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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.
Then we performed flow cytometry to measure cell cycle distribution.
The FUCCI system has been utilized to measure cell cycle progression in vitro and in vivo.
Indeed, it may be easier for routine diagnostic laboratories to measure cell cycle markers than DNA indices.
We describe a standard method to measure cell cycle profile by FACs in hESC and iPS cells using EdU substrate; and apoptosis using DilC mitochondrial membrane method in the same sample concurrently.
Experiments to measure cell cycle progression and ssDNA following telomere uncapping were carried out in bar1Δ cells-2 cdc13-1 cells and performed as described (Zubko et al, 2006).
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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].
To examine DNA replication, we measured cell cycle progression by cytometry analysis.
Inhibition of proliferation was further examined by measuring cell cycle distribution.
Effects of NOTCH1 restoration were followed by measuring cell cycle distribution, proliferation, clonogenicity and nuclear morphology.
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measure cell toxicity
measure cell membrane
measure cell traction
measure cell survival
measure cell mortality
measure cell contraction
measure cell adhesion
measure cell migration
measure cell apoptosis
measure cell motility
measure cell concentration
measure cell proliferation
measure cell death
measure cell envelope
measure cell density
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