Sentence examples for fiber cultures from inspiring English sources

By phase-contrast microscopy, SC clones were easily distinguished on the basis of their proliferation rate into LPC (Fig. 1c, left) and HPC (Fig. 1c, middle), similarly to what observed in single fiber cultures.

We placed the fiber cultures into a Zeiss Environmental incubation system (5% humidity, 95% O2) at 22°C.

In vivo activity of VLX40 was investigated in hollow fiber cultures of myeloid U-937 cells subcutaneously implanted in mice.

Using an innovative technique for single muscle fiber culture in suspension, adapted from embryoid-bodies cultures [30] we observed that not only SCs proliferate at different rates [52] but also that the ratio between clones with high (HPC) and low (LPC) proliferative rate was fixed at single fiber level.

To address this, we used primary single-fiber cultures in which myofibers are cultured with their associated satellite cells.

In 48 h, primary single-fiber cultures P-Fra-2 is expressed in Pax7-positive satellite cells, but myogenin expression does not appear until 72 h in culture and is not co-expressed with P-Fra-2.

Furthermore, during subsequent days, most of the fibers in cultures incubated with conjugated-GDNF became heavily myelinated.

Rat mesenchymal stromal cells (MSCs) were seeded on either PET or PU fiber-layered culture plates coated with laminin, collagen I, fibronectin, poly-d-lysine or gelatin.

The EPS-triggered changes of these genes in muscle fibers in culture were then compared to those in acutely exercised and trained mice, respectively.

Also, alterations in cell morphology were related to the presence of fibers in culture during the first 24 h and 48 h of chrysotile treatment and also after long periods of recovery.

We show in this study that the induction of aneuploidy in cells is chrysotile concentration-dependent, and as described above, that the percentage of aneuploid cells remained high compared with control cells after up to 8 days of recovery in fiber-free culture medium.