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Each midline was divided into 20 equal segments and the local angle at each of the inner 18 segments was calculated as shown in Figure 1A.
To normalize for differences in the tracing efficiency of the individual animals, the number of fibers crossing the midline was divided by the total number of labeled main CST fibers in the dorsal column.
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The midlines were divided into two regions of interest: fronto-central: (Fz, FC1, FC2, Cz) and parieto-occipital (CP1, CP2, Pz, Oz).
The cerebral cortex was divided down the midline and then further sectioned into anterior and posterior regions (frontal/parietal cortex and temporal/occipital cortex, respectively).
Each tissue block, corresponding to one embryo, was divided in the midline into two pieces to provide material for bilateral grafting into the striata of one MitoPark mouse.
The label set was divided along the midline to produce separate labels for each hemisphere, which were then used as seed regions for probabilistic tractography (Fig. 1 G, H).
After removal of the skin and muscles, the skull was divided into halves along the midline and the cerebral hemispheres were removed.
The triangle was divided into two parts along the midline, each part with a distinct color which was selected from a pool of seven colors.
For the corpus callosum, two ROIs were placed to either side of midline, on the slice ventral to the slice where it was divided by the longitudinal fissure.
Australia was divided.
All injections were made under visual guidance after the corpus callosum and fornix had been divided at the midline.
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CEO of Professional Science Editing for Scientists @ prosciediting.com