ライフサイエンスコーパス: ganglionic eminence

1 ls within the ventricular zone of the medial ganglionic eminence.

2 cell subpopulation derived from the lateral ganglionic eminence.

3 rn MSNs within their birthplace, the lateral ganglionic eminence.

4 that originate developmentally in the caudal ganglionic eminence.

5 cephalic ventricular zone and not the medial ganglionic eminence.

6 cal interneurons that derive from the medial ganglionic eminence.

7 ar zone of the third ventricle to the caudal ganglionic eminence.

8 cortical-striatal boundary into the lateral ganglionic eminence.

9 ene expression characteristic of the lateral ganglionic eminence.

10 several transcriptomic changes in the medial ganglionic eminence.

11 ulation resembles INs produced in the caudal ganglionic eminence.

12 liferation of interneuron progenitors in the ganglionic eminence.

13 sion of Nkx2-1 leads to a loss of the medial ganglionic eminence.

14 terneurons derived from the embryonic medial ganglionic eminence.

15 ibits cell migration from the MGE and caudal ganglionic eminence.

16 er from the medial (MGE) or the caudal (CGE) ganglionic eminences.

17 cal neuroepithelium but not medial or caudal ganglionic eminences.

18 tures such as the medial, lateral, or caudal ganglionic eminences.

19 itosis marker p-H3 showed down-regulation in ganglionic eminences.

20 medial (MGE), lateral (LGE) and caudal (CGE) ganglionic eminences.

21 ventrodorsally along a medial path from the ganglionic eminences.

22 neurons that populate the medial and lateral ganglionic eminences.

23 aracteristic of either the medial or lateral ganglionic eminences.

24 ontrols specification and differentiation of ganglionic eminences.

25 t vascular integrity and cause hemorrhage in ganglionic eminences.

26 how this might inform future research on the ganglionic eminences.

27 interneurons originating in the more distant ganglionic eminences.

28 inhibited in cortical ventricular zones and ganglionic eminences.

29 located outside the developing cortex in the ganglionic eminences(1-5).

30 arise from common lineages within the medial ganglionic eminence(4-11).

31 ented novel genetic evidence that the caudal ganglionic eminence, a distinct subpallial progenitor zo

32 LHX6+/DLX+ lineages derived from the medial ganglionic eminence, a progenitor domain in the ventral

33 eural progenitors in the cerebral cortex and ganglionic eminences, accompanied by induced apoptotic c

34 tion analysis, Gsh2 expression in the medial ganglionic eminence after E10.5 may negatively regulate

35 in the EC stream are derived from the caudal ganglionic eminence and become LAMP5(+)RELN(+) inhibitor

36 ic impairment in proliferation in the medial ganglionic eminence and caudal ganglionic eminence at E1

37 educe interneuron neurogenesis in the medial ganglionic eminence and diminish the population of parva

38 urons, are generated from the ventral medial ganglionic eminence and dorsal preoptic area based on fa

39 for inhibitory cells derived from the medial ganglionic eminence and few expressed VGAT, found in GAB

40 A and increased mitotic proliferation in the ganglionic eminence and fewer Gad1 + (glutamic acid deca

41 odeoxyuridine (BrdU) labeling in the lateral ganglionic eminence and frontal cortical neuroepithelium

42 genesis, single-cell transcriptome of medial ganglionic eminence and neurobehavioural functions.

43 al glial progenitors in the embryonic medial ganglionic eminence and preoptic area preferentially dev

44 p, develops domains equivalent to the medial ganglionic eminence and rhombic lip, resembling the gnat

45 The lateral ganglionic eminence and rostral migratory stream develop

46 an increase in cell death within the lateral ganglionic eminence and rostral migratory stream.

