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Liver samples in rats were collected and the tissue proteins were extracted by homogenization.
Rodent studies observed reduced total T4 levels in fetal plasma and brain samples in rats after pre-natal exposure to 4-OH-CB-107 4-OH-CB-107 4-OH-CB-107 4-OH-CB-107ture Aroclor 1254 (Meertset al. 1996).
Meerts et al. (2002) observed reduced levels of total thyroxine (T4) in fetal plasma and brain samples in rats after prenatal exposure to 4-OH-CB-107 4-OH-CB-107 4-OH-CB-107 4-OH-CB-107ites detected in humans.
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When the validated calibration curves of geniposide and genipin are used to determine spiked control samples in rat blood dialysates, the geniposide determination errors are within 15% accuracy and within 5.8% precision, respectively, and the genipin determination errors are within 23% accuracy and within 3.6% precision, respectively.
We have developed a unique system, which allows long-term simultaneous video-electroencephalography recording, drug infusion and blood sampling in rats.
We characterized basal and stress-induced HPA activity during lactation and experimental weaning using dynamic blood sampling in rats.
The differences in stimulus-induced activity could be due to a more homogenous biological sample in rats than in humans, or simply to higher sensitivity and faster signaling of NRBE cells compared with NHBE cells.
This difference could be owing to a more homogeneous biological sample in rats than in humans, or simply to higher sensitivity and faster signaling of the NRBE cells compared with NHBE cells.
More recently, using repeated blood sampling in rats, we have shown that acute iv injection of 2 mg methylprednisolone can both block the HPA response to 10 min noise stress 40 min later and suppress basal corticosterone levels when tested during the morning nadir (23) and that lower doses [500 μg (8) and 250 μg (9)] rapidly suppress basal corticosterone secretion at the diurnal acrophase.
As various cell types within the pancreas and other organs may modulate inflammatory responses during the course of AP, we attempted to clarify the origin of the inflammatory mediators and the inflammasome components that are upregulated during the early onset of sub-clinical AP, both in human AP samples and in rats treated with alcohol and LPS.
We describe an improved method for sampling CSF in rats that is easy to perform.
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