ライフサイエンスコーパス: interhemispheric

1 ory cortex to right primary auditory cortex (interhemispheric).

2 ty that structural dysconnectivity involving interhemispheric and fronto-thalamo-cerebellar networks,

3 eks postonset with widespread alterations of interhemispheric and intrahemispheric functional connect

4 that the effects of rTMS may depend on both interhemispheric and intrahemispheric interactions betwe

5 ing to examine the specific contributions of interhemispheric and intrahemispheric white matter fiber

6 Together, our results demonstrated that interhemispheric and intrahemispheric white matter fiber

7 in the switching process, intensification of interhemispheric and midline connectivity additionally o

8 ispheric ROIs, which revealed that decreased interhemispheric and right intrahemispheric FC was assoc

9 We show that loss of corticostriatal, interhemispheric, and intrahemispheric white matter conn

10 tter anomalies along many major association, interhemispheric, and projection tracts.

11 Steady-state interhemispheric anterior piriform cortex coherence is r

12 ident across species and have been linked to interhemispheric asymmetries in dopamine signaling, the

13 ent neuroimaging report, no population-based interhemispheric asymmetries of sulcal length existed th

14 A separate sample was used to consider interhemispheric asymmetry by volumetric assessment of t

15 The results obtained demonstrate a robust interhemispheric asymmetry in anterior piriform cortex a

16 e system dysfunction and, in one patient, an interhemispheric asymmetry in visual evoked potentials.

17 Therefore, we examined interhemispheric asymmetry of several different microstr

18 sleep experimental session involves regional interhemispheric asymmetry of sleep depth [9].

19 The interhemispheric asymmetry of sleep depth associated wit

20 The most marked leftward interhemispheric asymmetry of the human and great ape br

21 monkey brains to determine whether purported interhemispheric asymmetry of Tpt is manifested at the g

22 In addition, our data show that the interhemispheric atmospheric (14)C offset was close to z

23 Interhemispheric axons of the corpus callosum (CC) facil

24 emonstrate that L4 neurons develop transient interhemispheric axons.

25 These findings support the notion that the interhemispheric balance of activity across the DLPFCs i

26 The interhemispheric behaviour of the climate system during

27 ostoperatively, there was a striking loss of interhemispheric BOLD correlations with preserved intrah

28 e first time, a novel connective subcortical interhemispheric bridge of tissue in the posterior, but

29 lays an important role in the development of interhemispheric callosal connections, but little is kno

30 tween cortical asymmetry and the connecting, interhemispheric callosal white matter was also investig

31 acement, global cerebral autoregulation, and interhemispheric cerebral autoregulation asymmetry were

32 This revealed an interhemispheric circuit in which IL projects bilaterall

33 ndicate that the rat claustrum is part of an interhemispheric circuit that could be involved in the b

34 ously shown that the claustrum is part of an interhemispheric circuit that interconnects somesthetic-

35 This study identified disruption in interhemispheric circuitry (i.e., fractional anisotropy

36 esults demonstrate important features of the interhemispheric circuitry of the AON and suggest separa

37 Thus, L4 neurons discard alternative interhemispheric circuits as instructed by thalamic inpu

38 Understanding the timings of interhemispheric climate changes during the Holocene, al

39 in triggering, transmitting, and amplifying interhemispheric climate signals remains a key debate in

40 latory amplitudes (rho = 0.4, p = 0.009) and interhemispheric coherence (rho = 0.5, p = 0.002).

41 In addition, tDCS reduced EEG interhemispheric coherence in parietal areas and affecte

42 Similarly, transient, trial-related interhemispheric coherence increases with task competenc

43 Six of the networks included interhemispheric commissural bridges traversing the corp

44 born without the corpus callosum, the major interhemispheric commissure, lack the disconnection synd

45 ed specific behavioral deficits, and loss of interhemispheric communication across a set of regions w

46 splenium, the forceps major, which provides interhemispheric communication between regions of the oc

47 ort for hypotheses that focus on deficits in interhemispheric communication in stuttering.

