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Orientation-induced interaction between PET molecules may reduce the availability of sites that would otherwise interact with water.
GCK activators (GKAs) are currently in clinical trials as a potential treatment for Type 2 diabetes; however, these molecules may reduce plasma glucose concentrations at the expense of increased hepatic triglyceride biosynthesis (18– 20).
The reporters and contrast agents are often molecules and particles modified with fluorescent groups such as green fluorescent protein and Cyt. For ultraviolet and visible light, absorption by hemoglobin and other molecules may reduce optical signals by approximately 10-fold per centimeter of tissue, leading to poor tissue penetration (1 2 cm).
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As a result, CO-treated endothelial cells showed a reduced expression of adhesion molecules, which may reduce pro-inflammatory processes such as leukocyte adhesion and tissue infiltration of inflammatory cells.
If the root exudes some organic molecules which may reduce the metal salts, only then metal nanoparticles may be formed and transported.
The therapy targeting HIF-1α and associated molecules may profoundly reduce recurrence and prolong survival.
At higher flows the higher flux of signal molecules from structured communities may reduce signal concentration in the interior or core of the community.
Therefore, therapeutic strategies aimed at the molecules in these pathways may reduce TBI-induced inflammation and, by extension, post-TBI neuronal death.
By providing a long-term and localized source of active drug molecules, controlled release polymer implants may reduce the systematic side effects and dose-to-dose variability associated with conventional drug administration.
This decrease in Ka with increasing PnA concentration suggests that electrostatic repulsion between negatively charged PnA molecules and negatively charged immobilized GM1 may reduce the binding affinity at higher PnA concentrations.
We have previously shown that carboxyl terminus of Hsp70-interacting protein (CHIP), a co-chaperone molecule with E3 ubiquitin ligase activity, may reduce the levels of toxic α-syn oligomers.
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