47 iferation (e.g., the ventricular zone of the ganglionic eminence and septal area of the brain and the

48 racteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic r

49 sources such as the olfactory primordium and ganglionic eminence and via a massive subpial granular l

50 lation of Dlx1/2 genes in the ventral medial ganglionic eminences and adjacent regions of the septum,

51 We characterized the developing human ganglionic eminences and found that the subventricular z

52 tion and ERK signaling in progenitors of the ganglionic eminences and had fewer SST(+) and VIP(+) int

53 thalamus, parts of the hypothalamus, and the ganglionic eminences and their derivatives in the subpal

54 ative zone of the ventral telencephalon, the ganglionic eminence, and migrate into the developing neo

55 ain, abnormal interneuron migration from the ganglionic eminence, and reduced interneurons in the fro

56 uroepithelium had hemorrhages in the cortex, ganglionic eminence, and thalamus, as well as abnormal v

57 o cortical interneurons born from the caudal ganglionic eminence, and these cells were frequently rel

58 s, Dlx6(LacZ) is expressed in the developing ganglionic eminences, and their derivatives.

59 cular phenotypes were restricted to sporadic ganglionic eminence angiogenic defects, attributable to

60 h will generate the cerebral cortex, but the ganglionic eminences are not affected.

61 cular nucleus, and substantia nigra from the ganglionic eminence as development proceeds.

62 nterneurons that are derived from the medial ganglionic eminence, as most studies have examined this

63 in the medial ganglionic eminence and caudal ganglionic eminence at E13.5 and E17.5, respectively, co

64 Rodent interneurons originate in embryonic ganglionic eminences, but developmental origins in other

65 cal interneurons originate in the subpallial ganglionic eminences, but their developmental origins in

66 t these cells are specified within the human ganglionic eminences by transcriptional programs similar

67 ntral mesencephalon or porcine fetal lateral ganglionic eminence cells were also performed.

68 Ventral mesencephalon (VM) and lateral ganglionic eminence cells were isolated from fetal pigs

69 bset of NGCs lacking nNOS arises from caudal ganglionic eminence (CGE) progenitors.

70 m medial ganglionic eminence (MGE) or caudal ganglionic eminence (CGE) progenitors.

71 died; however, so far the role of the caudal ganglionic eminence (CGE), a posterior subpallial domain

72 the lateral ganglionic eminence (LGE) caudal ganglionic eminence (CGE), and septum, including loss of

73 the most posterior GE subregion, the caudal ganglionic eminence (CGE), highlighting what is known ab

74 In the hippocampal CA1, caudal ganglionic eminence (CGE)-derived interneurons are recru

75 lionic eminence (MGE)-derived but not caudal ganglionic eminence (CGE)-derived interneurons.

76 within the ventral telencephalon, the caudal ganglionic eminence (CGE).

77 interneurons that originate from the caudal ganglionic eminence (CGE).

78 t integration of INs derived from the caudal ganglionic eminence (CGE).

79 rons appear to derive mainly from the caudal ganglionic eminence (CGE).

80 ity arising from either the caudal or medial ganglionic eminences (CGE and MGE).

81 eral ganglionic eminences (LGEs), and caudal ganglionic eminences (CGEs) between preterm-born [born o

82 Our findings establish ganglionic eminence-dependent rules for early synaptic i

83 (CIG)) mice, conditionally deleting Arx from ganglionic eminence derived neurons including cortical i

84 each of which labels a subset of GABAergic, ganglionic eminence derived neurons.

85 tly expressed in the prethalamus and lateral ganglionic eminence-derived corridor and on corticofugal

86 Medial ganglionic eminence-derived inhibitory gamma-aminobutyri

87 ta suggest that Satb1 is required for medial ganglionic eminence-derived interneuron differentiation,

88 ates the differentiation of two major medial ganglionic eminence-derived interneuron populations and

89 tem neuroblastoma, FOXR2-activated to medial ganglionic eminence-derived interneurons, which could th

90 revealed that O-LM cells parse into a caudal ganglionic eminence-derived subpopulation expressing 5-H

91 5-HT(3A) receptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking 5-HT(3

92 , whereas ventral neuronal specification and ganglionic eminence development in the Shh(N/-) telencep

93 that the ITCs arise from the dorsal lateral ganglionic eminence (dLGE) and migrate in the lateral mi

94 We found that dorsal lateral ganglionic eminence (dLGE)-derived olfactory bulb intern

95 ventral pallium (VP) and the dorsal lateral ganglionic eminence (dLGE).

