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This model implies that the generator system creates primarily the Region-1 FACs of Iijima and Potemra at both hemispheres, while the Region-2 and Region-0 FACs form by spreading of the Region-1 currents through the ionosphere.
Stinear et al [6], applied TMS to both hemispheres while the ipsilateral hand performed isometric contractions at different force levels, however, no hemispheric differences were observed.
In addition, the right hippocampal activation was associated with activity in regions of both hemispheres, while the left hippocampal activation was mainly associated with activity in ipsilateral brain areas.
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By means of TMS they produced a transient virtual lesion of the dPMC in both hemispheres while a subject performed a precision grip-lift task with their right hand.
A larger number of neuroimaging metrics related with cortical atrophy with AUC>70% was found in CTRL-AD in both hemispheres, while in earlier stages, cortical metrics showed in more confined areas of the temporal region and mainly in LH, indicating an increasing of the spread of cortical atrophy that is characteristic of disease progression.
Production of plasma occurs during daylight hours when the sun illuminates the atmosphere at both conjugate hemispheres while the night-time production is small.
Indeed, even when the corpus callosum is surgically severed immediately after learning (to "disconnect" the two hemispheres), positive transfer will take place from one front paw to the other; manifestly, transfer of training takes place between connected hemispheres while the animal is learning.
Consistent with the previous report [43], GFP+ newborn neuron quantification shows no significant difference between the two hemispheres, while the dorsal blade has more newborn neurons than the ventral blade (Table S1).
Increased density of axons in the splenium subserve integration of visual field information from the two hemispheres, while the large heavily-myelinated callosal fibers of the midbody connect homotopic somatosensory and motor areas.
Since each eye sends some of its nerve impulses to both hemispheres of the cat's brain while each paw only directs impulses to the hemisphere of the brain on the same side of the animal's body, this procedure feeds the sensory information to just one hemisphere.
For motion stimuli, the N1 amplitudes were larger over the hemisphere contralateral to the origin of motion, while for static stimuli N1 amplitudes over both hemispheres were in the same range.
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