ライフサイエンスコーパス: dorsal-ventral

1 Grid cells recorded at different dorsal-ventral anatomical positions show systematic chan

2 Strain rate mapping of the dorsal, ventral and lateral epithelial cells proximal to

3 in development follows the determination of dorsal-ventral and anterior-posterior (A-P) body axes, a

4 e origins of mechanisms for establishing the dorsal-ventral and anterior-posterior axes in bilaterian

5 ilies" of LFC subregions organized along the dorsal-ventral and anterior-posterior axis with distinct

6 ed polarization aligned with principle axes (dorsal-ventral and anterior-posterior, m(22) = 0.64), wh

7 rn human forebrain regionalization along the dorsal-ventral and left-right (L-R) axes is likely to be

8 Vertebrate organisms are characterized by dorsal-ventral and left-right asymmetry.

9 sues polarized along the anterior-posterior, dorsal-ventral and medial-lateral axes.

10 -3/Robo receptor acts in anterior-posterior, dorsal-ventral and midline guidance decisions.

11 the glorund mutant phenotype, which includes dorsal-ventral and nuclear morphology defects, we search

12 n pathfinding decisions made by motoneurons, dorsal-ventral and pool-specific, depending on the sign

13 form a fat body that is expanded in both the dorsal/ventral and anterior/posterior axes.

14 egated into subregions of the PAG along both dorsal/ventral and rostral/caudal axes.

15 g gene expression along the adaxial-abaxial (dorsal-ventral) and proximal-distal polarity axes.

16 ial patterns, reflecting anterior-posterior, dorsal-ventral, and core-capsular relationships.

17 ed at spatially coherent anterior-posterior, dorsal-ventral, and medial-lateral coordinates that we i

18 emonstrating that Caulobacter cells maintain dorsal/ventral as well as anterior/posterior asymmetry.

19 We observed a similar dorsal/ventral asymmetry on membrane protrusions from SU

20 igher-order cognitive networks that included dorsal/ventral attention and default mode networks.

21 functional connectivity of default mode and dorsal/ventral attention networks, as well as reduced an

22 derm sample along the anterior-posterior and dorsal-ventral axes directly from its transcriptome.

23 l number of genes along the apical-basal and dorsal-ventral axes in the globular embryo, which tended

24 the formation of the anterior-posterior and dorsal-ventral axes, the development of the three germ l

25 establishment of the anterior-posterior and dorsal-ventral axes.

26 ir location along the anterior-posterior and dorsal-ventral axes.

27 es development of the anterior-posterior and dorsal-ventral axes.

28 inct cell types along their adaxial-abaxial (dorsal-ventral) axes.

29 for establishing the CNS and patterning the dorsal ventral axis.

30 h involves the shrinkage of junctions in the dorsal-ventral axis (vertical junctions) followed by jun

31 cted subpopulations of radial glia along the dorsal-ventral axis acquire different markers for neuron

32 cyte differentiation is regionalized along a dorsal-ventral axis and that this patterning occurs prio

33 establishing the cerebellar anlage along the dorsal-ventral axis are unknown.

34 emonstrate an inverse relationship along the dorsal-ventral axis compared with the rat.

35 Establishment of the dorsal-ventral axis depends on the precise restriction o

36 = 0.01949), adherens junction (P = 0.03134), dorsal-ventral axis formation (P = 0.03695), proteasome

37 n into distinct progenitor domains along the dorsal-ventral axis have provided an important framework

38 terobranchs, and chordates possess a defined dorsal-ventral axis imposed on their anterior-posterior

39 ) pathway that regulate establishment of the dorsal-ventral axis in embryos, for their ability to ind

40 rosophila homolog of NF-kappaB, patterns the dorsal-ventral axis in the blastoderm embryo.

41 Patterning of the dorsal-ventral axis in the early Drosophila embryo depen

42 tic influences on cortical thickness along a dorsal-ventral axis in the same cohort.

