ライフサイエンスコーパス: subventricular

1 ter, BrdU labeling was seen primarily in the subventricular and peripheral zones.

2 ared from progenitor cells obtained from the subventricular and the subgranular zones of adult mice b

3 Its filamentous pial, subventricular, and perivascular immunostaining pattern

4 adial glia (RG; neural stem cells) and their subventricular dispersion from the periventricular niche

5 tex increases the proportion of RG and their subventricular dispersion.

6 rs, such as the ventricular radial glia, the subventricular intermediate progenitors, and the subvent

7 cultured NSCs and inhibits proliferation of subventricular neural precursors in transgenic mice.

8 ll turnover in the RMS, but has no impact on subventricular neurogenesis.

9 Using subventricular neurosphere and matrigel cultures, we dem

10 that outer radial glia directly support the subventricular niche through local production of growth

11 SVZ cells also gave rise to proliferative subventricular nodules.

12 entricular intermediate progenitors, and the subventricular (outer) radial glia, have been identified

13 We also found that LLC in the subventricular region co-expressed beclin-1 or LC3, mark

14 n 2-immunolabeled neurons in the ventricular/subventricular region, periventricular white matter, cen

15 The rodent subventricular/subependymal zone (SVZ/SEZ) houses neural

16 Using this model, we show that a subventricular vascular plexus (SVP) extends through a h

17 red macrophages, adhered to the newly formed subventricular vascular plexus, and then divided into da

18 outer and inner subcompartments of the outer subventricular zone (OSVZ) in area 17 displayed unique m

19 Human outer subventricular zone (OSVZ) neural progenitors and Drosop

20 ransit-amplifying cells that forms the outer subventricular zone (OSVZ), a proliferative region outsi

21 largely linked to the emergence of the outer subventricular zone (OSVZ), a uniquely structured germin

22 show that neuroblasts born in the postnatal subventricular zone (SVZ) acquire NMDA receptors (NMDARs

23 that WIP1 is expressed in NPCs of the mouse subventricular zone (SVZ) and aged animals with genetica

24 nesis persists throughout life in the rodent subventricular zone (SVZ) and hippocampal dentate gyrus

25 ng and recently divided cells in the rostral subventricular zone (SVZ) and hippocampus of DCX-TK tran

26 rinting for murine adult neurogenesis in the subventricular zone (SVZ) and in the subgranular zone (S

27 ration of bromodeoxyuridine (+) cells in the subventricular zone (SVZ) and lesioned cortex in the str

28 ocyte progenitor cells (OPCs) arise from the subventricular zone (SVZ) and migrate into the developin

29 fying cells and neuroblasts in the postnatal subventricular zone (SVZ) and modulated the proliferatio

30 e correlation between protein changes in the subventricular zone (SVZ) and neurodegenerative diseases

31 olactin-stimulated adult neurogenesis in the subventricular zone (SVZ) and olfactory bulb (OB) mediat

32 diate progenitor cells that migrate into the subventricular zone (SVZ) and proliferate to increase ne

33 interleukin 6 (IL-6) in the amplification of subventricular zone (SVZ) and subgranular zone (SGZ) neu

34 d doublecortin (Dcx)-expressing cells in the subventricular zone (SVZ) and subgranular zone of dentat

35 und in various parts of the brain, e.g., the subventricular zone (SVZ) and substantia nigra (SN), hav

36 as been attributed to the elaboration of the subventricular zone (SVZ) and the associated increase in

37 TBI) increases neurogenesis in the forebrain subventricular zone (SVZ) and the hippocampal dentate gy

38 ral progenitor cells (NSCs/NPCs) in both the subventricular zone (SVZ) and the subgranular zone (SGZ)

39 brain plasticity in mammals occurring in the subventricular zone (SVZ) and the subgranular zone (SGZ)

40 directly to neural stem cells (NSCs) in the subventricular zone (SVZ) and to astrocytes in the adult

