ライフサイエンスコーパス: somatosensory cortex

1 or temporal sulcus, pSTS) and interoception (somatosensory cortex).

2 ion of sensory processing regions (secondary somatosensory cortex).

3 m (i.e. the anatomical site of the secondary somatosensory cortex).

4 ant anatomical and functional changes in the somatosensory cortex.

5 atter microstructure adjacent to the primary somatosensory cortex.

6 nal growth protein GAP43 in the ipsilesional somatosensory cortex.

7 dicted by a marker of iron content in second somatosensory cortex.

8 ices and between the dorsal striatum and the somatosensory cortex.

9 sensory periphery to activity in developing somatosensory cortex.

10 n ventrobasal thalamus, CA1 hippocampus, and somatosensory cortex.

11 the central pain matrix: the insula and the somatosensory cortex.

12 g ventrolateral prefrontal cortex and second somatosensory cortex.

13 or areas in the frontal lobe and portions of somatosensory cortex.

14 overlapping classes of interneurons in mouse somatosensory cortex.

15 ropriate digit representation in the primary somatosensory cortex.

16 , progressively increases after birth in the somatosensory cortex.

17 mus, thalamic reticular nucleus, and primary somatosensory cortex.

18 in 102 (SAP102), on development of the mouse somatosensory cortex.

19 e called "barrels" in layer 4 of the primary somatosensory cortex.

20 ze of cortical fields and the connections of somatosensory cortex.

21 halamic neurons that project directly to the somatosensory cortex.

22 ), thalamus, inferior visual cortex, and the somatosensory cortex.

23 s and single-unit action potentials from the somatosensory cortex.

24 fine the point representation in L2 of mouse somatosensory cortex.

25 d within primary, secondary, and associative somatosensory cortex.

26 of layer 5 (L5) pyramidal neurons of the rat somatosensory cortex.

27 ecorded with two-photon imaging in motor and somatosensory cortex.

28 he survival of divided cells in the deprived somatosensory cortex.

29 to form aggregates such as barrels in rodent somatosensory cortex.

30 n the brainstem, midbrain, thalamus, and the somatosensory cortex.

31 with injection of 4-aminopyridine (4-AP) in somatosensory cortex.

32 painful DSP phenotype and alterations in the somatosensory cortex.

33 perisomatic and dendritic inhibition in the somatosensory cortex.

34 d ventricles, and decreased thickness of the somatosensory cortex.

35 /-), 16p11.2(del/+), Tsc2(+/-)), focusing on somatosensory cortex.

36 inate mainly from 2 motor areas and adjacent somatosensory cortex.

37 In somatosensory cortex, activity related to movement of di

38 F1, F5, PEip, and somatosensory cortex also showed deactivations during sa

39 ain behavior, theta (4-8 Hz) oscillations in somatosensory cortex and burst firing in thalamic neuron

40 elligence implicate pyramidal neurons of the somatosensory cortex and CA1 region of the hippocampus,

41 he SDC criterion to data from rat visual and somatosensory cortex and discovered that the connectivit

42 Somatosensory inputs from the somatosensory cortex and dorsal column nuclei were found

43 nsory-evoked multiunit activity from primary somatosensory cortex and from the locus coeruleus (LC) (

44 lood volume (CBV) and neural activity in the somatosensory cortex and frontal cortex of head-fixed mi

45 ume alter the functional organization of the somatosensory cortex and how this relates to the various

46 euronal activity) in layer IV of the primary somatosensory cortex and increased immunoreactive cells

47 ludes phasic components, centered on primary somatosensory cortex and neighboring motor, premotor, an

48 sured from individual neurons in the primary somatosensory cortex and putamen strongly correlated wit

49 anatomical and functional changes within the somatosensory cortex and severity of the peripheral neur

50 at texture-sensitive activity in the primary somatosensory cortex and superior parietal lobule influe

51 Input from somatosensory cortex and thalamus converges in individua

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

53 rning-related plasticity is also observed in somatosensory cortex, and accordingly, it may also be in

54 ow locomotion modulates neuronal activity in somatosensory cortex, and how it is integrated with whis

55 eled by fear behavior, reduced activation of somatosensory cortex, and increased activation of the ba

56 ty of sensory regions, reduced activation of somatosensory cortex, and increased activation of the ba

57 d was used to locally disrupt the BBB in rat somatosensory cortex, and intravenous administration of

58 This information is processed in the somatosensory cortex, and it has long been presumed that

59 the ventral striatum, anterior cingulate and somatosensory cortex, and negatively in the precuneus an

60 uron packing include secondary visual areas, somatosensory cortex, and prefrontal granular cortex.

