ライフサイエンスコーパス: dorsoventral

1 Plants leaves develop proximodistal, dorsoventral (adaxial-abaxial), and mediolateral pattern

2 tion that is competent to be patterned along dorsoventral and anteroposterior axes.

3 of cell type-specific factors in response to dorsoventral and anteroposterior axis information.

4 ion factors have ancient bilaterian roles in dorsoventral and anteroposterior regionalisation of the

5 The dorsoventral and developmental gradients of entorhinal l

6 of Hh function in zebrafish does not affect dorsoventral and mediolateral otic patterning, we now sh

7 along which sensory neurons are guided: one dorsoventral and one anteroposterior.

8 t supply muscle groups located at restricted dorsoventral and proximodistal domains of the limb.

9 urons were distributed throughout the entire dorsoventral and rostrocaudal extent of the locus coerul

10 as the densest IGLE distribution in both the dorsoventral and the rostrocaudal extensions of the firs

11 sis for ternary interaction of the anterior, dorsoventral, and terminal patterning systems.

12 f RAD had a role in the generation of flower dorsoventral asymmetry.

13 wg varied along both the anteroposterior and dorsoventral axes of the embryo.

14 r firing fields increasing in size along the dorsoventral axes of the medial entorhinal cortex and hi

15 es development along the anteroposterior and dorsoventral axes of the vertebrate body, mainly by secr

16 e time was mapped along the rostrocaudal and dorsoventral axes.

17 activity spread along both rostrocaudal and dorsoventral axes.

18 he neural tube along its anteroposterior and dorsoventral axes.

19 on-activity spread along both horizontal and dorsoventral axes.

20 he horizontal (nasal-temporal) and vertical (dorsoventral) axes of visual space.

21 Concomitant with BMP activity patterning dorsoventral axial tissues, the embryo also undergoes dr

22 expression in both marginal cells along the dorsoventral axis and in the enveloping layer.

23 ning events such as the specification of the dorsoventral axis and primary germ layers.

24 Patterning of the dorsoventral axis by graded BMP signaling is conserved i

25 Specification of germ layers along the dorsoventral axis by morphogenetic gradients is an ideal

26 the embryonic cerebellum is patterned on the dorsoventral axis by opposing morphogens.

27 at is essential for proper patterning of the dorsoventral axis by regulating Bmp2 signaling.

28 bones mutant embryos also display defects in dorsoventral axis formation accompanied by a disorganize

29 Dorsoventral axis formation and patterning is then media

30 from genes important in anteroposterior and dorsoventral axis formation, including wingless (wg) and

31 fate proteoglycan provides a spatial cue for dorsoventral axis formation.

32 l begin and the opposite pole of the embryo (dorsoventral axis in amphibians and fish, anteroposterio

33 Toll-dependent patterning of the dorsoventral axis in Drosophila represents one of the be

34 adient of BMP specifies cell fates along the dorsoventral axis in species ranging from flies to mamma

35 ends on the location of the neuron along the dorsoventral axis in the entorhinal cortex, with dorsal

36 Specification of the dorsoventral axis in Xenopus depends on rearrangements o

37 The vertebrate embryonic dorsoventral axis is established and patterned by Wnt an

38 ntial patterns of gene expression across the dorsoventral axis of early embryos, thereby establishing

39 ies are differentially represented along the dorsoventral axis of the CA3 area of the rat hippocampus

40 dgehog and Wnt work in opposition across the dorsoventral axis of the cerebellum to regulate formatio

41 ) to define global gene expression along the dorsoventral axis of the developing arches.

42 ily transcription factor Dorsal patterns the dorsoventral axis of the Drosophila embryo by activating

43 The dorsoventral axis of the Drosophila embryo is patterned

44 hat is involved in gene regulation along the dorsoventral axis of the embryo.

45 of genes differentially expressed along the dorsoventral axis of the embryonic mouse trigeminal gang

46 nce for functional differentiation along the dorsoventral axis of the hippocampus, and supports the i

47 that, dependent on their position along the dorsoventral axis of the hippocampus, DG granule cells (

48 Gli2/3A is required along the length of the dorsoventral axis of the inner ear to mediate graded lev

49 ate the responses to Shh signaling along the dorsoventral axis of the inner ear.

50 al information at different scales along the dorsoventral axis of the MEC.

