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1 body titers between collection of acute- and convalescent-phase sera.
2 he carboxyl-terminal half of IpaD with a few convalescent-phase sera.
3 on of 2009 H1N1 virus-specific antibodies in convalescent-phase sera.
4 d aa 1 to 213 reacted specifically with SARS convalescent-phase sera but not with negative human sera
5 ole or fractionated bacterial proteomes with convalescent-phase sera can potentially accelerate ident
6 pneumonic plague models, passive transfer of convalescent-phase sera confers protection, as does acti
7 d rise in antibody titer from acute-phase to convalescent-phase sera for LukAB, the most recently des
8                                     By using convalescent-phase sera from 10 Shigella flexneri-infect
9                                              Convalescent-phase sera from 33 of 44 patients in the PS
10 epitope were highly reactive with all of the convalescent-phase sera from 40 SARS patients but not wi
11        The recombinant proteins reacted with convalescent-phase sera from dogs and human patients rec
12               In this study, we investigated convalescent-phase sera from H7N7-exposed individuals by
13                                              Convalescent-phase sera from NV-infected individuals sho
14 ), respectively, by Pepscan analyses against convalescent-phase sera from SARS patients and antisera
15 ts with seven different sera, including five convalescent-phase sera from these patients, one dog ant
16                                              Convalescent-phase sera from these primed mice conferred
17 mmunosorbent assays (ELISAs) with human HCMV-convalescent-phase sera from unselected donors confirmed
18 dian = 6.0) after the onset of symptoms, and convalescent-phase sera (n = 128) were collected >or=15
19 of human sera, including group C and group B convalescent-phase sera, normal sera with naturally occu
20  detection of babesial antibody in acute-and convalescent-phase sera, or identification of the organi
21 rediction model were significantly higher in convalescent-phase sera than in paired acute-phase sera.
22 gic study was conducted on stored acute- and convalescent-phase sera that had been submitted for Rock
23 pment of serological criteria for evaluating convalescent-phase sera that optimize detection of true
24                         When used to examine convalescent-phase sera, the IFA is positive in 93% of b
25  capsid and reacted with pig hyperimmune and convalescent-phase sera to PEC Cowden in enzyme-linked i
26                          The sensitivity for convalescent-phase sera was 93.8% by MAT, 84.4% by DST,
27                    In this study, acute- and convalescent-phase sera were evaluated against different
28 erved in 21 of 23 patients (91.3%) from whom convalescent-phase sera were obtained.

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