To investigate whether IMP3 could be one of these markers, we looked for a correlation between IMP3 immunohistochemical expression and Ki67 labeling index in the high-grade gliomas.
To monitor a potential perturbation in the expression of cardiomyocyte-specific markers, we looked at the expression levels of cardiac vmhc and of cardiac cmlc2 in 2-day MO1 Fam40b knockdown embryos.
Neanderthals and living people share derived polymorphisms regardless of recent interbreeding, yet these are the markers we look for as evidence of interbreeding.
It was a bit of a needle-in-a-haystack situation, because the marker we were looking for would need to map to a segment approximately equal to 1/3000 of the genome.
To investigate further the potential of the set as a source of new markers for genetic mapping we looked at the predicted number of markers it could provide in five existing populations.
Because there is no early marker for breast carcinoma, we looked for the presence of soluble Nectin-4 in the serum of patients with non-MBC.
We looked markers that might provide clues about NK cell differentiation in the following five NK subsets: CD56bright, CD56dimNKG2A+KIR−, CD56dimNKG2A+KIR+ and CD56dimNKG2A−KIR+.
In addition to these markers of cell death, we looked at other apoptosis-specific nuclear changes such as chromatin condensation as well as changes in mitochondrial potential.
In this study, we looked at markers on chromosomes 7 and 18. Research Genetics offers mouse MapPairs® Microsatellite Markers to detect SSRs throughout the entire genome.
First, we looked at markers that were discriminant between the 10 accessions with an open root cone angle and the rest of the panel (157 accessions).
