ライフサイエンスコーパス: telencephalon

1 differences in the neurogenic niches in the telencephalon.

2 genes expressed in particular regions of the telencephalon.

3 e ultrasensitivity and borders in the dorsal telencephalon.

4 to address this issue in the zebrafish adult telencephalon.

5 size of the precursor pool in the embryonic telencephalon.

6 psule requires Fz3 expression in the ventral telencephalon.

7 vely neurogenic radial glia of the embryonic telencephalon.

8 sue with characteristics of diencephalon and telencephalon.

9 l and that these embryos lack a fully formed telencephalon.

10 oth GABAergic and cholinergic neurons in the telencephalon.

11 on of cortical interneurons from the ventral telencephalon.

12 progenitors located throughout the embryonic telencephalon.

13 AptCB1R mRNA was highly expressed in the telencephalon.

14 selective elimination of Lhx2 in the dorsal telencephalon.

15 have affected or benefited from an enlarged telencephalon.

16 genitor cells (NPCs) in the mammalian dorsal telencephalon.

17 mediate evolutionary diversification of the telencephalon.

18 godendrogenesis within the embryonic ventral telencephalon.

19 ng interneurons derived from the subcortical telencephalon.

20 ized along their pathway through the ventral telencephalon.

21 odimer sites in the developing mouse ventral telencephalon.

22 ncers active in subregions of the developing telencephalon.

23 es of gamma-aminobutyric acid neurons in the telencephalon.

24 related (Area X) song regions of zebra finch telencephalon.

25 fy homologies between different parts of the telencephalon.

26 nscriptome of human, chimpanzee, and macaque telencephalon.

27 tem, or in a restricted manner in the dorsal telencephalon.

28 activities were also detected in the ventral telencephalon.

29 stretched along the rostrocaudal axis of the telencephalon.

30 ranscripts of these genes in the apteronotid telencephalon.

31 s that form the anterior head, including the telencephalon.

32 tion of limbic-associated areas in the avian telencephalon.

33 e inhibitory neuron diversity throughout the telencephalon.

34 riginate from progenitors within the ventral telencephalon.

35 ing oligodendrocyte formation in the ventral telencephalon.

36 cell populations in distinct regions of the telencephalon.

37 pulations function in different parts of the telencephalon.

38 ctor plays in the development of the ventral telencephalon.

39 nized clonal units in the developing ventral telencephalon.

40 ral ganglionic eminence (LGE) in the ventral telencephalon.

41 ctively] in radial glial cells of the dorsal telencephalon.

42 l levels of SHH signaling within the ventral telencephalon.

43 icient in Bmpr1a conditionally in the dorsal telencephalon.

44 iated with auditory areas in the caudomedial telencephalon.

45 d FoxG1 work together to specify the ventral telencephalon.

46 d extent of OPC production in the developing telencephalon.

47 orebrain has been poorly studied outside the telencephalon.

48 sis has been little investigated outside the telencephalon.

49 y bulb, subpallium, and preoptic area of the telencephalon.

50 Vv) and supracomissural (Vs) part of ventral telencephalon.

51 origin of cell types such as the vertebrate telencephalon.

52 uration and neurogenesis in developing human telencephalon.

53 reoptic area and ventral part of the ventral telencephalon.

54 ct tangential migratory routes in the dorsal telencephalon.

55 -1/3, and ARF6 accumulate in the RBX2 mutant telencephalon.

56 ssion dominates nuclei of the pallial dorsal telencephalon.

57 VZ) and intermediate zone (IZ) of the dorsal telencephalon.

58 ation sites in the preoptic area and ventral telencephalon.

59 ephalon migrate tangentially into the dorsal telencephalon.

60 ression to GABAergic interneurons within the telencephalon.

61 audal ganglionic eminences of the developing telencephalon.

62 0 transcription regulators (TR) in the adult telencephalon.

63 rom the Nkx2.1(+) progenitors of the ventral telencephalon.

64 he subcortical white matter of the mammalian telencephalon.

65 , the NG2(+) glia populate the entire dorsal telencephalon.

66 es are a conserved feature of amniote dorsal telencephalon.

67 y of peptides and receptors in the mammalian telencephalon.

