ライフサイエンスコーパス: primary somatosensory cortex

1 leus of the thalamus and subsequently to the primary somatosensory cortex.

2 teral lower and higher tier visual areas and primary somatosensory cortex.

3 m the callosum, the internal capsule, or the primary somatosensory cortex.

4 pain-related activation of the contralateral primary somatosensory cortex.

5 intracortical microstimulation (ICMS) of the primary somatosensory cortex.

6 in the whiskers' representations within the primary somatosensory cortex.

7 pillaries at different depths within the rat primary somatosensory cortex.

8 ng overproduction of transient spines in the primary somatosensory cortex.

9 ar thalamic nucleus, retrosplenial cortex or primary somatosensory cortex.

10 tation at the somatosensory periphery and in primary somatosensory cortex.

11 tools to study neurovascular coupling in rat primary somatosensory cortex.

12 l fraction of layer 2/3 neurons of the mouse primary somatosensory cortex.

13 cluding vibrissa-related 'barrel' columns in primary somatosensory cortex.

14 CM cells originate from area 3a, a region of primary somatosensory cortex.

15 t2 projection from the hypothalamus than the primary somatosensory cortex.

16 to the medial prefrontal cortex than to the primary somatosensory cortex.

17 stem, but a more general property of the rat primary somatosensory cortex.

18 lamus relays trigeminal sensory input to the primary somatosensory cortex.

19 tex but a more general characteristic of the primary somatosensory cortex.

20 0k injection into the contralateral motor or primary somatosensory cortex.

21 nt, which has also been localized to SI, the primary somatosensory cortex.

22 is: the medullary dorsal horn, thalamus, and primary somatosensory cortex.

23 icity of the whisker map in layer 2/3 of rat primary somatosensory cortex.

24 ned by their different representation in the primary somatosensory cortex.

25 dial barrel subfield (PMBSF) of rat layer IV primary somatosensory cortex.

26 pyramidal cells in organotypic slices of rat primary somatosensory cortex.

27 represented in the trunk region of the left primary somatosensory cortex.

28 array) normally found in layer IV of rodent primary somatosensory cortex.

29 body are conveyed by the spinal cord to the primary somatosensory cortex.

30 ally appropriate digit representation in the primary somatosensory cortex.

31 ry thalamus, thalamic reticular nucleus, and primary somatosensory cortex.

32 dules are called "barrels" in layer 4 of the primary somatosensory cortex.

33 white matter microstructure adjacent to the primary somatosensory cortex.

34 reserved OD plasticity after a stroke in the primary somatosensory cortex.

35 ine elevation on synaptic connections in the primary somatosensory cortex.

36 g--through intracortical microstimulation of primary somatosensory cortex.

37 olescent exposure than the earlier-maturing, primary somatosensory cortex.

38 tongue, teeth, and other representations in primary somatosensory cortex.

39 a region involved in mood disorders, and of primary somatosensory cortex.

40 g in the genital representation field of the primary somatosensory cortex.

41 spatially-organised, somatotopic map in the primary somatosensory cortex.

42 into each digit representation in area 3b of primary somatosensory cortex.

43 tive input to individual digits in the human primary somatosensory cortex [4].

44 ith decreased thalamic reticular nucleus and primary somatosensory cortex activity (quantitative arte

45 aracterize anatomical changes in layer IV of primary somatosensory cortex after a brief period of sen

46 y labeled cell bodies within area 1/2 of the primary somatosensory cortex after M1 injury.

47 Primary somatosensory cortex and adjoining somatosensory

48 located in the border of layers 1 and 2 from primary somatosensory cortex and found that practically

49 somatosensory-evoked multiunit activity from primary somatosensory cortex and from the locus coeruleu

50 he number of NGF-immunoreactive cells in the primary somatosensory cortex and magnocellular preoptic

51 key mediator of synaptic instability in the primary somatosensory cortex and may contribute to senso

52 work includes phasic components, centered on primary somatosensory cortex and neighboring motor, prem

53 long been thought to be accomplished by the primary somatosensory cortex and other structures associ

54 sional contralesional forelimb region of the primary somatosensory cortex and primary motor cortex at

55 ggest that texture-sensitive activity in the primary somatosensory cortex and superior parietal lobul

56 ACC and right M1, and decreased GM in right primary somatosensory cortex and thalamus.

57 e-induced Arc expression in the hippocampus, primary somatosensory cortex, and dorsal striatum of rat

58 he anterior mid-cingulate cortex (aMCC), the primary somatosensory cortex, and the posterior insula.

