ライフサイエンスコーパス: lateralization

1 ior Wernicke's area that exhibited rightward lateralization).

2 es and may indicate an early origin of brain lateralization.

3 mination, level discrimination, and binaural lateralization.

4 the evolutionary origins of vertebrate brain lateralization.

5 the corpus callosum helps to drive language lateralization.

6 ities provided qualitative information about lateralization.

7 etween handedness and the extent of language lateralization.

8 s, including individual differences in brain lateralization.

9 andedness in which we also measured language lateralization.

10 ction, from strong left-sided to symmetrical lateralization.

11 stent with well developed specialization and lateralization.

12 -surgical intellectual function and language lateralization.

13 pical lateralization, and degree of language lateralization.

14 glect and may relate to its right hemisphere lateralization.

15 r visual field, independent of the degree of lateralization.

16 uation of the structural bases of functional lateralization.

17 dominance modify the likelihood of atypical lateralization.

18 ed as a proxy for atypical brain hemispheric lateralization.

19 ties of core auditory areas lack hemispheric lateralization.

20 for attention, independently of the side of lateralization.

21 interfaces demonstrated increased connexin43 lateralization.

22 n, and 1 (4%) demonstrated right-hemispheric lateralization.

23 le one (2%) demonstrated a right-hemispheric lateralization.

24 etal drug exposure may alter normal cerebral lateralization.

25 or environmental mechanisms control cerebral lateralization.

26 del to study the genetic basis of functional lateralization.

27 o look for specializations that may underlie lateralization.

28 to their prey, constraining the evolution of lateralization.

29 t cerebral regions that are known to exhibit lateralization.

30 added to coral-reef waters, impaired visual-lateralization.

31 p size because of a lack of population-level lateralization.

32 (85%) demonstrated left-hemispheric language lateralization, 3 (11%) demonstrated symmetric activatio

33 ve video electroencephalographic recordings, lateralization accuracy was 88% with quantitative MR ima

34 Asymmetry, or cerebral lateralization, allows functional specialization of bila

35 en greater controversy surrounds hemispheric lateralization along the parasympathetic-sympathetic axi

36 Level-invariant decoding of sound lateralization also becomes possible in the active state

37 LQs, but individuals with atypical language lateralization also exhibited higher rates of atypical f

38 ers have been hypothesized to play a role in lateralization although mechanisms by which this occurs

39 Lateralization analyses demonstrated that the effect of

40 ight-handed children showed left-hemispheric lateralization and 3 (6%) demonstrated a symmetric activ

41 correlation between the degree of anatomical lateralization and asymmetry of performance on visuospat

42 of the association between atypical language lateralization and developmental disorders may benefit i

43 insights into mechanisms underlying cerebral lateralization and dyslexia.

44 se relationship between contralaterality and lateralization and elucidate similarities and difference

45 nce in favor of the hypothesis that language lateralization and handedness are related.

46 Copper rockfish exhibited reduced absolute lateralization and increased escape time at the lowest D

47 ment of the sensorimotor systems in language lateralization and its plasticity.SIGNIFICANCE STATEMENT

48 ers and are of interest given atypical brain lateralization and language development associated with

49 ions and languages, and examined hemispheric lateralization and learning-dependent plasticity of the

50 as to evaluate and optimize the performance (lateralization and lobar localization value of epileptic

51 688 BP(ND) and [(18) F]FDG uptake to compare lateralization and localization differences.

52 The accuracy of 3D VNE in lateralization and localization was 77.2% and 64.9%, res

53 level, we modeled the increased gap junction lateralization and lower conduction velocity due to down

54 ermine whether the side of deafness affected lateralization and magnitude of evoked blood oxygen leve

55 hat the direct associations between language lateralization and motor asymmetries are much weaker tha

56 Activation asymmetry, language lateralization and performance on preoperative neuropsyc

57 There was no correlation between language lateralization and planum temporale asymmetry in the con

58 anguage by establishing robust principles of lateralization and plasticity of the main language syste

59 verbally described hypotheses about language lateralization and recovery have been generated.

60 ellent, noninvasive alternative for language lateralization and should be considered for the initial

61 rong correlation between the degree of alpha lateralization and the magnitude of the cueing effect as

62 appeared in the right hemisphere, supporting lateralization and top-down inhibition theories of emoti

63 loud sounds to a symmetric preference across lateralizations and intensities, gain-modulation effecti

64 alue for the correct side of the adenoma(s) (lateralization) and the correct quadrant of the neck (lo

65 he brain region affected, (2) confirming its lateralization, and (3) demonstrating that a large part

66 were performed for left-handedness, atypical lateralization, and degree of language lateralization.

