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1 body specificity and titer were defined by a microneutralization and a pseudotype assay that could as
2               Serum samples were tested with microneutralization and hemagglutination inhibition assa
3 d vaccination were tested for H5 antibody by microneutralization and hemagglutination inhibition.
4 ibody positive if they were positive by both microneutralization and Western blot testing.
5                         In plaque reduction, microneutralization, and fusion-inhibition assays, MEDI-
6  A 2.7- and 3.5-fold rise in RSV/A and RSV/B microneutralization antibodies were noted at day 56.
7 nced seroconversion rates and geometric mean microneutralization antibody titers.
8 vaccine titer as assessed through a standard microneutralization assay (p<0.05, q <0.2).
9 ed 18 to 59 years were achieved by using the microneutralization assay combined with Western blotting
10     Direct comparison of an HI assay and the microneutralization assay demonstrated that the latter w
11             We have developed an alternative microneutralization assay for influenza virus using a qu
12 P)-based approach to develop a vaccine and a microneutralization assay for ZIKV.
13 ibition and microneutralization assays, with microneutralization assay titers >40 considered positive
14 was tested using a quantitative colorimetric microneutralization assay to demonstrate antibody titers
15     Therefore, we developed a more sensitive microneutralization assay to detect antibodies to avian
16                                            A microneutralization assay using an ELISA-based endpoint
17                                              Microneutralization assay was as sensitive as rtRT-PCR i
18             The sensitivity of the GFP-based microneutralization assay we developed was similar to th
19       The sensitivity and specificity of the microneutralization assay were compared with those of an
20                                The RVP-based microneutralization assay worked similarly to the PRNT a
21 ase chain reaction (rtRT-PCR), and serology (microneutralization assay).
22 lizing antibody responses were measured by a microneutralization assay, and hemagglutinin (HA)-specif
23 parable to that obtained by the conventional microneutralization assay, suggesting that the use of th
24                                      Using a microneutralization assay, we measured cross-reactive an
25 lizing antibody titers were measured using a microneutralization assay.
26  postpartum and tested using an RSV antibody microneutralization assay.
27 bition (HI) assay and, for a subset, also by microneutralization assay.
28  to test for H5N1 neutralizing antibodies by microneutralization assay.
29 mock-treated control ferrets, as assessed by microneutralization assay.
30 d for their ability to neutralize virus in a microneutralization assay.
31 with a clade 1 vaccine were characterized by microneutralization assays and modified hemagglutination
32  We recently developed high-throughput virus microneutralization assays using an endpoint assessment
33 cted in ELISA, hemagglutinin-inhibition, and microneutralization assays with these monoclonal antibod
34  (i.e., from hemagglutination inhibition and microneutralization assays) and HA protein sequences.
35  by means of hemagglutination inhibition and microneutralization assays, with microneutralization ass
36  measured by hemagglutination inhibition and microneutralization assays.
37 ssessed in hemagglutination inhibition (HI), microneutralization, ELISA, lymphoproliferative, ELISpot
38                                          The microneutralization GMTs after the first, second, third,
39 lt in higher hemagglutination inhibition and microneutralization GMTs, compared with the GMTs resulti
40 on and 227 nonexposed U.S. individuals using microneutralization (MN) and hemagglutination inhibition
41                                              Microneutralization (MN) and hemagglutination-inhibition
42        Hemagglutination inhibition (HAI) and microneutralization (MN) antibodies were measured on day
43  by hemagglutination inhibition (HAI) assay, microneutralization (MN) assay, and a newly standardized
44 ated by hemagglutination inhibition (HI) and microneutralization (MN) assays, H7 viruses and vaccines
45 y hemagglutination inhibition (HI) and virus microneutralization (MN) assays.
46 ults of hemagglutination inhibition (HI) and microneutralization (MN) assays.
47 ains by hemagglutination inhibition (HI) and microneutralization (MN) assays.
48 ed with hemagglutination inhibition (HI) and microneutralization (MN) titers (all P < 0.001).
49 crog dose of A/Vietnam vaccine induced virus microneutralization (MN) titers of >/=1:20 against the A
50                                   HI titers, microneutralization (MN) titers, and the frequency of ci
51 red by the hemagglutination inhibition (HI), microneutralization (MN), and single radial hemolysis (S
52             Antibody persistence (defined as microneutralization [MN] titer >/=1:40) 1 year after ini
53                                 A simplified microneutralization procedure is described that uses an
54  in standard hemagglutination inhibition and microneutralization serological assays.
55 sing enzyme-linked immunosorbent assays or a microneutralization test.
56                                              Microneutralization titers tended to be higher than HAI
57                                    ELISA and microneutralization titers were concordant.
58     Hemagglutinin inhibition (HI) responses, microneutralization titers, and antineuraminidase antibo
59 surement of haemagglutination inhibition and microneutralization titres.

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