ライフサイエンスコーパス: lateralized

1 e clockwise around their longest axis (right lateralized).

2 likely to be performed anti-clockwise (left lateralized).

3 ate control of processing functions that are lateralized.

4 ect an effect of top-down modulation that is lateralized.

5 o nostrils in the behavioral task was highly lateralized.

6 daptation to novel visuomotor conditions are lateralized.

7 e neural network subserving communication is lateralized.

8 n showed negligible change and remained left lateralized.

9 while sestamibi scintigraphy only correctly lateralized 90 of 122 adenomas (74%) as confirmed by exp

10 We have now demonstrated lateralized abnormalities of temporal cortex processing

11 Specifically, left lateralized activation in vOT does not necessarily indic

12 Whereas language-related areas kept their lateralized activation pattern independent of age in dif

13 with increasing age and maintenance of left-lateralized activation with age.

14 previous animal studies); and the LC showing lateralized activity during conflicting attentional dema

15 Right-lateralized activity has mainly been reported in ventral

16 b, depressed patients showed decreased right-lateralized activity in the precentral sulcus (PrCS) and

17 These results show that lateralized activity related to individual memories can

18 ditory spatial selective attention result in lateralized alpha (8-14 Hz) oscillatory power in parieta

19 n the present study, we found that a similar lateralized alpha effect is triggered by the appearance

20 Therefore, lateralized alpha may serve as a preparatory mechanism.

21 (i.e., the contralateral delay activity) and lateralized alpha power modulation as neural correlates

22 Although both lateralized alpha responses for selection and for suppre

23 ssion, we demonstrate that two sign-reversed lateralized alpha responses reflect target selection ver

24 o the target (which we call "target-elicited lateralized alpha suppression" or TELAS).

25 Here, we asked whether lateralized alpha-band activity is also evident in a pur

26 These results indicate that lateralized alpha-band activity is involved in active ta

27 ( approximately 100-200 ms) reactivation of lateralized alpha/beta (10-25 Hz) electroencephalographi

28 The left-lateralized alterations have not been identified in othe

29 ebellar and frontostriatal circuits and left-lateralized alterations of frontotemporal circuitry and

30 adigm suggests individuals are left or right lateralized, although the direction of this laterality c

31 selective engagement of M and P pathways and lateralized amygdala reactivity.

32 tal region showed significantly greater left lateralized amyloid uptake in the PPA group than the amn

33 ivity in depressive disorders, so aspects of lateralized anatomy may also be affected.

34 ls and line drawings of objects evoked right-lateralized and bilaterally specific responses, respecti

35 that the speech sensory-motor system is left lateralized and facilitates the transformation from sens

36 Such lateralized and focal results provide support for GWC as

37 Furthermore, these changes were lateralized and in proportion to the tactile allodynia e

38 d motor and feedback sensory signals is left-lateralized and lies at the junction of the supratempora

39 encoding phase in several predominantly left lateralized and medial areas of the PFC.

40 c activity induced by motor imagery was more lateralized and motor performance improved.

41 We found a strongly lateralized and regionally specific profile with reduced

42 e articulator-specific modulations were left-lateralized and remarkably early, occurring 60-100 ms af

43 visual periphery, preceded or followed by a lateralized and task-irrelevant sound at 4 stimulus-onse

44 These timing maps were partially left lateralized and widely spread, from occipital visual are

45 tal positive-going DM effect which was right-lateralized, and a later (onset at 800 ms) occipital neg

46 at boundary onset was accompanied by a left-lateralized anterior negative ERP effect, which likely r

47 Right-lateralized anticipatory activity selectively influenced

48 data suggest that "top-down" influences from lateralized areas within Ins and S1 selectively affect i

49 /right asymmetric manner in the functionally lateralized ASE neurons and are required to sense distin

50 e effect of focal seizures was inferred from lateralized atrophy common to both HS-TLE and MRI-neg TL

51 HS-TLE subjects had lateralized atrophy of most temporal lobe tracts, and hi

52 pture success because of specialization in a lateralized attack, but at the cost of increased predict

53 ry or visual) to attend, followed by a short lateralized auditory or visual stimulus.

