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We first derive the joint probability density of the data, for which the computation of the covariance matrix is critical.
Spatial distribution of cells within a three-dimensional matrix is critical for the success of any tissue-engineering construct.
The spatial distribution of nanoparticles as well as the interaction force between nanoparticles and matrix is critical important to structuring bionanocomposites with desirable properties.
To design a lumbar spine registry such that the accumulated data provide applicable guidance for clinical treatment, the incorporation of a functional diagnostic matrix is critical.
However thorough dispersion of nanomaterials in the cementitious matrix is critical for effective use of their distinct geometric and engineering properties towards development of higher-performance cementitious nanocomposites.
The capacity to engineer the extracellular matrix is critical to better understand cell function and to design optimal cellular environments to support tissue engineering, transplantation and repair.
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Interactions between cells and the surrounding matrix are critical to the development and engineering of tissues.
Amelogenins, the major protein component of the mineralizing enamel extracellular matrix are critical for normal enamel formation as documented in the linkage studies of a group of inherited disorders, with defective enamel formation, called Amelogenesis imperfecta.
The breakdown and remodeling of the extracellular matrix are critical steps in cancer cell invasion.
Matrix metalloproteinases (MMPs), which are initiators of the enzymatic degradation process of extracellular matrix, are critical in the tissue remodeling process [ 16, 17].
Furthermore, we assessed invasion in vitro using Matrigel as a surrogate basement membrane, as cancer cell interactions with the basement membrane matrix are critical, particularly for the peritoneal invasive route.
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