Exact(2)
The response for SCEs seen in the human cells was more complex, with genetic polymorphism for glutathione-S-transferases (GST) possibly modulating the response.
For SCEs, cells were either mock-treated or treated with 50 nM MMC and 5-bromodeoxyuridine (BrdU, 1 µg/ml, Sigma) was added to the medium for 72 h.
Similar(58)
Standard weights were used, with similar results obtained for SCE weights (not shown).
Because of the specificity of the large database required for the solution of various problems, thermodynamics is a fertile area for SCE-embedded applications designed for the storage of data in symbolic/ numerical form adapted for SCE processing.
To test further whether the cortical area had any effect on the force balance required for centrosome separation, we used a mutant for Sced protein, which shows defective actin organization at the cortex: in Sced mutants, smaller actin caps and absence of actin furrows were reported [18], [25].
To score for SCE, we used a magnification of 1,000×.
Clusters are smaller than for SCE or ME, in particular the periphery has on average only 4.4 vertices as opposed to 7.3 for SCE or 9.8 for ME.
For SCE analysis, cells were grown for 48 h in BrdU before irradiation.
For SCE, RCE and CI, a score of 0 means perfect and 1 means worst.
For SCE, running times show large variation (note the logarithmic scale).
CE outputs many nontrivial clusters, on average the cores and periphery are smaller than for SCE and ME.
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