ライフサイエンスコーパス: diencephalon

1 men, and diencephalon (thalamus plus ventral diencephalon).

2 wo distinct progenitor domains in the caudal diencephalon.

3 le compartmental boundaries within the mouse diencephalon.

4 ent boundary between telencephalon and basal diencephalon.

5 gination of the neuroectoderm in the ventral diencephalon.

6 located within the alar plate of the caudal diencephalon.

7 sed in the developing hippocampus and in the diencephalon.

8 es and few around the third ventricle in the diencephalon.

9 eity and differentiation kinetics within the diencephalon.

10 g centre for regional differentiation of the diencephalon.

11 ulation of wnt expression in the prospective diencephalon.

12 stablishing regional subdivisions within the diencephalon.

13 rd and a network in brainstem, midbrain, and diencephalon.

14 y inhibitory factors derived from the dorsal diencephalon.

15 iol were measured in the cerebral cortex and diencephalon.

16 epithelial (CPe) cells of the hindbrain and diencephalon.

17 neurons, which also derive from the ventral diencephalon.

18 ime when the optic axons first grow over the diencephalon.

19 cephalic vesicle and an abnormally patterned diencephalon.

20 ew into the subpallium but did not enter the diencephalon.

21 ut most stopped growing without entering the diencephalon.

22 halon and the anterior-ventral region of the diencephalon.

23 utants lack SFRP-2 expression in the PSB and diencephalon.

24 e when they integrate homotopically into the diencephalon.

25 he dorsal thalamic association nuclei of the diencephalon.

26 part of the nerve cord corresponding to the diencephalon.

27 to restore left-sided gene expression in the diencephalon.

28 en turn and extend anteriorly in the ventral diencephalon.

29 n within aspects of the ventral midbrain and diencephalon.

30 ell migration begins in the developing chick diencephalon.

31 erate correct dorsoventral patterning in the diencephalon.

32 eye, in the optic stalk, and in the ventral diencephalon.

33 most alar regions of the newly formed murine diencephalon.

34 als crossed the midline to the contralateral diencephalon.

35 cause ectopic lens formation in the ventral diencephalon.

36 ontact between this ectoderm and the ventral diencephalon.

37 and functional association with the ventral diencephalon.

38 ce Fgf8 expression in midbrain and posterior diencephalon.

39 induced in vivo by signals from the adjacent diencephalon.

40 d ventricular zones in the mesencephalon and diencephalon.

41 ired to maintain the appropriate size of the diencephalon.

42 5, TACC1, and RA signaling in the developing diencephalon.

43 odomain transcription factor, in the ventral diencephalon.

44 rome-positive cells reside within the caudal diencephalon.

45 xpression domains in the embryonic zebrafish diencephalon.

46 destined to form the eyes, telencephalon and diencephalon.

47 roepithelial domain in the alar plate of the diencephalon.

48 need-related phosphoprotein markers from the diencephalon.

49 prosomere organization of the alar and basal diencephalon.

50 part of the habenular complex in the dorsal diencephalon.

51 within the broader developing telencephalon/diencephalon.

52 fferent cell groups in the telencephalon and diencephalon.

53 telencephalic side of the TDJ but not in the diencephalon.

54 phalon and to more restricted regions of the diencephalon.

55 CP forms in the hindbrain (4th ventricle), diencephalon (3rd ventricle) and dorsomedial telencephal

56 ious subdivisions are established within the diencephalon--a complex integration center and relay sta

57 The retina as an extension of the diencephalon accessible to in vivo microcopy with spectr

58 [(123)I]ZIENT uptake in the diencephalon achieved transient equilibrium at 157 min.

59 It is still not known whether the ventral diencephalon acts as the initial inducer of pituitary de

60 expression in the ventral telencephalon and diencephalon and also appears to be unique for Dlx5 amon

61 monkey with [18F]1 showed high uptake in the diencephalon and brainstem with peak uptake achieved at

62 continuation of the alar territories of the diencephalon and brainstem, according to the prosomeric

63 ls, there were significantly greater ventral diencephalon and cerebellar gray matter volumes and sign

64 abnormal joining of the telencephalon to the diencephalon and defined the medial limit of the dorsal

65 rlapping domains, with pitx2c in left dorsal diencephalon and developing gut and pitx2a in left heart

