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This strategy permits one to account for the heterogeneity present in real reactors in both the abiotic and biotic phases.
In some cases, this strategy permits one to reduce the number of scans, i.e. the experiment time, by a factor of 100, depending on hardware, sample length and tolerable resolution loss.
However, this strategy permits deletion of genes only during development of the parasite in the mosquito.
As recently reported, this strategy permits efficient and sensitive detection of mutations.
Overall, this strategy permits a traceless entry into the fungal cells, thus guaranteeing that host integrity is not affected.
This strategy permits a more detailed exploration of the parameter space where the MC steps are taken in the sloppy directions.
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This strategy permitted to investigate the metabolomics data and their relation with botanic and genetic informations.
This strategy permitted us to induce immune complex glomerulonephritis in animals lacking normal systemic C3 synthetic capability, but with a hematopoietic system reconstituted from wild type mice.
This strategy permitted the identification of conserved sequences and apparently non conserved sequences that were able to elicit the same functions in different species.
This strategy permitted a simple yet flexible design as well as an adequate representation of the nonlinear nature of the optimized gradients within the framework of the standard LC control software (Chromeleon, version 6.80 SR11).
In addition, this strategy permitted the use of only one universal primer set suitable for all second step PCRs, resulting in a reduction of costs for the shortened ORF-specific primers.
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