ライフサイエンスコーパス: sensorimotor cortex

1 orimotor processing (dorsal dentate nucleus, sensorimotor cortex).

2 sal ganglia, thalamus, occipital cortex, and sensorimotor cortex).

3 performance and less EEG mu suppression over sensorimotor cortex.

4 le of the lateral ventricle and the forelimb sensorimotor cortex.

5 t neuronal correlates of handedness in human sensorimotor cortex.

6 ckness lesions of the forelimb region of the sensorimotor cortex.

7 same pattern was not seen after TMS of left sensorimotor cortex.

8 rized by intense activation of contralateral sensorimotor cortex.

9 t-spiking (FS) interneurons in slices of rat sensorimotor cortex.

10 of Betz cells and other pyramidal cells from sensorimotor cortex.

11 utely dissociated pyramidal neurons from rat sensorimotor cortex.

12 tomical connectivity involving primarily the sensorimotor cortex.

13 a chronic cortical stroke that involved the sensorimotor cortex.

14 old-spiking (LTS) cells in layer V of rodent sensorimotor cortex.

15 between craving and metabolism in the right sensorimotor cortex.

16 but instead was correlated with activity in sensorimotor cortex.

17 both cerebellar hemispheres and in the left sensorimotor cortex.

18 voked immediate-early gene expression in the sensorimotor cortex.

19 ed in a stereotaxically-identified region of sensorimotor cortex.

20 gamma-aminobutyric acid concentration in the sensorimotor cortex.

21 e anterior cingulate, prefrontal cortex, and sensorimotor cortex.

22 contralateral and ipsilateral activation of sensorimotor cortex.

23 nderwent unilateral aspiration lesion of the sensorimotor cortex.

24 e representations of different body parts in sensorimotor cortex.

25 e representations of different body parts in sensorimotor cortex.

26 y be used to detect functional activation of sensorimotor cortex.

27 , ephrin-A5 is transcribed abundantly in the sensorimotor cortex.

28 ing over the right premotor cortex or either sensorimotor cortex.

29 tence of a reward-like signal in the primary sensorimotor cortex.

30 refrontal cortex, right hippocampus and left sensorimotor cortex.

31 ing biotin-conjugated dextran amine into the sensorimotor cortex.

32 concurrently decreased in the contralateral sensorimotor cortex.

33 ted synchronization (ERS) over contralateral sensorimotor cortex.

34 n was observed with Broca's area, insula, or sensorimotor cortex.

35 and primary signal decreases in ipsilateral sensorimotor cortex.

36 ional functional connectivity in the primary sensorimotor cortex.

37 grid over the hand and arm area of the left sensorimotor cortex.

38 ions may depend on inhibitory release in the sensorimotor cortex.

39 coordinates depends on the plasticity in the sensorimotor cortex.

40 eta (13-30 Hz) band EEG in the contralateral sensorimotor cortex.

41 their relationship to functional changes in sensorimotor cortex.

42 through interhemispheric connections of the sensorimotor cortex.

43 callosal connections and the contralesional sensorimotor cortex.

44 rmed during functional MRI, showed increased sensorimotor cortex activation across the period of ther

45 h task, group average maps for contralateral sensorimotor cortex activation were generated.

46 Furthermore, the peak ipsilesional sensorimotor cortex activity shifted posteriorly in more

47 nce intervals -0.792, -0.014, P = 0.043) and sensorimotor cortex (adjusted difference = -0.385 mM, 95

48 ctivated by designer drug) receptor hM4Di in sensorimotor cortex and AAV-expressing Cre in C7/C8 dors

49 in the beta band may dynamically couple the sensorimotor cortex and basal ganglia after movements.

50 cAMP levels fall in the rostral spinal cord, sensorimotor cortex and brainstem after spinal cord cont

51 c reductions in the putamen/globus pallidus, sensorimotor cortex and cerebellar vermis, as well as in

52 nderwent photothrombotic stroke of the right sensorimotor cortex and chronic implantation of a stimul

53 Animals were lesioned in the left sensorimotor cortex and compared with age-matched naive

54 oherence between the bioelectric activity of sensorimotor cortex and contralateral muscles can be obs

55 hy were assessed by ex vivo pathology of the sensorimotor cortex and corpus callosum.

