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1 rotein Ags: hen egg white lysozyme, OVA, and listeriolysin O.
2 s not limited to CD8+ T cells that recognize listeriolysin O.
3 ecame ill had elevated levels of antibody to listeriolysin O.
4 erum samples were tested for IgG antibody to listeriolysin O.
6 accounted for by a decrease in LM-specific (listeriolysin O(91-99) tetramer(+)) effector CD8(+) T ce
7 aracterize changes in SUMOylation induced by listeriolysin O, a bacterial toxin that impairs the host
10 that pH-sensitive liposomes containing both listeriolysin O and gelonin were more effective than con
11 pression of the phagosome-lysing pore former listeriolysin O and on type I IFN receptor signaling.
12 atural L. monocytogenes-derived soluble Ags (listeriolysin O and p60) revealed that tethering of thes
14 xpression of other critical virulence genes (Listeriolysin O, and two phospholipases plcA and plcB) i
15 l liver kinase-1) to the microbial adjuvant, listeriolysin-O, and used Lm to deliver the Ags and elic
18 ; however, WTLM and L. monocytogenes lacking listeriolysin O (DeltahlyLM) induce similar levels of cy
19 In in vitro experiments, co-encapsulated listeriolysin O enabled liposomal gelonin-mediated B16 c
20 lipid biosynthesis, enhanced the toxicity of listeriolysin O expressed in the host cell cytosol, lead
23 smid containing the invasin gene Inv and the listeriolysin O gene HlyA, which encode two bacterial fa
24 partially dependent on the virulence factor listeriolysin O; however, WTLM and L. monocytogenes lack
25 irement for the essential pore-forming toxin listeriolysin O in mediating escape from phagocytic vacu
26 cytoplasmic entry of Listeria facilitated by listeriolysin O is an essential feature not only of the
27 anomer peptides amino acids (aa) 91 to 99 of listeriolysin O (LLO 91-99) and aa 217 to 225 of the p60
28 by the cholesterol-dependent cytolysin (CDC) listeriolysin O (LLO) acts within the infected cell, (ii
29 ast two critical secreted virulence factors: listeriolysin O (LLO) and a broad-specificity phospholip
33 tron microscopy that LM expressing truncated listeriolysin O (LLO) and amino acid fragments 311 to 66
34 on the expression of two secreted proteins: listeriolysin O (LLO) and phosphatidylcholine-preferring
35 virulence factors of Listeria monocytogenes, listeriolysin O (LLO) and phosphatidylinositol-specific
36 91 to 99 (aa91-99) immunodominant peptide of listeriolysin O (LLO) and to the aa217-225 immunodominan
37 n host cells by using the pore-forming toxin listeriolysin O (LLO) and two phospholipase C enzymes.
38 ) that are deficient in the virulence factor listeriolysin O (LLO) are highly attenuated and are thou
39 the Listeria monocytogenes virulence factor listeriolysin O (LLO) enhances the immunogenicity and an
49 ved cells tested, the pore-forming cytolysin listeriolysin O (LLO) is absolutely required for lysis o
52 ould be attributed partially to insufficient listeriolysin O (LLO) production, indicating a requireme
53 mediated, and a nonamer CTL epitope from the listeriolysin O (LLO) protein has been identified in BAL
55 ytogenes and its secreted pore-forming toxin listeriolysin O (LLO) to identify key signaling events a
56 uction of the hly-encoded secreted hemolysin listeriolysin O (LLO) was also found to significantly en
60 e with an Escherichia coli strain expressing listeriolysin O (LLO), a pore-forming toxin from L. mono
62 the Listeria monocytogenes virulence factor, listeriolysin O (LLO), induces an immune response that c
63 of L. monocytogenes, the pore-forming toxin listeriolysin O (LLO), is sufficient to induce L. monocy
64 ore-forming cholesterol-dependent cytolysin, listeriolysin O (LLO), mediates bacterial escape from ve
65 gen which secretes a pore-forming cytolysin, listeriolysin O (LLO), necessary for intracellular growt
68 e of macrophages from liposomes that contain listeriolysin O (LLO), the hemolytic protein of Listeria
69 ment of mice with a neutralizing mAb against listeriolysin O (LLO), the pore-forming toxin of Listeri
70 r PrfA, including the pore-forming cytolysin listeriolysin O (LLO), two phospholipases C (PlcA and Pl
71 rane is initiated by the secreted haemolysin listeriolysin O (LLO), which is essential for vacuolar e
86 CD8+ T cells specific for the immunodominant listeriolysin O (LLO91-99) epitope provide immunity to L
87 on uninfected cells and may be triggered by listeriolysin O-mediated activation of host response mec
89 -2Kb-restricted CD8 T cells specific for the listeriolysin O molecule mediate significant immunity in
90 cua and a mutant strain of L. monocytogenes (listeriolysin O negative), which do not enter the cytoso
91 provided only pore-forming activity because listeriolysin O of Listeria monocytogenes could substitu
92 ndent cytolysin (CDC) family, which includes listeriolysin O, perfringolysin O, and streptolysin O.
95 single LFn fusion protein containing NP and listeriolysin O protein epitopes in tandem mount a CTL r
96 r30 linked in frame to the L. monocytogenes listeriolysin O signal sequence and driven by the hly pr
97 nocytogenes and induced a subset of effector listeriolysin O-specific CD11a(+) CD8(+) T cells in sple
99 se animals is characterized by activation of listeriolysin O-specific CD8(+) T cells, which are capab
100 with L. monocytogenes dal dat/pRRR generated listeriolysin O-specific effector and memory CD8(+) T ce
101 specific cells were similar to those against listeriolysin O, the immunodominant Ag of L. monocytogen
102 n with WT, heat-killed, or mutant Lm lacking listeriolysin O, the pore-forming hemolysin that promote
103 apsulated inside pH-sensitive liposomes with listeriolysin O, the pore-forming protein that mediates
104 train was constructed in which expression of listeriolysin O was placed under the inducible control o
105 production of the critical virulence factor, listeriolysin O, was compromised by FA modulation, sugge
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