66 ns differentiate normally but scatter in the diencephalon and fail to properly gather close to the th

67 al thalamic axons extending down through the diencephalon and growing out through the internal capsul

68 ry for nonradial cell migration in the chick diencephalon and have provided a system to further explo

69 In general, the diencephalon and hypothalamus of the tree pangolin follo

70 nsive description of the organization of the diencephalon and hypothalamus using a range of standard

71 Given the interactions of the diencephalon and hypothalamus with virtually all portion

72 innervation patterns of RGC axons within the diencephalon and implicate the Slits as components of th

73 ye development, CE2 drives expression in the diencephalon and in the developing heart tube where Pax6

74 lsewhere in the dorsal telencephalon, in the diencephalon and in the ventral telencephalon, mutant ce

75 The mammalian thalamus is located in the diencephalon and is composed of dozens of morphologicall

76 region is topologically rostral to the basal diencephalon and is composed of the tuberal (rostral) an

77 urons have descending projections beyond the diencephalon and isthmus.

78 ft2 are expressed asymmetrically in the left diencephalon and left lateral plate respectively, sugges

79 The commonality of regions of mesencephalon, diencephalon and limbic/paralimbic areas involved in pri

80 stablishing regional subdivisions within the diencephalon and may also play a role in the development

81 Fgf15 shows Shh-dependent expression in the diencephalon and may participate in this interaction, at

82 cerebellum, as well as in cell bodies in the diencephalon and metencephalon.

83 th of both ventral and dorsal regions of the diencephalon and midbrain in early somite-stage mouse em

84 the hypothalamus and related regions of the diencephalon and midbrain was studied with retrograde an

85 Similarly, in the diencephalon and midbrain, prominent LAMP labeling was o

86 progenitors in the floor plate of the caudal diencephalon and midbrain.

87 d survival of dorsal cell populations in the diencephalon and midbrain.

88 the developing embryo, except for within the diencephalon and olfactory bulb.

89 mRNA and protein are localized in neurons of diencephalon and optic tectum, as well as in numerous fi

90 active cells were spread widely in the ovine diencephalon and overlapped with the known distribution

91 hFOXA2 in the neural tube, third ventricle, diencephalon and pancreas.

92 entral midbrain, the majority of the ventral diencephalon and parts of the telencephalon.

93 ich is expressed only in the rostral ventral diencephalon and pituitary gland, commencing on e11.5, m

94 as first expressed in groups of cells in the diencephalon and pretectum.

95 3 in mice causes abnormal development of the diencephalon and Rathke's pouch, the progenitor of the a

96 8); then in more caudal basal regions of the diencephalon and rostral mesencephalon (substantia nigra

97 and protein throughout the telencephalon and diencephalon and some mesencephalic structures of A. bur

98 forebrain, because the major features of the diencephalon and telencephalon were normal in the null m

99 C axons expressed in specific regions of the diencephalon and telencephalon, help regulate optic trac

100 l and retinal axons cross the midline of the diencephalon and telencephalon.

101 tral regions of CNS including the hindbrain, diencephalon and telencephalon.

102 instead forms tissue with characteristics of diencephalon and telencephalon.

103 urons situated at the midline of the ventral diencephalon and that function as intermediate targets f

104 s necessary for the formation of the rostral diencephalon and that Six3 activity is required for the

105 effect was statistically significant in the diencephalon and the cerebellum, while it was absent in

106 Shh is expressed throughout the ventral diencephalon and the oral ectoderm, but its expression i

107 the telencephalon and dorsal identity in the diencephalon and the retina.

108 elencephalon near to its boundaries with the diencephalon and the ventral telencephalon, mutant cells

109 ate in dorsal thalamus, project ventrally in diencephalon and then dorsolaterally in ventral telencep

110 ventrally from their position in the dorsal diencephalon and then turn and extend anteriorly in the

111 nglion cells (RGCs) within the embryonic rat diencephalon and whether the slits can account for a rep

112 d nucleus of the stria terminalis, amygdala, diencephalon, and brainstem.

113 nd protein were present in cortex, brainstem-diencephalon, and cerebellum.

114 gination of the neuroectoderm in the ventral diencephalon, and defects in the formation of the distin

115 on propagates between cortex, basal ganglia, diencephalon, and hippocampus in genetically susceptible

116 loping limbic structures of the cerebrum and diencephalon, and in the medulla of the brain stem.

