ライフサイエンスコーパス: cingulum

1 n altered white matter microstructure of the cingulum).

2 nferior fronto-occipital fasciculi and right cingulum.

3 fornix bilaterally and right dorsal-anterior cingulum.

4 SA in the orbitofrontal cortex and posterior cingulum.

5 uced mean and axial diffusivity in the right cingulum.

6 bundles, particularly in the left subgenual cingulum.

7 depression diagnosis maximally affecting the cingulum.

8 ffect on a second corticolimbic pathway, the cingulum.

9 and an ordering transition at the chimpanzee cingulum.

10 r longitudinal fasciculi and in the anterior cingulum.

11 arning deficits had hypoplasia or atresia of cingulum.

12 gulum; three patients had aberrant fibers of cingulum.

13 ronal structure and function in the anterior cingulum.

14 um, uncinate fasciculus, and parahippocampal cingulum.

15 nsula, thalamus, superior frontal gyrus, and cingulum.

16 ongitudinal fasciculus, corpus callosum, and cingulum.

17 difference = 0.011, p = 0.003) in the right cingulum.

18 and insular cortices, precentral gyrus, and cingulum.

19 ody of the corpus callosum, extending to the cingulum.

20 the SLF-I may be a separable tract from the cingulum.

21 ortex, the medial prefrontal cortex, and the cingulum.

22 for all cortical regions of interest, except cingulum.

23 tional anisotropy (FA) of the left and right cingulum.

24 in the limbic system, such as the fornix and cingulum.

25 ith seizure burden in the bilateral PWMB and cingulum.

26 impaired axonal integrity of the hippocampal cingulum.

27 perior and posterior corona radiata, and the cingulum.

28 s of 2.16% (95% CI, 0.49%-3.84%) in the left cingulum, 1.95% (95% CI, 0.43%-3.47%) in the left uncina

29 r fascicle of the septum pellucidum; (3) the cingulum; (4) the medial olfactory stria; (5) the ventra

30 ing the inferior longitudinal fasciculus and cingulum (61 272 mm3, P < .05).

31 ations were not found in the parahippocampal cingulum, a comparison temporal association pathway.

32 ited shared volume between the SLF-I and the cingulum, a controversy in recent literature.

33 and microstructure of connections within the cingulum, a major white matter tract and conduit of proj

34 reduced microarchitectural integrity of the cingulum, a white matter fiber that connects the entorhi

35 sults demonstrate that temporary blockade of cingulum activity at the time of nerve section reduces a

36 microglial activation in corpus callosum and cingulum along with severe astrogliosis and scar formati

37 For cingulum analysis from diffusion tensor MR imaging, trac

38 es in HS-TLE correlated with parahippocampal cingulum and anterior commissure atrophy, indicating an

39 calculating the DTI indices of the bilateral cingulum and cingulum hippocampal part for each subject.

40 y groups had bilateral atrophy of the dorsal cingulum and corpus callosum fibers, which we interpret

41 the white matter tracts of interest (fornix, cingulum and corpus callosum).

42 se error-corrected), mainly in the uncinate, cingulum and corpus callosum, whereas responders were in

43 ional anisotropy in the internal capsule and cingulum and decreases in the posterior thalamic radiati

44 n the SUV(mean) of the prefrontal cortex and cingulum and DKEFS-sequential tracking (DKEFS-TM4) z sco

45 matter abnormalities in the corpus callosum, cingulum and external capsule, with differing severity a

46 sclerosis in the ipsilateral parahippocampal cingulum and external capsule, with smaller effects acro

47 ct sizes, especially in the corpus callosum, cingulum and external capsule.

48 (fractional anisotropy, FA) of the bilateral cingulum and fornix after controlling for the nine poten

49 highlight the limbic system, especially the cingulum and fornix, as key regions associated with cogn

50 FA in several neural pathways, including the cingulum and frontal aslant tracts.

51 bundles (forceps minor, uncinate fasciculus, cingulum and fronto-striatal fibers).

52 Activations within anterior cingulum and insula correlated with better verbal and vi

53 Higher CRF was associated with higher FA in cingulum and lower MD in hippocampus and entorhinal cort

54 rostrum of the corpus callosum to enter the cingulum and merged with fibres of the lateral pathway w

55 gh 18F-flutemetamol retention (eg, posterior cingulum and precuneus, r = -0.72).

