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To assess the effect of fob1Δ on nucleolar morphology, we analyzed nucleoli in fob1Δ and eco1 fob1Δ strains.
In addition to describing the physiology and morphology, we analyzed the secretome and established genome-wide transcriptional profiles for three distinct starvation phases.
Taking advantage of the house mouse sperm morphology, we analyzed the variational modularity of the sperm head by testing several hypotheses related to its structural and functional organization.
To comparatively assess the effects of FGFR2 mutations on palate morphology, we analyzed patterns of palatal shape variation using geometric morphometric (GM) methods (Dryden and Mardia, 1998; Lele and Richtsmeier, 2001).
To quantify the effect of MVI depletion on the tube morphology, we analyzed the thickness of myotubes from 12 images collected randomly (more than 150 myotubes for each condition were analyzed in two independent experiments).
To investigate the possible role of PKCα in regulating cell morphology, we analyzed the morphology of selected mesenchymal and amoeboid cell lines in 3D collagen in the presence and absence of a PKCα activator or inhibitor.
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To quantitatively address mitochondrial morphology changes, we analyzed mitochondrial morphology using a computer-assisted morphometric analysis, which calculates form factor (FF) and aspect ratio (AR) as discussed above.
a) To address whether TERT rescues nuclear morphology defects, we analyzed two different HGPS-patient derived fibroblasts before and after transduction with hTERT, and cultured these cells for an extended period of time.
To determine whether an acute treatment of SAG has an effect on craniofacial morphology, we quantitatively analyzed the cranial form of adult euploid and Ts65Dn mice that were injected with either SAG or vehicle at birth.
To determine whether differential expression of these cell surface proteins and other differentially expressed orthologs either reflects species-specific adaptation in response to the environment or strictly correlates with morphology, we also analyzed the transcriptional profiles of C. albicans and C. dubliniensis during yeast to hyphae transition (Y-t-H), respectively.
To address the effects of reduced secretion at the morphological level, we analyzed tracheal morphology in more detail in γCOP mutants.
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format we analyzed
morphology we investigated
patterns we analyzed
morphology we visualized
morphology we compared
morphology we studied
morphology we tested
morphology we adapted
morphology we explored
morphology we speculated
morphology we determined
morphology we introduced
morphology we hypothesized
morphology we examined
morphology we denoted
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