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1 orimotor processing (dorsal dentate nucleus, sensorimotor cortex).
2 sal ganglia, thalamus, occipital cortex, and sensorimotor cortex).
3 4 Hz), and beta (15-25 Hz) oscillations over sensorimotor cortex.
4 grid over the hand and arm area of the left sensorimotor cortex.
5 ions may depend on inhibitory release in the sensorimotor cortex.
6 coordinates depends on the plasticity in the sensorimotor cortex.
7 eta (13-30 Hz) band EEG in the contralateral sensorimotor cortex.
8 their relationship to functional changes in sensorimotor cortex.
9 through interhemispheric connections of the sensorimotor cortex.
10 callosal connections and the contralesional sensorimotor cortex.
11 le of the lateral ventricle and the forelimb sensorimotor cortex.
12 t neuronal correlates of handedness in human sensorimotor cortex.
13 ckness lesions of the forelimb region of the sensorimotor cortex.
14 same pattern was not seen after TMS of left sensorimotor cortex.
15 rized by intense activation of contralateral sensorimotor cortex.
16 t-spiking (FS) interneurons in slices of rat sensorimotor cortex.
17 of Betz cells and other pyramidal cells from sensorimotor cortex.
18 utely dissociated pyramidal neurons from rat sensorimotor cortex.
19 tomical connectivity involving primarily the sensorimotor cortex.
20 a chronic cortical stroke that involved the sensorimotor cortex.
21 old-spiking (LTS) cells in layer V of rodent sensorimotor cortex.
22 between craving and metabolism in the right sensorimotor cortex.
23 but instead was correlated with activity in sensorimotor cortex.
24 both cerebellar hemispheres and in the left sensorimotor cortex.
25 teral geniculate nucleus of the thalamus and sensorimotor cortex.
26 voked immediate-early gene expression in the sensorimotor cortex.
27 ed in a stereotaxically-identified region of sensorimotor cortex.
28 e anterior cingulate, prefrontal cortex, and sensorimotor cortex.
29 contralateral and ipsilateral activation of sensorimotor cortex.
30 nderwent unilateral aspiration lesion of the sensorimotor cortex.
31 e representations of different body parts in sensorimotor cortex.
32 e representations of different body parts in sensorimotor cortex.
33 y be used to detect functional activation of sensorimotor cortex.
34 , ephrin-A5 is transcribed abundantly in the sensorimotor cortex.
35 ing over the right premotor cortex or either sensorimotor cortex.
36 t in the association cortex and least in the sensorimotor cortex.
37 cifically by CSN in medial, but not lateral, sensorimotor cortex.
38 e related to changes in the "hubness" of the sensorimotor cortex.
39 ere preceded by sources in the frontocentral sensorimotor cortex.
40 function of the speech areas of the primary sensorimotor cortex.
41 seven tasks, with mainly decreased GSCORR in sensorimotor cortex.
42 asal ganglia, thalami, and orbitofrontal and sensorimotor cortex.
43 postmovement clear-out of the motor plan in sensorimotor cortex.
44 o the large literature on beta recorded from sensorimotor cortex.
45 Rats received unilateral ischemic stroke in sensorimotor cortex.
46 al capsule, periventricular white matter and sensorimotor cortex.
47 raveled along opposite directions across the sensorimotor cortex.
48 face electric potentials recorded from human sensorimotor cortex.
49 performance and less EEG mu suppression over sensorimotor cortex.
50 y of anterior prefrontal inhibition over the sensorimotor cortex.
51 gamma-aminobutyric acid concentration in the sensorimotor cortex.
52 tence of a reward-like signal in the primary sensorimotor cortex.
53 refrontal cortex, right hippocampus and left sensorimotor cortex.
54 tion in the mouse visual thalamus as well as sensorimotor cortex.
55 ing biotin-conjugated dextran amine into the sensorimotor cortex.
56 concurrently decreased in the contralateral sensorimotor cortex.
57 ted synchronization (ERS) over contralateral sensorimotor cortex.
58 n was observed with Broca's area, insula, or sensorimotor cortex.
59 and primary signal decreases in ipsilateral sensorimotor cortex.
60 ional functional connectivity in the primary sensorimotor cortex.
