ライフサイエンスコーパス: lateralization

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

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

3 uation of the structural bases of functional lateralization.

4 dominance modify the likelihood of atypical lateralization.

5 ed as a proxy for atypical brain hemispheric lateralization.

6 ties of core auditory areas lack hemispheric lateralization.

7 for attention, independently of the side of lateralization.

8 interfaces demonstrated increased connexin43 lateralization.

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

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

11 to their prey, constraining the evolution of lateralization.

12 etal drug exposure may alter normal cerebral lateralization.

13 or environmental mechanisms control cerebral lateralization.

14 del to study the genetic basis of functional lateralization.

15 eye were compared to determine any potential lateralization.

16 that changes in eye position affect auditory lateralization.

17 by specific visual areas during task-driven lateralization.

18 t cerebral regions that are known to exhibit lateralization.

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

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

21 mination, level discrimination, and binaural lateralization.

22 the corpus callosum helps to drive language lateralization.

23 ities provided qualitative information about lateralization.

24 etween handedness and the extent of language lateralization.

25 s, including individual differences in brain lateralization.

26 andedness in which we also measured language lateralization.

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

28 stent with well developed specialization and lateralization.

29 -surgical intellectual function and language lateralization.

30 pical lateralization, and degree of language lateralization.

31 glect and may relate to its right hemisphere 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 example, through changes in interhemispheric lateralization, activity of association cortices linked

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

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

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

38 Lateralization analyses demonstrated that the effect of

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

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

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

42 insights into mechanisms underlying cerebral lateralization and dyslexia.

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

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

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

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

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

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

49 Activation asymmetry, language lateralization and performance on preoperative neuropsyc

50 robust inhibition, thereby reducing cerebral lateralization and permitting interference to influence

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 ous study has directly compared CC size with lateralization assessed by functional imaging data.

67 ditory cortex may be attributable to limited lateralization at the population level, despite what may

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

69 vocated as a potential marker for functional lateralization because its size is supposedly proportion

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

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

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

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

74 To test whether such neuroanatomical lateralization characterizes another species with comple

75 Further evidence of lateralization comes from morphological analyses of sail

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

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

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

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

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

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

82 Right lateralization during increased prosodic processing is c

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

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

85 or less likely to show differences in their lateralization (e.g., left vs right handers).

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

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

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

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

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

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

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

93 This lateralization extended to the receptor epithelium respo

94 able evidence suggests that left hemispheric lateralization for language comprehension in humans is a

95 ubjects who had a larger CC showed more left lateralization for language in posterior temporal and in

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

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

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

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

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

101 tal language disorders and atypical cerebral lateralization has been postulated since the 1920s, but

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

103 een histological architecture and behavioral lateralization has not yet been investigated.

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

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

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

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

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

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

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

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

112 ional deficits following stroke reflect this lateralization in control.

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

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

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

116 Motor lateralization in humans has primarily been characterize

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

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

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

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

121 ernicke's territories, with extreme leftward lateralization in more than half of the subjects and bil

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

142 and identified patients exhibiting defective lateralization including dextrocardia, asplenia and inte

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

144 t visual processing, can be estimated from a lateralization index of posterior alpha-activity.

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

146 When expressed as a lateralization index, these alpha-changes differed signi

147 Language lateralization indices were derived from functional magn

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

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

150 Lateralization is a fundamental principle of nervous sys

151 Cerebral lateralization is a fundamental property of the human br

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

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

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

155 Cerebral lateralization is expressed at both the structural and f

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

157 Lateralization is not exclusive to language because late

158 Functional MRI for language lateralization is now a clinical tool.

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

160 Lateralization is widespread throughout the animal kingd

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

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

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

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

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

166 Patients' abnormal hippocampal lateralization may play a role in the hippocampal-depend

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

168 However, lateralization might be costly because it increases pred

169 cally, bilateral representation, not extreme lateralization, might ultimately be advantageous for spe

170 The unusual lateralization of abnormalities in CHILD syndrome reflec

171 that the ASD group had significantly reduced lateralization of activation patterns in letter fluency

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

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

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

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

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

177 results suggest that estrogen influences the lateralization of an odor memory/discrimination task and

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

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

180 ary scenarios including: (1) microstructural lateralization of auditory cortical circuitry may be a u

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

182 tion regarding the normative development and lateralization of brain networks across time.

