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For this we analyzed expression of the marker CD107a, which is expressed at the plasma membrane of CD8+ T cells upon degranulation.

We then analyzed expression of the identified set of temperature or differentially expressed genes throughout differentiation (Fig. 5 C ). Nnat and Slc27a2 mRNA levels were undetectable at different time points in all cell lines.

Next, we analyzed expression of the Notch ligands DeltaA and DeltaD in asb11cul embryos.

We analyzed expression of the three genes by in situ hybridization in the ovary and in the developing pituitary.

We analyzed expression of the zinc-finger transcription factor Sp2 at early embryonic stages by whole-mount in situ hybridization on E7.5 to E9.5 mouse embryos (Figure 1).

As several chemotherapeutic drugs sensitize tumor cells for death ligand-mediated cell apoptosis (TRAIL) [34], we analyzed expression of the TRAIL receptor DR5 on AB1-HA tumor cells.

For analyzing expression of the β-xylosidase gene, we performed real-time PCR.

To analyze expression of the retinoic acid signaling pathway genes that are involved in retinol metabolism, transport, transcriptional activation, and transcriptional products in spontaneous human leiomyomas.

We used Clontech Cancer Profiling Arrays (19 different types of cancers, 395 samples) to analyze expression of the CHL1 gene.

We began by analyzing expression of the miR-290, miR-302, and miR-17∼92 miR-17∼92in staged embryos.

Phenotypic analysis of CD4+ and CD8+ T cells was performed by flow-cytometric analysis, analyzing expression of the memory markers such as CD45RO and CCR7.