56 mated arrival time of the afferent volley in sensorimotor cortex and decreased to 83% of baseline whe

57 tionship between focal reorganization in the sensorimotor cortex and everyday behavior.

58 t decrease in GABA level was observed in the sensorimotor cortex and lentiform nuclei contralateral t

59 l nonsignificant decrease in the ipsilateral sensorimotor cortex and lentiform nuclei.

60 ationship between time-dependent activity in sensorimotor cortex and movement velocity, independent o

61 th primary signal increases in contralateral sensorimotor cortex and primary signal decreases in ipsi

62 an imagined movement did within left primary sensorimotor cortex and right dorsal cerebellum, while i

63 circuit, significant decreases were noted in sensorimotor cortex and striatum, with associated increa

64 loss of brain activation in the ipsilesional sensorimotor cortex and that restoration of function is

65 of both hemispheres and between the primary sensorimotor cortex and the mesial premotor areas, proba

66 rtexes and between the contralateral primary sensorimotor cortex and the mesial premotor areas.

67 erent oscillatory coupling between the mouth sensorimotor cortex and the mouth muscles is strongest a

68 es corresponded to stereotactic locations in sensorimotor cortex and to the results of individual cli

69 F-2, on embryonic pyramidal neurons from the sensorimotor cortex and used time-lapse digital imaging

70 al cerebral blood flow increases in the left sensorimotor cortex and ventrolateral thalamus and in th

71 herically between the left and right primary sensorimotor cortexes and between the contralateral prim

72 eural oscillations originating from the left sensorimotor cortex, and directed toward auditory region

73 over the contralateral premotor and primary sensorimotor cortex, and functional coupling occurred be

74 tion of forebrain, including frontal cortex, sensorimotor cortex, and striatum, and transitioned the

75 on volumes in both occipital lobes, the left sensorimotor cortex, and the supplemental motor cortices

76 would increase COX activity in the striatum, sensorimotor cortex, and three hippocampal subfields.

77 results imply that 20 Hz oscillations in the sensorimotor cortex are at least partially produced by l

78 roscopy showed that GABA levels in the human sensorimotor cortex are quickly reduced within minutes o

79 lesions, but no direct damage to the primary sensorimotor cortex, are capable of longitudinally acqui

80 tions of biotinylated dextran amine into the sensorimotor cortex, assessing the distribution of DLCST

81 ng a large scale nonspecific organization of sensorimotor cortex based on a motif of large symmetrica

82 nalyses revealed a negative correlation over sensorimotor cortex between gamma-oscillatory activity a

83 ant correlation was found at the ipsilateral sensorimotor cortex between the NBR and EEG despite thei

84 the ventral premotor, Rolandic opercular and sensorimotor cortex bilaterally and Heschl's gyrus on th

85 nt of motor activation responses in the left sensorimotor cortex (Brodmann area [BA] 4), bilaterally

86 efrontal cortex, hippocampus, brainstem, and sensorimotor cortex, but not in the amygdala or hypothal

87 on of the limbic thalamic afferents from the sensorimotor cortex by mediating repulsive interactions.

88 cific structures (caudate, primary motor and sensorimotor cortex, CA1 hippocampus, subcortical white

89 nstrates that ECoG signals recorded from the sensorimotor cortex can be used for real-time device con

90 animals, sufficient unilateral damage to the sensorimotor cortex can cause impairments in the opposit

91 atterns suggest a model in which the primate sensorimotor cortex can target parvalbumin-containing in

92 ovements activated the contralateral primary sensorimotor cortex, caudal SMA and contralateral putame

93 Unilateral contusion injury to the sensorimotor cortex causes, among other symptoms, a tran

94 subjects, TMS-evoked cortical responses over sensorimotor cortex changed with different interstimulus

95 ntrinsic property of single neurons in mouse sensorimotor cortex, coinciding with the disappearance o

96 words in the temporal lobe, frontal lobe and sensorimotor cortex, consistent with previous findings i

97 ase in GAP-43 immunoreactivity in the intact sensorimotor cortex contralateral to cerebral infarcts f

98 We found activation in the primary sensorimotor cortex contralateral to the actual movement

99 dition, as well as activation in the primary sensorimotor cortex contralateral to the mirrored/virtua

100 stantial involvement of scalp areas over the sensorimotor cortex contralateral to the reaching hand.