59 d more robust pain-induced activation of the primary somatosensory cortex, anterior cingulate cortex,

60 hat spontaneously occurring UP states in the primary somatosensory cortex are 38-67% longer in Fmr1 K

61 showed that the whiskers and activity in the primary somatosensory cortex are involved during the dis

62 th contralateral M1 rostral, FR, AO, and the primary somatosensory cortex are lower than percentages

63 e representation of the reinnervated hand in primary somatosensory cortex area (area 3b) is quite ord

64 icroelectrode arrays in the hand area of the primary somatosensory cortex (area 1) in two awake macaq

65 extent of the hand representation in monkey primary somatosensory cortex (area 3b) interact, even wh

66 imaging (fMRI) of the hand representation in primary somatosensory cortex (area 3b) of macaque monkey

67 ations of the tongue, teeth, and face in the primary somatosensory cortex (area 3b) of macaque monkey

68 the hand representation in the contralateral primary somatosensory cortex (area 3b) of monkeys is lar

69 the hand representation of the contralateral primary somatosensory cortex (area 3b) unresponsive.

70 tions of the hand and arm representations in primary somatosensory cortex (area 3b), become responsiv

71 Other areas evoking movements included primary somatosensory cortex (area 3b), two lateral soma

72 the deafferented hand representation in the primary somatosensory cortex (area 3b), ventroposterior

73 the territory of the hand representations in primary somatosensory cortex (area 3b).

74 ses to hand stimulation in the contralateral primary somatosensory cortex (area 3b).

75 nnectivity within the hand representation of primary somatosensory cortex (areas 3b and 1) in anesthe

76 and in three regions post-mFPI: impact site, primary somatosensory cortex barrel field (S1BF), and a

77 trigger cross-modal synaptic changes in the primary somatosensory cortex barrel fields, but is insuf

78 ers; into the whisker-related regions of the primary somatosensory cortex (barrel field cortex [BC]),

79 long-range horizontally projecting axons in primary somatosensory cortex before and after selective

80 y between the spinal C6-DH and the thalamus, primary somatosensory cortex, bilateral insula, bilatera

81 ple levels of the sensory pathway, including primary somatosensory cortex, brainstem, and dorsal root

82 eted neurons, synchronous neural activity in primary somatosensory cortex can contribute to discrimin

83 The hand area of the primary somatosensory cortex contains detailed finger to

84 stimuli, we observed a signal change in the primary somatosensory cortex contralateral to the stimul

85 aration distance (P < 0.05) in contralateral primary somatosensory cortex, corroborating our previous

86 quently, the face representation area of the primary somatosensory cortex diminishes in size.

87 Activation in the primary somatosensory cortex displayed a laminar sequenc

88 Responses of neurons in the primary somatosensory cortex during movements are poorly

89 pendent integration of SPn neurites into the primary somatosensory cortex during the period of barrel

90 ng hand's individual fingers persists in the primary somatosensory cortex even decades after arm ampu

91 strength of excitatory synapses within mouse primary somatosensory cortex exhibit a critical period t

92 The primary somatosensory cortex exhibited significant 2DG u

93 ary motor cortex (face-M1) and adjacent face primary somatosensory cortex (face-S1) during OTM.

94 primary motor cortex (face-M1) and adjacent primary somatosensory cortex (face-S1) is crucial for un

95 the medial prefrontal cortex and 96% for the primary somatosensory cortex) followed by the hypothalam

96 atotopically distinct neuroplasticity in the primary somatosensory cortex following therapy.

