Distortions of the array of nanodots used as spot markers were analyzed near the triple junction.
Finally, the genes included in an interval of +/− 50 kb around the markers were analyzed.
A series of markers were analyzed during the differentiation of the macrophage cells to osteoclasts.
Secondarily, the distension properties of different frames by tracking markers were analyzed.
Genes underlying these QTLs (+/−50 kb from the significant markers) were analyzed.
A subset of 128 ISR markers were analyzed on a set of eight genotypes.
Two X- and Y-specific markers were analyzed to confirm the presence and percentages of cells containing a Y-chromosome.
Expressions of the hypertrophic and profibrotic markers were analyzed in TAC and MI mice with or without fasudil treatment.
The DCs were washed again with cold staining buffer for three times, and the cell surface markers were analyzed by flow cytometry.
Monocyte, dendritic cell, macrophage, endothelial cell, as well as smooth muscle cell markers were analyzed by real-time PCR, flow cytometry, and immunofluorescence staining.
When the new markers were analyzed in an experimental infection, absolute sequence conservation was found, indicating the stability of these markers during the course of infection.