61 rmed during functional MRI, showed increased sensorimotor cortex activation across the period of ther
64 anied by an increase in ipsilesional primary sensorimotor cortex activity following the intervention.
66 nce intervals -0.792, -0.014, P = 0.043) and sensorimotor cortex (adjusted difference = -0.385 mM, 95
67 ctivated by designer drug) receptor hM4Di in sensorimotor cortex and AAV-expressing Cre in C7/C8 dors
68 in the beta band may dynamically couple the sensorimotor cortex and basal ganglia after movements.
69 cAMP levels fall in the rostral spinal cord, sensorimotor cortex and brainstem after spinal cord cont
70 c reductions in the putamen/globus pallidus, sensorimotor cortex and cerebellar vermis, as well as in
71 nderwent photothrombotic stroke of the right sensorimotor cortex and chronic implantation of a stimul
73 oherence between the bioelectric activity of sensorimotor cortex and contralateral muscles can be obs
75 mated arrival time of the afferent volley in sensorimotor cortex and decreased to 83% of baseline whe
77 for changes in structural morphometry of the sensorimotor cortex and found that individuals with stro
79 LS) is the orofacial projection field of the sensorimotor cortex and is involved in the development o
80 t decrease in GABA level was observed in the sensorimotor cortex and lentiform nuclei contralateral t
82 ationship between time-dependent activity in sensorimotor cortex and movement velocity, independent o
83 th primary signal increases in contralateral sensorimotor cortex and primary signal decreases in ipsi
84 an imagined movement did within left primary sensorimotor cortex and right dorsal cerebellum, while i
85 circuit, significant decreases were noted in sensorimotor cortex and striatum, with associated increa
86 loss of brain activation in the ipsilesional sensorimotor cortex and that restoration of function is
87 of both hemispheres and between the primary sensorimotor cortex and the mesial premotor areas, proba
89 erent oscillatory coupling between the mouth sensorimotor cortex and the mouth muscles is strongest a
90 es corresponded to stereotactic locations in sensorimotor cortex and to the results of individual cli
91 edback from movements in driving activity in sensorimotor cortex and underscore the necessity of moni
92 F-2, on embryonic pyramidal neurons from the sensorimotor cortex and used time-lapse digital imaging
93 al cerebral blood flow increases in the left sensorimotor cortex and ventrolateral thalamus and in th
94 herically between the left and right primary sensorimotor cortexes and between the contralateral prim
95 eural oscillations originating from the left sensorimotor cortex, and directed toward auditory region
96 over the contralateral premotor and primary sensorimotor cortex, and functional coupling occurred be
98 tion of forebrain, including frontal cortex, sensorimotor cortex, and striatum, and transitioned the
99 on volumes in both occipital lobes, the left sensorimotor cortex, and the supplemental motor cortices
100 would increase COX activity in the striatum, sensorimotor cortex, and three hippocampal subfields.
101 linked to resting-state connectivity in the sensorimotor cortex, anterior cingulate cortex, and cere
102 results imply that 20 Hz oscillations in the sensorimotor cortex are at least partially produced by l
104 roscopy showed that GABA levels in the human sensorimotor cortex are quickly reduced within minutes o
105 lesions, but no direct damage to the primary sensorimotor cortex, are capable of longitudinally acqui
106 d by abnormal neuronal discharges within the sensorimotor cortex, as demonstrated by electrophysiolog
107 tions of biotinylated dextran amine into the sensorimotor cortex, assessing the distribution of DLCST
108 s, was observed concomitantly, involving the sensorimotor cortex, associative areas, and limbic struc
109 ng a large scale nonspecific organization of sensorimotor cortex based on a motif of large symmetrica
110 between the occurrence of beta bursts in the sensorimotor cortex before the go-cue and slowed movemen
111 nalyses revealed a negative correlation over sensorimotor cortex between gamma-oscillatory activity a
112 ant correlation was found at the ipsilateral sensorimotor cortex between the NBR and EEG despite thei
113 the ventral premotor, Rolandic opercular and sensorimotor cortex bilaterally and Heschl's gyrus on th
114 types in the low-to-mid auditory cortex and sensorimotor cortex bilaterally, with right-hemisphere d
115 nt of motor activation responses in the left sensorimotor cortex (Brodmann area [BA] 4), bilaterally
116 efrontal cortex, hippocampus, brainstem, and sensorimotor cortex, but not in the amygdala or hypothal
117 on of the limbic thalamic afferents from the sensorimotor cortex by mediating repulsive interactions.