97 3 and layer 5 pyramidal neurons in slices of primary somatosensory cortex from C57Bl6 mice on postnat

98 (2017) find a novel map of external space in primary somatosensory cortex, generated by multi-whisker

99 ectrode measurement of multiunit activity in primary somatosensory cortex in a sensory-evoked, in viv

100 (cTBS) to condition the excitability of the primary somatosensory cortex in healthy humans to examin

101 tile stimulation generated in area 3b of the primary somatosensory cortex in patients with schizophre

102 ar as 600 micrometers below the pia mater of primary somatosensory cortex in rat; this depth encompas

103 eep layers of the forelimb region of the rat primary somatosensory cortex in response to step stimuli

104 re, we used voltage-sensitive dye imaging of primary somatosensory cortex in the anesthetized rat in

105 nfluence of primary motor cortex activity on primary somatosensory cortex in the mouse whisker system

106 e a representation of eye position in monkey primary somatosensory cortex, in the representation of t

107 Expression was highest in layer IV of primary somatosensory cortex; in frontal and secondary s

108 ponses of topographically aligned neurons in primary somatosensory cortex, including antidromically i

109 ng) into layer VI or onto the surface of the primary somatosensory cortex induced increases in the ne

110 is factor alpha (TNFalpha) (150 ng) onto the primary somatosensory cortex induces state-dependent asy

111 n of pain-related brain regions, such as the primary somatosensory cortex, insular cortex, and ACC.

112 ons in the hand representation of area 3b of primary somatosensory cortex, interhemispheric interacti

113 spread beyond the PMBSF and sometimes beyond primary somatosensory cortex into the neighboring dysgra

114 ibited dramatically elevated activity of the primary somatosensory cortex ipsilateral to the lesioned

115 organization where nearly one-third (31%) of primary somatosensory cortex is devoted to the represent

116 Primary somatosensory cortex is located in the neocortex

117 Brodmann area (BA) 3a of the primary somatosensory cortex is part of an ascending pat

118 Barrel cortex, the whisker representation of primary somatosensory cortex, is required for the learni

119 h structural and functional anomalies in the primary somatosensory cortex may underlie orofacial tact

120 g and electrophysiology, we found that mouse primary somatosensory cortex neurons showed robust choic

121 In conclusion, primary somatosensory cortex neuroplasticity for median

122 question, we performed paired recordings in primary somatosensory cortex of mice lacking NL1 or NL2.

123 A major portion of the primary somatosensory cortex of rodents is characterized

124 tional and structural neuroplasticity in the primary somatosensory cortex of the brain.

125 a whisker's functional representation in the primary somatosensory cortex of the rat increases substa

126 In the primary somatosensory cortex of the rat vibrissa pathway

127 n-releasing hormone (CRH) was studied in the primary somatosensory cortex of the rat.

128 rray implanted in the hand representation of primary somatosensory cortex of two anesthetized owl mon

129 synapsin I and Golgi-Cox stained neurons in primary somatosensory cortex of unilaterally whisker-dep

130 to activate, among others, the contralateral primary somatosensory cortex on the postcentral gyrus to

131 within a large region of midrostral cortex (primary somatosensory cortex, or S1).

132 as much as 80% of the thalamic projection to primary somatosensory cortex originate in various relay

133 ogical recordings reveal that stimulation of primary somatosensory cortex potently suppresses SpVc re

134 e number of Fos- and IL1beta-IR cells in the primary somatosensory cortex relative to the contralater

135 alpha- and low beta-band (8-20 Hz) cycles in primary somatosensory cortex represent neurophysiologica

136 tion distance for each digit's contralateral primary somatosensory cortex representation was assessed

137 We found that neurons in bat primary somatosensory cortex respond with directional se

138 nd acute suppression of neuronal activity in primary somatosensory cortex resulted in a striking enla

139 e ventroposterior lateral thalamus (VPL) and primary somatosensory cortex (S1) 7 d after SCI.

