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The results shed light on the development of spatial representations for action in infancy.
At minimum, this activation of shared representations for action and emotion requires a variety of anatomical and functional circuits that together might be called the 'extended' mirror neuron system.
Although this computational division of labor is predicted by various theoretical accounts of navigation [ 8, 9], this is the first study to demonstrate that both of these direction coordinate frameworks are active at the same time, presumably acting together in order to translate stored representations into representations for action.
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However, space representation for object recognition is different from space representation for action [9], [13].
There is a need for greater integration in the domains of the development of sensory representations, the response of neural systems to damage, the integration of information from more than one sense and the transformation of sensory inputs to representations useful for action.
We use weak convergence methods which provide convenient representations for the action functional for all regimes.
To reduce the computational complexity for fulfilling the requirements of recognition, low-dimensional image vectors were used to generate low-dimensional block Hankel matrixes as representations for input action sequences.
The superior longitudinal fasciculus, white matter underlying motor areas, such as pre-SMA and the anterior corpus callosum, can carry sensorimotor representations for voluntary actions in frontoparietal motor areas, within and between the hemispheres.
The assumption that episodic memory was involved at Action is further supported by the fact that in the encoding phase, the subjects had to visualize themselves performing the tasks, elaborating then a representation for each action that was likely re-activated in the PM-VR experiment, and more particularly at Action.
How such experience changes neural representations of action remains unknown.
These results indicate that the mirrored ipsilateral finger representation during unimanual actions is located predominantly in caudal or "new" M1, whereas the ipsilateral finger representation for bimanual actions is shifted toward the rostral or "old" M1 (Rathelot and Strick 2009) and caudal PM.
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