51 ontrolled in specific cell cohorts along the dorsoventral axis of the neural tube.

52 en, sonic hedgehog (Shh), which patterns the dorsoventral axis of the neural tube.

53 ed expression of EphB and ephrin-B along the dorsoventral axis of the retina indicates a role for the

54 rting of axons according to origin along the dorsoventral axis of the retina is both spatially and ch

55 bone morphogenetic proteins (BMPs) along the dorsoventral axis of the spinal cord is necessary for th

56 e segregated into multiple domains along the dorsoventral axis of the vertebrate neural tube, and eac

57 nd mechanisms that establish and pattern the dorsoventral axis of the zebrafish embryo, including est

58 s specify major patterning domains along the dorsoventral axis of zebrafish pharyngeal arches.

59 P signaling through Smad2 mediates, in part, dorsoventral axis patterning in zebrafish embryos, where

60 hment of the Bmp gradient activity along the dorsoventral axis to induce distinct transcriptional out

61 inant of the oral-aboral axis (the embryonic dorsoventral axis), and is crucial for specification of

62 hanges of neural marker expression along the dorsoventral axis, as well as with expanded cranial neur

63 fined HDI types are set in columns along the dorsoventral axis, before migrating along well-defined t

64 cture that integrates cues not only from the dorsoventral axis, but also from the anteroposterior and

65 oglial translating mRNAs closely follows the dorsoventral axis, especially from cortex/hippocampus to

66 A profiles in astrocytes closely follows the dorsoventral axis, especially posteriorly from cortex/hi

67 2, a critical factor in the formation of the dorsoventral axis, is diminished in the Tgfbr2 mutant.

68 Based on their expression patterns along the dorsoventral axis, most of these genes can be classified

69 evelopmental Cell shows that, to pattern its dorsoventral axis, the beetle Tribolium utilizes many of

70 For the dorsoventral axis, the homeodomain gene, tinman, is a ke

71 onserved regulators of CNS pattern along the dorsoventral axis, the homeodomain protein Ind and the S

72 ace in multiple spatial scales along the MEC dorsoventral axis.

73 ling to pattern O and P cell fates along the dorsoventral axis.

74 poral properties of grid cells along the MEC dorsoventral axis.

75 ed in the egg and initiates formation of the dorsoventral axis.

76 getal axis as it relates to formation of the dorsoventral axis.

77 a that arise in specific positions along the dorsoventral axis.

78 is required to establish and/or pattern the dorsoventral axis.

79 e redundant with those of Chd in forming the dorsoventral axis.

80 motor behavior, but track normally along the dorsoventral axis.

81 egions of the retina, particularly along the dorsoventral axis.

82 ion, and after neural closure throughout the dorsoventral axis.

83 issue that is initially symmetric across its dorsoventral axis.

84 lly differentiation was also found along the dorsoventral axis.

85 ivity gradient patterns cell fates along the dorsoventral axis.

86 polarizing the retinal epithelium across its dorsoventral axis.

87 ignaling gradient patterns tissues along the dorsoventral axis.

88 potential of two equipotent cells along the dorsoventral axis.

89 stoderm embryo, they are able to pattern the dorsoventral axis.

90 istinct classes of ventral neurons along the dorsoventral axis.

91 egulates mesendoderm specification along the dorsoventral axis.

92 4GalT5 in Bmp2-mediated specification of the dorsoventral axis.

93 he sharing of Wingless among cells along the dorsoventral axis.

94 he cumulus) functions as an organizer of the dorsoventral axis.

95 MEC) grid fields increase in scale along the dorsoventral axis.

96 Dorsal (Dl), the morphogen that patterns the dorsoventral axis.

97 ntial for proper patterning of the zebrafish dorsoventral axis.

98 lds for a grid cell also increases along the dorsoventral axis.

99 with spatial scales that increase along the dorsoventral axis?