61 ingly from the primary motor cortex, primary somatosensory cortex, and secondary motor cortex, region

62 k to rat S1: primary motor cortex, secondary somatosensory cortex, and secondary somatosensory thalam

63 ove, or below the resonance frequency of the somatosensory cortex, and tested subjects' accuracy and

64 ensory processing and integration (fusiform, somatosensory cortex, and thalamus), salience detection

65 abnormal homeostatic activity regulation of somatosensory cortex, and that enhancing cortical excita

66 Conversely, SCl, M2, somatosensory cortex, and the granular retrospenial cort

67 Corticostriatal neurons in motor and somatosensory cortex are implicated in these symptoms, y

68 uts from distinct somatotopic regions of the somatosensory cortex are integrated at the level of sing

69 hat the whiskers and activity in the primary somatosensory cortex are involved during the discriminat

70 3-fold between species ranging from 0.5% of somatosensory cortex area in chipmunks to 1.7% in rats.

71 f the tongue, teeth, and face in the primary somatosensory cortex (area 3b) of macaque monkeys.

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

73 neurons in the hand region in contralateral somatosensory cortex (areas 3b and 1).

74 Using human somatosensory cortex as a model, we investigated the eff

75 ariability in perceptual acuity, using human somatosensory cortex as a model.

76 We find that neurons in the somatosensory cortex, as well as in the motor cortex, pr

77 hree regions post-mFPI: impact site, primary somatosensory cortex barrel field (S1BF), and a remote r

78 epresentation of the whiskers in the primary somatosensory cortex (barrel field) of adult mice with d

79 neural modules represent each whisker in the somatosensory cortex ("barrels"), thalamus ("barreloids"

80 nge horizontally projecting axons in primary somatosensory cortex before and after selective whisker

81 n addition, we found close correspondence in somatosensory cortex between connectivity that we reveal

82 n the spinal C6-DH and the thalamus, primary somatosensory cortex, bilateral insula, bilateral striat

83 te cortex (ACC), left insula, left secondary somatosensory cortex, bilateral thalamus, and decreased

84 on for observed touch in the hand regions of somatosensory cortex but rather in superior and inferior

85 f thalamocortical (TC) axons innervating the somatosensory cortex, but did not affect the segregation

86 ons and pyramidal cells are prominent in the somatosensory cortex by postnatal day (P) 7.

87 Relative to cathodal tDCS over the left somatosensory cortex, cathodal tDCS over the left vlPFC

88 arge and robust hemodynamic responses in the somatosensory cortex, characterized by fast arterial act

89 the left vlPFC versus a control region, left somatosensory cortex, concurrently with neuroimaging.

90 ponsive hand representation in contralateral somatosensory cortex confirmed the effectiveness of the

91 The hand area of the primary somatosensory cortex contains detailed finger topography

92 The tCDA manifests over somatosensory cortex contralateral to task-relevant tact

93 ivity component with a scalp topography over somatosensory cortex contralateral to the cued hand.

94 In the putative somatosensory cortex contralateral to the stimulus, 2 we

95 , we observed a signal change in the primary somatosensory cortex contralateral to the stimulus.

96 h spike-rate and spike-timing information in somatosensory cortex contribute to their perceptual deci

97 also had significantly greater mean primary somatosensory cortex cortical volume and functional conn

98 L2 neurons projecting to motor and secondary somatosensory cortex differed in whisker tuning and resp

99 y for neural control of movement whereby the somatosensory cortex directly influences motor behavior,

100 ns in the juvenile (P18 to 27) mouse whisker somatosensory cortex, distinguished by expression of the

101 coupling in layer 2/3 of the mouse vibrissal somatosensory cortex during active tactile discriminatio

102 neurons in the prefrontal and primary motor--somatosensory cortex during mid-fetal development in aut

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

104 m to record neuronal network activity in the somatosensory cortex during sensory stimulation.

105 Recording in vivo from neurons in primary somatosensory cortex during tactile stimulation, we foun

106 ays critical roles in the development of the somatosensory cortex during the neonatal period.