43 During formation of the dorsal-ventral axis Kek1 is expressed in dorsal follicle

44 ne Morphogenetic Proteins (BMPs) pattern the dorsal-ventral axis of bilaterian embryos; however, thei

45 formed whole-cell patch recordings along the dorsal-ventral axis of EC in bats.

46 t change in the opposite direction along the dorsal-ventral axis of entorhinal cortex, suggesting tha

47 ls showed an abnormal gradient along the CA1 dorsal-ventral axis of excessive free radical production

48 stematically in neurons positioned along the dorsal-ventral axis of MEC, suggesting that these intrin

49 physiology of neurons distributed along the dorsal-ventral axis of MEC.

50 grid cells changes systematically along the dorsal-ventral axis of MEC.

51 of differential modulation of I(h) along the dorsal-ventral axis of mEC.

52 ontribute to grid cell periodicity along the dorsal-ventral axis of medial entorhinal cortex.

53 Dorsal establishes three tissues across the dorsal-ventral axis of precellular Drosophila embryos: m

54 limbs, expression of Fgf8 is expanded in the dorsal-ventral axis of the apical ectodermal ridge and s

55 precursor formation and patterning along the dorsal-ventral axis of the developing CNS and include ve

56 ein is required for the establishment of the dorsal-ventral axis of the egg and future embryo.

57 edgehog signaling caused redeployment of the dorsal-ventral axis of the injured neural tube, allowing

58 l and environmental stimuli varies along the dorsal-ventral axis of the medial EC (mEC) in a manner t

59 ripheral axis of olfactory airspace onto the dorsal-ventral axis of the MOB, encompassing a greater t

60 igands, receptors, and antagonists along the dorsal-ventral axis of the neural tube.

61 k of transcription factors that patterns the dorsal-ventral axis of the pharyngeal arches.

62 Precise patterning of cell types along the dorsal-ventral axis of the spinal cord is essential to e

63 or cells become properly organized along the dorsal-ventral axis of the vertebrate neural tube in a c

64 iod that depends on neuronal location on the dorsal-ventral axis of themedial entorhinal cortex, and

65 late BMP gradient formation during embryonic dorsal-ventral axis patterning.

66 the oscillation frequency gradient along the dorsal-ventral axis previously shown in juvenile rats al

67 Mapping along the dorsal-ventral axis requires interactions between EphB a

68 ch that the differences within CA1 along the dorsal-ventral axis rivaled differences across distinct

69 In the frog Xenopus laevis, dorsal-ventral axis specification involves cytoskeleton-

70 he pre-gastrula axis historically called the dorsal-ventral axis, and a dorsal-to-ventral progression

71 o regulate gene expression across the entire dorsal-ventral axis, and the robustness of gene expressi

72 ions of retinal spatial patterning along the dorsal-ventral axis, consistent with a known function of

73 ting the earliest zygotic patterns along the dorsal-ventral axis, have revealed a gradient that is to

74 as diverse as establishment of the embryonic dorsal-ventral axis, induction of neural tissue, formati

75 ical, and functional dissociations along the dorsal-ventral axis, theta oscillations were simultaneou

76 protein controls pattern formation along the dorsal-ventral axis.

77 ession and cell fate specification along the dorsal-ventral axis.

78 establish gene expression domains along the dorsal-ventral axis.

79 ularly distinct microdomains arranged on the dorsal-ventral axis.

80 ctive axis is homologous with the bilaterian dorsal-ventral axis.

81 efects along both the anterior-posterior and dorsal-ventral axis.

82 ed molecules guides axons along the metazoan dorsal-ventral axis.

83 change in grid-field spacing shown along the dorsal-ventral axis.

84 tral nerve cord into three columns along the dorsal-ventral axis.

85 genes is the differential expression in the dorsal-ventral axis.

86 rula BMP activity gradient that patterns the dorsal-ventral axis.

87 the amnioserosa strongly shortens along its dorsal-ventral axis.

