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1 mpared to resting-state patterns in the same motor region.
2 elated with MEP amplitudes in the upper limb motor region.
3 l prefrontal cortex, functions as a visceral motor region.
4 NMDA) receptors following stimulation of non-motor regions.
5 g task-relevant information in visual and/or motor regions.
6 oss much of the brain, including sensory and motor regions.
7  movement representations in spared cortical motor regions.
8 ional connectivity with subcortical and (pre)motor regions.
9  and dose-dependent thinning of the cortical motor regions.
10 similarity of paralimbic and primary sensory/motor regions.
11 higher energetic costs than those in sensory-motor regions.
12 ring would be associated with high forces in motor regions.
13 er-order brain regions and either sensory or motor regions.
14 piratory modulation, with highest density in motor regions.
15 iii) elicit stronger effects of TMS on these motor regions.
16 corticography was recorded over auditory and motor regions.
17 rocal interactions with temporal and frontal motor regions.
18 as actions are produced by modality-specific motor regions.
19 these deep-layer cells also target brainstem motor regions.
20 s, lateral frontal cortex, and somatosensory/motor regions.
21  densely connected with other frontal cortex motor regions.
22 ngulate gyrus and right sensorimotor and pre-motor regions.
23 2% identity to MYO3 across the motor and non-motor regions.
24 y inactivated, indicating plasticity in song motor regions.
25 g frontal and parietal areas [10, 11], other motor regions [12-15], and also the existence of multise
26     Consistent with prior data, the cortical motor regions activated during the motor task showed gre
27 s also densely connected with frontal cortex motor regions, albeit to a lesser extent than the M1 gra
28 activity pulses that appeared in the disused motor regions and CON control regions.
29  well established in humans for language and motor regions and correlate with handedness.
30 mal anticorrelation between dorsal attention/motor regions and default-mode/frontoparietal regions, p
31           31P-MRS was acquired from cerebral motor regions and from tibialis anterior during rest and
32 ciation cortices relative to primary sensory/motor regions and have implications for understanding po
33 ved stronger recruitment of primary auditory-motor regions and low visual engagement.
34 wed impaired connectivity between cerebellar motor regions and neocortical visuomotor and premotor re
35  between the left precentral gyrus and other motor regions, and between Broca's and Wernicke's areas.
36 already in early sensory, somatosensory, and motor regions, and only for political content.
37 actions between auditory, somatosensory, and motor regions, and the hemispheric lateralization patter
38 One metastate is associated with sensory and motor regions, and the other involves areas related to h
39 ge-scale circuit model suggests that sensory-motor regions are a driver of FC dynamics.
40 parietal, higher-order language regions, and motor regions are involved in beta.
41                                    Secondary motor regions are less efficient at generating motor out
42 cted by an associative account, responses in motor regions are observed for novel and/or abstract vis
43 rdless of age group, stronger coupling among motor regions, as well as between language/speech region
44  temporal, fronto-insular, and supplementary motor regions, as well as between the amygdala and dorsa
45  of upper-limb casting revealed that disused motor regions became more strongly connected to the cing
46 h and language processing, where sensory and motor regions better align with the model's speech embed
47 yses revealed higher sodium concentration in motor regions (bilateral precentral gyri, corticospinal
48 in striatal areas but also in extrastriatal "motor" regions, bilaterally.
49 nd closely in unimodal, primary sensory, and motor regions, but diverge in transmodal cortex, particu
50 mispheric inhibitory effects between primary motor regions can explain subjective post-stroke fatigue
51 nd more balanced between visual and auditory-motor regions compared with the spatial pathway.
52 nnectivity among a bilateral network of core motor regions comprising M1, lateral premotor cortex, an
53 and inter-hemispheric interactions among key motor regions constitute an important pathophysiological
54 tigated the hypothesis that areas beyond the motor regions could participate in RtG planning and exec
55 the medial frontal cortex, salience network, motor regions, default mode network, and cerebellum.
56 the cortex concentrated in visual and somato-motor regions, distinct from the pattern of intersubject
57 nduced changes in coupling within or between motor regions during motor preparation may affect cortic
58  3-33 Hz) broadband oscillatory activity) in motor regions during movement compared to rest, as well
59 d the activation and interaction of cortical motor regions during simple, internally paced and extern
60 and the increased activation in the cortical motor regions during the dopamine-replete state was posi
61 s task have revealed selective activation of motor regions during the perception of 'natural' versus
62               Truncation mutants lacking the motor region failed to localize to filopodial tips but s
63                            The divergent non-motor regions flanking the ATPase domain are critical in
64 ntal, premotor, supplementary, and cingulate motor regions, following training of a challenging dynam
65 did not consistently distinguish sensory and motor regions from paralimbic and association regions: (
66                                         Each motor region has unique terminations in the ipsilateral
67              Responses within the stimulated motor region have previously been found to correlate wit
68 lved correlated activity throughout multiple motor regions; however, we found no evidence for plastic
69 ever, it is difficult to target the cervical motor region in a rodent using a non-penetrating stimulu
70 y regulates kinesin-1 via the amino-terminal motor region in the context of the incoming viral partic
71 overy in a number of primary and non-primary motor regions in all patients, but no session effects we
72  movement-related activation in ipsilesional motor regions in chronic subcortical stroke patients.