101 ups, specifically in the WM subjacent to the sensorimotor cortex contralateral to the trained limb.

102 with motor execution [contralateral primary sensorimotor cortex, contralateral thalamus, ipsilateral

103 at either 10 or 20 Hz and was imposed on the sensorimotor cortex contralaterally or ipsilaterally to

104 Vibrissae-related sensorimotor cortex controls whisking movements indirect

105 alysis of T1-weighted images focusing on the sensorimotor cortex corresponding to the hand area.

106 tomical borders between cortical modalities, sensorimotor cortex could therefore be viewed as a conti

107 signal in both contralateral and ipsilateral sensorimotor cortex depends on the poststimulus synchron

108 Microbeam irradiation of sensorimotor cortex did not affect weight gain and motor

109 stical parametric mapping), localized to the sensorimotor cortex, dorsal premotor cortex, supplementa

110 cterized by covarying neural activity in the sensorimotor cortex, dorsal premotor cortex, supplementa

111 ed greater leftward gray matter asymmetry of sensorimotor cortex, due in large part to more pronounce

112 nt signal in posterior parts of ipsilesional sensorimotor cortex during hand grip, corresponding to t

113 movement and abnormal processing in primary sensorimotor cortex during imagined movement; and (iii)

114 ts reveal the dynamic organization of speech sensorimotor cortex during the generation of multi-artic

115 pecific and only occurred over contralateral sensorimotor cortex during unilateral limb movements (al

116 compared oscillatory activity in the primary sensorimotor cortex [EEG of sensorimotor cortex (SMC-EEG

117 e potential early stages in the evolution of sensorimotor cortex, electrophysiological studies were c

118 expression pattern suggests that the primate sensorimotor cortex exerts a differential influence on t

119 y to the forelimb representation area of the sensorimotor cortex (FL-SMC) in adult rats causes over-r

120 y to the forelimb-representation area of the sensorimotor cortex (FL-SMC) in adult rats results in us

121 s of the forelimb representation area of the sensorimotor cortex (FL-SMC) in rats increase in size su

122 lateral damage to the forelimb region of the sensorimotor cortex (FLsmc) in adult rats has previously

123 ateral lesions of the forelimb region of the sensorimotor cortex (FLsmc) in rats, or callosal transec

124 x opposite unilateral damage to the forelimb sensorimotor cortex (FLsmc).

125 female mice and reduced MAP-2 levels in the sensorimotor cortex following ACP-105 treatment might co

126 Regional EEG modulations at the sensorimotor cortex further predicted a spatially distri

127 Reward modulation of the primary sensorimotor cortex has yet to be characterized at the l

128 mulus-induced activation in the ipsilesional sensorimotor cortex; however, local tissue and perfusion

129 Although those in executive sensorimotor cortex (i.e., SM1 and adjacent PMd) depend

130 s-identified regions of left perisylvian and sensorimotor cortex impaired performance, whereas rTMS t

131 ipsilateral SEP components in the remaining sensorimotor cortex in 10 of the 17 patients (five with

132 broadly and nearly uniformly distributed in sensorimotor cortex in a pattern similar to that in post

133 Aspiration lesions of the sensorimotor cortex in adult rats induced a transient do

134 ilateral lesions of the forelimb area of the sensorimotor cortex in adult rats resulted in time-depen

135 , mirrored movements differentially activate sensorimotor cortex in amputees with and without phantom

136 bles to determine the organization of speech sensorimotor cortex in humans.

137 MR images is located exactly in the anatomic sensorimotor cortex in normal brains, whereas a mismatch

138 or five subdivisions of the somatosensory or sensorimotor cortex in North American opossums (Didelphi

139 Following stroke-like lesions to the sensorimotor cortex in rats, experience with the ipsi-to

140 r, an information drive appeared from STN to sensorimotor cortex in the first phase of the adaptation

141 as do the somatotopic representations of the sensorimotor cortex in the subthalamus.

