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The difference in the gene expression breadth between gbM and unmethylated genes was due to a higher proportion of the gbM genes (82.4 vs. 72% unmethylated genes) having a maximal expression breadth.
We have developed a simple and rapid method for the expression of mutated proteins with comprehensive single amino acid substitutions from single mutated genes having a four-base codon in a cell-free translation system.
It can be stated that genes having a lot of mutations also have a very high number of ontologies, except for EIF1AY.
Within our stringent parameters, we found eight of the genes, having a function in regulating yield, to be differentially regulated in response to one or more abiotic stress conditions (Figures3 and4).
Genes having a Z ratio >1.5 and p value <0.05 were considered significant.
(3) Applying a statistical test to determine whether genes having a relationship are over represented in a group.
Is there any random gene (white signal) or a group of random genes having a flat PSD?
Only those genes having a 3 fold or higher change in expression were examined (GEO accession number GSE18537).
Accumulating evidence suggests that multiple candidates, including p73, CDH5, and KIF1β, for genes having a NB-suppressive role within the 1p36-critical region [1] [3], [38] [40].
Genes having a probability > = 0.95 for differential regulation combined with an absolute fold-change > = 0.5 were finally considered as differentially expressed.
We established that these 9 genes are repressed by the Fur repressor and that they are the only TBDR genes having a Fur-box in their promoter region.
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