96 om common precursors generated in the medial ganglionic eminence during embryogenesis.

97 ors and neuroblasts in the medial and caudal ganglionic eminences during development, with a peak of

98 V)-expressing cells, are born in the ventral ganglionic eminences during mid-gestation and then migra

99 ncer (Dlx5/6ei) in embryonic day 13.5 medial ganglionic eminence (E13.5 MGE).

100 (E11, E0 = day of conception) when a lateral ganglionic eminence emerges surrounding the lateral and

101 The medial ganglionic eminence exhibited unique patterns of progeni

102 re hippocampus as well as lateral and medial ganglionic eminences exhibited a 20-30% reduction in mit

103 pmental literature on embryonic mouse medial ganglionic eminence exists (with some additional charact

104 tiation of neurons that populate the lateral ganglionic eminence express different combinations of th

105 al GPe neurons originate from lateral/caudal ganglionic eminences, express the transcription factor F

106 ominantly localised in the developing medial ganglionic eminences, flanking a Fgf8-positive midline r

107 forebrain progenitors of the dorsal lateral ganglionic eminence from Pax6 mutant Small Eye (Pax6(Sey

108 the frequency of embryonic day 14.5 (E14.5) ganglionic eminence (GE) progenitors that grew into neur

109 only RG cells isolated from the subpallium (ganglionic eminence) generate CalR(+) or GABA(+) cells,

110 tering, and markers revealed that the caudal ganglionic eminence generated a greater proportion of co

111 sponding to the mammalian medial and lateral ganglionic eminences generated medium spiny neurons foun

112 taining and single-nucleus RNA sequencing of ganglionic eminence germinal zones, the EC stream and th

113 ortical interneurons (CINs) originate in the ganglionic eminences (GEs) and migrate tangentially to t

114 the VZ and subventricular zone (SVZ) of the ganglionic eminences (GEs), the source of all forebrain

115 erated during embryonic development from the ganglionic eminences (GEs).

116 x genes that migrate ventrodorsally from the ganglionic eminences has not been explored in vivo.

117 that multipotential precursor cells from E13 ganglionic eminence have several orders of magnitude hig

118 genitors and neuroblasts in the human medial ganglionic eminence (hMGE).

119 between intermediate zones of the thalamus, ganglionic eminence, hypothalamus, and cortical preplate

120 s of the developing brain, including cortex, ganglionic eminence, hypothalamus, and inferior collicul

121 ingle-cell transcriptomic analyses of medial ganglionic eminence identified a distinct subpopulation

122 re GABAergic interneurons originating in the ganglionic eminence in the ventral telencephalon.

123 In vivo prenatal Foxr2 targeting to the ganglionic eminences in mice induced postnatal cortical

124 Cortical interneurons arise from the ganglionic eminences in the ventral telencephalon and mi

125 ors, found in the proliferative zones of the ganglionic eminences in the ventral telencephalon, in th

126 an cortical interneurons are produced in the ganglionic eminences, including an enormous contribution

127 dicate that the volumes of basal ganglia and ganglionic eminence increase along with that of the whol

128 Transplanting medial ganglionic eminence interneuron progenitors to introduce

129 -type embryonic interneurons from the medial ganglionic eminence into the prefrontal cortex of neonat

130 kx2.1, which is expressed only in the medial ganglionic eminence, is not.

131 architecture of the human SVZ at the lateral ganglionic eminence late in the second trimester of deve

132 the progenitor zones in the pallium, lateral ganglionic eminence (LGE) and medial ganglionic eminence

133 f3 in the subventricular zone of the lateral ganglionic eminence (LGE) at embryonic day 13.5 may unde

134 tion phenotypes, particularly in the lateral ganglionic eminence (LGE) caudal ganglionic eminence (CG

135 ere we report that activin A induces lateral ganglionic eminence (LGE) characteristics in nascent neu

136 uction in the size of the Tlx mutant lateral ganglionic eminence (LGE) from embryonic day 14.5 onward

137 essed in neuronal progenitors of the lateral ganglionic eminence (LGE) in the ventral telencephalon.