88 f the limb: the proximal-distal axis and the dorsal-ventral axis.

89 anisms can pattern the neural tube along its dorsal-ventral axis.

90 variation in the trisynaptic loop across the dorsal-ventral axis.

91 o regulate gene expression across the entire dorsal-ventral axis.

92 ppaB homolog transcription factor, along the dorsal-ventral axis.

93 -Admp signaling controls regeneration of the dorsal-ventral axis.

94 rphogen gradient that patterns the embryonic dorsal-ventral axis.

95 n within the retina are asymmetric about the dorsal/ventral axis and that Tbx2b mediates this process

96 important clues about the orientation of the dorsal/ventral axis in the embryo.

97 The inner ear is partitioned along its dorsal/ventral axis into vestibular and auditory organs,

98 hese results support a proposal to align the dorsal/ventral axis of the mesendoderm with the animal/v

99 hich retinal neurons are patterned along the dorsal/ventral axis remain largely unknown, yet this pat

100 he Dorsal (Dl) morphogen, which patterns the dorsal/ventral axis.

101 map revised the assignment of the embryonic dorsal/ventral (back-to-belly) axis in pre-gastrula embr

102 al for patterning the anterior-posterior and dorsal-ventral body axes.

103 c left-right body flexions (LR) and rhythmic dorsal-ventral body flexions (DV).

104 A distinct dorsal/ventral border nevertheless is maintained in the

105 specific developmental process of Drosophila dorsal-ventral boundary formation.

106 e posterior compartment, and can distort the dorsal-ventral boundary in either the dorsal or ventral

107 Finally, our data indicate the presence of a dorsal/ventral boundary established by stage 16 that is

108 that slowing the frequency by half perturbed dorsal-ventral but not pool-specific pathfinding, shows

109 protein (BMP) signalling regulates embryonic dorsal-ventral cell fate decisions in flies, frogs and f

110 all regions of the subpallium (including the dorsal, ventral, central, and lateral nucleus of the are

111 otch signaling controls both the mosaic, and dorsal/ventral changes in expression, and is controlled,

112 It helps specify the dorsal-ventral compartment border, and it is needed for

113 ty differences at the anterior-posterior and dorsal-ventral compartment boundaries of the wing disc.

114 nt is the establishment of pattern along the dorsal-ventral (D-V) and anterior-posterior (A-P) axes.

115 tions along the anterior-posterior (A-P) and dorsal-ventral (D-V) axes of neural tube during developm

116 aphically along anterior-posterior (A-P) and dorsal-ventral (D-V) axes to innervate their primary tar

117 ments cause the germband to narrow along the dorsal-ventral (D-V) axis and more than double in length

118 At the Drosophila wing dorsal-ventral (D-V) border, the mechanism by which an F

119 , picrotoxin, resulted in motoneurons making dorsal-ventral (D-V) pathfinding errors in the limb and

120 Several of these genes have a dorsal-ventral (D-V) pattern of expression similar to th

121 In Xenopus, dorsal-ventral (D-V) patterning can self-regulate after

122 esis of the vertebrate head relies on proper dorsal-ventral (D-V) patterning of neural crest cells (N

123 d select a longitudinal fascicle at specific dorsal-ventral (D-V) positions.

124 ue axonal behaviors required for mapping the dorsal-ventral (D-V) retinal axis along the lateral-medi

125 e vertebrate body plan follows stereotypical dorsal-ventral (D-V) tissue differentiation controlled b

126 pographic axes, anterior-posterior (A-P) and dorsal-ventral (D-V).

127 the establishment of the anterior-posterior, dorsal-ventral (D/V) and proximal-distal axes.

128 ing in the conversion of the L/R axis to the dorsal-ventral (D/V) axis of the linear heart.

129 terior (A/P) axis; later, signaling acquires dorsal-ventral (D/V) polarity.

