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We next checked the interactions between corto and the gain-of-function allele Scr Antp Scx (Table 2).
We checked the interactions between blood lead and urinary cadmium on the levels of oxidative stress markers; however, there was no reportable result (data not shown).
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To provide further evidence that the N-terminus of DLC1 interacted with tensin2 through a PTB domain-dependent mechanism, we checked the interaction between DLC1 1–400 and the aforementioned tensin2 deletion mutants.
In addition, we also checked the interaction terms of the variables included in the models which were likely to interact.
When we checked the interaction term to understand better what this result meant, we found that the interaction of spending per child and GDP per capita has also a negative effect.
We checked the interaction terms of HBV with sex, HBV with age, and HBV with age and sex, all of which were statistically significant.
To test whether OA regulated HIF1 α via SIRT3 through a similar mechanism, we checked the interaction of SIRT1 or SIRT3 with HIF1 α.
For both regressions we checked the interaction assumptions by using unweighted regressions, and adding to the model three interaction terms, which are the product of the three martial arts dichotomies and the prescore for classroom behavior.
To further examine the specificity of chromatin interaction between the AF-associated region and Pitx2c, we checked the interaction of a fragment containing the promoter of Enpep, the next neighbouring gene distal to Pitx2 in both mouse and humans.
We checked the interaction of the variables with each other and with time to event (time of death or censoring time) to find those variables with a time-varying effect on the risk of mortality.
Whether the inhibitory effect of the ETO1 family in planta is limited to type 2 is still unknown; we have not yet checked the interaction of ETO1 with LE-ACS2 and LE-ACS4 in planta.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com