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1 three TonB systems within the human pathogen Vibrio vulnificus.
2 idase (PGI-LysAP) activity was identified in Vibrio vulnificus.
3 ansferase, termed Bpt, in the human pathogen Vibrio vulnificus.
4 nesis of an encapsulated, virulent strain of Vibrio vulnificus 1003(O) led to the identification of f
6 n applied to a collection of 120 isolates of Vibrio vulnificus, a water-born species common in shellf
7 ibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account for the majority of Vibrio inf
8 , we established a conformational map of the Vibrio vulnificus add adenine riboswitch that reveals fi
9 mily toxins are produced by Vibrio cholerae, Vibrio vulnificus, Aeromonas hydrophila and other Gram-n
13 ficient mice with the siderophilic bacterium Vibrio vulnificus and found that hepcidin deficiency res
15 gh October, mostly due to the seasonality of Vibrio vulnificus and Vibrio parahaemolyticus infections
16 useful insights into other bacteria, such as Vibrio vulnificus and Vibrio parahaemolyticus, that have
18 charide (CPS) is a major virulence factor in Vibrio vulnificus, and encapsulated strains have an opaq
20 rs also exist in Vibrio parahaemolyticus and Vibrio vulnificus, and thus these genes may represent a
42 xtracellular capsule polysaccharide (CPS) of Vibrio vulnificus is a primary virulence factor which al
55 from two different effector domains from the Vibrio vulnificus MARTX toxin restored RID activity, ind
59 ocessing repeats-in-toxin (MARTXVv) toxin of Vibrio vulnificus plays a significant role in the pathog
63 structure of a complex of EspI and EpsJ from Vibrio vulnificus represents the first atomic resolution
65 ot unexpectedly, Vibrio parahaemolyticus and Vibrio vulnificus strains formed out-groups; we also ide
66 ibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus, the only members of the Vibrionaceae
69 (MARTX) toxin-effector domain DUF5(Vv) from Vibrio vulnificus to be a site-specific endopeptidase th
70 nse to iron in the broad-range host pathogen Vibrio vulnificus under the hypothesis that iron is one
71 ram-negative bacteria, including the species Vibrio vulnificus, Vibrio parahaemolyticus and Vibrio ch
72 nce for L-ornithine, whereas the enzyme from Vibrio vulnificus (VvL/ODC) had dual specificity functio
73 x genes of the only known luminous strain of Vibrio vulnificus, VVL1 (ATCC 43382), were evolutionaril
74 se gene sequence shows 80% homology with the Vibrio vulnificus VvpD type 4 prepilin peptidase require
78 e and elucidated the structure of VvPL2 from Vibrio vulnificus YJ016, which represents a transitional
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