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To assess the relative importance of each cell type and the potential overlap with mouse gonadal expression profiles we compared our screen and three high throughput microarray screens carried out on embryonic mouse gonads/cells at a similar stage of differentiation [ 32– 32].
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To our knowledge, we report here the largest microarray screening carried out so far between human and bacterial extracellular proteins using two different approaches.
To further characterize the agp6 agp11 mutant line a differential microarray screen was carried out to identify genes with modified expression in the 8 h-grown pollen tubes of agp6 agp11 compared to wild type pollen tubes.
The microarray screens were conducted at the DNA Microarray facility of UCLA, Los Angeles.
Microarray screens for upstream regulators of cVg1.
Microarray analysis was carried out to screen the tumor cells and NPC with the goal to find putative genes involved in glioma growth and invasion.
Small-molecule microarray manufacture and screening were carried out as described (Casalena et al., 2012).
Microarray was carried out using the NimbleGen microarray service.
RT constructed the microarray and carried out the microarray experiments.
mRNA microarray was carried out by Microarray facility in Sanford-Burnham Institute.
Two different microarray screening setups were designed for the two pathogens, trying to answer different biological questions.
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