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1 Yop protein production in the intracellular yersiniae.
2 er, Yops were produced only by extracellular yersiniae.
3 rs of T3SS gene expression in the pathogenic yersiniae.
4 ogy to proteins of unknown function in other yersiniae.
5 that is translocated into mammalian cells by Yersiniae.
6 o activate type III secretion than wild-type yersiniae.
9 ficient for bacteriostasis of Ca(2+)-starved yersiniae and suggest that abrupt restriction of Y. pest
10 op targeting at the extracellular surface of yersiniae and that the protective efficacy of LcrV-speci
11 contact-activated, extracellularly localized yersiniae and were targeted to the HeLa cell cytosol.
13 oes not decrease survival of YadA-expressing Yersiniae because C3b becomes readily inactivated by fac
14 in lcrV reduced type III targeting of mutant yersiniae but did not promote secretion into the extrace
15 heterogeneity of size and sequence among the yersiniae, but the functional consequences of this varia
16 estis lacking effector Yops, even though the yersiniae could strongly express LcrV, suggesting that Y
19 odulate and evade host immune systems, these yersiniae inject effector proteins into host macrophages
25 no significant effect of the iron status of yersiniae or of the pigmentation locus on invasion and l
27 pe III targeting pathway in the cytoplasm of yersiniae, presumably by preventing the export of YopN.
28 Thus, competition studies with wild-type yersiniae reveal critical roles of Yops in combating hos
31 at during infection of tissue culture cells, yersiniae secrete small amounts of LcrV into the extrace
32 We show here that the type III machines of yersiniae secrete three proteins into the extracellular
33 such as Salmonella spp., Shigellae spp. and Yersiniae spp., use specialized virulence factors to ove
35 en grown at 21 degrees C, however, the three yersiniae synthesized LPS containing predominantly hexa-
36 ut mutations in both genes caused DeltalcrGV yersiniae to display a Los phenotype similar to that of
37 contact with host cells and is necessary for Yersiniae to establish a replicative niche and cause dis
39 hat knockout mutations of lcrG caused mutant yersiniae to prematurely secrete Yops into the extracell
42 tasis of Y. pestis (but not enteropathogenic yersiniae) was abrupt in Ca(2+)-deficient medium at neut
43 ovided evidence that the Deltalpp mutants of yersiniae were significantly attenuated and could be use
46 the injection of Yop proteins by tyeA mutant yersiniae with the digitonin fractionation technique.
47 or more of Y. pestis or the enteropathogenic yersiniae Yersinia enterocolitica and Yersinia pseudotub
48 ce (complement resistance) in the pathogenic Yersiniae (Yersinia pestis, Y. enterocolitica, and Y. ps
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