Sentence examples for marks were reduced from inspiring English sources

Fig. 5 AFM images (40 μm × 10 μm) of a diamond turned surface before and after one IBP run on sample A. The amplitudes of the tool marks were reduced from 20 nm to 2.5 4 nm (height scale 80 nm).

At the latter time-point, H3K27me3 marks were reduced in control birds from both lines, but line L63 displayed increased H3K27me3 levels in infected birds.

In contrast, H3K4me3 enrichments correlated well with those of H3K9ac [ 24]; signals for both activating marks were reduced in genomic regions where AML1-ETO and N-CoR were elevated (data not shown).

Both increased and decreased numbers of H3K4me3 sites were found in different parts of the Ncoa2 gene (responsible for steroid-dependent gene activation): H3K4me3 marks were reduced at exon 2 and increased near the TSS region in treated animals (Fig.  7a); expression of the latter gene was downregulated.

These marks are reduced in the BWS cells, and increased becoming biallelic in the SRS cells.

It is an inevitable feature of the way that reliability is calculated, that if the range of marks is reduced then the reliability must go down.

Interestingly, both active euchromatin marks are reduced in Scl Δ19/Δ19 fetal liver cells, indicating that the Scl +19 element is required for enhanced activity of the Scl promoter.

Recent findings have suggested that epigenetic 'ON' marks are reduced in evolution, while the 'OFF' signs have significantly increased; unicellular organisms contain more marks associated with transcriptional activation, whereas mammals contain more modifications associated with repression [ 5, 6].

However, whether the epigenetic marks are reduced or masked, our findings reveal a significant new property of nonrandomly co-segregating chromosomes in DSCs that is likely to manifest mechanisms of asymmetric DSC fate specification and/or mechanisms of nonrandom co-segregation.

The H3K4me3 mark is reduced by CYP33 overexpression at the promoter regions of CDKN1B and HOXC8.

While the H3K4me3 (activating) mark is increased in both activation states (more so during TLR4 engagement), the appearance of the H3K27me3 (repressive) mark is reduced on BCR-responsive genes but remains relatively unchanged in LPS-responsive genes [ 3].