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This study supports that approximation as the measured overall hydrolysis rate of A does not differ from the formation rate of D. The measured rate for the formation of D from A (T1/2 = 37 h) is 10 times faster than the rate for the formation of B from A (T1/2 = 297 h) indicating that the overall rate of ethephon hydrolysis is governed by the rate of phosphate formation (k3).
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Measured rates for fast (τfast) and slow (τslow) components of deactivation, in addition to the relative contributions of these components are given in Table S2.
Early stochastic microscopic models showed that measured rates for growth, capping, and depolymerization are consistent with the formation of an actin comet tail on coated beads [ 409, 410].
The updated model includes kinetics for cetuximab binding to EGFR's extracellular domain and for intracellular GRB2 binding to the phosphorylated receptor, and assumes that GRB2-bound receptors internalize at experimentally measured rates for EGFR endocytosis.
The experiment used a toroidal magnetic spectrometer instrumented with drift chambers and time-of-flight detectors to measure rates for elastic scattering over the polar angular range of approximately 25° 75°.
This categorization allowed us to measure rates for different types of microsatellites.
By independently measuring these three processes under identical experimental conditions, we were able to readily decouple internalization, phagosomal acidification and phagosomal-endosomal/lysosomal fusion by simply measuring the lag between the measured rate curves for these three processes.
Glass soap bubble flow meter was employed for measuring rate of permeate stream.
We also searched for studies measuring rates of screening for tobacco use among persons with SMI.
We also measure rates of environmental turnover for North America using Macrostrat and the principals of macrostratigraphy [31].
We exploited the equivalence of kcat and k2(4) to efficiently measure rate constants for Wt and mutant enzymes.
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