Cartilage matrix is continuously turned over during development and tissue homeostasis.
This matrix is continuously remodelled in a process controlled by the NP cells and closely regulated by anabolic growth factors and catabolic cytokines.
While the FN matrix is continuously assembled, remodeled and turned over by cells, a more mature and stable ECM network assembles on this FN-matrix scaffold [ 61, 85, 88].
Over the years, always new doping substances are synthesized and, as a consequence, the list of prohibited compounds is continuously updated and new suitable analytical methods for their detection and determination in biological matrices are continuously required.
The genome-wide set of gene family matrices is continuously displayed.
At the same time, new treatments (growth factors, bioengineered skin substitutes, extracellular matrix proteins, and various other products) are continuously being explored (Jeffcoate et al 2004; Petrova and Edmonds 2006).
Depending on the new values of weight, mean and standard deviation, the solution matrix table is continuously updated.
Among them, amelogenin is the most abundant protein in enamel matrix and is continuously expressed throughout amelogenesis.
Technical improvements regarding the cell density, the composition of the culture medium or the use of different matrices on which to seed hepatocytes are continuously developed to circumvent the limitations of these models.
Once assembled, FN fibrils are continuously polymerized and remodeled within the fibrillar matrix on the cell surface [ 61].
