Circularity as a quantitative descriptor of cell shape complexity has been used for characterization of several cell types in plants.
Western blotting was used to analyze the expression of several cell cycle regulators in aortic EC.
The effect of carnosine was studied using two-dimensional cell monolayers of several cell lines with endogenous CA IX expression as well as Madin Darby canine kidney transfectants, three-dimensional HeLa spheroids, and an in vivo model of HeLa xenografts in nude mice.
In a recent study, we profiled the chromatin states of several cell lines using ChromHMM [ 2], which revealed the presence of large gene control elements that we designated "stretch enhancers" (referred to as SEs in this paper) [ 3].
This cohort was used to identify differences in expression of several cell cycle and apoptotic markers, including Ki67 and p53 (CM McNeil et al, manuscript in preparation), between LA and B cancers using the following definitions: LA: ER+ and/or PR+ and HER2− and LB: ER+ and/or PR+ and HER2+.
To identify mechanisms controlling cellular reactions to DNA damage, we measured the protein levels of several cell cycle regulators using specific antibodies in Western blots.
Furthermore, some of the assumptions underlying the earlier work were more pessimistic, whereas here we have refined the model to be more realistic, such as allowing for a delay between infection and the onset of infectivity, a lower susceptibility in non-MM genotypes and the use of several red cell units in a single transfusion, reducing the values of the basic reproduction number further.
Simultaneous operations of multiple cells using a parallel-cell testing system have made it possible to compare the performance of several cells with high reliability.
Therefore, this review discusses on the use of several biomaterials at cell electrode interfaces of a living cell based chip together with their influence on cellular adhesion as well as on the electrochemical measurements.
Many studies relying on the use of several putative stem cell markers to determine a method by which these cells can be isolated from a full-depth articular chondrocyte population [27], [28], [29].
