ライフサイエンスコーパス: internal capsule

1 asal ganglia, occipital WM, thickness of the internal capsule).

2 1 (brainstem and cerebrum) to 0.74 +/- 0.06 (internal capsule).

3 r the hippocampus and posterior limbs of the internal capsule.

4 orpus callosum (CC), optic chiasm (Och), and internal capsule.

5 alamic radiations, and posterior limb of the internal capsule.

6 ially the frontal parts of the brain and the internal capsule.

7 for thalamic axons that failed to enter the internal capsule.

8 or commissure, subcortical fiber tracts, and internal capsule.

9 ductions in the frontal lobe, cerebellum and internal capsule.

10 neurons during electrical stimulation of the internal capsule.

11 the corticospinal tracts at the level of the internal capsule.

12 ar connections, all of which are part of the internal capsule.

13 01 to <.03) except the posterior limb of the internal capsule.

14 lly medially across the inferior edge of the internal capsule.

15 ventromedial putamen, on either side of the internal capsule.

16 e zone, and, by P5, they reach the primitive internal capsule.

17 me fraction within the posterior limb of the internal capsule.

18 mporal lobe, and right posterior limb of the internal capsule.

19 es in the putamen, thalamus, insula, and the internal capsule.

20 erally implanted in the anterior limb of the internal capsule.

21 of the striatum and the anterior limb of the internal capsule.

22 homolog of the primate anterior limb of the internal capsule.

23 ed white matter volumes in pyramids and left internal capsule.

24 and inferior fronto-occipital fasciculi, and internal capsule.

25 wing the fornix and the anterior limb of the internal capsule.

26 e ventral border of the anterior limb of the internal capsule.

27 m, and to subcortical structures through the internal capsule.

28 te cells with an axon projecting through the internal capsule.

29 p=0.01), and abnormal posterior limb of the internal capsule (0.38, 0.17-0.85; p=0.02).

30 the corpus callosum and anterior limb of the internal capsule (-0.02; p =.01) at hospital discharge.

31 e, 130 x 10(-5) mm(2)/sec; posterior limb of internal capsule, 109 x 10(-5) mm(2)/sec) and three gray

32 10(-5) mm(2)/sec at birth; anterior limb of internal capsule, 130 x 10(-5) mm(2)/sec; posterior limb

33 th irregular tails, often extending into the internal capsule; 22 of these patients experienced at le

34 , associations with the anterior limb of the internal capsule, a subcortical white matter region, rem

35 ly lower axial diffusion in the thalamus and internal capsule across groups (P = .02).

36 sed atrophy in the anterior limb of the left internal capsule adjacent to the head of the left caudat

37 ccipital cortices, and posterior limb of the internal capsules after TBI.

38 cle, the anterior and posterior limbs of the internal capsule (ALIC and PLIC), the external capsule,

39 Pe), nucleus accumbens, anterior limb of the internal capsule (ALIC) and anterior lateral anterior co

40 rocedures targeting the anterior limb of the internal capsule (aLIC) can be effective in patients wit

41 fibers that are part of the anterior limb of internal capsule (ALIC) in MDD and diabetic subjects usi

42 Disconnection of the anterior limb of the internal capsule (ALIC) was assessed via individual and

43 at underwent DBS to the anterior limb of the internal capsule (ALIC), the nucleus accumbens or the su

44 the diencephalon and growing out through the internal capsule among groups of back-labelled cells tha

45 ter effect size in the posterior limb of the internal capsule and a tendency for decreased fractional

46 kB-immunostained fibers were observed in the internal capsule and as two distinct fascicles within th

47 of fractional anisotropy in the genu of the internal capsule and bilateral increase of overall water

48 We show that striatonigral axons pioneer the internal capsule and cerebral peduncle and are temporall

49 atonigral (direct) pathway in pioneering the internal capsule and cerebral peduncle, and in guiding a

50 for corticofugal outputs passing through the internal capsule and cerebral peduncle, there is accumul

51 ts (corticofugal) as they extend through the internal capsule and cerebral peduncle.

