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In order to examine gene expression changes that occur as a result of conversion into L-form colonies, we performed microarray experiments utilizing E. coli 2.0 Genome Genechip arrays (Affymetrix).
Current studies are under way in patients with depression to examine gene expression changes following moderate exercise tasks, found to differentiate patients with CFS and FM from controls.
By collecting pretreatment biopsies, we attempted to identify biomarkers that could predict chemotherapy response, whereas collecting post-treatment tissue samples allowed us to examine gene expression changes in response to treatment.
To examine gene expression changes occurring during its intracellular passage, we extracted a list of genes that were differentially expressed (determined by ANOVA) between times 2 h and 6 h after internalization.
In an effort to examine gene expression changes during experimental arthritis, we found that three members of the endothelin system - namely ET-1, ET-2, and ETA - were markedly upregulated during the acute phase of AIA.
Gene expression profiles were analysed in MCF7 and BT474 cells at 0 and 2 days, 6 weeks and 10 months after estrogen deprivation in order to examine gene expression changes in response to estrogen deprivation (see Figure 1, experimental overview).
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This is the first study to examine gene expression change in the kidney of a large animal model that exhibits AKI in response to a common clinical injury; CPB.
We have globally examined gene expression changes in tumor-infiltrating T-cells both in the presence and absence of anti-PD-1 therapy, and identified a cohort of >100 genes with significantly enhanced expression in the dysfunctional state both in mouse and human samples.
Therefore, we examined gene expression changes of many PcG and Trithorax Group (TrxG) genes upon Pc RNAi in the embryo.
We began a search for candidate genes by examining gene expression changes in any genes known to be generally involved in chromatin binding and genetic regulation.
We sought to better understand how LPA in the microenvironment impacts molecular ovarian cancer progression by examining gene expression changes induced by LPA in ovarian cancer cell lines.
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