41 wofold increase in cell proliferation in the subventricular zone (SVZ) at P17 and a threefold increas

42 neural precursor cells (NPCs) from the adult subventricular zone (SVZ) can also generate new oligoden

43 We challenged subventricular zone (SVZ) cells in vivo with low concent

44 In the postnatal forebrain, the subventricular zone (SVZ) contains a pool of undifferent

45 The subventricular zone (SVZ) continuously supplies new inte

46 ding that NK cells are retained in the brain subventricular zone (SVZ) during the chronic phase of mu

47 uman ganglionic eminences and found that the subventricular zone (SVZ) expanded massively during the

48 liferation and neuroblast chain formation in subventricular zone (SVZ) explants are compromised when

49 neural stem cells (NSCs) in the adult mouse subventricular zone (SVZ) express the histone methyltran

50 Neurons arise in the adult forebrain subventricular zone (SVZ) from Type B neural stem cells

51 After birth, stem cells in the subventricular zone (SVZ) generate neuroblasts that migr

52 ities of the stem cell niche in the affected subventricular zone (SVZ) in aging mice.

53 quired for postnatal neurogenesis within the subventricular zone (SVZ) in the rodent model.

54 gement of subdomains within the adult neural subventricular zone (SVZ) in vivo, we show distinct resp

55 Immature cells of the neonatal forebrain subventricular zone (SVZ) infected in vivo with a retrov

56 s edematous T2 abnormality, mass effect, and subventricular zone (SVZ) involvement-were independently

57 The fetal development of the anterior subventricular zone (SVZ) involves the transformation of

58 The lateral ventricle subventricular zone (SVZ) is a frequent and consequentia

59 The subventricular zone (SVZ) is a principal site of adult n

60 ordinated regulation of the adult neurogenic subventricular zone (SVZ) is accomplished by a myriad of

61 The subventricular zone (SVZ) is greatly expanded in primate

62 The subventricular zone (SVZ) is one of the two major neurog

63 The subventricular zone (SVZ) is the largest germinal zone o

64 so shown that PEDF enhances renewal of adult subventricular zone (SVZ) neural precursors.

65 es are continuously generated from nestin(+) subventricular zone (SVZ) neural progenitor cells (NPCs)

66 negatively regulates neurogenesis from adult subventricular zone (SVZ) neural stem cells (NSCs) in cu

67 Here, we report that loss of Tsc1 in mouse subventricular zone (SVZ) neural stem/progenitor cells (

68 to guide and contain newly generated rodent subventricular zone (SVZ) neuroblasts as they transit al

69 Subventricular zone (SVZ) neurogenesis continuously prov

70 cription factor PAX6 in the control of adult subventricular zone (SVZ) neurogenesis in rodents.

71 Postnatal and adult subventricular zone (SVZ) neurogenesis is believed to be

72 ular zone (SGZ) of the dentate gyrus and the subventricular zone (SVZ) next to the lateral ventricles

73 neural progenitor cells (NPCs) of the adult subventricular zone (SVZ) niche are fairly well understo

74 ads to the expansion of these cells in their subventricular zone (SVZ) niches but fails to maintain s

75 low cytometry, adult mouse lateral ventricle subventricular zone (SVZ) NICs as Glast(mid)EGFR(high)Pl

76 ated cells in the dentate gyrus (DG) and the subventricular zone (SVZ) of 6 and 18 week-old GK and WK

77 d ischemic neural progenitor cells or in the subventricular zone (SVZ) of ischemic animals significan

78 as Srrt) is expressed by adult NSCs from the subventricular zone (SVZ) of mice, and that selective kn

79 ingle cell electroporation in the neurogenic subventricular zone (SVZ) of neonatal mice, we deleted T

80 isease (PD), neurogenesis is impaired in the subventricular zone (SVZ) of postmortem human PD brains,

81 Neural stem cells (NSCs) persist in the subventricular zone (SVZ) of the adult brain.

82 The subventricular zone (SVZ) of the adult mouse brain has a

83 e conditionally expressed Idh1(R132H) in the subventricular zone (SVZ) of the adult mouse brain.