48 Here we report unprecedented interhemispheric communication in the midbrain dopamine

49 Today, the study of interhemispheric communication is facilitated by a batte

50 In the auditory cortex (AC), interhemispheric communication is involved in sound loca

51 Our study demonstrates that interhemispheric communication is sensitive to locus-spe

52 We also measured interhemispheric communication speed and bimanual coordi

53 ore, we found opposing relationships between interhemispheric communication speed and bimanual perfor

54 handedness, motor cortical organization, and interhemispheric communication speed.

55 a genetically defined type of interneuron in interhemispheric communication.

56 providing an unprecedented means of decoding interhemispheric communication.

57 accordance with classic models of reciprocal interhemispheric competition ('rivalry').

58 and provide a neural basis in support of an interhemispheric competition account of spatial attentio

59 etic stimulation (TMS) to causally test this interhemispheric competition account.

60 ts agree only partially with the influential interhemispheric competition model of spatial neglect an

61 he right hemisphere and others supporting an interhemispheric competition theory.

62 se neural processing capacity and to prevent interhemispheric conflict.

63 Associations were strongest for the interhemispheric connecting fibers of the corpus callosu

64 ies increase our knowledge of the pattern of interhemispheric connection of PMv.

65 atic dependence on retinal influences is the interhemispheric connection through the corpus callosum.

66 nsory cortices, the functional properties of interhemispheric connections between auditory cortical f

67 elucidate the functional specificity of the interhemispheric connections between the claustrum and p

68 r corpus callosum (splenium), which contains interhemispheric connections between the occipital, pari

69 ecent theories emphasizing the importance of interhemispheric connections for language, particularly

70 As many of the interhemispheric connections in the olfactory system ari

71 am, which was activated by letter judgments, interhemispheric connections mediated asymmetric informa

72 The sparse interhemispheric connections of the forelimb sector of M

73 n of functional recovery is mediated through interhemispheric connections of the sensorimotor cortex.

74 es to cTBS is determined by the integrity of interhemispheric connections within the corpus callosum,

75 Furthermore, we hypothesized that interhemispheric connections would be most vulnerable to

76 processing arises from imbalanced intra- and interhemispheric connections.

77 e connections involving peripheral nodes and interhemispheric connections.

78 rupted processing in the left hemisphere via interhemispheric connections.

79 thin motor functional networks, particularly interhemispheric connections.

80 itative or quantitative differences in their interhemispheric connections.

81 s thought a total absence of corpus callosal interhemispheric connective tissues in the BTBR mice may

82 mbination of anatomical measures of temporal interhemispheric connectivity (through the splenium of t

83 ait and vulnerability marker of BD1, whereas interhemispheric connectivity appears to be a disease ma

84 d, unilateral maps to bilateral responses as interhemispheric connectivity becomes established.

85 two, and predominantly encompassed decreased interhemispheric connectivity between cortical motor net

86 difference was driven mostly by decreases in interhemispheric connectivity between the primary motor

87 e cerebral cortex, but whether EMX1 mediates interhemispheric connectivity by controlling corpus call

88 individual's pattern distortion in homotopic interhemispheric connectivity correlated significantly w

89 n functionally repurposed to also facilitate interhemispheric connectivity essential for high order c

90 This study shows there is novel abnormal interhemispheric connectivity in the BTBR strain of mice

91 est that there is more intrahemispheric than interhemispheric connectivity in the sensorimotor area o

92 Increased levels of interhemispheric connectivity with age were diminished b

93 ce on the grooved pegboard did not relate to interhemispheric connectivity, but rather was inversely

94 Hence, in neglect patients with intact interhemispheric connectivity, cTBS over the contralesio

95 under conditions of symmetric and asymmetric interhemispheric connectivity.

96 to assess sensorimotor network strength and interhemispheric connectivity.

97 exploiting robotic devices and modulation of interhemispheric connectivity.

98 , at least in part, by preserving the normal interhemispheric control dynamics with which the basal g

99 findings indicate that intrahemispheric and interhemispheric cooperation between brain regions lying

100 glect and suggest an additional component of interhemispheric cooperation in the compensation of negl

101 Finally, cortico-cortical interhemispheric coordination among bilateral sensorimot

102 h schizophrenia also had a disruption of the interhemispheric coordination among the cortical regions

103 ative functional modules defined by coherent interhemispheric coordination come online in a transient

104 sly unapproachable insights into the role of interhemispheric coordination in cognition.

