ライフサイエンスコーパス: body axis

1 served role in patterning the dorsal-ventral body axis.

2 idual limbs in relation to the front-to-rear body axis.

3 ep290 MO-injected embryos exhibited a curved body axis.

4 convergent-extension process elongating the body axis.

5 elopment, and a shortened anterior-posterior body axis.

6 tructures during the development of the main body axis.

7 d autonomic nervous system targets along the body axis.

8 e behavior as they initiate extension of the body axis.

9 one cells and the continued extension of the body axis.

10 noid signalling in the newly generated chick body axis.

11 odels of pattern formation in the developing body axis.

12 ts is the duplication of the anteroposterior body axis.

13 entiation and pattern onset in the extending body axis.

14 order with their expression patterns on the body axis.

15 cterized by severe eye defects and shortened body axis.

16 driving force elongating the anteroposterior body axis.

17 t in the position of the limb along the main body axis.

18 t are influenced by the embryonic left-right body axis.

19 -to-right and right-to-left inversion of the body axis.

20 t occurs in a stereotypic position along the body axis.

21 rs within the VNC and along the dorsoventral body axis.

22 ation and in patterning the lower end of the body axis.

23 in an asymmetric fashion about its secondary body axis.

24 llel or perpendicular to the anteroposterior body axis.

25 that establishes the anterior-posterior (AP) body axis.

26 of RB neurons differs along the rostrocaudal body axis.

27 critical for the formation of the vertebrate body axis.

28 l differentiation along the antero-posterior body axis.

29 e main fin axis seems to lie parallel to the body axis.

30 lopmental programs along the anteroposterior body axis.

31 fferent body regions along the C. elegans AP body axis.

32 dorsoventral locations along the vertebrate body axis.

33 establish the anteroposterior pattern of the body axis.

34 hrough its differential expression along the body axis.

35 ivisions all along the anteroposterior (A/P) body axis.

36 mutant embryos exhibit a truncated posterior body axis.

37 is involved in the establishment of a major body axis.

38 e directions along the anteroposterior (A/P) body axis.

39 al and temporal patterning of the vertebrate body axis.

40 th directions as long fibers parallel to the body axis.

41 e formation of blastopores and the wild-type body axis.

42 a failure to promote full elongation of the body axis.

43 elopment requires extension from the primary body axis.

44 ulating embryo that induces and patterns the body axis.

45 in a row along the anterior-posterior (A/P) body axis.

46 men asymmetrically along the left-right (LR) body axis.

47 the establishment of the anterior-posterior body axis.

48 eir normal domains of function along the A/P body axis.

49 odal in a pathway determining the left-right body axis.

50 s along the anteroposterior and dorsoventral body axis.

51 , as well as establishment of the left-right body axis.

52 etic flows to shape the extending vertebrate body axis.

53 and endodermal derivatives along the primary body axis.

54 permitted to form along the anteroposterior body axis.

55 meristems allow continuous growth along the body axis.

56 ipositors in any direction relative to their body axis.

57 the Gram-negative Curvibacter sp., along the body axis.

58 o guide patterning of the anterior-posterior body axis.

59 order as their expression domains along the body axis.

60 egardless of their positions relative to the body axis.

61 a blueprint for segmental identity along the body axis.

62 ocalised to establish the anterior-posterior body axis.

63 terior-posterior elongation of the embryonic body axis.

64 cues are coordinated to generate a segmented body axis.

65 4-cell stage to establish the C. elegans LR body axis.

66 ctors regulating development along the major body axis.

67 cell rearrangements during elongation of the body axis.

68 ons early in the establishment of left-right body axis.

69 o drive patterning of regeneration along the body axis.

70 consequently establish the mammalian primary body axis.

71 es in various species as they elongate their body axis.

72 r177 exhibit defects in establishment of the body axis, a phenotype highly reminiscent to the loss of

73 have lost a large intermediate region of the body axis-a region corresponding to the entire thorax an

74 did not exhibit downstream craniofacial and body axis abnormalities.

75 of ccm2 alone, and also leads to substantial body axis abnormalities.

76 shown developmental defects such as abnormal body axis and brain malformation, implying disrupted cil

77 that drives axial lengthening of the primary body axis and depends on the planar cell polarity (PCP)

78 'Freeing' fins from the body axis and establishing a separate 'limb' axis has be

79 c changes in such contexts as the vertebrate body axis and external Drosophila melanogaster tissues.