100 Epistatic experiments suggested that the dorsoventral (BMP) and anteroposterior (Wnt/GSK3) patter

101 Moreover, using these coordinates, the dorsoventral boundary for S-opsin expressing cones close

102 In plants the dorsoventral boundary of leaves defines an axis of symme

103 expression is normally upregulated along the dorsoventral boundary of the developing wing, and is res

104 n (e.g. the midbrain-hindbrain boundary, the dorsoventral boundary), its perturbations resulting in a

105 Both processes paralleled the dorsoventral changes in fibroblast growth factor recepto

106 ration in turn disrupts the formation of the dorsoventral channels within the VNC, further highlighti

107 Genetically altering the dorsoventral character of the limb mesenchyme elicits a

108 sed the abnormally low levels of hippocampus dorsoventral connectivity and phase coherence.

109 for ray axon growth cones to respond to the dorsoventral cue.

110 hown previously to cause motoneurons to make dorsoventral (D-V) pathfinding errors and to alter the e

111 mals, whereas VD commissure growth along the dorsoventral (D/V) axis occurred normally in these anima

112 are established according to position in the dorsoventral (D/V) axis of the embryo.

113 tterning the mammalian spinal cord along its dorsoventral (D/V) axis through the activation of Glioma

114 excitatory inputs that were related to their dorsoventral dendritic expanse.

115 The other was the absence of the dorsoventral diencephalic tract in Alligator which lacks

116 Overall, our results highlight the dorsoventral differences in dendritic computation that c

117 These dorsoventral differences in neuronal output and spatial

118 ritic computation that could account for the dorsoventral differences in spatial representation.SIGNI

119 Together, these dorsoventral differences in the threshold for LTP induct

120 in layer I; and 3) run preferentially in the dorsoventral direction similar to isofrequency axes.

121 The dorsoventral distribution of HCN1 and HCN2 subunits and

122 enular asymmetry and consequently alters the dorsoventral distribution of innervating axons.

123 gle-cell labeling approaches to quantify the dorsoventral distribution of V2a axonal projections and

124 ibit segmental differences in proportion and dorsoventral distribution.

125 ls expressed in restricted proximodistal and dorsoventral domains of the developing limb.

126 dh18, and Pcdh19 are expressed in restricted dorsoventral domains of the neuroepithelial layer at ear

127 the projection of sensory axons to discrete dorsoventral domains of the spinal cord without regard f

128 ich forms orthogonally to previously defined dorsoventral (DV) and anteroposterior (AP) axes.

129 LR patterning with the establishment of the dorsoventral (DV) axes and midline determination in earl

130 xis relative to the anteroposterior (AP) and dorsoventral (DV) axes is central to the organization of

131 a melanogaster, the anteroposterior (AP) and dorsoventral (DV) axes of the oocyte and future embryo a

132 g distinct pre-skeletal identities along the dorsoventral (DV) axes of the pharyngeal arches.

133 viously established anteroposterior (AP) and dorsoventral (DV) axes remain poorly understood.

134 pulations along the anteroposterior (AP) and dorsoventral (DV) axes.

135 establishing rudimentary anteroposterior and dorsoventral (DV) axes.

136 How dorsoventral (DV) axial patterning relates to AP tempora

137 The forebrain is patterned along the dorsoventral (DV) axis by Sonic Hedgehog (Shh).

138 ignaling establishes cell identity along the dorsoventral (DV) axis during gastrulation.

139 plays a very specific developmental role in dorsoventral (DV) axis formation during Drosophila oogen

140 spatial positioning of structures along the dorsoventral (DV) axis is essential for proper embryonic

141 spatial domains of gene expression along the dorsoventral (DV) axis of Drosophila melanogaster embryo

142 By contrast, reversing the dorsoventral (DV) axis of the hindbrain results in chang

143 pears to be regionally dissociated along the dorsoventral (DV) axis of the hippocampus.

144 Wg and Dpp are also required to pattern the dorsoventral (DV) axis of the leg.

145 , BMP signaling, controls development of the dorsoventral (DV) axis throughout the Bilateria.

146 rects differential gene expression along the dorsoventral (DV) axis, translating it into distinct dom

147 crest-derived skeletal precursors along the dorsoventral (DV) axis.

148 vation of the Notch receptor is required for dorsoventral (DV) compartmentalization of the Drosophila

149 determined the genome-wide occupancy of the dorsoventral (DV) determinants Dorsal, Twist, and Snail

150 nizers that control anteroposterior (AP) and dorsoventral (DV) development are known, and the regulat

151 Both genes display dorsoventral (DV) gradients of expression due to differe

152 proximodistal (PD), anteroposterior (AP) and dorsoventral (DV) limb axes.