142 post-movement beta activity (13-30 Hz) over sensorimotor cortex in young healthy subjects indexes th

143 much reduced, e.g. 4-8% of normal in primary sensorimotor cortex, in the setting of twice normal vari

144 ha power facilitate early registration, with sensorimotor cortex including the sensorimotor face area

145 voked potentials decrease over contralateral sensorimotor cortex, indicative of local synaptic depres

146 We show that the microstimulation of sensorimotor cortex induces Fos and Jun B expression in

147 rtices and motor-related areas including the sensorimotor cortex, inferior-frontal gyrus, supplementa

148 lpha-band oscillatory power increased in the sensorimotor cortex ipsilateral to the arm used for imag

149 Using fMRI, we show that the deprived sensorimotor cortex is employed by whichever limb indivi

150 The orofacial sensorimotor cortex is known to play a role in motor lea

151 ted, led to decreased activation of the left sensorimotor cortex, lateral premotor cortex, and pariet

152 Following a unilateral sensorimotor cortex lesion in the adult rat, amphetamine

153 aching) forelimb received ischemic bilateral sensorimotor cortex lesions, or unilateral lesions, with

154 This is the first study of sensorimotor cortex local field potentials in the three

155 aining induces significant plasticity in the sensorimotor cortex, manifested as improved discriminabi

156 Fifty nanomoles of NMDA were injected in the sensorimotor cortex of 6-day-old rats.

157 d by cortical evoked potentials (EPs) in the sensorimotor cortex of awake, behaving monkeys.

158 tional coupling occurred between the primary sensorimotor cortex of both hemispheres and between the

159 < 0.005) in the subgyral white matter of the sensorimotor cortex of DYT1 carriers.

160 vation of this PCD pathway in the MNs of the sensorimotor cortex of G93A transgenic mice.

161 latory activity in the 15-30 Hz range in the sensorimotor cortex of human subjects and monkeys during

162 ron spiking with substantial accuracy in the sensorimotor cortex of humans and nonhuman behaving prim

163 phosphatase and tensin homolog (PTEN) in the sensorimotor cortex of neonatal mice enables regeneratio

164 ng biotinylated dextran amine (BDA) into the sensorimotor cortex of one hemisphere either at the time

165 ct injury delivered by a piston to the right sensorimotor cortex of the anesthetized rat, we evaluate

166 mptive inhibitory synapses in layer 2 of the sensorimotor cortex of the Brown Norway x Fisher 344 rat

167 lled cortical impact (CCI) over the forelimb sensorimotor cortex of the rat (FL-SMC) is neuroprotecti

168 the age of 3 years) showed activation in the sensorimotor cortex of the remaining hemisphere with pas

169 Moreover, metabolic activity in the sensorimotor cortex of these animals was closely correla

170 us) was invariably coherent with that in the sensorimotor cortex or contracting muscle in the 8-27 Hz

171 d from more caudally placed contacts and the sensorimotor cortex or contracting muscle was negligible

172 iMSNs) and optically stimulated inputs from sensorimotor cortex or intralaminar thalamus in brain sl

173 etween RTs and activation volume in the left sensorimotor cortex (P =.048).

174 olitional inspiration included inferolateral sensorimotor cortex, prefrontal cortex and striatum (the

175 portions of the motor pathway, including the sensorimotor cortex, putamen, pallidum, and substantia n

176 dings, we tested whether beta-gamma PAC over sensorimotor cortex, recorded noninvasively with EEG, di

177 nd beta-band oscillatory brain activity over sensorimotor cortex reflected decision variables such as

178 roencephalographic (EEG) beta power over the sensorimotor cortex reflects neural processes that evalu

179 In vivo expression of p53 in the sensorimotor cortex rescued and enhanced the sprouting p

180 he modular activation of striatal neurons by sensorimotor cortex seems likely.

181 In contrast, activity in sensorimotor cortex shifted to a more dorsal locus, cons

182 EEG recordings from sensorimotor cortex show oscillations around 10 and 20 H

183 gue task (although the signal of the primary sensorimotor cortex showed a clear trend of decline).

184 r insula/secondary somatosensory cortex, the sensorimotor cortex (SI/MI), and the caudal ACC was spec

185 the layer V neurons in the wide areas of the sensorimotor cortex simultaneously control STN and ZI ne

186 reased activity in the contralateral primary sensorimotor cortex (SM1).

