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Further evaluation of these cells by electron microscopy demonstrated a decrease in wrapped viruses (WV) compared to wild type control.
Scanning electron microscopy demonstrated a mesothelial cell layer covering the mesh after 4 weeks.
Assessments of cell viability and imaging with transmission electron microscopy demonstrated a much higher efficacy of the HCPT-ND complex compared with HCPT alone.
In situ quartz crystal microbalance (QCM) experiments and fluorescence microscopy demonstrated a complete lack of Psl adsorption on the PslGh-bound surfaces.
Electron microscopy demonstrated a predominance of collagen and fibroblasts.
Transmission electron microscopy demonstrated a differentiated phenotype, showing elongated cells with clearly organized contractile sarcomeres in the cytoplasm (Fig. 5W).
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In addition, laser confocal microscopy demonstrated an open porosity and loosely packed structure throughout the depth of the cotton ball-like scaffold, contrasting the superficially porous and tightly packed structure of the traditional electrospun scaffold.
METHODS AND RESULTS: Scanning electron microscopy demonstrated an immediate decrease in vein graft endothelial cell density associated with vein graft wall stretch, followed by a return to baseline by postoperative day 3. En face detection of bromodeoxyuridine incorporation confirmed a rapid endothelial proliferation by 48 hours.
NIR scanning and confocal microscopy demonstrated an elevated level of pAktser473 in the MAS98.12 basal-like xenograft model.
Light microscopy demonstrated an increase in mesangial cell number and expanded mesangial areas due to amorphous deposits.
Contact angle goniometry, X-ray photoelectron spectroscopy (XPS), and microscopy demonstrate a spontaneous accumulation of these additives at the film surface without lateral phase segregation.
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