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 y form as continuous subdivisions around the lateral ventricle.

4 that later formed specific folds around the lateral ventricle.

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

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

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

8 the speed of neuroblast migration along the lateral ventricle.

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

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

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

12 tors in different regions of the zebra finch 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 h Ommaya-reservoirs to the frontal horn of a lateral ventricle.

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

19 distinct localization within the mouse brain-lateral ventricle.

20 formation of ciliated ependymal cells in the lateral ventricle.

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

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

23 dentate gyrus and subventricular zone of the lateral ventricles.

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

25 D11b/IBA1 positive microglia surrounding 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 zation transfer ratio-increases close to the lateral ventricles.

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

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

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

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

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

43 .001), white matter (26 mL; P < .001), mean lateral ventricles (2.2 mL; P < .001), and mean summated

44 ar/periaqueductal, 32.7% periependymal along lateral ventricles, 3.4% large hemispheric, 6.0% diencep

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

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

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

48 NTF), and the implantation of eMSCs into the lateral ventricle activated relevant pathways associated

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 distance between occipital horn of the left lateral ventricle and internal surface of the cranium an

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

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

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

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

62 Neuroanatomical analysis suggested greater lateral ventricle and putamen volume in duplication carr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 = 0.005) and brain tissue (P = 0.004) to the lateral ventricles and significantly lower (11)C-PiB sig

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

82 euN) in the subventricular zone (SVZ) of the lateral ventricles and striatum of mice with genetic del

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

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

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

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

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

88 , 34 cortical thickness and 34 surface area, lateral ventricles and total intracranial volume measure

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

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

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

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

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

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

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

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

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

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

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

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

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

102 e identified the choroid plexus of the mouse lateral ventricle as the major source of miR-204 that is

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

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

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

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

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

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

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

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

115 ippocampus, and amygdala volumes and greater lateral ventricle, caudate, and accumbens volumes (Cohen

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 ools to interrogate these functions in adult lateral ventricle ChP in whole-mount explants and in awa

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

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

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

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

123 tation of encapsulated MSCs (eMSCs) into the lateral ventricle counteracted depressive-like behavior

124 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

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

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

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

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

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

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

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

132 and presence of periependymal lesions along lateral ventricles discriminated neuromyelitis optica pa

133 , posterior horn width of the right and left lateral ventricle, distance between occipital horn of th

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

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

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

137 Reduction in lateral ventricle enlargement using anti-secretory facto

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

139 ests that the implantation of eMSCs into the lateral ventricle exerted antidepressant effects likely

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

141 that patients had significant enlargement of lateral ventricles (F(1,59) = 48.89; p < 0.001) and redu

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

143 min) was infused in vivo into the CSF-filled lateral ventricle followed by ex vivo high-resolution MR

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

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

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

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

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

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

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

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

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

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

154 duction of these cytotoxic amyloids into the lateral ventricle impairs learning and memory in mice.

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

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

157 ricular microglia, that are located near the lateral ventricle in the prenatal neocortex.

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

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

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

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

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

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

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

165 (via intravenous injection), and brain (via lateral ventricle infusion).

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

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

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

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

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

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

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

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

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

175 The structural variability of lateral ventricles is poorly understood notwithstanding

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

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

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

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

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

181 1229U91 or the MC3/4R agonist MTII into the lateral ventricle (LV) dose-dependently decreased high-f

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

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

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

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

186 supratentorial ventricular structures, i.e., lateral ventricle (mean % change +/- SE = 13.3 +/- 1.9),

187 h still residual increases in volume for the lateral ventricle (mean % change +/- SE = 7.7 +/- 1.6; P

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

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

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

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

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

193 The anterior chamber and lateral ventricle of anaesthetized Brown-Norway rats wer

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

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

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

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

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

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

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

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

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

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

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

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

206 vator (SRT2104) is injected into the mPFC or lateral ventricle of wild-type mice, it reverses chronic

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

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

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

210 the magnitude of (11)C-PiB PET signal in the lateral ventricles of an independent group of Alzheimer

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

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

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

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

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

216 (2016) show that choroid plexus, within the lateral ventricles of the adult brain, secretes signals

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

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

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

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

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

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

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

224 sfect SVZ NPCs when directly injected in the lateral ventricles of uninjured mice.

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

226 lower (11)C-PiB signal clearance out of the lateral ventricles (P = 0.002) in Alzheimer subjects tha

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

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

229 he anterior horn width of the right and left lateral ventricle, posterior horn width of the right and

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

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

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

233 Lateral ventricle regions of interest were generated man

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

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

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

237 hesus macaques had persistent enlargement of lateral ventricles, smaller volumes and altered function

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

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

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

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

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

243 We demonstrate that lateral ventricle subventricular zone NSCs are molecular

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

263 Lateral ventricle volume increased 280% in the first yea

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

265 Increased lateral ventricle volume was associated with heart disea

266 otal gray matter and amygdala volume, larger lateral ventricle volume, and lower structural connectiv

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

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

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

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

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

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

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

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

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

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

277 1.14; p = 0.036; CVR, 1.30; p < 0.001), and lateral ventricles (VR, 1.56; p = 0.004).

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

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

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

281 The magnitude of (11)C-PiB signal in the lateral ventricles was calculated as area under the curv

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

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

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

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

286 The lateral ventricles were significantly larger in the pati

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

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

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

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

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

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

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

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

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

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

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

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

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

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