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Hydrogen-bonding networks in proteins considered as structural tensile elements are in balance separately from any other stabilising interactions that may be in operation.
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Structural property tensile testing of the isolated ALL utilising similar specimen setup and crosshead speed (20 mm/min) has produced mean ultimate load values of 189 Newtons (N) and stiffness of 31 N/mm, when averaging the values of all 29 unpaired specimens [33, 46].
The extracellular matrix (ECM) in this region consists mainly of collagens I and II, in a 2 3 ratio, which are responsible for providing structural and tensile properties to the tissue [ 9, 10].
Their natural 3D structure provides structural support and tensile strength, attachment sites for cell surface receptors, and a reservoir for signaling factors that modulate angiogenesis, cell migration, cell proliferation, and orientation in wound healing [ 1].
Both structural and material tensile properties were determined, with the latter presented in Table 1.
Type XXVII collagen, encoded by COL27A1, is responsible for the key structural framework and tensile strength of the interstitial matrices.
This is followed by discussion of major loadings need to be considered for tensile structural.
The fracture behavior of adhesively-bonded structural joints under tensile constant amplitude fatigue has been investigated.
Furthermore, the model is applied to the structural analyses of tensile and compressive failure.
To this end, experiments were performed to evaluate the complex structural behaviour under tensile loading of single-lap bolted joints.
However, when analyzing remodeling of ECM, it is important to take into account substrates of proteolytic enzymes [39] and the contribution of the structural protein to tensile strength of the aortic wall.
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