153 al features of and the molecules involved in dorsoventral (DV) patterning in the neural tube.

154 Dorsoventral (DV) patterning is essential for growth of

155 ein (BMP) signaling is broadly implicated in dorsoventral (DV) patterning of bilaterally symmetric an

156 The dorsoventral (DV) patterning of the Drosophila embryo de

157 Dorsoventral (DV) patterning of the Drosophila embryo is

158 , we show that Mkif5Ba is also essential for dorsoventral (DV) patterning.

159 Drosophila embryo dorsoventral (DV) polarity is defined by serine protease

160 Next, we studied the dorsoventral (DV) positional identity of subpopulations

161 Bauplan defined by anteroposterior (AP) and dorsoventral (DV) subdivisions, characterized by largely

162 We have previously shown that dorsoventral (DV) tissues are temporally patterned progr

163 atic disruption of azimuthal topography, the dorsoventral (elevation) map was relatively normal, indi

164 genetic Protein (BMP) signaling patterns the dorsoventral embryonic axis of vertebrates and invertebr

165 ecifically, Hoxa2 loss of function induced a dorsoventral enlargement of the Olig2/Nkx2.2-expressing

166 enables making accurate inferences about the dorsoventral expression domains of engrailed in the trun

167 the left habenula terminate along the entire dorsoventral extent of the IPN, whereas axons from the r

168 CRTC1 expression was detected throughout the dorsoventral extent of the SCN in the middle of the subj

169 and metabolic differences within the entire dorsoventral extent of the striatum and thalamus.

170 N1 protein localisation, and is modulated by dorsoventral gene activity.

171 on in the shoot, leading to a model in which dorsoventral genes coordinate to regulate plant developm

172 At later stages, CUP is activated by dorsoventral genes in an intermediary region of the coro

173 iffuse illumination dominates and a smoother dorsoventral gradation is found.

174 rences were not paralleled by changes to the dorsoventral gradient in parvalbumin staining or neurode

175 hese alterations corresponded to a flattened dorsoventral gradient in theta-gamma cross-frequency cou

176 In all species, rods follow a pronounced dorsoventral gradient with highest densities in the vent

177 anatomically arranged to express functional dorsoventral gradients in a variety of neuronal properti

178 Dorsoventral gradients in certain intrinsic membrane pro

179 at the onset of neurogenesis revealed clear dorsoventral gradients in the emergence of two types of

180 d the effects of tau pathology on functional dorsoventral gradients in the mEC.

181 an peak SMU frequencies and rostrocaudal and dorsoventral gradients of activity during HF-SCS were no

182 Similar rostrocaudal and dorsoventral gradients of activity were observed during

183 Dorsoventral gradients of V(r) were present in healthy s

184 ECs, and the resultant flattening of certain dorsoventral gradients, may contribute to disturbances i

185 disrupted, resulting in a flattening of some dorsoventral gradients.

186 trin-UNC-40/DCC pathway provides the primary dorsoventral guidance cue to ray axon growth cones.

187 on range from narrow to broad along both the dorsoventral (i.e., tonotopic) and the rostrocaudal dime

188 shape entorhinal theta rhythmicity and the (dorsoventral) integration of information across grid sca

189 om the right habenula adopt a more extensive dorsoventral IPN projection pattern typical of left habe

190 Our results clearly demonstrate a dorsoventral laminar organization of projections from th

191 In maize, adaxial/abaxial (dorsoventral) leaf polarity is established by an abaxial

192 atterning of the gut along its longitudinal, dorsoventral, left-right, and radial axes is one of the

193 Here, we test whether different dorsoventral levels in the NT have similar or differenti

194 precisely labeled NT precursors at specific dorsoventral levels of the chick NT using fluorescent dy

195 in the ability of precursors from different dorsoventral levels of the NT to contribute to NC deriva

196 f these areas was mapped by rostrocaudal and dorsoventral location within the DR.

197 ns of overlaps spatially organized along the dorsoventral, mediolateral, and anteroposterior striatal

198 for all eight delta-protocadherins along the dorsoventral, mediolateral, and rostrocaudal dimensions

199 these bidirectional signalling molecules in dorsoventral-mediolateral retinocollicular mapping.

200 x1-expressing domain of the VZ, spanning the dorsoventral midline.