56 rom hippocampus to thalamus to the posterior cingulum and shows promise as a distinct biomarker of si

57 ely, of the total white matter tracts in the cingulum and superior and inferior longitudinal fascicul

58 wed decreased activation particularly in the cingulum and thalamus during both the encoding and recal

59 In particular, the anterior part of the cingulum and the cingulate gyrus isthmus, as well as the

60 mentioned regions and, in addition, with the cingulum and the left hippocampus (cluster level, P < .0

61 hanges were regionally specific to the right cingulum and the right superior and inferior longitudina

62 in the mid-body of the corpus callosum, the cingulum and the superior longitudinal fasciculus (p < 0

63 hild-reported anxiety symptoms and FA in the cingulum and uncinate fasciculus.

64 and long segments of the arcuate fasciculus, cingulum and uncinate--predominantly in the left hemisph

65 er changes, which were most prominent in the cingulum and which correlated with disease severity.

66 st-injury, NFC was observed primarily in the cingulum, and appeared as swollen axons and terminal bul

67 gions, including the right precentral gyrus, cingulum, and bilateral amygdala, contribute to dysregul

68 work (inferior frontal-occipital fasciculus, cingulum, and corpus callosum).

69 ncinate fasciculus, fornix/stria terminalis, cingulum, and corticospinal tract following NBT that wou

70 nate fasciculi, anterior thalamic radiation, cingulum, and corticospinal tract.

71 ly myelinated white matter (corpus callosum, cingulum, and deep cortical white matter).

72 the callosal genu, thalamus, right posterior cingulum, and fornix crus (seven studies; largest cluste

73 oups in subdivisions of the corpus callosum, cingulum, and fornix were measured as indicators of trai

74 wer structural connectivity in the splenium, cingulum, and fronto-occipital fasciculus (t score >2.5;

75 basal forebrain and temporofrontal, insula, cingulum, and hippocampal regions, and with modest corre

76 Injured cortex, striatum, cingulum, and hippocampus also demonstrated significant

77 m in the striatum, as well as in the cuneus, cingulum, and parietal lobe, in all SCA17 patients and p

78 splenium of the corpus callosum, the fornix, cingulum, and superior and inferior longitudinal fascicu

79 atter tracts, including the corpus callosum, cingulum, and superior longitudinal fasciculus (ps < .00

80 normalities observed in the corpus callosum, cingulum, and temporal lobe likely constitute the neural

81 he splenium of the corpus callosum, the left cingulum, and the anterior part of the left arcuate fasc

82 ry networks: the fornix, the parahippocampal cingulum, and the uncinate fasciculus.

83 asciculus, superior longitudinal fasciculus, cingulum, and uncinate underlie these associations.

84 nferior longitudinal, superior longitudinal, cingulum, and uncinate) tracts were quantified using tra

85 o FA values in the corpus callosum and right cingulum; and eye-hand coordination sub-scores to FA val

86 synchronization in the thalamus; cerebellum; cingulum; and insular, prefrontal, and parieto-occipital

87 the cerebellum; basal ganglia; hippocampus; cingulum; and temporo-occipital, insular, frontal, and p

88 tology, suggesting that abnormalities in the cingulum angular bundle might reflect "scarring" effects

89 us, and middle portion of the left and right cingulum angular bundle).

90 Significant cingulum architectural disturbances were observed in tra

91 ing, because characteristics of the anterior cingulum are shown to be related to impulse, attention,

92 nectivity within the corpus callosum and the cingulum are strongly associated with BD.

93 the amygdala, insula, precentral gyrus, and cingulum, as well as in the right frontal superior gyrus

94 periodontal probing depth of 8 mm below the cingulum, associated with a developmental groove.