187 The relative hemispheric lateralization of sensorimotor cortex (SMC) activation decreased in direct

188 in the adult motor cortex after a unilateral sensorimotor cortex (SMC) lesion and treatment with mono

189 Areas of interest included the sensorimotor cortex (SMC), primary motor area (M1), prim

190 y in the primary sensorimotor cortex [EEG of sensorimotor cortex (SMC-EEG)] and a motor neuronal pool

191 current models of broad, rather than focal, sensorimotor cortex somatotopic representation.

192 degeneration following a large lesion of the sensorimotor cortex, some rubrospinal and reticulospinal

193 After photothrombotic stroke in the forelimb sensorimotor cortex, SPARC nulls demonstrate enhanced mi

194 Inosine applied with a minipump to the rat sensorimotor cortex stimulated intact pyramidal cells to

195 gether with the disturbances reported in the sensorimotor cortex, striatum, and globus pallidus, supp

196 ases in the efficiency of neural processing (sensorimotor cortex, striatum, vermis) and an increased

197 sults from maladaptive reorganization of the sensorimotor cortex, suggesting that experimental induct

198 regional CBF (rCBF) in the cingulate gyrus, sensorimotor cortex, superior temporal cortex, occipital

199 the contralateral left hemisphere, including sensorimotor cortex, supplementary motor area, and rostr

200 hin established nodes of the tremor circuit: sensorimotor cortex, thalamus, contralateral cerebellar

201 rize corticostriatal projections from rodent sensorimotor cortex, the anterograde tracers biotinylate

202 and functional degeneration in the deprived sensorimotor cortex, the experience of persistent pain i

203 oduced equivalent activation within the left sensorimotor cortex, the right cerebellum (dorsal dentat

204 myelin basic protein (MBP) and myelin in the sensorimotor cortex, the stratum radiatum, the corpus ca

205 val activity in midline cortical structures, sensorimotor cortex, the striatum, and the medial tempor

206 CP-105 reduced MAP-2 immunoreactivity in the sensorimotor cortex, there was a trend towards increased

207 n the insula and toward low frequency in the sensorimotor cortex to a greater extent than male IBS su

208 tran amine (BDA) was injected into the right sensorimotor cortex to anterogradely label the CST.

209 dition, the observed capacity of the primary sensorimotor cortex to exhibit operational heterogeneity

210 njected into either the hindlimb or forelimb sensorimotor cortex to label corticospinal axons project

211 ortex was dominated by information flow from sensorimotor cortex to STN.

212 n the alpha frequency range, particularly in sensorimotor cortex, to processing of social actions.

213 he result of the characterization of the rat sensorimotor cortex tolerance to microradiosurgical para

214 The CCI was centered over the forelimb sensorimotor cortex, unilaterally, in the adult mouse.

215 icipant was able to voluntarily activate his sensorimotor cortex using attempted movements, with dist

216 motor skill learning on WM structure within sensorimotor cortex using both diffusion MRI fractional

217 we recorded local field potentials from hand sensorimotor cortex using subdural electrocorticography

218 formation encoded by neurons in the hindlimb sensorimotor cortex was assessed.

219 The language and sensorimotor cortex was identified by standard mapping m

220 The sensorimotor cortex was located by identifying the centr

221 Functional activity in the primary sensorimotor cortex was not affected by handedness.

222 thalamus, and cerebellum, while activity in sensorimotor cortex was noted with motor tics.

223 a survival period of 12 weeks, the opposite sensorimotor cortex was stereotaxically injected with th

224 ing a unilateral injury model limited to the sensorimotor cortex, we show that inosine triples the nu

225 Finally, specific subregions of sensorimotor cortex were identified in which deep brain

226 sensory evoked potentials recorded over the sensorimotor cortex were larger and detectable over a mo

227 Partially isolated islands of sensorimotor cortex were made in 28- to 30-day-old male

228 Partially isolated islands of rat sensorimotor cortex were treated with Elvax polymer cont

229 d clinical task (localization of the primary sensorimotor cortex) were used.

230 stal area, namely the anterior sector of the sensorimotor cortex, when participants observe videos of

231 ts with stronger alpha suppression over left sensorimotor cortex, whereas the Taylor illusion correla

232 Thermal-ischemic lesions (TCL) of sensorimotor cortex, which induce axonal sprouting, prod

233 of activation responses in the ipsilesional sensorimotor cortex, which was related to T2 lesion size

234 We found that activation of the ipsilateral sensorimotor cortex with simple hand movements was incre