105 trate the use of these techniques to examine interhemispheric coordination in healthy human participa

106 We find that interhemispheric coordination is greater when lexical in

107 This novel method of examining interhemispheric coordination may yield insights regardi

108 rodent claustrum is probably involved in the interhemispheric coordination of the MI and SI whisker r

109 esults demonstrate functional differences in interhemispheric coordination related to the brain's hie

110 le is known about regional variation in this interhemispheric coordination.

111 ing astroglial guidepost cells essential for interhemispheric corpus callosum (CC) axon navigation.

112 s with a data-driven approach, and ICA-based interhemispheric correlation analysis.

113 alized resting-state network and showed high interhemispheric correlation of activity at rest, as is

114 In contrast, the interhemispheric correlation of resting activity in extr

115 y specific reductions both in activation and interhemispheric correlation within the restrosplenial c

116 Specifically, there was a gradient of interhemispheric correlation, with highest correlations

117 substantial regional variation in homotopic interhemispheric correlations that was highly consistent

118 e to detect circuitry alterations underlying interhemispheric cortical reorganization.

119 cell-specific, synaptic mechanism underlying interhemispheric cortical reorganization.

120 With 'stimulation on', interhemispheric cortico-cortical coherence in the beta

121 ditory and visual system thalamocortical and interhemispheric corticocortical connections was estimat

122 in resting and walking states, and increased interhemispheric coupling (phase lag index) that was mor

123 in response to somatosensory stimulation and interhemispheric coupling of auditory cortices is prefer

124 ere we demonstrate that, in the human brain, interhemispheric coupling of somatosensory regions is pr

125 n individuals who exhibited a naturally weak interhemispheric coupling.

126 Observed changes in the interhemispheric difference of (13)C effectively exclude

127 Results A significant interhemispheric difference was found between the activa

128 In addition, interhemispheric differences in entrained phase were fou

129 [(11) C]ABP688 BP(ND) showed interhemispheric differences of higher magnitude and dis

130 ct, and demonstrate an implication of caudal interhemispheric disconnection in chronic neglect.

131 ity in BPI and further underscore a role for interhemispheric disconnectivity in the pathophysiologic

132 y and excitatory function in maintaining the interhemispheric dynamics that underlie the allocation o

133 ls and slow-wave sleep (SWS) with a striking interhemispheric EEG asymmetry (asymmetrical SWS or ASWS

134 tric levels of serotonin are compatible with interhemispheric EEG asymmetry in the fur seal.

135 , we examined the age-related changes in the interhemispheric effects from the dorsolateral prefronta

136 errestrial mammals, and slow-wave sleep with interhemispheric electroencephalogram (EEG) asymmetry, r

137 al areas do not participate by themselves in interhemispheric exchange in birds.

138 otor, parietal, and occipital regions, while interhemispheric expression profiles are associated with

139 ed with improvements of previously depressed interhemispheric FC across attention, sensory, and motor

140 Consistent with previous findings, interhemispheric FC between homotopic regions were signi

141 In the attention network, disruption of interhemispheric FC was significantly correlated with ab

142 In the somatomotor network, disruption of interhemispheric FC was significantly correlated with up

143 pheric FC to the behavioral correlation with interhemispheric FC.

144 ctography showed that of the three groups of interhemispheric fibres within the splenium, only those

145 f prepontine cistern - 0.034-0.067; index of interhemispheric fissure width - 0.044-0.127; index of S

146 t-right stretch around the temporal lobe and interhemispheric fissure, anterior-posterior stretch in

147 We previously reported increased interhemispheric functional and structural connectivity

148 Indices of interhemispheric functional and structural neural connec

149 elopmental timeline of the transition toward interhemispheric functional asymmetry during the first 2

150 imaging scans to delineate the trajectory of interhemispheric functional asymmetry in language-relate

151 the early language-related transition toward interhemispheric functional asymmetry in the brain using