140 provide new details for the organization of primary somatosensory cortex (S1) and identify cortical

141 de recordings in postnatal day 3 (P3)-P5 rat primary somatosensory cortex (S1) and M1 in vivo, we obs

142 of the contralateral body, corresponding to primary somatosensory cortex (S1) and secondary somatose

143 ase were used to determine the topography of primary somatosensory cortex (S1) and the location and s

144 continuity was found to be disturbed at the primary somatosensory cortex (S1) and the supplementary

145 iring within both the distinct layers of the primary somatosensory cortex (S1) and the ventral poster

146 we investigate neuronal responses in the rat primary somatosensory cortex (S1) and ventral posterior

147 p sensory digit representations in the human primary somatosensory cortex (S1) at the level of indivi

148 The primary somatosensory cortex (S1) can be subdivided cyto

149 The primary somatosensory cortex (S1) contains a complete bo

150 ld, the responsiveness and somatotopy of the primary somatosensory cortex (S1) contralateral to the h

151 Pyramidal neurons in layers 2/3 and 5 of primary somatosensory cortex (S1) exhibit somewhat modes

152 Studies of human primary somatosensory cortex (S1) have placed a strong e

153 Recordings from primary somatosensory cortex (S1) in anesthetized mice i

154 er associative plasticity is abnormal in the primary somatosensory cortex (S1) in FHD and whether PAS

155 leus (VPL) of the somatosensory thalamus and primary somatosensory cortex (S1) in two macaque monkeys

156 etic response adaptation patterns within the primary somatosensory cortex (S1) in young adult humans.

157 atotopic barrel pattern in developing rodent primary somatosensory cortex (S1) is not prevented by ac

158 , are encoded in the responses of neurons in primary somatosensory cortex (S1) is unknown.

159 ted functional response observed in deprived primary somatosensory cortex (S1) may be the result of a

160 Prominent 7-12 Hz oscillations in the primary somatosensory cortex (S1) of awake but immobile

161 e modular "barrel" organization found in the primary somatosensory cortex (S1) of mice and rats, but

162 ce in sculpting an inhibitory circuit in the primary somatosensory cortex (S1) of mice by using optog

163 used ultrasound (tFUS) targeted to the human primary somatosensory cortex (S1) on sensory-evoked brai

164 GdDOTA-CTB was injected into the primary somatosensory cortex (S1) or the olfactory pathw

165 Whether primary somatosensory cortex (S1) participates in tempor

166 Primary somatosensory cortex (S1) receives two distinct

167 Neurons of the primary somatosensory cortex (S1) respond as functions o

168 nucleus of the somatosensory thalamus and in primary somatosensory cortex (S1) respond to vibrotactil

169 In a parallel analogous pathway, the whisker primary somatosensory cortex (S1) strongly projects to t

170 by a periodic ICMS pattern delivered to the primary somatosensory cortex (S1) through a pair of impl

171 w that the topography of the projection from primary somatosensory cortex (S1) to the SC is establish

172 tomy around a representational border in rat primary somatosensory cortex (S1), a novel in vivo/in vi

173 One of the representations appears to be primary somatosensory cortex (S1), and it contained cyto

174 e lack of inputs from the face region of the primary somatosensory cortex (S1), and only about half a

175 representation in primary motor cortex (M1), primary somatosensory cortex (S1), and supplementary mot

176 he production of spindle bursts (SBs) within primary somatosensory cortex (S1), most notably during p

177 a shared somatosensory representation in the primary somatosensory cortex (S1), putatively involved i

178 isocortical motor area (ProM), ventrolateral primary somatosensory cortex (S1), rostral insula, and p

179 In primary somatosensory cortex (S1), the transition from o

180 Single neurons located in the primary somatosensory cortex (S1), the ventroposterior m

181 eport that the primary motor cortex (M1) and primary somatosensory cortex (S1), two adjacent but func

182 fect of subplate removal in the neonatal rat primary somatosensory cortex (S1).

183 orepaw stimulation excited the contralateral primary somatosensory cortex (S1).

184 o the contralateral side of the brain in the primary somatosensory cortex (S1).

185 provide a panoramic view of IR sources, into primary somatosensory cortex (S1).

186 ization of the finger representations in the primary somatosensory cortex (S1).

187 as delineated a neural network that bypasses primary somatosensory cortex (S1).

188 as identified a neural network that bypasses primary somatosensory cortex (S1).

