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1 haracterize modified peptide-cytidylate from Yersinia pseudotuberculosis.
2 vasion factor in Yersinia enterocolitica and Yersinia pseudotuberculosis.
3 onal pathogen that has recently emerged from Yersinia pseudotuberculosis.
4 tal structure of residues 1-129 of YopH from Yersinia pseudotuberculosis.
5  Salmonella enterica serovar Typhimurium and Yersinia pseudotuberculosis.
6 ogenic relatives Yersinia enterocolitica and Yersinia pseudotuberculosis.
7  translocation into HeLa cells infected with Yersinia pseudotuberculosis.
8 lows efficient entry into mammalian cells by Yersinia pseudotuberculosis.
9 ogenic yersiniae Yersinia enterocolitica and Yersinia pseudotuberculosis.
10 inv gene product (invasin) on the surface of Yersinia pseudotuberculosis.
11 osely related pathogens, Yersinia pestis and Yersinia pseudotuberculosis.
12 duced by the gram-negative, enteric pathogen Yersinia pseudotuberculosis.
13 uring primary infection of C57BL/6 mice with Yersinia pseudotuberculosis.
14 of the T3SS in the gastrointestinal pathogen Yersinia pseudotuberculosis.
15 , evolved from the gastrointestinal pathogen Yersinia pseudotuberculosis.
16 L-10) in sera of C57BL/6J mice infected with Yersinia pseudotuberculosis.
17 y pathogenic Escherichia coli strains and by Yersinia pseudotuberculosis.
18 ired for the virulence of the enteropathogen Yersinia pseudotuberculosis.
19 nt of plague, has only recently evolved from Yersinia pseudotuberculosis.
20 , regulates virulence in Yersinia pestis and Yersinia pseudotuberculosis.
21 2, inhibit beta1 integrin-promoted uptake of Yersinia pseudotuberculosis.
22 is genomes and the corresponding features in Yersinia pseudotuberculosis.
23 ffected in T cells exposed to low numbers of Yersinia pseudotuberculosis.
24 in the biosynthesis of 3,6-dideoxyhexoses in Yersinia pseudotuberculosis.
25  diverged recently from the enteric pathogen Yersinia pseudotuberculosis.
26 elated food- and waterborne enteric pathogen Yersinia pseudotuberculosis A combination of population
27            Y. pestis and the closely related Yersinia pseudotuberculosis also make biofilms on the cu
28 acterial pathogen that evolved recently from Yersinia pseudotuberculosis, an enteric pathogen transmi
29 the causative agent of plague, diverged from Yersinia pseudotuberculosis, an enteric pathogen, an est
30 secreted in a type III-dependent manner from Yersinia pseudotuberculosis and also secreted from C. tr
31  similarity with YopJ of the animal pathogen Yersinia pseudotuberculosis and AvrRxv of the plant path
32                    Enteric pathogens such as Yersinia pseudotuberculosis and enteropathogenic Escheri
33                                 Nonpigmented Yersinia pseudotuberculosis and Escherichia coli strains
34 s the products of the psaEFABC genes in both Yersinia pseudotuberculosis and Escherichia coli.
35 etermine if YopE is a protective antigen for Yersinia pseudotuberculosis and if primary infection wit
36 RIFosome) mediates cell death in response to Yersinia pseudotuberculosis and LPS.
37  the activity of Cif from the human pathogen Yersinia pseudotuberculosis and selected variants, and t
38  other bacterial pathogens, the dam genes of Yersinia pseudotuberculosis and Vibrio cholerae were dis
39 different receptors and for phages infecting Yersinia pseudotuberculosis and Vibrio cholerae.
40  a role in recognition of the enteropathogen Yersinia pseudotuberculosis and whether this results in
41                            Previous study in Yersinia pseudotuberculosis and Yersinia enterocolitica
42                           The binding of the Yersinia pseudotuberculosis and Yersinia enterocolitica
43                The enteropathogenic bacteria Yersinia pseudotuberculosis and Yersinia enterocolitica
44                                              Yersinia pseudotuberculosis and Yersinia enterocolitica
45  Yersinia pestis and pYV in enteropathogenic Yersinia pseudotuberculosis and Yersinia enterocolitica)
46                                           In Yersinia pseudotuberculosis and Yersinia enterocolitica,
47 nia pestis and two enteropathogenic species, Yersinia pseudotuberculosis and Yersinia enterocolitica.
