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For reasons not yet clear to scientists, exposing cells to these genes appears to turn back the developmental clock.
In addition, we analyzed the response of histamine-producing cells to these inhibitors.
Adaptation of cells to these products prior to fermentation increased overall fermentation rate.
In this paper, the mechanism of adhesion of smooth muscle cells to these materials was investigated.
Therefore, aurilide and aurilide B are considered to have therapeutic potential, prompting us to identify potential combinatorial drug targets by screening for a gene(s) whose downregulation sensitizes cells to these compounds.
Future studies should explore the role of neoantigens and non-mutated proteins in eliciting cancer-killing CD8+ T cells, as well as the relative importance of responses of CD4+ T cells compared with CD8+ T cells to these proteins.
Significantly, co-treatment with both the sugar pharmacophore and the existing TKI drugs resulted in strong synergy, in essence re-sensitizing the SW1990 cells to these drugs.
They introduced S. aureus cells to these structures, gave the cells time to stick, and then rinsed the structures with deionized water to remove all but the most solidly bound bacteria.
All the coatings are tested for their suitability as biocompatible coatings, and hence, the adherence of osteoblast progenitor cells to these coatings was investigated in correlation with deposition parameters and surface morphology.
Researchers have looked for ways to awaken immune cells to these antigens' presence.
There was little reduction in cell viability following repeated exposure of human endocervical cells to these compounds, although a reduction in secretory leukocyte protease inhibitor levels was observed.
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CEO of Professional Science Editing for Scientists @ prosciediting.com