54 t the long and anterior arcuate segments are lateralized before adolescence and their lateralization

55 Here, we show the earliest evidence of lateralized behavior in a fossil reptile based on repeat

56 To understand if this unusual lateralized behavior may have coevolved with genital mor

57 Lateralized behavior was strongly sex related.

58 Captorhinus aguti indicate that it exhibited lateralized behavior, preferring to feed using the right

59 may therefore lie at the foundation of other lateralized behavioral choices.

60 l ganglion cells in cockatoos reflects their lateralized behaviors and microhabitat diversity.

61 Lateralized behaviors benefit individuals by increasing

62 Because lateralized behaviors have been linked to hemispheric (b

63 Lateralized behaviors have been reported in a variety of

64 In contrast, cockatoo species that show no lateralized behaviors have equivalent retinal ganglion c

65 ion in some vertebrates [11-15], evidence of lateralized behaviors in ancient vertebrates might yield

66 However, evidence of lateralized behaviors in extinct vertebrates is rare, pr

67 species that have strong left eye-left foot lateralized behaviors.

68 By contrast, lateralized beta-band power (10-30 Hz) overlying human m

69 with damage to a distributed network of left lateralized brain areas, including regions of frontal an

70 ntal language disorders result from a poorly lateralized brain, but until recently, evidence has been

71 in cognitive functions have been known to be lateralized, but the provenance and flexibility of hemis

72 try and how the Nodal-Pitx2 pathway controls lateralized cell differentiation, migration, and other a

73 n and spatial attention are the most salient lateralized cerebral functions, and their complementary

74 tivity within each hemisphere and discovered lateralized circuit-motifs that are hearing experience-d

75 the affective and default mode and the right lateralized cognitive control networks compared with hea

76 stic function considered to be strongly left-lateralized, combining measures of tissue integrity, neu

77 However, evidence for the lateralized computation of sensory-motor speech transfor

78 with disrupted hedonic function, abnormally lateralized connectivity through ventromedial prefrontal

79 ing MEG suggested that there is also a right-lateralized contribution from the auditory cortex at the

80 ctive mechanisms are implemented in the left-lateralized "core language network", whereas domain-gene

81 ial motor and autonomic control, than to the lateralized cortical activation manifested in asymmetric

82 century, but the mechanisms underlying this lateralized cortical function are poorly understood.

83 for the first time, we examined regional and lateralized cortical thickness in a sample of 71 chimpan

84 n over both hemispheres - but robustly right-lateralized - could reflect distorted hands as emotional

85 In AF animals, controls had reduced and lateralized Cx43 expression, and Cx43 gene transfer rest

86 Administering peptide mimetics to inhibit lateralized Cx43 function prior to challenge protected m

87 Conforming to predominantly left-lateralized damage in sv-PPA and accounts of interhemisp

88 They also showed lateralized deficits in procedural learning and open-loo

89 gs of similar visual complexity, with a left-lateralized distribution.

90 ols demonstrated Cx43 remodeling from IDs to lateralized distributions.

91 lization of human speech that is due to left-lateralized dopaminergic modulation of brain activity an

92 th (1) aggravated hypo-function of the right-lateralized dorsal attention and salience networks and (

93 nnectivity analyses revealed a largely right-lateralized dorsolateral prefrontal cortex-cingulate-par

94 Subjects viewed a lateralized drifting grating stimulus, presented at mult

95 found that cortical acetylcholine release is lateralized during ASWS in the northern fur seal, with g

96 eport that cortical serotonin release is not lateralized during ASWS.

97 a classifier on sleep EEG data (focusing on lateralized EEG features that discriminated left- vs rig

98 In two experiments, we measured a lateralized EEG response (N2pc) previously associated wi

99 HS-TLE and MRI-neg TLE, suggesting a common lateralized effect of focal seizures.

100 ffects of NPTN mutations, accounting for the lateralized effect of rs7171755 found in our study.

