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The biological activity of mouse mesenchymal stem cells in contact with the new materials was measured.
These scaffolds were biocompatible with mouse mesenchymal stem cells.
Specificity and heterogeneity of terahertz radiation effect on gene expression in mouse mesenchymal stem cells.
The tMP surface was examined for its differentiation efficiency using mouse mesenchymal stem cells, C3H10T1/2.
These nanoparticles were not cytotoxic and induced an osteogenic response in mouse mesenchymal stem cells.
Lei, Y.,Gojgini, S. & Segura, T. The spreading, migration and proliferation of mouse mesenchymal stem cells cultured inside hyaluronic acid hydrogels.
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The viability of mouse fibroblast cells (NIH-3T3) on the modified PEEK was determined to study cytotoxicity, and bone-marrow-derived mouse pluripotent mesenchymal stem cells (D1) were cultured to evaluate the mineralization capability through cell adhesion, proliferation, and differentiation on the modified PEEK substrates.
Matsukura, Y. et al. Mouse synovial mesenchymal stem cells increase in yield with knee inflammation.
In order to estimate the biocompatibility of PCL/GO composite scaffolds, mouse marrow mesenchymal stem cells (mMSCs) and low-differentiated rat pheochromocytoma (PC12-L) cells were cultured.
In vitro cell culture experiments verify that mouse bone mesenchymal stem cells can proliferate on the porous scaffolds well, indicating the good biocompatibility of porous scaffolds.
It has been shown in the mouse that mesenchymal stem cells from adipose tissue can spontaneously differentiate into skeletal muscle, and that their conversion to a myogenic phenotype is enhanced by co-culture with primary myoblasts [ 27].
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