84 ing neuronal recruitment from the neurogenic subventricular zone (SVZ) of the adult mouse striatum.

85 The subventricular zone (SVZ) of the brain constitutes a nic

86 ncreased neurogenesis in the hippocampus and subventricular zone (SVZ) of the brain of animals has be

87 neuronal numbers in the cortex, striatum and subventricular zone (SVZ) of the ischemic rat brain, whi

88 ) and neural progenitor cells (NPCs) are the subventricular zone (SVZ) of the lateral ventricle and t

89 ein (sAPP) as a vascular niche signal in the subventricular zone (SVZ) of the lateral ventricle of th

90 In adult mammals, the subventricular zone (SVZ) of the lateral ventricles and

91 uced nestin lineage neural stem cells in the subventricular zone (SVZ) of the lateral ventricles and

92 egions where neurogenesis takes place is the subventricular zone (SVZ) of the lateral ventricles.

93 dentified a novel population of cells in the subventricular zone (SVZ) of the mammalian brain that ex

94 The subventricular zone (SVZ) provides a constant supply of

95 of nestin-positive neural progenitors in the subventricular zone (SVZ) region of mouse brain.

96 Through adulthood, the rodent subventricular zone (SVZ) stem cell niche generates new

97 cursor cells (NPCs) from the early postnatal subventricular zone (SVZ) to become OPCs in an autonomou

98 iption factors increase in stem cells of the subventricular zone (SVZ) upon oncogenic stress, whereas

99 urogenesis persists postnatally in the human subventricular zone (SVZ) where slow-growing tumors cont

100 Here we show that the VZ, subventricular zone (SVZ), and CP contain distinct molec

101 progenitor cell (NSPC) proliferation in the subventricular zone (SVZ), and migration of newly formed

102 e cell types in the preplate, marginal zone, subventricular zone (SVZ), and ventricular zone (VZ).

103 In the subventricular zone (SVZ), B1 cells contact transit ampl

104 lls (IPC) and mitosis showed that NSC in the subventricular zone (SVZ), but not in the ventricular zo

105 In the adult mammalian subventricular zone (SVZ), GFAP-positive neural stem cel

106 In adult mice, new neurons born in the subventricular zone (SVZ), lining the lateral ventricles

107 Aging and PD impair the subventricular zone (SVZ), one of the most important bra

108 1 (cD1) and D2 (cD2) in ventricular zone and subventricular zone (SVZ), respectively, suggests that a

109 dant in the neurogenic regions including the subventricular zone (SVZ), rostral migratory stream (RMS

110 In the postnatal subventricular zone (SVZ), S phase entry of neural proge

111 calization of beta-galactosidase outside the subventricular zone (SVZ), subarachnoid hemorrhage, and

112 ate neural stem cell quiescence in the adult subventricular zone (SVZ), the function of ECM in the de

113 re, we addressed microglial functions in the subventricular zone (SVZ), the major postnatal neurogeni

114 urogenic regions of the adult brain like the subventricular zone (SVZ), the rostral migratory stream

115 migration, we deleted RhoA and Cdc42 in the subventricular zone (SVZ), where more fate-restricted pr

116 Subventricular zone (SVZ)-derived adult neural precursor

117 We show that CNTF controls the migration of subventricular zone (SVZ)-derived neural progenitors tow

118 Adult subventricular zone (SVZ)-derived neural stem cells (NSC

119 We used adult brain subventricular zone (SVZ)-derived NPC cultures transduce

120 uired for injury-induced neurogenesis in the subventricular zone (SVZ).

121 egion-specific actions of FGF2 on the VZ and subventricular zone (SVZ).