101 However, these two lateralized effects had different time courses and they

102 periodic discharges (also known as periodic lateralized epileptiform discharges), subjects with foca

103 om generalized slowing to bilateral periodic lateralized epileptiform discharges.

104 ow cues elicits a characteristic sequence of lateralized ERP components.

105 nectivity in the hindbrain important for the lateralized escape behavior of zebrafish and then test t

106 We found lateralized event-related potentials during task trainin

107 thy control (n = 15) participants with their lateralized event-related potentials during the performa

108 dominantly, long-range connectivity was left lateralized (except anterior Wernicke's area that exhibi

109 These findings indicate that right lateralized face-selective processes emerge well before

110 Tcf7l2 is essential for lateralized fate selection by habenular neurons that can

111 differentiated, with male-biased numbers and lateralized favoring the right in the rat MePD.

112 ,6], and we posit that the specialization of lateralized feeding strategies may enhance foraging effi

113 re examined separately, Arc/Arg3.1 level was lateralized following novel taste learning.

114 poral (vOT) activation is more strongly left lateralized for written words than other visual stimuli.

115 lar to gesture are processed within the left-lateralized frontal-temporal network used for spoken lan

116 erage reduction in the engagement of a right-lateralized fronto-parietal functional network, while an

117 A left-lateralized fronto-parietal network was recruited for co

118 anguage control is thought to involve a left-lateralized fronto-temporal-parietal (FTP) system.

119 rent stimulation dynamically modulated right-lateralized fronto-visual theta oscillations compared to

120 d signaling of temporal predictions in right-lateralized frontoparietal associative regions.

121 eration between the DMN and a specific right-lateralized frontoparietal component of the EAS is assoc

122 ual stimuli increased activations in a right-lateralized frontoparietal system, when they were presen

123 Aside from the language-selective left-lateralized frontotemporal network, language comprehensi

124 A left-lateralized FTP network was activated during Speech and

125 A mirror right-lateralized FTP network was activated in the Count and D

126 to study normal and abnormal development of lateralized function in the developing brain and have co

127 but only to NaCl, suggesting some degree of lateralized function.

128 and that this reduction correlates with left-lateralized functional and structural frontoinsular and

129 that seems to be at odds with the notion of lateralized functions in cerebral cortex.

130 gamma oscillators bilaterally, synchronizing lateralized gamma strings to converge optimally on CA1 t

131 to first initiate and then actively maintain lateralized gene expression in the gustatory system of t

132 Once established during development, lateralized gene expression patterns need to be maintain

133 cted human volunteers to classify words with lateralized hand responses while falling asleep.

134 This left-lateralized hierarchy originated near primary auditory c

135 Here we examined whether lateralized hippocampal memory processing is present in

136 Furthermore, we observed two lateralized human frontoparietal networks in the cortica

137 subliminal threat induced a pattern of right-lateralized hyperactivation in the amygdala and fusiform

138 tivity in temporal language regions was left-lateralized in 66.7% and 58.3% of individuals during wor

139 specialized brain networks that are usually lateralized in adult population.

140 including those that will eventually become lateralized in adulthood.

141 including those that will eventually become lateralized in adulthood.

142 he 4-8 Hz coupling remained right-hemisphere lateralized in both conditions.

143 Postmortem cortical pathology was left-lateralized in both FTLD-TDP (beta = -0.15, standard err

144 al (posterior segment) connections are right lateralized in childhood, but become progressively bilat

145 ous resting state oscillations are similarly lateralized in children.

146 that sensory responses to light and odor are lateralized in larval zebrafish habenulae and that loss

147 This tract is left lateralized in right-handed subjects, suggesting a possi

148 proportion of opioid receptors are strongly lateralized in the spinal cord, interregional coexpressi

149 Most likely, sexual hormone effects are lateralized in this brain region, leading to higher syna

150 and angry prosody conditions exhibited right lateralized increases in HbO compared to the neutral con

151 one) changes that alter word meaning is left-lateralized indicating that linguistic function and lang

152 More strongly lateralized individuals had a higher capture success.

153 that simply mirrors that of typical leftward lateralized individuals.

