to enable the use of just 2 aliquots of starting library, and its 96-well microplate
211                                              Aliquots of the alveolar macrophages were also treated w
212 BAL fluid can be reliably determined in 2-ml aliquots of the biological fluid with <10% error.
213  and the expression of SpeA in the aspirated aliquots of the chamber fluid was analyzed on successive
214                                              Aliquots of the crude membrane fraction were run on mult
215 ion structural images are obtained by adding aliquots of the evolving reaction to BzCN and then 'wait
216                                              Aliquots of the exudates were metabolized by soil bacter
217                  Analyses of three different aliquots of the Gibeon (IVA) iron meteorite obtained ove
218                                              Aliquots of the incubating research blood culture fluid
219 firmed by exoglycosidase array digestions of aliquots of the N-glycan pool.
220 strument was set to disperse the appropriate aliquots of the reagents and sample on a Whatman paper s
221 sing 120 mL of ambient air based on multiple aliquots of the same air sample.
222 -CH4 is 0.05/1000 (1sigma) on multiple 60-mL aliquots of the same ambient air sample.
223  biochemical profiling to be performed using aliquots of the same cell populations employed for the t
224                                              Aliquots of the same cells transfected with a plasmid co
225                                    Different aliquots of the same saffron sample were subjected to va
226 or carbonates that are believed to represent aliquots of the same solutions that precipitated the ore
227  sera was determined following incubation of aliquots of the sera with human serum albumin (HSA), lip
228          In the fluorescence detection step, aliquots of the supernatant are concentrated onto a prot
229                                              Aliquots of the ultrafiltrate were analyzed for monomeri
230                  By covalently cross-linking aliquots of the walker to its track in successive walkin
231                                        Small aliquots of these adducts were separated for characteriz
232                                              Aliquots of these DAGK stock solutions were diluted 200-
233 osensory thalamus in rats, we injected small aliquots of tracer into each nucleus and analyzed the pa
234      The latter approach only requires small aliquots of unroasted cocoa beans, can be automatated, r
235          DBS were created by spotting 50-mul aliquots of whole blood on 903 filter paper.
236                                              Aliquots of WNV were removed from the 37 degrees C ELISA
237 additive solutions and administered in small aliquots over the shelf life of the product to decrease
238 is of genomic integrity gels, than untreated aliquots (P<.0005).
239 aliquot) than untreated aliquots (7.6 microg/aliquot) (P<.0005) and were more likely to have smaller
240                   To prepare DSS samples, we aliquoted precisely 20 microL serum per spot on filter p
241 entrifugation and clarification of a 500-mul aliquot prior to sample lysis (protocol A) and direct ly
242 is (protocol A) and direct lysis of a 50-mul aliquot (protocol B).
243                                          The aliquot punches were extracted by liquid/liquid extracti
244 ements under relatively dilute conditions by aliquot quenching kinetics and by relative rate measurem
245                            Ensemble-decision aliquot ranking (eDAR) is a sensitive and high-throughpu
246    This technology, termed ensemble decision aliquot ranking (eDAR), recovered spiked-in cancer cells
247 ibuted into multiple aliquots such that each aliquot receives a fraction of a haploid copy.
248                                   Irradiated aliquots showed poorer PCR amplification of a 989-bp bet
249 th Poisson-distributed experimental error in aliquoting starting copies, a theoretical limit to instr
250 utomatic collection of a given number of its aliquots (subfractions) exposed to the solid sample.
