259) ons had substantially declined, extensive cell migration from the neurospheres as we |
260) Chemotactically induced cell migration is also addressed. |
261) intimately related to healing events and cell migration while promoting apoptosis. |
262) tivity of T-lymphocytes and T-dependent B-cell response in cultures stimulated with |
263) red on collagen-coated fibres to evaluate cell response dependence on substrate topo |
264) r applications, their microstructure, the cell response to polymeric fibres and the |
265) Cell-seeded scaffolds were transplanted in |
266) The 3D cell-printed scaffolds of PCL-alginate gel |
267) used to fabricate three-dimensional (3D) cell-printed scaffolds using layer-by-laye |
268) human hepatocytes represent an important cell source for in vitro investigation of |
269) o-expanded ECFCs are a novel, very potent cell source for scaffold-based tissue engi |
270) eved that ADRCs are a useful and feasible cell source not only for cosmetic therapy |
271) The most common are germ cell tumors (39%). |
272) Granular cell tumors (GCTs) are uncommon soft tissu |
273) Malignant granular cell tumors (MGCTs) comprise less than 2 |
274) milar and overlapping actions on the same cell type and one cytokine shows a wide ra |
275) In addition, calcium deposition was cell type dependent and decreased for BM-M |
276) riers and adipocytes, an abundant stromal cell type in breast tissue, to investigate |
277) Cell viability, surface roughness, and wet |
278) rm and high-content-imaging endpoints for cell viability, oxidative stress and DNA d |
279) Cytocompatibilty was evaluated using cell viability, total DNA, collagen and GA |
280) Glial cell activation and oxidative stress are i |
281) at least in part, to reduce spinal glial cell activation. |
282) Cell aggregation and expression of chondra |
283) iscosity (KSPV 1 Fresenius) and Red blood cell aggregation in stasis and under low s |
284) rved that, like BC, MBC scaffolds support cell attachment and proliferation. |
285) We analyzed cell attachment four days post seeding via |
286) Our strategy has been to integrate stem cell biology and cell sheet engineering, i |
287) n of specific miRNAs as key regulators of cell biology has opened new clinical avenu |
288) mmediate sufficient performance, complete cell coating, proliferation, engraftment, |
289) echnologies resulted in complete valvular cell-plus-matrix coating, excellent engraf |
290) t bendiocarb treatment leads to increased cell death, liver perisinusoidal fibrosis, |
291) veal the cellular mechanism of osteoblast cell death, which is served for the pursui |
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