154 these experiments confirm that being highly lateralized is ecologically advantageous, exposure to ch

155 ticular, gain access to a predominantly left-lateralized language and semantic system.

156 anguages, while language production was left lateralized, lateralization for language comprehension w

157 In contrast to strongly lateralized left hemisphere activations for language in

158 Whether the speech sensory-motor system is lateralized, like higher-order language processes, or bi

159 ral activity in visual cortex in a spatially lateralized manner even in visually deprived individuals

160 s is increased if stimuli are presented in a lateralized manner so that they are incongruous with the

161 spiral fiber neurons excite the M-cell in a lateralized manner.

162 logy in one sex correlates or coevolves with lateralized mating behavior in the other sex remains lar

163 While lateralized mating behaviors are taxonomically widesprea

164 Asymmetric genitalia and lateralized mating behaviors occur in several taxa, yet

165 lateralization can be dissociated from other lateralized measures of target selection, indicating tha

166 essary to precisely identify these distinct, lateralized mechanisms.

167 ribution of resources amongst systematically lateralized memory items.

168 Remarkably, a model incorporating this lateralized memory predicted that the nondominant arm wo

169 etries in the TGF-beta signaling pathway and lateralized methylation of CpG islands.

170 information, zebrafish larvae show intrinsic lateralized motor behavior that is mediated by a cluster

171 ent electrophysiological signal triggered by lateralized movements to robustly demonstrate the retrie

172 fast RTs were preceded by earlier and larger lateralized N2pc waves, reflecting faster and stronger a

173 evealed the recruitment of a partially right-lateralized network comprising lateral occipitotemporal

174 associated with grey matter loss in a right-lateralized network including insula (P < 0.05 corrected

175 thy adults demonstrate involvement of a left-lateralized network of frontal, temporal, and parietal r

176 tual learning modulates activation in a left-lateralized network, including inferior frontal gyrus (I

177 cts for both modalities were found in a left-lateralized network, including left posterior middle tem

178 ement) revealed the activation of a strongly lateralized network, where the infra-parietal lobule (IP

179 ation in a communicative paradigm recruits a lateralized network, with left fronto- and right parieta

180 s identify, for the first time, distinct and lateralized neural substrates critical for correcting un

181 The disappearance of a lateralized neural trace for the relevant S1 pulse did n

182 Altered lateralized neurodevelopment may therefore be a feature

183 n, is sufficient to develop specialized left lateralized neuronal circuits, thereby pointing to an ea

184 n eccentric dot) or auditory attention (with lateralized noise) while they performed an auditory spat

185 Covert tracking of lateralized objects evokes a difference between slow-wav

186 ally specific TMS pulses were delivered over lateralized occipital cortex at 100, 200, or 400 ms into

187 Voxel-based morphometry showed left-lateralized occipito-temporal atrophy in both patients,

188 These results provide evidence for left-lateralized occipito-temporo-parieto-frontal network of

189 t olfactory system is symmetric, with highly lateralized odor flow and neuronal responses.

190 PC) using ex vivo slices from rat pups given lateralized odor preference training.

191 In pups, the lateralized olfactory networks are independent, permitti

192 lus: (1) contralateral; (2) bilateral highly lateralized; or (3) at the center near 0 ILD.

193 connections between IP and LDTg displayed a lateralized organization, with LDTg inputs to IP being p

194 first to demonstrate that mammary glands are lateralized organs, and, moreover, that mammary glands h

195 characterizing effective connectivity during lateralized orienting and reorienting of attention, resp

196 Motor cortex (M1) has lateralized outputs, yet neurons can be active during mo

197 Though this approach revealed a lateralized parieto-occipital negative slow wave (i.e.,

198 group (p < 0.007), consistent with the left lateralized pattern of neurodegeneration in PPA.

199 failure, and we suggest that discordant and lateralized patterns of associativity in SC and FC may p

200 lness, a proportion similar to subjects with lateralized periodic discharges (57%) and significantly

201 with LRDA and comparison with subjects with lateralized periodic discharges (also known as periodic

202 Lateralized periodic discharges (LPDs) had the highest a

203 Most patients (80%-90%) in the LRDA and lateralized periodic discharges groups who had seizures

204 ith other focal EEG abnormalities, including lateralized periodic discharges in 44%of cases.

