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1 mutations of psaE and psaF caused defective haemagglutination.
2 inia pseudotuberculosis pH6 antigen mediates haemagglutination and adhesion to cultured mammalian cel
4 n of these surface structures, which mediate haemagglutination and have a demonstrated role in virule
5 binding by B. burgdorferi is associated with haemagglutination and we have identified a 26 kDa protei
7 significant inhibition of P fimbria-mediated haemagglutination assay of uropathogenic Escherichia col
9 antibodies that inhibited mannose-resistant haemagglutination by ETEC expressing CFA/I, CS4 and CS14
10 E. coli chi7122 conferred mannose-resistant haemagglutination (HA) and curli production to E. coli H
11 ed that the psaABC genes were sufficient for haemagglutination if they were expressed by a heterologo
12 s formed high levels of A/Cal-specific serum haemagglutination-inhibiting antibodies and were solidly
14 In the baseline serum samples from 2008, haemagglutination inhibition and microneutralisation ant
16 tal transfer of antibodies by measurement of haemagglutination inhibition and microneutralization tit
18 this influenza nanoparticle vaccine elicited haemagglutination inhibition antibody titres more than t
19 y and efficacy of anti-influenza plasma with haemagglutination inhibition antibody titres of 1:80 or
20 and compared the proportion of samples with haemagglutination inhibition titre 1:32 or more (deemed
22 difference in the proportion of samples with haemagglutination inhibition titre equal to or above 1:3
24 ted participants had a four-fold increase in haemagglutination inhibition titres (group geometric mea
25 he placebo group had a four-fold increase in haemagglutination inhibition titres (group geometric mea
29 r, and one person of eleven seroconverted by haemagglutination inhibition, microneutralisation, H5N3
30 ccine gave the highest seroconversion rates: haemagglutination inhibition, six of ten; microneutralis
31 unogenicity endpoints were seroconversion by haemagglutination-inhibition (HAI), defined as a four-ti
32 subsequent immunisation were evaluated using haemagglutination-inhibition and microneutralisation ass
36 vaccinated with LAIV H5N2 had an increase in haemagglutination-inhibition titre of greater than four-
37 ants in the vaccine group had an increase in haemagglutination-inhibition titre of more than four-fol
40 by the organism which are biofilm formation, haemagglutination properties and capsule production.
41 strains exhibited a strong mannose-sensitive haemagglutination reaction with guinea pig erythrocytes,
42 ctive combined serology (positive T pallidum haemagglutination test and rapid plasmin reagin titre of
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