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These studies are used to support a kinetic model based on nucleic acid end fraying that describes dissociation for both short (<10 bp) and long (>10 bp) DNA duplexes.
These data support a kinetic proofreading model where the principle binding parameter controlling T cell activation is the TCR off-rate or mean dwell-time.
The second part is the supporting experimental evidence (Ingestion), and the third contains a kinetic model of the theoretical equilibrium (Gas-Solid Equilibrium Kinetic Simulations).
The objective of this work was to develop a kinetic model for Cr VI) biosorption, for supporting our mechanism.
A kinetic model was developed.
In this study, a kinetic model for S. stipitis/S.
To simulate gasification process, a kinetic model was used which comprises chemical kinetic and flow hydrodynamics.
These results were described by a kinetic model [22], [28].
Finally, a kinetic model is presented that is consistent with the observed improvement in sensitivity.
A kinetic model for Nodal morphogen interpretation.
In contrast, a kinetic model requires all kinetic parameters to simulate the dynamics of the system.
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