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In this study, we evaluated the gene expression profiles in the olfactory bulbs of normal rats and naris-occluded rats using the gene microarray technique.
In a previous study, we evaluated the gene expression of placental samples from PE patients and controls using a self-designed gene array that targeted critical signaling pathways.
In addition, we evaluated the gene expression and protein secretion of amphiregulin from hBMSCs and hTBCs and assessed the biologic activity and possible mechanism of amphiregulin in our system.
In this paper we have evaluated the gene expression programming (GEP) methodology for modeling the effect of different variables (continuous and nominal) and their interactions on the properties of direct compression formulations.
However, the characteristics of gene expression in beta-cells of T2D subjects, which determines the cell phenotype, are largely unknown; only a few studies have evaluated the gene expression of islets isolated from T2D subjects [8] [15].
We eventually evaluated the gene expression profiles combining different criteria, such as PD-relevant pathway analysis as previously described [12], computational gene-term association networking, and comparative data mining from published literature on PD pathogenesis and PD-associated gene lists.
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When evaluating the gene expression trends observed in the macrophages, there was a highly significant increase in TNF-α expression for the 50-nm topography.
Studies designed to evaluate the gene expression profiles induced by these compounds have the potential to provide further information to test this hypothesis.
Microarray data analysis of RNA samples from tick infested skin was used to evaluate the gene expression at 0, 24 and 48 h after R. microplus larvae attachment.
(H) Quantitative reverse transcription PCR (qRT PCR) assay was used to evaluate the gene expression profile of pFind1 insertion neighboring genes in pFind1-iPSC lines and control OKS-iPSC lines.
The clinical relevance of livin/BIRC7 expression is still controversial in different types of malignancies, therefore this study was designed to evaluate the gene expression of livin in Egyptian adult AML and ALL.
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