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We used an oligonucleotide array spotted with 135 apoptotic and anti-apoptotic genes (see Materials and methods section) and identified a panel of genes differentially expressed, which were subjected to hierarchical clustering to reveal expression trends.
Finally, polymorphism studies reveal expression quantitative trait loci in the PGC-1β gene that correlate with tanning ability and protection from melanoma in humans.
Further analysis of the upstream regions of responsive transcripts and accompanying changes in alternative splicing may reveal expression networks underlying Pi homeostasis in plants.
The RT-PCR analysis did not reveal expression of sensory neuron specific markers (Figure S3).
Methods designed to reveal expression changes at the level of the single gene are powerful, but depend on that change being high with low variance across samples.
A comparison of APOE splicing and promoter use in the frontal lobe and total brain did not reveal expression pattern differences as seen in the temporal lobe.
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Isoform-selective genome editing revealed expression and nociceptive function of Drosophila TrpA1 channel.
Immunohistochemistry revealed expression of UCN in the cytotrophoblast, the EVT and decidual cells.
All (8/8) normal HGF cultures revealed expression of the wild-type APC protein.
Our earlier DNA microarray analysis revealed expression of putative tumour suppressor exostosin 1 (EXT-1) in odontoblasts.
The transcriptomes of single infected macrophages and phagocytosed C. albicans displayed a tightly coordinated shift in gene expression co-stages and revealed expression bimodality and differential splicing that may drive infection outcome.
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