ライフサイエンスコーパス: telencephalon

1 uration and neurogenesis in developing human telencephalon.

2 ct tangential migratory routes in the dorsal telencephalon.

3 AptCB1R mRNA was highly expressed in the telencephalon.

4 selective elimination of Lhx2 in the dorsal telencephalon.

5 have affected or benefited from an enlarged telencephalon.

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

7 mediate evolutionary diversification of the telencephalon.

8 godendrogenesis within the embryonic ventral telencephalon.

9 ng interneurons derived from the subcortical telencephalon.

10 ized along their pathway through the ventral telencephalon.

11 ncers active in subregions of the developing telencephalon.

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

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

14 fy homologies between different parts of the telencephalon.

15 nscriptome of human, chimpanzee, and macaque telencephalon.

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

17 activities were also detected in the ventral telencephalon.

18 ssion dominates nuclei of the pallial dorsal telencephalon.

19 stretched along the rostrocaudal axis of the telencephalon.

20 ranscripts of these genes in the apteronotid telencephalon.

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

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

23 e inhibitory neuron diversity throughout the telencephalon.

24 riginate from progenitors within the ventral telencephalon.

25 ing oligodendrocyte formation in the ventral telencephalon.

26 cell populations in distinct regions of the telencephalon.

27 pulations function in different parts of the telencephalon.

28 ctor plays in the development of the ventral telencephalon.

29 nized clonal units in the developing ventral telencephalon.

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

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

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

33 l levels of SHH signaling within the ventral telencephalon.

34 icient in Bmpr1a conditionally in the dorsal telencephalon.

35 iated with auditory areas in the caudomedial telencephalon.

36 d FoxG1 work together to specify the ventral telencephalon.

37 d extent of OPC production in the developing telencephalon.

38 ruited to promote neural repair in the adult telencephalon.

39 h the highest levels of expression in dorsal telencephalon.

40 y abnormal structures particularly in dorsal telencephalon.

41 to mediate organizer activity for the whole telencephalon.

42 other birds possess a significantly smaller telencephalon.

43 ephalon migrate tangentially into the dorsal telencephalon.

44 f promoters in GABAergic interneurons of the telencephalon.

45 ression to GABAergic interneurons within the telencephalon.

46 audal ganglionic eminences of the developing telencephalon.

47 0 transcription regulators (TR) in the adult telencephalon.

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

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

50 es are a conserved feature of amniote dorsal telencephalon.

51 y of peptides and receptors in the mammalian telencephalon.

52 differences in the neurogenic niches in the telencephalon.

53 reoptic area and ventral part of the ventral telencephalon.

54 genes expressed in particular regions of the telencephalon.

55 e ultrasensitivity and borders in the dorsal telencephalon.

56 to address this issue in the zebrafish adult telencephalon.

57 size of the precursor pool in the embryonic telencephalon.

58 psule requires Fz3 expression in the ventral telencephalon.

59 vely neurogenic radial glia of the embryonic telencephalon.

60 sue with characteristics of diencephalon and telencephalon.

61 oth GABAergic and cholinergic neurons in the telencephalon.

62 on of cortical interneurons from the ventral telencephalon.

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

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

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

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

67 ormation of the compartment boundary between telencephalon and basal diencephalon.

68 otropin-releasing hormone (GnRH) in the male telencephalon and cerebellum (p < 0.005, one-way ANOVA)

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

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

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

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

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

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

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

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

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

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

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

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

81 1 and ERbeta2 were robustly expressed in the telencephalon and hypothalamus in vocal-acoustic and oth

82 ) in the forebrain structures, including the telencephalon and hypothalamus.

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

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

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

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

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

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

89 SCA is highly expressed in chicken and mouse telencephalon and peripheral ganglia and correlates with

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

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

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

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

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

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

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

97 zebrafish, dispatched 2 is expressed in the telencephalon and ventral hindbrain and is essential for

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

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

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

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

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

103 pocampus and cortical hem, while the ventral telencephalon appears to expand.