189 mal neuronal hypoactivity in the non-injured primary somatosensory cortex (S1).

190 ere recorded from primary motor cortex (M1), primary somatosensory cortex (S1, areas 3a and 2), poste

191 sponse to stimulation of the barrel field in primary somatosensory cortex (S1BF), which was eliminate

192 euronal responses in the barrel field of the primary somatosensory cortex (S1bf).

193 ion encompassing the dysgranular zone of the primary somatosensory cortex (S1DZ).

194 ional connectivity was detected in bilateral primary somatosensory cortex (S1FL) of the resting brain

195 which is classically considered part of the primary somatosensory cortex, should be reclassified as

196 found in major somatosensory regions, i.e., primary somatosensory cortex SI, secondary somatosensory

197 odification of the response of contralateral primary somatosensory cortex (SI and SII) to skin mechan

198 the intensity of cerebral activation in the primary somatosensory cortex (SI) (bilateral) and left m

199 was mainly generated from the contralateral primary somatosensory cortex (SI) and bilateral secondar

200 ion of laser-induced activity in ipsilateral primary somatosensory cortex (SI) and contralateral oper

201 on perception in visual motion area V5/hMT+, primary somatosensory cortex (SI) and posterior parietal

202 cortical connections in lamina IV of the rat primary somatosensory cortex (SI) are most dense outside

203 d oscillations (GBOs) induced over the human primary somatosensory cortex (SI) by nociceptive stimuli

204 The rodent primary somatosensory cortex (SI) contains a map of the

205 stimulation of the hand was observed in the primary somatosensory cortex (SI) hand area, which was c

206 Thirty-eight neurons in the primary somatosensory cortex (SI) in alpha-chloralose/Ne

207 least up to and including the input stage of primary somatosensory cortex (SI) in primates, area 3b.

208 ve fields in the stump representation of the primary somatosensory cortex (SI) in rats that sustained

209 en blood flow and glucose consumption in rat primary somatosensory cortex (SI) in vivo.

210 racterization by showing that 5 Hz rTMS over primary somatosensory cortex (SI) induces a reconfigurat

211 The primary somatosensory cortex (SI) is topographically org

212 ibrissa resonance in trigeminal ganglion and primary somatosensory cortex (SI) neurons (regular and f

213 specificity to trigeminal ganglion (NV) and primary somatosensory cortex (SI) neurons during suprath

214 oposterior medial thalamic nucleus (VPM) and primary somatosensory cortex (SI) of awake, freely movin

215 ss the development of projections within the primary somatosensory cortex (SI) of rats aged between p

216 veloping thalamocortical afferents (TCAs) in primary somatosensory cortex (SI) of rats and mice.

217 in and extent of axons within layer I of the primary somatosensory cortex (SI) of rats by using retro

218 ateral peripheral nerve injury, the deprived primary somatosensory cortex (SI) responds to stimulatio

219 Orderly topographic maps in the primary somatosensory cortex (SI) serve as an anchor for

220 tion in the forepaw barrel subfield (FBS) of primary somatosensory cortex (SI) that follows forelimb

221 f the global neuronal population response of primary somatosensory cortex (SI) that has been demonstr

222 ng in the major proprioceptive region of the primary somatosensory cortex (SI) that is conventionally

223 topography of the cortical pathway from the primary somatosensory cortex (SI) that may deliver vibri

224 show with optical imaging in area 3b of the primary somatosensory cortex (SI) that simultaneous stim

225 intrinsic signal response of squirrel monkey primary somatosensory cortex (SI) to 25 Hz vibrotactile

226 al contrast in the response of contralateral primary somatosensory cortex (SI) to mechanical skin sti

227 fMRI, a reduced centrality of contralateral primary somatosensory cortex (SI) was found, which appea

228 ded in each layer of the whisker area of the primary somatosensory cortex (SI) while rats performed a

229 nt activations in contralateral insula, SII, primary somatosensory cortex (SI), inferior parietal lob

230 or nociceptive inputs to the digits in human primary somatosensory cortex (SI).

