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1  the sodium-powered polar flagellar motor in Vibrio parahaemolyticus.
2 acterial pathogens, followed by Shigella and Vibrio parahaemolyticus.
3 ancreatic Necrosis Disease (AHPND) caused by Vibrio parahaemolyticus.
4 to the COD homologs from Vibrio cholerae and Vibrio parahaemolyticus.
5 ystems to combat the causative agent of EMS, Vibrio parahaemolyticus.
6 odium hypochlorite (NaOCl) solutions against Vibrio parahaemolyticus.
7  VopS-dependent manner during infection with Vibrio parahaemolyticus.
8 at ParP is integral to array localization in Vibrio parahaemolyticus.
9 present the crystal structure of a TrkH from Vibrio parahaemolyticus.
10 ome and stimulates motility and virulence of Vibrio parahaemolyticus.
11 nknown function from Pyrococcus furiosus and Vibrio parahaemolyticus.
12 ted by the lateral flagellar (laf) system in Vibrio parahaemolyticus.
13 S2 gene cluster found in a pandemic clone of Vibrio parahaemolyticus.
14 ter-regulator operons of Vibrio cholerae and Vibrio parahaemolyticus.
15 d encode a protein highly similar to NorM of Vibrio parahaemolyticus.
16  of P. aeruginosa is most similar to FlgM of Vibrio parahaemolyticus.
17 yme, yielding a limit of detection of 62 CFU Vibrio parahaemolyticus, 86 CFU Salmonella Typhimurium,
18                                              Vibrio parahaemolyticus, a biofouling marine bacterium a
19                                              Vibrio parahaemolyticus, a causative agent of gastroente
20 hogenesis of the diarrheal disease caused by Vibrio parahaemolyticus, a leading cause of seafood-asso
21                                          For Vibrio parahaemolyticus, a marine bacterium and pathogen
22                                              Vibrio parahaemolyticus, a marine bacterium, is the caus
23                                           In Vibrio parahaemolyticus, a significant enteric pathogen
24 outer protein S) from the bacterial pathogen Vibrio parahaemolyticus and the human protein HYPE (hunt
25 ia, including the species Vibrio vulnificus, Vibrio parahaemolyticus and Vibrio cholerae, grow in war
26                            Not unexpectedly, Vibrio parahaemolyticus and Vibrio vulnificus strains fo
27            Homologous clusters also exist in Vibrio parahaemolyticus and Vibrio vulnificus, and thus
28    Pathogenic non-cholera Vibrio spp., e.g., Vibrio parahaemolyticus and Vibrio vulnificus, cause gas
29 lmonella Typhimurium, Staphylococcus aureus, Vibrio parahaemolyticus) and their mixtures in water and
30 ng antimicrobial activity for fish pathogen, Vibrio parahaemolyticus, and identified surfactin as the
31 n = 30 form each group) were challenged with Vibrio parahaemolyticus, and survival rates were subsequ
32 at cause human diseases are Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus, the only
33 Of these 12, three species--Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account f
34 abdus luminescens, Aeromonas hydrophila, and Vibrio parahaemolyticus are also sensitive to mutations
35  swarming-proficient and virulent strains of Vibrio parahaemolyticus are silenced for the vibrio arch
36                          Some bacteria, like Vibrio parahaemolyticus, are social and swarm in groups
37 ven different strains of the marine pathogen Vibrio parahaemolyticus as a model system.
38 ophilus somni at tyrosine 32 or by VopS from Vibrio parahaemolyticus at threonine 35.
39 TDH), an exotoxin of the food-borne pathogen Vibrio parahaemolyticus, can be exported through the typ
40                         The marine bacterium Vibrio parahaemolyticus causes gastroenteritis in humans
41 s of this nucleotide promote a more adhesive Vibrio parahaemolyticus cell type.
