ライフサイエンスコーパス: lateral ventricle

1 ippocampus, pallidum, putamen, thalamus, and lateral ventricle).

2 ) and dorsomedial telencephalon bilaterally (lateral ventricles).

3 ts (pinwheels) along the lateral wall of the lateral ventricle.

4 formation of ciliated ependymal cells in the lateral ventricle.

5 etry and with a guide cannula aimed into the lateral ventricle.

6 the speed of neuroblast migration along the lateral ventricle.

7 emetry and with a guide cannula aimed into a lateral ventricle.

8 re injected (30 microL over 30 minutes) into lateral ventricle.

9 l precursors along the lateral border of the lateral ventricle.

10 tors in different regions of the zebra finch lateral ventricle.

11 distinct localization within the mouse brain-lateral ventricle.

12 ed within the brainstem, olfactory bulb, and lateral ventricle.

13 euroblasts at the subventricular zone of the lateral ventricle.

14 n substantia nigra and areas surrounding the lateral ventricle.

15 of vehicle or 100 mug 6-OHDA into the right lateral ventricle.

16 itor U0126 (100 microg) was infused into the lateral ventricle.

17 t brain, the subependymal layer (SEL) of the lateral ventricle.

18 a 350-m-wide layer of tissue adjacent to the lateral ventricle.

19 into the fourth ventricle as compared to the lateral ventricle.

20 into the hippocampus and a cannula into the lateral ventricle.

21 y form as continuous subdivisions around the lateral ventricle.

22 that later formed specific folds around the lateral ventricle.

23 ncluding a T3 dose to the preoptic region or lateral ventricle.

24 ts were measured 1-5 mm and 6-10 mm from the lateral ventricles.

25 days after birth to evaluate the size of the lateral ventricles.

26 Z), a specialized cell layer surrounding the lateral ventricles.

27 raquat were seen in the pineal gland and the lateral ventricles.

28 gliogenesis, which occurs in the SVZ of the lateral ventricles.

29 subependymal zone of the lateral wall of the lateral ventricles.

30 along the length of the lateral wall of the lateral ventricles.

31 icular epithelium (PVE) lining the embryonic lateral ventricles.

32 which derive from the region surrounding the lateral ventricles.

33 obes, but a larger right caudate nucleus and lateral ventricles.

34 3) samples of the lateral walls of the human lateral ventricles.

35 cortical regions of NAWM at the level of the lateral ventricles.

36 also had a 42.0% increase in the size of the lateral ventricles.

37 s and in the ependymal cells surrounding the lateral ventricles.

38 he difference was not attributable to larger lateral ventricles.

39 es through the upper and lower halves of the lateral ventricles.

40 ospinal fluid (CSF), which flows through the lateral ventricles.

41 ocampus, globus pallidus, putamen, thalamus, lateral ventricles.

42 zation transfer ratio-increases close to the lateral ventricles.

43 localize in the region of the bodies of the lateral ventricles.

44 lace is the subventricular zone (SVZ) of the lateral ventricles.

45 dentate gyrus and subventricular zone of the lateral ventricles.

46 ACSF) or placebo was injected into the brain lateral ventricle 45 min before scans.

47 We previously identified in the lateral ventricles a rare ependymal subpopulation (E2) w

48 We tracked the volume of the lateral ventricles across baseline, 1-year, and 2-year f

49 aromatase was localized to cells lining the lateral ventricle adjacent to the lesioned hippocampus.

50 FP, into the mouse ventral midbrain and into lateral ventricle, allowed us to fluorescently visualize

51 d cells were integrated into the wall of the lateral ventricle and expressed vimentin, a marker also

52 NSCs) reside in widespread regions along the lateral ventricle and generate diverse olfactory bulb (O

53 t least 1 lesion adjacent to the body of the lateral ventricle and in the inferior temporal lobe; or

54 al and third ventricle volumes, with reduced lateral ventricle and increased anterior cortical gray m

55 ells, leading to enlargement of the cerebral lateral ventricle and infection of the brain parenchyma.

56 temporal lobe cortical thickness and greater lateral ventricle and inferior lateral ventricle volumes

57 Z), lies adjacent to the lateral wall of the lateral ventricle and is responsible for replacement of

58 We believe that the position of the lateral ventricle and its associated mesopallium lamina

59 elopmental cell domains that wrap around the lateral ventricle and its extension through the middle o

60 lar zone and in the white matter between the lateral ventricle and neocortex; some of the latter cell

61 the experimental measures were seen in both lateral ventricle and preoptic region groups, but these

62 Cs) are the subventricular zone (SVZ) of the lateral ventricle and the dentate gyrus of the hippocamp

63 egions: the subventricular zone (SVZ) of the lateral ventricle and the dentate gyrus subgranular zone

64 ite matter between the external angle of the lateral ventricle and the forelimb sensorimotor cortex.

