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1 nt series of experiments where adenosine triphosphate (ATP) concentrations were determined by a luciferase-linked lumines
2                                              Thrombomodulin concentrations were determined by an enzyme-linked immunosorb
3                                                  Equivalent concentrations were determined by both enzymatic and chromato
4                                          Endogenous protein concentrations were determined by comparing MS/MS peak areas
5                                       The relative CAM cDNA concentrations were determined by comparing the density of MI
6                                           Luminal bacterial concentrations were determined by culture and counting chambe
7                                                     Protein concentrations were determined by densitometry and/or spectro
8 vo and proliferation in vitro were quantified, and cytokine concentrations were determined by ELISA.
9         Anti-H. pylori immunoglobulin G and immnoglobulin A concentrations were determined by enzyme immunoassay on prein
10                       Serum cytokine and C-reactive protein concentrations were determined by enzyme-linked immunosorbent
11                                                        IL-6 concentrations were determined by enzyme-linked immunosorbent
12                                               Methylmercury concentrations were determined by gas chromatography.
13                                            MTX and 7-OH-MTX concentrations were determined by high-performance liquid chr
14                                        Plasma catecholamine concentrations were determined by high-performance liquid chr
15              The filter was rinsed with water and albuterol concentrations were determined by high-performance liquid chr
16                                                     Analyte concentrations were determined by high-resolution gas chromat
17 was collected and carotenoid, retinol, and alpha-tocopherol concentrations were determined by HPLC.
18                                                  Antibiotic concentrations were determined by LC-MS/MS measurements.
19                                         The final certified concentrations were determined by liquid chromatography (LC)
20                                              Plasma 5-MTHFA concentrations were determined by liquid chromatography-mass
21                                                       Ester concentrations were determined by liquid-liquid-extraction- o
22 ic cells were incubated with HDEs, and supernatant cytokine concentrations were determined by means of ELISA.
23                                                  Plasma KTP concentrations were determined by means of high-performance l
24                           Fasting and postchallenge insulin concentrations were determined by oral-glucose-tolerance test
25                                               Plasma folate concentrations were determined by radioassay.
26                               Retinol binding protein (RBP) concentrations were determined by radioimmunoassays, and tran
27                                           Blood T. pallidum concentrations were determined by real-time polymerase chain
28                                                      Plasma concentrations were determined by sandwich immunoassay; lower
29 ng affinity and binding free energy, for three bulk protein concentrations were determined by SHCS.
30                      Skeletal muscle interstitial adenosine concentrations were determined by the microdialysis technique
31  Intrahepatic lipid (IHL) and intramyocellular lipid (IMCL) concentrations were determined by using (1)H-MRS before and 3
32                                                     Element concentrations were determined by using inductively coupled p
33 ablished from serum cotinine levels, and serum IgG subclass concentrations were determined by using radial immunodiffusio
34                             Aortic wall PAI-1, uPA, and tPA concentrations were determined by western blot analyses.

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