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To examine DNA replication, we measured cell cycle progression by cytometry analysis.
Flow cytometry measured cell cycle events and the Affymetrix exon array platform was used to identify the gene expression and alternate exon usage changes.
To assess the effect of fob1Δ on cell cycle progression in the eco1 strain, we measured cell cycle progression in fob1Δ and eco1 fob1Δ strains.
To test this possibility, we measured cell cycle distribution, changes in p21 expression, and the capability of MB cells to grow clonally following the restoration of miR-9.
We also measured cell cycle progression of DS progenitors vs euploid cells and we did not find any significant difference [Additional file 3: Supplemental Figure S1C].
In addition, we could check other commonly measured cell cycle properties of mutants: for example, cell size at division, and duration of the unbudded phase of the cell cycle.
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In the present study we have used flow cytometric DNA measurements on synchronised human NHIK 3025 cells to measure cell cycle progression under various conditions of reduced oxygenation.
GO biocompatibility with fibroblast viability was assessed by measuring cell cycle and apoptosis.
To dissect the effect of γ irradiation on induction of cell apoptosis and further examine the correlation between the BRCA1 degradation and apoptosis, we tested the effect of γ irradiation on cell apoptosis using three different assays, including measuring cell cycle profile (sub-G1 peak), PARP cleavage and Annexin-V staining [36].
Then we performed flow cytometry to measure cell cycle distribution.
Inhibition of proliferation was further examined by measuring cell cycle distribution.
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demonstrated cell cycle
moderate cell cycle
assess cell cycle
measured cell area
measured load cycle
measured cell suspension
measured cell viability
measured drive cycle
measured cell number
measured cell adhesion
measured cell death
measured threshold cycle
measured cell potential
measured cell length
measured cell size
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