Sentence examples for marker we noted from inspiring English sources

Neuro-inflammation is also an important component of many lysosomal diseases [22], and upon IHC staining of CD68, a CNS inflammatory marker, we noted reduced labeling in brains of end-stage CD-treated Npc1−/− mice compared to end-stage untreated Npc1−/− mice (data not shown).

An additional marker we noted as characteristic of "false" saccades was that the disparity between the positions reported by the left and right eyes was larger than normal.

Another marker we noted for "false saccades" was that they often occurred during segments in which the reported POG appeared to be inaccurate over sustained periods.

When we measured glucose accumulation in PMN using 2-NBDG, a fluorescent glucose marker, we noted somewhat lower levels of glucose in PMN of older adults at baseline that did not reach statistical significance (Fig 5B, ns).

The four criteria we implemented to identify false positive saccades were the following: One marker we noted for "false saccades" was that the location of the "fixation" after the "saccade" was the same as that before the "saccade".

Additionally, we noted that LAMP1 (lysosomal marker) was also associated with the damaged mitochondria, supporting the association of mitochondria around lysosomes when Q74 was expressed (Fig 1D).

That is, we noted that the distinct markers and their states evidence variability of diverse functional features of LTR retroelements.

In contrast, for the downregulated MSC marker gene CXCL12 we note the disappearance of H3K9ac and H3K36me3 and a restriction in H3K4me3 occupancy to the vicinity of the TSS.

Since both PDZK1 and PR are surrogate markers for ER activity, we note that the strength of this panel may be skewed by the presence of PDZK1 protein in the panel.

We note that SNP marker IAAV5782 -log100 P = 38.60) originates from the same wheat contig as a marker (BE498831) previously shown to cosegregate with Snn1 (Reddy et al. 2008).

We note that INDEL markers in the real-time PCR assay strengthen the SNP marker information at the main phylogenetic nodes (Figure 3).