205 y or generalized periodic discharges and any lateralized periodic discharges or electrographic seizur

206 Lateralized periodic discharges were associated with sei

207 Lateralized rhythmic delta activity and lateralized periodic discharges were both associated wit

208 harges (B[I]RDs) (2 points); (2) presence of lateralized periodic discharges, lateralized rhythmic de

209 ients has a similar clinical significance as lateralized periodic discharges.

210 ange reaction times are associated with left-lateralized phonological processing and good CI outcome.

211 l cortex in the context of reorganized right-lateralized phonological processing compromises its avai

212 er of feature-based selection is the N2pc, a lateralized posterior negativity emerging around 180-200

213 ave divergent anatomic distributions of left-lateralized postmortem pathology that relate to antemort

214 face encoding, control subjects showed right lateralized prefrontal cortex and bilateral hippocampal

215 MN, as well as in DMN connections with right lateralized prefrontal regions (in frontoparietal networ

216 It is unclear whether left-lateralized processing of faster rhythms and right-later

217 ging the conventional view of segregated and lateralized processing of music versus language.

218 lized processing of faster rhythms and right-lateralized processing of slower rhythms bases upon hemi

219 ological evidence that risk-taking bias is a lateralized push-pull neural system governing counterint

220 ort that the visual system alone can recruit lateralized, rapid escape motor programs, similar to tho

221 timing of the stimulus- and response-locked lateralized readiness potential (indexing motor-response

222 and the EEG exhibited an abrupt rise in the lateralized readiness potential (LRP) on a subset of bia

223 The lateralized readiness potential (LRP), an electrophysiol

224 both the stimulus-locked and response-locked lateralized readiness potentials (LRPs).

225 potentials synchronized to stimulus, but not lateralized readiness potentials synchronized to respons

226 which were accompanied by prolonged PCN and lateralized readiness potentials synchronized to stimulu

227 focal-attentional selection times, while the lateralized readiness potentials synchronized to stimulu

228 tern analysis revealed a network of six left-lateralized regions largely outside of category-selectiv

229 uppression following tactile stimulation was lateralized relative to the stimulated hand over central

230 of the arcuate fasciculus are left and right lateralized, respectively, and remain lateralized throug

231 present the first noninvasive evidence for a lateralized response to noxious and non-noxious stimuli

232 on-making in these tasks relied on spatially lateralized responses, confounding the ability to genera

233 visual' cortex was not recruited to the left-lateralized resting-state network and showed high interh

234 ipital cortex was also recruited into a left-lateralized resting-state network that usually comprises

235 Generalized periodic discharges (GPDs) and lateralized rhythmic delta activity (LRDA) were associat

236 Lateralized rhythmic delta activity and lateralized peri

237 Lateralized rhythmic delta activity in critically ill pa

238 s defined as greater than or equal to 1.5 Hz lateralized rhythmic delta activity or generalized perio

239 n multivariable analyses in the lobar group, lateralized rhythmic delta activity predicted electrogra

240 Lateralized rhythmic delta activity was an independent p

241 s with lobar intraparenchymal hemorrhage and lateralized rhythmic delta activity were six times as li

242 presence of lateralized periodic discharges, lateralized rhythmic delta activity, or bilateral indepe

243 Cross-sectional prevalence of lateralized rhythmic delta activity; EEG characteristics

244 We found that in patients with left lateralized seizure onset zones, spikes outside the seiz

245 ory system or whether asymmetry results from lateralized sensorimotor interactions.

246 on strategies typically involve balanced and lateralized sensory input and early neuronal processing.

247 This allowed us to track the reactivation of lateralized sensory memory traces during retrieval.

248 kable switch of BOLD activity within a right lateralized set of brain regions related to awareness an

249 Lateralized shifts in alpha-band activity were indeed ob

250 Moreover, these lateralized signals increased with postcue sleep spindle

251 h directed deflections can be triggered by a lateralized source of odor.