107 eduction in neuronal activity in the primary somatosensory cortex dysgranular zone (S1DZ), the hypera

108 hypothalamic nucleus, primary and secondary somatosensory cortex, ectorhinal cortex, and dorsolatera

109 s individual fingers persists in the primary somatosensory cortex even decades after arm amputation.

110 Intracortical microstimulation (ICMS) of the somatosensory cortex evokes vivid tactile sensations and

111 In controls, a region of secondary somatosensory cortex exhibited attenuated activation whe

112 r cortex (face-M1) and adjacent face primary somatosensory cortex (face-S1) during OTM.

113 motor cortex (face-M1) and adjacent primary somatosensory cortex (face-S1) is crucial for understand

114 r, the degree of amplified reactivity within somatosensory cortex following sleep deprivation signifi

115 ally distinct neuroplasticity in the primary somatosensory cortex following therapy.

116 implicit learning processes, suppression of somatosensory cortex following training almost entirely

117 ns simultaneously in slice cultures of mouse somatosensory cortex for 1 h at a time.

118 BF with laser Doppler flowmetry in the rat's somatosensory cortex for both resting state and forepaw

119 The digital reconstruction of a slice of rat somatosensory cortex from the Blue Brain Project provide

120 l insula, medial cingulate cortex, secondary somatosensory cortex, frontal areas, and cerebellum.

121 Similar to observations in the somatosensory cortex, FS V1 cells received less specific

122 KEY POINTS: It has long been known that the somatosensory cortex gates sensory inputs from the contr

123 ind a novel map of external space in primary somatosensory cortex, generated by multi-whisker interac

124 studies of area 2, a proprioceptive area of somatosensory cortex, have simply compared neurons' acti

125 We identified genital responses in rat somatosensory cortex in a region previously assigned as

126 to condition the excitability of the primary somatosensory cortex in healthy humans to examine its po

127 ulness on neuronal activity in the motor and somatosensory cortex in mice.

128 nctional disorganisation was reported in the somatosensory cortex in patients.

129 sed voltage-sensitive dye imaging of primary somatosensory cortex in the anesthetized rat in response

130 the origins of sensory input to the neonatal somatosensory cortex in the natural environment remain l

131 on on GABAergic synaptic transmission in rat somatosensory cortex in vitro.

132 (2+) also induce similar plasticity in mouse somatosensory cortex in vivo.

133 ed to activation in several areas, including somatosensory cortex, insula, superior temporal gyrus, s

134 We confirmed that cTBS to somatosensory cortex interfered with normal sensory func

135 Increased alpha-band power in the somatosensory cortex ipsilateral to the selected arm was

136 ring critical period (CP) development in the somatosensory cortex is delayed, but it is unclear how t

137 We show that TC synaptic transmission in somatosensory cortex is enhanced in FHM1 mice.

138 shows that the spatial map of the fingers in somatosensory cortex is largely preserved in chronic com

139 Primary somatosensory cortex is located in the neocortex just an

140 Brodmann area (BA) 3a of the primary somatosensory cortex is part of an ascending pathway fro

141 paper shows that activity in rodent forelimb somatosensory cortex is related to the animal's behavior

142 portant principle in the organization of the somatosensory cortex is that it processes afferent infor

143 ortex, the whisker representation of primary somatosensory cortex, is required for the learning of a

144 The role of the ipsilateral somatosensory cortex (iS1) in sensory gating in humans r

145 examined the contribution of the ipsilateral somatosensory cortex (iS1) to sensory gating during inde

146 ateral motor cortex and unilateral, ischemic somatosensory cortex, lateral thalamus, and hippocampal

147 ural and functional anomalies in the primary somatosensory cortex may underlie orofacial tactile sens

148 females, and increased ventral striatum and somatosensory cortex metabolism in males.

149 rectifies the chloride imbalance in layer IV somatosensory cortex neurons and corrects the developmen

150 ectrophysiology, we found that mouse primary somatosensory cortex neurons showed robust choice-relate

151 Here we show that at this synapse in the somatosensory cortex of 2- to 3-week-old rats and mice,

152 assive 25-Hz vibrotactile stimulation in the somatosensory cortex of 20 typically developing individu

153 strocytes in layers 1 through 4 of the adult somatosensory cortex of a FXS mouse model, the FMR1 knoc

154 of layer V pyramidal neuron activity in the somatosensory cortex of a mouse model of neuropathic pai

155 med time lapse in vivo two photon imaging in somatosensory cortex of adult mice to define the kinetic

156 y motor cortex, corpus callosum, and primary somatosensory cortex of adult mice.