183 Lateralization of cerebral activity during emotional str

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

185 The findings suggest that lateralization of color CP changes with color term acqui

186 purpose of this study was to investigate the lateralization of contraction anisocoria in young female

187 Such right-side lateralization of contraction anisocoria is much greater

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

189 Right lateralization of cortical regions mobilized for prosody

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

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

192 in posterior fiber tract course, and reduced lateralization of fiber coherence in WS.

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

194 Lateralization of function in auditory cortex has remain

195 especially information concerning prefrontal lateralization of function.

196 Dopamine-induced lateralization of functional activity and networks durin

197 We show lateralization of functional connectivity of bilateral v

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

199 To examine the extent of lateralization of gcy gene expression patterns in the AS

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

201 rying rates of stimulus change and rightward lateralization of increasing spectral information.

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

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

204 account of the consequences of a failure of lateralization of language functions to the right as wel

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

206 Lateralization of language to the left hemisphere is con

207 The lateralization of language via invasive methods may not

208 tudy revealed change in anatomic location or lateralization of language-receptive (Wernicke) (28% of

209 unction was correlated with right hemisphere lateralization of language.

210 Future studies of abnormal lateralization of left hemisphere language functions nee

211 s coeruleus, additional studies examined: 1) lateralization of locus coeruleus efferents to these reg

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

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

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

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

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

217 rotaxy, a disorder characterized by abnormal lateralization of normally asymmetric thoracic and abdom

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

219 These results suggest that lateralization of pain in migraine is due to lateralized

220 These findings suggest that the degree of lateralization of perisylvian pathways is heterogeneous

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

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

223 Parkinson's disease patients did not lead to lateralization of power suppression at lower frequencies

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

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

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

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

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

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

230 ontralateral to movement, so we posited that lateralization of subcortical gamma reactivity should oc

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

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

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

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

235 The lateralization of the CRT-FA correlation to right visual

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

237 o the left hemisphere, whereas the degree of lateralization of the imitation circuitry in humans is u

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

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

240 e dopamine depletion might contribute to the lateralization of the nigrostriatal system observed in s

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

242 e presence of KV, suggesting roles for KV in lateralization of the pharyngeal skeleton when fgf8 is a

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

244 Lateralization of the ventricular gap junction protein c

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

246 ociation areas is consistent with functional lateralization of these regions.

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

248 The lateralization of this defect led us to investigate the

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 reased in ischemic hearts; despite extensive lateralization of total Cx43, pS368-Cx43 remained predom

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

253 ultidimensionality and consider variation in lateralization over developmental time.

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

255 = 5.202; 95% CI = (1.665, 16.257)], seizure lateralization [P = 0.001; OR of right versus left = 2.0

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 Because our model of lateralization predicts that contralesional deficits wil

260 The degree of lateralization present in these distinct systems selecti

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

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

263 sensitive to sensory processing demands and lateralizations related to shifting of covert attention

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

265 evealed that, as CC size increased, stronger lateralization resulted from more left hemisphere activa

266 Furthermore, our lateralization results suggest left hemisphere specifici

267 her factors such as seizure localization and lateralization, seizure duration, contralateral spread o

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 hesis that aging reduces functional cerebral lateralization through corpus callosum (CC) degradation.

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

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

276 tical responses showed the expected leftward lateralization to varying rates of stimulus change and r

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

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

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

280 Lateralization value and performance of lobar localizati

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

282 ampal activation during TP, and greater left lateralization was associated with better performance on

283 Language lateralization was clearly observed to be a dynamic proc

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

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

286 This lateralization was more pronounced with higher anxiety.

287 This alpha power lateralization was not maintained steadily but fluctuate

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

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

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

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

292 ory fluency, no between-group differences in lateralization were found, in light of greater bilateral

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

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

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

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 cue and during the delay period showed clear lateralization with larger responses to trials in which

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.