95 CD200R(+) /Iba1(+) ameboid microglia in the cingulum at P1-P5 were the only CD200R(+) cells in the n

96 n contrast, developmental differences in the cingulum at the level of the parahippocampal region were

97 that a temporary anesthetic blockade of the cingulum at the time of nerve section delayed the onset

98 s Test score by radial diffusivity along the cingulum (beta = -4.3 x 10(4); P < .01), and T2* in the

99 ornix: beta = -1.069; P < .001) and decline (cingulum: beta = -0.115; P < .001; fornix: beta = -0.153

100 t associations with both memory performance (cingulum: beta = -0.718; P < .001; fornix: beta = -1.069

101 tracts, particularly in the corpus callosum, cingulum, bilateral superior and inferior longitudinal f

102 n fibers of the uncinate fasciculus (UF) and cingulum bundle (CB) among MDD subjects.

103 The cingulum bundle (CB) is one of the brain's major white m

104 e superior longitudinal fasciculus (SLF) and cingulum bundle (CB) predicted deviations from the optim

105 The cingulum bundle (CB), specifically the dorsal anterior p

106 A) were measured for the dorsal and inferior cingulum bundle (CB), uncinate, and fornix using probabi

107 et bundles: either the forceps minor (FM) or cingulum bundle (CB).

108 sciculus (ILF), uncinate fasciculus (UF) and cingulum bundle (CB).

109 ssociated with altered microstructure of the cingulum bundle (t274 = 3.48; beta = 0.21; corrected P =

110 ximately 1-cm span along the anterior dorsal cingulum bundle above genu of the corpus callosum.

111 Atypical microstructure of the cingulum bundle and anterior thalamic radiation was asso

112 greater fractional anisotropy in the dorsal cingulum bundle and better performance on measures of re

113 e tracts (crossing between anterior parts of cingulum bundle and body of corpus callosum), which show

114 C) and structural decrements in the anterior cingulum bundle and hippocampus.

115 ildhood to early adulthood, higher FA of the cingulum bundle and inferior frontooccipital fasciculus

116 but also in 5-HT axonal bundles such as the cingulum bundle and medial forebrain bundle.

117 Deficits in the cingulum bundle and mid-hippocampus and ventral prefront

118 with limbic pathways including the posterior cingulum bundle and the fornix were also found.

119 (a measure of white matter integrity) in the cingulum bundle and uncinate fasciculus.

120 of a local anesthetic (bupivacaine) into the cingulum bundle at the time of nerve section could reduc

121 e-abnormalities in fiber collinearity of the cingulum bundle could distinguish 48 adults with OCD (me

122 Among them, the uncinate fasciculus and the cingulum bundle have been associated with aggression and

123 ter disruptions at specific locations of the cingulum bundle may be a hallmark for the early predicti

124 esults indicate that higher FA of the dorsal cingulum bundle may be an acquired feature of persistent

125 The cingulum bundle may play a critical role in protracted m

126 Lower FA within the cingulum bundle of hippocampus and cerebrospinal tracts

127 natomical regions such as the fornix and the cingulum bundle or corpus callosum.

128 right superior longitudinal fasciculi, right cingulum bundle projecting to the hippocampus, left infe

129 ical stimulation of the left dorsal anterior cingulum bundle promoted a positive (mirthful) effect an

130 rlap with the end points of the parolfactory cingulum bundle rather than the parahippocampal cingulum

131 During the procedure, cingulum bundle stimulation enhanced positive affect and

132 demonstrates a robust anxiolytic response to cingulum bundle stimulation in 3 patients with epilepsy.

133 a specific fiber tract, the corpus callosum/cingulum bundle that conveys reciprocal connections betw

134 Results revealed that greater cingulum bundle volume was significantly associated with

135 erently organised within the parahippocampal cingulum bundle was also linked with autobiographical me

136 FA of the cingulum bundle was correlated with functional connectiv

137 ical stimulation of the left dorsal anterior cingulum bundle was discovered to reliably evoke positiv

138 conduction velocity, of the parahippocampal cingulum bundle were associated with autobiographical me

139 sterior, and parahippocampal portions of the cingulum bundle were reconstructed separately using dete

140 g impairments and in the hippocampal part of cingulum bundle which accounted for long-term memory bin

141 eps minor, anterior thalamic radiation(ATR), cingulum bundle(CB), and uncinate fasciculus(UF).

142 ropy genu of corpus callosum and hippocampal cingulum bundle), and cognition.

143 culus) and to the cingulate cortex (via left cingulum bundle), whereas behaviorally salient but nonbe

144 fasciculus, splenium of corpus callosum, and cingulum bundle).

