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Instead, PEG gels can be engineered from the bottom up to incorporate desired or key aspects of the native extracellular matrix (ECM) microenvironment in which cells naturally reside (e.g., integrin binding adhesive sites, enzymatically degradable cross-links).
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Although CDH1 (E-cadherin), a classical member of the cadherin superfamily, was downregulated, THBS4 encoding calcium-binding adhesive glycoprotein, thrombospondin-4, was upregulated in all lobular carcinomas.
Some of the benefits and challenges of finite element modeling of lipid bilayer systems are discussed, and it is indicated how this framework is natural for future investigation of biologically realistic bilayer structures involving nonaxisymmetric geometries, binding and adhesive interactions, heterogeneous mechanical properties, cytoskeletal interactions, and complex loading arrangements.
Synthetic extracellular matrices (ECMs) provide a blank slate that can ostensibly be populated with specific bioactive cues, including growth factors, growth factor binding motifs, adhesive peptides and peptide crosslinks susceptible to proteases, thereby enabling a degree of customization for specific applications.
Moreover, endothelial cells in the extracellular matrix need binding to adhesive proteins to initiate invasion and migration (McCathy et al, 1990).
The genetic polymorphism concerning the ß3-subunit of platelet integrin receptor glycoprotein IIIa is held responsible for enhanced binding of adhesive proteins resulting in increased thrombogenic potential.
Here, inspired by the fundamental roles of decorin, a collagen-targeting proteoglycan, in collagen remodeling, we created a scar-preventive collagen-targeting glue consisting of a newly designed collagen-binding mussel adhesive protein and a specific glycosaminoglycan.
Osteonectin or secreted protein acidic and rich in cysteine is a calcium-binding, anti-adhesive and bone-specific glycoprotein with high affinity to collagen and hydroxyapatite.
It is well-known that differential adhesion, whereby two cell types having different adhesive binding strengths between cells of the same type versus cells of different type, can cause cells to physically sort themselves into two distinct populations [ 47].
The capacity for cadherins to organize into lateral clusters was observed nearly 20 years ago when it was identified as a mechanism that could strengthen cadherin-based adhesion, probably by increasing the avidity of adhesive binding between cadherins and their ligands.
Vendome, J. et al. Structural and energetic determinants of adhesive binding specificity in type I cadherins.
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