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The results in Tables 4 and 5 achieved with this modification are marked with an asterisk, for example ITKrMM*.
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All modifications that are marked as significant in a particular region of the genome are significant at a q-value of 0.05.
It has become apparent that functional chromatin elements such as promoters or enhancers are marked by characteristic modification signatures [ 8].
But in the cis-NAT gene group, more than 35% TEs are marked by histone modifications from G1.
At distal regulatory regions that are marked by histone modifications and transcription factors, H3.3 steady-state levels are substantially higher in proximal regions compared to distal regions.
This indicates that those TEs, which are marked by histone modifications from G1 and are less methylated, may play an important role in systemic resistance.
We have previously shown that genes for the two largest classes of mammalian transcription factors are marked by distinct histone modifications; homeobox genes are marked by H3K27me3 and zinc finger genes are marked by H3K9me3.
During early differentiation genes are marked by permissive histone modifications.
Cis-NAT pairs are mostly marked by group G1_G1, and trans-NAT pairs are marked by G2_G2, which indicate the two genes share a common histone modification pattern.
All modification will be marked on the CRFs.
This adaptation was marked by the modification in LPS PAMP connected features (i.e., acyl chains and charged groups) and had as a result that LPS no longer needed stabilizing agents in the OM.
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