80 /- embryos lacking RA synthesis that exhibit body axis and forelimb defects.

81 ial for patterning of the anterior-posterior body axis and germ cell function.

82 tors provide instructions for key aspects of body axis and germ layer patterning; however, the comple

83 t roles in the development of the vertebrate body axis and gut epithelium.

84 or involved in multiple functions, including body axis and hand/foot development in tetrapods.

85 ponsible for establishment of the left-right body axis and head formation.

86 Dkk1 on the induction and patterning of the body axis and heart.

87 arget genes already known to be required for body axis and limb formation, thus validating our approa

88 poral order is critical to patterning of the body axis and limbs during embryonic development.

89 ntagonists are involved in patterning of the body axis and numerous aspects of organogenesis.

90 rack the origin of tendon progenitors of the body axis and reveal the molecular events and tissue int

91 nockdown of RP2 in zebrafish causes a curved body axis and small eye phenotype, associated with incre

92 an analogous step in the extending embryonic body axis and so identify attenuation of Fgf signalling

93 sner fiber for the maintenance of a straight body axis and spine morphogenesis in adult zebrafish.

94 a shared toxicity phenotype characterized by body axis and swim bladder defects and hyperactivity.

95 The establishment of the main body axis and the determination of left-right asymmetry

96 rs are important in the establishment of the body axis and the development of tissues from all three

97 t of the rhombomeres caused by the shortened body axis and the kink in the neural tube.

98 0 during development and regeneration of the body axis and the limbs of axolotls.

99 ntations of fluorescence intensity along the body axis and throughout development from early larvae t

100 position in lateral plate mesoderm along the body axis and thus for determining where limbs are forme

101 nstrated previously unknown requirements for body axis and/or limb formation.

102 y structured by dynamic cytodifferentiation, body-axis and cell-proliferation gene sets that were fur

103 erally to a paraxial position (alongside the body axis) and segment into epithelial somites.

104 on in the amount of bone laid down along one body axis, and it arises at or shortly after the onset o

105 neuron subpopulations along the rostrocaudal body axis, and local signals within the neural tube can

106 are segmented along the anteroposterior (AP) body axis, and the segmental identity of the vertebrae i

107 sed in a staggered fashion along its primary body axis, and the transforming growth factor-beta gene

108 n in the striatum caused rotation around the body-axis, and stimulation near the ridge between ventra

109 cation of the spleen on the left side of the body axis appears to result from preferential developmen

110 events that initially orient the left-right body axis are beginning to be understood, the mechanisms

111 enetic pathway that establish the left-right body axis are conserved in vertebrates.

112 sion at later stages on the left side of the body axis are controlled by a 600-bp intronic enhancer.

113 ating somites, the segments of the embryonic body axis, are absent or irregular.

114 ll is believed to rotate clockwise about the body axis as shown for the Leptospiraceae.

115 biased, regardless of the origin of the left body axis, as seen in many instances of experimentally i

116 her congestion forms within the flow and the body axis becomes contorted.

117 ent show a severe reduction of the posterior body axis; both these classes of affected embryos die in

118 Markers of the early body axis, Brachyury (BRA) and FOXA2, usually showed a c

119 p70b morphants exhibited broader and shorter body axis but cell fate specification appeared normal.

120 nserved domains along the anterior-posterior body axis, but whether they are performing the same func

121 cription factors that regionalize the animal body axis by controlling complex developmental processes

122 Elongation of the head-to-tail body axis by convergent extension is a conserved develop

123 , which is termed the organizer, pattern the body axis by specifying the fates of neighbouring cells.

124 n is fundamental to the establishment of the body axis, cell migration, synaptic plasticity, and a va

125 opmental processes such as patterning of the body axis, central nervous system and limbs, and the reg

126 In the mouse embryo, the body axis continues to develop after gastrulation as a t

127 rt and abdominal organs externalized and the body axis contorted.

128 turbations that included a notably shortened body axis, convoluted anterior neuroepithelium, caudal d

129 1) a group of twelve mutants with defects in body axis curvature and manifesting the most rapid and s

130 ression resulted in pronephric kidney cysts, body axis curvature, organ laterality defects, and hydro

131 turb the entire length of the pronephros and body axis curvature.