130 ear concentration gradient that patterns the dorsal/ventral (D/V) axis of the embryo.

131 The anterior/posterior (A/P) and dorsal/ventral (D/V) compartment borders that subdivide

132 Bone morphogenetic proteins (BMPs) regulate dorsal/ventral (D/V) patterning across the animal kingdo

133 a of the cephalochordate amphioxus expresses dorsal/ventral (D/V) patterning genes (for example, bone

134 maternal transcripts for the germ layer and dorsal/ventral determinants VegT and Wnt11.

135 importance of core promoter functions in the dorsal-ventral developmental gene regulatory network.

136 Together, our findings indicate that a dorsal-ventral difference in SK channel regulation of NM

137 We observed a robust dorsal-ventral dissociation within the mPFC with cogniti

138 Here, we discovered a dorsal-ventral distinction of actions in LOTC: dorsal LO

139 ational framework outlined only a bipartite, dorsal/ventral, division of striatum.

140 evelopment, localized Notch signaling at the dorsal ventral (DV)-midline promotes growth of the entir

141 ndamental importance of patterning along the dorsal-ventral (DV) and anterior-posterior (AP) axes dur

142 d a global brain-patterning defect along the dorsal-ventral (DV) and anterior-posterior (AP) axes.

143 legume, Lotus japonicus, the development of dorsal-ventral (DV) asymmetric flowers is mainly control

144 sion pattern the anterior-posterior (AP) and dorsal-ventral (DV) axes of the early Drosophila embryo.

145 expression along anterior-posterior (AP) or dorsal-ventral (DV) axes, respectively, by spatially lim

146 cell fates along anterior-posterior (AP) and dorsal-ventral (DV) axes, respectively, of sea urchin em

147 le progenitors were specified broadly on the dorsal-ventral (DV) axis and subsequently formed a clust

148 By analyzing enhancers during dorsal-ventral (DV) axis formation in the Drosophila emb

149 affects patterning of the Drosophila embryo dorsal-ventral (DV) axis is not known.

150 The Drosophila dorsal-ventral (DV) axis is polarized when the oocyte nu

151 rsal boundaries of genes expressed along the dorsal-ventral (DV) axis of early Drosophila embryos, wh

152 mplex patterns of gene expression across the dorsal-ventral (DV) axis of the early Drosophila embryo.

153 buted in a broad nuclear gradient across the dorsal-ventral (DV) axis of the early Drosophila embryo.

154 1 (Edn1) and Jagged/Notch, which pattern the dorsal-ventral (DV) axis of the pharyngeal arches.

155 the early Drosophila embryo, patterning the dorsal-ventral (DV) axis to specify mesoderm, neurogenic

156 dorsal anterior region for induction of the dorsal-ventral (DV) axis, but regulation of Grk localiza

157 ead to neural tube-like patterning along the dorsal-ventral (DV) axis.

158 ents, which led to the identification of the dorsal-ventral (DV) border ectoderm exclusive of the api

159 zation pattern of the limb, indicate altered dorsal-ventral (DV) boundaries.

160 ogen proteins (BMPs) are distributed along a dorsal-ventral (DV) gradient in many developing embryos.

161 The genetic network controlling early dorsal-ventral (DV) patterning has been extensively stud

162 t completely lack endoderm, reveals that the dorsal-ventral (DV) patterning of jaw skeletal precursor

163 Dorsal-ventral (DV) patterning of the Drosophila embryo

164 coordination of anterior-posterior (AP) and dorsal-ventral (DV) patterning of the mesencephalon (mes

165 The establishment of dorsal-ventral (DV) polarity in the Drosophila embryo de

166 Drosophila embryonic dorsal-ventral (DV) polarity is controlled by a group of

167 The establishment of Drosophila embryonic dorsal-ventral (DV) polarity relies on serine proteolyti

168 is a key event that specifies progeny embryo dorsal-ventral (DV) polarity.

