Exact(1)
Multimodal neuroimaging has also been used in many non-clinical applications, such as building brain machine interface (BMI) [44], tracing neural activity pathways [45] and mapping mind and behavior to brain anatomy [46, 47, 48].
Similar(58)
There is a wide range of applications of multimodal neuroimaging, clinical and non-clinical, including building a brain machine interface (BMI) [19], tracing neural activities and information pathways [20], mapping mind and behavior to brain regions [21, 22, 23], evaluating the effects of pharmacological treatments [24, 25], and image-guided therapy (IGT) [26, 27, 28].
This would allow mapping neural connectivity using optical tools, rapidly, in scalable manner, and without tracing neural projections.
To trace neural crest derivatives, we performed genetic fate-mapping studies with a recent Wnt1-Cre2 line that does not induce ectopic Wnt1 activity (Lewis et al., 2013).
Overall, by showing how different optical factors interact to affect signal quality, our treatment offers a valuable guide to experimental design and provides measures of confidence to assess optically extracted traces of neural activity.
Perceptual symbols are believed to be multimodal traces of neural activity that contain at least some of the motor information present during actual sensorimotor experience (Barsalou, 1999).
Such a mechanism is wide-ranging in its explanatory capacity and resembles other accounts, such as Barsalou's (1999) perceptual symbol systems, where "multimodal traces of neural activity that contain at least some of the motor information present during actual sensorimotor experience" (Goldin-Meadow & Beilock, 2010, p. 665) can ground meaning in simulation.
This is a first report of spatiotemporal dipole source analysis on healthy adolescent ERP data tracing the sequence of neural activity within the first 500 ms of categorizing emotion from faces.
Neural activity actively regulates muscle gene expression.
This is a first report of high-density ERP dipole source analysis in healthy adolescents which traces the sequence of neural activity within the first 500 ms of categorizing emotion from faces.
Representative traces from active electrodes exhibiting neural activity (i.e., action potential spikes) for these cultures are shown in Fig. 2b.
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