65 mi-1 transgenic mice were born with enlarged lateral ventricles and a minority developed idiopathic h

66 ransgenic mice showed an increased number of lateral ventricles and a reduced number of parvalbumin-s

67 move tangentially close to the walls of the lateral ventricles and along blood vessels.

68 ng the lateral body and frontal horns of the lateral ventricles and by PMG most severe in the posteri

69 e III Nrg1 (Nrg1(tm1.1Lwr+/-)) have enlarged lateral ventricles and decreased dendritic spine density

70 excessive cell extrusion, enlargement of the lateral ventricles and hydrocephalus.

71 ular abnormalities, such as asymmetry of the lateral ventricles and hypoplasia of the septum, reminis

72 urogenesis in the subventricular zone of the lateral ventricles and in the dentate gyrus of the hippo

73 the neurogenic zones of the hippocampus and lateral ventricles and in the olfactory bulb.

74 In addition, PDE11A KO mice show enlarged lateral ventricles and increased activity in CA1 (as per

75 In contrast, anterior lateral ventricles and insula showed an isotropic stretc

76 ells in the subventricular zone (SVZ) of the lateral ventricles and nestin expressing NeuN positive n

77 that are distributed along the walls of the lateral ventricles and often associated with increased p

78 f C terminus of murine S100A9 protein in the lateral ventricles and PFCTX but not somatosensory barre

79 d that BDI patients had significantly larger lateral ventricles and smaller hippocampus and amygdala

80 ume, with reciprocal volume increases in the lateral ventricles and sulcal (especially frontal and te

81 Lateral ventricles and temporal horns were also delineat

82 identified in the subventricular zone of the lateral ventricles and the subdentate gyrus of the hippo

83 within the subventricular zone (SVZ) of the lateral ventricles and the subgranular zone (SGZ) of the

84 ammals, the subventricular zone (SVZ) of the lateral ventricles and the subgranular zone of the denta

85 (SVZ) neuroblasts as they transit along the lateral ventricles and then through the anterior forebra

86 lained by CSF-brain transport from the large lateral ventricles and we confirm this route of uptake w

87 olume expansion in right frontal sulci, left lateral ventricle, and bilateral prefrontal and posterio

88 ntate gyrus (DG), subventricular zone of the lateral ventricle, and olfactory bulb.

89 rvous system: the subventricular zone of the lateral ventricle, and the subgranular zone of the hippo

90 te gyrus, ventricular/subventricular zone of lateral ventricles, and ependymal layer of 3rd ventricle

91 abnormal development of the corpus callosum, lateral ventricles, and hippocampus.

92 predominantly in the posterior horns of the lateral ventricles, and midcallosal, posterior cingulate

93 rigones, temporal and posterior horns of the lateral ventricles, and PMG most severe in the temporo-p

94 nges in volumes of frontal lobe gray matter, lateral ventricles, and sulcal CSF.

95 primarily in the ventrolateral region of the lateral ventricles, and the ventricles of olfactory bulb

96 measure midline structures and the width of lateral ventricles, and to visualize the tip of the vent

97 ar to multiciliated ependymal cells from the lateral ventricles, and uniciliated and biciliated epend

98 isplayed a distorted ependymal lining of the lateral ventricles, and we found evidence of misplaced n

99 SVZ of the anterior horn and the body of the lateral ventricle appear to proliferate based on prolife

100 matter infarctions, arranged parallel to the lateral ventricle, are associated with severe hemodynami

101 er group of males was exposed at PND270, and lateral ventricle area, glial activation, CNS cytokines,

102 uorescent protein reporter in utero into the lateral ventricle at embryonic day 15.5 to transfect pro

103 a maximal decrease skewed on the side of the lateral ventricles at around a mean distance of 9 mm.

104 s serotype 2 (AAV2) vector into the cerebral lateral ventricles at birth and mapped its distribution

105 ory ventricle and subventricular zone of the lateral ventricle, both of which are rich sources of neu

106 When infused into the lateral ventricle, BTC induces expansion of NSCs and neu

107 from multiply affected families had enlarged lateral ventricles but no other volumetric deviations.

