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1 transcription polymerase chain reaction, and enzyme-linked immunoassay.
2 and tetanus toxoid were measured by indirect enzyme-linked immunoassay.
3 ne attack complex C5b-9 concentrations using enzyme-linked immunoassay.
4 e changes validated by mass spectrometry and enzyme-linked immunoassay.
5 d by real-time polymerase chain reaction and enzyme-linked immunoassay.
6 LA2 was measured in plasma aliquots using an enzyme-linked immunoassay.
7 drolysis of cyclic (c)GMP levels with a cGMP enzyme-linked immunoassay.
8 by PDE inhibitors were quantitated by a cGMP enzyme-linked immunoassay.
9 protein C (pepC10) were evaluated by kinetic enzyme-linked immunoassay.
10 eceptors were performed on plasma samples by enzyme-linked immunoassay.
11 rs by end-point dilution by use of an HTLV-I enzyme-linked immunoassay.
12 or estradiol and progesterone metabolites by enzyme-linked immunoassay.
13 ntigens was determined by flow cytometry and enzyme-linked immunoassay.
14    Plasma c-erbB-2 levels were quantified by enzyme-linked immunoassay.
15 and 15 normal donors was determined using an enzyme-linked immunoassay.
16 d IL-6 concentrations were measured using an enzyme-linked immunoassay.
17 d PACAP and its receptor (PAC1) levels using enzyme-linked immunoassay.
18 matic activity in a solution compatible with enzyme-linked immunoassays.
19 often a necessary step in the development of enzyme-linked immunoassays.
20 analyzed using cell-proliferation assays and enzyme-linked immunoassays.
21 erferon (IFN-gamma), as measured by cytokine enzyme-linked immunoassays.
22  and NS4a and E2-HVR-1 peptides were used in enzyme-linked immunoassays.
23               The pool was narrowed using an enzyme-linked immunoassay: 370 clones were tested, and s
24         Western blotting and antigen capture enzyme-linked immunoassay also confirmed an increase in
25                                              Enzyme-linked immunoassay analysis revealed increased ba
26  apoB-100] were measured by chemiluminescent enzyme-linked immunoassay and commercial assays, respect
27 avidity assay by modifying the Ortho 3.0 HCV enzyme-linked immunoassay and tested 997 serum or plasma
28     The presence of OxPL was confirmed using enzyme-linked immunoassays and immunohistochemistry of c
29        Serum myeloperoxidase was measured by enzyme-linked immunoassay, and brachial artery flow-medi
30 ar MUC5AC concentration was quantified using enzyme-linked immunoassay, and conjunctival goblet cell
31 unoblots, glycosidase digestion, intact cell enzyme-linked immunoassay, and extracellular calcium-sti
32       Serum 25(OH)D was measured by using an enzyme-linked immunoassay, and serum albumin-corrected c
33                              On the basis of enzyme-linked immunoassays as well as cross-linking expe
34 of receptor phosphorylation determined in an enzyme-linked immunoassay, as well as by Western blottin
35 4 into the culture medium was assessed using enzyme-linked immunoassay-based antibody arrays.
36                                              Enzyme-linked immunoassay-based protein interaction assa
37 st homologous virus-like particles (VLPs) by enzyme-linked immunoassay but did not react with denatur
38 etion was shown, with immunofluorescence and enzyme-linked immunoassay, by loss of binding of PF sera
39 d seven respiratory viruses through culture, enzyme-linked immunoassay (EIA) and polymerase chain rea
40 rization and use of a sensitive and specific enzyme-linked immunoassay (EIA) for BDNF protein.
41 he conventional radioimmunoassay (RIA) to an enzyme-linked immunoassay (EIA) for the measurement of H
42 positive results in the Platelia Aspergillus enzyme-linked immunoassay (EIA), due to contamination wi
43 atitis B surface antigen (anti-HBs) by AUSAB enzyme-linked immunoassay (EIA).
44 ter using a whole-virus IgG measles-specific enzyme-linked immunoassay (EIA).
45  to HCV (anti-HCV) using a second-generation enzyme-linked immunoassay (EIA-2), followed by recombina
46                              We evaluated an enzyme-linked immunoassay (EIA; BioWhittaker) and a late
47 s with chronic HCV infection were assayed in enzyme-linked immunoassays (EIAs) for antibody binding t
48       We first describe the validation of an enzyme-linked immunoassay (ELISA) for quantifying adipon
49            We describe the development of an enzyme-linked immunoassay (ELISA) for quantifying insuli
50                                        Last, enzyme-linked immunoassay (ELISA) was used to demonstrat
51 n tears, feces and serum were measured using enzyme-linked immunoassays (ELISA) after topical and sys
52         Using intracellular TSH staining and enzyme-linked immunoassay for detection of secreted TSH,
53                        Using immunoblots and enzyme-linked immunoassay for ICE, we demonstrate that a
54                ECD was centrally measured by enzyme linked immunoassay in available samples at baseli
55                                     Using an enzyme-linked immunoassay, in vitro expression of E-sele
56 on of cell surface proteins, and intact cell enzyme-linked immunoassay indicated that disruption of a
57                     Results are validated by enzyme-linked immunoassays of the sera in a certified la
58 ese devices have been used to perform simple enzyme linked immunoassays on paper.
59 ted generation of cyclic AMP, as measured by enzyme-linked immunoassay (p = .05 polynomial regression
60 uorescent microbead-based immunoassay and/or enzyme-linked immunoassay platform to characterize the a
61 evels, as determined by Western blotting and enzyme-linked immunoassays, respectively.
62 ty shift assays, Western immunoblotting, and enzyme-linked immunoassays, respectively.
63 on occurs is presently unknown, quantitative enzyme-linked immunoassay showed the presence of the equ
64 sence of antibodies to HCV was determined by enzyme-linked immunoassay, supplementary recombinant imm
65                          A Toxoplasma gondii enzyme-linked immunoassay that detects strain-specific a
66 ha and interleukin-6 levels were analyzed by enzymes-linked immunoassay using randomly selected plasm
67                                       A cGMP enzyme-linked immunoassay was used to assess phototransd
68                           Using a microarray enzyme-linked immunoassay, we found that exposure to TNF
69                                 By use of an enzyme-linked immunoassay, we measured the in-vitro prod
70 ith reactive rapid test results were offered enzyme-linked immunoassay, Western blot, and plasma HIV-
71                                              Enzyme-linked immunoassay with Px44-TRAIL showed deliver

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