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To illustrate the different partial relationship matrices, we analysed the small pedigree in Table 1.
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To ensure efficient cell growth and adhesion, as well as optimal ligand distribution within the matrix, we analysed cell morphology and signalling dynamics in this culture system.
For each of these matrices, we conducted analyses of complete plastomes (non-coding and protein coding) and protein-coding sequence (cds).
To determine if the defects in O-glycan secretion are accompanied by defects in luminal extracellular matrix assembly, we analysed the SGs of γCOP mutant embryos by TEM.
To understand sources of variance in these matrices, we performed PERMANOVA analyses (adonis function in vegan) with 10,000 permutations.
We analysed a matrix of 131 species × 158 relevés via detrended correspondence analyses (DCA) using the R statistical software (R Core Team 2014 Vegan package; Oksanen et al. 2013).
In particular, we analysed the extracellular matrix organisation, inflammatory infiltration and expression of matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) using immunhistochemistry and electron microscopy.
Finally, to investigate the ability to degrade the extracellular matrix, we also performed analyses of MMP-9 levels by RT-PCR.
To answer this question, we analyse matrices of language co-occurrences based on a 6.5% random sample of the data (200,748 concepts).
In this work, we analyse the confusion matrices presented in [7].
The next matrix component we have analysed is the link protein HAPLN-1.
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CEO of Professional Science Editing for Scientists @ prosciediting.com