68 The ventral telencephalon acts as an instructive tissue, but the imp

69 ed dendritic spine densities within auditory telencephalon, an effect blocked by WIN pretreatments.

70 er name), a premotor nucleus of the songbird telencephalon analogous to premotor cortical regions in

71 axonal mistargeting by neurons of the dorsal telencephalon and abnormal itch-like behavior.

72 Cre-mediated Ctcf deletion in the telencephalon and anterior retina at embryonic day 8.5 t

73 cations, contrary to what is observed in the telencephalon and cerebellum.

74 aracteristic slope, which is highest for the telencephalon and cerebellum.

75 maging at cellular resolution throughout the telencephalon and deep into the cerebellum and optic tec

76 one receptor mRNA and protein throughout the telencephalon and diencephalon and some mesencephalic st

77 rvations indicate that the separation of the telencephalon and diencephalon depends on interactions b

78 in the ventral forebrain (including both the telencephalon and diencephalon) revealed a unique role f

79 Further, the border between the telencephalon and diencephalon, the telencephalic/dience

80 tion of the cells destined to form the eyes, telencephalon and diencephalon.

81 rom a number of different cell groups in the telencephalon and diencephalon.

82 cation, growth, and patterning of the dorsal telencephalon and displays highest correlation with that

83 However, its roles in the ventral telencephalon and during oligodendrogenesis in the telen

84 control of cell proliferation in the dorsal telencephalon and for the formation of its normal lamina

85 o express either Gsx1 or Gsx2 throughout the telencephalon and found that Gsx1 functions similarly to

86 -evoked activity in two forebrain areas: the telencephalon and habenula.

87 1 and ERbeta2 were robustly expressed in the telencephalon and hypothalamus in vocal-acoustic and oth

88 ts in incomplete segregation of the eyes and telencephalon and in defective evagination of the optic

89 expression in avian as compared to mammalian telencephalon and in other regions that show the most di

90 inhibitory interneurons arise in the ventral telencephalon and migrate tangentially to enter the deve

91 from the ganglionic eminences in the ventral telencephalon and migrate tangentially to the cortex.

92 l GABAergic neurons are generated in ventral telencephalon and migrate up to developing cortex where

93 al cortex and dorsoventral patterning of the telencephalon and neural tube were partially rescued in

94 nighttime in tissue samples inclusive of the telencephalon and POA, but remains stable in other brain

95 ype that originates in the embryonic ventral telencephalon and populates the cortex through long-dist

96 c, send ascending projections to the ventral telencephalon and prominent descending projections to vo

97 NPY expressing neurons are localized also in telencephalon and rhombencephalon; (c) HCRT expressing n

98 pression of a series of genes in the ventral telencephalon and severe impairment in the tangential mi

99 cts in the generation of OPCs throughout the telencephalon and subsequent reductions in white matter

100 RT-qPCR revealed that the telencephalon and thalamus were characterized by the mos

101 expression defined the boundary between the telencephalon and the hypothalamus.

102 a marked loss of huC-positive neurons in the telencephalon and throughout the spinal cord axis.

103 rimary extrabulbar projections widely in the telencephalon and to more restricted regions of the dien

104 laminated encephalic regions, the forebrain (telencephalon) and hindbrain (cerebellum) separately.

105 e severe in the caudo-lateral portion of the telencephalon, and do not survive past birth.

106 on, proliferation and differentiation of the telencephalon, and is expressed from the earliest stages

107 ABAergic interneurons arising from the basal telencephalon, and may help to unravel the pathogenesis

108 tory bulb, pallium, and preoptic area of the telencephalon, and the subpallium is devoid of these cel

109 d gene expression changes in adult zebrafish telencephalon are affected by chronic stress experience.

