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Methods: A rat sodium deoxycholate-induced pancreatitis model was used.
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To further illustrate the performance and the application of our method, a rat pineal gland RNA-Seq dataset with 6 sampling time points was analyzed (GSE46069) [ 36].
To investigate the effects of GnRH antagonist (GnRH-ant) and agonist (GnRH-a) in the prevention of postoperative pelvic adhesions by a visual scoring system and immunohistochemical methods in a rat uterine horn model.
Yüksel et al. [ 18] reported that in both morphometric and gait analysis, the repair with the side-to-side method was better than with the end-to-side method in a rat model.
Although the degree of inflammation and joint swelling can also be determined by measuring the volume of the paws using a water displacement method in a rat model of CIA [ 18, 19], this method is less practical in mice given the small size and volume of the paws.
In a recent study, L-MSTL was used to embed BMP-2 within poly DL-lactic-co-glycolic acid) (poly DL-lactic-co-glycolicly(poly DL-lactic-co-glycolicolymer, which enhanced MT3T-E1 cell differentiation in vitro and outpoly DL-lactic-co-glycolicacidlds and scaffolds made by the PLGAiculate leaching/gas foamicrospheresin an rat cranial injury repair monel [ 63].
Materials and methods We designed a rat study to investigate lithium-induced encephalopathy and correlate its severity to plasma, erythrocyte, cerebrospinal fluid and brain lithium concentrations previously determined in rat models mimicking human poisoning patterns.
The effects of aerosolised PPS delivered by this new method were evaluated in a rat model with severe ALI induced by oleic acid (OA).
Data presented in this paper provide a baseline for selecting the adequate end-point and methods of recovery assessment for a rat sciatic nerve crush study and suggest that the combined use of functional and morphological analysis should be recommended in this experimental model.
Immunohistochemical staining for blood vessels was carried out by the indirect immunoperoxidase method as described above using a rat monoclonal antibody to mouse CD31 (MEC 13.3; BD Biosciences Pharmingen) as the primary antibody.
To date, only a single report [24] exists describing the successful generation of a rat by this method.
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