ライフサイエンスコーパス: subventricular zone

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

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

3 constantly being generated in the postnatal subventricular zone.

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

5 rphology while passing through the transient subventricular zone.

6 dictates postnatal neurogenesis in the mouse subventricular zone.

7 inactivate Gabra2 in precursor cells of the subventricular zone.

8 olfactory bulb after their generation in the subventricular zone.

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

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

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

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

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

14 upts tangential interneuron migration in the subventricular zone.

15 , followed by symmetric divisions within the subventricular zone.

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

17 eurotoxins via increased neurogenesis in the subventricular zone.

18 gents that may stimulate neurogenesis in the subventricular zone.

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

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

21 neate their locations in the ventricular and subventricular zones.

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

23 eural progenitors within the ventricular and subventricular zones.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 the Tbr2(+) INPs from the ventricular to the subventricular zones is unknown.

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

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

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

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

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

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

89 In the ventricular and subventricular zones, monomethyl-lysine 9 of H3 (H3K9me1

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

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

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

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

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

95 Subventricular zone neuroblasts are aligned in tightly b

96 ved, but Dlx2, a key downstream regulator of subventricular zone neurogenesis, is not expressed.

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

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

99 Astroglia outside the subventricular zone niche can support NSC differentiatio

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

101 with NPCs we found evidence of elevated host subventricular zone NPC proliferation, neurogenesis, and

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

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

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

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

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

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

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

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

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

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

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

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

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

115 t neural stem cells (aNSCs) derived from the subventricular zone of the brain show therapeutic effect

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

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

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

119 , putative neural stem cells (NSCs) from the subventricular zone of the lateral ventricle can differe

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

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

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

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

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

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

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

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

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

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

130 c protein-positive cells in the hippocampus, subventricular zone or cortex of mice heterozygous for t

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

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

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

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

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

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

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

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

142 Although outer subventricular zone radial glia may generate the majorit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 throughout life in two forebrain areas: the subventricular zone (SVZ) and the hippocampus.

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

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

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

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

167 feration of neuronal progenitor cells in the subventricular zone (SVZ) by 40-50% and migration of new

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

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

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

171 In mice and in young adult humans, the subventricular zone (SVZ) contains multipotent, dividing

172 The subventricular zone (SVZ) continuously supplies new inte

173 drocyte precursor cell (OPC) arises from the subventricular zone (SVZ) during early vertebrate develo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 The subventricular zone (SVZ) is the largest neurogenic nich

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

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

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

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

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

198 Subventricular zone (SVZ) neurogenesis continuously prov

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

226 s at hatching contains a thick proliferative subventricular zone (SVZ) that extends from the subpalli

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

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

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

230 reased proliferation in both the SGZ and the subventricular zone (SVZ), a source of adult-generated o

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

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

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

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

235 ling molecule regulating neurogenesis in the subventricular zone (SVZ), but its functional consequenc

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

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

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

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

240 1 (cD1) and D2 (cD2) in ventricular zone and subventricular zone (SVZ), respectively, suggests that a

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

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

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

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

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

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

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

248 Subventricular zone (SVZ)-derived adult neural precursor

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

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

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

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

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

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

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

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

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

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

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

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

261 onal progenitor cells in the postnatal mouse subventricular zone (SVZ).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.