118 cific structures (caudate, primary motor and sensorimotor cortex, CA1 hippocampus, subcortical white
119 nstrates that ECoG signals recorded from the sensorimotor cortex can be used for real-time device con
120 animals, sufficient unilateral damage to the sensorimotor cortex can cause impairments in the opposit
121 atterns suggest a model in which the primate sensorimotor cortex can target parvalbumin-containing in
122 ovements activated the contralateral primary sensorimotor cortex, caudal SMA and contralateral putame
124 subjects, TMS-evoked cortical responses over sensorimotor cortex changed with different interstimulus
125 ntrinsic property of single neurons in mouse sensorimotor cortex, coinciding with the disappearance o
127 CD and AAV1-eGFP, or AAV1-eGFP alone, in the sensorimotor cortex concurrent with a C4 dorsal SCI.
128 words in the temporal lobe, frontal lobe and sensorimotor cortex, consistent with previous findings i
129 ase in GAP-43 immunoreactivity in the intact sensorimotor cortex contralateral to cerebral infarcts f
131 dition, as well as activation in the primary sensorimotor cortex contralateral to the mirrored/virtua
132 stantial involvement of scalp areas over the sensorimotor cortex contralateral to the reaching hand.
133 ups, specifically in the WM subjacent to the sensorimotor cortex contralateral to the trained limb.
134 with motor execution [contralateral primary sensorimotor cortex, contralateral thalamus, ipsilateral
135 at either 10 or 20 Hz and was imposed on the sensorimotor cortex contralaterally or ipsilaterally to
138 alysis of T1-weighted images focusing on the sensorimotor cortex corresponding to the hand area.
139 tomical borders between cortical modalities, sensorimotor cortex could therefore be viewed as a conti
140 signal in both contralateral and ipsilateral sensorimotor cortex depends on the poststimulus synchron
142 stical parametric mapping), localized to the sensorimotor cortex, dorsal premotor cortex, supplementa
143 cterized by covarying neural activity in the sensorimotor cortex, dorsal premotor cortex, supplementa
144 ed greater leftward gray matter asymmetry of sensorimotor cortex, due in large part to more pronounce
146 nt signal in posterior parts of ipsilesional sensorimotor cortex during hand grip, corresponding to t
147 movement and abnormal processing in primary sensorimotor cortex during imagined movement; and (iii)
149 ta-band rhythms modulate excitability of the sensorimotor cortex during psychophysically-controlled m
151 ts reveal the dynamic organization of speech sensorimotor cortex during the generation of multi-artic
152 pecific and only occurred over contralateral sensorimotor cortex during unilateral limb movements (al
153 on cause of disability, which often leads to sensorimotor cortex dysfunction above the spinal injury
154 compared oscillatory activity in the primary sensorimotor cortex [EEG of sensorimotor cortex (SMC-EEG
155 e potential early stages in the evolution of sensorimotor cortex, electrophysiological studies were c
156 ving distal upper limbs, linked to increased sensorimotor cortex excitability, as seen in cortical my
157 expression pattern suggests that the primate sensorimotor cortex exerts a differential influence on t
158 y to the forelimb representation area of the sensorimotor cortex (FL-SMC) in adult rats causes over-r
159 y to the forelimb-representation area of the sensorimotor cortex (FL-SMC) in adult rats results in us
160 s of the forelimb representation area of the sensorimotor cortex (FL-SMC) in rats increase in size su
161 lateral damage to the forelimb region of the sensorimotor cortex (FLsmc) in adult rats has previously
162 ateral lesions of the forelimb region of the sensorimotor cortex (FLsmc) in rats, or callosal transec
164 female mice and reduced MAP-2 levels in the sensorimotor cortex following ACP-105 treatment might co
165 s in directed functional connectivity across sensorimotor cortex further distinguished the sustained
167 seed-based functional connectivity from the sensorimotor cortex, globus pallidus internus, ventral i
168 senting an animal's position and movement in sensorimotor cortex has been found to continually reconf
170 mulus-induced activation in the ipsilesional sensorimotor cortex; however, local tissue and perfusion
172 s-identified regions of left perisylvian and sensorimotor cortex impaired performance, whereas rTMS t
173 ipsilateral SEP components in the remaining sensorimotor cortex in 10 of the 17 patients (five with
