Sentence examples for murine fibroblast cell from inspiring English sources

Two plasma deposited acrylic acid (pdAA) surfaces with very different surface density of COOH groups, wettability and stability in water were compared about their suitability to support adhesion and growth of 3T3 murine fibroblast cell lines.

Potentiodynamic polarization, in vitro human osteoblasts and murine fibroblast cell adhesion tests were employed to assess the corrosion performances of Ti6Al4V alloy coated with the films in Tyrode's solution, and the biocompatibility of Ti-incorporated a-CNx films, respectively.

Based on the fact that green silanized QDs have the characteristics of high affinity with nuclei, Alivisatos et al. directly marked murine fibroblast cell nuclei using the QDs [50].

Less advanced cell spreading was observed for L929 (murine fibroblast cell line) cells during the first 5 h in culture which was accompanied by retarded recruitment of αvβ3-integrin into focal adhesions (FAs).

Significantly, whereas the antibacterial films containing high loadings of silver were found to be toxic to a murine fibroblast cell line (NIH-3T3), the polymeric films containing ∼0.4 μg/cm2 of silver were not toxic and allowed attachment, and growth of the mammalian cells.

The murine fibroblast cell line NIH3T3 was cultured in DMEM in the presence of 10% FBS.

MTT assay suggested that the extract of the Si coated WE43 alloys was harmless to murine fibroblast cells (L 929).

Results indicate that negative pressure enhanced Wnt signaling and migration into a simulated wound in vitro in NIH-3T3 murine fibroblast cells.

Murine fibroblast cells (NIH-3T3) expressing endogenous murine CD1d were seeded in a 96 well plate at 8,000 cells per well and incubated for 1 3 h to adhere.

HeLa human cervical epithelial cells and LTA murine fibroblast cells [35] were maintained at 37°C, 5% CO2 in DMEM (Invitrogen/Gibco BRL) supplemented with 10% (v/v) heat inactivated FCS (JRH Biosciences) and 100 U/ml streptomycin and penicillin.

Microarray analyses have been used previously to investigate the global effects of interferon stimulation in human non-immune cells after 6 h incubation in a fibrosarcoma cell line [29], in murine fibroblast cells [30], in primary endothelial cells after 18 h treatment [31], and in epithelial cells using ChIP-chip technology to investigate STAT1/STAT2 binding events [32].