157 pocampal slices exposed to NH4(+) and in the somatosensory cortex of anesthetized mice in response to

158 hanges in cerebral blood volume (CBV) in the somatosensory cortex of awake, head-fixed mice during pe

159 In vivo two-photon microscopy of the somatosensory cortex of Cdkl5(-/y) mice was applied to m

160 in vivo two-photon Ca(2+) imaging data from somatosensory cortex of Fmr1 knock-out (KO) mice, a mode

161 ital reconstruction of the microcircuitry of somatosensory cortex of juvenile rat.

162 ic slices, and layer 2/3 pyramidal neuron in somatosensory cortex of living mice.

163 ices, and layer 2/3 pyramidal neurons in the somatosensory cortex of living mice.

164 nses of single units in the nerve and in the somatosensory cortex of primates to the same textures sc

165 Single cells in the motor and somatosensory cortex of rats were stimulated in vivo wit

166 The barrel cortex is within the primary somatosensory cortex of the rodent, and processes signal

167 ingle-unit recordings were made in secondary somatosensory cortex of three non-human primates while a

168 imulus-evoked population spiking activity in somatosensory cortex of urethane anesthetized rats.

169 n increase in neuronal activation in primary somatosensory cortex of young mice and behavioral hypera

170 ZIKV microinjection into the somatosensory cortex on one side of the normal mouse bra

171 ere was no effect of cTBS over the secondary somatosensory cortex on STDT, although it reduced the N1

172 ate, among others, the contralateral primary somatosensory cortex on the postcentral gyrus together w

173 rding the role of activity in the developing somatosensory cortex, one persistent debate concerns the

174 In somatosensory cortex, only CR(+) neurons showed changes,

175 y placing a powerful magnetic field over the somatosensory cortex overcomes the natural decline in de

176 the first direct evidence that plasticity in somatosensory cortex participates in the consolidation o

177 t from the posterior medial (POm) nucleus to somatosensory cortex plays an unexpected role in plastic

178 xpression, becoming restricted to CPN of the somatosensory cortex postnatally.

179 ecordings reveal that stimulation of primary somatosensory cortex potently suppresses SpVc responses

180 itional brain regions in bilateral secondary somatosensory cortex, premotor cortex, primary motor cor

181 t are significantly delayed across secondary somatosensory cortex, premotor, and motor areas when dec

182 y postsynaptic structure and function in the somatosensory cortex prior to signs of neurodegeneration

183 toward the occipital pole, whereas alpha in somatosensory cortex propagates from associative regions

184 We first found that alpha in both visual and somatosensory cortex propagates from higher-order to low

185 minently found in the apical dendrite of S1 (somatosensory cortex) pyramidal neurons.

186 the hypothesis that in adaptation learning, somatosensory cortex rather than motor cortex is involve

187 sing neurogliaform interneurons in the mouse somatosensory cortex receive afferent innervation from b

188 lantation, host neurons in the contralateral somatosensory cortex receive monosynaptic inputs from gr

189 at describes how the responses of neurons in somatosensory cortex-recorded from awake, behaving monke

190 DCS over the left vlPFC relative to the left somatosensory cortex reduces reward expectancy-related a

191 nd low beta-band (8-20 Hz) cycles in primary somatosensory cortex represent neurophysiological correl

192 at the peak of status epilepticus, motor and somatosensory cortex, retrosplenial cortex, and insular

193 re reduced to a similar degree as in primary somatosensory cortex, revealing differential low-pass fi

194 observed strong signal activation in primary somatosensory cortex (S1) and frontal cortices, includin

195 ent on the communication between the primary somatosensory cortex (S1) and higher-order integrative c

196 ity was found to be disturbed at the primary somatosensory cortex (S1) and the supplementary motor ar

197 ponses collected simultaneously from primary somatosensory cortex (S1) and ventral premotor cortex (v

198 d that temporally precise photoinhibition of somatosensory cortex (S1) applied concurrently with the

199 ching the primary motor cortex (M1) from the somatosensory cortex (S1) are likely involved in fine mo

200 yer (L) 2/3 pyramidal neurons in the primary somatosensory cortex (S1) are sparsely active, spontaneo

