ライフサイエンスコーパス: somatosensory cortex

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

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

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

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

5 halamic neurons that project directly to the somatosensory cortex.

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

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

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

9 atter microstructure adjacent to the primary somatosensory cortex.

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

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

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

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

14 and with local field potentials in the rat's somatosensory cortex.

15 the function of PV-neurons in mouse forelimb somatosensory cortex.

16 ment of two different microECoG grids on the somatosensory cortex.

17 nal growth protein GAP43 in the ipsilesional somatosensory cortex.

18 OD plasticity after a stroke in the primary somatosensory cortex.

19 c currents and receptive fields (RFs) in the somatosensory cortex.

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

21 evented the formation of "barrel" columns in somatosensory cortex.

22 induces representational map changes in the somatosensory cortex.

23 on of cortical astrocytes in the adult mouse somatosensory cortex.

24 ns between the finger pad representations in somatosensory cortex.

25 bolic couplings vary vertically in the rat's somatosensory cortex.

26 recise anatomical connections in the primate somatosensory cortex.

27 ation on synaptic connections in the primary somatosensory cortex.

28 ntaneous neuronal ensemble activity in mouse somatosensory cortex.

29 gh intracortical microstimulation of primary somatosensory cortex.

30 osensory cortex and two barrels in the right somatosensory cortex.

31 exposure than the earlier-maturing, primary somatosensory cortex.

32 teeth, and other representations in primary somatosensory cortex.

33 f cortex, and greater in the VPM than in the somatosensory cortex.

34 n involved in mood disorders, and of primary somatosensory cortex.

35 genital representation field of the primary somatosensory cortex.

36 ly-organised, somatotopic map in the primary somatosensory cortex.

37 h digit representation in area 3b of primary somatosensory cortex.

38 eling intensity for PSD95) were found in the somatosensory cortex.

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

40 ordings in thalamocortical slices from mouse somatosensory cortex.

41 the thalamus and subsequently to the primary somatosensory cortex.

42 ts and after-effects of tDCS observed in the somatosensory cortex.

43 n the functional responsiveness of the adult somatosensory cortex.

44 prominent form of activity in the developing somatosensory cortex.

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

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

47 g ventrolateral prefrontal cortex and second somatosensory cortex.

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

49 overlapping classes of interneurons in mouse somatosensory cortex.

50 ropriate digit representation in the primary somatosensory cortex.

51 , progressively increases after birth in the somatosensory cortex.

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

53 ut to individual digits in the human primary somatosensory cortex [4].

54 eased thalamic reticular nucleus and primary somatosensory cortex activity (quantitative arterial spi

55 In somatosensory cortex, activity related to movement of di

56 ze anatomical changes in layer IV of primary somatosensory cortex after a brief period of sensory dep

57 d evidence of rapid neural reorganization in somatosensory cortex after brain damage [1] and amputati

58 the long-term depression (LTD) evoked in the somatosensory cortex after cathodal tDCS.

59 to evaluate patterns of the reactivation of somatosensory cortex after sensory loss produced by spin

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

61 Primary somatosensory cortex and adjoining somatosensory areas c

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

63 rupts the formation of barrel columns in the somatosensory cortex and cortical lamination, providing

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

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

66 in the border of layers 1 and 2 from primary somatosensory cortex and found that practically all ChC

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

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

69 a seed revealed increased connectivity with somatosensory cortex and lateral inferior parietal lobe

70 iator of synaptic instability in the primary somatosensory cortex and may contribute to sensory and c

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

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

73 Input from somatosensory cortex and thalamus converges in individua

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

75 position of the entire vibrissal area in rat somatosensory cortex and thalamus.

76 fied one putative trident barrel in the left somatosensory cortex and two barrels in the right somato

77 y laminar distributions of synapses in mouse somatosensory cortex and validate the classification pro

78 amplitude was source localized to secondary somatosensory cortex, and attributed to feedforward proc

79 silateral striatum, periaqueductal gray, and somatosensory cortex, and in contralateral amygdala, ven

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

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

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

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

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

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

86 ior mid-cingulate cortex (aMCC), the primary somatosensory cortex, and the posterior insula.

87 eld potential in the limb representations in somatosensory cortex, and was accompanied by increases i

88 ndicate that areas 3a, 3b, 1, and 2-5 of the somatosensory cortex are extensively reactivated after l

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

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

91 3-fold between species ranging from 0.5% of somatosensory cortex area in chipmunks to 1.7% in rats.

92 trode arrays in the hand area of the primary somatosensory cortex (area 1) in two awake macaque monke

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

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

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

96 ty within the hand representation of primary somatosensory cortex (areas 3b and 1) in anesthetized sq

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

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

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

100 tion are not associated with synapse loss in somatosensory cortex (as might be expected) but with alt

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

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

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

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

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

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

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

108 in other parts of the frontal cortex and in somatosensory cortex, but no reduction was apparent in t

109 ard processing between primary and secondary somatosensory cortex by means of dynamic causal modeling

110 s indicate that early neural activity in the somatosensory cortex can reflect the subjective quality

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

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

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

114 tex that triggered electrical stimulation in somatosensory cortex continuously over subsequent weeks.

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

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

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

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

119 ncreased c-Fos expression in the ipsilateral somatosensory cortex, contralateral amygdala and globus

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

121 distance (P < 0.05) in contralateral primary somatosensory cortex, corroborating our previous prelimi

122 ee of this behavioral effect correlated with somatosensory cortex density across individuals.

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

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

125 elated potentials (ERPs) measured over early somatosensory cortex diverge for detected and missed per

126 studied local L2/3 recurrent networks in rat somatosensory cortex during deprivation-induced whisker

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

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

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

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

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

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

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

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

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

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

137 ng of dendritic spines and axonal boutons in somatosensory cortex for up to 1 year in thy1 GFP mice t

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

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

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

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

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

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

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

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

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

147 we experimentally imaged brain tissue of the somatosensory cortex in six mice.