174 rocorticography signals from the ipsilateral sensorimotor cortex in 10 patients undergoing deep brain
175 igh-density surface recordings of the speech sensorimotor cortex in a clinical trial participant with
176 broadly and nearly uniformly distributed in sensorimotor cortex in a pattern similar to that in post
179 ilateral lesions of the forelimb area of the sensorimotor cortex in adult rats resulted in time-depen
180 , mirrored movements differentially activate sensorimotor cortex in amputees with and without phantom
181 aimed to investigate the causal role of the sensorimotor cortex in generating movement and bodily se
182 ate volitional suppression of beta bursts in sensorimotor cortex in healthy motor control better than
184 MR images is located exactly in the anatomic sensorimotor cortex in normal brains, whereas a mismatch
185 or five subdivisions of the somatosensory or sensorimotor cortex in North American opossums (Didelphi
187 r, an information drive appeared from STN to sensorimotor cortex in the first phase of the adaptation
189 post-movement beta activity (13-30 Hz) over sensorimotor cortex in young healthy subjects indexes th
190 less of the effector used in the association sensorimotor cortex, in the left intraparietal sulcus an
191 much reduced, e.g. 4-8% of normal in primary sensorimotor cortex, in the setting of twice normal vari
192 ha power facilitate early registration, with sensorimotor cortex including the sensorimotor face area
193 voked potentials decrease over contralateral sensorimotor cortex, indicative of local synaptic depres
195 rtices and motor-related areas including the sensorimotor cortex, inferior-frontal gyrus, supplementa
197 lpha-band oscillatory power increased in the sensorimotor cortex ipsilateral to the arm used for imag
200 ndergoing awake craniotomy has revealed that sensorimotor cortex is functionally organized for signin
202 ted, led to decreased activation of the left sensorimotor cortex, lateral premotor cortex, and pariet
204 aching) forelimb received ischemic bilateral sensorimotor cortex lesions, or unilateral lesions, with
206 aining induces significant plasticity in the sensorimotor cortex, manifested as improved discriminabi
207 anguage, whereas nonheritable asymmetries of sensorimotor cortex may manifest as consequences of hand
210 tional coupling occurred between the primary sensorimotor cortex of both hemispheres and between the
213 latory activity in the 15-30 Hz range in the sensorimotor cortex of human subjects and monkeys during
214 ron spiking with substantial accuracy in the sensorimotor cortex of humans and nonhuman behaving prim
215 phosphatase and tensin homolog (PTEN) in the sensorimotor cortex of neonatal mice enables regeneratio
216 ng biotinylated dextran amine (BDA) into the sensorimotor cortex of one hemisphere either at the time
217 ed electrocorticographic recordings from the sensorimotor cortex of people with refractory epilepsy a
218 ate that a unilateral injury of the hindlimb sensorimotor cortex of rats with completely transected t
219 ct injury delivered by a piston to the right sensorimotor cortex of the anesthetized rat, we evaluate
220 mptive inhibitory synapses in layer 2 of the sensorimotor cortex of the Brown Norway x Fisher 344 rat
221 lled cortical impact (CCI) over the forelimb sensorimotor cortex of the rat (FL-SMC) is neuroprotecti
222 the age of 3 years) showed activation in the sensorimotor cortex of the remaining hemisphere with pas
224 us) was invariably coherent with that in the sensorimotor cortex or contracting muscle in the 8-27 Hz
225 d from more caudally placed contacts and the sensorimotor cortex or contracting muscle was negligible
226 iMSNs) and optically stimulated inputs from sensorimotor cortex or intralaminar thalamus in brain sl
228 olitional inspiration included inferolateral sensorimotor cortex, prefrontal cortex and striatum (the
229 portions of the motor pathway, including the sensorimotor cortex, putamen, pallidum, and substantia n
231 dings, we tested whether beta-gamma PAC over sensorimotor cortex, recorded noninvasively with EEG, di
232 nd beta-band oscillatory brain activity over sensorimotor cortex reflected decision variables such as
233 roencephalographic (EEG) beta power over the sensorimotor cortex reflects neural processes that evalu
238 gue task (although the signal of the primary sensorimotor cortex showed a clear trend of decline).
