ライフサイエンスコーパス: ventricular zone

1 pression profiles in specific domains in the ventricular zone.

2 l plate at a time when axons grow toward the ventricular zone.

3 genes regulating progenitor identity in the ventricular zone.

4 lf-renewal of neuronal precursors within the ventricular zone.

5 increased the number of S-phase cells in the ventricular zone.

6 nal, despite strong reelin expression in the ventricular zone.

7 ot observed in nonmigrating cells within the ventricular zone.

8 mmigration of new neurons from the overlying ventricular zone.

9 ell cycle and migrated out of the cerebellar ventricular zone.

10 neural progenitors of the mitotically active ventricular zone.

11 normally expressed by cells in the embryonic ventricular zone.

12 cells expressed MASH-1 also expressed in the ventricular zone.

13 ced proliferation of progenitor cells in the ventricular zone.

14 on, which is downregulated as cells exit the ventricular zone.

15 e the cerebral wall rather than in the local ventricular zone.

16 stin-positive progenitors in the neocortical ventricular zone.

17 born from apical progenitors located in the ventricular zone.

18 drocyte precursor migration from the ventral ventricular zone.

19 the fraction of cells expressing Sox2 in the ventricular zone.

20 ginate in a restricted domain of the ventral ventricular zone.

21 of neurons into the cortical plate from the ventricular zone.

22 neocortex that migrate towards the cortical ventricular zone.

23 precursors arise in distinct domains of the ventricular zone.

24 recursor cells residing in the proliferating ventricular zone.

25 ogenitor cells of the prenatal telencephalic ventricular zone.

26 enerated by precursor cells of the embryonic ventricular zone.

27 ls that migrate radially from the underlying ventricular zone.

28 found among cells already detached from the ventricular zone.

29 ction of Dlx-positive cells increases in the ventricular zone.

30 , suggesting premature delamination from the ventricular zone.

31 state and transcriptional repression in the ventricular zone.

32 to their ectopic localization outside of the ventricular zone.

33 eptors of neural precursors in the embryonic ventricular zone.

34 ion of progenitor cells occurs at the apical ventricular zone.

35 neurons, including in the brain stem and the ventricular zone.

36 with their embryonic sites of origin in the ventricular zone.

37 heir primary ventral migration away from the ventricular zone.

38 otch3 mRNAs are more highly localized to the ventricular zones.

39 %], p < 0.01) zones, with a similar trend in ventricular zone (-7.1% [1.9%], p = 0.07).

40 ecursors appear in the metencephalic ventral ventricular zone adjacent to the midline, consistent wit

41 The waves in the outer retina (ventricular zone) also showed stage-dependent pharmacolo

42 strocyte precursors: radial glia (RG) in the ventricular zone and a second cell type we call an 'inte

43 Cell proliferation in the ventricular zone and cell migration to the developing co

44 mination of neural progenitor cells from the ventricular zone and exit from cell cycle, which is asso

45 ng and differentiating neuronal cells of the ventricular zone and external granular layer of the deve

46 ultifunctional guidance cue expressed in the ventricular zone and floor plate of the embryonic neural

47 ast, alphaN-catenin expression is low in the ventricular zone and high in the developing cortical pla

48 ration of neural progenitor cells within the ventricular zone and is required for normal brain histog

49 gradually leads to disruption of the apical ventricular zone and loss of radial glia alignment.

50 Consequently, the ventricular zone and lumen of the dysplastic region are

51 pool of neurons stays in the vicinity of the ventricular zone and matures in situ within 7 days.

52 PrV neurons are born along the hindbrain ventricular zone and migrate radially for a short distan

53 cells of the cerebral cortex are born in the ventricular zone and migrate through the intermediate zo

54 e, GFP expression was found prominent in the ventricular zone and neural progenitor cells from embryo

55 -9(-/-) embryonic mice exhibited an expanded ventricular zone and neuronal malformations identical to

56 from radial glial cells in the telencephalic ventricular zone and not the medial ganglionic eminence.

57 romoter to express Reelin ectopically in the ventricular zone and other brain regions in transgenic m

58 he neocortex, are located in two niches: the ventricular zone and outer subventricular zone.