138 The lateral ganglionic eminence (LGE) is known to give rise to stria

139 e is considerable agreement that the lateral ganglionic eminence (LGE) is the origin of striatal proj

140 The embryonic lateral ganglionic eminence (LGE) is thought to be the site of o

141 known as Aldh1a3), is reduced in the lateral ganglionic eminence (LGE) of Gsh2 mutants.

142 glionic eminence (MGE), but not from lateral ganglionic eminence (LGE) or neocortex, dispersed and di

143 ns (MSNs), which arise from a common lateral ganglionic eminence (LGE) progenitor.

144 tinct neuronal subtypes derived from lateral ganglionic eminence (LGE) progenitors at specific embryo

145 es neural progenitor identity in the lateral ganglionic eminence (LGE), despite upregulating the neur

146 ell cycle of progenitor cells in the lateral ganglionic eminence (LGE), the neuroepithelial precursor

147 rgic interneurons (GABA INs), or the lateral ganglionic eminence (LGE), which generate GABA INs that

148 d such that they acquire a subset of lateral ganglionic eminence (LGE)-specific properties at the exp

149 direct pathways are generated in the lateral ganglionic eminence (LGE).

150 ity defined by their position in the lateral ganglionic eminence (LGE).

151 elopment of neurons derived from the lateral ganglionic eminence (LGE).

152 ns from an extracortical origin, the lateral ganglionic eminence (LGE).

153 wave of OLPs from the lateral and/or caudal ganglionic eminences (LGE and CGE).

154 ates of cells born in the lateral and medial ganglionic eminences (LGE and MGE) in 13.5-day-old mouse

155 ion of progenitors in the lateral and medial ganglionic eminences (LGE and MGE).

156 essed later in the forebrain itself (lateral ganglionic eminence; LGE) starting at E12.5, suggesting

157 medial ganglionic eminences (MGEs), lateral ganglionic eminences (LGEs), and caudal ganglionic emine

158 MENT Here we demonstrate that porcine medial ganglionic eminence, like rodents, exhibit a distinct tr

159 nversion of some MGE progenitors to a caudal ganglionic eminence-like, bipolar calretinin-expressing

160 ation and organisation into neural rosettes, ganglionic eminence marker expression at early developme

161 nd ectopic persistence of the dorsal lateral ganglionic eminence marker Sp8.

162 lly expressed ventrally in the telencephalic ganglionic eminences (Mash1, Dlx2 and Gsh2) are upregula

163 that the first OLPs originate in the medial ganglionic eminence (MGE) and anterior entopeduncular ar

164 precursors--including those from the medial ganglionic eminence (MGE) and OB--fail to generate neuro

165 Progenitor cells in the medial ganglionic eminence (MGE) and preoptic area (PoA) give r

166 ortical) telencephalon, including the medial ganglionic eminence (MGE) and preoptic area.

167 rupts interneuron neurogenesis in the medial ganglionic eminence (MGE) and, more importantly, that es

168 hermore, Nkx2.1(+) progenitors in the medial ganglionic eminence (MGE) are misspecified such that the

169 terneuron precursors derived from the medial ganglionic eminence (MGE) can induce a second period of

170 ed GABAergic precursor cells from the medial ganglionic eminence (MGE) can migrate and differentiate

171 gic progenitor cells derived from the medial ganglionic eminence (MGE) can reverse mechanical hyperse

172 Embryonic medial ganglionic eminence (MGE) cells transplanted into the ad

173 en described, a system modeling human medial ganglionic eminence (MGE) development, a critical ventra

174 rneurons originating in the embryonic medial ganglionic eminence (MGE) diverge into a range of differ

175 itory interneuron precursors from the medial ganglionic eminence (MGE) enhances GABAergic signaling i

