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Second, as the newly induced mutation should not be found in either of the laboratory background strains (C57BL/6J or FVB/NJ) used, we next ruled out variants found in these strains from further consideration.
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For the survival network to be of potential use, we next explored its power in prognosis and druggability.
Where the medical records of these control cases were unavailable we used the next available appropriate case.
We used the next generation matrix method to calculate the basic reproductive ratio and performed elasticity analyses.
Using Corollary 5.1, we next study the problem of minimizing a convex function.
Using Corollary 4.3, we next show the following result; see also [21, 24].
Using our model, we next investigated the TRAM-dependent pathway in wildtype and MyD88 KO conditions.
Using these assays, we next evaluated requirement of RNAi for centromere activity in N. castellii.
Using this assay, we next determined the distribution of initial SRP-RNC binding events.
Using these particles, we next tested whether misfolded Ubc9ts or luciferase could recruit stress granule components.
When we don't have the precise answer we need, we use the next best thing: a factual anchor.
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CEO of Professional Science Editing for Scientists @ prosciediting.com