59 expression of LacZ mRNA was confined to the ventricular zone and perdurance of LacZ protein served a

60 recursor cells (NPCs) populate the embryonic ventricular zone and persist in the subependymal zone of

61 cal properties of proliferative cells of the ventricular zone and postmitotic neurons of the PP at E1

62 y arise from two sources: radial glia in the ventricular zone and progenitors in the subventricular z

63 ced tyrosine phosphorylation of Dab-1 in the ventricular zone and rescued some, but not all, of the n

64 pinal cord oligodendrocytes originate in the ventricular zone and subsequently migrate to white matte

65 pression of cyclins D1 (cD1) and D2 (cD2) in ventricular zone and subventricular zone (SVZ), respecti

66 promoted retention in progenitor layers, the ventricular zone and subventricular zone.

67 t NSCs and INPs coexist in the telencephalic ventricular zone and that they can be prospectively sepa

68 ed region between proliferating cells of the ventricular zone and the deepest neuronal layers of the

69 A is strongly expressed in the proliferative ventricular zone and the developing cortical plate, yet

70 were surprisingly heterogeneous in both the ventricular zone and the motor columns.

71 hat CoupTFI is required for RA rescue of the ventricular zone and the neurogenic phenotypes in Foxc1-

72 and migrating cells, including the embryonic ventricular zone and the postnatal rostral migratory str

73 pecification of populations arising from the ventricular zone and the rhombic lip, two distinct germi

74 igated the neurogenesis derived from the sub-ventricular zone and the sub-granular zone of the dentat

75 or Olig3 is expressed in the entire thalamic ventricular zone and the zona limitans intrathalamica (Z

76 oid structure with two progenitor zones, the ventricular zone and upper rhombic lip, which give rise

77 Mfsd7c-KO embryos was inhibited in cortical ventricular zones and ganglionic eminences.

78 s identified were highly enriched in the CNS ventricular zones and not widely expressed in other prol

79 compared with that of both normal adult VZ (ventricular zone) and E/nestin:GFP (green fluorescent pr

80 xtending from the subventricular zone to the ventricular zone), and some short-range (filopodia-like)

81 d from progenitor cells in the proliferative ventricular zone, and control of progenitor division is

82 D1-like effects are prominent in the ventricular zone, and D2-like effects are prominent in t

83 ed proliferating, migrated radially from the ventricular zone, and differentiated into neurons in the

84 to maintain precursors in the proliferative ventricular zone, and suggest an unexpected function for

85 ved from the neuroepithelium in the cortical ventricular zone, and use the processes of radial glia i

86 ortical development, progenitor cells in the ventricular zone are multipotent, producing neurons of m

87 Our studies indicate that PCs in the ventricular zone are sensitive to loss of Tlx in caudal

88 We propose that DLX-negative cells in the ventricular zone are specified progressively to become D

89 he subventricular zone (SVZ), but not in the ventricular zone, are reduced in MAO AB-deficient mice.

90 We describe the hypothalamic ventricular zone as a key site of neuroendocrine regulat

91 godendrocyte precursors arise in the ventral ventricular zone as a result of local signals.

92 owever, the heterogeneity of the neocortical ventricular zone as well as the contribution of lineage-

93 ord, cell-cell coupling is widespread in the ventricular zone at E11, and the extent of coupling decr

94 hindbrain, but later become confined to the ventricular zone at rhombomere centers, whereas the prot

95 We analyzed the early postnatal ventricular zone at the EM and found a subpopulation of

96 of cells that were finishing division in the ventricular zone at the time of harvest.

97 thelial-like neural stem cells divide in the ventricular zone at the ventricles of the embryonic brai

98 led cells were identified around the ventral ventricular zone at W7.

99 , while a small number of RGCs on the apical ventricular zone (aVZ), expressed cytoplasmic GR.

100 he expression level of ectopic reelin in the ventricular zone became very weak (E18.5) were SPN found

101 tate granule cell progenitors in the dentate ventricular zone before the emigration of the earliest d

102 l regulator into embryonic mouse neocortical ventricular zone before the usual onset of OPC productio

103 Expression extends dorsally to the ventricular zone beginning at E5.

104 lation size of neural precursor cells in the ventricular zone, both in the healthy brain and in the c

105 ls intrinsic to the early embryonic cortical ventricular zone by a process of radial migration, where

106 genitors, we overexpressed BDNF in the adult ventricular zone by transducing the forebrain ependyma t

107 eeping through cohorts of radial glia in the ventricular zone can modulate their proliferation during

108 on of anti-ELF, nestin and dystrophin in sub ventricular zone cells and in stellate-like cells of the

109 al cells constitute a sizeable proportion of ventricular zone cells during late stages of cortical ne

110 actor Ascl1 (previously Mash1) is present in ventricular zone cells in restricted domains throughout

111 exhibit an increased number of proliferative ventricular zone cells that express progenitor cell mark

112 eath and inhibited proliferation of cortical ventricular zone cells, resulting in the generation of f

113 s and Mpp5 at the apical surface of cortical ventricular zone compared with wild type.