252 ible sine-wave speech engaged a typical left-lateralized speech processing network.

253 gh connecting fibre tracts, forming the left lateralized speech sensory-motor system.

254 suggests a close relationship between (left-lateralized) speech production areas and the implementat

255 ssection for nodal relapse) in patients with lateralized stage T1 or T2 oral squamous-cell carcinomas

256 development and cell motility genes in right-lateralized structures.

257 havior and neuronal generation genes in left-lateralized structures; and (iii) nervous system develop

258 ect a target at a specific location produces lateralized suppression in the contralateral hemisphere.

259 plasticity by asking whether a strongly left-lateralized system can successfully reorganize to the ri

260 Second, a specific lateralized system learns "consummatory" limb-withdrawal

261 ntal Eye Field (FEF) prior to the onset of a lateralized target.

262 slowing of response times to left and right lateralized targets.

263 e to speech sounds and have abnormally right-lateralized temporal cortex response to language; this d

264 e previously observed a trend for abnormally lateralized temporal responses to language (i.e. greater

265 o highly interactive routes--a strongly left lateralized temporosylvian language network for verbal c

266 While the mouse MePD is generally less lateralized than in rats, we did find that the sex diffe

267 Four-dimensional CT lateralized the abnormal glands with 93.7% accuracy (134

268 olume nor metabolite deviations consistently lateralized the epileptogenic hippocampus.

269 nally, we show that the more left hemisphere-lateralized the pedunculopontine nucleus tract volume, t

270 Odor preference memory can be lateralized through naris occlusion as the anterior comm

271 right lateralized, respectively, and remain lateralized throughout adolescence and early adulthood.

272 We conclude that, while language is left-lateralized throughout life, the RH contribution to lang

273 tory cortices of a group of 14 patients with lateralized tinnitus (eight left ear) and 14 controls ma

274 dings and MRI findings, 50 patients with EEG lateralized TLE and normal structural Magnetic Resonance

275 neous epileptiform discharges were initially lateralized to ipsilateral neocortex but became bilatera

276 suggests an effect of TMEM106B on functions lateralized to the dominant hemisphere, such as language

277 We have long known that language is lateralized to the left hemisphere (LH) in most neurolog

278 arger in March than in December or May/June, lateralized to the left hemisphere and specific to behav

279 left hand recruit a common network strongly lateralized to the left hemisphere especially during pla

280 anguage-selective network, which is robustly lateralized to the left hemisphere, these responses were

281 They are also specifically lateralized to the left hemisphere.

282 VC shows that control of syllables is mostly lateralized to the left HVC, whereas transition probabil

283 e infra-parietal lobule (IPL) activation was lateralized to the left, while the infero-frontal gyrus

284 t vestibular cortical processing is strongly lateralized to the non-dominant hemisphere.

285 Lateralized top-down motor influences can affect asymmet

286 he N2pc event-related potential component, a lateralized transient EEG response that has been tightly

287 Following four spaced lateralized trials, the AMPA receptor-mediated fEPSP is

288 nclude an opacified and hypoplastic sinus, a lateralized uncinate process, depression of the orbital

289 d anxiety-related hyper-function of the left-lateralized ventral attention and salience networks.

290 on to invalidly cued targets engages a right-lateralized ventral frontoparietal network comprising th

291 e consistent with the highly replicable left-lateralized ventral visual processing stream.

292 s that normally enable integration of highly lateralized visual and motor processes.

293 Most species display strong lateralized visual behaviors using their left eye/foot t

294 ticipants attended selectively to one of two lateralized visual-stimulus streams while task-irrelevan

295 ults have implications for interpreting left lateralized vOT activation during reading.

296 Here, we investigated whether left lateralized vOT responses for words were the consequence

297 WM) capacity have been characterized using a lateralized VWM task in which participants had to rememb

298 Neural responses to pup calls were lateralized, with co-tuned and temporally precise excita

299 It is also highly lateralized, with the right MePD larger than the left in

300 his method, we confirm that speech is highly lateralized, with the vast majority of behavioral effect