ライフサイエンスコーパス: ganglionic eminence

1 that originate developmentally in the caudal ganglionic eminence.

2 cephalic ventricular zone and not the medial ganglionic eminence.

3 liferation of interneuron progenitors in the ganglionic eminence.

4 cal interneurons that derive from the medial ganglionic eminence.

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

6 cortical-striatal boundary into the lateral ganglionic eminence.

7 ene expression characteristic of the lateral ganglionic eminence.

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

9 terneurons derived from the embryonic medial ganglionic eminence.

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

11 cell subpopulation derived from the lateral ganglionic eminence.

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

13 cal neuroepithelium but not medial or caudal ganglionic eminences.

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

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

16 ventrodorsally along a medial path from the ganglionic eminences.

17 neurons that populate the medial and lateral ganglionic eminences.

18 aracteristic of either the medial or lateral ganglionic eminences.

19 interneurons originating in the more distant ganglionic eminences.

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

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

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

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

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

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

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

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

28 The lateral ganglionic eminence and rostral migratory stream develop

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 5-HT(3A) receptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking 5-HT(3

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

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

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

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

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

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

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

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

71 The medial ganglionic eminence exhibited unique patterns of progeni

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

89 Transplanting medial ganglionic eminence interneuron progenitors to introduce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 2 in the ventricular zone (VZ) of the medial ganglionic eminence (MGE) using Olig2-Cre mice causes mo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 Enforced collapse of ganglionic eminence vessels and resultant periventricula

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

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

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

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