114 eloping brain ATF5 expression is high within ventricular zones containing neural stem and progenitor

115 Parallel in vitro studies showed that ventricular zone cultures, enriched in aggrecan-expressi

116 Furthermore, En1/2 function in ventricular zone-derived cells plays a more significant

117 nd abnormal differentiation and migration of ventricular zone-derived neurons and Bergmann glia.

118 onal differentiation, such that cells in the ventricular zone differentiate into post-mitotic neurons

119 and tangential migration of neurons, but not ventricular zone-directed migration.

120 ckdown and found that silencing Cenpj in the ventricular zone disrupts centrosome biogenesis and rand

121 Netrin 1 is expressed at the ventral ventricular zone during oligodendrocyte precursors emigr

122 e midgestation cortex and classified them as ventricular zone-enriched RG (vRG) that express ANXA1 an

123 ess activated beta-catenin in the cerebellar ventricular zone exhibit increased proliferation of NSCs

124 Precursors within the cerebral cortical ventricular zone exhibit robust beta-catenin-mediated tr

125 Ventricular zone expressed PH domain-containing 1 (VEPH1

126 ecific gene expression and a decrease in the ventricular zone expression of motor neuron patterning g

127 Very little ventricular zone expression was observed for Foxp2 and F

128 the adult human hippocampus, we transfected ventricular zone-free dissociates of surgically-excised

129 est expression in proliferating cells of the ventricular zone from E12.5 to E14.5; N-myc was absent f

130 in the number of proliferative cells in the ventricular zone from embryonic day 14 to day 18.

131 lucidating the role of Ptf1a as a cerebellar ventricular zone GABerigic fate switch were actually pre

132 tor LPA1/VZG-1 (lysophospholipid receptor A1/ventricular zone gene-1), revealed a major locus of expr

133 ugh there is cellular disorganization in the ventricular zone, gross morphology of the cortex was una

134 ation, after primary neurogenesis in compact ventricular zones has commenced, individual postmitotic

135 es of GBM, based on its proximity to the sub-ventricular zone, have been reported to have different p

136 Strong expression in the ventricular zone, home of neural progenitor cells during

137 In the ventricular zone, immunoreactivity for both alphaE-caten

138 neuronal phenotype were observed within the ventricular zone in close proximity to the mantle layer

139 eurons compared to neural progenitors of the ventricular zone in the mouse developing cortex.

140 h species, these cells occupy ~60 mum of the ventricular zone in the tangential axis and make contact

141 1 gene expression was observed mainly in the ventricular zone in the ventral parts of the prosencepha

142 ve growth of corticofugal axons into the sub-ventricular zone in vivo.

143 detected in the lateral marginal and ventral ventricular zones in both rodent species.

144 sed in opposing gradients in the neocortical ventricular zone, in specifying areas.

145 We found that neurogenesis in the ventricular zone, in the olfactory bulb, and in a newly

146 and a distorted cellular organization in the ventricular zone, including reduced cellular polarity bu

147 n primates, most SP neurons generated in the ventricular zone initially migrate radially, together wi

148 f Ptf1a, cells originating in the cerebellar ventricular zone initiate a more ventral brainstem expre

149 We analyzed sections of cortex (ventricular zone, intermediate zone, and cortical plate

150 similarities in gene expression between the ventricular zones, intermediate zone, and subplate, and

151 ifferentiate precociously, the proliferative ventricular zone is lost and differentiation markers bec

152 e duration and reduced neurogenesis from the ventricular zone neural precursor population.

153 In ventricular zone neural precursors, beta-catenin signali

154 ession of active nuclear YAP1 (nlsYAP5SA) in ventricular zone neural progenitor cells using condition

155 ort here that purines drive the expansion of ventricular zone neural stem and progenitor cells, and t

156 nces the generation and survival of cortical ventricular zone neuroblasts.

157 only Puma deficiency protected telencephalic ventricular zone NPCs from death in vivo.