117 e telencephalon, moderate binding within the diencephalon, and mild binding within the mesencephalon

118 of the infundibulum, a region of the ventral diencephalon, and Rathke's pouch, a derivative of oral e

119 talk and nerve, the optic chiasm and ventral diencephalon, and the anterior midline zones that abut d

120 ains of BMP and FGF signaling in the ventral diencephalon, and the second mechanism is the restrictio

121 f their production in neurons of the rostral diencephalon, and their axonal localization in brain sit

122 eta species in the hippocampus and brainstem/diencephalon ( approximately 1.5-fold).

123 In diencephalon, AptCB1R RNA probe weakly stained the centr

124 tein into the anterior midbrain or posterior diencephalon are consistent with it being at least part

125 ion in which the embryonic hindbrain and the diencephalon are flattened out, allowing a birds-eye vie

126 Several brain areas in the diencephalon are involved in the activation and expressi

127 and SPNs are ubiquitous in the brainstem and diencephalon, areas that together contain <1% of the neu

128 ei, indicating that laterality of the dorsal diencephalon arises in a step-wise fashion.

129 We identify a DA cell group in the diencephalon as a common source for innervation of both

130 IL)-4 and interferon-gamma (IFNgamma) in the diencephalon, as well as lower levels of hippocampal IFN

131 key, radioactivity was reduced by 39% in the diencephalon at 101 min following injection of citalopra

132 ell proliferation or death in the developing diencephalon at embryonic day 10.5 (e10.5) or e11.5.

133 Fgf8 and Wnt3a expression are induced in the diencephalon at the ZLI, reminiscent of the Fgf8/Wnt1-ex

134 t, and that antagonizing its function in the diencephalon attenuates thalamic specification.

135 rted to be detected only in the midbrain and diencephalon, become elevated.

136 Olg genes are expressed at the telencephalon-diencephalon border and adjacent to the floor plate, a s

137 en the medial temporal lobe (MTL) and medial diencephalon, both of which are critical for episodic me

138 ically specific nuclei in the basal ganglia, diencephalon, brainstem and cerebellum, with restricted

139 sion of gnih was particularly evident in the diencephalon, but also in the olfactory bulbs/cerebral h

140 GC axon pathfinding and targeting within the diencephalon by regulating their fasciculation, preventi

141 st a mechanism by which damage to the medial diencephalon can impact upon learning and memory process

142 ex above the basal ganglia, cortex above the diencephalon], caudate-putamen, basal forebrain, hypotha

143 Lateral diencephalon cell conditioned medium inhibits growth of

144 it reduced growth in the presence of lateral diencephalon cell membranes.

145 e and involved the medial temporal lobe, the diencephalon, cerebral cortex, basal ganglia, and cerebe

146 cantly different between groups overall; and diencephalon, cerebral white matter, cerebellum and glob

147 n had greater 3alpha,5alpha-THP formation in diencephalon compared to other groups.

148 dorsal and ventral hypothalamus) and caudal diencephalon, confirming results of Garcia-Fernandez et

149 e co-cultures in which a region of embryonic diencephalon containing the ZI is maintained adjacent to

150 The teleostean diencephalon contains a relatively large number of dopam

151 necdotal expression studies suggest that the diencephalon contains multiple developmental compartment

152 ate here that Gbx2-expressing cells in mouse diencephalon contribute to the entire thalamic nuclear c

153 , lefty1 and pitx2 are expressed in the left diencephalon; cyclops, lefty2 and pitx2 are expressed in

154 that the separation of the telencephalon and diencephalon depends on interactions between Shh and Gli

155 The diencephalon-derived optic stalk (OS) and neural retina

156 n was investigated in Alligator during early diencephalon development.

157 The pattern of cell proliferation in the diencephalon differed from that observed in the rhombenc

158 As in the mammalian telencephalon and chick diencephalon, dispersion among clonally related cells in

159 loarchitecture, and chemoarchitecture of the diencephalon (dorsal thalamus, ventral thalamus, and epi

160 The diencephalon (dorsal thalamus, ventral thalamus, and epi

161 Noggin is expressed in the ventral diencephalon during Rathke's pouch induction, in the und

162 ssed in VT retina, as well as in the ventral diencephalon during the formation of the optic chiasm.