201 originally taken as evidence of the directed dorsoventral migration of melanoblasts (the embryonic pr

202 and provides a direct link between two major dorsoventral morphogenetic signalling pathways.

203 ated cuticular plates, longitudinal muscles, dorsoventral muscles, and ganglia.

204 bject behavioral performance and patterns of dorsoventral neuronal activity were assessed before and

205 bination with other markers, olig2 reveals a dorsoventral organization of cerebellar neurons in embry

206 f neurogenesis can therefore account for the dorsoventral organization of nIII and may play a primary

207 We describe a dorsoventral organization of the four nIII motoneuron po

208 ization of superficial layers of the MEC and dorsoventral organization of the scale of spatial repres

209 irectional firing fields, have a laminar and dorsoventral organization that corresponds to a similar

210 brain structures and reveals its laminar and dorsoventral organization.

211 increased in the AP orientation, compared to dorsoventral orientation or to either orientations more

212 and chick, Hh is predominantly required for dorsoventral otic patterning.

213 d) or by combined activation of both imd and dorsoventral pathways.

214 al, a transcription factor that controls the dorsoventral pattern of the Drosophila embryo.

215 tor Pt-Ets4 is needed for cumulus integrity, dorsoventral patterning and for the activation of Pt-hun

216 sults suggest a role for translation in leaf dorsoventral patterning and indicate that ribosomes are

217 t characterized for their roles in mediating dorsoventral patterning and the innate immune response.

218 r we also find that auxin levels feedback on dorsoventral patterning by spatially organizing HD-ZIPII

219 Mutant females are sterile and show dorsoventral patterning defects during oogenesis.

220 tions secondary to early anteroposterior and dorsoventral patterning defects, or to misspecification

221 In addition to dorsoventral patterning defects, split top mutants displ

222 ges over time, with BMPs required for global dorsoventral patterning during early gastrulation and fo

223 Indicating that the hem regulates dorsoventral patterning in the cortical hemisphere, the

224 ired for the establishment or maintenance of dorsoventral patterning in the retina, as we observe nor

225 genetic proteins (BMPs) are key mediators of dorsoventral patterning in vertebrates and are required

226 gative regulatory point during LRP6-mediated dorsoventral patterning in zebrafish and in allograft mo

227 Dorsoventral patterning is mediated by two organizer reg

228 This indicates that dorsoventral patterning is not dependent upon Dorsal-med

229 gradient in the early Drosophila embryo, the dorsoventral patterning of a frog embryo by bone morphog

230 in (BMP) signaling is an essential factor in dorsoventral patterning of animal embryos but how BMP si

231 Previous work has suggested that the dorsoventral patterning of O and P fates differs in the

232 We have discovered a new role for SMA-9 in dorsoventral patterning of the C. elegans post-embryonic

233 Dorsoventral patterning of the Drosophila embryo is regu

234 th the gene regulatory network that controls dorsoventral patterning of the Drosophila embryo.

235 al C and trailer hitch are both required for dorsoventral patterning of the Drosophila oocyte.

236 iation by tuning the DPP receptor Saxophone, dorsoventral patterning of the egg shell by regulating t

237 Dorsoventral patterning of the embryonic neural tube giv

238 identify TGIF2 as the molecular link between dorsoventral patterning of the endoderm and pancreatic s

239 a BMP family member previously implicated in dorsoventral patterning of the eye.

240 is important to regulate Wg signaling during dorsoventral patterning of the larval wing.

241 pathway function independently in regulating dorsoventral patterning of the M lineage, with LIN-12/No

242 ate the molecular mechanisms associated with dorsoventral patterning of the neural tube and acquisiti

243 prechordal plate functions as a morphogen in dorsoventral patterning of the neural tube.

244 ed excess Hh signaling and resultant altered dorsoventral patterning of the neural tube.

245 erived Sonic Hedgehog (Shh) is essential for dorsoventral patterning of the overlying neural tube.

246 gnals through Ednra proteins to direct early dorsoventral patterning of the skeletogenic neural crest

247 d temporal requirements for Tolloid (Mfn) in dorsoventral patterning of the tail.