48 how that PNPase also enhances the ability of Yersinia pseudotuberculosis and Yersinia pestis to withs
49 was required for optimal T3SS functioning in Yersinia pseudotuberculosis and Yersinia pestis.
50 um and to binding of the biofilm produced by Yersinia pseudotuberculosis and Yersinia pestis.
51 nteric pathogens, Salmonella typhimurium and Yersinia pseudotuberculosis, and the second vector teste
52 ch as Escherichia coli, Salmonella enterica, Yersinia pseudotuberculosis, and Vibrio cholerae, among
53 in Escherichia coli, Salmonella typhimurium, Yersinia pseudotuberculosis, and Vibrio cholerae, each o
54 e and are fully conserved between Y. pestis, Yersinia pseudotuberculosis, and Yersinia enterocolitica
55                          Yersinia pestis and Yersinia pseudotuberculosis are closely related facultat
56 nse to pathogenic Listeria monocytogenes and Yersinia pseudotuberculosis as well as commensal bacteri
57 structures, we mapped the RNA structurome of Yersinia pseudotuberculosis at three different temperatu
58 age and apoptosis against L. pneumophila and Yersinia pseudotuberculosis but preferentially activate
59 s modest catalase activity, and is shared by Yersinia pseudotuberculosis, but not Yersinia enterocoli
60  and core metabolism in the enteric pathogen Yersinia pseudotuberculosis by integrated transcriptome
61 ary for efficient invasin-promoted uptake of Yersinia pseudotuberculosis by nonphagocytic cells.
62 e, has arisen from a less virulent pathogen, Yersinia pseudotuberculosis, by a rapid evolutionary pro
63                         The enteric pathogen Yersinia pseudotuberculosis causes the disease yersinios
64 tifying a potential association site for the Yersinia pseudotuberculosis chaperone-effector pair SycE
65                  We previously reported that Yersinia pseudotuberculosis colonizes the intestinal muc
66 virulence genes found in Yersinia pestis and Yersinia pseudotuberculosis compared to other Yersinia s
67  Yersinia pestis, unlike the closely related Yersinia pseudotuberculosis, constitutively produces iso
68 nfected with a different bacterial pathogen, Yersinia pseudotuberculosis, contain damaged DNA.
69                                 In cell-free Yersinia pseudotuberculosis culture supernatants, we hav
70                                              Yersinia pseudotuberculosis delivers several Yop effecto
71                           The virulence of a Yersinia pseudotuberculosis Delta yopM mutant in mice vi
72 ion with hyperyersiniabactin (Ybt) producing Yersinia pseudotuberculosis Deltafur mutant (termed Delt
73           The gram-negative enteric pathogen Yersinia pseudotuberculosis employs a type III secretion
74 -borne and water-borne transmission route of Yersinia pseudotuberculosis, from which Y. pestis diverg
75                          The closely related Yersinia pseudotuberculosis, from which Y. pestis recent
76                           The enteropathogen Yersinia pseudotuberculosis, from which Y. pestis recent
77                 After infection of mice with Yersinia pseudotuberculosis, IL-33 expression was increa
78 ucture of CDP-D-glucose 4,6-dehydratase from Yersinia pseudotuberculosis in the resting state.
79                          M-cell targeting by Yersinia pseudotuberculosis in vivo may, therefore, be m
80 ained ancestral genomic variation present in Yersinia pseudotuberculosis, including virulence factors
81              The oral LD50 for a yopJ mutant Yersinia pseudotuberculosis increases 64-fold compared w
82                           Cell extracts from Yersinia pseudotuberculosis induced multinucleation in H
83                          Using this tool for Yersinia pseudotuberculosis-infected lymphatic tissues,
84  lymph nodes and associated lymphatics after Yersinia pseudotuberculosis infection and clearance.
85                     Quantitative analysis of Yersinia pseudotuberculosis infection of murine gut loop
86 esponses within SLOs during gastrointestinal Yersinia pseudotuberculosis infection to limit pathogen
87 vated with lipopolysaccharide (LPS) prior to Yersinia pseudotuberculosis infection, caspase-1 is acti
88                          In a mouse model of Yersinia pseudotuberculosis infection, we show that at l
89 ensal microbiota or animal susceptibility to Yersinia pseudotuberculosis infection.
90 s also been demonstrated in a mouse model of Yersinia pseudotuberculosis infection.