108 ression was increased in white matter around lateral ventricles but not in neurons of LXRalphabeta ko

109 ells, not only in the SVZ lining the infused lateral ventricle, but moreover, in specific parenchymal

110 ents is also relatively widespread along the lateral ventricles, but migration is largely restricted

111 entral canal (Ecc) resembled E2 cells of the lateral ventricles, but their basal bodies were differen

112 eled cells could still be observed along the lateral ventricles, but very few were observed within th

113 s (NSCs) from the subventricular zone of the lateral ventricle can differentiate into functional SGNs

114 erature/activity transponders and unilateral lateral ventricle cannulae or bilateral preoptic region

115 we revealed leftward asymmetry for thalamus, lateral ventricle, caudate and putamen volumes, and righ

116 Lateral ventricle, caudate, and hippocampal volumes were

117 omponent of the V-SVZ stem cell niche is the lateral ventricle choroid plexus (LVCP), a primary produ

118 en's d=-0.11, % difference=-1.23) and larger lateral ventricles (Cohen's d=0.12, % difference=5.11).

119 uorescent protein-tagged retrovirus into the lateral ventricles confirmed that newly generated neurob

120 dents and humans, the ependymal layer of the lateral ventricle contains cells with proliferative pote

121 nd the subventricular zone (SVZ) next to the lateral ventricles, continuously self-renew and differen

122 mus (d=-0.148; P=4.27 x 10(-3)) and enlarged lateral ventricles (d=-0.260; P=3.93 x 10(-5)) in patien

123 cluded ovoid lesions adjacent to the body of lateral ventricles, Dawson's fingers, T1 hypointense les

124 genitor cells that migrate medially from the lateral ventricle dentate notch neuroepithelium to popul

125 ocortin 2 infusion into the medial septum or lateral ventricle did not affect anxiety measures.

126 PACAP38 infused into the lateral ventricles did not alter weight, suggesting that

127 Lateral ventricle dilation (i.e., ventriculomegaly) was

128 developmentally important neurochemicals and lateral ventricle dilation may be mechanistically relate

129 We observed ventriculomegaly (i.e., lateral ventricle dilation) preferentially in male mice

130 domain of either EphB2 or ephrin-B2 into the lateral ventricle disrupted migration of neuroblasts and

131 derive from the ventral germinal zone of the lateral ventricle during late gestation and require the

132 Bipolar disorder was associated with lateral ventricle enlargement (effect size = 0.39; 95% c

133 Our results implicate lateral ventricle enlargement as a major cause of mortal

134 Reduction in lateral ventricle enlargement using anti-secretory facto

135 of a healthy brain, MDD was associated with lateral ventricle enlargement; larger cerebrospinal flui

136 ciated with a decline in episodic memory and lateral ventricle expansion.

137 retrograde tracer fluorogold (FG) following lateral ventricle FG injection, and (2) GLP-1-immunoreac

138 eotaxic surgery, a cannula was placed in the lateral ventricle for convulsant agent administration (2

139 mote plasticity inosine was infused into the lateral ventricles for 28 days.

140 oped a whole-mount preparation of the entire lateral ventricle from postnatal day (P) 20-25 DCX-GFP m

141 rogenitor (B1) cells within the walls of the lateral ventricles generate different types of neurons f

142 hreshold for effect when administered to the lateral ventricle, GLP-1 significantly reduced food inta

143 new neurons in the walls of the adult brain lateral ventricles has captured the attention of many ne

144 ired t-test), indicating that cells from the lateral ventricle have a greater surface area.

145 right caudate, putamen, pallidum, thalamus, lateral ventricles, hippocampus, and amygdala.

146 rior forebrain in MRL mice revealed enlarged lateral ventricles; however, little neurodegeneration wa

147 c) or ethanol (0.25 ml) and infused into the lateral ventricle (ICV) for 4 h with 40 microg T (TF and

148 Along the walls of the lateral ventricles, immature neuronal progeny migrate in

149 mitters were implanted to monitor ICP in the lateral ventricle in nine light-dark-entrained Sprague-D

150 The lateral wall of the lateral ventricle in the human brain contains neural ste

151 were used to measure the caudate nucleus and lateral ventricles in 15 right-handed male subjects with

152 ells are scattered throughout the SVZ of the lateral ventricles in adult human brain and are signific

153 Volumetric analyses of the lateral ventricles in native image data space confirmed

154 germinal niche adjacent to the walls of the lateral ventricles in the adult brain.

