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DCE-MRI is a potentially powerful technique for measuring kinetic parameters, which are important in determining progression of disease and effectiveness of treatments.
The recommendations for measuring kinetic parameters are reported together with the benefits/disadvantages using the three mentioned approaches.
The review and discussion concentrate on the preparation and coating of various photocatalytic catalysts; different kinetic experiments and models; novel methods for measuring kinetic parameters; reaction pathways; intermediates generated by PCO; and an overview of various PCO reactors and their models described in the literature.
While network information has been compiled in public databases [ 7], there are currently limited methods for measuring kinetic parameters [ 8].
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Owing to the extremely fast kinetics, it was not possible to measure kinetic parameters for most of the APL, but in the few instances where off-rates could be estimated, they correlated with equilibrium dissociation constant measurements.
Computer simulations of the global catalytic model using the measured kinetic parameters produced results that mimicked the measured outcomes, and this provided further insights on the catalytic behaviors of the chimeras and basis of their increased NO dioxygenase activities.
Hence, it is fundamental that the rate constants used in the model arise from directly measured kinetic parameters rather than rely on equilibrium data such as affinity measurements.
From the combinations of the measured kinetic parameters, we inferred that one of the two charge carriers moved much faster than the other.
Potential step chronocoulometric methods were used to measure kinetic parameters for the oxidation of ferrocene at platinum vitreous carbon electrodes in acetonitrile.
The model incorporates recently measured kinetic parameters, intra- and extra-particle heat transfer, and particle shrinkage as gaseous products are formed.
The experimentally measured kinetic parameters and equilibrium transition profiles suggest a highly specific two-state transition in which the folding and unfolding of the first G3T monomer is rate-limiting for both annealing and melting processes.
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