110 Interestingly, endothelial cells of the telencephalon are not homogeneous in their gene expressi

111 populations in the dogfish hypothalamus and telencephalon are notable in comparison with those of th

112 he ventricular neuroepithelium of the dorsal telencephalon are the progenitor cells for neocortical p

113 Here, we used the developing mouse telencephalon as an example to study the role of the FRS

114 r signal, and its source in the rostromedial telencephalon as an organizer of the neocortical area ma

115 oxG1 regulates neurogenesis in the embryonic telencephalon as well as a number of other neurodevelopm

116 dissected regions of the mid-gestation human telencephalon, as well as microdissected upper and deep

117 naling centers were identified in the ferret telencephalon, as were expression gradients of the patte

118 indicating a morphological alteration of the telencephalon associated with the return to the marine e

119 The telencephalon-associated intercellular adhesion molecule

120 es of neurosphere cultures prepared from the telencephalon at different embryonic and postnatal ages

121 ent in early NSPCs of the dorsal and ventral telencephalon at E11.5 and primarily occupies the nucleu

122 lice variants and beta(2)AR in the embryonic telencephalon at E17.

123 of neural stem cells (NSC) in the developing telencephalon beginning in late gestation [embryonic day

124 sh brain, particularly the memory associated telencephalon brain region, is unclear.

125 expression profile typical of the embryonic telencephalon but not that of other CNS regions.

126 -) cells contributed to the chimeric ventral telencephalon, but that they retained abnormal specifica

127 eurons are both generated within the ventral telencephalon, but their migratory journey takes them to

128 gate the subdivisions of the adult zebrafish telencephalon by analyzing the expression pattern of con

129 the olfactory bulbs-terminal nerve, ventral telencephalon, caudal preoptic area, dorsal mesencephali

130 were present in the olfactory bulbs, ventral telencephalon, caudal preoptic area, dorsal tegmentum an

131 Human studies demonstrate visual associated telencephalons communicate with higher order brain areas

132 ions of brain neurons located in the pallial telencephalon compared with primates or other mammals an

133 The subpallial region of the avian telencephalon contains neural systems whose functions ar

134 Interneuron complexity within the telencephalon could be simplified by viewing them as ela

135 +/+) chimeric embryos that contained ventral telencephalon created by normally patterned wild-type ce

136 The central region of dorsocentral telencephalon (DC(core) ) strongly expressed CB1R mRNA;

137 In developing telencephalons deficient for Brg, Shh target genes were

138 factors, in the development of these ventral telencephalon derived neurons.

139 use deficits in glutamatergic neurons of the telencephalon-derived neocortex.

140 investigating gene regulatory mechanisms of telencephalon development and enable studies of the role

141 ionality remain poorly defined in vivo Using telencephalon development as an example, we show here th

142 To address the role of Six3 in telencephalon development, we analyzed zebrafish embryos

143 of Lhx6 and Lhx8 in the control of mammalian telencephalon development.

144 ar to the role of Hedgehog (Hh) signaling in telencephalon development.

145 hat results, at least in part, from abnormal telencephalon development.

146 re;COUP-TFII(F/F)), to study its function in telencephalon development.

147 ating the dorsalmost neuronal lineage of the telencephalon, DG granule neurons, and in the developmen

148 ps of cholinergic cells were observed in the telencephalon, diencephalon, mesencephalon, and hindbrai

149 tify and localize proliferation zones in the telencephalon, diencephalon, mesencephalon, and rhombenc

150 pressed predominantly in the olfactory bulbs/telencephalon, diencephalon, midbrain tegmentum, retina,

151 of this region within the broader developing telencephalon/diencephalon.

152 The morphology of the telencephalon displays great diversity among different v

153 e do not understand how evolution has shaped telencephalon diversity.

154 cally, radial glial stem cells of the dorsal telencephalon divide asymmetrically to produce excitator

155 The rostral division of the dorsomedial telencephalon (DM1) highly expresses AptCB1R mRNA.

156 auditory systems, including portions of the telencephalon, dorsal thalamus, hypothalamus, posterior

157 ells were prematurely depleted in the dorsal telencephalon due to accelerated differentiation, impair

158 e efforts have largely focused on generating telencephalon due to its direct relevance in a variety o

159 r Sufu have increased numbers of OPCs in the telencephalon during development.

160 ory elements, including a noncoding intronic telencephalon enhancer of DCHS1 The functions of the gen

161 eater rescue efficiency than Pax6(5a) in the telencephalon even though the latter was identical to Pa

162 ionalization of this area into eye-field and telencephalon fates are still unknown.