158 ndent progressive thinning of the cortex and ventricular zone occurred by programmed cell death.

159 e is a 20-fold increase in cell death in the ventricular zone of fh/fh neocortex, and at postnatal da

160 pment, enhanced apoptosis is observed in the ventricular zone of PIKE knock-out (PIKE(-/-)) cortex.

161 In the ventricular zone of PS1(-/-) mice, expression of the Not

162 The rhombencephalic ventricular zone of the alar plate expressed Pax7.

163 accrues from germinal cell divisions in the ventricular zone of the brain.

164 lly improved proviral gene expression in the ventricular zone of the brain.

165 rom the nucleus at the apical surface of the ventricular zone of the cerebral cortex(5-8).

166 R56 protein, which is highly enriched in the ventricular zone of the cerebral cortex, EGFP is mostly

167 glial precursor somal translocation from the ventricular zone of the corticoseptal boundary (CSB) to

168 icant reduction in cell proliferation in the ventricular zone of the developing cerebral cortex, as r

169 Neural progenitor cells in the ventricular zone of the developing mammalian cerebral co

170 nockdown of Fut10 expression in the cortical ventricular zone of the embryonic brain by in utero elec

171 ltransferase 10 (Fut10), is expressed in the ventricular zone of the embryonic brain.

172 At later stages of development, as the ventricular zone of the embryonic spinal cord is reduced

173 ll mitosis at the ventricular surface of the ventricular zone of the hippocampus [to 56+/-14% (se) hi

174 adial glia-like neural stem cells within the ventricular zone of the medial ganglionic eminence.

175 In the absence of Id4, the ventricular zone of the neocortex, future hippocampus as

176 eveloping skeletal muscles, and later in the ventricular zone of the nervous system.

177 pression in the developing neural retina and ventricular zone of the optic stalk.

178 Two waves of oligodendrogenesis in the ventricular zone of the spinal cord (SC-VZ) during rat d

179 lation of precursor cells within the ventral ventricular zone of the spinal cord.

180 lls are derived from a region connecting the ventricular zone of the third ventricle to the caudal ga

181 ssed in all of the subpallium, including the ventricular zones of (all three subvidisions of) the dor

182 d Musashi-1, are dramatically reduced in the ventricular zones of brg1 mutant mice.

183 natal periods, radial glial cells in various ventricular zones of the brain differentiate into ependy

184 ecoverin-positive cells were apparent in the ventricular zone on the day of birth [postnatal day 0 (P

185 ting from the nuclear transitory zone or the ventricular zone, or both.

186 e developing forebrain, Pax6 is expressed in ventricular zone precursor cells and in specific subpopu

187 natomical origins for GABAergic neurons from ventricular zone precursors and glutamatergic cell from

188 vation functions in the decision of cortical ventricular zone precursors to proliferate or differenti

189 Early progenitor cells in the ventricular zone produce deep layer neurons that express

190 with RA signaling to regulate both cortical ventricular zone progenitor cell behavior and cortical n

191 nd DDR markers are upregulated in cerebellar ventricular zone progenitors.

192 th defects in the transcriptional program of ventricular zone progenitors.

193 oepithelia of the retina and cerebrocortical ventricular zones provide a platform for progenitor cell

194 rons are generated from the Ptf1a-expressing ventricular zone (Ptf1a domain).

195 devastating decrease in embryonic cerebellar ventricular zone radial glial proliferation and concurre

196 However, in the ventricular zone, removal of MPP3 resulted in randomizat

197 mainly in the rhombic lip and the cerebellar ventricular zone, respectively.

198 or compartments (the subventricular zone and ventricular zone) rises and falls with cortical plate ne

199 l plate and cellular heterotopias within the ventricular zone, similar to the phenotypes of mutant mi

200 Proliferating cells in the ventricular zone stem cell compartment are also depleted

201 ains in the lateral and dorsal metencephalic ventricular zone subsequently generate oligodendrocyte p

202 Remarkably, along the germinal ventricular zone-subventricular zone and corpus callosum

203 scl1 promoted tangential migration along the ventricular zone/subventricular zone (VZ/SVZ) and interm

204 3 was detected within the cortical plate and ventricular zone suggesting possible roles in cell proli

205 rkinetic nuclear migration and divide at the ventricular zone surface.

206 rom neural stem cells located within the Sub-Ventricular Zone (SVZ).

