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1  requires the presence of pore-forming toxin listeriolysin O.
2 ecame ill had elevated levels of antibody to listeriolysin O.
3 erum samples were tested for IgG antibody to listeriolysin O.
4  requires the presence of pore-forming toxin listeriolysin O.
5 rotein Ags: hen egg white lysozyme, OVA, and listeriolysin O.
6 s not limited to CD8+ T cells that recognize listeriolysin O.
7                          Mice immunized with listeriolysin O 91-99-coated BMDCs are protected against
8  accounted for by a decrease in LM-specific (listeriolysin O(91-99) tetramer(+)) effector CD8(+) T ce
9 aracterize changes in SUMOylation induced by listeriolysin O, a bacterial toxin that impairs the host
10                            Immunization with listeriolysin O, a potent inducer of cell death, also pr
11       Cellular immune responses specific for listeriolysin O, a secreted bacterial protein required f
12  that pH-sensitive liposomes containing both listeriolysin O and gelonin were more effective than con
13 pression of the phagosome-lysing pore former listeriolysin O and on type I IFN receptor signaling.
14 atural L. monocytogenes-derived soluble Ags (listeriolysin O and p60) revealed that tethering of thes
15 ree of these exotoxins: anthrolysin O (ALO), listeriolysin O, and pneumolysin.
16 xpression of other critical virulence genes (Listeriolysin O, and two phospholipases plcA and plcB) i
17 l liver kinase-1) to the microbial adjuvant, listeriolysin-O, and used Lm to deliver the Ags and elic
18              HD-5 was very effective against listeriolysin O but less effective against the other tox
19 when the matrix protein was coexpressed with listeriolysin O, but not when expressed alone.
20 ; however, WTLM and L. monocytogenes lacking listeriolysin O (DeltahlyLM) induce similar levels of cy
21     In in vitro experiments, co-encapsulated listeriolysin O enabled liposomal gelonin-mediated B16 c
22 lipid biosynthesis, enhanced the toxicity of listeriolysin O expressed in the host cell cytosol, lead
23                               Infection with listeriolysin O-expressing, cytosolic Bacillus subtilis
24                                           Lm-listeriolysin-O-fetal liver kinase-1 was able to eradica
25 smid containing the invasin gene Inv and the listeriolysin O gene HlyA, which encode two bacterial fa
26  partially dependent on the virulence factor listeriolysin O; however, WTLM and L. monocytogenes lack
27 irement for the essential pore-forming toxin listeriolysin O in mediating escape from phagocytic vacu
28 ncentrations fractions significantly reduced listeriolysin O-induced haemolysis (p < 0.05), and ameli
29 cytoplasmic entry of Listeria facilitated by listeriolysin O is an essential feature not only of the
30 anomer peptides amino acids (aa) 91 to 99 of listeriolysin O (LLO 91-99) and aa 217 to 225 of the p60
31 by the cholesterol-dependent cytolysin (CDC) listeriolysin O (LLO) acts within the infected cell, (ii
32 ast two critical secreted virulence factors: listeriolysin O (LLO) and a broad-specificity phospholip
33                                              Listeriolysin O (LLO) and a phosphatidylinositol-specifi
34                                              Listeriolysin O (LLO) and ActA are essential virulence d
35              Listeria monocytogenes requires listeriolysin O (LLO) and ActA, the products of hly and
36 tron microscopy that LM expressing truncated listeriolysin O (LLO) and amino acid fragments 311 to 66
37  on the expression of two secreted proteins: listeriolysin O (LLO) and phosphatidylcholine-preferring
38 virulence factors of Listeria monocytogenes, listeriolysin O (LLO) and phosphatidylinositol-specific
39 to 200 nm, containing the pore-forming toxin listeriolysin O (LLO) and phosphatidylinositol-specific
40 91 to 99 (aa91-99) immunodominant peptide of listeriolysin O (LLO) and to the aa217-225 immunodominan
41 n host cells by using the pore-forming toxin listeriolysin O (LLO) and two phospholipase C enzymes.
42 ) that are deficient in the virulence factor listeriolysin O (LLO) are highly attenuated and are thou
43  the Listeria monocytogenes virulence factor listeriolysin O (LLO) enhances the immunogenicity and an
44                                              Listeriolysin O (LLO) is a cholesterol-dependent cytolys
45                       The pore-forming toxin listeriolysin O (LLO) is a major virulence factor implic
46                       The pore-forming toxin listeriolysin O (LLO) is a major virulence factor secret
47                                              Listeriolysin O (LLO) is a pore-forming cytolysin that m
48           The Listeria monocytogenes protein listeriolysin O (LLO) is a pore-forming protein essentia
49                                              Listeriolysin O (LLO) is a pore-forming toxin of the cho
50                                              Listeriolysin O (LLO) is a pore-forming toxin that media
51                                              Listeriolysin O (LLO) is a secreted pore-forming protein
52                                              Listeriolysin O (LLO) is a secreted pore-forming toxin o
53 ved cells tested, the pore-forming cytolysin listeriolysin O (LLO) is absolutely required for lysis o
54                                              Listeriolysin O (LLO) is an essential determinant of pat
55                                              Listeriolysin O (LLO) is an essential virulence factor f
56              The secreted pore-forming toxin listeriolysin O (LLO) of the intracellular pathogen List
57 ould be attributed partially to insufficient listeriolysin O (LLO) production, indicating a requireme
58 mediated, and a nonamer CTL epitope from the listeriolysin O (LLO) protein has been identified in BAL
59 ,258) fused to the first 441 residues of the listeriolysin O (LLO) protein.