248 ell proliferation in the cerebral cortex and dorsoventral patterning of the telencephalon and neural

249 particular, loss of Shh has little effect on dorsoventral patterning of the telencephalon when Gli3 i

250 During embryonic development, appropriate dorsoventral patterning of the trachea leads to the form

251 A widely accepted model of dorsoventral patterning postulates that a morphogenetic

252 analyze multiple morphogen gradients in the dorsoventral patterning system.

253 vents involving outgrowth, proximodistal and dorsoventral patterning, and epithelial tubulogenesis.

254 Similarly, the maternal regulation of dorsoventral patterning, and in particular the maternal

255 proteoglycan is involved in pipe function in dorsoventral patterning, we generated females carrying f

256 of pituitary progenitors but not for initial dorsoventral patterning.

257 e ventral wall closure indicative of altered dorsoventral patterning.

258 ies Axin overexpression resulting in altered dorsoventral patterning.

259 dient of BMP signaling that is essential for dorsoventral patterning.

260 odal gene cyclops (cyc) are not required for dorsoventral patterning.

261 ised trunk development but did not eliminate dorsoventral patterning.

262 tant background, results in abnormal retinal dorsoventral patterning.

263 understanding of the maternal regulation of dorsoventral patterning.

264 e found homozygous missense mutations in the dorsoventral-patterning gene WNT7A and confirmed their f

265 repeated gills, nephridia, and eight sets of dorsoventral pedal retractor muscles.

266 ssion patterns with both anteroposterior and dorsoventral polarities.

267 plays a central role in the establishment of dorsoventral polarity during early embryogenesis, wherea

268 lation of PDB leads to a significant loss of dorsoventral polarity in large body bends.

269 d by EGFR and essential for establishing the dorsoventral polarity of the embryo.

270 mouse embryos lacking sonic hedgehog (Shh), dorsoventral polarity within the otic vesicle is disrupt

271 Dorsoventral polarity, stress fibers, and focal adhesion

272 pithelium, is a key determinant of embryonic dorsoventral polarity, suggesting that Pipe-mediated sul

273 ated apical tuft cilia and no indications of dorsoventral polarity.

274 daxial or abaxial fates function to maintain dorsoventral polarity.

275 roperties were found to be predictive of the dorsoventral position of a neuron's input zone relative

276 ation of the somites, determines the correct dorsoventral position of mammary epithelium along the fl

277 n order in the optic tract that reflects the dorsoventral position of the parent RGCs in the eye.

278 ple parameters of axon morphology, including dorsoventral position, midline crossing and collateral b

279 spatial distributions with mediolateral and dorsoventral positional biases.

280 ifferent progenitor cell domains in distinct dorsoventral positions around the central canal are acti

281 l (two or three segments), mediolateral, and dorsoventral (reaching laminae III-IV) distribution.

282 t and right axons terminate within different dorsoventral regions of the midbrain target.

283 B:ephrin-B interactions have a major role in dorsoventral retinal ganglion cell axon termination alon

284 xperiments show that BMP signaling regulates dorsoventral RGC cell fate, RGC axon behavior in the asc

285 rated occurrence of different types of trunk dorsoventral segmental mismatch in several phylogenetica

286 phase-locked to the local field theta at all dorsoventral segments.

287 By implication, the clustering and dorsoventral settling position of motor neuron pools ser

288 The dorsoventral settling position of motor pools in the spi

289 Under the influence of a common dorsoventral signal, sonic hedgehog, and distinct anteri

290 In the embryonic neural tube, dorsoventral signaling has emerged as a fundamental mech

291 ticular, the intracellular components of the dorsoventral signaling pathway (except for dorsal) and t

292 Thus, two dorsoventral signaling pathways, mediated by Shh and Wnt

293 hat the specification of MMC fate involves a dorsoventral signaling program mediated by three Wnt pro

294 o required for hippocampal specification and dorsoventral telencephalic patterning.

295 inal axes-proximodistal, anteroposterior and dorsoventral-that are established via the organization o

296 ignaling evolved with fundamental changes in dorsoventral tissue differentiation is unclear.

297 with perturbations in the spatial pattern of dorsoventral Toll signaling.

298 Along the dorsoventral, tonotopic axis of DCN, the mean position o

299 e) and longer spatial extent, whereas in the dorsoventral (vertical) plane, electrical coupling domin

300 estingly, asymmetry develops in a protracted dorsoventral wave, whereas lamination does so in a rapid