152 ivity and functional connectivity: we tested interhemispheric functional connectivity before and afte

153 atory domain, as well as a dynamic effect on interhemispheric functional connectivity between primary

154 increased posterior superior temporal gyrus interhemispheric functional connectivity during story co

155 everal reports have documented nearly intact interhemispheric functional connectivity in individuals

156 Interhemispheric functional connectivity in relation to

157 d in Plp-Nf1 (fl/+) corpus callosum and that interhemispheric functional connectivity in the motor co

158 This suggests that interhemispheric functional connectivity is one potentia

159 Additionally, interhemispheric functional connectivity of the bilatera

160 significantly more correlated with abnormal interhemispheric functional connectivity patterns within

161 significantly more correlated with abnormal interhemispheric functional connectivity within the dors

162 fected and unaffected sensorimotor cortices (interhemispheric functional connectivity).

163 at forebrain commissurotomy severely reduced interhemispheric functional connectivity, but surprising

164 inated, particularly for corticocortical and interhemispheric functional connectivity.

165 onnections play a role in the maintenance of interhemispheric functional connectivity.

166 tion of the corpus callosum markedly reduced interhemispheric functional connectivity.

167 d sensory-motor networks showed: (i) reduced interhemispheric functional connectivity; (ii) reduced a

168 sing functional connectivity, we demonstrate interhemispheric functional somatotopic connectivity of

169 erally, our findings suggest that increasing interhemispheric functional symmetry in the first year m

170 erally, our findings suggest that increasing interhemispheric functional symmetry in the first year m

171 We derived the trajectory of interhemispheric functional symmetry of the inferior fro

172 We found enhanced interhemispheric gamma-band coherence in typically devel

173 ic intracortical circuits mediating SICI and interhemispheric glutamatergic projections between M1s c

174 Here, using measurements of the interhemispheric gradient of atmospheric carbon dioxide

175 tered deep ocean circulation, which enhanced interhemispheric heat and salt transport, thereby contri

176 coherence, rs14429078 and parieto-occipital interhemispheric high theta coherence, and rs116445911 w

177 We show that FC between interhemispheric homotopic cortical and hippocampal area

178 The presence of a low- to mid-latitude interhemispheric hydrologic seesaw is apparent over orbi

179 The impacts of such an interhemispheric hydrologic seesaw on higher-latitude re

180 ndicates that the sphere of influence of the interhemispheric hydrologic seesaw over the past 550,000

181 An interhemispheric hydrologic seesaw--in which latitudinal

182 ndent refinement result in mature functional interhemispheric hyperconnectivity, demonstrating the pl

183 be exceptionally strong compared with other interhemispheric (i.e., heterotopic) connections.

184 activity between geometrically corresponding interhemispheric (i.e., homotopic) regions, is a fundame

185 d from the removal of subglacial regolith or interhemispheric ice sheet phase-locking.

186 These results suggest that interhemispheric imbalance is not a cause of poor motor

187 atients might be based on an increase of the interhemispheric information transfer between the bilate

188 regions are known to contribute to abnormal interhemispheric information transfer, heteromodal senso

189 citability of TC pathways was measured using interhemispheric inhibition (IHI) and the ipsilateral si

190 tional changes within M1(ipsilateral) and in interhemispheric inhibition (IHI) associated with parame

191 racortical inhibition (LICI) in right M1 and interhemispheric inhibition (IHI) from right to left M1.

192 e have been shown to have failure to release interhemispheric inhibition (IHI) from the intact to the

193 Interhemispheric inhibition (IHI) is essential for dexte

194 Interhemispheric inhibition between S1s and intracortica

195 Note that changes in interhemispheric inhibition between S1s correlated with

196 Our results indicate that modulation of interhemispheric inhibition between the M1 areas may, as

197 Notably, changes in interhemispheric inhibition correlated with changes in P

198 Interhemispheric inhibition increased the amplitude of t

199 one influential account of spatial neglect, interhemispheric inhibition is impaired and leads to a p

