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1 c IgM or IgG antibody titers from acute- and convalescent-phase sera.
2 body titers between collection of acute- and convalescent-phase sera.
3 he carboxyl-terminal half of IpaD with a few convalescent-phase sera.
4 on of 2009 H1N1 virus-specific antibodies in convalescent-phase sera.
5 In conclusion, we show high sensitivity in convalescent-phase sera and high specificity for the Abb
6 d aa 1 to 213 reacted specifically with SARS convalescent-phase sera but not with negative human sera
7 ole or fractionated bacterial proteomes with convalescent-phase sera can potentially accelerate ident
8 pneumonic plague models, passive transfer of convalescent-phase sera confers protection, as does acti
9 d rise in antibody titer from acute-phase to convalescent-phase sera for LukAB, the most recently des
12 epitope were highly reactive with all of the convalescent-phase sera from 40 SARS patients but not wi
16 ), respectively, by Pepscan analyses against convalescent-phase sera from SARS patients and antisera
17 ts with seven different sera, including five convalescent-phase sera from these patients, one dog ant
19 mmunosorbent assays (ELISAs) with human HCMV-convalescent-phase sera from unselected donors confirmed
20 dian = 6.0) after the onset of symptoms, and convalescent-phase sera (n = 128) were collected >or=15
21 of human sera, including group C and group B convalescent-phase sera, normal sera with naturally occu
22 detection of babesial antibody in acute-and convalescent-phase sera, or identification of the organi
24 rediction model were significantly higher in convalescent-phase sera than in paired acute-phase sera.
25 gic study was conducted on stored acute- and convalescent-phase sera that had been submitted for Rock
26 pment of serological criteria for evaluating convalescent-phase sera that optimize detection of true
28 capsid and reacted with pig hyperimmune and convalescent-phase sera to PEC Cowden in enzyme-linked i