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In addition, although we have categorized cells here based only on their peptide profiles, morphological information generated during optical cell finding may contribute another dimension for cell classification.
We analyzed the mean number of cells in each layer (6 sections from each of the 6 control mice and 4 KO mice) the diameter of each cell counted (6 sections from each of the 4 control mice and 4 KO mice), and categorized cells as vertical and horizontal fusiform, pyriform, marginal (round), and multipolar cells according to the previous studies [ 56, 57].
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To assess the association between the categorical variables, Pearson's χ-test or Fisher's exact test was applied to cumulative categorized cell divisions data collected from four independent shake-off experiments.
(K) Mitochondrial clustering was analyzed by categorizing cells based on the criteria of complete clustering, partial clustering, or no clustering.
DOI: http://dx.doi.org/10.7554/eLife.06197.009 We then used a temperature-controlled microfluidic device that enabled us to categorize cells depending on their pre-stress age-associated protein deposit-status, and monitor them under the microscope prior to, during and after undergoing acute proteotoxic stress conditions.
In such tests, we also assessed the binaural interactions potentially underlying the ILD sensitivity function, categorizing cells based on their binaural input characteristics into EE, EI, IE, predominantly binaural (PB), and EO/mon, using the notation introduced by Goldberg & Brown (1969), and based on characteristics described in detail by Irvine et al.
The fundamental idea of recent studies on drug resistance has been to categorize cell lines into sensitive, resistant and intermediate groups based on drug dose response experiments and subsequently to generate a genetic classifier or signature based on microarray analysis.
The software CellQuestPro was used to categorize cell cycle distribution based on the relative DNA content.
Historically, lectins have been used in low-throughput agglutination assays to categorize cell surfaces.
A rank-order plot of IC50s for NVP-CFC218 showed a natural cut-off of 4 μM, which was used to categorize cell lines.
Since CD44 and CD24 expression alone could not be used to classify cell lines based on tumor subtype, we examined whether together these markers might be able to categorize cell lines.
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