251 DNA is diluted and distributed into multiple aliquots such that each aliquot receives a fraction of a
252                       For direct testing, an aliquot taken from BD BACTEC Plus and/or BD BACTEC Lytic
253 ions of individual samples, the volume of an aliquot taken from each sample is adjusted so that the s
254                                              Aliquots taken at various time points were analyzed.
255 clinical samples was verified by analysis of aliquots taken directly from BacT/Alert blood culture bo
256 ixture, but instead are only introduced into aliquots taken from the reaction at regular time interva
257 uots had lower median DNA yields (3.7 microg/aliquot) than untreated aliquots (7.6 microg/aliquot) (P
258 nce between the mean bacterial abundances in aliquots that were subjected to only DTT treatment and t
259 ach centre sent nine new cerebrospinal fluid aliquots that were used to measure total tau, phosphoryl
260                  After reprocessing of a new aliquot, the final h-IC inhibition rates were 0% (EM) an
261           Each fraction then is split in two aliquots: The first is digested with trypsin for peptide
262 bility to signal average spectra of the same aliquot, thereby improving the signal-to-noise in a stop
263 tistep pathway that was elucidated by taking aliquots throughout the course of the reaction and study
264 lization period, animals were hemorrhaged in aliquots to 10, 20, 30, 35, 40, 45, and 50% of total blo
265 f blood was obtained and inoculated in 10-ml aliquots to aerobic and anaerobic culture vials.
266 wed by resequencing separately amplified DNA aliquots to confirm each mutation.
267  propionaldehyde at -78 degrees C in THF, an aliquot transferred to a flask at approximately 30 degre
268 ) of this pipettor have been demonstrated to aliquot/transport nanoliter-to-picoliter solutions.
269  NAFLD ingested heavy water ((2) H2 O, 50-mL aliquots) two to three times daily for 3-5 weeks prior t
270 few microliters of sample, it is possible to aliquot up to 40 replicates within seconds, each aliquot
271 analyzed breast cancer cell line derived RNA aliquots using Agilent cDNA and Affymetrix oligonucleoti
272               Lp-PLA2 was measured in plasma aliquots using an enzyme-linked immunoassay.
273 on curves or measurements of compound masses/aliquot volumes are required.
274                                     A 10 muL aliquot was determined by gas chromatography with chemic
275 r to heat treatment of the swab specimen, an aliquot was removed and cytocentrifuged onto a slide.
276                 When growth was detected, an aliquot was removed and plated onto CHROMagar Candida.
277                 For the rRNA assay, a 0.4-ml aliquot was removed, and the cells were pelleted by cent
278  measured the total urine volume (Uvol), the aliquot was stored for the later determination of Uosm a
279                                   A separate aliquot was used to quantify levels of pro-surfactant pr
280                                          Two aliquots were continuously agitated with or without MAPK
281 K) pathway from treated and untreated sample aliquots were determined using a bead-based immunoassay.
282                                              Aliquots were digested with pepsin, trypsin, or GluC and
283                                              Aliquots were extracted and tested for DNA yields (e.g.,
284                           At this time, cell aliquots were grafted into nude mice to study in vivo fu
285 wabbed, and prepared in suspension, and 1 mL aliquots were inoculated onto test plates in triplicate.
286                         Following treatment, aliquots were plated for viability determination and com
287       The vials were incubated for 72 h, and aliquots were removed for HPLC analysis by using the She
288                                              Aliquots were removed over a period of 3 weeks and analy
289                                   Two sample aliquots were simultaneously injected onto a dual column
290  alteplase was diluted to 1 mg/mL and 2.5-mL aliquots were stored at -20 degrees C until use.
291                                              Aliquots were stored at room temperature before being fr
292                                          Two aliquots were subjected to 48 hours of interruption of a
293                                              Aliquots were subjected to short pressure pulses of 690,
294                          During irradiation, aliquots were taken and analyzed by a flow injection sys
295                                       Sample aliquots were tested for dissolved and total arsenic by
296                                          The aliquots were then treated with iodo[(14)C]acetamide and
297                                              Aliquots were withdrawn hourly to assess apoptosis and v
298 ected to only DTT treatment and those of the aliquots which included an MH step (all bacteria, P = 0.
299               A sample was divided into four aliquots which were analyzed in parallel by 1D isoelectr
300  mouthwash rinses, and were split into equal aliquots, with one aliquot irradiated by electron-beam (
301 d-transfer system is used to transfer sample aliquots without fear of plugging.

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