231 terminate in largely separate regions of the primary somatosensory cortex (SI).

232 somatosensory information from the VP to the primary somatosensory cortex (SI).

233 important front teeth, accounting for 30% of primary somatosensory cortex (SI).

234 as induced by collagenase injection into the primary somatosensory cortex (SI).

235 understanding of these processes in the rat primary somatosensory cortex (SI).

236 medial nucleus (VPM) of the thalamus and the primary somatosensory cortex (SI).

237 the mystacial vibrissae in lamina IV of the primary somatosensory cortex (SI).

238 as 3a (proprioception) and 3b (cutaneous) of primary somatosensory cortex (SI).

239 ond stimulation relative to the first in the primary somatosensory cortex (SI).

240 Top-down axons projecting from secondary to primary somatosensory cortex signaled choice.

241 we show, in awake monkeys, that a subset of primary somatosensory cortex single units consistently f

242 n neuronal activity in the vibrissal area of primary somatosensory cortex: single units responded dif

243 study further suggests that improvements in primary somatosensory cortex somatotopy can predict long

244 rd dorsal horn neurons to stimulation of the primary somatosensory cortex (SSC).

245 cal cell cultures and microinjected into the primary somatosensory cortex (SSctx) of rats.

246 cases targeting primary motor cortex (MOp), primary somatosensory cortex (SSp), and caudoputamen (CP

247 As these primary somatosensory cortex subregions are distinctly t

248 x and in the whisker-barrel fields of rodent primary somatosensory cortex suggest common organizing p

249 These studies of spine dynamics in the primary somatosensory cortex suggest that experience pla

250 ular within the parietal association and the primary somatosensory cortex, suggesting that the closer

251 g four main functions: sensation-perception (primary somatosensory cortex, thalamus and insula); atte

252 We found a select population of neurons in primary somatosensory cortex that are transiently excite

253 The reorganisation of primary somatosensory cortex that occurs after lesioning

254 made electrophysiological recordings in rat primary somatosensory cortex that was undergoing experie

255 (M1), the rostromedial motor area (M2), the primary somatosensory cortex, the insula and other regio

256 y gray matter protoplasmic astrocytes of the primary somatosensory cortex, the thalamic ventrobasal n

257 In the primary somatosensory cortex, these binding sites were a

258 ns of cortical microstimulation delivered to primary somatosensory cortex through chronically implant

259 Specifically, we deliver ICMS to primary somatosensory cortex through chronically implant

260 ogram (EEG) were obtained in the vicinity of primary somatosensory cortex, time-locked to repetitive

261 Granger causal influences were observed from primary somatosensory cortex to both motor cortex and in

262 ubiquitous on and off responses observed in primary somatosensory cortex to complement slowly varyin

263 he hindpaw representational area of the left primary somatosensory cortex to electrical stimulation o

264 well-characterized development of the murine primary somatosensory cortex to examine cortical maturat

265 nctional topography, and connectivity of the primary somatosensory cortex using psychophysics and fun

266 resonance imaging assessed somatotopy in the primary somatosensory cortex using vibrotactile stimulat

267 ellular activity of up to 135 neurons in the primary somatosensory cortex, ventral posterior medial n

268 areas similar to rectal stimulation, but the primary somatosensory cortex was activated at a more sup

269 ortical separation distance in contralateral primary somatosensory cortex was associated with worse s

270 oreover, activity in the left BA44, BA6, and primary somatosensory cortex was correlated with subject

271 Second, when pain-related activation of the primary somatosensory cortex was examined during left- a

272 dual thalamocortical axons in developing rat primary somatosensory cortex was studied using lipophili

273 measure responses of networks of neurons in primary somatosensory cortex, we discovered that associa

274 touch to the face activated the head area of primary somatosensory cortex, whereas observation of tou

275 ling in the posteromedial barrel subfield of primary somatosensory cortex, which can be divided into

276 earning-related changes were observed in the primary somatosensory cortex, which mediates the uncondi

277 percepts, begins as early as area 3b in the primary somatosensory cortex with the involvement of int

278 on defined by dense innervation from whisker primary somatosensory cortex (wS1).