60 ytogenes and its secreted pore-forming toxin listeriolysin O (LLO) to identify key signaling events a
61 uction of the hly-encoded secreted hemolysin listeriolysin O (LLO) was also found to significantly en
62                                              Listeriolysin O (LLO), a cholesterol-binding cytolysin o
63                               Among these is listeriolysin O (LLO), a pore-forming hemolysin that is
64                  We prove in this study that listeriolysin O (LLO), a pore-forming molecule and a maj
65 e with an Escherichia coli strain expressing listeriolysin O (LLO), a pore-forming toxin from L. mono
66 which is dependent on the pore-forming toxin listeriolysin O (LLO), followed by rupture.
67 the Listeria monocytogenes virulence factor, listeriolysin O (LLO), induces an immune response that c
68  of L. monocytogenes, the pore-forming toxin listeriolysin O (LLO), is sufficient to induce L. monocy
69 ore-forming cholesterol-dependent cytolysin, listeriolysin O (LLO), mediates bacterial escape from ve
70 gen which secretes a pore-forming cytolysin, listeriolysin O (LLO), necessary for intracellular growt
71               Here, the pore-forming protein listeriolysin O (LLO), secreted by Listeria monocytogene
72                  We report here that the CDC listeriolysin O (LLO), secreted by the facultative intra
73 e of macrophages from liposomes that contain listeriolysin O (LLO), the hemolytic protein of Listeria
74 ment of mice with a neutralizing mAb against listeriolysin O (LLO), the pore-forming toxin of Listeri
75 r PrfA, including the pore-forming cytolysin listeriolysin O (LLO), two phospholipases C (PlcA and Pl
76                    Using a prototypical CDC, listeriolysin O (LLO), we provide a microscopic connecti
77 o reduced cytokine production in response to Listeriolysin O (LLO), which activates MC by a TLR2-inde
78 hat secretes a pore-forming cytolysin called listeriolysin O (LLO), which disrupts the phagosomal mem
79 rane is initiated by the secreted haemolysin listeriolysin O (LLO), which is essential for vacuolar e
80  amino acid 91 to 99 (aa91-99) sequence from listeriolysin O (LLO).
81 tion through the secreted pore-forming toxin listeriolysin O (LLO).
82 intracellular life cycle that is mediated by listeriolysin O (LLO).
83 osol by secreting the pore-forming cytolysin listeriolysin O (LLO).
84 om the phagosome using a secreted cytolysin, listeriolysin O (LLO).
85 otein with a truncated, nonhemolytic form of listeriolysin O (LLO).
86 actions of the pore-forming virulence factor listeriolysin O (LLO).
87 diated by the bacterial pore-forming protein listeriolysin O (LLO).
88 lls via the action of the pore-forming toxin listeriolysin O (LLO).
89 as a fusion protein joined to a nonhemolytic listeriolysin O (LLO).
90 (PI-PLC), a broad-range phospholipase C, and listeriolysin O (LLO).
91 T cells is the secreted bacterial hemolysin, listeriolysin O (LLO).
92 pecific for the L. mono cytogenes-encoded Ag listeriolysin O (LLO).
93              T cell populations specific for listeriolysin O (LLO)91-99, the immunodominant epitope r
94 CD8+ T cells specific for the immunodominant listeriolysin O (LLO91-99) epitope provide immunity to L
95  on uninfected cells and may be triggered by listeriolysin O-mediated activation of host response mec
96                     The pore-forming protein listeriolysin O mediates escape from host vacuoles and u
97 -2Kb-restricted CD8 T cells specific for the listeriolysin O molecule mediate significant immunity in
98 cua and a mutant strain of L. monocytogenes (listeriolysin O negative), which do not enter the cytoso
99  provided only pore-forming activity because listeriolysin O of Listeria monocytogenes could substitu
100 ndent cytolysin (CDC) family, which includes listeriolysin O, perfringolysin O, and streptolysin O.
101              Nonetheless it is possible that listeriolysin O potentiates the effect(s) of an other mo
102                      These data suggest that listeriolysin O production by infecting L. monocytogenes
103  single LFn fusion protein containing NP and listeriolysin O protein epitopes in tandem mount a CTL r
104  r30 linked in frame to the L. monocytogenes listeriolysin O signal sequence and driven by the hly pr
105 nocytogenes and induced a subset of effector listeriolysin O-specific CD11a(+) CD8(+) T cells in sple
106       However, significant levels of Gag and listeriolysin O-specific CD8(+) T cells were observed in
107 se animals is characterized by activation of listeriolysin O-specific CD8(+) T cells, which are capab
108 with L. monocytogenes dal dat/pRRR generated listeriolysin O-specific effector and memory CD8(+) T ce
109 specific cells were similar to those against listeriolysin O, the immunodominant Ag of L. monocytogen
110 n with WT, heat-killed, or mutant Lm lacking listeriolysin O, the pore-forming hemolysin that promote
111 apsulated inside pH-sensitive liposomes with listeriolysin O, the pore-forming protein that mediates
112 train was constructed in which expression of listeriolysin O was placed under the inducible control o
113 production of the critical virulence factor, listeriolysin O, was compromised by FA modulation, sugge

 
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