42                             The success of a Vibrio parahaemolyticus clone (VpST3) in Latin America-
43 im (PAS)-like fold highly similar to that of Vibrio parahaemolyticus CpxA as determined by X-ray crys
44                                              Vibrio parahaemolyticus differentiates from a polarly fl
45                        Here we show that the Vibrio parahaemolyticus effector protein VopQ is a poten
46 w that the actin-binding repeat (ABR) of the Vibrio parahaemolyticus effector VopV binds to cytoplasm
47                            The flaA locus of Vibrio parahaemolyticus encodes one of the four polar fl
48 two example sets of Escherichia/Shigella and Vibrio parahaemolyticus genomes, we show that iterative-
49                                              Vibrio parahaemolyticus harbors two type III secretion s
50                                              Vibrio parahaemolyticus has dual flagellar systems adapt
51  controlling swarmer cell differentiation of Vibrio parahaemolyticus identified a novel three-gene op
52 e activities, and disease resistance against Vibrio parahaemolyticus in Pacific white shrimp (Penaeus
53 egulatory cascade is poorly characterized in Vibrio parahaemolyticus, in part because swarming and vi
54                                              Vibrio parahaemolyticus infections are associated with c
55               In May and June 1998, reported Vibrio parahaemolyticus infections increased sharply in
56  to the seasonality of Vibrio vulnificus and Vibrio parahaemolyticus infections.
57                                              Vibrio parahaemolyticus is a common marine bacterium and
58                                              Vibrio parahaemolyticus is a facultative intracellular p
59                                              Vibrio parahaemolyticus is a Gram-negative bacterium res
60                                              Vibrio parahaemolyticus is a halophile that inhabits bra
61                                              Vibrio parahaemolyticus is a halophilic bacterium capabl
62                                              Vibrio parahaemolyticus is a marine microorganism that c
63 erial Na(+)/galactose cotransporter vSGLT of Vibrio parahaemolyticus is a member of the sodium:solute
64                                              Vibrio parahaemolyticus is a naturally occurring bacteri
65                                              Vibrio parahaemolyticus is a ubiquitous, gram-negative m
66                                              Vibrio parahaemolyticus is an emerging food- and waterbo
67                                              Vibrio parahaemolyticus is an important human foodborne
68                                              Vibrio parahaemolyticus is an important human pathogen w
69                                              Vibrio parahaemolyticus is an organism well adapted to c
70                                              Vibrio parahaemolyticus is one of only two marine pathog
71                                              Vibrio parahaemolyticus is one of the most important foo
72                                              Vibrio parahaemolyticus is the leading cause of bacteria
73                                              Vibrio parahaemolyticus is the leading cause of food-bor
74                                              Vibrio parahaemolyticus is the leading cause of seafood-
75                                              Vibrio parahaemolyticus is the leading worldwide cause o
76                                              Vibrio parahaemolyticus is the most common cause of seaf
77                                              Vibrio parahaemolyticus isolates display variation in co
78     In this study, 77 clinical and 67 oyster Vibrio parahaemolyticus isolates from North America were
79                   When exposure challenge of Vibrio parahaemolyticus, it is indicated that the PI3K-A
80 : Vibrio cholerae HapR, Vibrio harveyi LuxR, Vibrio parahaemolyticus OpaR and Vibrio vulnificus SmcR.
