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VEGF VEGFR binding process is the key point of neovascularization.
The kinetics study of fatty acid binding to different FABPs indicates that the rate-limiting step in the binding process is the entry or release of ligand through the portal.
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This study clearly demonstrates that the binding process is weakened by the clustering of the GM1 molecules.
The binding process is based on the autonomous nature of interactions between DNA and the target molecule, so that DNA probes are useful for sensing of a variety of biomolecules.
The effect of nonnative hydrophobic interactions on the binding process is dependent on the contact distance σhφ because lengthening σhφ will enhance nonnative hydrophobic interactions under the same interaction strength KHP.
However, the substrate binding process is most likely the rate limiting step.
Previous studies have indicated that fluoroquinolones inhibit the activity of the DNA gyrase complex by binding to the QBP; the binding process is shape-dependent, and mutations in the QRDRs modify the geometry of the QBP.
It is also observed that the visual feature binding process is synchronized with the gamma band [18, 32].
The effect of temperature on the binding process is not considered in the study.
Also, from Fig. 4 it is clear that the binding process is much more effective in the smaller volumes.
An example of adding another compartment before the binding process is adding a depot to the model.
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