67 alization, early seizure onset with temporal lateralization, and left hemisphere focus with a unilate

68 EG imaging findings and the IAP for language lateralization, and provide new insights into the spatio

69 erties, their relations with gestures, their lateralization, and their neurofunctional correlates as

70 phy of activation, the extent of hemispheric lateralization, and what aspects of the stimulus are nec

71 etween these encoding schemes and functional lateralization are not fully understood.

72 strate that two distinct forms of functional lateralization are present in the left vs. the right cer

73 Relationships to timing and their lateralization are supported by parallels in the microst

74 ation was the only clinical effect showing a lateralization, as they were evoked only in the non-domi

75 uppression-related alpha oscillations, alpha lateralization at the individual, single-trial level was

76 We also suggest that the conclusions about lateralization based on an unselected sample of the popu

77 s an effective tool for determining language lateralization before electrode implantation and is espe

78 ORNs, providing a structural basis for odor lateralization behavior.

79 found differences in the extent of language lateralization between males and females with males exhi

80 of the two eyes involve not only a dominant lateralization but also some avenue of bilaterality.

81 between individuals (i.e., population-level lateralization), but evidence for this effect is mixed.

82 Moreover, we found that alpha lateralization can be dissociated from other lateralized

83 alternating attacks, individual-level attack lateralization can evolve, without the negative conseque

84 Further evidence of lateralization comes from morphological analyses of sail

85 other brain functions and whether defects in lateralization contribute to neurological deficits.

86 These findings suggest that Cx43 lateralization contributes significantly to DMD arrhythm

87 gree of stimulation-related change in neural lateralization correlated with the stimulation-related c

88 09, SE = 0.04, p = 0.015), but the degree of lateralization decreased with greater overall dementia s

89 In middle vOT, lateralization depended on a combination of visual exper

90 In anterior vOT, lateralization depended on the semantic demands of the t

91 In posterior vOT, lateralization depended on the spatial frequency of the

92 e cues, suggesting that posterior alpha-band lateralization does not index automatic tactile transfor

93 Right lateralization during increased prosodic processing is c

94 r neurotransmitter, dopamine, on hemispheric lateralization during real-life speaking using a multimo

95 f inter-hemispheric dissociation of language lateralization (e.g. Broca's area in the left, and Werni

96 ons in humans show an asymmetric hemispheric lateralization--e.g., right brain specialization for spa

97 TEMENT Cortical motor control exhibits clear lateralization: each hemisphere controls the motor outpu

98 ed an association of handedness with frontal lateralization, early seizure onset with temporal latera

99 Strikingly, the lateralization effect was dependent upon the subjects' h

100 Importantly, these lateralization effects were stronger when the memory ite

101 represented a priori in both hemispheres and lateralization emerges via cross-hemispheric communicati

102 ses this hierarchy suggests that hemispheric lateralization enables specialized tracking of acoustic

103 This lateralization extended to the receptor epithelium respo

104 le language production was left lateralized, lateralization for language comprehension was highly var

105 The development of hemispheric lateralization for language is poorly understood.

106 studies in infants and children indicate LH lateralization for language.

107 lateralize independently), we determined the lateralization for spatial attention in a group of indiv

108 for temporal modulations and a weaker right lateralization for spectral modulations.

109 s with known atypical right hemispheric (RH) lateralization for speech production, based on a previou

110 ributions from both hemispheres, with a left lateralization for temporal modulations and a weaker rig

111 eaders, our paradigm compared activation and lateralization for words and nonlinguistic stimuli durin

112 We found that increased left lateralization for words relative to pictures was the co

113 ound localization commonly assume that sound lateralization from interaural time differences is level

114 there is little evidence that weak cerebral lateralization has common genetic origins with language

115 Our results indicate that loss of brain lateralization has significant consequences upon sensory

116 Lateralization, i.e. the preferential use of one side of

117 individual differences, for example in tract lateralization, important to understand heterogeneity of

118 indicating typical left-hemispheric language lateralization in 82.1% of the participants.

119 riatal dopamine and a complete recovery from lateralization in a test of sensorimotor behavior.

120 vide a more mechanistic basis to account for lateralization in auditory cortex.

121 atively simple olfactory system demonstrates lateralization in both human and non-human animals.