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

149 of primary motor cortex activity on primary somatosensory cortex in the mouse whisker system.

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

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

152 (2+) also induce similar plasticity in mouse somatosensory cortex in vivo.

153 iogenesis in the subventricular zone and the somatosensory cortex in vivo.

154 pling and endothelium-dependent responses in somatosensory cortex induced by hypertension.

155 e with our framework, we could show that the somatosensory cortex is "more efficiently" integrated in

156 Primary somatosensory cortex is located in the neocortex just an

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

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

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

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

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

162 ti cells, the axons of SOM INs in layer 4 of somatosensory cortex largely remain within layer 4.

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

164 reactive profiles was observed in layer V of somatosensory cortex: Met-labeled spines were rare and a

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

166 t motor cortex activity can drive changes in somatosensory cortex network state.

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

168 In conclusion, primary somatosensory cortex neuroplasticity for median nerve in

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

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

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

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

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

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

175 Whisker removal deprives the somatosensory cortex of experience-dependent input and r

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

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

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

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

180 dritic spines and axonal varicosities in the somatosensory cortex of mice lacking Nogo Receptor 1 (Ng

181 ound a marked reduction in axonal pruning in somatosensory cortex of mice with a knock-out of the DR6

182 activity of individual L2/3 neurons from the somatosensory cortex of mice.

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

184 nd structural neuroplasticity in the primary somatosensory cortex of the brain.

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

186 ecifically ADCY1 and BDNF - increased in the somatosensory cortex of transected animals that received

187 n I and Golgi-Cox stained neurons in primary somatosensory cortex of unilaterally whisker-deprived ad

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

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

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

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

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

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

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

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

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

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

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

199 Furthermore, failure to attenuate secondary somatosensory cortex processing was predicted by current

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

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

202 The somatosensory cortex remodels in response to sensory dep

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

204 tance for each digit's contralateral primary somatosensory cortex representation was assessed.

205 as a seed showed stronger connectivity with somatosensory cortex, right insula, OFC, and striatum.

206 The primary and secondary somatosensory cortex (S1 and S2), anterior cingulate cor

207 dings in postnatal day 3 (P3)-P5 rat primary somatosensory cortex (S1) and M1 in vivo, we observed th

208 ic FGF8 in the caudalmost NP could duplicate somatosensory cortex (S1) and primary visual cortex (V1)

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

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

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

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

213 The primary somatosensory cortex (S1) can be subdivided cytoarchitec

214 The primary somatosensory cortex (S1) contains a complete body map t

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

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

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

218 L) of the somatosensory thalamus and primary somatosensory cortex (S1) in two macaque monkeys perform

219 The human somatosensory cortex (S1) is not among the brain areas u

220 coded in the responses of neurons in primary somatosensory cortex (S1) is unknown.

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

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

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

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

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

226 of the somatosensory thalamus and in primary somatosensory cortex (S1) respond to vibrotactile stimul

227 allel analogous pathway, the whisker primary somatosensory cortex (S1) strongly projects to the brain

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

229 t of a head-mounted infrared sensor to their somatosensory cortex (S1) via intracortical microstimula

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

231 somatosensory representation in the primary somatosensory cortex (S1), putatively involved in unders

232 cal motor area (ProM), ventrolateral primary somatosensory cortex (S1), rostral insula, and pregenual

233 Single neurons located in the primary somatosensory cortex (S1), the ventroposterior medial, a

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

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

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

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

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

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

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

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

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

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

244 ere is a pure and independent involvement of somatosensory cortex (SCx) during face processing over a

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

246 The mammalian somatosensory cortex shows marked species-specific diffe

247 n major somatosensory regions, i.e., primary somatosensory cortex SI, secondary somatosensory cortex

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

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

250 the forepaw barrel subfield (FBS) of primary somatosensory cortex (SI) that follows forelimb amputati

251 e major proprioceptive region of the primary somatosensory cortex (SI) that is conventionally referre

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

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

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

255 eptive inputs to the digits in human primary somatosensory cortex (SI).

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

257 , primary somatosensory cortex SI, secondary somatosensory cortex SII, posterior parietal cortex, and

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

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

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

261 In somatosensory cortex specifically, many studies did not

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

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

264 As these primary somatosensory cortex subregions are distinctly targeted

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

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

267 P70S6K was hyperphosphorylated in Tg1 somatosensory cortex, suggesting that elevated mTOR sign

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

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

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

271 osterior and anterior insulae, the secondary somatosensory cortex, the anterior cingulate cortex, the

272 atter protoplasmic astrocytes of the primary somatosensory cortex, the thalamic ventrobasal nucleus,

273 Consistent with studies of the somatosensory cortex, these data point to hyper-responsi

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

275 ous on and off responses observed in primary somatosensory cortex to complement slowly varying pressu

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

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

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

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

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

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

282 s the facial sensations to the contralateral somatosensory cortex via the ventrobasal thalamus.

283 nformation ascends from the brainstem to the somatosensory cortex via two major parallel pathways, le

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

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

286 Gray matter density of the somatosensory cortex was found to be greater in children

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

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

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

290 The terminal territory from the somatosensory cortex was significantly smaller compared

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

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

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

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

295 ynaptic inputs into layer 4 neurons from rat somatosensory cortex while altering the depth of anesthe

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

297 In the vibrissal area of rodent somatosensory cortex, whisker-related "barrel" columns h

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

299 s, begins as early as area 3b in the primary somatosensory cortex with the involvement of intrinsic l

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

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