169 control the unique mechanisms in mapping the dorsal-ventral (DV) retinal axis along the lateral-media

170 Dorsal/ventral (DV) patterning of the sea urchin embryo

171 resented here identify the non-AER border of dorsal-ventral ectoderm as a new signaling center in lim

172 nd across much of the anterior-posterior and dorsal-ventral ectoderm.

173 Establishment of dorsal-ventral epidermal identities and functions, in re

174 On the basis of the asymmetry in the dorsal-ventral expression patterns of several members of

175 rucial role for BMP signaling in determining dorsal/ventral fates in ectoderm and mesoderm.

176 l regulation of Sox2 and Nkx2.1 during early dorsal/ventral foregut patterning.

177 nd ChIP-seq we show that BMP/Smad1 regulates dorsal-ventral gene expression in both the endoderm and

178 The findings reveal a dorsal-ventral gradient for I(Kv) regulation and a novel

179 s in control adult mice, indicating that the dorsal-ventral gradient generalizes across age and speci

180 Our results show a dorsal-ventral gradient in the expression of melanopsin

181 -1 mEGF10 is required for the formation of a dorsal-ventral gradient of CED-3 caspase activity within

182 Knock-out of the HCN1 channel flattens the dorsal-ventral gradient of the membrane potential oscill

183 nsiveness to gamma frequency inputs follow a dorsal-ventral gradient similar to the topographical org

184 S- and M-opsin are expressed in an opposing dorsal-ventral gradient.

185 umerous neuroimaging studies reveals a clear dorsal/ventral gradient in both left inferior frontal co

186 distribution of pRGCs, which, combined with dorsal-ventral gradients in ultraviolet-sensitive and me

187 on patterns, many of which occur in opposing dorsal-ventral gradients.

188 Here we present evidence that dorsal-ventral growth of the developing spinal cord is r

189 Based on the dorsal-ventral hypothesis, and language and auditory fin

190 roepithelia, patterned to rostral-caudal and dorsal-ventral identities with the same morphogens used

191 ted developmental controls, conferring mixed dorsal-ventral identity.

192 ventral superior temporal sulcus (STSv) and dorsal/ventral inferotemporal gyrus (TEd, TEv).

193 erior-posterior junctions before the loss of dorsal-ventral junctions.

194 endothelium in particular proximal/distal or dorsal/ventral limb regions.

195 r muscles within specific proximal/distal or dorsal/ventral limb regions.

196 stinct classes of cells that form at precise dorsal-ventral locations and express specific combinatio

197 te cells in entorhinal slices from different dorsal-ventral locations.

198 for them, including EphB/ephrin-B control of dorsal-ventral mapping, bidirectional signaling of EphAs

199 ral distinct abnormalities, including random dorsal/ventral meandering of fibers in the stratum optic

200 Each circumferential half of the MOB (dorsal/ventral, medial/lateral) contained about 50% of t

201 d AP axis, the pre-existing midline, and the dorsal-ventral median plane.

202 This disruption of dorsal-ventral neural patterning permits a new wave of m

203 thway is disrupted, as evidenced by abnormal dorsal-ventral neural tube patterning and diminished exp

204 posterior mesoderm in spt(-);ntl(-) embryos, dorsal-ventral neural tube patterning is relatively norm

205 throughout the entire anterior-posterior and dorsal-ventral neuraxes, and levels of thymidine labelin

206 The dorsal-ventral organization of intrinsic theta-likemembr

207 This arrangement, coupled with dorsal/ventral organization of thalamic/brainstem fibers

208 adjacent to the third ventricle between the dorsal, ventral, paraventricular, and arcuate hypothalam

209 d, motor axons correctly executed the binary dorsal-ventral pathfinding decision but failed to make t

210 rons to accurately execute their first major dorsal-ventral pathfinding decision.

211 Proper dorsal--ventral pattern formation of the optic cup is es

212 not localized within the posterior pole, and dorsal-ventral pattern abnormalities are observed.

