In addition to analysis of covariates associated with ethnicity, obesity, fast-food chains, and other potential confounders, using U.S. Census Divisions, we analyzed the relationship after eliminating, individually and together, the East South, East North Central, and the South Atlantic Census Divisions (19).
Reasoning that different tubular architectures may impose discrete mechanistic constraints on endothelial cell division, we analyzed and compared the sequential steps of cell division, namely mitotic rounding, cytokinesis, actin re-distribution and adherence junction formation, in different blood vessels.
Since it is at the 16-cell stage that the first two cell lineages can be observed for the first time, and because this is dependent upon the setting up of cell polarity and the existence of asymmetric cell divisions, we analyzed this phenotype in more details.
As these data suggest that CAPNb2 might affect cell division, we analyzed MDA-MB-231-CAPNb cells with flow cytometry.
To further address the consequence of these imprecise divisions, we analyzed our metaphase spreads from AB control and homozygous mutant embryos for the number of chromatids present.
To determine whether the reduction of root length is due to reduced cell division or reduced cell elongation, we analyzed the size of the meristematic and elongation zone of 6-day-old seedlings.
We analyzed the divisions of the gonadal precursor cells at the L1 stage in cye-1 mutants and found that they divided twice with the same timing and orientation as in wild type (n>10, data not shown).
In order to explain the relationship between the recognition performance and the division ways, we analyze the case of 4 sub-band and 2 sub-band.
To test this hypothesis, we analyzed the orientation of granulosa cell division, in 10-week-old mice.
We analyzed the mechanisms that may drive the residual cell division cycle in estrogen-deprived cells.