155 Zc3h14Deltaex13/Deltaex13 mice show enlarged lateral ventricles in the brain as well as impaired work

156 ing the formation of the lateral wall of the lateral ventricles in the brain.

157 eurogenic in the adult brain, the SEL of the lateral ventricle, in zones adjacent to the caudate puta

158 contrast, central injection of NMDA into the lateral ventricle increased plasma LH levels in both Kis

159 of GDNF per day for 2 months into the right lateral ventricle initially increased hand movement spee

160 e implanted into 23 C57BL/6 mice before left lateral ventricle injection of antibody-positive (test)

161 , because rats depleted of histamine through lateral ventricle injections of alpha-fluoromethylhistid

162 This resulted in severe damage to brain lateral ventricle integrity and identified roles for Num

163 ntracerebroventricularly to migrate from the lateral ventricles into the brain parenchyma in mice.

164 Recent work indicates that the wall of the lateral ventricle is highly regionalized, with progenito

165 The subventricular zone (SVZ) of the lateral ventricle is the major site of neurogenesis in t

166 A similar enlargement in the lateral ventricles is found in a subpopulation of herpes

167 The subependymal zone (SEZ) of the lateral ventricles is one of the areas of the adult brai

168 The structural variability of lateral ventricles is poorly understood notwithstanding

169 extensive germinal layer in the walls of the lateral ventricles is the site of birth of different typ

170 led MCH (R-MCH), when microinjected into the lateral ventricle, is internalized in serotonergic and n

171 alis (BNST) lies immediately adjacent to the lateral ventricle, is rich in CGRP receptors, and has it

172 Brains from transgenic animals have enlarged lateral ventricles lined with neuroepithelial precursor

173 clear (Hb)/dorsal third ventricle (D3 V) and lateral ventricle (LV) areas were identified as CL "hot

174 1229U91 or the MC3/4R agonist MTII into the lateral ventricle (LV) dose-dependently decreased high-f

175 Injection of AngII into the lateral ventricle (LV) increases water intake, but a sim

176 The lateral ventricle (LV) is a preferential location for br

177 carbocyanine perchlorate) injection into the lateral ventricle (LV) of early postnatal mice demonstra

178 e substantia nigra pars compacta (SNpc), the lateral ventricle (LV) or the striatum (or combinations

179 Ventricle stenosis and fusion of the lateral ventricle (LV) walls is associated with a massiv

180 Urocortin infusion into neighboring sites (lateral ventricle, medial caudate) had no effects.

181 in the subventricular zone (SVZ), lining the lateral ventricles, migrate tangentially into the olfact

182 c low-grade glioma, third ventricle, but not lateral ventricle, NSCs hyperproliferate in response to

183 CSF from the lateral ventricle of affected foetal brains not only inh

184 e receptor agonists and antagonists into the lateral ventricle of AGSs at different times of the year

185 hat blocks connexin 43 hemichannels into the lateral ventricle of chronically instrumented fetal shee

186 and cannula guides were implanted above the lateral ventricle of male Wistar rats.

187 russide or selective PKG activators into the lateral ventricle of mouse brain induced PDE5 phosphoryl

188 ronidase were injected unilaterally into the lateral ventricle of MPS VII mice with established disea

189 of NSC migration, we injected HNSCs into the lateral ventricle of null reeler and wild-type mice.

190 ee effective antibodies or controls into the lateral ventricle of P301S mice for 3 months.

191 When injected into the lateral ventricle of rats and macaques, Abeta oligomers

192 molecule (NCAM) (5 microg, i.c.v.) into the lateral ventricle of rats and tested them on the forced

193 anxiety-like responses when infused into the lateral ventricle of rats.

194 EARCH DESIGN AND A cannula was placed in the lateral ventricle of Sprague-Dawley rats for intracerebr

195 gnal in the subventricular zone (SVZ) of the lateral ventricle of the adult mouse brain.

196 ters were stereotactically inserted into the lateral ventricle of the brain in C57BL/6 mice and evalu

197 ntities of (+/-)Bay K 8644 directly into the lateral ventricle of the brain, suggesting a central eff

198 al cells of choroid plexus isolated from the lateral ventricle of the rat brain.