122 Here, we explored functional lateralization in both primary olfactory cortex - a regi

123 onversely, the posterior segment shows right lateralization in childhood but becomes progressively bi

124 in the human brain, in relation to language lateralization in children with left-sided focal epileps

125 e right hemisphere, demonstrating functional lateralization in enhanced envelope coding in SNHL liste

126 s only on the right because of a significant lateralization in females, with significantly fewer astr

127 lanum temporale may be unrelated to language lateralization in healthy individuals, but the size of t

128 Motor lateralization in humans has primarily been characterize

129 right, providing further evidence of sensory lateralization in invertebrates.

130 presence of similar mechanisms for language lateralization in left- and right-handed children.

131 udy investigated the development of language lateralization in left- and righthanded children between

132 rates of atypical right-hemispheric language lateralization in left-/mixed-handers, an accurate estim

133 The incidence of atypical language lateralization in left-handed children in this study was

134 rent gold standard for preoperative language lateralization in neurosurgical candidates.

135 eature of the human brain and drives symptom lateralization in Parkinson's disease (PD), but its mole

136 titative relationships between the degree of lateralization in particular brain regions and the level

137 Hemispheric asymmetry and symptom lateralization in PD is linked to genes affecting neurod

138 n the evolution of cortical organization and lateralization in primates.

139 gene level of expression, for the role of IC lateralization in processing novel taste information and

140 provide evidence for individual-level attack lateralization in sailfish.

141 Comparison of lateralization in social and non-social bees tests the h

142 iors have been linked to hemispheric (brain) lateralization in some vertebrates [11-15], evidence of

143 also showed opposite patterns of hemispheric lateralization in the connectivity of dorsomedial and do

144 atomotor (and not auditory) areas determined lateralization in the dorsal auditory pathway.

145 emisphere was the main predictor of language lateralization in the epilepsy group, accounting for 48%

146 a strong trend (P=.059) toward greater left lateralization in the leukoaraiosis group.

147 peri-Sylvian area associated with structural lateralization in the mature brain.

148 increased redirected behavior and a left-eye lateralization in the negative condition.

149 s to sustain the posterior hemispheric alpha lateralization in the period before the target for the l

150 whether there is similar song memory-related lateralization in the songbird brain.

151 onal network and support a context-sensitive lateralization in the top-down (backward) mediation of a

152 heritability of left-handedness and language lateralization in these pedigrees is 0.24 and 0.31, resp

153 been a centrepiece for theories of anomalous lateralization in this disorder.

154 olvement of S1, and its possible hemispheric lateralization, in encoding the affective valence of emo

155 The strength of this hemispheric alpha lateralization, in turn, predicted an individual's atten

156 We have proposed a model of motor lateralization, in which the left and right hemispheres

157 Moreover, the determinants of lateralization include both visual and semantic factors

158 Left-hemispheric language lateralization increased with age in both groups but som

159 For each patient a regional lateralization index was calculated separately for Broca

160 Language lateralization indices were derived from functional magn

161 ed within vertebrate neural circuits and how lateralization influences processing of information in t

162 Even though functional lateralization is a common feature of many nervous syste

163 Lateralization is a fundamental principle of nervous sys

164 Cerebral lateralization is a fundamental property of the human br

165 Asymmetry in the form of left-hemisphere lateralization is a striking characteristic of the cereb

166 tial ability, providing direct evidence that lateralization is associated with enhanced cognitive abi

167 ry preservation, indicating that hemispheric lateralization is central for processing taste saliency

168 Cerebral lateralization is expressed at both the structural and f

169 Our findings demonstrate that alpha power lateralization is modulated in tune with the sensory inp

170 Lateralization is not exclusive to language because late

171 Hence, population-level lateralization is present only for social interactions c

172 Lateralization is widespread throughout the animal kingd

173 e much scientific attention, the function of lateralization, its possible dependence on experience, a

174 ioral experiments, we demonstrate that human lateralization judgments are consistent with predictions

175 characteristic of individuals; rather, weak lateralization may be a consequence of impaired language

176 eral volume differences, subcortical disease lateralization may have been overlooked thus far.

177 Contrary to popular belief, cerebral lateralization may not be a highly heritable, stable cha

178 in three previous studies in which language lateralization measured via dichotic listening, handedne

179 reased only in the semantic group, anomalous lateralization mechanisms might instead be related to fr

180 However, lateralization might be costly because it increases pred

181 individuals with atypical rightward language lateralization (N = 30, 25 LH) do not rely on an organiz

182 The unusual lateralization of abnormalities in CHILD syndrome reflec

183 riteria to define successful cannulation and lateralization of aldosterone production.

