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We did not specifically evaluate whether the increased ultrasound numbers translated into improved image acquisition or interpretation or whether the scans were clinically relevant or changed patient management.
The purpose of this study was to evaluate whether the increased risk of placental abruption among women with chronic hypertension is modified by ischemic placental disease, specifically pregnancy-induced hypertension (PIH) and fetal growth restriction (FGR).
To evaluate whether the increased MCP-1 secretion was functional, macrophage migration was assayed in vitro.
Support vector machines were selected to evaluate whether the increased accessibility of the RSA-based methods involves a trade-off in accuracy.
To evaluate whether the increased dehiscence rate in the control group for this study is statistically significant (12.5 % in the control group and 0%% in the NPWT group) at least 31 animals would be required in each group.
To address these issues we used data from the EchoCardiography and Heart Outcome Study (ECHOS) study to evaluate whether the increased mortality risk observed in HF patients with renal dysfunction potentially could be explained by severe diastolic dysfunction.
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We then evaluated whether the increased collagen secretion induced by B cells is due to soluble or cell-membrane factors.
We evaluated whether the increased deposition of lysozyme with male UV chroma could have been caused by correlations between male and female phenotypes.
We evaluated whether the increased mitochondrial activity and the reduction in H2O2-induced ROS generation and cytotoxicity following treatment with EH-201 in astrocytes and PC12 cells were dependent on EPO.
To evaluate whether the increase in DNA binding observed in the presence of AICAR was the result of increased protein expression, we measured USF-1 and GATA-4 protein by western blotting.
To further evaluate whether the increase of miR-21 also increased VEGF expression at mRNA level, the expression of VEGF and GAPDH was tested by semi-quantitative RT-PCR and real-time RT-PCR.
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CEO of Professional Science Editing for Scientists @ prosciediting.com