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Currently a role of cortactin at the NMJ in vivo cannot be directly tested because suitable models – viable animals with global or muscle-specific cortactin gene deletion – are unavailable.
This cannot be directly tested because of different methodologies between the present and previous studies [ 21, 29].
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The two loci that were previously determined to be associated with differentiating resident from anadromous life-history forms (Omy_ndk-152 and Omy_LDHB-2_i6; Narum et al. 2011) could not be directly tested for association with life-history forms because most populations in our analyses were field identified as anadromous (e.g., juvenile smolt or adult steelhead phenotypes).
This cannot be directly tested if assignment is based on more covariates than the researcher observes, because then the marginal treatment recipient is not identified.
This will be directly tested in the coming years.
The law may be directly tested in the Dunn case.
But the idea needs to be directly tested.
Because of all these concerns, the concept of longer vaccinations leading to better protection remains a conjecture which must be directly tested in a future experiment.
However, because AFLPs are dominant markers and heterozygotes are not observed, Hardy-Weinberg equilibrium cannot be directly tested.
Because they are based on specific, organic molecules, these predictions may be directly tested by an experimental assay on the same molecules that articulate them.
The ERK phosphorylation was directly tested in human iPSCs because the Essential 8 medium contains bFGF, which is required for growth of human iPSCs.
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CEO of Professional Science Editing for Scientists @ prosciediting.com