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1                                              Neisserial adhesin A (NadA), a trimeric autotransporter
2 tched reference strain (5/99, which included neisserial adhesin A), both of which were used in vaccin
3      The functions of type IV pili and other neisserial adhesins are discussed in the specific contex
4                                        Thus, neisserial adhesion via either of at least two different
5                               Genome-derived neisserial Ag (GNA) 1870 is a meningococcal vaccine cand
6 of polysaccharide-specific Ig in response to neisserial and other gram-negative porin-expressing bact
7 ain engineered to overexpress genome-derived neisserial antigen (GNA) 1870, a lipoprotein discovered
8                               Genome-derived neisserial antigen 2132 (GNA2132) is a novel vaccine can
9 t activities in DNA repair: one is a typical Neisserial AP endonuclease (NApe), whereas the other is
10 ly conserved 9-bp core sequence, whereas the neisserial apparatus binds a 10-bp motif.
11             Genetic recombination impacts on neisserial biology in two ways: (i) specific loci underg
12  orders Xanthomonadales, Burkholderales, and Neisseriales carry a type IV secretion system (T4SS) spe
13              Based on these frequencies, six Neisserial clinical isolates could be grouped into three
14 tudy, we found that DNA derived from various neisserial co-colonizers of the human nasopharynx increa
15  in understanding the mechanisms that enable neisserial colonisation, in terms of the role of type IV
16  microenvironment, and a multistep model for neisserial colonization of mucosal epithelia is proposed
17  the cell, the earliest demonstrable step in neisserial competence.
18  fusion proteins, suggesting that additional neisserial components are involved.
19 ey are a long-standing, integral part of the neisserial dcw gene cluster.
20 ociated with the development of disseminated neisserial disease, and did not require opacity outer me
21 ng frequencies, indicating that heterologous neisserial DNA modulates phase variation in a transforma
22  ermC, the vector contains two copies of the neisserial DNA uptake sequence to facilitate high-freque
23 ncies were also increased in the presence of neisserial DNA.
24  other is a specialised 3'-phosphodiesterase Neisserial exonuclease (NExo).
25                         We have identified a neisserial gene, hemO, that is essential for heme, hemog
26 ith differences in repeat length between the neisserial genome sequences is further corroborative evi
27 sts it is an essential gene (engA, essential neisserial GTPase).
28                   When the gene encoding the neisserial heme oxygenase, hemO, was replaced with pigA,
29    The deduced amino acid sequences of these neisserial hemoglobin receptors were also highly related
30 factor H binding protein [fHbp]-GNA2091, and Neisserial heparin binding antigen [NHBA]-GNA1030).
31     In the current study, we investigate the neisserial heparin-binding antigen (NHBA) of N. gonorrho
32  against factor H-binding protein (fHbp) and Neisserial Heparin-Binding Antigen (NHBA), two major ant
33 ntigens (factor H-binding protein [fHbp] and neisserial heparin-binding antigen).
34 o-glutamine exchange in the active center of neisserial HtrA.
35  Several lines of evidence indicate that the neisserial IgA1 protease is directly responsible for thi
36 pe IV pili play an active role in initiating neisserial infection of the mucosal surface in vivo.
37 t in innate immune defenses against invasive neisserial infections.
38 s the transcriptional activity of two common neisserial intergenic components.
39 egy for vaccine development has targeted the neisserial iron import systems.
40              Evidence for the role of Fur in neisserial iron regulation has been indirect because of
41 f predominantly "transparent" (Opa-negative) neisserial isolates from persons with invasive disease,
42                   Approximately 95 different neisserial isolates tested positive by Western blotting
43 eity of this protein, the 2086 genes from 63 neisserial isolates were sequenced.
44                     Human IgGs that bind the neisserial L7 lipooligosaccharide (LOS) are bactericidal
45                      Thus, the Opa family of neisserial ligands may interact with several members of
46                            The inner core of neisserial lipooligosaccharide (LOS) contains heptose re
47                                              Neisserial lipooligosaccharide (LOS) contains three olig
48  and phosphoethanolaminylation of lipid A on neisserial lipooligosaccharide (LOS), a major cell-surfa
49                                              Neisserial lipooligosaccharides (LOSs) are a family of c
50 identification and characterization of nlaB (neisserial LPA acyltransferase B), the second LPA acyltr
51 d sequence from the previously characterized neisserial LPA acyltransferase homologue nlaA.
52 risingly, picogram-per-milliliter amounts of neisserial LPS were also found to be highly synergistic
53             Overexpressing components of the neisserial mismatch repair system partially alleviated D
54                                              Neisserial mod alleles also contained a hypervariable re
55                                              Neisserial Opa proteins function as a family of adhesins
56 receptor-binding function in the majority of neisserial Opa proteins.