184 This study tested whether the hemispheric lateralization of alpha power codes not just the spatial

185 netoencephalogram, spatial attention induced lateralization of alpha power in parietal, but notably a

186 We tested whether lateralization of alpha- and beta-band oscillatory brain

187 Accordingly, lateralization of alpha-band activity in parietal region

188 a potential mechanism for right hemispheric lateralization of amygdala function in pain processing.

189 ted with taste familiarity, whereas the high lateralization of Arc/Arg3.1 expression observed followi

190 rlap, referred to by Vaesen; but also (2) co-lateralization of asymmetric cognitive functions and (3)

191 A right-lateralization of attention effects, but not predictabil

192 d plasticity provides a biological basis for lateralization of auditory cortical processing.

193 ic variants contribute to neurodevelopmental lateralization of brain organization, which in turn infl

194 ogram fractionation, increased fibrosis, and lateralization of cardiomyocyte connexin-40.

195 The hemispheric lateralization of certain faculties in the human brain h

196 ional, and heterogeneous with respect to the lateralization of control in the DLPFC.

197 Right lateralization of cortical regions mobilized for prosody

198 observed reduced gap junction remodeling and lateralization of Cx43 immunosignals, protection against

199 ion of Cx43 and exacerbated ischemia-induced lateralization of Cx43 in isolated adult cardiomyocytes.

200 We also found indices of lateralization of different attention networks: PPI incr

201 eus consistent with previous observations of lateralization of emotionally evoked activity to right v

202 e provide evidence that the well-known right lateralization of face processing arises from imbalanced

203 rentially contributes to both the anatomical lateralization of frontoparietal attentional networks an

204 In contrast, findings on lateralization of function during development are more c

205 especially information concerning prefrontal lateralization of function.

206 Dopamine-induced lateralization of functional activity and networks durin

207 We show lateralization of functional connectivity of bilateral v

208 Significant left-hemispheric lateralization of functional networks during simple but

209 We show that volumetric hemispheric lateralization of globus pallidus (GP) and thalamus (Th)

210 mechanistic explanation for left-hemispheric lateralization of human speech that is due to left-later

211 to NH irrespective of RE/LE stimulation and lateralization of inputs.

212 We finally observed strong lateralization of intrinsic signal responses from the gl

213 explanation for the bilateral yet asymmetric lateralization of language in healthy participants, chro

214 Age-related reductions in left-lateralization of language responses were observed betwe

215 The lateralization of language via invasive methods may not

216 unction was correlated with right hemisphere lateralization of language.

217 specialization at birth characterized by the lateralization of memory functions: the interplay betwee

218 ly, we present evidence of right hemispheric lateralization of mGluR5 modulation of amygdalar nocicep

219 the human brain has been linked with normal lateralization of motor and cognitive functions, disrupt

220 rence in metabolic patterns depending on the lateralization of MTLE may represent distinct epileptic

221 Although the concept of left-hemispheric lateralization of neural processes during speech product

222 humans and songbirds, there is evidence for lateralization of neural responsiveness in these brain r

223 tary specialization has a causal origin (the lateralization of one function causes the opposite later

224 modulating task-specific anticipatory neural lateralization of oscillatory brain activity in a modali

225 ces between PD hemispheres correspond to the lateralization of PD symptoms, with abnormalities being

226 ributions to speech as well as the extent of lateralization of phonological representations within au

227 we investigated the regional specificity and lateralization of potential beneficial stimulation effec

228 as an important factor contributing to right lateralization of prosody.

229 emifields under central fixation, we found a lateralization of reach-related signals with respect to

230 This preference was correlated with lateralization of signal-dependent noise: the direction

231 The source imaging data revealed a clear lateralization of source activation in the 70-120 Hz ran

232 in these regions and drives left-hemispheric lateralization of speech production network.

233 networks during speaking is not dependent on lateralization of structural nigro-striatal and nigro-mo

234 ention paradigm, we show that the volumetric lateralization of subcortical structures (specifically g

235 particularly interested in understanding how lateralization of the arcuate fasciculus impacts on seve

236 Preliminary twin analysis suggested that lateralization of the arcuate fasciculus is a heterogene

237 The extent of functional lateralization of the ASE neurons and genes responsible

238 of evolutionary conservation or convergence, lateralization of the brain is found in both vertebrates

239 the basis for the poorly understood, unique lateralization of the cutaneous and bone malformations o

240 uidance receptors Unc-5 or Robo-2 results in lateralization of the dbd axon, which forms anatomical a

241 olic patterns were observed depending on the lateralization of the epileptogenic TL.