145 ount for these 100 different segments of the cingulum bundle, a repeated measures analysis of varianc

146 l (middle portion) within the left and right cingulum bundle, although did not correlate with symptom

147 perior and inferior longitudinal fasciculus, cingulum bundle, and corpus callosum).

148 er tracts including the uncinate fasciculus, cingulum bundle, and inferior longitudinal fasciculus.

149 d microstructural integrity of the posterior cingulum bundle, as measured by diffusion tensor imaging

150 Notably, the cingulum bundle, being the major white matter tract conn

151 arity and/or white matter integrity), in the cingulum bundle, bilaterally.

152 rations in white matter (in corpus callosum, cingulum bundle, corona radiata, and superior fronto-occ

153 pared to matched controls in the left dorsal cingulum bundle, splenium of the corpus callosum, right

154 The dorsal and hippocampal cingulum bundle, stria terminalis, and fornix were inves

155 development of fractional anisotropy in the cingulum bundle, superior longitudinal fasciculus, inter

156 This change was more marked within the cingulum bundle, the tract connecting the parahippocampa

157 FBA metrics were decreased in the entire cingulum bundle, uncinate fasciculus and anterior thalam

158 and childhood trauma exposure, including the cingulum bundle, uncinate fasciculus, and corpus callosu

159 ibition functions typically subserved by the cingulum bundle.

160 asciculus; and from the cingulate gyrus, the cingulum bundle.

161 re extensively damaged on the dorsal part of cingulum bundle.

162 of AF64A on the cholinergic elements of the cingulum bundle.

163 flow, and mean fractional anisotropy in the cingulum bundle.

164 rostral and dorsal cingulate cortex via the cingulum bundle; and 3) subcortical nuclei.

165 he middle cerebellar peduncles (P<0.001), in cingulum bundles (P=0.002), and in the right orbitofront

166 ted positively with FA in the right and left cingulum bundles (r = .342, p = .052; r = .477, p = .005

167 c radiations, corpus callosum, and bilateral cingulum bundles after controlling for the same possible

168 h altered white matter microstructure in the cingulum bundles and uncinate fasciculi.

169 had 3% to 5% lower FA in the right and left cingulum bundles than FH- individuals (p = .012, p = .05

170 associated with reduced FA in the bilateral cingulum bundles, particularly in the left subgenual cin

171 te fasciculus and hippocampal portion of the cingulum bundles.

172 one-induced demyelination selectively in the cingulum, but not in the corpus callosum.

173 ecrease in fractional anisotropy in the left cingulum-callosal bundle.

174 ) and CBF(mean) of the prefrontal cortex and cingulum can serve as quantitative measures for detectin

175 as associated with decreased FA in the genu, cingulum cingulate gyri, centrum semiovale, inferior lon

176 terations at specific locations on the right cingulum cingulate, the right cingulum hippocampus and a

177 corpus callosum, left fornix, and subgenual cingulum compared with control subjects.

178 ndividual tracts, including the uncinate and cingulum, contributed to this global association.

179 sivity in the amygdala-frontal tract and the cingulum, controlling for postpartum depression.

180 sor imaging abnormalities of the cerebellum, cingulum, corpus callosum, internal capsule, thalamus, b

181 le, the NTRK1-T effect was replicated in the cingulum, corpus callosum, superior and inferior longitu

182 eta = -4.3 x 10(4); P < .01), and T2* in the cingulum cortical projection at 25% depth (beta = -1.7;

183 ities in parahippocampal gyrus and posterior cingulum, extending laterally into adjacent temporo-pari

184 ld-reported anxiety symptoms predicted lower cingulum FA, and this effect was moderated by pubertal s

185 he rodent thalamus, retrosplenial cortex and cingulum fiber bundle are tuned to conjunctive combinati

186 Posterior cingulum fiber integrity predicted the degree of PCC dea

187 erior corona radiata, cortico-spinal tracts, cingulum fibre bundles, external capsule, forceps minor

188 mbic association tracts such as the anterior cingulum, fornix and uncinate fasciculus.

