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We further assessed the changes in the frequencies of functionally distinct T cell subsets.
We further assessed the inversion sensitivity to different observing sites and model sampling strategies.
We further assessed the ability of the SA129, SA138, and SA157* to antagonize the activation of ELR+ CXC chemokine receptors.
Field validation trials further assessed the efficacy of heat treatment within a replica sea chest environment.
We further assessed the across-site transferability of the best allometric equations.
Further, assessed the activities of enzymatic antioxidants and measured the levels of nonenzymatic antioxidants.
We further assessed the effect of re-expressing NF1-LRD in GPCs that did not express neurofibromin (i.e., NNI-19 and NNI-24).
We further assessed the mechanism of uptake of EN2 by co-culturing PC3 or WPMY-1 cells transfected with EN2-GFP with untransfected cells labelled using LifeAct (red).
We further assessed the difference in surface temperature anomalies between the positive PCT (PCT+) and the negative phase of the NAM (NAM–; Fig. 10b).
We further assessed the druggability potential of the shortlisted targets by comparing them with the DrugBank Database (DBD).
We further assessed the effects of each drug on various aspects of HUVEC function.
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