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1 , V. parahaemolyticus, V. vulnificus, and V. mimicus).
2 , V. parahaemolyticus, V. vulnificus, and V. mimicus.
3 erae and the heat-labile hemolysin of Vibrio mimicus.
4 0 strains), V. metschnikovii (9 strains), V. mimicus (10 strains), V. parahaemolyticus (30 strains),
5 ium sporogenes, Bacillus subtilis and Vibrio mimicus, allowing interpretation of the extensive body o
6 othesis that, in the course of evolution, V. mimicus and V. cholerae diverged from a common ancestor
8 ome contained virulence genes shared with V. mimicus and/or V. cholerae, with those associated with s
11 integrated at different sites within the V. mimicus genome whereas V. mimicus strains PT48, 523-80,
20 uences of VPIPhi genes aldA and toxT from V. mimicus strain PT5 and V. cholerae N16961 were identical
21 quences of CTXPhi genes orfU and zot from V. mimicus strain PT5 and V. cholerae strain N16961 were id
23 ites within the V. mimicus genome whereas V. mimicus strains PT48, 523-80, and 9583 each contain tand
24 including some not previously reported in V. mimicus, such as mannose-sensitive hemagglutinin (MSHA),
26 man intestinal pathogenic Vibrio species, V. mimicus, V. fluvialis, and V. parahaemolyticus, display
27 , with probabilities averaging 10%, while V. mimicus was a major problem with the Crystal E/NF, which