189 actions for FA were found in the hippocampal cingulum, fornix, and stria terminalis, posterior corona

190 coordination sub-scores to FA values in the cingulum, fornix, anterior commissure, corpus callosum a

191 have differential effects on the hippocampal cingulum, fornix, stria terminalis, posterior corona rad

192 ippocampal volume (beta = 10.598; P < .001), cingulum FW and SPARE-AD index (beta = -0.532; P < .001)

193 tracts including the in uncinate fasciculus, cingulum-gyrus, and forceps major and minor, with eviden

194 he DTI indices of the bilateral cingulum and cingulum hippocampal part for each subject.

195 ion, as well as the WM integrity of the left cingulum hippocampal part.

196 white matter (WM) microstructure of the left cingulum hippocampal part.

197 uperior longitudinal fasciculi and the right cingulum-hippocampal projection compared with their coun

198 d significantly lower FA values in the right cingulum-hippocampal projection than their counterparts

199 s on the right cingulum cingulate, the right cingulum hippocampus and anterior corpus callosum (CC) i

200 The CBF(mean) of the cingulum, hippocampus, and prefrontal cortex correlated

201 ded cerebral cortex, lateral septal nucleus, cingulum, hippocampus, thalamus, amygdala, and vestibula

202 which allows us to optimize the location of cingulum in a global sense based on the diffusion measur

203 ith reduced FC mainly in the parahippocampal cingulum in Abeta-positive individuals.

204 greater decrease in FA in the left posterior cingulum in bipolar disorder.

205 tified between VMIQ and avgERD of the middle cingulum in the beta band and with avgERD of the left in

206 investigations into the role of the anterior cingulum in the development of psychopathology in VPT in

207 sotropic intracellular diffusion in the left cingulum, in the left superior longitudinal fasciculus,

208 ediate values in the amygdala, white matter, cingulum, insula, frontal cortex, putamen, temporal and

209 45 on neuropsychological performance and the cingulum integrity in Chinese Han population.

210 lative intervention techniques targeting the cingulum, internal capsule, and other limbic regions.

211 Cingulum is widely studied in healthy and psychiatric su

212 ociated with lower FA in the right posterior cingulum, left callosal splenium, right inferior fronto-

213 ropy in the left cingulate gyrus part of the cingulum, left posterior thalamic radiation, and bilater

214 Specifically, greater bilateral cingulum length predicted lower PGBI-10M at follow-up.

215 thway of the brain, the limbic fibers of the cingulum, lesions of which have been associated with sev

216 c features, such as large dental dimensions, cingulum-like structures at the dentine level in the pos

217 ences were found in the ASD group in the mid-cingulum longitudinal and u-fibers, the corpus callosum

218 Cingulum, longitudinal fasciculus, optic radiation, forc

219 as associated with ACC threat reactivity via cingulum microstructural changes (index of moderated med

220 ere related, additionally, to right anterior cingulum microstructure.

221 a strong decrease of oligodendrocytes in the cingulum of Cx43/Cx32dKO mice.

222 lesions in limbic system structures (eg, the cingulum) on the right than did subjects who did not mee

223 cts, such as the callosal genu and splenium, cingulum, optic radiations, and the superior longitudina

224 , and was correlated with FIQ and PIQ in the cingulum, optic radiations, superior fronto-occipital fa

225 r medial temporal regions and contralesional cingulum or pallidum contribute to long-term verbal and

226 SP MS group had abnormal recruitment of the cingulum or precuneus.

227 TSD patients had increasing FA of the dorsal cingulum over time, and at reassessment these FA values

228 be (P = .004), precuneus (P = .02), anterior cingulum (P = .002), and superior parietal lobule (P = .

229 ns in the microarchitecture of the posterior cingulum (PC), a white matter tract proximal to the hipp

230 odifications of the activity of the anterior cingulum, PCC and/or precuneus, left dorsolateral PFC, a

231 on other tracts, notably the parahippocampal cingulum (PHC).

232 ntervention group had an increased FC in the cingulum, precuneus, and bilateral parietal cortex and a

233 FW in limbic tracts, such as the cingulum, presented the strongest associations with both

234 with alterations in diffusivity in the left cingulum (r = -0.66, P = .01) and superior longitudinal

235 .005, respectively), and the left subgenual cingulum (r = .500, p = .003).