52 ending and descending axon tracts within the internal capsule and cerebral peduncle.SIGNIFICANCE STAT

53 ed increases in fractional anisotropy in the internal capsule and cingulum and decreases in the poste

54 and myelin content in the right genu of the internal capsule and clusters of mineral depositions, co

55 se an updated model of tinnitus, wherein the internal capsule and corpus callosum play important role

56 w images for differentiation of GPi from the internal capsule and external globus pallidus, respectiv

57 e normally situated in the ventral thalamus, internal capsule and hypothalamus, were more dispersed i

58 e effects of DBS in the anterior limb of the internal capsule and nucleus accumbens region (ALIC-NAcc

59 tropy (FA) in the right anterior limb of the internal capsule and right uncinate fasciculus.

60 he DTI analysis revealed fiber damage in the internal capsule and somatosensory cortex.

61 t on thalamic axons as they grow through the internal capsule and subplate but is not present in the

62 hich attracts initial axon growth toward the internal capsule and that this activity may be due to Ne

63 ns of white matter, particularly in the left internal capsule and the left frontal lobe (P = .02-.05)

64 ODI was reduced in the right anterior internal capsule and the right PCG.

65 ostly in and around the anterior limb of the internal capsule and ventral striatum.

66 the ventral part of the anterior limb of the internal capsule and were followed for at least 3 years

67 the ventral part of the anterior limb of the internal capsule and were followed for at least 3 years

68 imulated thalamic axons coursing through the internal capsule and, as a control, the basolateral (BL)

69 ding white matter density differences in the internal capsules and left centrum semiovale.

70 tter (anterior and posterior subcortical and internal capsule) and four of gray matter (cortex, thala

71 y low within areas of white matter (fimbria, internal capsule) and select neuronal fields (hippocampa

72 h frontal lobes, posterior limb of the right internal capsule, and both cerebellar hemispheres in pat

73 white matter tracts of the corpus callosum, internal capsule, and brain stem.

74 l external capsule and posterior limb of the internal capsule, and corona radiata.

75 ly in white matter tracts of the cerebellum, internal capsule, and corpus callosum.

76 ing confirmed that striatum but also insula, internal capsule, and external capsule were associated w

77 tria terminalis, medial amygdala, claustrum, internal capsule, and globus pallidus.

78 trum semiovale, in the posterior limb of the internal capsule, and in the cerebral peduncle; the thal

79 lly located in the cerebral white matter and internal capsule, and infrequently in the brain stem.

80 le, bilateral retrolenticular region part of internal capsule, and left posterior thalamic radiation.

81 ped myelination of the posterior limb of the internal capsule, and more immature gyral folding than t

82 ervention techniques targeting the cingulum, internal capsule, and other limbic regions.

83 ed increased volume in the basal ganglia and internal capsule, and otherwise normal brain volumes.

84 diffusivity measures of the corpus callosum, internal capsule, and posterior thalamic radiation contr

85 um bundle, superior longitudinal fasciculus, internal capsule, and splenium of the corpus callosum.

86 c radiation, the retrolenticular part of the internal capsule, and the sagittal stratum (p<.05, corre

87 l globus pallidus, the ventral pallidum, the internal capsule, and the substantia innominata.

88 of the frontal lobes, posterior limbs of the internal capsules, and cerebellar hemispheres in patient

89 , caudate nuclei, lentiform nuclei, thalami, internal capsules, and cerebellar hemispheres.

90 eviation was related to connections with the internal capsule (anterior limb) and the pallidum.

91 (subcortical white matter, corpus callosum, internal capsule, anterior commissure), gray matter (glo

92 Fibers in the internal capsule are organized according to destination.

93 motor system through the corona radiata and internal capsule are well described in non-human primate

94 ein (MBP) at the fimbria hippocampus and the internal capsule areas in the 7-day-old BACO rat brain w

95 matter in the corpus callosum, subcortex and internal capsule areas while largely spared cortical neu

96 rmation in the corpus callosum, external and internal capsule areas.

97 knock-out mice pioneer the projection to the internal capsule as they do in wild-type mice.

98 xons show increased fasciculation within the internal capsule, as well as abnormal turning and branch

99 ractional anisotropy in the anterior limb of internal capsule at discharge and in genu of corpus call

100 reatest regional effects in the external and internal capsules, B(FA)= -0.12 to -0.14).

101 -0.03 to 0.02) in the posterior limb of the internal capsule between the two groups.

