ライフサイエンスコーパス: subventricular zone

1 yrus, superior temporal gyrus, thalamus, and subventricular zone).

2 (E-protein) interactions predominate in the subventricular zone.

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

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

5 upts tangential interneuron migration in the subventricular zone.

6 , followed by symmetric divisions within the subventricular zone.

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

8 eurotoxins via increased neurogenesis in the subventricular zone.

9 gents that may stimulate neurogenesis in the subventricular zone.

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

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

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

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

14 constantly being generated in the postnatal subventricular zone.

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

16 rphology while passing through the transient subventricular zone.

17 dictates postnatal neurogenesis in the mouse subventricular zone.

18 inactivate Gabra2 in precursor cells of the subventricular zone.

19 olfactory bulb after their generation in the subventricular zone.

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

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

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

23 delamination process in the formation of the subventricular zone.

24 al progenitor numbers (Ki67 positive) in the subventricular zone.

25 abling cells to both enter and remain in the subventricular zone.

26 s showed no staining in the striatum besides subventricular zone.

27 neate their locations in the ventricular and subventricular zones.

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

29 eural progenitors within the ventricular and subventricular zones.

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

31 nhanced neurogenesis in both subgranular and subventricular zones.

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

33 In mice, Chi3l3 is highly expressed in the subventricular zone, a stem cell niche of the adult brai

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

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

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

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

38 al stem cells located in the ventricular and subventricular zones along the lateral forebrain ventric

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

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

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

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

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

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

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

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

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

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

49 -diffraction-limit resolution-in the cortex, subventricular zone and olfactory bulb of mouse brain, u

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

69 mbic lip primary progenitor zones to include subventricular zones containing basal progenitors.

70 mined stem cells residing in the ventricular-subventricular zone continuously generate progenitors th

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

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

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

74 accumulation of neuronal progenitors in the subventricular zone during corticogenesis, and impaired

75 accompanied by a relative enlargement of the subventricular zone during development.

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

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

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

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

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

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

82 enitors(1) that delaminate and settle in the subventricular zone in enlarged brain regions(2).

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

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

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

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

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

88 The length of time that cells stay in the subventricular zone is essential for controlling further

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

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

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

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

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

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

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

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

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

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

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

100 Here, subventricular zone neural stem cells that generate olfa

101 Subventricular zone neuroblasts are aligned in tightly b

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

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

104 wild-type NSCs isolated from the adult mouse subventricular zone niche.

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

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

107 shRNA mediated knockdown of Rab27a in dorsal subventricular zone NSCs and astrocytes increased the nu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 l neurons in the dramatically enlarged outer subventricular zone (oSVZ).

137 hin the brain, endothelial cells (EC) of the subventricular zone play a critical role in neural stem

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

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

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

141 Although outer subventricular zone radial glia may generate the majorit

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

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

144 h glioblastoma that contacts the ventricular-subventricular zone stem cell niche (VSVZ + GBM) have a

145 hey became transcriptionally very similar to subventricular zone stem cells, progressing through a ne

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

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

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

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

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

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

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

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

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

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

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

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

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

159 enhanced the endogenous neurogenesis in the subventricular zone (SVZ) and the dentate gyrus (DG) of

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

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

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

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

164 velopmental processes in the early postnatal subventricular zone (SVZ) are critical for proper brain

165 method, neural stem and progenitor cells of subventricular zone (SVZ) are isolated and expanded usin

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

167 on of LIN28 in progenitor cells of the mouse subventricular zone (SVZ) caused several distinct effect

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

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

170 The subventricular zone (SVZ) continuously supplies new inte

171 rogenitor cells (NSPCs) originating from the subventricular zone (SVZ) contribute to brain repair dur

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

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

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

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

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

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

178 neural progenitor cells (NPCs) found in the subventricular zone (SVZ) have prompted strategies targe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

194 Subventricular zone (SVZ) neurogenesis continuously prov

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

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

197 derived neurotrophic factor (BDNF) level and subventricular zone (SVZ) neurogenesis.

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

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

200 the neural stem cell (NSC) pool in the adult subventricular zone (SVZ) niche by preventing premature

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

218 in), and (d) neuronal maturity (NeuN) in the subventricular zone (SVZ) of the lateral ventricles and

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

220 ortex via either modulation drives increased subventricular zone (SVZ) progenitor proliferation, migr

221 Dopaminergic signalling is necessary for subventricular zone (SVZ) proliferation and olfactory bu

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

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

224 l precursor cells (eNPCs) located within the subventricular zone (SVZ) since this latter area is cons

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

226 The adult subventricular zone (SVZ) stem cell niche is comprised o

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

228 eural precursor cells (eNPCs) located in the subventricular zone (SVZ) to generate new OPCs in the le

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

230 odel in which neural stem cells (NSC) of the subventricular zone (SVZ) were temporarily expanded by c

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

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

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

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

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

236 es and normal Pten/chr19 are observed in the subventricular zone (SVZ), but are distantly segregated

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

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

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

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

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

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

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

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

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

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

247 Subventricular zone (SVZ)-derived adult neural precursor

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

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

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

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

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

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

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

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

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

257 e production of reactive astrocytes from the subventricular zone (SVZ).

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

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

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

261 A certain fraction also homed in the subventricular zone (SVZ).

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

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

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

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

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

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

268 and 8 months of age, whilst others, like the subventricular zones, these differences were more eviden

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

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

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

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

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

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

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

276 stem cells (NSCs) persist in the ventricular-subventricular zone (V-SVZ) and the subgranular zone (SG

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

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

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

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

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

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

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

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

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

286 entiation in the young postnatal ventricular-subventricular zone (V-SVZ), in which neural stem cells

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

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

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

290 city and NSC number in the adult ventricular-subventricular zone (V-SVZ).

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

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

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

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

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

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

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

298 Moreover, AKNA regulates the exit from the subventricular zone, which reveals the pivotal role of c

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

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