163 y from specific proliferative regions of the telencephalon (for example, the cortical hem (CH)) to po

164 We found that telencephalon forms in six3b;six7-deficient embryos; how

165 rdium from a discrete source in the anterior telencephalon, forms a protein gradient across the entir

166 on factor Rx3, thereby protecting the future telencephalon from acquiring eye identity.

167 E2 is co-expressed with FoxG1 in the ventral telencephalon from the early neural plate stage and func

168 ic eminences, two protrusions of the ventral telencephalon from which the basal ganglia and olfactory

169 genitor zones of the embryonic mouse ventral telencephalon give rise to GABAergic and cholinergic neu

170 In the telencephalon, Gly-ir cells were observed in the olfacto

171 neurogenic niches of adult brain, the dorsal telencephalon, habenula, preoptic area, hypothalamus, an

172 reached the olfactory bulbs, ventral/dorsal telencephalon, habenula, ventral thalamus, pretectum, ro

173 The adult zebrafish telencephalon has become a model to study neurogenesis.

174 In particular, the adult telencephalon has been an intensely studied structure in

175 nsically incompetent to generate the ventral telencephalon has remained untested.

176 The teleost telencephalon has subpallial and pallial components.

177 profile was observed throughout the ventral telencephalon, hippocampus and olfactory bulb, with NSPC

178 cells and GABAergic neurons of the embryonic telencephalon; however, while the neuronal GABA pathway

179 throughout most of the late-stage embryonic telencephalon (i.e. E15.5-18.5) result in a significant

180 glia cells in the medial zone of the dorsal telencephalon (i.e., the teleostan pallial amygdala).

181 n reported for the organization of the basal telencephalon in amniotes, and most characteristics were

182 ated from multiple progenitor domains in the telencephalon in developmental succession from ventral t

183 By contrast, the telencephalon in non-mammalian vertebrates, including re

184 ggests a homologous similarity of the caudal telencephalon in sauropsids.

185 1 is required for development of the ventral telencephalon in the embryonic mammalian forebrain.

186 ate timing of neurogenesis in the developing telencephalon in vivo and in cultured NPCs, and that the

187 n in the developing mouse ventral and dorsal telencephalon in vivo.

188 s are the direct targets of COUP-TFII in the telencephalon in vivo.

189 hP) of the developing hindbrain, but not the telencephalon, in both mouse and human.

190 cell-type diversity in the developing human telencephalon, including distinct excitatory lineages em

191 inate signals between diverse regions of the telencephalon, including the neocortex, hippocampus, amy

192 n a newly identified parenchymal zone of the telencephalon indeed declines as the fish ages and that

193 substantially different in the dorsolateral telencephalon, intermediate layers of the optic tectum,

194 oup of nuclei in the avian posterior ventral telencephalon is comparable to the mammalian amygdala.

195 Morphogenesis of the rostral telencephalon is controlled in part by Fgf signaling fro

196 How Fgf signaling is regulated in the telencephalon is critical for understanding cerebral cor

197 puts from all glomeruli, whereas the ventral telencephalon is diffusely innervated by axons from part

198 During embryonic development, the telencephalon is specified along its axis through morpho

199 The telencephalon is the most complex brain region, controll

200 c protein (BMP) signaling in the dorsomedial telencephalon, is the embryonic organizer for the hippoc

201 Inactivation of afadin or CDH2 in the dorsal telencephalon leads to a phenotype resembling subcortica

202 In the developing telencephalon Lmx1a is expressed in the cortical hem, an

203 In the telencephalon, members of the distal-less (Dlx) homeobox

204 ical interneurons generated from the ventral telencephalon migrate tangentially into the dorsal telen

205 germinative zones in the ventral forebrain (telencephalon), migrate tangentially in two spatially di

206 er species-high intensity binding within the telencephalon, moderate binding within the diencephalon,

207 er the lesion, were increased in the damaged telencephalon, mostly suddenly after the lesion.

208 iments showed that outside the most anterior telencephalon, neocortical progenitor cells did not expr

209 Here we identify a hypothalamus to telencephalon neural pathway for regulating impulsivity

210 ay (the entopallium) with their higher order telencephalon, nidopallium caudolateral (NCL) were simul

211 In the developing telencephalon, NMDA receptors (NMDARs) are composed of G

212 t an expression map of 1,202 TR genes in the telencephalon of adult zebrafish.

