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In order to test our hypothesis, we have examined 41 healthy subjects using incident dark field video microscopy and assessed TVD and microcirculatory flow velocity before and after the topical application of ACH and NG both by manual computer-assisted video analysis and by a newly developed, fully automated algorithm.
The intracellular lipid droplets were easily observed by phase-contrast microscopy and assessed using Oil Red O (Sigma) staining.
Zingg et al used high power field light microscopy and assessed the number of lymphocytes in two different locations, at the periphery and in the center of the tumors [ 29].
Morphological evidence of epithelial damage such as cilia disappearance, disruption of epithelium or inflammatory cell infiltrates, fibrosis, and edema was looked for under light microscopy and assessed according to the scale represented in Table 1.
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In addition, we performed confocal fluorescence microscopy analysis and assessed the mitochondrial membrane potential by JC-1 staining to show that TfR-lytic peptide causes stimulation of the cell surface, suggesting that these cascades are all activated swiftly and simultaneously.
A novel implementation of structured illumination microscopy has been described and assessed theoretically in this Paper.
The present morphometric study was designed to assess the dimensions and shape of keratocytes and their nuclei by transmission electron microscopy, and to assess these features in relation to the stromal lamellae.
Each core collected was rinsed and assessed by microscopy (Zeiss Axiophot, Thornwood, NY, USA) to ensure that microspheres were dispersed.
Thus, it would be required to perform further study, such as that using immunoelectron microscopy and that assessing blood-testis barrier permeability.
Using fluorescence microscopy, we assessed spontaneous and radiation-induced foci of γ-H2AX and 53BP1 in peripheral blood mononuclear cells derived from unselected RC patients (n = 53) undergoing neoadjuvant chemo- and RT.
By studying the immunolabeling for different markers and using confocal microscopy, we assessed the expression of Smad3 at specific stages of neuronal maturation: in quiescent RGL (Type-1) cells, intermediate progenitor cells (Type-2 cells), neuroblasts (Type-3 cells), immature neurons, and in mature granule neurons [ 10].
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