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Therefore, each antimicrobial drug was carefully investigated relative to NTSEC and M. haemolytica to identify appropriate CLSI interpretive criteria when possible and published acceptable alternatives when CLSI criteria were not defined (Tables 1, 2, 3 and 4).
Using the new CV terms we defined (Tables 1 and 2), the interdependencies between the interactions that mediate phosphorylation of Cdc6 by Cyclin A-Cdk2 can be captured in the PSI-MI format to reflect the complexity involved in regulation of such molecular systems.
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Two different activity distributions were defined (Table 1).
At the end of these two steps, contextual elements were defined (Table 1).
The analysis of the results allowed us to identify that strong and moderate degrees are fairly well defined (Table 3).
Statistic data indicate that both structures are well defined (Table 1).
Therefore, new criteria were defined (Table 2).
Confident was not consistently defined (Table 3).
First, the distribution of each parameter was defined (Table 1).
Most of the structure is well defined (Table 1).
Three separate groups of febrile episodes were defined (table 2).
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