122 lls in the ovine brain was injected into the subventricular zone (SVZ).

123 -positive neural progenitor cells within the subventricular zone (SVZ).

124 lb (OB), rostral migratory stream (RMS), and subventricular zone (SVZ).

125 xpense of neurogenesis in neonatal and adult subventricular zone (SVZ).

126 velopment, the ventricular zone (VZ) and the subventricular zone (SVZ).

127 or progenitor populations in the adult mouse subventricular zone (SVZ).

128 genous neural progenitor cells (NPCs) in the subventricular zone (SVZ).

129 umbers of neural precursors (NPs) within the subventricular zone (SVZ).

130 d to restricted brain regions, including the subventricular zone (SVZ).

131 NPCs derived from the subventricular zone (SVZ-NPCs) were also included in the

132 t neural stem cells (NSCs) within the rodent subventricular zone (SVZ; also called subependymal zone)

133 Neuronal progenitor cells of the anterior subventricular zone (SVZa) migrate along the rostral mig

134 c niches in the adult brain, the ventricular-subventricular zone (V-SVZ) and the subgranular zone (SG

135 Adult neural stem cells in the ventricular-subventricular zone (V-SVZ) contact the cerebrospinal fl

136 NSCs in the adult mouse ventricular-subventricular zone (V-SVZ) exhibit a regional identity

137 The ventricular-subventricular zone (V-SVZ) is an extensive germinal nic

138 diate progenitors persist in the ventricular-subventricular zone (V-SVZ) of the adult mammalian brain

139 SCs) in different domains of the ventricular-subventricular zone (V-SVZ) of the adult rodent brain ge

140 The mammalian ventricular-subventricular zone (V-SVZ) presents the highest neuroge

141 neural stem cells (NSCs) in the ventricular-subventricular zone (V-SVZ) produce diverse olfactory bu

142 Neurogenesis in the ventricular-subventricular zone (V-SVZ) shortly after birth was also

143 he adult neurogenic niche of the ventricular-subventricular zone (V-SVZ), beyond serving as a potenti

144 In the adult ventricular-subventricular zone (V-SVZ), NSCs are a specialized form

145 In the ventricular-subventricular zone (V-SVZ), quiescent neural stem cells

146 nal region of the forebrain, the ventricular-subventricular zone (V-SVZ), replenish olfactory neurons

147 ent adult NSCs that populate the ventricular-subventricular zone (V-SVZ).

148 gential migration along the ventricular zone/subventricular zone (VZ/SVZ) and intermediate zone (IZ)

149 l (RG) cells, in the neocortical ventricular/subventricular zone (VZ/SVZ), generate cortical projecti

150 yrus of the hippocampal formation and in the subventricular zone adjacent to the wall of the lateral

151 DeltaTK-GFP) transgene that labels quiescent subventricular zone adult neural stem cells also labels

152 e progenitor cells (OPCs) migrating from the subventricular zone after focal demyelination of adult m

153 d can similarly improve gene transfer to the subventricular zone after intraventricular injection.

154 Expansion of the subventricular zone and appearance of oRG cells may have

155 arkably, along the germinal ventricular zone-subventricular zone and corpus callosum there is reduced

156 ng immature neurons in human early postnatal subventricular zone and cortex.

157 e quiescent neural stem cells from the adult subventricular zone and demonstrate their stem cell char

158 Endogenous neurogenesis and glia in the subventricular zone and dentate gyrus neurogenic niches

159 sing and BrdU-labeled cells from the rostral subventricular zone and dentate gyrus, and abolished neu

160 neurogenesis in the adult lateral ventricle subventricular zone and dentate gyrus.

161 tex and loss of doublecortin(+) cells in the subventricular zone and hippocampal dentate gyrus.

162 was detected in progenitors of the cortical subventricular zone and in cortical OPCs.

163 neural stem cells were not maintained in the subventricular zone and neurogenesis was lost.