132 pletion of sdccag8 causes kidney cysts and a body axis defect in zebrafish and induces cell polarity

133 mbryos, elongation of the anterior-posterior body axis depends on convergent extension, a process tha

134 es, reveals frequent evolutionary changes of body axis determinants and a remarkable opportunity to s

135 Cilia are required for left/right body axis determination and second heart field (SHF) Hed

136 taining genes play an important role in both body axis determination and specific organ development.

137 adherins, actin organization through fascin, body axis determination through Wnt signaling, tumor sup

138 morphogen involved in regulating left-right body axis determination.

139 and lung function, fertility, and left-right body-axis determination.

140 s contain protein-coding genes that regulate body axis development and microRNA (miRNA) genes whose f

141 dressing the cell and morphological basis of body axis development in embryos of the cnidarian Clytia

142 ncluding the Nodal-related gene cyclops, and body axis dorsalization.

143 microinjection of mRNA encoding a variety of body axis duplicating proteins, including members of the

144 tional identity along the anterior-posterior body axis during animal development.

145 mediating extension and straightening of the body axis during development, and highlight open questio

146 Patterning of the anterior-posterior body axis during Drosophila development depends on the r

147 a Reissner fiber and fail to form a straight body axis during embryonic development [3].

148 is required outside of the limb field in the body axis during forelimb induction but that RA is unnec

149 or coordinating stepping and stabilizing the body axis during movements.

150 or coordinating stepping and stabilizing the body axis during movements.

151 setting the normal polarized features of the body axis during regeneration.

152 ed the ability of Wnt8 to induce a secondary body axis during Xenopus embryonic development.

153 l eyes, diminished pharyngeal arches, curved body axis, edema, underdeveloped intestine and cell deat

154 an overview of CE as a general strategy for body axis elongation and discuss conserved and divergent

155 different posterior tissues during zebrafish body axis elongation change their physical state, the re

156 ish that notochord vacuoles are required for body axis elongation during embryonic development and id

157 e, the results indicate that chato regulates body axis elongation in all embryonic tissues through a

158 ated as a mechanism driving gastrulation and body axis elongation in mouse embryos, the cellular mech

159 Body axis elongation represents a common and fundamental

160 A key mechanism triggering body axis elongation without additional growth is conver

161 serving bilateral symmetry during Drosophila body axis elongation, a process driven by cell rearrange

162 both tissue flows and shape during zebrafish body axis elongation, we show that the observed morphoge

163 nd the paraxial mesoderm in concert with the body axis elongation.

164 xtension that drives neural tube closure and body axis elongation.

165 ing retinoid activity underlies cessation of body axis elongation.

166 Body-axis elongation constitutes a key step in animal de

167 annelids and chordates, segmentation of the body axis encompasses both ectodermal and mesodermal der

168 mmalian embryogenesis for anterior-posterior body axis establishment and subsequent spinal cord devel

169 the mesoderm of vertebrate embryos controls body axis extension by downregulating Fgf8 expression in

170 of FGF8 signaling during the early stages of body axis extension provides an environment permissive f

171 eterochronic changes in Oct4 activity during body axis extension, which may have derived from differe

172 gh without a directional bias, drives caudal body axis extension.

173 aterally intercalative behavior required for body axis extension.

174 n cause dramatic tissue deformations such as body axis extension.

175 at an extrinsic tensile force contributed to body axis extension.

176 -field stimulus rotating around the vertical body axis, flies display a following behavior called "op

177 Formation of the vertebrate postcranial body axis follows two sequential but distinct phases.

178 the cerebrospinal fluid (CSF) contributes to body axis formation and brain development.

179 Vertebrate body axis formation depends on a population of bipotenti

180 that inhibition of sirtuins interferes with body axis formation in Arabidopsis.

181 Asymmetric body axis formation is central to metazoan development.

182 The genetic systems controlling body axis formation trace back as far as the ancestor of

183 processes, including neural differentiation, body axis formation, and organogenesis.

184 other species is required for ciliogenesis, body axis formation, and renal function.

185 mitive streak and tail-bud regression during body axis formation.

186 lpha signal emitted by the oocyte to control body axis formation.

187 t-7 influence caudal vertebrae number during body axis formation.

188 nin in early Xenopus embryos is required for body axis formation.

189 embryology has revealed deep similarities in body-axis formation and organization across deuterostome

190 polarity that defines the anterior-posterior body axis frequently fails.

191 zes the organ precursors along the embryonic body axis, giving rise to the blueprint of organ formati

192 l which were planar, wrapped around the cell body axis in a right-handed sense.

