Sentence examples for markers we described from inspiring English sources

The observations in this study moreover, show that the superficial dermal microvessels in c-GVHD differ from those seen in SSc by having neither capillary rarefaction nor the loss of endothelial cell specific markers we described before [12].

The microsatellite markers we described here are the first for P. mistassinica.

The diagnostic value of the candidate markers we described can be judged in any future study where subjects have a well-defined lung disease.

As these correlations are made the candidate markers we described would be ready for validation studies and eventually, translation into clinical trials.

Using autoimmunity (at least one of two diabetes autoantibodies) and insulin sensitivity (equation validated against hyperinsulinemic-euglycemic clamps) as the main etiologic markers, we described four categories along a bidimensional spectrum: autoimmune plus insulin-sensitive (IS), autoimmune plus insulin-resistant (IR), nonautoimmune plus IS, and nonautoimmune plus IR.

Using different methods of microscopy, immunolabelling and a number of molecular markers, we describe the neural and mesodermal structures of the pygidium of Platynereis dumerilii.

For the case of infections caused by strains of B. pseudomallei, which exhibit substantial genetic variability and contrasting pathologies, a more extensive analysis of additional tissues will be required before the final utility of the specific markers we describe can be determined.

This indicates that the panel of senescent markers that we describe here could be used as a prognostic tool in cancer and underscores the clinical relevance of our findings.

For identification of the MNC hUCB cells in the cervical/lumbar spinal cords and blood smears, staining with the human-specific marker (HuNu) as we described previously [31].

Small variations or decreasing marker levels, as we described in case of CEA may be attributable to differences in venous versus arterial blood levels.

Tumor cryosections (5  μm thick) were analyzed for CD31 (specific marker for endothelial cells) as we described in the study by Filleur et al. Cryosections were fixed for 10 min in acetone, 1 : 1 acetone/chloroform and acetone; and blocked with 2% donkey serum (Jackson ImmunoResearch, West Grove, PA, USA).