164 nal progenitor cells located in the neonatal subventricular zone and persist in the adult murine cent

165 Here we find that the infant human subventricular zone and RMS contain an extensive corrido

166 ust proliferation and migration in the human subventricular zone and RMS.

167 feration and an increase in apoptosis in the subventricular zone and rostral migratory stream of ERK5

168 inactivated in migrating neuroblasts in the subventricular zone and rostral migratory stream, and ac

169 the PI3K-Akt-mTorc1 pathway and an enlarged subventricular zone and rostral migratory stream.

170 stin, and doublecortin, such as those in the subventricular zone and rostral migratory stream.

171 ted Rad-NSCs were observed to persist in the subventricular zone and secondary Rad-NSCs were isolated

172 ls were also found to have migrated into the subventricular zone and the corpus callosum.

173 ls labeled from E12.5 contribute to both the subventricular zone and the dentate gyrus of the hippoca

174 ed in the adult brain, the lateral ventricle subventricular zone and the dentate gyrus subgranular zo

175 in the adult mammalian brain, including the subventricular zone and the dentate gyrus, which act to

176 striatal neuroglia, with gliogenesis in the subventricular zone and the somatosensory cortex in vivo

177 urogenesis, not all new neurons in the human subventricular zone are destined for the olfactory bulb-

178 adult neural stem cells resident within the subventricular zone are known sources of remyelinating c

179 Some of these subventricular zone astrocytes can function as neural st

180 rounds of transit amplification in the outer subventricular zone before producing neurons.

181 In contrast, in Mll1-deficient subventricular zone cells, chromatin at Dlx2 is bivalent

182 In differentiating wild-type subventricular zone cells, Mash1, Olig2 and Dlx2 loci ha

183 rates that Dlx2 is a direct target of MLL in subventricular zone cells.

184 Another deletion removes a forebrain subventricular zone enhancer near the tumour suppressor

185 the CNS only when the germinal niche of the subventricular zone functions properly.

186 roughout life, stem cells in the ventricular-subventricular zone generate neuroblasts that migrate vi

187 Cells generated in the subventricular zone give rise to neuroblasts that migrat

188 Here we show that ZIKV infects the subventricular zone in human fetal brain tissues and tha

189 rter NKCC1 (shNKCC1) in NPCs of the neonatal subventricular zone in mice to reduce GABA(A)-induced de

190 d by ventricular radial glial (RG) cells and subventricular zone intermediate progenitor (IP) cells.

191 ontinuous supply of new neuroblasts from the subventricular zone is necessary for both the restoratio

192 rogenesis in the subgranular zone and/or the subventricular zone is responsible for the social abnorm

193 liferation of neural progenitor cells in the subventricular zone leads to the continuous generation o

194 om microarrays, and FACS purification of the subventricular zone lineage, we stringently identify lnc

195 and adult CNS, Plexin-B2 is expressed in the subventricular zone lining the telencephalic ventricles

196 temness promoting actions of IGF-II on mouse subventricular zone neural precursors.

197 (ANG2), a proangiogenic gene, expression in subventricular zone neural progenitor cells.

198 Consistent with the integral role of subventricular zone neural progenitors in generation and

199 nalyze lncRNA expression for the adult mouse subventricular zone neural stem cell lineage.

200 Mll1-deficient subventricular zone neural stem cells survive, prolifera

201 Subventricular zone neuroblasts are aligned in tightly b

202 nterior forebrain.SIGNIFICANCE STATEMENT The subventricular zone neurogenic stem cell niche generates

203 acts NPCs proliferation and migration at the subventricular zone niche and results, for the first tim

204 as-homolog enriched in brain (Rheb(CA)) into subventricular zone NPCs increased mTOR activity in newb

205 We demonstrate that lateral ventricle subventricular zone NSCs are molecularly and functionall

206 ultured as neurospheres and, in vivo, in the subventricular zone of adult mice.

