Sentence examples for dead lymphocytes from inspiring English sources

Baize et al., [ 19] demonstrated similar increase in the percentage of dead lymphocytes in patients suffering from sepsis.

The present study revealed that either 20S proteasome or the percentage of dead lymphocytes had not any significant correlation separately to the prognosis in both septic and non-septic critically ill patients, while correlation of both 20S proteasome or the percentage of dead lymphocytes was found to have moderate positive correlation in both sepsis and non-sepsis groups.

Hotchkiss et al., [ 1] and Bourboulis et al., [ 18] demonstrated a statistically significant increase in the percentage of dead lymphocytes in septic patients infected with Gram-negative bacteria in comparison to the control group.

Activated T lymphocyte death in response to FK866 was typically a slowly progressing form of cell demise as an increase in the rate of dead T lymphocytes was normally observed starting from 72 h treatment (Figure 1F).

Six weeks after weaning, involuted mammary glands were processed to single cells, and luminal and basal MEC populations were identified by staining for CD24 and α6-integrin (CD49f) [ 21, 29], after exclusion of doublets, dead cells, and lymphocytes.

Basal and luminal subsets were identified by using CD24 and CD49f (α6-integrin; Figure 4A), after exclusion of debris, doublets, dead cells, and lymphocytes, as outlined in Additional file 2. This was followed by discrimination of alveolar progenitor- and hormone sensing-enriched fractions by using Sca1 (Ly6andand CD49b (α2-integrin, Figure 4B).

Simply measuring extracellular HSP72, however, it may not be clear whether this release comes from live neutrophils, monocytes, lymphocytes, or dead cells.

Following this, degraded products of dead myoepithelial cells attract lymphocyte infiltration that physically disrupts the BM.

On one occasion most of the residual circulating lymphocytes were apparently dead.

In Region R2, granulocytes were excluded according to their high SSC and lymphocytes, monocytes, and dead cells were excluded according to their CD19, CD14, and propidium iodide staining.

This effect was even more evident when directly comparing the ratio between living lymphocytes and all dead cells based on the separation obtained from the FSC/SSC properties of these two cell populations (Supporting Information Fig. S3A).