193 ctors specify the spatial coordinates of the body axis in all animals with bilateral symmetry, but a

194 The dorsoventral body axis in amphibian embryos is established by a rotat

195 ows for divergence along the anteroposterior body axis in arthropods.

196 ed function in patterning the dorsal-ventral body axis in Bilateria and the directive axis in anthozo

197 en shown to regulate Hox loci along the main body axis in embryonic development, but the extent to wh

198 ole as a Nodal co-receptor for patterning of body axis in embryonic development.

199 ential for specifying the anterior/posterior body axis in insects, the fate of early-born pioneer neu

200 ental diversity along the anterior-posterior body axis in metazoans.

201 red to polarize the anterior-posterior (a-p) body axis in one-cell zygotes, but it remains unknown ho

202 ne expression domains are expanded along the body axis in python embryos, and that this can account f

203 is critical for establishing the left-right body axis in several vertebrate embryos.

204 en proposed to establish the left-right (LR) body axis in vertebrate embryos by creating a directiona

205 acid influences the formation of the primary body axis in vertebrates and that this may occur through

206 ory for normal orientation of the left-right body axis in Xenopus.

207 her7 is essential for the development of the body axis in zebrafish embryos.

208 and shows a fixed "polarity" with respect to body axis, independent of the precise location of the cl

209 n zebrafish embryos led to short, dorsalized body axis induced by elevated apoptosis.

210 ront of determination which sweeps along the body axis interacting as it moves with the segmentation

211 The periodic segmentation of the vertebrate body axis into somites, and later vertebrae, relies on a

212 Patterning the avian left-right (L/R) body axis involves the establishment of asymmetric molec

213 Formation of the left/right body axis is a critical early step in embryogenesis.

214 ages at appropriate levels along the primary body axis is a hallmark of the body plan of jawed verteb

215 Elongation of the body axis is a key aspect of body plan development.

216 Elongation of the body axis is accompanied by the assembly of a polarized

217 body pattern along the anteroposterior (A/P) body axis is achieved largely by the actions of conserve

218 omes and their domains of function along the body axis is conserved between arthropods and vertebrate

219 Differentiation onset in the vertebrate body axis is controlled by a conserved switch from fibro

220 n of reiterated somites along the vertebrate body axis is controlled by the segmentation clock, a mol

221 The left-right body axis is coordinately aligned with the orthogonal do

222 During vertebrate gastrulation, the body axis is established by coordinated and directional

223 ins to specify distinct structures along the body axis is frequently dependent on interactions with o

224 In most animal species, the anteroposterior body axis is generated by the formation of repeated stru

225 ta suggest that nearly the entire tardigrade body axis is homologous to just the head region of arthr

226 ow animals establish and pattern the primary body axis is one of the most fundamental problems in bio

227 dal genes is diminished and extension of the body axis is prematurely terminated.

228 sequential and rhythmic segmentation of the body axis is regulated by a "segmentation clock".

229 determination of the vertebrate dorsoventral body axis is regulated in the extracellular space by a s

230 mbryonic development, the anterior-posterior body axis is specified in part by the combinatorial acti

231 The vertebrate body axis is subdivided into repeated segments, best exe

232 the QR descendants along the anteroposterior body axis, is mediated through a cell-autonomous process

233 d with ciliary anomalies including shortened body-axis, kinked tail, hydrocephaly and edema but does

234 elopment, defective head organs, and reduced body axis length, providing compelling evidence for the

235 The Caenorhabditis elegans body axis, like that of other animals, is patterned by t

236 n the development of the mammalian secondary body axis (limb).

237 aspects such as shortened anterior-posterior body axis, limb, and frontonasal process.

238 ion (CE) movements simultaneously narrow the body axis mediolaterally and elongate it from head to ta

239 ent extension mutants, including a shortened body axis, mediolaterally extended somites and an open n

240 nction in the zebrafish results in shortened body axis, microphthalmia with disorganized lens, microc

241 tebrates, the Reissner fiber, which controls body axis morphogenesis in the zebrafish embryo.

242 CSF-cNs and thereby contributes to establish body axis morphogenesis, and suggest it does so by contr

243 iber-signaling pathway to CSF-cNs and rescue body axis morphogenesis.

244 ion such as their origin, position along the body axis, number and identity.

245 t of the embryonic axis foreshadows the main body axis of adults both in plants and in animals, but u

246 that assign positional identities along the body axis of animal embryos.

