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1 etectable in the cell-free extracts needs to be checked.
2 l against which data in journal articles can be checked.
3 mality all feature sets of a given size must be checked.
4 both groups, and references in these reports were checked.
5 CT, mortality dates of all surgical patients were checked.
6 -dependent patients and 102 healthy controls were checked.
7 n reducing activities of different fractions were checked.
8  the reference lists from published articles were checked.
9 ed sample were determined, and linear trends were checked.
10                         Three critical steps were checked: (1) influence of atmospheric CO2 remaining
11 omen in the 4400-IU group whose blood levels were checked, 289 (74.9%) had 25-hydroxyvitamin D levels
12 basis in the clinical setting, but it should be checked after every other patient for more precise re
13 roblem in two settings: U.S. visa applicants are checked against a list of visa holders to detect vis
14 t visa fraud, and visitors entering the U.S. are checked against a watchlist of criminals and suspect
15 continuum model; the reliability of TD-M052X is checked against CASPT2 calculations regarding the beh
16                              All mortalities were checked against the Social Security Death Index.
17 origin and biological species, which have to be checked and guaranteed, not only in order to avoid mi
18  Based on our review H. pylori status should be checked and treated only in certain autoimmune diseas
19 stane, a sensitive assay for serum estradiol was checked and returned at 16 pg/mL (61 pmol/L); postme
20 m 45 epidemiological studies in 21 countries were checked and analysed centrally.
21                               After the data were checked and cleaned, linkage analysis was performed
22         For each model, assumptions validity were checked and compared as to how this fitted to the d
23                               The alignments were checked and curated to make them specific to the ta
24                              Reference lists were checked and hand-searching was undertaken for 2 jou
25                      Interobserver agreement was checked, and diagnostic accuracy of radiologic featu
26                The selectivity of the system was checked, and other pathogens, including Salmonella t
27                Several of the gene responses were checked, and in each case confirmed by reverse-tran
28 -induced changes in the backbone of N-TIMP-1 were checked as one possible source of conformational en
29                                      HBV DNA was checked at baseline, at the start of each cycle of c
30 stry, hematologic, and liver function tests) were checked at regular intervals and 1 and 7 days after
31 arathyroidism, calcium concentrations should be checked before and during treatment.
32                   Glomerular filtration rate was checked before conversion and 1 year later.
33                                 Calibrations were checked before, during, and after each day's field
34        The protein complexes in this dataset are checked by a literature search to confirm that they
35                            Planning bias can be checked by comparing propensity to report contracepti
36 eory is doubtful, significance levels should be checked by simulations.
37 gans are considered promising, their use has been checked by concerns about the transmission of porci
38 ducibility and robustness of the method have been checked by various means: (1) the comparison with c
39                      Hepatic arterial signal is checked by CONDOR at least six times per day for the
40              The model quality and stability was checked by 100 ns of molecular dynamics simulations
41              The model quality and stability was checked by 100 ns of molecular dynamics simulations.
42 tion: Study data extracted by 1 investigator was checked by a second reviewer; 2 reviewers independen
43 ccuracies impacting the present observations was checked by additional molecular dynamics simulations
44                   The accuracy of the method was checked by analysing a certified reference material;
45  Validity and accuracy of the desired method was checked by analysis of certified reference materials
46                Method accuracy and precision was checked by analyzing an AFM1 certified reference mat
47         The accuracy of the developed method was checked by analyzing certified reference material.
48                          The film morphology was checked by atomic force microscopy, and the results
49             The existence of imprinted sites was checked by comparing a SPAM modified surface to a ne
50               The accuracy of the SOLiD data was checked by conventional PCRs directed at 11 SNPs and
51  a metallic corrosion method, and the purity was checked by energy-dispersive X-ray spectroscopy (EDS
52 g methods, and the quality of cell fractions was checked by flow cytometry.
