These observations prompted us to carry out DNA microarray experiments to study global gene expression under these conditions.
Towards the identification of impaired downstream pathway and elements, we carried out microarray experiments to compare this mutant and wild type controls using the Agilent 8X60K microarray.
By first examining how biological mechanisms are reflected in mRNA transcript abundance, investigators can better design microarray experiments to answer the most interesting questions.
We performed microarray experiments to further study the effect of Hcl1 on mycobacteria.
Ren et al., (2002) performed a ChIP analysis combined with microarray experiments to determine transcriptional targets of E2F4.
In this study, we conducted a series of whole blood microarray experiments to evaluate variations of correlation among individuals and ages using specific pathogen-free (SPF) miniature pigs.
Smirnov et al. performed microarray experiments to measure human gene expression levels in CEPH [23] (data accessible at NCBI GEO database [24], accession GSE12626).
A more ambitious approach has been to use observational microarray experiments to infer which genes are driving the observed expression patterns [2] [4].
We use hundreds of microarray experiments to infer the nature of the regulatory interactions among genes, and implement these data into the Boolean models of the genetic networks.
Having seen the effect of Hcl1 on M. tuberculosis growth and cell morphology, we next performed microarray experiments to further explore the effects of Hcl1 on mycobacterial cells.
We conclude therefore that the One-Direct system can further push the lower limits of material required for probe synthesis for microarray experiments to 50 pg of input when using high quality RNA, without significant impact on resulting information generated.