199 line, senktide, or NPY was injected into the lateral ventricle of unanesthetized rats and serial bloo

200 hat infusion of 100 ng of HIV-1 Tat into the lateral ventricle of yellow fluorescent protein-expressi

201 rly, continuous PEDF administration into the lateral ventricles of adult glial fibrillary acidic prot

202 Using whole mounts of the walls of the lateral ventricles of adult mice and three cell cycle an

203 DNF:IRES:hGFP (AdBDNF) was injected into the lateral ventricles of adult rats, who were treated for 1

204 ion of CTZ (5 micromol in 5 microl) into the lateral ventricles of anaesthetized rats also induces sp

205 tered stereotaxically, bilaterally, into the lateral ventricles of Fischer albino male rats (1 nmol/2

206 :Abeta complex is directly injected into the lateral ventricles of mice, it is rapidly cleared from t

207 st human SOD1 was injected into the cerebral lateral ventricles of neonatal SOD1(G93A) mice, and impa

208 mia were infused for 12 weeks into the brain lateral ventricles of streptozotocin-diabetic adult rats

209 (2016) show that choroid plexus, within the lateral ventricles of the adult brain, secretes signals

210 neural stem cells (NSCs) in the walls of the lateral ventricles of the adult brain.

211 scribe a ribbon of SVZ astrocytes lining the lateral ventricles of the adult human brain that prolife

212 The subependymal zone (SEZ) of the lateral ventricles of the adult mouse brain hosts neurog

213 es of neurons, ectopically located along the lateral ventricles of the brain.

214 al nodules, ectopically positioned along the lateral ventricles of the cerebral cortex.

215 l plexus of serotonin axons in the third and lateral ventricles of the human and monkey brains that i

216 erestingly, upon intracranial injection into lateral ventricles of the neonatal mouse brain, a low-af

217 ventral bundle pathways or infused into the lateral ventricle or both.

218 g activity or pain responses; infusions into lateral ventricle or nucleus of the diagonal band had no

219 nfusion of 5 or 15 micro g/day GDNF into the lateral ventricle or the striatum, using programmable pu

220 o MRI of the DN-DISC1 mice detected enlarged lateral ventricles particularly on the left side, sugges

221 ical neurons in proliferative zones near the lateral ventricles (periventricular heterotopia).

222 cursor cell populations lining the embryonic lateral ventricles produce the projection neurons.

223 receptors (losartan) microinjected into the lateral ventricle reduced BP level of HS, but not of Con

224 Disc1(tr) transgenic mice display enlarged lateral ventricles, reduced cerebral cortex, partial age

225 ctosidase (betagal) or rAAV4betagal into the lateral ventricle resulted in stable transduction of epe

226 ction of a small molecule dimerizer into the lateral ventricle resulting in localized, acute oligoden

227 ated that the microinjection of MCH into the lateral ventricle results in a significant decrease in t

228 They further exhibit an expansion of lateral ventricle size, an atrophy of the olfactory bulb

229 Whole mounts of the lateral wall of the lateral ventricle stained for the neuroblast marker doub

230 The lateral ventricle subventricular zone (SVZ) is a frequen

231 and isolated by flow cytometry, adult mouse lateral ventricle subventricular zone (SVZ) NICs as Glas

232 ll maintenance and neurogenesis in the adult lateral ventricle subventricular zone and dentate gyrus.

233 have been described in the adult brain, the lateral ventricle subventricular zone and the dentate gy

234 We demonstrate that lateral ventricle subventricular zone NSCs are molecular

235 Interestingly, a ventral extension of the lateral ventricle suggests the presence of a putative RM

236 ned effects on both volumetric expansion and lateral ventricle surface morphology.

237 Regional analysis along the lateral ventricle surface revealed that the age-dependen

238 s persists in the subventricular zone of the lateral ventricles (SVZ) and the dentate gyrus (DG) of t

239 ing cells in the subventricular zones of the lateral ventricles (SVZ) migrate into the gray and white

240 Minimal effects of lateral ventricle T3 microinjection were demonstrated (N

241 expression, we defined the transcriptome of lateral ventricle (telencephalic) versus fourth ventricl

242 cs have a stronger influence on the shape of lateral ventricles than do the disease-related changes i

243 nd SEGA-like structural abnormalities in the lateral ventricle, the consequence of abnormal migration

244 mpus and from the subventricular zone of the lateral ventricle, the rostral migratory stream to the o

245 The subventricular zone (SVZ) of the lateral ventricles, the largest remaining germinal zone

246 ei, the cerebellum, the cerebral cortex, the lateral ventricles, the lentiform nuclei, the thalami, t

247 e was active in vivo by injection into mouse lateral ventricle, thereby suppressing water-drinking be

248 Volumetric measurements of the cerebrum, lateral ventricles, third ventricle, and hippocampus wer

249 campus and in the subventricular zone of the lateral ventricles throughout life.

