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Differences in the rise times of the two Ca2+ indicators (OGB-1 and GCaMP6s) precluded a meaningful analysis of signal onsets in motile cilia versus the cytoplasm.
The differences in the rise and decay phase kinetics could be attributed to differences in the abundance of thapsigargin-insensitive IP3-releasable Ca2+ stores (i.e. Golgi Ca2+ stores).
Thereby it is observed that slow and fast contractile characteristics of motor units are reflected by differences in the (electric) firing pattern of the innervating motoneuron and concentration differences in the rise of myocellular calcium with excitation [ 7].
An explanation for the differences in the rise value and peak shape between the isw2 and reference samples may be found considering the role of the isw2-remodelling enzymes in S. cerevisiae.
Beyond the differences in amplitude there were also differences in the rise kinetics that can be related to stoichiometric differences in the composition of the photosynthetic electron transport chain [ 39].
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Figure 2c illustrates the temporal differences in the rising portions of the SC and LGN responses using the normalized mean BOLD signals.
We note that Tian et al. focused their study on the temporal differences in the rising portion of the signal and did not examine the return to baseline as closely.
This suggests that the two parties may be arguing over a year's difference in the rise.
However, considerable variability was observed in this regard between journals in specific subject categories; the difference in the rise of the impact factor between European and US journals was particularly seen in the medical subject categories (Critical Care Medicine and Infectious Diseases) and Cell Biology, whereas the opposite was observed for Biology.
This sex difference in the rise in Na+ was increased if hearts were treated with isoproterenol prior to ischemia.
Under this condition, we no longer observed a difference in the rise in [Ca2+] i between WT and Trpm4− / − myocytes during the Ca2+ re-addition phase (Fig. 6e).
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