102 m, bilateral anterior and posterior limbs of internal capsule, bilateral retrolenticular region part

103 e we demonstrate that a set of neurons in an internal-capsule bordering regions of the primate dorsal

104 fected 293T cells, as it had been toward the internal capsule, but not toward control-transfected 293

105 tical axon outgrowth was directed toward the internal capsule, but outgrowth was nondirected and supp

106 tions, superior fronto-occipital fasciculus, internal capsule, callosal isthmus, and the corona radia

107 alamo-cortical loop, brainstem, external and internal capsules, callosal and cerebellar structures.

108 igma)) were measured in the corpus callosum, internal capsule, caudate nucleus, lentiform nucleus, an

109 ontrol subjects in the posterior limb of the internal capsule, corona radiata, posterior frontal whit

110 st in the centrum semiovale, corona radiata, internal capsule, corpus callosum, and subcortical white

111 Major central WM tracts, including internal capsule, corpus callosum, anterior commissure,

112 addition, reduced FA in anterior limb of the internal capsule correlated significantly with an increa

113 ctional anisotropy with age was found in the internal capsule, corticospinal tract, left arcuate fasc

114 f basal ganglia circuits can drive secondary internal capsule defects and thereby may contribute to t

115 Parietal operculum, corona radiata, and internal capsule differences between cases and controls

116 ed FA values were located bilaterally in the internal capsule extending into the globus pallidus and

117 nferior longitudinal fasciculi, limbs of the internal capsule, external capsule and cerebellum (p < 0

118 ngs in the putamen into the rostral putamen, internal capsule, external capsule, caudate nucleus, and

119 beta = -0.01 (P = .04)] and retrolenticular internal capsule [FA, beta = -0.01 (P = .002); RD, beta

120 ralateral side (FAcontra) and to that in the internal capsule (FAint) was calculated.

121 We further demonstrated that the internal capsule features could be trained as a motif de

122 Development of anterior cortical and internal capsule fibers may be particularly vulnerable t

123 te matter for HT+M versus HT (p = 0.036) and internal capsule for HT+M compared to HT (p = 0.001) and

124 mulation of the ventral anterior limb of the internal capsule for obsessive-compulsive disorder and p

125 for Isl1 in diencephalic cells bordering the internal capsule for the normal development of the stria

126 ntal contributions of striatonigral axons to internal capsule formation, we have made use of Sox8-EGF

127 Striatonigral axon defects can thus disrupt internal capsule formation.

128 VPN neurons by electrical stimulation of the internal capsule from P3.

129 m, cortical plate, hemispheric white matter, internal capsule, ganglionic eminence, ventricular zone,

130 out the striatal neuropil, as well as in the internal capsule, globus pallidus, and substantia nigra.

131 of myelination in the posterior limb of the internal capsule, gyral maturation, signal intensity abn

132 fiber tracts within the anterior limb of the internal capsule have a significantly higher (P < 0.01)

133 S) trials targeting the anterior limb of the internal capsule have shown promising results.

134 n began at postnatal day 5 (P5) (E36) in the internal capsule (IC) and at P11 in the medial corpus ca

135 tor regions through the corona radiata (CR), internal capsule (IC) and crus cerebri of the cerebral p

136 udinal fasciculus (LF), corona radiata (CR), internal capsule (IC) and external capsule (EC).

137 nd inversely varied with FA in the bilateral internal capsule (IC) at 2-weeks (p = 0.0294, FDR correc

138 al projection in the corona radiata (CR) and internal capsule (IC) can assist in evaluating a patient

139 Only the posterior limb of the internal capsule (IC), comprised primarily of corticofug

140 upon DA application or by stimulation of the internal capsule (IC), which also supports self-stimulat

141 the pallial-subpallial boundary to form the internal capsule (IC).

142 ly and orthodromically by stimulation of the internal capsule (IC; conduction velocity, 2.4 +/- 0.2 m

143 ite matter volume around the optic tract and internal capsule in anophthalmic subjects showed a large

144 including the corpus callosum, fimbria, and internal capsule in the brain, and pyramidal tracts and

145 y increased ODI in the posterior limb of the internal capsule in unmedicated patients (242 voxels; x

146 major CNS axon tracts including those of the internal capsule, in part via cell-nonautonomous mechani

147 the ventral part of the anterior limb of the internal capsule is effective and tolerable for treatmen

148 In rats, the internal capsule is pioneered on E14, but the corpus cal

149 ns pioneer the pathway from neocortex to the internal capsule, leading to the proposal that they are

150 1.17 x10(3)mum(2)/sec), anterior limb of the internal capsule (left, 1.11 x10(3)mum(2)/sec; right, 1.