163 ce paced mating but younger rats had greater diencephalon E(2) than did middle-aged rats.

164 TCF4 is expressed in the ventral diencephalon early in pituitary development, rostral to

165 neural differentiation within the developing diencephalon, emphasizing the contribution of recent lar

166 ebral cortex, striatum, basal forebrain, and diencephalon express the dopamine D5 receptor.

167 Within the diencephalon, Fgf3 and Fgf8 act synergistically to patte

168 oping axons of the fasciculus retroflexus, a diencephalon fiber tract associated with limbic function

169 The embryonic diencephalon forms integration centers and relay station

170 In addition, in the Foxd1 deficient ventral diencephalon, Foxg1 invades the Foxd1 domain, Zic2 and I

171 We provide evidence that the ventral diencephalon from 2- to 4-day-old chick embryos is able

172 Finally, we demonstrate that the ventral diencephalon from e9.5-e11.5 mouse embryos is also an ef

173 hypothalamus, and the more caudally located diencephalon [from rostral to caudal: the prethalamus, t

174 The embryonic diencephalon gives rise to the vertebrate thalamus and h

175 In the diencephalon, Gly-ir neurons were observed in the pretha

176 Here we studied development of the diencephalon, hypothalamus and eyes in mutant mice in wh

177 complex role of cilia in development of the diencephalon, hypothalamus and eyes via the region-speci

178 t of the NMDA-R is widely distributed in the diencephalon, implicates it in a wide variety of functio

179 an Unc5c ligand, is expressed in the ventral diencephalon in a pattern that is consistent with impedi

180 e ventral midbrain and dorsal midline of the diencephalon in Gbx2-deficient mice.

181 Nevertheless, damage to the medial diencephalon in humans is associated with both retrograd

182 nstructive tissue, but the importance of the diencephalon in TCA mapping is unknown.

183 t the ventral midline of the spinal cord and diencephalon in the developing rodent CNS, respectively.

184 alar hypothalamus was located rostral to the diencephalon in the secondary prosencephalon and represe

185 ene, zic2a, during formation of the anterior diencephalon in zebrafish.

186 alis (SP) in the midbrain, almost the entire diencephalon including nucleus dorsomedialis posterior t

187 ensively expressed in the developing ventral diencephalon, including the infundibulum and the posteri

188 n of ligand binding sites in the fetal sheep diencephalon indicated that the highest levels of bindin

189 disruption of the normal architecture of the diencephalon indicating nonradial cell migration is nece

190 P and WNT signals emanating from the ventral diencephalon influence pouch growth and development.

191 n the retina, gene expression in the ventral diencephalon influences chiasm formation.

192 ch and by inductive signals from the ventral diencephalon/infundibulum.

193 ry appears normal, patterning in the ventral diencephalon is disrupted; Bmp4 activity is expanded res

194 urons from either the cerebral cortex or the diencephalon is largely lacking.

195 ion in the PSB, but Wnt-7b expression in the diencephalon is preserved.

196 Nodal signaling within the developing dorsal diencephalon is required for determining the direction o

197 the 15- to 17-somite stage, the prospective diencephalon is the most-anterior structure in the Six3-

198 observe that the nuclear organization of the diencephalon is very similar in the two species, and sim

199 rojections from field CA1 to the interbrain (diencephalon) is analyzed here with the Phaseolus vulgar

200 ral thalamus (vTh), two major regions of the diencephalon, is characterized by their parcellation int

201 pretoral nucleus, contralateral NC, tectum), diencephalon (lateral preglomerular, central posterior,

202 itional deletion of Lhx6 from the developing diencephalon leads to decreases in both NREM and REM sle

203 They show reciprocal connections with the diencephalon (mainly the thalamus), project to the midbr

204 central progestogen formation in midbrain or diencephalon may contribute to some variability in expre

205 eminence and dorsal hypothalamic area in the diencephalon; medial region of the superior colliculus,

206 NS (olfactory bulbs, pallium, basal ganglia, diencephalon, mesencephalic tegmentum, rhombencephalon,

207 f these isoforms were found in the thalamus, diencephalon, mesencephalon, and brainstem.

208 ic cells were observed in the telencephalon, diencephalon, mesencephalon, and hindbrain.

