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Covariance matrices are key tools in the study of the genetics and evolution of quantitative traits.
Selection at subinhibitory concentrations and assay development for environmental matrices are key areas of research that need to be addressed.
From this point of view, partial relationship matrices are key when constructing a single-step method for both purebred and crossbred performances.
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The discovery of new carbon sources, design of novel porous carbon structures, and effective hetero-atom doping of the sulfur matrix are key to overcome this dilemma.
Proper deformability and uniform suspension of coarse aggregate particles in the matrix are key parameters to ensure successful casting and adequate in situ performance.
While cell migratory behavior has been traditionally studied using simple assays on culture dishes, in recent years it has been increasingly realized that the physical, mechanical, and chemical aspects of the matrix are key determinants of the migration mechanism.
In fact, mutual interactions among endothelial cells (ECs), supporting mural cells and organ-specific cells, as well as between ECs and the extracellular matrix, are key driving forces for vascularization.
Proteolysis of phagosome contents and damaged extracellular matrix are key PMN actions in inflammation.
We show that patterned constraints exerted on the tissue by the extracellular matrix are key to force the tissue into the right shape.
Computation of sparse matrix is key in a wide range of applications of science and engineering.
Matrix metalloproteases are key regulatory molecules in the breakdown of extracellular matrix and in inflammatory processes.
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