236 fornix crus [AD, beta = 0.02 (P = .046)] and cingulum [RD, beta = -0.01 (P = .02); MD, beta = -0.01 (

237 functional significance of the uncinate and cingulum relationships, we found that the resulting imba

238 callosum (R(2) = 0.041, P(corr) < 0.001) and cingulum (right: R(2) = 0.041, left: R(2) = 0.040, P(cor

239 l volume effect, and extract the skeleton of cingulum robustly and reliably.

240 osed method provides an approach to localize cingulum robustly, which is a very important feature for

241 tensors' information throughout the tract of cingulum simultaneously, which is quite different from t

242 he greatest change within right paracallosal cingulum (sporadic bvFTD, FA: -6.7%/yr, p < 0.001; MD: 3

243 the need for further evaluation of anterior cingulum stimulation to reduce anxiety during awake surg

244 f the dorsomedial SLF (SLF-I) is part of the cingulum subsystem.

245 gulum bundle rather than the parahippocampal cingulum, suggesting that the limbic HAP-wave may travel

246 nate fasciculus, superior cingulum, temporal cingulum, superior longitudinal fasciculus, arcuate fasc

247 participants had lower cortical ReHo in the cingulum, superior temporal lobe, frontal lobe, and seve

248 lowing tracts: uncinate fasciculus, superior cingulum, temporal cingulum, superior longitudinal fasci

249 rs was examined by applying DiI to the right cingulum; the labeled fibers ran throughout the CC and r

250 patients had defects within fornices and/or cingulum; three patients had aberrant fibers of cingulum

251 tural connectivity produced by damage to the cingulum tract explained the compensatory increases in f

252 s in white matter tract properties along the cingulum tract predicted memory and cognitive functionin

253 related to the level of injury to the dorsal cingulum tract, which connects medial frontal and pariet

254 chanisms to the structural maturation of the cingulum tract.

255 0.002) cingulum tracts, bilateral descending cingulum tracts (P < 0.001) and left uncinate tracts (P

256 descending (left P < 0.001; right P = 0.003) cingulum tracts, and uncinate tracts (left P < 0.001; ri

257 terior (P = 0.003) and posterior (P = 0.002) cingulum tracts, bilateral descending cingulum tracts (P

258 fic fibre tracts (including corpus callosum, cingulum, uncinate and corticospinal tracts) as well as

259 Fractional anisotropy (FA) was computed for cingulum, uncinate and superior longitudinal fasciculi.

260 racts in emotional regulation circuitry (ie, cingulum, uncinate fasciculus, and forceps minor) and (1

261 oduce an approach to extract the skeleton of cingulum using active contour model, which allows us to

262 Structurally, the dorsal cingulum volume and hindrance-modulated orientational an

263 e amygdala, fornix, uncinate fasciculus, and cingulum was assessed using fractional anisotropy and me

264 crostructural variation in the left anterior cingulum was closely related to interindividual control

265 aled that fractional anisotropy of the right cingulum was inversely correlated with AD PRSs (p = .009

266 usivity in the parahippocampal region of the cingulum was negatively associated with verbal memory de

267 ty in the left parahippocampal region of the cingulum was negatively associated with visuospatial mem

268 d by fractional anisotropy) of the posterior cingulum was observed in participants with PTSD (p<0.05)

269 nd corticolimbic projection, the hippocampal cingulum, was not associated with maternal unpredictabil

270 For more accurate localization of cingulum, we attempt to define it by skeleton extraction

271 ffusivity (MD) within the right paracallosal cingulum were greatest (FA: -6.8%/yr, p < 0.001; MD: 2.9

272 temporal pole, amygdala, insula, and dorsal cingulum, were aberrant in FXS and iAUT as compared with

273 white matter integrity in the left posterior cingulum, which may contribute to cognitive impairment d

274 Altered cingulum white matter architecture is implicated in the

275 ety is associated with disruptions in girls' cingulum white matter microstructure and that this relat

276 al properties of the uncinate fasciculus and cingulum with behavioral hierarchy measures while contro

277 uggest that abnormal uncinate fasciculus and cingulum WM structure may underlie emotional, but not be

278 Left and right rostral anterior cingulum WM volume loss correlated with changes in neuro