91                                              Yersinia pseudotuberculosis infects many mammals and bir
92   We demonstrate that, in addition to MyD88, Yersinia pseudotuberculosis inhibits TRIF signaling thro
93                                              Yersinia pseudotuberculosis initiates systemic disease a
94 sequences of wild-type and mutant strains of Yersinia pseudotuberculosis interactions with the macrop
95                          Efficient uptake of Yersinia pseudotuberculosis into cultured mammalian cell
96                                 The entry of Yersinia pseudotuberculosis into cultured mammalian cell
97             Efficient entry of the bacterium Yersinia pseudotuberculosis into mammalian cells require
98 ency entry of the enteropathogenic bacterium Yersinia pseudotuberculosis into nonphagocytic cells is
99                                              Yersinia pseudotuberculosis inv mutant strains cured of
100 munoglobulin-like (Big) domains, such as the Yersinia pseudotuberculosis invasin and Escherichia coli
101  localization to an amino terminal-truncated Yersinia pseudotuberculosis invasin derivative.
102                              Transfer of the Yersinia pseudotuberculosis invasin gene into E.coli DH1
103           To determine if recognition of the Yersinia pseudotuberculosis invasin protein and natural
104                                          The Yersinia pseudotuberculosis invasin protein promotes bac
105                                          The Yersinia pseudotuberculosis invasin protein promotes bac
106  fused EHEC intimin to a homologous protein, Yersinia pseudotuberculosis invasin, or to maltose-bindi
107                       Quorum sensing (QS) in Yersinia pseudotuberculosis involves two pairs of LuxRI
108    Mating pair formation proteins (Trb) from Yersinia pseudotuberculosis IP31758 are the mostly close
109                                              Yersinia pseudotuberculosis is a foodborne pathogenic ba
110                                              Yersinia pseudotuberculosis is a Gram-negative bacterial
111                                              Yersinia pseudotuberculosis is a Gram-negative enteropat
112 e dimeric [2Fe-2S] protein, E 1, cloned from Yersinia pseudotuberculosis, is the only known enzyme wh
113 fied IS100 sequences in a specific subset of Yersinia pseudotuberculosis isolates that were also sens
114 osum and periarthritis due to infection with Yersinia pseudotuberculosis IV was followed 13 months la
115                                              Yersinia pseudotuberculosis lcrF-null mutants showed att
116                                              Yersinia pseudotuberculosis LcrQ is a transcriptional re
117 onary steps that led to its emergence from a Yersinia pseudotuberculosis-like progenitor; however, th
118                                              Yersinia pseudotuberculosis localizes to the distal ileu
119       To test these models, we constructed a Yersinia pseudotuberculosis mutant expressing YopD devoi
120                       Here, we constructed a Yersinia pseudotuberculosis mutant strain with arabinose
121 ordingly, caspase-1-dependent clearance of a Yersinia pseudotuberculosis mutant was enhanced in BCAP-
122                                              Yersinia pseudotuberculosis mutants deficient for the ad
123                                              Yersinia pseudotuberculosis mutants that overproduce the
124                                              Yersinia pseudotuberculosis mutants that overproduce the
125 e found that only a small fraction of either Yersinia pseudotuberculosis or Yersinia pestis bacteria
126  cytotoxicity induced by Yersinia pestis and Yersinia pseudotuberculosis paradoxically leads to decre
127 n this study, a novel recombinant attenuated Yersinia pseudotuberculosis PB1+ strain (chi10069) engin
128                                          The Yersinia pseudotuberculosis pH6 antigen mediates haemagg
129 itating biofilm on Caenorhabditis elegans by Yersinia pseudotuberculosis represents a tractable model
130 have suggested that rfaH may be required for Yersinia pseudotuberculosis resistance to antimicrobial
131 fection during C. trachomatis infections, in Yersinia pseudotuberculosis resulted in its secretion vi
132           We report that oral infection with Yersinia pseudotuberculosis results in the development o
133 nfection with the RIPK1-activating pathogen, Yersinia pseudotuberculosis, results in enhanced RIPK1-c
134         The gram-negative bacterial pathogen Yersinia pseudotuberculosis secretes into macrophages a
135 the mechanism(s) of complement resistance in Yersinia pseudotuberculosis showed that the outer membra