239 r insula/secondary somatosensory cortex, the sensorimotor cortex (SI/MI), and the caudal ACC was spec
240 the layer V neurons in the wide areas of the sensorimotor cortex simultaneously control STN and ZI ne
243 The relative hemispheric lateralization of sensorimotor cortex (SMC) activation decreased in direct
244 in the adult motor cortex after a unilateral sensorimotor cortex (SMC) lesion and treatment with mono
247 y in the primary sensorimotor cortex [EEG of sensorimotor cortex (SMC-EEG)] and a motor neuronal pool
249 degeneration following a large lesion of the sensorimotor cortex, some rubrospinal and reticulospinal
250 After photothrombotic stroke in the forelimb sensorimotor cortex, SPARC nulls demonstrate enhanced mi
251 Inosine applied with a minipump to the rat sensorimotor cortex stimulated intact pyramidal cells to
252 gether with the disturbances reported in the sensorimotor cortex, striatum, and globus pallidus, supp
253 ases in the efficiency of neural processing (sensorimotor cortex, striatum, vermis) and an increased
254 eals increased intrinsic connectivity in the sensorimotor cortex, suggesting neuronal dysfunction in
255 sults from maladaptive reorganization of the sensorimotor cortex, suggesting that experimental induct
256 regional CBF (rCBF) in the cingulate gyrus, sensorimotor cortex, superior temporal cortex, occipital
257 the contralateral left hemisphere, including sensorimotor cortex, supplementary motor area, and rostr
258 atrophy in specific regions, notably primary sensorimotor cortex, temporal white and gray matter, tha
259 hin established nodes of the tremor circuit: sensorimotor cortex, thalamus, contralateral cerebellar
261 rize corticostriatal projections from rodent sensorimotor cortex, the anterograde tracers biotinylate
262 and functional degeneration in the deprived sensorimotor cortex, the experience of persistent pain i
263 While neural activity was recorded from sensorimotor cortex, the participant produced a large va
264 oduced equivalent activation within the left sensorimotor cortex, the right cerebellum (dorsal dentat
265 myelin basic protein (MBP) and myelin in the sensorimotor cortex, the stratum radiatum, the corpus ca
266 val activity in midline cortical structures, sensorimotor cortex, the striatum, and the medial tempor
267 CP-105 reduced MAP-2 immunoreactivity in the sensorimotor cortex, there was a trend towards increased
268 n the insula and toward low frequency in the sensorimotor cortex to a greater extent than male IBS su
269 tran amine (BDA) was injected into the right sensorimotor cortex to anterogradely label the CST.
270 dition, the observed capacity of the primary sensorimotor cortex to exhibit operational heterogeneity
271 njected into either the hindlimb or forelimb sensorimotor cortex to label corticospinal axons project
272 alternating current stimulation (tACS) over sensorimotor cortex to modulate theta-gamma activity dur
275 n the alpha frequency range, particularly in sensorimotor cortex, to processing of social actions.
276 he result of the characterization of the rat sensorimotor cortex tolerance to microradiosurgical para
278 icipant was able to voluntarily activate his sensorimotor cortex using attempted movements, with dist
279 motor skill learning on WM structure within sensorimotor cortex using both diffusion MRI fractional
280 we recorded local field potentials from hand sensorimotor cortex using subdural electrocorticography
287 a survival period of 12 weeks, the opposite sensorimotor cortex was stereotaxically injected with th
288 ing a unilateral injury model limited to the sensorimotor cortex, we show that inosine triples the nu
290 sensory evoked potentials recorded over the sensorimotor cortex were larger and detectable over a mo
294 stal area, namely the anterior sector of the sensorimotor cortex, when participants observe videos of
295 ts with stronger alpha suppression over left sensorimotor cortex, whereas the Taylor illusion correla
296 VTS modulates neuronal synchronization over sensorimotor cortex, which can induce short-term improve
298 of activation responses in the ipsilesional sensorimotor cortex, which was related to T2 lesion size
299 We found that activation of the ipsilateral sensorimotor cortex with simple hand movements was incre
300 to volitionally suppress beta bursts in the sensorimotor cortex, with training being accompanied by