200 Moreover, interhemispheric inhibition of SII source activity corre

201 This interhemispheric inhibition of the contralateral SII sou

202 the contralesional cortex exerts an enhanced interhemispheric inhibition over the perilesional tissue

203 of ipsilateral silent periods indicated that interhemispheric inhibition plays a role in mediating th

204 barrel cortex in lightly sedated mice, while interhemispheric inhibition reduces activity in the ipsi

205 These may reflect a change in interhemispheric inhibition that could contribute to mai

206 ponents) and paired-pulse SSEPs between S1s (interhemispheric inhibition) and within (intracortical i

207 sensory streams, refine representations via interhemispheric inhibition, and demix locomotor instruc

208 lateralized damage in sv-PPA and accounts of interhemispheric inhibition, we applied left hemisphere

209 irroring" motor representations, and reduced interhemispheric inhibition.

210 ring M1 and cerebellum, and markedly reduced interhemispheric inhibition.

211 ing that of the ipsilateral cortex to reduce interhemispheric inhibition.

212 regions of the AON have distinct patterns of interhemispheric innervation; contralateral fibers were

213 However, the interhemispheric input also changed the contrast sensiti

214 examining directly the functional effects of interhemispheric inputs to specific pyramidal neurons in

215 The mechanisms underlying interhemispheric integration (IHI) remain poorly underst

216 etwork dysfunction consisting of decrease of interhemispheric integration and intrahemispheric segreg

217 or stroke, this functional loss disrupts the interhemispheric interaction between intact and deprived

218 As a result of this interhemispheric interaction, a large or rapid Northern

219 these regions, suggesting an involvement of interhemispheric interaction.

220 regulating homotopic as well as heterotopic interhemispheric interactions (IHIs) are assumed to be r

221 her by complex network modulations involving interhemispheric interactions and areas associated with

222 This finding reveals the importance of interhemispheric interactions and network adaptations fo

223 These results indicate that interhemispheric interactions are common in area 3b, som

224 The findings suggest that interhemispheric interactions between bilateral SMA play

225 Interhemispheric interactions between the primary motor

226 ea, in a longitudinal study, we investigated interhemispheric interactions by tracking patients' prem

227 aimed to clarify the timing and magnitude of interhemispheric interactions during early integration o

228 of area 3b of primary somatosensory cortex, interhemispheric interactions have been reported to vary

229 litation strategy of attempting to rebalance interhemispheric interactions in order to improve motor

230 he putative pathway that mediated inhibitory interhemispheric interactions in SII was a transcallosal

231 al magnetic stimulation (dsTMS) has revealed interhemispheric interactions mainly at early latencies.

232 Here we give a detailed description of the interhemispheric interactions of a period of theta burst

233 ks, the cBCT is more specifically reliant on interhemispheric interactions of lateralized motor contr

234 Thus, long-latency interhemispheric interactions, likely reflecting indirec

235 arietal cortex, emphasizing the relevance of interhemispheric interactions.

236 stem, we developed a simple model of lateral interhemispheric interactions.

237 r recent proposal of an age-related shift in interhemispheric interactions.

238 rom stroke, and underscore the importance of interhemispheric interactions.

239 processing and highly interacting by strong interhemispheric intrinsic connectivity and larger corpu

240 region may reflect a 'reserve capacity' for interhemispheric language reorganization in the presence

241 al recovery, for example, through changes in interhemispheric lateralization, activity of association

242 uced fractional anisotropy (FA) primarily in interhemispheric, left frontal and temporal WM.

243 le, BPI patients had reduced WM integrity in interhemispheric, limbic, and arcuate WM tracts.

244 formations, including frontonasal dysplasia, interhemispheric lipoma, agenesis of the corpus callosum

245 omosome 18q23 were associated with posterior interhemispheric low theta EEG coherence (3-5 Hz).

246 ivation), and cortical connectivity (greater interhemispheric M1-M1 connectivity).

247 ic winter sea ice cover, which steepened the interhemispheric meridional temperature gradient.