136 fore, self-adjuvanting OMVs from a remodeled Yersinia pseudotuberculosis strain as a type of plague v
137 ium evolved from an ancestral enteroinvasive Yersinia pseudotuberculosis strain by gene loss and acqu
138          Infection assays carried out with a Yersinia pseudotuberculosis strain producing YopER144A d
139 ersinia enterocolitica strains and 2 (of 10) Yersinia pseudotuberculosis strains at the restrictive t
140                                              Yersinia pseudotuberculosis strains expressing the mutan
141 PS)-primed murine macrophages with DeltayopM Yersinia pseudotuberculosis strains expressing wild-type
142 expressing these proteins were infected with Yersinia pseudotuberculosis strains that secrete functio
143 ith a panel of different Yersinia pestis and Yersinia pseudotuberculosis strains to determine whether
144 lar delivery of IcsA in Escherichia coli and Yersinia pseudotuberculosis, suggesting that the mechani
145                                          The Yersinia pseudotuberculosis surface protein invasin bind
146                       Following clearance of Yersinia pseudotuberculosis, sustained inflammation and
147 ia coli expressing invA, a gene product from Yersinia pseudotuberculosis that mediates cellular invas
148                                              Yersinia pseudotuberculosis, the closely related food-an
149                                              Yersinia pseudotuberculosis, the relatively recent proge
150 ed a systematic deletion analysis of YopM in Yersinia pseudotuberculosis to determine which regions a
151 es and synthesizing the invasin protein from Yersinia pseudotuberculosis to enhance cellular entry we
152                                    YscU is a Yersinia pseudotuberculosis type III secretion system pr
153                                              Yersinia pseudotuberculosis uses a plasmid (pYV)-encoded
154                                              Yersinia pseudotuberculosis uses a type III secretion sy
155                       The bacterial pathogen Yersinia pseudotuberculosis uses type III secretion mach
156 itor identified by in vitro screening, using Yersinia pseudotuberculosis Using a mouse model of P. ae
157                    The lipopolysaccharide of Yersinia pseudotuberculosis V includes a 3,6-dideoxyhexo
158 oxyhexose found in the lipopolysaccharide of Yersinia pseudotuberculosis V, have shown that the C-3 d
159 trasaccharide of the lipopolysaccharide from Yersinia pseudotuberculosis V.
160 he L-colitose biosynthetic gene cluster from Yersinia pseudotuberculosis VI.
161 seudomonas aeruginosa, Erwinia chrysanthemi, Yersinia pseudotuberculosis, Vibrio cholerae (30-70% seq
162 he evolution of Y. pestis from the ancestral Yersinia pseudotuberculosis was a significant reduction
163                        In mice infected with Yersinia pseudotuberculosis, we found that PP barrier dy
164 es of YopB, YopD, and YopE (BDE) secreted by Yersinia pseudotuberculosis were purified by affinity ch
165   During 2001, 89 culture-confirmed cases of Yersinia pseudotuberculosis were reported in Finland; 55
166 stis (the plague bacillus) and its ancestor, Yersinia pseudotuberculosis (which causes self-limited b
167 to colonization by another enteric pathogen, Yersinia pseudotuberculosis, which normally invades the
168 ulated by RovA in both Y. enterocolitica and Yersinia pseudotuberculosis while negatively regulated b
169                             Dissemination of Yersinia pseudotuberculosis within mice after oral inocu
170 ic plague, evolved from the enteric pathogen Yersinia pseudotuberculosis within the past 20,000 years
171  protein YtfE contributes to the survival of Yersinia pseudotuberculosis within the spleen following
172 ying degrees of homology to genomic DNA from Yersinia pseudotuberculosis, Yersinia enterocolitica, an
173 as the Yersinia pestis, which causes plague, Yersinia pseudotuberculosis, Yersinia enterocolitica.
174              After oral inoculation of mice, Yersinia pseudotuberculosis yopE and yopH mutants coloni
175  N-terminal domain (residues 1-129) from the Yersinia pseudotuberculosis YopH (YopH-NT) in complex wi
176                       The bacterial pathogen Yersinia pseudotuberculosis (Yp) blocks innate inflammat
177 iI complexes from Escherichia coli EC869 and Yersinia pseudotuberculosis YPIII to explore the evoluti
178 lysaccharide (LPS) for the enteric pathogens Yersinia pseudotuberculosis (Ypt) and Yersinia enterocol
179 infection sites, we established a system for Yersinia pseudotuberculosis (Yptb) growth in microfluidi
180 nal peptide generated by auto-proteolysis of Yersinia pseudotuberculosis YscU, is secreted by the T3S

 
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