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We also characterised the various bioluminescence reactions by varying the integration time and substrate concentration, and by measuring the kinetics of light output.
We also characterised the expression of SSEA-3 and SSEA-4 antigens on the surface of hESC by using two different staining methods.
We also characterised the effects of temsirolimus on CD8 memory cell formation.
We also characterised the expression of HIF-1 α, a biochemical marker of hypoxia.
We also characterised the consequence of reducing MIF expression in B16-F10 cells in vitro in response to hypoxia, where MIF was proposed to play a role.
We also characterised the between-state changes from standing-to-exercise and exercise-to-recovery. SBP and DBP were significantly altered in the Exercise group when changing from exercise-to-recovery in the postpartum period.
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We also characterise the functions that operate in the modulation space M1,1(Rn).
We also characterised (4) the morphology and discuss the origin of the scours previously identified in the study area.
Here, we also characterised, for the first time in the brown bear, DQB sequences, encoding the β chain, which forms a biding groove in a dimer with the α chain coded by DQA.
We have also characterised the predicted set of secreted proteins encoded by each genome and identified a set of protein families which are significantly over-represented in the secretomes of plant pathogenic fungi, including putative effector proteins that might perturb host cell biology during plant infection.
We have also characterised the distribution of prostaglandin pathway proteins throughout the constituent cells of the uterus using immunohistochemistry.
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