53 d on chemical bonding of the cofactor (which was checked by infrared spectroscopy) led to good perfor
54 group composition of the individual polymers was checked by MALDI-TOF MS and by nuclear magnetic reso
55             The purity of the title compound was checked by matrix-assisted laser desorption ionizati
56  receptors of each compound class by acetate was checked by measuring their acidities (DeltapKa value
57                          The final structure was checked by restrained and free molecular dynamic cal
58         The validity of each complementation was checked by showing that the yeast cells stop their g
59                                 Its validity was checked by the analysis of four certified reference
60             One reviewer extracted data that were checked by 3 others.
61        Data were extracted independently and were checked by double entry.
62      The validity of the obtained structures were checked by measuring and analyzing the vibrational
63 and genetic regulators (for DNA methylation) were checked by quantitative real-time RT-PCR.
64                            These suggestions were checked by radioligand and electrophysiology experi
65 he BACTEC 460 method, and discrepant results were checked by the conventional proportion method.
66           Most putative IRESs still have not been checked carefully to determine whether the dicistro
67 ric feasibility of the chosen set of helices is checked during the folding process using a highly coa
68                             Blood cell count was checked every 2 wk after the first and every 4 wk af
69                                       Safety was checked every 2 wk by laboratory tests, the prostate
70 ests, the prostate-specific antigen response was checked every 4 wk, and other effects were assessed
71 tation of the correlation intensities should be checked for consistency with the general trend of eac
72                The consistency of the method is checked for small model systems.
73           The validity and optimal procedure is checked for those materials most often found on the s
74                                     Semolina was checked for Falling Number (533-644s), protein conte
75                             The DNA sequence was checked for mutations.
76           References from extracted articles were checked for any additional relevant articles.
77             References from extracted papers were checked for any additional relevant papers.
78                       The OCT thickness maps were checked for areas of retinal thinning, appearing as
79                                  The mutants were checked for defects in swimming through liquids, sw
80                                      Animals were checked for diarrhea daily after lactose intake.
81                              Identified SNPs were checked for flanking sequences of >/= 60 bp along b
82 le and reference lists of retrieved articles were checked for further relevant studies.
83                                 Nonhost data were checked for similarity to known organisms using BLA
84  phrases were coded, and earlier transcripts were checked for the emerging codes.
85                                      Strains were checked for their ability to differentiate by using
86 ons to static or free-fall pH control should be checked in advance, particularly when undertaking lar
87 n problems for which a proposed solution can be checked in polynomial time), are distinct in the stan
88 he ability of lanthanum in different formats is checked in the selective phosphopeptides enrichment.
89 tions kinetics in bulk reactors in mind, and was checked in terms of linearity, limits of detection a
90          Chlorophyll a fluorescence emission was checked in treated and nontreated samples of all the
91                            Their specificity was checked in twenty more species of those most commonl
92 t receptor potential ankyrin (TRPA)1 channel was checked in vivo by the use of TRPA1(-/-) mice and in
93                       Serum T3 and T4 levels were checked in Alb/AEG-1 mice and human HCC patients.
94 fects (transcriptional-reporter gene assays) were checked in bottled water extracts using bacteria (S
95 hiatric hospitalizations for substance abuse were checked in national registers.
96 were 34 years of age, their arrest histories were checked in the Danish National Criminal Register.
97 h intravitreal anti-VEGF agents, proteinuria be checked monthly, and there should be a low threshold
98 The alignment of the device does not need to be checked on a regular basis in the clinical setting, b
99 es whose structures have not been determined are checked to see if they have binding-site signatures
100                This performance equalization was checked to ensure it was not due solely to the redun
101                        Residual of the model was checked to examine whether there was an added effect
102                              Final estimates were checked to ensure that numbers of deaths in specifi
103       Reference lists from retrieved studies were checked to identify any further studies.
104 ir effect on Ca(2+) binding capacity of cCSQ was checked using equilibrium dialysis and atomic absorp
105                          The gene expression was checked using qRT-PCR, and none of the genes encodin
106 heir immersion in simulated body fluid (SBF) was checked using SEM and pH measurements.
107 irring speed, pH and dilution of the sample) were checked using the Simplex method approach.
108                                     Accuracy was checked via an EC-sponsored interlaboratory trial.
109                                         Mice were checked weekly for the presence of palpable urinary
110                    The validity of the model was checked with a test set of 43 additional compounds t
111 age growth in diameter of fast muscle fibres was checked with fasting and significant fibre hypertrop
112  The quantification of the inhibitory effect was checked with the agar well diffusion method.
113 cibility) and measurement uncertainty, which were checked within the validation protocol, while the m

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