250 distances from the subependymal zone of the lateral ventricles to the olfactory bulb (OB) within the

251 ntricular zone migrate from the walls of the lateral ventricles to the olfactory bulb.

252 VZ), neuroblasts migrate in chains along the lateral ventricle towards the olfactory bulb.

253 d in NPH, with an abnormal gradient from the lateral ventricles towards the subcortical WM.

254 ved neurotrophic factor was infused into the lateral ventricle via the implanted osmotic minipump.

255 In mixed-effect model analysis, the lateral ventricle volume (P = .005), accumulation of CE

256 oth disorders were associated with increased lateral ventricle volume and increased rates of subcorti

257 Lateral ventricle volume increased 280% in the first yea

258 d for intracranial, cerebrum, cerebellum, or lateral ventricle volume or for head circumference.

259 During water loading, total VBR and lateral ventricle volume significantly decreased by 13.1

260 Slopes relating lateral ventricle volume to age were steeper in alcoholi

261 Increased lateral ventricle volume was associated with heart disea

262 h total brain gray matter, white matter, and lateral ventricle volume.

263 12), as well as larger pallidum (d=0.21) and lateral ventricle volumes (d=0.37).

264 decrease in thalamic volumes and increase in lateral ventricle volumes (P = .009) were MR imaging var

265 In the SPD group, larger lateral ventricle volumes correlated with more severe sy

266 ignificantly smaller white matter and larger lateral ventricle volumes than healthy comparison subjec

267 s and greater lateral ventricle and inferior lateral ventricle volumes were seen in the AC+ participa

268 cranial, CSF, gray matter, white matter, and lateral ventricle volumes, and for neonatal diffusion pr

269 nsignificantly larger intracranial, CSF, and lateral ventricle volumes.

270 ger bilateral caudate, putamen, pallidum and lateral ventricle volumes.

271 er intracranial, CSF, total gray matter, and lateral ventricle volumes; the female high-risk neonates

272 e to adult-born neurons are generated is the lateral ventricle wall of the brain.

273 st, fractones, similar to those found in the lateral ventricle wall, were regularly arranged along th

274 that basal bodies in ependymal cells in the lateral ventricle walls of adult mice are polarized in t

275 hite matter lesions arranged parallel to the lateral ventricle was observed only in symptomatic patie

276 Effacement of the lateral ventricle was used as a radiographic surrogate f

277 Having larger lateral ventricles was associated with a higher number o

278 After injection of UII and URP in the lateral ventricle, we observed c-Fos-positive cell nucle

279 ventricular zone adjacent to the wall of the lateral ventricles, we and others have recently reported

280 sal hippocampus and a cannula into the right lateral ventricle were used to investigate the ECoG freq

281 7 BCAO rat brains and significantly enlarged lateral ventricles were found in five out of seven P14 B

282 forebrain cross-sectional area but that the lateral ventricles were significantly larger in IBA trea

283 The lateral ventricles were significantly larger in the pati

284 tial scans showed narrowing of the third and lateral ventricles when compared with follow-up.

285 ltiple regions of interest, particularly the lateral ventricles where the left was larger than the ri

286 sions were in the right and left body of the lateral ventricle, where the volumes of schizophrenic su

287 is restricted to the ependymal cells of the lateral ventricles, where FXR2 is not expressed.

288 a small subset of FoxJ1(+) astrocytes in the lateral ventricles, where these cells form a postnatal n

289 iche in the adult subventricular zone of the lateral ventricles, where they regulate neurogenesis and

290 An angular configuration of the lateral ventricles, which is seen in fetuses with neural

291 ere established for the size of the neonatal lateral ventricles, which may allow for early identifica

292 Comparisons were made for prenatal lateral ventricle width and head circumference, for neon

293 ith schizophrenia did not differ in prenatal lateral ventricle width or head circumference.

294 d computed tomography was found in measuring lateral ventricles width (intraclass correlation coeffic

295 By stereotaxic puncture of the lateral ventricle with a microneedle, ICP was 9.5 +/- 1.

296 d filled with cerebrospinal fluid connecting lateral ventricle with the subarachnoid space.

297 tabolites in a white matter region above the lateral ventricles with (1)H-MRS and WMH volume in this

298 LXRalphabeta ko mice is the occlusion of the lateral ventricles with age.

299 developed hydrocephalus and grossly dilated lateral ventricles, with accumulation of 2-hydroxyglutar

300 ) delivered, respectively, to the fourth and lateral ventricles yielded substantial suppression of fo