176 In the developing telencephalon, the medial ganglionic eminence (MGE) generates many cortical and vi

177 The medial ganglionic eminence (MGE) gives rise to the majority of

178 BAergic interneurons derived from the medial ganglionic eminence (MGE) impacts their synaptic and int

179 lateral ganglionic eminence (LGE) and medial ganglionic eminence (MGE) in the subpallium has been wel

180 cursors of GABAergic neurons from the medial ganglionic eminence (MGE) into adult mouse spinal cord a

181 of precursor cells from the embryonic medial ganglionic eminence (MGE) into early postnatal neocortex

182 embryonic inhibitory neurons from the medial ganglionic eminence (MGE) into postnatal visual cortex m

183 GABAergic interneurons from the mouse medial ganglionic eminence (MGE) into the adult mouse spinal co

184 In the ventral telencephalon, the medial ganglionic eminence (MGE) is a major source of cortical

185 The medial ganglionic eminence (MGE) is an embryonic forebrain stru

186 Young neurons born in the medial ganglionic eminence (MGE) migrate a long distance dorsal

187 report that mosaic elimination in the medial ganglionic eminence (MGE) of Smo, a key effector of SHH

188 groups originate primarily within the medial ganglionic eminence (MGE) of the subcortical telencephal

189 urons targeting cells by lineage from medial ganglionic eminence (MGE) or caudal ganglionic eminence

190 neurons tangentially migrate from the medial ganglionic eminence (MGE) or the adjacent preoptic/anter

191 omprises cryopreserved, post-mitotic, medial ganglionic eminence (MGE) pallial-type GABAergic interne

192 The medial ganglionic eminence (MGE) produces both locally-projecti

193 ar to rodents, delineating a distinct medial ganglionic eminence (MGE) progenitor domain.

194 show that Prdm16 expression in mouse medial ganglionic eminence (MGE) progenitors is required for ma

195 Caudally situated medial ganglionic eminence (MGE) progenitors receive high level

196 ) IvCs and NGCs are both derived from medial ganglionic eminence (MGE) progenitors under control of t

197 based on transplantation of embryonic medial ganglionic eminence (MGE) progenitors.

198 e the two major subtypes generated by medial ganglionic eminence (MGE) progenitors.

199 y, it resulted in a partial rescue of medial ganglionic eminence (MGE) properties, including interneu

200 ST(+)) interneuron (IN) production in medial ganglionic eminence (MGE) secondary progenitors in mice.

201 king ALK4 in GABAergic neurons of the medial ganglionic eminence (MGE) showed marked deficits in dist

202 tor of interneuron migration from the median ganglionic eminence (MGE) to the pallium, including the

203 2 in the ventricular zone (VZ) of the medial ganglionic eminence (MGE) using Olig2-Cre mice causes mo

204 ibitory interneurons derived from the medial ganglionic eminence (MGE), a germinal zone in the embryo

205 several cIN subtypes derive from the medial ganglionic eminence (MGE), a transient ventral telenceph

206 is regulated by blood vessels of the medial ganglionic eminence (MGE), an interneuron progenitor dom

207 ient embryonic structure known as the medial ganglionic eminence (MGE), but how the remarkable divers

208 ed neuronal precursors from embryonic medial ganglionic eminence (MGE), but not from lateral ganglion

209 rgic interneuron progenitors from the medial ganglionic eminence (MGE), can overcome the mechanical h

210 cid (GABA) interneurons, derived from medial ganglionic eminence (MGE), is implicated in disorders of

211 RNA sequencing on the mouse embryonic medial ganglionic eminence (MGE), the major birthplace for CINs

212 cycle regulation was examined in the medial ganglionic eminence (MGE), the major source of PV intern

213 BAergic precursors from the embryonic medial ganglionic eminence (MGE), the source of neocortical par

214 ortical interneurons originate in the medial ganglionic eminence (MGE), where the signaling molecule

215 eurons, but not by progenitors in the medial ganglionic eminence (MGE), which generate cortical GABAe