248 s correlated with direction and degree of an interhemispheric metabolism bias in the inferior parieta

249 In particular, interhemispheric modulation of alpha band (8-13 Hz) osci

250 f subcortical structural asymmetries predict interhemispheric modulation of alpha power during a spat

251 onfirming and extending the view of impaired interhemispheric neural communications mediated by CC, p

252 t feature of ALS, studies directly examining interhemispheric neural connectivity are still lacking.

253 tracts in combination with reinstatement of interhemispheric neuronal signal synchronization and nor

254 on of the transcallosal projections, showing interhemispheric neuroplasticity and thus, setting a fou

255 could be a manifestation of a multi-decadal interhemispheric or bipolar seesaw pattern, which is wel

256 The shallower interhemispheric overturning circulation makes room for

257 ogether with a weakening and shoaling of the interhemispheric overturning circulation, again consiste

258 ct current stimulation-induced modulation of interhemispheric parietal balance may be used clinically

259 Analysis of interhemispheric pathways (in particular, connections be

260 Interhemispheric pathways are more disrupted in patients

261 r hippocampal commissure constitute the only interhemispheric pathways at the telencephalic level in

262 mber of epilepsy-related factors may promote interhemispheric plasticity, it has remained unexplored

263 We discuss the complex interhemispheric processes that might underlie this effe

264 Our novel findings suggest that interhemispheric projections between S1s and intracortic

265 the substantia nigra, sends dense intra- and interhemispheric projections to the OFC, which in turn h

266 d that this effect is exerted by influencing interhemispheric reciprocal networks.

267 We found that the degree of interhemispheric rs-FC within fronto-temporal auditory n

268 We here present Pliocene Atlantic interhemispheric sea surface temperature and salinity gr

269 Such interhemispheric sea-level forcing may explain the synch

270 urprisingly, many patients fail to show such interhemispheric shift of language despite having major

271 xamined the relationship between TMS-induced interhemispheric signal propagation and anatomical prope

272 Our data suggest that early interhemispheric somatosensory integration primarily occ

273 tica, which suggests that dust generation in interhemispheric source regions exhibited a common respo

274 In the present study, we related interhemispheric structural and functional connectivity

275 present study aims to examine alterations of interhemispheric structural and functional connectivity

276 the analysis has also revealed reductions of interhemispheric structural connectivity through the CC

277 ion of the transcallosal connections removes interhemispheric suppression from retino-geniculate affe

278 Long-term variations in interhemispheric surface temperature anomalies coexist w

279 Interhemispheric symmetry of connectivity was assessed i

280 s with autism exhibited significantly weaker interhemispheric synchronization (i.e., weak "functional

281 are associated with an increase in local and interhemispheric synchronization.

282 l deprivation consistent with the model that interhemispheric takeover supports intact whisker proces

283 s thermal equator, initiated by an increased interhemispheric temperature contrast, may well produce

284 warming in the northern hemisphere create an interhemispheric temperature gradient that enhances the

285 of the rainbelt over the oceans to regional interhemispheric temperature gradients, which is opposit

286 urning in the North Atlantic led to a strong interhemispheric thermal gradient during late-glacial ti

287 sence of chronic ischemic lesions within the interhemispheric tracts and thalamic radiation (P < .05,

288 only necessary for a better understanding of interhemispheric transfer in birds, but also for a compa

289 dence for their functional role in preserved interhemispheric transfer of complex tactile information

290 ne, with partial compensatory effects to the interhemispheric transfer of cortical function.

291 tructures, and also provides a route for the interhemispheric transfer of olfactory information.

292 We assessed CC function through interhemispheric transfer time (IHTT) as measured using

293 the rat claustrum are structured for rapid, interhemispheric transmission of information needed for

294 ic transport model that accurately describes interhemispheric transport and modelled emissions.

295 egulators of neuronal cell fate that control interhemispheric versus corticofugal connections respect

296 visual and emotional processing, as well as interhemispheric visual information transfer.

297 ractography analyses of intrahemispheric and interhemispheric white matter bundles were performed.

298 dren might reflect injury to major intra- or interhemispheric white matter pathways connecting fronta

299 hing cortical connectivity by regulating the interhemispheric wiring of a subpopulation of neurons wi

300 maging indices from the long-associative and interhemispheric WM tracts were obtained.