151 1.17 x10(3)um(2)/sec), anterior limb of the internal capsule (left, 1.11 x10(3)um(2)/sec; right, 1.0

152 02) and a lower FA of the cranial CST at the internal capsule level (p = 0.001).

153 putamen, corpus callosum, posterior limb of internal capsule), level of brainstem, grey- white matte

154 Results The posterior limb of the internal capsule (mean ADC: left hemisphere, 1.18 x10(3)

155 Results The posterior limb of the internal capsule (mean ADC: left hemisphere, 1.18 x10(3)

156 onal anisotropy in the posterior limb of the internal capsule, measured with magnetic resonance spect

157 y of the deep gray matter nuclei, brainstem, internal capsule, motor cortex and corticospinal pathway

158 =47), nucleus accumbens/anterior limb of the internal capsule (n=4) or a combination of targets (n=8)

159 timulation of the human anterior limb of the internal capsule/NAcc region for treatment-resistant obs

160 timulation (DBS) of the anterior limb of the internal capsule/NAcc region for treatment-resistant obs

161 anatomy, except for larger basal ganglia and internal capsule, not explained by antipsychotic dose.

162 imulation targeting the anterior limb of the internal capsule/nucleus accumbens.

163 tently lower diffusivity in the thalamus and internal capsule of all tobacco-exposed infants suggests

164 ore were detected for the right putamen, and internal capsules of both hemispheres.

165 ion restriction in the posterior limb of the internal capsule, often also optic radiation, brainstem

166 In contrast, bilateral involvement of the internal capsule on brain MRI was associated with poorer

167 ury was prominent in the corpus callosum and internal capsule on day 3 and then partially recovered o

168 ls form long-range axonal projections to the internal capsule or callosum.

169 oring, closed-loop direct stimulation of the internal capsule or striatum, especially the dorsal site

170 = 50) receiving DBS to anterior limb of the internal capsule or subthalamic nucleus zones, optimal f

171 gets of cortical efferent axons, the nascent internal capsule, or the medial wall of the dorsal telen

172 bocyanine dye tracing from the callosum, the internal capsule, or the primary somatosensory cortex.

173 ventral portion of the anterior limb of the internal capsule over a 20-year period using the Leksell

174 ccumbens (P = .03), and anterior limb of the internal capsule (P = .02).

175 ells) throughout the whole brain, and in the internal capsule, periventricular white matter and senso

176 and the contralateral posterior limb of the internal capsule (PLIC) after age correction and were co

177 and abnormal signal in the posterior limb of internal capsule (PLIC) had an AUC of 0.82 (0.76-0.87).

178 The posterior limb of the internal capsule (PLIC) showed a significant diagnostic

179 l tracts (CSTs) in the posterior limb of the internal capsule (PLIC).

180 corpus callosum (SPCC) and posterior limb of internal capsule (PLIC).

181 orpus callosum (SCC), posterior limbs of the internal capsules (PLIC), superior longitudinal fascicul

182 d white matter, increased myelination of the internal capsule, poorer motor performance, and profound

183 und mainly in the left posterior limb of the internal capsule, posterior corona radiata, and partly i

184 ttern beginning in the cerebellum, pons, and internal capsule; proceeding caudocranially from the spl

185 ared with hypothermia alone in the thalamus, internal capsule, putamen and caudate, and there was red

186 mid, and anterior cingulate, as well as the internal capsule, putamen, and globus pallidus and basal

187 nd vessel walls of the posterior limb of the internal capsule, putamen, globus pallidus and cerebellu

188 mulation of the ventral anterior limb of the internal capsule rapidly improves mood and anxiety with

189 hen cocultured with MDT, suggesting that the internal capsule releases a chemoattractant for cortical

190 icothalamic and thalamocortical axons in the internal capsule requires Fz3 expression in the ventral

191 ateral amydalofugal pathway and ventromedial internal capsule, respectively).

192 the cortical afferents arriving through the internal capsule, respectively.