213 are important mediators in the regulation of dorsal-ventral pattern formation during vertebrate devel

214 l cord shows only very subtle alterations in dorsal-ventral pattern in Noggin mutants.

215 g of new tissues, and the maintenance of the dorsal-ventral pattern of existing adult tissue in homeo

216 ar mechanisms responsible for specifying the dorsal-ventral pattern of neuronal identities in dorsal

217 The prevailing model of dorsal ventral patterning of the amphibian embryo predic

218 of Shh from the third pouch is required for dorsal-ventral patterning and for parathyroid specificat

219 The first round is associated with dorsal-ventral patterning and is necessary for designati

220 de apparent differences in the mechanisms of dorsal-ventral patterning and limb identity specificatio

221 insights into the progression of Drosophila dorsal-ventral patterning and raises new issues about th

222 ostic information, and support disruption of dorsal-ventral patterning as a mechanism underlying rhom

223 Thus, although dorsal-ventral patterning begins during the first cell c

224 n of Bmp2 and Bmp4 is required for digit and dorsal-ventral patterning but surprisingly not for limb

225 Our experiments reveal that cic controls dorsal-ventral patterning by regulating pipe expression

226 -B, activate a meiotic checkpoint leading to dorsal-ventral patterning defects in the egg and an abno

227 auses lethality during embryogenesis but not dorsal-ventral patterning defects, indicating that fusil

228 is required for the proper secretion of the dorsal-ventral patterning factor Gurken, as well as the

229 erm, consistent with the hypothesis that the dorsal-ventral patterning function of Toll arose from th

230 titative perturbation analysis targeting the dorsal-ventral patterning gene regulatory network (GRN)

231 Moreover, expression of dorsal-ventral patterning genes including Shh, Pax6 and

232 The analysis of approximately 20 different dorsal-ventral patterning genes suggests that the initia

233 In Xenopus embryos, a dorsal-ventral patterning gradient is generated by diffu

234 Bone morphogenetic proteins (BMP) direct dorsal-ventral patterning in both invertebrate and verte

235 However, during embryonic dorsal-ventral patterning in Drosophila, two members of

236 ating cells and is important for maintaining dorsal-ventral patterning in other organs.

237 However, during dorsal-ventral patterning in the Drosophila embryo, an i

238 f the endomesoderm in sea urchin embryos and dorsal-ventral patterning in the Drosophila embryo.

239 se molecules are critical for some aspect of dorsal-ventral patterning in the eye; however, it has be

240 o identify novel factors that could regulate dorsal-ventral patterning in the Xenopus embryo, we isol

241 Dorsal-ventral patterning in vertebrate and invertebrate

242 t transcription is required prior to MBT for dorsal-ventral patterning in XENOPUS:

243 During vertebrate embryogenesis, dorsal-ventral patterning is controlled by the BMP/Chord

244 olutionary modifications in the well-defined dorsal-ventral patterning network led to the wholesale d

245 Computational modeling of the dorsal-ventral patterning network recapitulates these va

246 nts of a signaling pathway that controls the dorsal-ventral patterning of many animal embryos: a BMP1

247 tissues at the midline of regeneration, the dorsal-ventral patterning of new tissues, and the mainte

248 The dorsal-ventral patterning of the Drosophila embryo is co

249 Dorsal-ventral patterning of the early Drosophila embryo

250 Changes in dorsal-ventral patterning of the hyoid arch also might n

251 role of Tlx, an orphan nuclear receptor, in dorsal-ventral patterning of the mouse telencephalon.

252 cts, including neural tube defects, abnormal dorsal-ventral patterning of the spinal cord, a defect i

253 In the developing vertebrate embryo, proper dorsal-ventral patterning relies on BMP antagonists secr

254 he integration of the anterior-posterior and dorsal-ventral patterning systems.

