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1 ons of sire alleles with progeny response to S. enterica serovar Enteritidis.
2 s an important aspect in the transmission of S. enterica serovar Enteritidis.
3 inacin genes with the phenotypic response to S. enterica serovar Enteritidis, an F1 population of chi
4 100% correlation among Dice similarities for S. enterica serovar Enteritidis and S. enterica serovar
5 9% and 96% for five-enzyme combined PFGE for S. enterica serovar Enteritidis and S. enterica serovar
6 SfiI, PacI, and NotI) for 74 strains each of S. enterica serovar Enteritidis and S. enterica serovar
9 e that YafD provides a survival advantage to S. enterica serovar Enteritidis in eggs by repairing DNA
11 for bacterial colonization after pathogenic S. enterica serovar Enteritidis inoculation and for circ
12 A unique epidemiological characteristic of S. enterica serovar Enteritidis is its association with
13 creased substantially in recent decades, and S. enterica serovar Enteritidis is now one of the leadin
14 NPs as molecular markers for the response to S. enterica serovar Enteritidis may result in the enhanc
15 ause infection in different hosts, including S. enterica serovar Enteritidis (multiple hosts), S. Gal
16 gg albumen, while disruption of this gene in S. enterica serovar Enteritidis rendered the organism mo
18 scriminatory PFGE-based subtyping scheme for S. enterica serovar Enteritidis that relies on a single
19 how that arcA is essential for resistance of S. enterica serovar Enteritidis to nitrosative and oxida
21 olecular basis for the RNI/ROI resistance of S. enterica serovar Enteritidis, we transformed a genomi
22 ontrast, S. enterica serovar Typhimurium and S. enterica serovar Enteritidis, which are usually linke
23 BlnI, SfiI, and PacI as most concordant for S. enterica serovar Enteritidis, while XbaI, BlnI, and S
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