216 apoptosis is mediated by inputs from medial ganglionic eminence (MGE)-derived but not caudal ganglio

217 mbryos harboring tdTomato-fluorescent medial ganglionic eminence (MGE)-derived cortical GABAergic int

218 Interestingly, compared with medial ganglionic eminence (MGE)-derived cortical interneuron p

219 Medial ganglionic eminence (MGE)-derived GABAergic cortical int

220 or the differentiation of a subset of medial ganglionic eminence (MGE)-derived neurons, but are dispe

221 Medial ganglionic eminence (MGE)-derived somatostatin (SST)+ an

222 development represents an ancestral, medial ganglionic eminence (MGE)-derived striatal population th

223 o telencephalic excitatory neurons or medial ganglionic eminence (MGE)-like inhibitory neurons.

224 Medial ganglionic eminence (MGE)-like interneuron precursors de

225 irected differentiation of hPSCs into medial ganglionic eminence (MGE)-like progenitors and their mat

226 ortical interneurons generated in the medial ganglionic eminence (MGE).

227 enitors that primarily resides in the medial ganglionic eminence (MGE).

228 s, including those originating in the medial ganglionic eminence (MGE).

229 rneurons (CINs) that originate in the medial ganglionic eminence (MGE).

230 of immature neurons derived from the medial ganglionic eminence (MGE).

231 e embryonic subpallium, including the medial ganglionic eminence (MGE).

232 enitor cells from embryonic medial or caudal ganglionic eminence (MGE, CGE) were made in a well-chara

233 igin in the embryo from the medial or caudal ganglionic eminences (MGE and CGE).

234 nic lineage from either the medial or caudal ganglionic eminences (MGE and CGE).

235 fate-mapping of the mouse medial and caudal ganglionic eminences (MGE and CGE, respectively), from w

236 basal telencephalon: the medial and lateral ganglionic eminences (MGE and LGE).

237 ineages in mouse medial, lateral, and caudal ganglionic eminences (MGE, LGE, and CGE) at embryonic da

238 ared interneuronal progenitors in the medial ganglionic eminences (MGEs), lateral ganglionic eminence

239 erative areas examined: embryonic neocortex, ganglionic eminence, midbrain, retina, hindbrain, and sp

240 ogenitors, derived from the embryonic medial ganglionic eminence, migrate long distances following tr

241 al ganglia arise from the medial and lateral ganglionic eminences, morphologically distinct structure

242 Nkx2.1+ and Dlx2+ progenitors in the medial ganglionic eminence of both humans and rabbits by attenu

243 he anterior entopeduncular area-basal medial ganglionic eminence of mammals).

244 ole in oligodendrogenesis, within the medial ganglionic eminence of Nkx2.1 mutants, the early express

245 In addition, unlike in the ganglionic eminence of the embryonic forebrain where Oli

246 rototypic GPe neurons derive from the medial ganglionic eminence of the embryonic subpallium and expr

247 f the corpus striatum arise from the lateral ganglionic eminence of the telencephalic neuroepithelium

248 uman brain, a contingent of neurons from the ganglionic eminence of the telencephalon migrate to the

249 n of pulvinar neurons has been observed, the ganglionic eminence of the telencephalon.

250 GABAergic interneurons that originate in the ganglionic eminence of the ventral forebrain and incorpo

251 he GABAergic neurons and originates from the ganglionic eminence of the ventral forebrain.

252 epithelium: the majority is derived from the ganglionic eminence of the ventral telencephalon.

253 ricular zone similar to that observed in the ganglionic eminences of mammalian embryos.

254 al interneurons within the medial and caudal ganglionic eminences of the developing telencephalon.

255 t in the hindbrain and within the developing ganglionic eminences of the forebrain.

256 tected in the differentiating regions of the ganglionic eminences on embryonic day 12.5 (E12.5).

257 lls within the caudate nucleus adjoining the ganglionic eminence, potentially a waiting compartment.