255 Dorsal-ventral patterning was not affected in these mice

256 ereby Wnt and Shh signaling promote distinct dorsal-ventral patterning while also having broader effe

257 actor 7 (Xnf7), a developmental regulator of dorsal-ventral patterning, as a microtubule-binding prot

258 pituitary development by maintaining normal dorsal-ventral patterning, cell survival, and normal exp

259 orepressors meditate embryonic segmentation, dorsal-ventral patterning, neurogenesis, and Notch and W

260 isted gastrulation (TSG) is also involved in dorsal-ventral patterning, yet the mechanism of its func

261 f3 is required for mesendoderm formation and dorsal-ventral patterning.

262 rulation Defective to exert their effects on dorsal-ventral patterning.

263 amatically affect neural tube maturation and dorsal-ventral patterning.

264 plicing regulator for anterior-posterior and dorsal-ventral patterning.

265 d source-sink mechanism underlying zebrafish dorsal-ventral patterning.

266 th a physiological role in the regulation of dorsal-ventral patterning.

267 cell survival but show evidence of defective dorsal-ventral patterning.

268 by the BMP2/4 ortholog DPP during embryonic dorsal-ventral patterning.

269 luding neural tube closure defects, abnormal dorsal/ventral patterning of the central nervous system

270 f some Dlx genes as well as other markers of dorsal/ventral patterning of the neural crest.

271 ion and/or epithelial patterning rather than dorsal/ventral patterning.

272 g abnormal compaction of the AER with normal dorsal/ventral patterning.

273 2 (P2), SCN oscillators displayed the daily, dorsal-ventral phase wave in clock gene expression typic

274 Finally, the dorsal-ventral phase wave of PER2 typical of the adult S

275 ient in Serpin-27A produce embryos that lack dorsal-ventral polarity and show uniform high levels of

276 actors that establish proliferation rate and dorsal-ventral polarity in the developing neural tube; f

277 ppaB pathway, first identified in studies of dorsal-ventral polarity in the early Drosophila embryo,

278 many genes responsible for the formation of dorsal-ventral polarity in the early embryo, the innate

279 Drosophila embryonic dorsal-ventral polarity is generated by a series of seri

280 reotypic cell division pattern, formation of dorsal-ventral polarity, and endogenous initiation of th

281 n pathway that controls Drosophila embryonic dorsal-ventral polarity.

282 ng through the Toll receptor is required for dorsal/ventral polarity in Drosophila embryos, and also

283 The establishment of dorsal/ventral polarity, especially dorsal specification

284 models incorporating a second activator and dorsal/ventral polarized modification of activator signa

285 joints that normally form at an intermediate dorsal-ventral position.

286 top of a signaling cascade that establishes dorsal-ventral positional information in the retina and

287 nal ganglion cell (RGC) axons from different dorsal-ventral positions showed graded and biphasic resp

288 ular niche specification by antagonizing the dorsal-ventral regulatory limits of VEGF.

289 signaling mediate axon attraction to control dorsal-ventral retinal mapping along the lateral-medial

290 stablishing central, anterior-posterior, and dorsal-ventral retinal patterning has given us insights

291 ng depends upon the correct establishment of dorsal-ventral retinal polarity.

292 , the anterior domain first disassembles the dorsal-ventral sarcomere region and develops filopodia t

293 genesis with a second, local inhibitor and a dorsal/ventral signal gradient within the feather.

294 level of individual maps to map clusters to dorsal-ventral streams.

295 seradish peroxidase (WGA-HRP) were made into dorsal/ventral striatum (DS/VS), basolateral amygdala (B

296 signals establish evolutionary divergence in dorsal-ventral telencephalon patterning.

297 Increasing dorsal-ventral tension resulted in vertex resolution per

298 transported label showed rostral-caudal and dorsal-ventral topographic arrangement of claustrum conn

299 ns from stochastic processes.We suggest that dorsal-ventral tuning of theta-like membrane potential a

300 pe swimming behaviors consisting of repeated dorsal-ventral whole-body flexions.