247 mental fates to cells on the anteroposterior body axis of animal embryos.

248 gical diversity along the anterior-posterior body axis of animals, but the cellular processes they di

249 ole to the apical tuft and defines the major body axis of both the planula larva and adult polyp.

250 lls that lie along the anteroposterior (A/P) body axis of C. elegans.

251 differential identity of segments along the body axis of insects.

252 of cell fates along the anteroposterior (AP) body axis of many organisms.

253 the animal, control morphologies on the main body axis of nearly all metazoans.

254 e rotation of the propulsive force about the body axis of the bacterium.

255 gn and intercalate to establish the physical body axis of the developing embryo.

256 Patterning of the anterior-posterior body axis of the Drosophila embryo requires production o

257 ntal potencies at different levels along the body axis of the embryo.

258 temporal and spatial colinearity in the main body axis of the mouse embryo.

259 Neural crest populations along the embryonic body axis of vertebrates differ in developmental potenti

260 The body axis of vertebrates is composed of a serial repetit

261 The head-to-tail body axis of vertebrates is elongated in embryonic stage

262 Here, in the context of the elongating body axis of Xenopus embryos, we combine tools from cell

263 yo, revealed by the formation of a secondary body axis or dorsalization of the ventral mesoderm expla

264 embryo is a key embryonic region involved in body axis organization and neural induction.

265 code transcription factors which function in body axis patterning in the developing embryo.

266 During animal ontogenesis, body axis patterning is finely regulated by complex inte

267 Silencing of mekk3 rescues the big heart and body axis phenotype, suggesting cross-talk between the C

268 nary shifts in Hox gene expression along the body axis provided a transcriptional mechanism allowing

269 LIP1 in Xenopus embryos induces a secondary body axis, providing further evidence for a functional l

270 Xenopus development: establishing the dorsal body axis; regulating mesoderm induction; and subsequent

271 The alignment of the left-right (LR) body axis relative to the anteroposterior (AP) and dorso

272 al cleavage, anteroposterior axis formation, body axis segmentation, and head versus trunk distinctio

273 illator ensemble linked to vertebrate embryo body axis segmentation.

274 Body axis specification is a crucial event in animal emb

275 nt of many organs and tissues, including the body axis, spinal cord, forelimbs, heart, eye and reprod

276 ascade originating from this fiber to ensure body axis straightening is not understood.

277 eads to BBS with randomization of left-right body axis symmetry, a known defect of the nodal cilium.

278 ary afferents from the anterior to posterior body axis terminate in different areas in the mediolater

279 hine-induced rotations and with the extended body axis test.

280 to correctly specify the anterior-posterior body axis, that are not caused by changes in proliferati

281 s oscillator with a wave traveling along the body axis (the clock-and-wavefront model) is generally b

282 Along the body axis, the neural crest is heterogeneous, with diffe

283 mechanosensory neuron is reversed along the body axis: the long PLM process, PLM growth cone, and sy

284 by its motion at an angle to the horizontal body axis; the vortex directs water backwards and downwa

285 e level of MIG-13 determines where along the body axis these migrating cells stop.

286 Tbx3 in positioning the limb along the main body axis through a genetic interplay between dHand and

287 inter-tissue forces in coordinating distinct body axis tissues during their co-elongation.

288 een one another transverse to the elongating body axis to form a narrower, longer array.

289 ants migrate along the anteroposterior (A/P) body axis to positions that are not associated with any

290 ural differentiation in the elongating chick body axis to provide the first analysis of transcriptome

291 s that close the blastopore and elongate the body axis, to examine the role of myosin IIB in converge

292 ed force-producing tissues in the elongating body axis, we show that TiFM quantitatively captures str

293 ions of the treadmill motion relative to the body axis were used (0, +/- 45, +/- 90, and 180 degrees

294 ivity and is capable of inducing a secondary body axis when ectopically expressed.

295 e vertebrate organizer can induce a complete body axis when transplanted to the ventral side of a hos

296 erized by an elongated antero-posterior (AP) body axis, which forms by progressive cell deposition fr

297 s the sequential segmentation of the primary body axis, which is conserved in all vertebrates and man

298 ion, disruption of somitogenesis, and curved body axis with bent tail.

299 pha5 display somite defects along the entire body axis, with a complete loss of the mesenchymal-to-ep

300 according to their level of origin along the body axis, with only cranial neural crest cells contribu