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Each segment crosses a number of model cells, and each cell where the segment crosses is called a reach.
We propose that this may be due to the large difference between the passive time constant of our model cells and the period of the swim oscillation.
On the one hand, the SWI2 allows a vertically integrated variable-density groundwater flow and seawater intrusion in coastal multi-aquifer systems, and a reduction in number of required model cells and the elimination of the need to solve the advective-dispersive transport equation, which leads to substantial model run-time savings.
HSp17 was present in the cytoplasm and on the cell surface in these model cells, and induced a significant increase in HO8910 migration by a transwell assay.
According to this model, cells and tissues respond to increasing levels of oxidative stress via antioxidant enzyme systems upon NP exposure.
We did not use a sensitivity analysis because we attempt to realistically model cells and this immediately implies that not all parameter space is available.
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Note that we performed extensive model studies to justify the parameters describing the model (cell and mesh sizes, number of anomalous layers, values for seawater and land conductivities).
In these calculations, we note that a single diode laser bar both deforms the model cell and imparts a net translation force and cell movement.
Cell culture models lack the natural environment of an intact organism and, in mouse models, cells and proteins are difficult to track without intervention.
In this model, cell-cell and cell-extracellular matrix (ECM) interactions are preserved.
When we overexpressed CYB5R2 in NPC cells and implanted these cells into a CAM model, cell proliferation and angiogenesis were suppressed.
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