201 y digit representations in the human primary somatosensory cortex (S1) at the level of individual par

202 tical microstimulation (ICMS) of the primary somatosensory cortex (S1) can produce percepts that mimi

203 Direct cortical stimulation (DCS) of primary somatosensory cortex (S1) could help restore sensation a

204 How the somatosensory cortex (S1) encodes complex patterns of to

205 midal neurons in layers 2/3 and 5 of primary somatosensory cortex (S1) exhibit somewhat modest synapt

206 Studies of human primary somatosensory cortex (S1) have placed a strong emphasis

207 Recordings from primary somatosensory cortex (S1) in anesthetized mice indicated

208 pothesis that synaptic structures of primary somatosensory cortex (S1) neurons in Fragile X syndrome

209 Performance was tested in whisker somatosensory cortex (S1) of anesthetized mice in vivo.

210 r "barrel" organization found in the primary somatosensory cortex (S1) of mice and rats, but it is un

211 ulpting an inhibitory circuit in the primary somatosensory cortex (S1) of mice by using optogenetics

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

213 field potential (LFP) recordings in primary somatosensory cortex (S1) of the awake mouse, we optimiz

214 rasound (tFUS) targeted to the human primary somatosensory cortex (S1) on sensory-evoked brain activi

215 Whether primary somatosensory cortex (S1) participates in temporal integ

216 Neurons of the primary somatosensory cortex (S1) respond as functions of freque

217 us (ventral posterolateral nucleus, VPL) and somatosensory cortex (S1) sharing the same cutaneous rec

218 rged, expressed via alpha modulations in the somatosensory cortex (S1) that characterized an automati

219 an postoperative neocortex, in vivo in mouse somatosensory cortex (S1), and in a mouse kainic acid (K

220 f inputs from the face region of the primary somatosensory cortex (S1), and only about half as much i

221 In contrast, in somatosensory cortex (S1), excitatory neurons were mostl

222 at the primary motor cortex (M1) and primary somatosensory cortex (S1), two adjacent but functionally

223 investigate the projection from the primary somatosensory cortex (S1), which encodes the sensory pai

224 ntralateral side of the brain in the primary somatosensory cortex (S1).

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

226 eated a neural network that bypasses primary somatosensory cortex (S1).

227 ified a neural network that bypasses primary somatosensory cortex (S1).

228 onal hypoactivity in the non-injured primary somatosensory cortex (S1).

229 equency of spontaneous network events in the somatosensory cortex (S1).

230 d how OFC dynamically interacts with primary somatosensory cortex (S1).

231 presentation of the affected limb in primary somatosensory cortex (S1).

232 mpassing the dysgranular zone of the primary somatosensory cortex (S1DZ).

233 1BC, primary motor cortex (M1) and secondary somatosensory cortex (S2) may underlie beneficial adapta

234 eport that higher-order area 1 and secondary somatosensory cortex (S2) underwent similar spatial reor

235 a, 1 and 2, parietal ventral (PV), secondary somatosensory cortex (S2), and primary motor cortex (M1)

236 feedback connections from area 1, secondary somatosensory cortex (S2), parietal ventral area (PV), a

237 the mid- and posterior insula and secondary somatosensory cortex (S2).

238 On every touch, the somatosensory cortex sends a packet of texture informati

239 midal neurons in acute brain slices of mouse somatosensory cortex show that excitatory synaptic trans

240 The mammalian somatosensory cortex shows marked species-specific diffe

241 nly generated from the contralateral primary somatosensory cortex (SI) and bilateral secondary somato

242 ption in visual motion area V5/hMT+, primary somatosensory cortex (SI) and posterior parietal cortex

243 Barrel subfields in rodent primary somatosensory cortex (SI) are important model systems fo

244 reduced centrality of contralateral primary somatosensory cortex (SI) was found, which appeared to b

245 ulation relative to the first in the primary somatosensory cortex (SI).

246 roprioception) and 3b (cutaneous) of primary somatosensory cortex (SI).

247 n axons projecting from secondary to primary somatosensory cortex signaled choice.

248 that cebus monkeys have a relatively complex somatosensory cortex, similar to that of macaques and hu

249 al activity in the vibrissal area of primary somatosensory cortex: single units responded differentia

250 urther suggests that improvements in primary somatosensory cortex somatotopy can predict long-term cl

251 In somatosensory cortex specifically, many studies did not

252 In the somatosensory cortex, SRPX2(-/Y) mice show decreased tha

253 ampus (HPC), basolateral amygdala (BLA), and somatosensory cortex (SSCTX).