57                                          The neisserial opacity (Opa) proteins are a family of antige
58                                          The neisserial opacity (Opa) proteins are phase-variable, an
59  Omp31, Agrobacterium tumefaciens Omp25, and neisserial opacity proteins (Opa).
60 ing infections caused by multidrug-resistant neisserial or streptococcal strains.
61                                          The neisserial outer membrane protein, PorB, is a TLR2 ligan
62 y designated FrpB, an iron-regulated, 76-kDa neisserial outer membrane protein, shows sequence homolo
63  constitute the vast majority of channels in neisserial outer membranes and can be subdivided within
64                         PorB is required for neisserial pathogenesis and can elicit a Toll-like recep
65 is the most dissimilar of the three types of neisserial pilE loci.
66 eat sequence, a feature present in all other neisserial pilin genes examined to date.
67 th the N-terminal conserved regions of other neisserial pilin proteins.
68 ivariable and hypervariable regions of other neisserial pilins and displays a large deletion in a hyp
69 icited when CPS is conjugated to the class 3 neisserial porin (CPS-porin).
70                                PorB is a pan-neisserial porin expressed regardless of organisms' path
71                                          The neisserial porin P.I is a GTP binding protein that forms
72                                The effect of neisserial porin PorB on activation-induced cell death w
73                                       Due to neisserial porin's ability to activate B cells and poten
74 nificant for elucidating the mechanism(s) of neisserial porin's immune stimulatory activity.
75 y effect on the B-cell-stimulatory effect of neisserial porins (essential for the adjuvant activity o
76                                              Neisserial porins are strong immune adjuvants and B cell
77                                          The neisserial porins are the major protein components of th
78                                 Furthermore, neisserial porins co-localize with mitochondria of targe
79 The mechanism of the antiapoptotic effect of neisserial porins could be explained by the protein-prot
80                                              Neisserial porins have been shown to act as adjuvants in
81                                              Neisserial porins have been shown to act as B cell mitog
82                                              Neisserial porins increased the surface expression of th
83             In addition, incubation with the neisserial porins increased the T lymphocyte costimulato
84                                              Neisserial porins interact with target cells to localize
85  potent adjuvant activity, the effect of the neisserial porins on T-B cell interactions and T cell co
86                                The effect of neisserial porins on the immune system also involves int
87 a support the hypothesis that the ability of neisserial porins to improve the immune response to poor
88 does not significantly affect the ability of neisserial porins to induce the costimulatory ligand B7-
89 rins (essential for the adjuvant activity of neisserial porins), B cells from both murine strains wer
90           The immunopotentiating activity of neisserial porins, the major outer membrane protein of t
91 sm behind the immunopotentiating activity of neisserial porins.
92 ent reports of the crystal structures of the neisserial receptor proteins TbpA and TbpB, each solved
93 tified one small RNA, herein named NrrF (for neisserial regulatory RNA responsive to iron [Fe]), whic
94                                The commensal neisserial species were identified as reservoirs for all
95 GAA) present frequently in the chromosome of neisserial species.
96 evotella spp), and Bacillales, and increased Neisseriales spp.
97  Although FetA is commonly expressed by most neisserial strains and is a potential vaccine candidate
98  is present in different copy numbers in the neisserial strains examined.
99                     Unexpectedly, none of 10 Neisserial strains tested bound native properdin.
100 by NmUC to infect UECs are shared with other neisserial strains, hybrid mechanisms unique to the clad
101 of Hb receptors or the general mutability of Neisserial strains.
102 f a complement down-regulator protein to the neisserial surface by specific Ab may enhance intrinsic
103                                              Neisserial surface protein A (NspA) is a highly conserve
104                                              Neisserial surface protein A (NspA) is currently being i
105 c acid, factor H binding protein (fHbp), and neisserial surface protein A (NspA) to regulate the alte
106 g expression of capsule (select serogroups), Neisserial surface protein A (NspA), factor H (fH) bindi
107 gand for both FH and FHL-1 was identified as neisserial surface protein A (NspA), which has previousl
108 rected against the highly conserved protein, neisserial surface protein A (NspA).
109 ein currently undergoing clinical trials and Neisserial surface protein A.
110      In contrast to type IV pili, many other neisserial surface structures are not involved in cortic
111                  Little is known about other neisserial targets for complement proteins C3 and C4, wh
112   Complementation studies indicated that the neisserial Ton system cannot interact with the E. coli F
113                                          The neisserial transferrin binding proteins (Tbps) comprise
114 region with potential cleavage sites for the neisserial type 1 and type 2 IgA1 proteases.
115                                              Neisserial type 2 IgA1 protease cleaves purified LAMP1 i
116  to induce cortical plaques, indicating that neisserial type IV pili are required for cortical plaque
117  was delineated by a 33-bp repeat containing neisserial uptake sequences located downstream of col.
118 ream of this promoter is an inverted pair of neisserial uptake signal sequences, which are commonly c
119 the choice of complement sources to evaluate neisserial vaccine candidates.
120 the choice of complement sources to evaluate neisserial vaccine candidates.

 
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