207 ort for their role as precursor cells in the ventricular zone that generate cortical neurons and glia

208 ed in a restricted domain of the spinal cord ventricular zone that sequentially generates motoneurons

209 and that local environmental factors in the ventricular zone, the floor plate, or other tissues coor

210 In the ventricular zone, the radial glial cell population remai

211 opositive (BrdU+) cells to be distributed in ventricular zones throughout the brain.

212 hanges from the mitotic germinal zone in the ventricular zone to become distributed in cell groups in

213 ronal differentiation and migration from the ventricular zone to form the mantle layer.

214 and that interneurons may seek the cortical ventricular zone to receive layer information.

215 Migration of post-mitotic neurons from the ventricular zone to the cortical plate during embryogene

216 progenitors as they migrate from the dentate ventricular zone to the dentate gyrus proper, resulting

217 the relocation of neural precursors from the ventricular zone to the forming dentate pole to produce

218 radial migration of newborn neurons from the ventricular zone to the mantle regions.

219 Projection neurons migrate from the ventricular zone to the neocortical plate during the dev

220 al neurons, migrating from the proliferative ventricular zone to the overlaying cortical plate, assum

221 Embryonic CNS neurons can migrate from the ventricular zone to their final destination by radial gl

222 , and a rostral pathway along the cerebellar ventricular zone toward the brainstem.

223 d to the surface of the embryonic ventricle (ventricular zone) until a subset of dividing cells (basa

224 eus of the arcopallium (RA), and the ventral ventricular zone (VVZ), which may provide neurons to Are

225 of IE2-expressing cells was detected in the ventricular zone (VZ) and cortical plate (CP) compared t

226 nitor divisions relative to the plane of the ventricular zone (VZ) and find that this does not correl

227 BrdU+ cells were found predominantly in the ventricular zone (VZ) and immediately adjacent to the VZ

228 rise directly from radial glial cells in the ventricular zone (VZ) and indirectly from intermediate p

229 The CP and the GZ including ventricular zone (VZ) and outer and inner subcompartment

230 erated from two germinal neuroepithelia: the ventricular zone (VZ) and rhombic lip.

231 strate that ATF5 regulates the conversion of ventricular zone (VZ) and subventricular zone (SVZ) neur

232 cipal germinal zones during development, the ventricular zone (VZ) and the subventricular zone (SVZ).

233 with strongest expression observed along the ventricular zone (VZ) and to a lesser degree in postmito

234 cle progression of apical progenitors in the ventricular zone (VZ) at different stages of mouse cereb

235 w increased tangential growth of the rostral ventricular zone (VZ) but decreased Wnt3a and Lef1 expre

236 and diffuse in the cytoplasm and nucleus of ventricular zone (VZ) cells, whereas it is nuclear in th

237 ave unique transcriptional signatures in LGE ventricular zone (VZ) cells.

238 precursors (SNPs) in the murine neocortical ventricular zone (VZ) challenges the widely held view th

239 ial (high Pax6+) and subpallial (high Gsx2+) ventricular zone (VZ) compartments.

240 which are induced throughout the spinal cord ventricular zone (VZ) concomitantly with the induction o

241 T2 mice we demonstrated that the neocortical ventricular zone (VZ) contains radial glial cells (RGCs)

242 n is transiently expressed in the cerebellar ventricular zone (VZ) during a period when PCs are speci

243 ural progenitor cells of the telencephalonic ventricular zone (VZ) has been reported in several studi

244 ally active radial progenitors away from the ventricular zone (VZ) in the upper cerebral wall.

245 neural stem-cell proliferation in the nearby ventricular zone (VZ) increased shortly thereafter.

246 absence, proliferation of stem cells in the ventricular zone (VZ) is compromised.

247 developing cerebral cortex revealed that the ventricular zone (VZ) is divided into p19(INK4d)(+) and

248 The proliferative ventricular zone (VZ) is the main source of projection n

249 migration of differentiated neurons from the ventricular zone (VZ) is well established.

250 el, promotes the growth and proliferation of ventricular zone (VZ) neural precursor cells (NPCs) in v

251 ctor Pax6 is expressed by progenitors in the ventricular zone (VZ) of dorsal telencephalon (dTel), wh

252 show impairments in proliferation within the ventricular zone (VZ) of early DS fetal cortex and in cu

253 Prophase cells in the ventricular zone (VZ) of embryonic day 13.5 Lis1(+/-) mo

254 cell proliferation within the telencephalic ventricular zone (VZ) of juvenile and adult birds to loo

255 increased cellular proliferation within the ventricular zone (VZ) of juvenile male songbirds may con

256 ete floxed-Rac1 alleles in the telencephalic ventricular zone (VZ) of mouse embryos.

