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Emerging clones with undifferentiated morphology were counted and examined for eGFP expression.
Cells with blast and promyelocyte morphology were counted as primitive; those with myelocyte/metamyelocyte morphology as intermediate myeloid; those with band, segmented neutrophil, monocyte, and macrophage morphology as mature myeloid; those with intermediate hemoglobinization as intermediate erythroid; and those with full hemoglobinization as mature erythroid.
Only neurons with a clearly visible nuclear morphology were counted.
Only cells with a monocytoid/macrophage-like morphology were counted.
For brightfield immunohistochemistry, only MAP2-positive cells with unambiguous neuronal morphology were counted as neurons.
After four days, wells containing cells with hematopoietic morphology were counted.
Similar(49)
After 12 days culture, colony number and morphology was counted using inverted microscope.
The number of cells with nuclear apoptotic morphology was counted in five fields of 100 cells.
However, only those that appear mature in their morphology are counted.
Condensed or fragmented nuclei (apoptotic nuclear morphology type II) were counted as dead cells as described by Yuste et al. The quantification of cell death by chromatin condensation was performed in blind testing, counting at least 300 cells for each data point, and was repeated at least three times in independent experiments.
Morphology was analyzed and chromosomes were counted and compared to the standard Bos indicus karyotype pattern.
More suggestions(15)
patterns were counted
morphology was counted
morphology were correlated
morphology were tested
morphology were selected
morphology were determined
morphology were seen
morphology were followed
morphology were recorded
morphology were investigated
morphology were noticed
morphology were assessed
morphology were obtained
morphology were visualized
morphology were isolated
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