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1 ch by verifying a predicted effector TseC in Aeromonas hydrophila.
2 . of Vibrio cholerae, Vibrio vulnificus, and Aeromonas hydrophila.
3 d gene (vacB) from a clinical isolate SSU of Aeromonas hydrophila.
4 , or TagA, from a diarrheal isolate, SSU, of Aeromonas hydrophila.
5 t of a Type IIH R-M system from the pathogen Aeromonas hydrophila.
6 mal operon from the diarrheal isolate SSU of Aeromonas hydrophila.
7 onal responses to a cytotoxic enterotoxin of Aeromonas hydrophila.
8 holerae and by the closely related bacterium Aeromonas hydrophila.
9 hromosomal DNA of a diarrheal isolate SSU of Aeromonas hydrophila.
10 ng the various virulence factors produced by Aeromonas hydrophila, a type II secretion system (T2SS)-
13 s a toxin secreted by the bacterial pathogen Aeromonas hydrophila and is capable of killing target ce
14 duced by Vibrio cholerae, Vibrio vulnificus, Aeromonas hydrophila and other Gram-negative bacteria.
15 in the virulence of diarrheal isolate SSU of Aeromonas hydrophila and showed that VasH, a sigma(54) a
16 bp), isolated in 1971 from the fish pathogen Aeromonas hydrophila, and of the cryptic IncA/C plasmid
17 ne expression from Photorhabdus luminescens, Aeromonas hydrophila, and Vibrio parahaemolyticus are al
18 five septic groups receiving an infusion of Aeromonas hydrophila at 0.2 mL/kg/hr, gradually increasi
20 ressed enolase from diarrheal isolate SSU of Aeromonas hydrophila bound to human plasminogen and faci
22 tx) of an environmental isolate ATCC 7966 of Aeromonas hydrophila consists of six genes (rtxACHBDE) o
24 pestris (xps), Pseudomonas aeruginosa (xcp), Aeromonas hydrophila (exe), and Vibrio cholerae (eps).
25 product displayed 87% sequence similarity to Aeromonas hydrophila ExeE, a member of the PulE (GspE) f
27 ody group (n = 5), which received continuous Aeromonas hydrophila infusion plus antiprostacyclin anti
28 otoxin Act from a diarrheal isolate, SSU, of Aeromonas hydrophila is aerolysin related and crucial to
30 iron transport in the fresh water bacterium Aeromonas hydrophila is found to occur by means of an in
31 a isolates, 1 Serratia marcescens isolate, 1 Aeromonas hydrophila isolate, 1 Aeromonas veronii isolat
32 during transit through turtles colonized by Aeromonas hydrophila, leading to the hypothesis that Sdi
34 ompetent individual with multiple strains of Aeromonas hydrophila (NF1-NF4), the latter three constit
35 irus or M. rosenbergii nodovirus), bacteria (Aeromonas hydrophila or Vibrio harveyi) or heavy metals
37 lysin-related cytotoxic enterotoxin (Act) of Aeromonas hydrophila possesses multiple biological activ
41 ng multiple pathogens, including a strain of Aeromonas hydrophila resistant to amikacin, tobramycin,
43 Polar and lateral flagellin proteins from Aeromonas hydrophila strain AH-3 (serotype O34) were fou
44 a 5.4-kb pil gene cluster that resembles the Aeromonas hydrophila tap gene cluster and other type IV-
46 ated strains of a diarrheal isolate, SSU, of Aeromonas hydrophila that exhibited a 50 to 53% reductio
48 antagonism against Edwardsiella ictaluri and Aeromonas hydrophila, the causative agents of enteric se
49 ated with the cytotoxic enterotoxin (Act) of Aeromonas hydrophila to examine global cellular transcri
50 mposed of EpsL and its homologue, ExeL, from Aeromonas hydrophila together with either EpsE or its Ae
53 ncoding the cytotoxic enterotoxin (Act) from Aeromonas hydrophila was hyperexpressed with the pET, pT
54 ptic control group (n = 6), in which 1010/mL Aeromonas hydrophila was infused intravenously at 0.2 mL
55 bacterial viability of Escherichia coli and Aeromonas hydrophila were compared to spherical nanostru
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