207 increased infiltration of microglia into the subventricular zone of both FIP200hGFAP conditional knoc

208 NSCs harvested from the subventricular zone of fetal rats were preconditioned wi

209 Neural stem cells harvested from the subventricular zone of foetal mice were preconditioned w

210 proteins) 1, 5, and 8, were elevated in the subventricular zone of human infants with HIE compared t

211 lar zone (SGZ) of dentate gyrus, ventricular/subventricular zone of lateral ventricles, and ependymal

212 The subventricular zone of many adult non-human mammals gene

213 NPCs were isolated from the subventricular zone of neonatal cats and implanted at th

214 treatment on primary cells obtained from the subventricular zone of postnatal BALB/c mice.

215 Newly generated neuroblasts from the subventricular zone of the adult brain migrate as neuron

216 t mouse brain contain neural stem cells: the subventricular zone of the anterior forebrain and the su

217 ural stem and progenitor cells reside in the subventricular zone of the brain, intraventricular injec

218 y are required for AKT activation within the subventricular zone of the developing MGE.

219 Reduced expression of Fgf3 in the subventricular zone of the lateral ganglionic eminence (

220 entate gyrus of the hippocampus and from the subventricular zone of the lateral ventricle, the rostra

221 mmalian brains, neurogenesis persists in the subventricular zone of the lateral ventricles (SVZ) and

222 re part of the neurogenic niche in the adult subventricular zone of the lateral ventricles, where the

223 genesis in the hippocampal dentate gyrus and subventricular zone of the lateral ventricles.

224 decrease in neurogenesis is observed in the subventricular zone of the LGE at mid-stages of embryoge

225 eural stem/progenitor cell population in the subventricular zone of the post-natal brain.

226 aled that the migration and proliferation of subventricular zone OPCs is decreased in the Cav1.2(KO)

227 lls) were observed in the cortex but not the subventricular zone or hippocampus of the transgenic com

228 ling, or exits the cycle and migrates to the subventricular zone or the developing cortical plate.

229 oma multiforme when transduced either in the subventricular zone or the hippocampus.

230 tively regulated both OPC specification from subventricular zone progenitors as well as the balance b

231 We found that Cited2 functions within subventricular zone progenitors to both broadly regulate

232 An initial report found few subventricular zone proliferating cells and rare migrati

233 ad little effect on CNS stem cell frequency, subventricular zone proliferation, olfactory bulb neurog

234 Although outer subventricular zone radial glia may generate the majorit

235 ime-lapse imaging of multipolar cells in the subventricular zone revealed that downregulating levels

236 Delocalized RGPs did not become outer subventricular zone RGPs (oRGs).

237 d GCs by sparse retroviral delivery in mouse subventricular zone that allows functional analysis of s

238 lls with a migratory morphology in the adult subventricular zone that coexpressed markers of neural s

239 Neuronal precursors produced in the subventricular zone throughout an animal's life migrate

240 show that these cells are recruited from the subventricular zone to populate demyelinated lesions in

241 n and migration of newly formed cells in the subventricular zone to the olfactory bulb.

242 ostral migratory stream (RMS) connecting the subventricular zone to the olfactory bulb.

243 me apparently long-range (extending from the subventricular zone to the ventricular zone), and some s

244 glial cells and seed formation of the outer subventricular zone via horizontal divisions, which occu

245 Neural precursors from the subventricular zone were propagated in vitro in culture

246 These data suggest that in the subventricular zone where Reelin is not present but ApoE

247 oliferating neural stem cells located in the subventricular zone within 24 h after infection.

