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To test if the morphological traits characterizing G. henleyi and G. a. allenbyi are geographically structured, we analyzed the log-transformed measurements of their hind foot length, tail length, and body mass using a multivariate analysis of variance (i.e. MANOVA) followed by univariate tests (i.e. ANOVAs), both conducted using SYSTAT v.11.
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To study in detail the full-length protein structure, we analyzed the low-resolution architecture of Swt1 in solution using small angle X-ray scattering (SAXS) method.
Based on the electronic band structure, we analyzed the relationship between the electronic structure and the nature of the Schottky rectifier, and revealed the potential of utilizing GBM Schottky diode for the higher rectification characteristic devices.
To assess whether a baz mutant enhancer screen would identify regulators of epithelial structure, we analyzed the effects of loss of function of four candidate genes on the baz zygotic mutant phenotype in a pilot screen.
As the known NLRR3 (FIGLER 5) and Pal (FIGLER 9) genes have been shown to have an unusual three exon structure, we analyzed the predicted exon structure of the entire FIGLER gene family.
To understand how gene responses to stimuli relate to gene size and other structural features, we analyzed the structure of housekeeping and hypervariable genes.
All cluster structures we analyzed in the present work are listed in (Additional file 1: Table S1).
Through a structured quantitative survey approach, we analyzed the relationships between consumers in China, Germany, Spain, and the United States and more than 200 brands in 11 industries, including hair care, airlines, cars, and media.
To assess the effect of loss of Id1 on skeletal structure and function, we analyzed the bones of Id1−/− mice.
In order to investigate whether other PD-related CNS structures were affected, we analyzed the SN and the striatum of rotenone-treated and control mice.
To obtain a better insight into the structure-function relationship, we analyzed the results based on PONDR (Predictors of Natural Disordered Regions) methods for predicting the disorder regions (DRs) in proteins [24].
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