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

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

106 progressively more severe truncations of the telencephalon are observed in FGFR single, double and tr

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

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

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

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

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

112 The telencephalon-associated intercellular adhesion molecule

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

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

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

116 mplete loss of her right hemisphere (di- and telencephalon) at birth, the patient's remaining hemisph

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

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

119 mpal volume relative to the remainder of the telencephalon, but not at the expense of neuron numbers.

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

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

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

123 In addition, passerines enlarged their telencephalon by decreasing the proportional size of the

124 regulation of angiogenesis in the embryonic telencephalon, call for a revision of the current models

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

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

127 RAR403 expression throughout the developing telencephalon causes pronounced hypoplasia resulting fro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 (125)I]OVTA labeled receptors throughout the telencephalon, diencephalon, midbrain, and brainstem, wi

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

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

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

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

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

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

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

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

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

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

157 R mutant mice exhibit a complete loss of the telencephalon, except the dorsal midline.

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

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

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

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

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

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

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

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

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

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

168 n the nucleus of the stria terminalis in the telencephalon; habenular nucleus, paraventricular nucleu

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

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

171 o induce different cell types in the ventral telencephalon has been controversial.

172 NE) and radial glial (RG) cells in the mouse telencephalon has been shown to have a significant impac

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

174 The teleost telencephalon has subpallial and pallial components.

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

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

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

178 e;R26R;Bmpr1aflox/flox mice showed collapsed telencephalon in association with impaired clearing of b

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

180 mechanisms underlie the evolution of a large telencephalon in passerines.

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

182 1 is required for development of the ventral telencephalon in the embryonic mammalian forebrain.

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

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

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

186 Elsewhere in the dorsal telencephalon, in the diencephalon and in the ventral te

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

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

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

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

191 In Gli3(-/-) embryos the dorsal telencephalon is abnormally small and fails to develop d

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

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

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

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

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

197 The telencephalon is the most complex brain region, controll

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

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

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

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

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

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

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

205 daries with the diencephalon and the ventral telencephalon, mutant cells express sets of transcriptio

206 alon, in the diencephalon and in the ventral telencephalon, mutant cells express sets of transcriptio

207 e misspecified: in those parts of the dorsal telencephalon near to its boundaries with the diencephal

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

209 In the developing mammalian basal telencephalon, neural progenitors from the subpallium ge

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

211 ult zebra finches (Taeniopygia guttata), the telencephalon occupies 64% of the entire brain.

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

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

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

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

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

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

221 ctroporation of Nkx2.1 cDNA into the ventral telencephalon of slice cultures from Nkx2.1-/- mouse emb

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 finding to emerge from this work is that the telencephalon of zebra finches at hatching contains a th

228 Slices generated from the telencephalons of 17-d-old rat fetuses were treated with

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

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

231 idely distributed throughout the zebra finch telencephalon, overlapping with song control regions.

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

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

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

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

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

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

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

239 sh evolutionary divergence in dorsal-ventral telencephalon patterning.

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

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

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

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 r tract formation was also documented in the telencephalon, secondary prosencephalon, and midbrain du

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 pocampal volumes relative to the rest of the telencephalon than captive birds with or without memory-

268 d a subpopulation of CR cells in the rostral telencephalon that expresses Er81, a downstream target o

269 (2-fold) and Hs6st1(-/-) (6-fold) embryonic telencephalon that was most striking at the midline, whe

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

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

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

273 sed to play multiple roles in patterning the telencephalon, the precursor to the cerebrum.

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

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

276 In human telencephalon, this malformation is most commonly associ

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

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

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

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

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

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

283 ere were no differences in neuron numbers or telencephalon volume.

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

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

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

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

288 ing all Gli genes and found that the ventral telencephalon was highly disorganized with intermingling

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

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

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

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

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

294 tle effect on dorsoventral patterning of the telencephalon when Gli3 is also removed.

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

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

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

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