Sentence examples for high levels of release from inspiring English sources

In in vitro cultures, the Δ isp1/2/3 mutant contained more haptomonad, nectomonad and leptomonad promastigotes with elongated flagella and reduced motility compared with Δ isp2/3 populations, moreover it was characterized by very high levels of release of exosome-like vesicles from the flagellar pocket.

In a study of U.S. Medicare beneficiaries, Willis et al. (2010) used county-level data from the U.S. Environmental Protection Agency EPAA) Toxic Release Inventory (TRI) (U.S. EPA 2010b) on copper, lead, and manganese and found significant associations between residence in urban counties with high levels of release of manganese and PD.

As stated above, this might also be responsible for the high levels of released H2O2.

This current study showed that levels of S100B are raised in female patients diagnosed with schizophrenia and correlate with BMI, which is possibly linked to higher levels of release from adipocytes.

Highest levels of released mediators were measured in animals of the group being immunized ip. with the triggering allergen OVA.

At high levels of dopamine release, results suggest that refinements of the model will be required to consistently describe the PET and fMRI data.

Previous in vitro studies have found high levels of antibiotic release in the days immediately following implantation of antibiotic loaded articulating spacers.

However, as we also observed high levels of IFNγ release by MLN neonatal cells that can be severely reduced by in vitro IL-12 neutralisation, this suggests that neonate produce more bioactive IL-12p70.

It could be postulated that high levels of apoptosis release signals which could induce cell migratory behaviour in the hemocyte population as a whole.

Again, the close binding proximity of ofatumumab to the cell membrane likely results in highly efficient complement deposition on B cell membranes, without high levels of systemic release of activated complement components.

On the other hand, the oral treatment of AF or C3G, 1 h after i.p. injection of cg, did not induce any modification in the high levels of PGE2 release by cg).