242 gest that the age-related differences in the lateralization of the language perisylvian pathways are

243 ntly, it remains unclear the extent to which lateralization of the nervous system is important for no

244 lization of one function causes the opposite lateralization of the other) or rather is a statistical

245 l cortex, consistent with the putative right lateralization of the stopping network.

246 Lateralization of the ventricular gap junction protein c

247 ors relate to the age-related differences in lateralization of these language pathways is still not k

248 Here we studied response strength and lateralization of this activation using event-related po

249 Moreover, the left hemisphere lateralization of this operation remains controversial.

250 by mislocalization of cell polarity markers, lateralization of tight junctions, deterioration of desm

251 g pathways that impose underlying functional lateralization on a broadly symmetric nervous system are

252 ft-handed individuals with atypical language lateralization on the categorical level, we only detecte

253 zone remodeling (i.e., Gj reduction and Cx43 lateralization) on theta(T).

254 ultidimensionality and consider variation in lateralization over developmental time.

255 reathing showed significant left-hemispheric lateralization (p < 0.0005).

256 The conventional lateralization paradigm suggests individuals are left or

257 sory, and motor regions, and the hemispheric lateralization pattern is largely unknown.

258 ) over sensorimotor areas to modulate neural lateralization patterns induced by unilateral mental mot

259 ontrast to previous studies, we focus not on lateralization per se but rather on patterns of left-hem

260 Because our model of lateralization predicts that contralesional deficits wil

261 The degree of lateralization present in these distinct systems selecti

262 itive correlation between dichotic listening lateralization quotients (LQs) and handedness LQs using

263 ferred hand, and that strength of behavioral lateralization (rather the direction) on this task would

264 have proposed an alternative view that motor lateralization reflects proficiency of each arm for comp

265 are lateralized before adolescence and their lateralization remains stable throughout adolescence and

266 Furthermore, our lateralization results suggest left hemisphere specifici

267 hen the target was fixed in the front, alpha lateralization reversed in direction for the suppression

268 Atypical language lateralization showed suggestive linkage in the 7q34 reg

269 Furthermore, both entrainment and alpha lateralization significantly affected task performance.

270 being among the most overt aspects of human lateralization, studies of this healthy analogue of left

271 henomenon in the neurobiology of language is lateralization: the dominant role of one hemisphere in a

272 nto the developmental mechanisms of language lateralization, this study reveals language-related func

273 nement of the hypothesis linking directional lateralization to social behaviour.

274 conductances' traces gap detection and sound lateralization to their cellular and biophysical origins

275 th age in both groups but somewhat different lateralization trajectories were observed in girls when

276 Activation was affected by tumor lateralization (unilateral or bilateral), macular involv

277 tudy was to examine the dynamics of language lateralization using magnetoencephalographic (MEG) imagi

278 Lateralization value and performance of lobar localizati

279 We also found that the determinants of lateralization varied with the subregion of vOT tested.

280 Language lateralization was clearly observed to be a dynamic proc

281 A significant left-hemispheric lateralization was found in the AR reconstruction of the

282 Moreover, Arc/Arg3.1 lateralization was inversely correlated with taste famil

283 Edinburgh Handedness Inventory, and language lateralization was measured with functional transcranial

284 This lateralization was more pronounced with higher anxiety.

285 This alpha power lateralization was not maintained steadily but fluctuate

286 Left hemispheric lateralization was observed 250 ms earlier in IPL and vC

287 Atypical language lateralization was observed in 19 patients (38%) and in

288 nd contralateral to the cathode, hemispheric lateralization was reduced.

289 For strength of language lateralization, we observed suggestive linkage in the 6p

290 Here, only 0.4% of the variance in language lateralization were explained by handedness.

291 tion-related increase and decrease in neural lateralization were negatively related.

292 The strength and direction of individuals' lateralization were related to where and how the whales

293 ve a failure in sustaining hemispheric alpha lateralization when cued to the left, resulting in an at

294 x differences seem to be present in language lateralization when the power of the study is adequate s

295 es in exploratory behavior and turning bias (lateralization), whereas physiological tests focused on

296 d of P less than 0.001 provided 100% correct lateralization, which was better than visual assessment

297 tes of increase in left-hemispheric language lateralization with age between groups (i.e., independen

298 In addition, these patterns show lateralization, with disassortative mixing within FC sub

299 whether c-Src/ZO-1 interactions affect Cx43 lateralization within the epicardial border zone, we per

300 mation processing were linked to hemispheric lateralization within the IFOF.