81                                              Vibrio parahaemolyticus possesses dual flagellar systems
82                                              Vibrio parahaemolyticus possesses two types of flagella,
83 s required for normal flagellar synthesis in Vibrio parahaemolyticus, Pseudomonas putida, and Shewane
84 o alter intracellular cyclic-di-GMP pools in Vibrio parahaemolyticus revealed that these genes also a
85                                          The Vibrio parahaemolyticus Scr system modulates decisions p
86                                           In Vibrio parahaemolyticus, scrC participates in controllin
87                                   Pathogenic Vibrio parahaemolyticus senses bile acids and induce pat
88                                              Vibrio parahaemolyticus senses surfaces via impeded rota
89                                              Vibrio parahaemolyticus sequence type 36 (ST36) strains
90                 The crystal structure of the Vibrio parahaemolyticus SGLT showed that residue Gln(428
91 vSGLT), a solute-sodium symporter (SSS) from Vibrio parahaemolyticus, shares a common structural fold
92           The crystal structure of TrkH from Vibrio parahaemolyticus showed that TrkH resembles a K(+
93 r of the solute sodium symporters (SSS), the Vibrio parahaemolyticus sodium/galactose symporter (vSGL
94 ed into the external face of a cysteine-less Vibrio parahaemolyticus sodium/glucose cotransporter for
95                                          The Vibrio parahaemolyticus sodium/glucose transporter (vSGL
96                            Recently isolated Vibrio parahaemolyticus strains have displayed multiple
97         The present method of characterizing Vibrio parahaemolyticus strains involves serotyping or d
98                                          The Vibrio parahaemolyticus T3SS effector VopQ targets host-
99 _1663), is conserved only in V. cholerae and Vibrio parahaemolyticus T3SS-positive strains and has no
100 ting technology with the cytotoxicity of two Vibrio parahaemolyticus T3SSs (T3SS1 and T3SS2) to ident
101 The Na(+)/galactose cotransporter (vSGLT) of Vibrio parahaemolyticus, tagged with C-terminal hexahist
102 ly emergent penaeid shrimp disease caused by Vibrio parahaemolyticus that has already led to tremendo
103             VopL is an effector protein from Vibrio parahaemolyticus that nucleates actin filaments.
104 ther bacteria, such as Vibrio vulnificus and Vibrio parahaemolyticus, that have syp-like loci and con
105                                           In Vibrio parahaemolyticus, the leading cause of bacterial
106                                              Vibrio parahaemolyticus, the leading cause of seafood-as
107  reveal that the BPD of the newly identified Vibrio parahaemolyticus Type III effector VopR is unfold
108                                          The Vibrio parahaemolyticus type III effector VopS is implic
109 iplasmic bile acid sensor that activates the Vibrio parahaemolyticus type III secretion system adopts
110                          Herein we show that Vibrio parahaemolyticus uses the type III effector VopQ
111 rovide evidence supporting that the pathogen Vibrio parahaemolyticus uses transertion to assemble its
112  Vibrio alginolyticus, Vibrio fluvialis, and Vibrio parahaemolyticus utilized heme and hemoglobin as
113                       The bacterial pathogen Vibrio parahaemolyticus utilizes a type III secretion sy
114                                              Vibrio parahaemolyticus (V. para) is a Gram-negative bac
115                                              Vibrio parahaemolyticus (V. para), a Gram-negative halop
116 e chain reaction for the prevalence of total Vibrio parahaemolyticus, V. vulnificus and V. cholerae a
117 l regulation of the polar flagellar genes of Vibrio parahaemolyticus, Vibrio cholerae, and Pseudomona
118 io species, with a focus on Vibrio cholerae, Vibrio parahaemolyticus, Vibrio vulnificus and Vibrio fi
119 mined the structure of the first W domain of Vibrio parahaemolyticus VopL cross-linked to actin Cys37
120      One of these pathogens, disease-causing Vibrio parahaemolyticus (VP(AHPND)) which induces acute
121 y designed to have a complementary region in Vibrio parahaemolyticus (VP) genome and to make differen
122 the first structure of a bacterial ATL, from Vibrio parahaemolyticus (vpAtl).
123 udy of the sodium/galactose transporter from Vibrio parahaemolyticus (vSGLT), consisting of molecular
124                           We discovered that Vibrio parahaemolyticus VtrC, along with VtrA and VtrB,
125            In Gram-negative enteric pathogen Vibrio parahaemolyticus, we found that polar flagella ca
126 acteriophages of an environmental isolate of Vibrio parahaemolyticus were isolated and sequenced.
127  including the pathogens Vibrio cholerae and Vibrio parahaemolyticus, were found to produce such acti
128  similarities to the TDH and TRH proteins of Vibrio parahaemolyticus, where they have been shown to c
129 nome of the closely related marine bacterium Vibrio parahaemolyticus, which is a human pathogen, show
130  function of an effector protein secreted by Vibrio parahaemolyticus, which is an enteric pathogen fo

 
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