258 d then patterned to NKX2.1-expressing medial ganglionic eminence progenitors by simple treatment with

259 rk has established that INs originate in the ganglionic eminence regions in mice, recent studies have

260 embryonic inhibitory neurons from the medial ganglionic eminence reinstate ocular dominance plasticit

261 ibitory interneurons derived from the medial ganglionic eminence represent the largest cohort of GABA

262 present in cortex and inhibitory lineages in ganglionic eminence, revealing both distinct and shared

263 The mutant lateral ganglionic eminences showed an abnormal absence of Dlx 2

264 rived from the cortical anlage (CTXOE03) and ganglionic eminence (STROC05), as well as an adult EC li

265 Dlx-2 in the lateral (LGE) and medial (MGE) ganglionic eminences, subpallial embryonic structures, i

266 rast with the cortex, most stem cells in the ganglionic eminence SVZ did not maintain radial fibers o

267 interneurons, most of which originate in the ganglionic eminences, take distinct tangential migratory

268 restricted to neural progenitor cells in the ganglionic eminence that are fated to differentiate into

269 ions of the rat embryonic telencephalon--the ganglionic eminence that the anlage of the cerebral cort

270 rises from progenitor cells in the embryonic ganglionic eminences that also produce inhibitory neuron

271 erse interneurons from the medial and caudal ganglionic eminences that migrate into the frontal, cing

272 re as the homologue of the mammalian lateral ganglionic eminence (the adult caudatoputamen in mammals

273 ere as the homologue of the mammalian medial ganglionic eminence (the adult pallidum in mammals).

274 lantation of cells from the embryonic medial ganglionic eminence (the major origin of cerebral cortic

275 ventral neurons characteristic of the medial ganglionic eminence, the embryonic structure which gives

276 In the medial ganglionic eminence, the NKX2-1 transcription factor con

277 s that mark early development of the lateral ganglionic eminence, the striatal anlage.

278 the emergence of cell diversity in the human ganglionic eminences, the transitory structures of the h

279 l lateral geniculate nucleus from the caudal ganglionic eminence, there is no obvious new source of p

280 hand, disrupting specification of the medial ganglionic eminence through loss of Nkx2.1 homeobox func

281 ring their migration from the dorsal lateral ganglionic eminence through maturity.

282 onic basal telencephalon (lateral and medial ganglionic eminences) through loss of Dlx1/2 homeobox fu

283 pment, interneurons migrate from the ventral ganglionic eminence to the cerebral cortex within severa

284 evelopment from progenitors in the embryonic ganglionic eminences to progeny in the striatum.

285 neuron migration from the medial and caudal ganglionic eminences to the cerebral cortex in slice pre

286 cells migrate tangentially from the ventral ganglionic eminences to the developing cortex.

287 nterneurons from their place of birth in the ganglionic eminences to their place of terminal differen

288 iption factors normally found in the lateral ganglionic eminence, to prevent precocious differentiati

289 neural progenitors of the lateral and median ganglionic eminences, two protrusions of the ventral tel

290 neurons, from their generation in the medial ganglionic eminence up to their settlement in the AC, ex

291 estricted progenitors are located within the ganglionic eminences, using Dlx5/6-Cre-ires-EGFP (Dlx5/6

292 hemispheric white matter, internal capsule, ganglionic eminence, ventricular zone, corpus callosum,

293 Enforced collapse of ganglionic eminence vessels and resultant periventricula

294 m progenitors located in the ventral lateral ganglionic eminence (vLGE).

295 In the forebrain the lateral ganglionic eminence was reduced in size.

296 d the ventricular-subventricular zone of the ganglionic eminences, whereas at midgestation (20 GW), t

297 The PL develops next to the caudal ganglionic eminence, which generates inhibitory interneu

298 We deleted mouse Nf1 from the medial ganglionic eminence, which gives rise to both oligodendr

299 se cells in mice reduces angiogenesis in the ganglionic eminences, which correspond to the human germ

300 everely impaired proliferation in the medial ganglionic eminence without grossly altering differentia