Sentence examples for trigger adverse effects from inspiring English sources

Several AhR agonists, including BP, trigger adverse effects, including formation of DNA adducts or induction of oxidative stress.

Pro-atherogenic and pro-oxidant, oxidised LDL trigger adverse effects on pancreatic beta cells, possibly contributing to diabetes progression.

Current serum dioxin concentrations in the U.S. and European general populations of infants are far below levels that would trigger adverse effects.

However, when ROS accumulate in excess for prolonged periods as observed for all the environmental stressors related to diabetes, they trigger adverse effects [ 18, 36– 36].

The geno-protective effect of lovastatin is independent of changes in doxorubicin transport and, furthermore, is not related to ROS, which are often discussed to trigger adverse effects of anthracyclines.

The concentration of Thyroid-stimulating Hormone (TSH) in the mother (in the first and third trimester of gestation) and in the blood of the umbilical cord are lower and the T3 levels are higher which may trigger adverse effects for both [ 15, 16].

So far, numerous clues support a role for oxidised LDL in triggering adverse effects in beta cells and thereby contributing to the pathophysiology of diabetes.

However, application of high doses of allergen to large areas of barrier-disrupted skin for prolonged periods of time may trigger local adverse effects 24.

Pentamidine, another drug currently used for leishmaniasis treatment, is highly toxic and triggers important adverse effects, such as diabetes mellitus, severe hypoglycemia, hypotension, myocarditis, and renal toxicity and can ultimately cause death [ 1, 24].

Both compounds triggered specific adverse effects in the MINC assay (in the absence of cytotoxicity) at the relatively low concentrations of > 50 µM (74 ± 6%, triadimefon) and > 25 µM (72 ± 9%, triadimenol. The antiepileptic drug VPA is a human reproductive toxicant, and also has adverse effects on the NC of several species during early stages of development (Pennati et al. 2001).

The current study extends these findings, showing that repeated instillations of fine particulate matter trigger systemic adverse effect.