193 Early in the study, heating of the internal capsule resulted in 2 cases (8%) of mild hemipa

194 ion of thalamic/brainstem fibers through the internal capsule, results in a complex mingling of thala

195 ial corticospinal tracts at the level of the internal capsule (right Z score 5.21, p=0.0081; left Z s

196 us callosum, the right posterior limb of the internal capsule, right external capsule, and the right

197 nal capsule, the retrolenticular part of the internal capsule (RLIC), the body and splenium of the co

198 to Broca's area (RR, 2.5; 95% CI, 1.3-5.0), internal capsule (RR, 2.2; 95% CI, 1.1-4.4), Wernicke's

199 Labeled fibers descend in the internal capsule (SMA in anterior limb and genu; M1 in p

200 oscillations became the typical response to internal capsule stimulation at P12.

201 fic brain regions (including corona radiata, internal capsule, superior and inferior longitudinal fas

202 sterior limb and the retrolenticular part of internal capsule, superior and posterior corona radiata,

203 ut adolescence (in the posterior limb of the internal capsule, superior corona radiata, and cerebella

204 d to pain processing (e.g., corpus callosum, internal capsule, superior longitudinal fasciculus and s

205 WM loss was concentrated in the brainstem, internal capsule, temporal and frontal regions and the m

206 rticospinal tract), corpus callosum, fornix, internal capsule (thalamocortical and corticothalamic tr

207 f the cerebellum, cingulum, corpus callosum, internal capsule, thalamus, basal forebrain, occipital,

208 tures (corpus callosum, anterior commissure, internal capsule, thalamus, caudoputamen, and cortex).

209 sociated with increased FA of regions of the internal capsule that contain auditory thalamocortical a

210 lsive Scale, one in the anterior limb of the internal capsule that overlapped with a previously ident

211 -compared with controls-in the pyramids, the internal capsule, the cerebral peduncle and the hand are

212 ntricular regions, the posterior limb of the internal capsule, the external capsule, and the pyramida

213 defined and topographic anterior limb of the internal capsule, the specific locations and organizatio

214 These include the anterior limb of the internal capsule, the ventral striatum, the subthalamic

215 th abnormalities in the anterior limb of the internal capsule, the white matter (WM) bundle carrying

216 ither through the ventrolaterally positioned internal capsule to subcortical targets or through the d

217 eral DBS of the ventral anterior limb of the internal capsule (vALIC) between April 2005 and October

218 targeted at the ventral anterior limb of the internal capsule (vALIC) in 25 patients with TRD during

219 echanisms may lie in the efficacy of ventral internal capsule/ventral striatum (VCVS) DBS in both maj

220 Deep brain stimulation (DBS) of the ventral internal capsule/ventral striatum (VCVS) is an emerging

221 showed cerebral cortex, corpus callosum, or internal capsule volume differences from control.

222 ng the ventral striatum/anterior limb of the internal capsule (VS/ALIC) in 10 patients with poststrok

223 Notably, microstructure of the internal capsule was consistently implicated across all

224 Myelination of the posterior limb of the internal capsule was less developed, and gyral maturatio

225 FA of the posterior limb of the left internal capsule was positively correlated with reaction

226 nisotropy (FA) in the posterior limbs of the internal capsules was determined with diffusion-weighted

227 Automated GWR_si (putamen/posterior limb of internal capsule) was performed with an area under the c

228 chemoattractant Netrin-1 is expressed in the internal capsule, we cocultured cortical explants with E

229 us pallidus and the adjacent optic tract and internal capsule were identified with microelectrode rec

230 The basal ganglia, cortex and lobar, and internal capsule were the frequently involved areas of t

231 Dysmorphic basal ganglia with an abnormal internal capsule were the most consistent feature.

232 the corpus callosum, the frontal WM, and the internal capsule; were compared with those of five age-m

233 substantia innominata, globus pallidus, and internal capsule, where PHA-L-labeled terminals abutted

234 l axon growth is directed toward the nascent internal capsule, which could account for the timing dif

235 Converging evidence suggests the ventral internal capsule white matter tracts traversing the rost

236 actional anisotropy and lower diffusivity in internal capsule white matter; lower regional blood flow

237 nderwent DBS to the ventral anterior limb of internal capsule with subsequent programming uninformed

238 orticospinal tract at the level of the right internal capsule (Z score 4.01, p<0.0001).

239 l capsule (Z score 4.30, p=0.0021), the left internal capsule (Z score 4.27, p=0.0278), and left cere

240 rticospinal tracts at the level of the right internal capsule (Z score 4.30, p=0.0021), the left inte

241 d growth of dorsal thalamic axons toward the internal capsule zone of ventral telencephalic explants