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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 0k injection into the contralateral motor or primary somatosensory cortex.

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

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

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

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

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

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

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

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

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

39 white matter microstructure adjacent to the primary somatosensory cortex.

40 ally appropriate digit representation in the primary somatosensory cortex.

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

42 dules are called "barrels" in layer 4 of the 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 ker of neuronal activity) in layer IV of the primary somatosensory cortex and increased immunoreactiv

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

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

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

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

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

56 udes measured from individual neurons in the primary somatosensory cortex and putamen strongly correl

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

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

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

60 verwhelmingly from the primary motor cortex, primary somatosensory cortex, and secondary motor cortex

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

81 raphic representation of the whiskers in the primary somatosensory cortex (barrel field) of adult mic

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

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

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

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

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

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

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

89 idocaine also had significantly greater mean primary somatosensory cortex cortical volume and functio

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

91 Activation in the primary somatosensory cortex displayed a laminar sequenc

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

93 Recording in vivo from neurons in primary somatosensory cortex during tactile stimulation,

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

95 d by a reduction in neuronal activity in the primary somatosensory cortex dysgranular zone (S1DZ), th

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

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

98 The primary somatosensory cortex exhibited significant 2DG u

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

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

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

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

103 3 and layer 5 pyramidal neurons in slices of primary somatosensory cortex from C57Bl6 mice on postnat

104 (2017) find a novel map of external space in primary somatosensory cortex, generated by multi-whisker

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 Primary somatosensory cortex is located in the neocortex

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

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

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

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

126 In conclusion, primary somatosensory cortex neuroplasticity for median

127 secondary motor cortex, corpus callosum, and primary somatosensory cortex of adult mice.

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

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

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

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

132 In the primary somatosensory cortex of the rat vibrissa pathway

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

134 The barrel cortex is within the primary somatosensory cortex of the rodent, and processe

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

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

137 caused an increase in neuronal activation in primary somatosensory cortex of young mice and behaviora

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

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

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

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

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

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

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

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

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

147 e ACC were reduced to a similar degree as in primary somatosensory cortex, revealing differential low

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

149 uli, we observed strong signal activation in primary somatosensory cortex (S1) and frontal cortices,

150 y dependent on the communication between the primary somatosensory cortex (S1) and higher-order integ

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

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

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

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

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

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

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

158 onal responses collected simultaneously from primary somatosensory cortex (S1) and ventral premotor c

159 Layer (L) 2/3 pyramidal neurons in the primary somatosensory cortex (S1) are sparsely active, s

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

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

162 Intracortical microstimulation (ICMS) of the primary somatosensory cortex (S1) can produce percepts t

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

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

165 Direct cortical stimulation (DCS) of primary somatosensory cortex (S1) could help restore sen

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

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

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

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

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

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

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

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

174 d the hypothesis that synaptic structures of primary somatosensory cortex (S1) neurons in Fragile X s

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

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

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

178 In primary somatosensory cortex (S1) of mice, layer 5 (L5)

179 el local field potential (LFP) recordings in primary somatosensory cortex (S1) of the awake mouse, we

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

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

182 Whether primary somatosensory cortex (S1) participates in tempor

183 Primary somatosensory cortex (S1) receives two distinct

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

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

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

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

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

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

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

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

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

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

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

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

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

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

198 Here, we investigate the projection from the primary somatosensory cortex (S1), which encodes the sen

199 estigated how OFC dynamically interacts with primary somatosensory cortex (S1).

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

201 topic representation of the affected limb in primary somatosensory cortex (S1).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

221 Barrel subfields in rodent primary somatosensory cortex (SI) are important model sy

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

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

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

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

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

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

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

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

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

231 The primary somatosensory cortex (SI) is topographically org

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

265 avior is mediated by the projection from the primary somatosensory cortex (SSp) to the ventral sector

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

267 As these primary somatosensory cortex subregions are distinctly t

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

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

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

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

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

273 The reorganisation of primary somatosensory cortex that occurs after lesioning

274 for a direct corticospinal pathway from the primary somatosensory cortex that synapses with cervical

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

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

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

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

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

280 Here we show that neuronal activity in the primary somatosensory cortex tightly correlates with the

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

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

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

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

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

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

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

288 vivo population calcium imaging in vibrissa primary somatosensory cortex (vS1) revealed increased sp

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

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

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

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

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

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

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

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

297 raining enhances stimulus selectivity in the primary somatosensory cortex while maintaining perceptua

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

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

300 in reactivity within human (male and female) primary somatosensory cortex yet blunts pain reactivity