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The surface scale composition and morphology were analysed by optical metallography and SEM.
The surface scale composition and morphology were analysed with a variety of analysis techniques.
Cell adhesion and morphology were analysed by SEM while the cell viability and proliferation were assessed by MTS test and DNA quantification.
Then, chondrocytes morphology were analysed by measuring main parameters of the cell shape, including: the area, Feret's diameter, perimeter, and circularity index.
Influenza virus and VLP morphology were analysed by visual inspection on NSTEM micrographs, and the concentration of VLP particles were assessed for the comparison of VLP production efficiency in both cellular platforms.
Nanoparticle size and morphology were analysed via scanning electron microscopy and a Nanosight imaging/sizing system.
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The morphology was analysed in 51 knees at 10, 15, 20, and 25 mm below the centre of the lateral tibial plateau.
Finally the stability of the blend morphology was analysed by high temperature isothermal annealing in the presence and absence of compatibiliser.
Cell morphology was analysed using optical microscopy.
Brain morphology was analysed by using Nissl staining (53).
Three weeks post-rotenone treatment retinal morphology was analysed.
More suggestions(15)
patterns were analysed
morphology were determined
morphology were noticed
morphology were investigated
morphology were synthesized
morphology were obtained
morphology were visualized
morphology were isolated
morphology were confirmed
morphology were generated
morphology were performed
morphology were correlated
morphology were selected
morphology were followed
morphology were recorded
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