213 nar functional modules in laminated auditory telencephalon of an avian species (Gallus gallus).

214 ization that is so conspicuous in the dorsal telencephalon of birds and other reptiles.

215 potential (LFP) recordings from the ventral telencephalon of dominant and subordinate male cichlids

216 bly different morphology from the evaginated telencephalon of nonray-finned fishes and other vertebra

217 d fishes and their relation to nuclei in the telencephalon of other vertebrates has been reached yet.

218 number of new neurons is still formed in the telencephalon of posthatch domestic chicks, whereas subt

219 omparison between the different parts of the telencephalon of ray-finned fishes and other vertebrates

220 o consensus on the subdivisions of the adult telencephalon of ray-finned fishes and their relation to

221 Particularly the everted telencephalon of ray-finned fishes shows a noticeably di

222 Emx1, Lhx2, Lhx9, and Tbr1 in the embryonic telencephalon of the lacertid lizard Psammodromus algiru

223 Shh expression is diminished in the ventral telencephalon of the mutants, while Tcfap2a expression i

224 ephalic connections of regions of the dorsal telencephalon of the weakly electric fish Apteronotus le

225 In summary, the small telencephalon of the zebrafish shows a remarkable comple

226 es the anatomical organization of the dorsal telencephalon of two gymnotiform fish: Gymnotus sp. and

227 to thalamic-recipient sensory neurons of the telencephalon or in the thalamic sensory input neurons t

228 omical defects appeared in the double mutant telencephalon outside the DG, our observations support a

229 in of lungfishes, in distinct regions of the telencephalon (pallium and subpallium), diencephalon, me

230 ibes the extrinsic connections of the dorsal telencephalon (pallium) of gymnotiform fish.

231 In the dorsal telencephalon (pallium) of vertebrates, it remains unres

232 The appearance of TH-ir cells in the telencephalon (pallium) was rather late (stage [S]31) wi

233 ies show that these abilities require dorsal telencephalon (pallium).

234 However, the roles of Six3 in telencephalon patterning and differentiation are not wel

235 nce (CGE), a posterior subpallial domain, in telencephalon patterning remains poorly understood.

236 sh evolutionary divergence in dorsal-ventral telencephalon patterning.

237 ting a novel Hh-independent role for Six3 in telencephalon patterning.

238 , with strong expression in the ventromedial telencephalon, periventricular regions of the thalamus a

239 The mammalian telencephalon plays critical roles in cognition, motor f

240 reactive cells/fibers in the olfactory bulb, telencephalon, preoptic area (POA), hypothalamus, midbra

241 telencephalon, the medial zone of the dorsal telencephalon, preoptic area and hypothalamus.

242 n cave Astyanax in the olfactory bulb, basal telencephalon, preoptic nuclei, ventral thalamus, poster

243 ependymal cells of different regions of the telencephalon, preoptic region, hypothalamus, and thalam

244 mRNA-containing cells in the olfactory bulb, telencephalon, preoptic region, hypothalamus, mesencepha

245 mechanism initiates the establishment of the telencephalon prior to the involvement of Wnt antagonist

246 ze that efferents from the dorsocentral (DC) telencephalon project to the dorsal torus semicircularis

247 Distinct from those in the dorsal telencephalon, radial glial progenitors (RGPs) in the ve

248 The central portion of posterior telencephalon receives non-selective, interspersed input

249 ives indirect input from limbic areas of the telencephalon, relayed by the habenula via the fasciculu

250 ephalon and during oligodendrogenesis in the telencephalon remain largely unknown.

251 ssing/Lhx9-negative area at the front of the telencephalon, resembling the avian hyperpallium.

252 nd ventral progenitor zones of the embryonic telencephalon, respectively.

