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We used transmission electron microscopy and light microscopy to compare parallel fibers in mammals of different brain sizes.
Explanted hearts were analyzed by 2,3,5-triphenyltetrazolium chloride stain and tissue electron microscopy to compare infarct, BZ, and remote myocardium.
We purified the MukB homodimer and the MukBEF complex and analyzed them by electron microscopy to compare both structures.
We applied several fluorescence imaging modes, such as wide-field and confocal one-photon and two-photon microscopy, to compare photochemical and biophysical properties of various iRFPs.
Study Design: To differentiate the effect of implantation from the disease process that originally destroyed the hearing, 11 pairs of temporal bones from unilateral implantees were studied with light microscopy to compare the vestibular damage in the implanted ears with that in the nonimplanted ears.
To assess the role of FLNa in cell migration we used time-lapse microscopy to compare the random migration of FLNaKD and wild-type HT1080 cells.
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Atomic force microscopy (AFM) was used to study membrane roughness and we correlate this with scanning electron microscopy (SEM) to compare results of both the techniques with the RBCs of healthy individuals.
The surface roughness was analyzed by atomic force microscopy (AFM) to compare the coating surface roughness before and after the laser surface treatments.
The aims of the present study were to analyze the ovary cord structure and oogenesis in Erpobdella johanssoni under light, fluorescent and transmission electron microscopy and to compare the obtained results with other clitellate annelids, especially with other arhynchobdellid leeches.
Using embryonic flies, some native (normal) and others genetically altered to lack a member of the semaphorin gene family or the receptor that binds to the semaphorin and signals within the responding neuron, the team labeled particular classes of neurons and then observed them at high resolution using various microscopy strategies to compare their axon projections.
To explore the cytological mechanism which led to the reduction of spikelet hulls, we used scanning electron microscopy (SEM) to compare the cell lengths of the inner and outer epidermal cells in spikelet hulls in R498 and 08sg2 (Fig. 2b-e).
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CEO of Professional Science Editing for Scientists @ prosciediting.com