254 BOLD responses in the forepaw region of the somatosensory cortex (SSFP) of an anesthetized rat.

255 mediated by the projection from the primary somatosensory cortex (SSp) to the ventral sector of zona

256 argeting primary motor cortex (MOp), primary somatosensory cortex (SSp), and caudoputamen (CP) showed

257 As these primary somatosensory cortex subregions are distinctly targeted

258 cells from layers II-VI of the juvenile rat somatosensory cortex suggest common design principles, d

259 nsmission in the frontal cortex, but not the somatosensory cortex, suggesting that earlier puberty ca

260 llow the organisation of topographic maps in somatosensory cortex, suggesting that tactile localisati

261 hin the parietal association and the primary somatosensory cortex, suggesting that the closer a regio

262 irect corticospinal pathway from the primary somatosensory cortex that synapses with cervical excitat

263 d homeostatic plasticity mechanism in rodent somatosensory cortex that transiently maintains whisker-

264 ectrophysiological recordings in rat primary somatosensory cortex that was undergoing experience-depe

265 Specifically, we deliver ICMS to primary somatosensory cortex through chronically implanted elect

266 pare the response times to DCS of human hand somatosensory cortex through electrocorticographic grids

267 e show that neuronal activity in the primary somatosensory cortex tightly correlates with the onset a

268 ural correlates ranging from activity within somatosensory cortex to activation of widely distributed

269 tracings, and reconstructions of PTs in rat somatosensory cortex to show that PT structure and activ

270 rom barrel-specific blood flow in the rodent somatosensory cortex to the human cortex, where BOLD-fMR

271 group of layer 2/3 pyramidal neurons in the somatosensory cortex triggered long-term plasticity of c

272 activity in layer 5 pyramidal neurons of the somatosensory cortex using an optical fiber imaging appr

273 topography, and connectivity of the primary somatosensory cortex using psychophysics and functional

274 e imaging assessed somatotopy in the primary somatosensory cortex using vibrotactile stimulation over

275 pulation calcium imaging in vibrissa primary somatosensory cortex (vS1) revealed increased spontaneou

276 OVX-associated reduction of spine density in somatosensory cortex was accompanied by a reduction in m

277 OVX-associated spine loss in somatosensory cortex was also rescued by an agonist of t

278 ntation dispersion in the left primary motor-somatosensory cortex was associated with increased Expan

279 separation distance in contralateral primary somatosensory cortex was associated with worse symptomat

280 Optogenetic inactivation showed that the somatosensory cortex was necessary for sequence discrimi

281 read, connectivity between these regions and somatosensory cortex was not as severely affected.

282 In vivo two-photon microscopy of the somatosensory cortex was performed to monitor structural

283 bumin-positive interneuron occurrence in the somatosensory cortex was shifted from layers II/III to V

284 cally in the primary (S1) and secondary (S2) somatosensory cortex, was reduced in the autism group (P

285 investigate the representation of texture in somatosensory cortex, we scanned a wide range of natural

286 ectrophysiological data recorded from rodent somatosensory cortex, we show that a signal from a posts

287 cerebellum and negative connectivity to the somatosensory cortex were specific markers for cervical

288 ndings challenge the automatic engagement of somatosensory cortex when observing touch, suggest mislo

289 id homeostasis in layer 2/3 (L2/3) of rodent somatosensory cortex, where D-row whisker deprivation dr

290 target detection are restricted to secondary somatosensory cortex, whereas activity in insular, cingu

291 the olfactory bulb glomerular layer and the somatosensory cortex, whereas there are large capillary

292 n scheme compared with the same cell type in somatosensory cortex, which has important implications f

293 howed reduced functional connectivity in the somatosensory cortex, which was paralleled by fear behav

294 enhances stimulus selectivity in the primary somatosensory cortex while maintaining perceptual stabil

295 s been previously reported to project to the somatosensory cortex, while the PEc receives additional

296 s in M1 are similar to their counterparts in somatosensory cortex, whose activity is driven primarily

297 apped individual vessels penetrating the rat somatosensory cortex with 100-ms temporal resolution by

298 or infection restricted to the contralateral somatosensory cortex without any infection of midline br

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

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