257 , using Foxg1-Cre mice to delete Rac1 in the ventricular zone (VZ) of telencephalon and Dlx5/6-Cre-IR

258 The embryonic ventricular zone (VZ) of the cerebral cortex contains mi

259 The ventricular zone (VZ) of the developing cerebral cortex

260 differentiating cells simultaneously in the ventricular zone (VZ) of the developing neocortex.

261 the majority of neuroepithelial cells in the ventricular zone (VZ) of the early embryonic CNS.

262 They first appear in the ventricular zone (VZ) of the embryonic spinal cord in mi

263 SOX9 and GLAST at the wound site and in the ventricular zone (VZ) of the injured tecta indicated an

264 Aergic neuronal migration and found that the ventricular zone (VZ) of the LGE is repulsive to GABAerg

265 e we show that loss of RhoA and Cdc42 in the ventricular zone (VZ) of the medial ganglionic eminence

266 netrin1 is also produced by ventricular zone (VZ) progenitors along the axons' route

267 ord are derived from a region of the ventral ventricular zone (VZ) that also gives rise to motoneuron

268 ta1 promotes cell cycle exit in the cortical ventricular zone (VZ) through modulation of cell cycle p

269 (E10.5), primarily in the dorsal part of the ventricular zone (VZ) throughout the hindbrain and spina

270 ic mouse cerebral cortex, progenitors in the ventricular zone (VZ) undergo a developmental change bet

271 al cortical neurogenesis, neuroblasts in the ventricular zone (VZ) undergo a shape change termed "int

272 cal analysis revealed that the volume of the ventricular zone (VZ) was increased by more than two fol

273 om the more medial portion of the cerebellar ventricular zone (VZ) were observed to spread preferenti

274 ession of Dct was primarily localized to the ventricular zone (VZ) where neuronal stem cells reside.

275 ed at high levels by progenitor cells of the ventricular zone (VZ) within the hippocampal primordium.

276 responding receptors in the embryonic murine ventricular zone (VZ) within which the NSCs undergo symm

277 in the adult songbird brain occurs along the ventricular zone (VZ), a specialized cell layer surround

278 ojection neurons originate from the cortical ventricular zone (VZ), and then migrate radially into th

279 differentiated precursors in the spinal cord ventricular zone (VZ), as well as in the progenitors of

280 in mice, we show that Ntn1 derived from the ventricular zone (VZ), but not the FP, is crucial for CA

281 lso present in neural progenitors within the ventricular zone (VZ), raising the question of which sou

282 division in the telencephalic proliferative ventricular zone (VZ), the nuclei of the neural precurso

283 minative zones, the rhombic lip (RL) and the ventricular zone (VZ), which generate different types of

284 rebellar primordium, later localizing to the ventricular zone (VZ), with the hgf1 and hgf2 ligand gen

285 with ependymal cells, forming a unique adult ventricular zone (VZ).

286 al and neuron cell types that arise from the ventricular zone (vz).

287 al glial cells in the proliferative cortical ventricular zone (VZ).

288 ial glial progenitors (RGPs) residing in the ventricular zone (VZ).

289 , which define a "protomap" in the embryonic ventricular zone (VZ).

290 arginal zone, subventricular zone (SVZ), and ventricular zone (VZ).

291 rily derived from immature cortical regions [ventricular zone (vz)/subventricular zone (svz)].

292 the two neural progenitor populations in the ventricular zones (VZs) and subventricular zones (SVZs)

293 position and number of mitotic cells in the ventricular zone were more abnormal as LIS1 levels decre

294 f later developmental stages, but not in the ventricular zone where neural stem cells reside and divi

295 are present in motor neurons and the ventral ventricular zone where they likely exert their influence

296 ation, HFGFR1 was expressed primarily in the ventricular zone, whereas HEGFR was expressed in the sub

297 -4 expression, however, were elevated in the ventricular zone which only weakly stained for complex g

298 arise from restricted domains of the pallial ventricular zone, which are associated with signalling c

299 l precursor cells in the developing cortical ventricular zone, with markedly reduced expression in th

300 Tlx is expressed broadly in the ventricular zone, with the exception of the dorsomedial