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 her than PEDF and included some cortical and subventricular areas.

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

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

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

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

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

10 Using subventricular neurosphere and matrigel cultures, we dem

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

12 SVZ cells also gave rise to proliferative subventricular nodules.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 The subventricular zone (SVZ) continuously supplies new inte

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Subventricular zone (SVZ) neurogenesis continuously prov

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 Subventricular zone (SVZ)-derived adult neural precursor

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 Here, subventricular zone neural stem cells that generate olfa

198 Subventricular zone neuroblasts are aligned in tightly b

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

227 Although outer subventricular zone radial glia may generate the majorit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

264 upts tangential interneuron migration in the subventricular zone.

265 , followed by symmetric divisions within the subventricular zone.

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

267 eurotoxins via increased neurogenesis in the subventricular zone.

268 gents that may stimulate neurogenesis in the subventricular zone.

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

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

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

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

273 constantly being generated in the postnatal subventricular zone.

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

275 rphology while passing through the transient subventricular zone.

276 dictates postnatal neurogenesis in the mouse subventricular zone.

277 inactivate Gabra2 in precursor cells of the subventricular zone.

278 olfactory bulb after their generation in the subventricular zone.

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

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

281 delamination process in the formation of the subventricular zone.

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

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

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

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

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

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

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

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

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

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

297 neate their locations in the ventricular and subventricular zones.

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

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

300 nhanced neurogenesis in both subgranular and subventricular zones.