248 sis by outer radial glial cells in the outer subventricular zone, a region present in humans but not

249 on molecule Contactin2, defasciculate in the subventricular zone, and fail to grow toward the midline

250 of the hippocampal formation, but not in the subventricular zone, and, as a novel finding, affected m

251 al stem cells (NSC) harvested from Mut3 mice subventricular zone, and, in vivo, there was increased p

252 born pyramidal neurons migrating through the subventricular zone, but not in those migrating through

253 he number of newly formed neuroblasts in the subventricular zone, corpus callosum and the peri-infarc

254 Unlike glial progenitors in the subventricular zone, differentiated astrocytes undergo s

255 dly by progenitors in the embryonic day 15.5 subventricular zone, during the peak of superficial laye

256 The adult human subventricular zone, in contrast, contains a hypocellula

257 ised when clusterin, which is present in the subventricular zone, is blocked in vitro.

258 precursors, generated throughout life in the subventricular zone, migrate through the rostral migrato

259 Prominin-1(+) precursor cells from the adult subventricular zone, no information about the expression

260 losum and reduced cell division in the mouse subventricular zone, the hippocampal dentate gyrus, and

261 postnatal day 4 NSCs and adult NSCs from the subventricular zone, transplanted Rad-NSCs differentiate

262 the addition of new neurons generated in the subventricular zone, were observed in the injured bulb.

263 the ventricular zone and progenitors in the subventricular zone, with the contribution from each reg

264 t hours of neuronal differentiation of adult subventricular zone-derived stem/progenitor cells, we de

265 vRG) that express ANXA1 and CRYAB, and outer subventricular zone-localized RG (oRG) that express HOPX

266 quired for stem cell activation in the adult subventricular zone.

267 opulations of adult neural stem cells in the subventricular zone.

268 iR-124 is a neuronal fate determinant in the subventricular zone.

269 constantly being generated in the postnatal subventricular zone.

270 s (GCs) are generated throughout life in the subventricular zone.

271 rphology while passing through the transient subventricular zone.

272 dictates postnatal neurogenesis in the mouse subventricular zone.

273 inactivate Gabra2 in precursor cells of the subventricular zone.

274 olfactory bulb after their generation in the subventricular zone.

275 ood into the striatal region adjacent to the subventricular zone.

276 n the human brain, which reside in the outer subventricular zone.

277 al brain's neural progenitor cell (NPC)-rich subventricular zone.

278 born granule cells (GCs), migrating from the subventricular zone.

279 n two niches: the ventricular zone and outer subventricular zone.

280 upts tangential interneuron migration in the subventricular zone.

281 , followed by symmetric divisions within the subventricular zone.

282 in the dentate gyrus of the hippocampus and subventricular zone.

283 eurotoxins via increased neurogenesis in the subventricular zone.

284 gents that may stimulate neurogenesis in the subventricular zone.

285 em cells [aNSCs]) from the adult ventricular-subventricular zone.

286 umulation of these newly born neurons at the subventricular zone/intermediate zone border.

287 ave defects in postnatal neurogenesis in the subventricular zone: a developmental continuum that resu

288 ermal growth factor receptor (EGFR)-positive subventricular-zone (SVZ) astrocytes are activated stem

289 ursors in the embryonic ventricular (VZ) and subventricular zones (SVZ), which give rise to excitator

290 imal differences between the inner and outer subventricular zones even though the outer zone is expan

291 s in the transient embryonic ventricular and subventricular zones generate neurons that migrate acros

292 ial glia cells (RGCs) in the ventricular and subventricular zones of developing human brain.

293 zed that neurogenesis in the ventricular and subventricular zones of the cerebral cortex would contin

294 idal neurons are born in the ventricular and subventricular zones of the pallium and migrate along ra

295 to cellular retention in the ventricular and subventricular zones, whereas overexpression of Botch dr

296 neate their locations in the ventricular and subventricular zones.

297 s, is mainly confined to the subgranular and subventricular zones.

298 eural progenitors within the ventricular and subventricular zones.

299 al layers and accumulated at the ventricular/subventricular zones.

300 oliferative compartment (the ventricular and subventricular zones; S/VZ) and the postproliferative co