253 dial glial progenitors (RGPs) in the ventral telencephalon responsible for producing neocortical inte

254 Conditional inactivation of Isl1 in the telencephalon resulted in a smaller striatum with fewer

255 misexpression of Irx3 in the prethalamus or telencephalon results in ectopic induction of thalamic m

256 Transcriptome analysis of the telencephalon revealed 155 differentially expressed gene

257 es within the ventral nucleus of the ventral telencephalon should have a positive relationship with a

258 Only Pax6 was found in the telencephalon, specifically the olfactory bulbs, striatu

259 e such tremendous morphological variation in telencephalon structure.

260 eurons concentrated in high densities in the telencephalon substantially contribute to the neural bas

261 genitor zone, contributes cells to the basal telencephalon, such as the BMA nucleus.

262 similar expression of Sox2 and Sox19 in the telencephalon, supporting conserved roles for both genes

263 TLE2 disrupts the development of the ventral telencephalon, supporting the idea that endogenous TLE2

264 e two visual pathways from the retina to the telencephalon: thalamofugal terminating in the Wulst, an

265 perikarya in specific nuclear groups in the telencephalon, thalamus, hypothalamus and brainstem, man

266 rotocadherins is similar in the ventromedial telencephalon, thalamus, hypothalamus, facial, and vagal

267 (2-fold) and Hs6st1(-/-) (6-fold) embryonic telencephalon that was most striking at the midline, whe

268 a relatively novel source within the ventral telencephalon, the caudal ganglionic eminence (CGE).

269 From the rostral patterning center in the telencephalon, the Fibroblast Growth Factor, FGF8, dispe

270 In the developing telencephalon, the medial ganglionic eminence (MGE) gene

271 ns such as the dorsal nucleus of the ventral telencephalon, the medial zone of the dorsal telencephal

272 vides the two main progenitor domains in the telencephalon: the pallium, the major source of excitato

273 to sensory input neurons of the thalamus and telencephalon; they further suggest that this regulation

274 signals, Foxg1 acts cell-autonomously in the telencephalon to ensure that cells develop the competenc

275 f 5-HT(4)R expression in the mouse embryonic telencephalon to prenatal maternal stress and altered se

276 itly links graded morphogen signaling in the telencephalon to switch-like cellular responses and has

277 vertebrates that extend from the forebrain (telencephalon) to the midbrain (mesencephalon), constitu

278 In the developing dorsal telencephalon, two distinct populations of neural progen

279 nd sand-dwellers in the relative size of the telencephalon versus the thalamus is correlated with gen

280 em, input from the beak and head reaches the telencephalon via a disynaptic pathway, involving projec

281 tical role in patterning the spinal cord and telencephalon via the regulation of Hedgehog/Gli signali

282 grate toward the pial surface of the ventral telencephalon (VT).

283 ocortical axon subpopulations at the ventral telencephalon (VTe), an intermediate target for thalamic

284 al axons (TCAs) navigate through the ventral telencephalon (VTel) to reach their target regions in th

285 tween diencephalic gustatory centers and the telencephalon was also investigated.

286 Specifically, the radial thickness of dorsal telencephalon was significantly decreased in Cln5-/- mou

287 In the telencephalon, we found regions where the responses over

288 In the telencephalon, we show for the first time that fezf2 mut

289 ty and parvalbumin in the anterior zebrafish telencephalon, we show that against previous assumptions

290 studying Ngn2, a Pax6 direct target gene in telencephalon, we showed that the level of Ngn2 expressi

291 originating from progenitors in the ventral telencephalon were generated, but oligodendrocyte progen

292 In addition, axonal tracts in the telencephalon were severely defective in the absence of

293 been localized to the embryonic subcortical telencephalon where distinct neuroepithelial precursors

294 citatory neurons are derived from the dorsal telencephalon, whereas inhibitory interneurons are gener

295 cl1) plays important roles in the developing telencephalon, whether Ascl1 regulates tangential migrat

296 n dominates nuclei of the subpallial ventral telencephalon, while glutamatergic expression dominates

297 review the origin and diversification of the telencephalon with a focus on key evolutionary innovatio

298 nally inactivate Gsx2 throughout the ventral telencephalon with the exception of the dorsal (d)LGE, w

299 the pallial and subpallial divisions of the telencephalon, with a focus on the hippocampus, somatose

300 cer was placed into individual layers of the telencephalon within the cortical region that is similar