209 ndrograms from the secondary prosencephalon, diencephalon, mesencephalon, and isthmus showed some dev

210 ze proliferation zones in the telencephalon, diencephalon, mesencephalon, and rhombencephalon that we

211 mRNA is expressed in discrete regions of the diencephalon, mesencephalon, and rhombencephalon.

212 gnals over much of the turkey telencephalon, diencephalon, mesencephalon, cerebellum, pituitary, and

213 labeling over much of the rat telencephalon, diencephalon, mesencephalon, cerebellum, spinal cord, an

214 the telencephalon (pallium and subpallium), diencephalon, mesencephalon, hindbrain, spinal cord, and

215 nantly in the olfactory bulbs/telencephalon, diencephalon, midbrain tegmentum, retina, and gonads.

216 d, contributing to diverse structures in the diencephalon, midbrain, and brainstem and extensively po

217 eled receptors throughout the telencephalon, diencephalon, midbrain, and brainstem, with a similar di

218 CN-complex projection targets throughout the diencephalon, midbrain, and hindbrain, in addition to th

219 on of sleep and wake in the basal forebrain, diencephalon, midbrain, and pons of the minke whale, a m

220 ed to sleep and wake in the basal forebrain, diencephalon, midbrain, and pons of the river hippopotam

221 branes from brain stem, cortex, hippocampus, diencephalon, midbrain, and spinal cord, but not basal g

222 brate ancestor of the vertebrates included a diencephalon, midbrain, hindbrain, and spinal cord.

223 rea and in the periventricular region at the diencephalon/midbrain junction.

224 e eye to the optic stalk (OS), and cross the diencephalon midline at the optic chiasm en route to the

225 Tumor locations were diencephalon (n = 58), cerebral hemisphere (n = 3), and

226 of the cholinergic tone to the brainstem and diencephalon necessary for physiological arousal.

227 g cells failed to move anteriorly, a ventral diencephalon never formed, and the eyes remained fused.

228 placeable brain uptake (i.e., V3"=[brainstem-diencephalon-occipital]/occipital), a measure proportion

229 measure Mecp2e1 and Mecp2e2 abundance in the diencephalon of adult mice, demonstrating significantly

230 ctor influencing brain development, then the diencephalon of Alligator may be built differently from

231 ed with the idea of a common bauplan for the diencephalon of anamniote and amniote vertebrates from f

232 transcriptomes of dissociated cells from the diencephalon of E12.5 mouse embryos.

233 absent from the rostral midbrain and caudal diencephalon of embryos carrying a dominant-negative tra

234 ctions, we localized the NR2B subunit in the diencephalon of the adult male rat using immunoperoxidas

235 the lateral plate mesoderm (LPM) and dorsal diencephalon of the brain.

236 d neuropeptide, predominantly located in the diencephalon of vertebrates, and associated with a wide

237 In the diencephalons of the adult zebrafish brain, all catechol

238 val or transplant replacement of the lateral diencephalon optic tract entry zone in GAP-43-deficient

239 uding the pallium, subpallium, hypothalamus, diencephalon, optic tectum, midbrain tegmentum, and rhom

240 cortical axons (TCAs) also fail to leave the diencephalon or abnormally project toward the amygdala.

241 p explain why pathology in either the medial diencephalon or the medial temporal lobes can result in

242 The dorsal diencephalon (or epithalamus) of larval zebrafish displa

243 sfunction or injury involving the brainstem, diencephalon, or cerebral cortex and are associated with

244 In the diencephalon, overlap was observed in several hypothalam

245 sion to portions of the ventral midbrain and diencephalon, overlaps both temporally and spatially wit

246 ease in the number of dividing cells in male diencephalon (p < 0.05, Kruskal-Wallis test).

247 support the idea that there are distinct MTL-diencephalon pathways that subserve differing memory pro

248 In the diencephalon, Pax6 and Pax7 were distinct in the alar an

249 In the diencephalon, PITX2 is expressed in neurons of the zona

250 s of the adult cerebral cortex, hippocampus, diencephalon, pons/medulla, and cerebellum.

251 ebellar cell populations were located in the diencephalon (pretectum and thalamus), mesencephalon (re

252 organisms, and in a small domain in the left diencephalon, providing the first observation of asymmet

253 organ, a neuroendocrine gland on top of the diencephalon, remains enigmatic.

