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1 S. dysenteriae 1 shares characteristics with other Shige
2 S. dysenteriae 1 strains obtained in locations throughou
5 in all strains examined, suggesting that all S. dysenteriae 1 isolates derive from a clone that resul
8 strain induced robust serum and mucosal anti-S. dysenteriae 1 lipopolysaccharide (LPS) responses and
9 vaccine to protect against disease caused by S. dysenteriae 1 and potentially to protect against the
12 of STEC are highly mobile, the stx genes in S. dysenteriae 1 have been believed to be chromosomally
13 quences flanking the haem transport locus in S. dysenteriae matched those at the 78.7 minute region o
15 locus has an organization similar to that in S. dysenteriae, and it is located in the same relative p
16 ins tested were nearly identical to those in S. dysenteriae, indicating that, in these strains, the h
20 n clinical studies, we developed a series of S. dysenteriae 1 vaccine candidates containing the funda
28 Disruption of this open reading frame on the S. dysenteriae chromosome by marker exchange yielded a s
30 ses and cytokine production were measured to S. dysenteriae whole-cell preparations and to purified r
32 (2) gene were identified by RAM assay, while S. dysenteriae and nonpathogenic E. coli isolates were u
33 um retinol was independently associated with S. dysenteriae type 1, high serum C-reactive protein con
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