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In this work we utilize surgical phase events recognized in surgical device data to learn prediction models and trigger online predictions for remaining intervention times in operating rooms.
While looking over the events that were initially highlighted during the previous phase, events that would further convey the complexity of how each parent interacted with professionals and negotiated the process were selected.
The present paper will review recent observations implicating cephalic phase events in the control of enterocyte lipid transport, the impact of varying the composition of meals on subsequent fat metabolism, and the means by which dietary lipid carried in chylomicrons can lead to elevated postprandial non-esterified fatty acid concentrations.
The resultant voltage unbalance associated with open phase events can cause excessive heating in transformer core and coil assemblies and tanks, reduce the available starting and running torque of motors, increase motor acceleration time, cause inadvertent tripping of critical loads, and thermally damage plant equipment.
Furthermore, as the bumps are minimum phase events [53], the dead-time, seen in the phase-shift and impulse response data (cf. Figs. 3F and 5G), comes from the latency distribution.
The interaction of Tim with mitotic kinases can be detected in G2 and M phases (Fig. 4D), and therefore may provide a mechanism for regulation of M phase events, including sister-chromatid cohesion [46], [53].
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These data, combined with simulations based on established models for the aqueous-phase events leading to radical entry into particles in emulsion polymerizations, suggest that the induced decomposition of persulfate seen at high initiator concentrations arises from transfer to initiator.
With respect to S-phase events both mouse models and studies on cancer-derived cells revealed that accumulation of cyclin D1/CDK4 complexes triggers DNA re-replication [36] and, thus, could be specifically targeted in cancer cells.
In this way, these two critical S-phase events can be intimately coupled by redox signalling.
This enables studying events occurring in the middle phase (dsDNA and its various functions) and their separation from early-phase events (entry, uncoating, transport to the nucleus, etc).
The physiological responses of the mouse uterus to E2 consist of both early- and late-phase events (Hewitt et al. 2003).
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