73                 Crucially, however, distinct motor regions in the precentral gyrus sparked by articul
74                        Overall, the forelimb motor region included: (1) a large caudal forelimb area
75 ves the SMA and cortical regions outside the motor regions, including prefrontal and parietal regions
76                      The enzyme was found in motor regions, including the dorsal motor nucleus of the
77 try of connectivity was assessed in the hand motor region, incorporating tumor position, perfusion, g
78  whereas activity in insular, cingulate, and motor regions is best explained in terms of stimulus unc
79 we have found that cholinergic input to both motor regions is required for task acquisition.
80  that a network of auditory and superior pre/motor regions is universally activated in the process of
81 ynchronized brain activity among sensory and motor regions may also play a critical role.
82                         These activations in motor regions may possibly reflect volitional effort to
83            These molecules share a conserved motor region of approximately 340 amino acids, which is
84  dyslexics relative to the controls in a pre-motor region of Broca's area (BA 6/44).
85       The general structural features of the motor region of myosin superfamily members are now well
86 ivity between frontal cortical areas and the motor region of the striatum as a putative substrate for
87 ucleus is a specialized autonomic-projecting motor region of the striatum, whereas the lateral and an
88 ic carrot DNA, DcKRP120-1, homologous to the motor region of tobacco TKRP125.
89 models N-terminal scaffolding and C-terminal motor regions of DnaB to produce a clear break in the he
90 blood oxygen level dependent signal of three motor regions of interest in each hemisphere.
91 ends of white matter volume loss in relevant motor regions of the brain as measured via MRI.
92 d with a unique gene expression signature in motor regions of the brain implicated in neurodegenerati
93 s linking sound perception and production in motor regions of the brain, so this ability is not speci
94 ty in the motor cortex and striatum, two key motor regions of the brain.
95 s the immature networks in children included motor regions of the brain.
96 nitive-behavioural dysfunction affecting non-motor regions of the brain.
97 em, decreasing response times and activating motor regions of the brain.
98 I, and VIII bilaterally corresponding to the motor regions of the cerebellum (z score = 3.96 and 3.42
99 rain correlates of stuttering are the speech-motor regions of the non-dominant (right) cerebral hemis
100 ally, it is thought that action selection in motor regions originates from a competitive process that
101 ed a buildup of choice-selective activity in motor regions over time reflecting the integrated sensor
102 , fast spindles (13.5-15 Hz) at task-related motor regions predicted overnight enhancement in procedu
103 ies on a distributed network of temporal and motor regions rather than any specific anatomical landma
104 t predominantly contralateral frontoparietal motor regions, recordings in patients revealed that move
105 gined transformations to the equation or the motor region reflecting manual programming.
106 in the proportion of activated voxels in any motor region (relative to the total number of activated
107                           The recruitment of motor regions requires modulatory input to shape circuit
108 e cognitive control, less is known about how motor regions respond to rapid and unexpected changes in
109 model of increasing degrees of damage to the motor regions responsible for gait i.e. IUGR, IUGR + hyp
110 culate nucleus and primary visual cortex) to motor regions (secondary and primary motor cortex and gi
111                  We demonstrate that, beyond motor regions, several areas, such as the visual and the
112 evels, including auditory, sensorimotor, and motor regions, suggesting the representation of sensorim
113 tions between basal ganglia circuits and the motor regions that directly control performance.
114  in several identical primary and nonprimary motor regions that is independent of time after stroke.
115 r expression in the cerebellum and striatum, motor regions that may contribute to the improved behavi
116  PMd and remote right-hemispheric and mesial motor regions that was only present during arbitrary vis
117                            Among the brain's motor regions, the cortico-basal ganglia circuit is part
118  recorded from neurons in the red nucleus, a motor region thought to be important for initiating move
119 e, sport novices recruit lower-level sensory-motor regions, thought to support the instantiation of m
120 ral cingulate (M3) and caudal cingulate (M4) motor regions through the corona radiata (CR), internal
121 chimeric kinesin-1 that fuses the N-terminal motor region to the tail and a tail variant unable to in
122 luctuation of functional connectivity in all motor regions to a level closer to that of healthy parti
123 onal gradients extending from perceptual and motor regions to cortical areas representing more abstra
124 put, and show that the cells projecting from motor regions to insular cortex are engaged shortly befo
125 k together with right-hemispheric and mesial motor regions to sustain visuomotor mapping performed wi
126 tients with FND exhibited increased SFC from motor regions to the bilateral posterior insula, TPJ, mi
127  and raphespinal innervation to the cervical motor region was promoted by C'ase plus transplant.
128 ansient synchronization between auditory and motor regions was observed.
129 uctuation of functional connectivity between motor regions were associated with improvements in tremo
130 sions positive for p62 immunostaining in non-motor regions were strongly over-represented in the C9OR
131 d following stimulation, particularly in non-motor regions where less is known about TMS physiology.
132 ndings suggest that PPTg input to downstream motor regions, where it can be integrated with other rel
133 s observed mainly in the primary sensory and motor regions, whereas low GSCORR was seen in the associ
134       The caudal ZI primarily connected with motor regions, while the rostral ZI received a topograph
135 recurring activation patterns of interacting motor regions (whole-brain intrinsic motor network state
136 FC that included only hypothesized value and motor regions with models trained on whole-brain FC.
137  molecular basis for the function of the non-motor regions within the context of full-length MCAK is
138          We hypothesized that recruitment of motor regions would shift from primary to secondary moto

 
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