254 oop with FGF8/FGF10 signaling in the ventral diencephalon, required to prevent induction of multiple

255 We conclude that proper maturation of the diencephalon requires ZLI-derived Hh signalling.

256 CE2 is shown to be autoregulated in the diencephalon, responding to absence of Pax6.

257 ebrain (including both the telencephalon and diencephalon) revealed a unique role for Isl1 in diencep

258 In the future diencephalon, several genes with patterned expression ha

259 At the time RGC axons extend over the diencephalon, slit1 and slit2 are expressed in hypothala

260 In the diencephalon, substantial secondary olfactory projection

261 cord, hindbrain, rostral midbrain and caudal diencephalon, suggesting that multiple transcriptional r

262 lls appeared in the hypothalamus and rostral diencephalon (suprachiasmatic, posterior recess and post

263 (M), medial striatum (MSt), septum, Area X, diencephalon, telencephalic subventricular zone (SVZ), a

264 e nucleus, globus pallidus plus putamen, and diencephalon (thalamus plus ventral diencephalon).

265 crete neuroepithelial domains, including the diencephalon, the insertion of the eminentia thalami int

266 duced in frontal cortex and cortex overlying diencephalon, the olfactory bulbs, caudate-putamen, hipp

267 rating the eyes, and formed ventral anterior diencephalon, the presumptive hypothalamus.

268 ess also induced activation of mast cells in diencephalon, the site where most mast cells are found i

269 er, the border between the telencephalon and diencephalon, the telencephalic/diencephalic junction (T

270 issue is located in a small region of caudal diencephalon-this region is necessary to retain response

271 -negative GABAergic progenitors in the early diencephalon through sequential waves of tangential migr

272 from each eye sort in the developing ventral diencephalon to project to ipsi- or contralateral target

273 ed from their various sites of origin in the diencephalon to the synaptic termination sites on differ

274 ry periphery and brainstem) to sensorimotor (diencephalon) to motor (forebrain) components of a behav

275 nd place, in both the retina and the ventral diencephalon, to be able to influence RGC axon guidance.

276 ptake in the diencephalon, which resulted in diencephalon-to-cerebellum ratios of 2.12 at 190 min.

277 in the vertebrate forebrain that bisects the diencephalon transversely, expresses the secreted factor

278 with transcriptome sequencing of the hamster diencephalon under winter and summer conditions, and in

279 hh is a direct target of Six3 in the rostral diencephalon ventral midline (RDVM).

280 nregulation of Shh expression in the rostral diencephalon ventral midline, the alobar phenotype is ca

281 Beck Depression Inventory, bilateral ventral diencephalon volume, and expression levels of the RNF123

282 d transverse and longitudinal borders of the diencephalon was investigated in Alligator embryos begin

283 ucleus of the ansa lenticularis in the avian diencephalon was renamed the subthalamic nucleus, both f

284 of adenosine A(2A) receptors in fetal sheep diencephalon, we have used a receptor autoradiographic t

285 Steroid levels in the diencephalon were altered by age mainly in females, and

286 l, posterior cingulate, thalamus and ventral diencephalon were independently associated with telomere

287 )I-FP-CIT binding ratios in the midbrain and diencephalon were significantly higher 2 h after injecti

288 in the patterning of the developing ventral diencephalon where the optic chiasm forms.

289 ereby helping define the site in the ventral diencephalon where the optic chiasm forms.

290 Forebrain labeling was restricted to the diencephalon, where distinctive terminal fields were obs

291 Cells in the ventral diencephalon, where Sox3 is usually highly expressed, ha

292 l correlates, of structures in brainstem and diencephalon which regulate the sleep-wake cycle, and of

293 rodevelopmental gene mostly expressed in the diencephalon, which contains a region previously reporte

294 The medial habenular nuclei of the zebrafish diencephalon, which lie bilateral to the pineal complex,

295 to monoamine transporters in the midbrain or diencephalon, which may reflect predominantly serotonin

296 al lamination, and cell death in the ventral diencephalon, which resulted in cyclopia.

297 emonstrated high [(123)I]ZIENT uptake in the diencephalon, which resulted in diencephalon-to-cerebell

298 ound to be widely distributed in the ventral diencephalon, with high densities in the preopticoseptal

299 sed on the left side of the embryonic dorsal diencephalon, within a region corresponding to the presu

300 In diencephalon, WNT2b expression is restricted to medial d