ライフサイエンスコーパス: anterior-posterior axis

1 , thoracic, and abdominal segments along the anterior posterior axis.

2 om pair-rule to segmental patterns along the anterior-posterior axis.

3 es appropriate organ specification along its anterior-posterior axis.

4 le dislocations of notochord cells along the anterior-posterior axis.

5 d asymmetric cell divisions along the entire anterior-posterior axis.

6 aces in mirror image symmetry, with a common anterior-posterior axis.

7 rganization of these subpopulations along an anterior-posterior axis.

8 lts in abnormal gastrulation and a shortened anterior-posterior axis.

9 Strikingly, phenotypes are graded along the anterior-posterior axis.

10 nes spaced at an absolute distance along the anterior-posterior axis.

11 defined dorsal-ventral axis imposed on their anterior-posterior axis.

12 icantly biased to the right, relative to the anterior-posterior axis.

13 sed within the pharyngeal endoderm along the anterior-posterior axis.

14 arget genes at different positions along the anterior-posterior axis.

15 resents a crucial event in patterning of the anterior-posterior axis.

16 dline of the developing CNS along its entire anterior-posterior axis.

17 intricate scaffold of cables parallel to the anterior-posterior axis.

18 ole in establishing distinct fates along the anterior-posterior axis.

19 sor function in restricting induction of the anterior-posterior axis.

20 the dorso-ventral axis and in patterning the anterior-posterior axis.

21 of the MTL, but patterns differed along the anterior-posterior axis.

22 is known to be required for formation of the anterior-posterior axis.

23 m induction and results in truncation of the anterior-posterior axis.

24 sts play in the patterning of the vertebrate anterior-posterior axis.

25 e of signals from adjacent repeats along the anterior-posterior axis.

26 ween neighboring blast cell clones along the anterior-posterior axis.

27 skar mRNA are key events in establishing the anterior-posterior axis.

28 pecify aspects of segment identity along the anterior-posterior axis.

29 s, particularly in those patterned along the anterior-posterior axis.

30 izer development, and the positioning of the anterior-posterior axis.

31 growth and patterning of the limbs along the anterior-posterior axis.

32 ns that are ubiquitously expressed along the anterior-posterior axis.

33 alternative developmental pathways along the anterior-posterior axis.

34 is the first overt morphological sign of the anterior-posterior axis.

35 mation of segment specific structures in the anterior-posterior axis.

36 n do mammals, despite less complexity in the anterior-posterior axis.

37 the longitudinal fibres, oriented along the anterior-posterior axis.

38 on that result in dramatic shortening of the anterior-posterior axis.

39 proximal-distal asymmetry into an orthogonal anterior-posterior axis.

40 polarised microtubule array that defines the anterior-posterior axis.

41 for DPP, show shifts in cell fate along the anterior-posterior axis.

42 iption factors, control cell fates along the anterior-posterior axis.

43 n Drosophila embryonic development along the anterior-posterior axis.

44 ted for six PP that span along the embryonic anterior-posterior axis.

45 zed their physiological properties along the anterior-posterior axis.

46 shows a polarized location along the cell's anterior-posterior axis.

47 emphasizing tonotopic organization along the anterior-posterior axis.

48 maintenance is crucial for completion of the anterior-posterior axis.

49 pecification of body segment identity in the anterior-posterior axis.

50 tions) followed by junction extension in the anterior-posterior axis.

51 ctive properties of callosal axons along the anterior-posterior axis.

52 which define different identities along the anterior-posterior axis.

53 genesis, the egg chamber elongates along the anterior-posterior axis.

54 pecialization for these properties along its anterior-posterior axis.

55 gut looping defects and shortening along the anterior-posterior axis.

56 e pathology was generalized along the entire anterior-posterior axis.

57 causes the egg chamber to rotate around its anterior-posterior axis.

58 striking regional differentiation along its anterior-posterior axis.

59 fferences in notochord cell volume along the anterior-posterior axis.

60 is responsible for correctly orientating the anterior-posterior axis.

61 d for coordinated neural signaling along the anterior-posterior axis.

62 l body organisation along all or part of the anterior-posterior axis.

63 s in an inhibition of neurogenesis along the anterior-posterior axis.

64 This Dicer mutant exhibits a reduced anterior-posterior axis.

65 A)] in the brainstem project axons along the anterior-posterior axis.

66 d by shifts in Hox gene expression along the anterior-posterior axis.

67 nt of neuronal polarity along the C. elegans anterior-posterior axis.

68 in opposite orientations with respect to the anterior/posterior axis.

69 ors associated with their position along the anterior/posterior axis.

70 lly to specify positional identity along the anterior/posterior axis.

71 characteristic of their positions along the anterior/posterior axis.

72 oss of other domains of expression along the anterior/posterior axis.

73 ted in an embryo dorsalized along the entire anterior/posterior axis.

74 aterians: elongation of the embryo along the anterior-posterior axis [1].

75 The establishment of the anterior-posterior axis(8,9) further regulates basement

76 ne-cell embryo of C. elegans establishes the anterior--posterior axis (A-P), and is necessary for the

77 The polarization of the anterior-posterior axis (A-P) of the Caenorhabditis eleg

78 is the polarization of the oocyte along the anterior-posterior axis, a process induced by an unknown

79 embryonic structures is polarized along the anterior/posterior axis, a subdivision first distinguish

80 genes are essential to the patterning of the anterior-posterior axis along the developing Drosophila

81 bserved across most cortical areas along the anterior-posterior axis and (2) a discrete, abrupt bound

82 lls in the ventral midline arrayed along the anterior-posterior axis and 6 of these cells become the

83 in overlapping transverse stripes along the anterior-posterior axis and act in combination to direct

84 the alignment of cell division planes to the anterior-posterior axis and acts in parallel to known po

85 ress Smad2(Deltaexon3) correctly specify the anterior-posterior axis and definitive endoderm, and are

86 ase activity and disrupted elongation of the anterior-posterior axis and differentiation of skeletal

87 he extent to which hb is expressed along the anterior-posterior axis and displayed a reduced ability

88 set of embryos also show a shortening of the anterior-posterior axis and frequent duplication of axia

89 s anterior and posterior expansion along the anterior-posterior axis and medial-lateral compression a

90 Pax9 plays a crucial role in patterning the anterior-posterior axis and outgrowth of the developing

91 imensional stem cell aggregates that form an anterior-posterior axis and structures resembling the ma

92 wnstream signaling pathways differ along the anterior-posterior axis and suggests a functional role f

93 robustly recapitulate the patterning of the anterior-posterior axis and the formation of cells refle

94 Although the specification of the anterior-posterior axis and the initial response to meso

95 nal gradients, one of Wnt activity along the anterior-posterior axis and the other of BMP signals alo

96 bditis elegans is necessary to establish the anterior-posterior axis and to ensure the proper identit

97 (TCF/LEF) transcriptional activity along the anterior-posterior axis, and 3) coelomocyte competence f

98 is, where the embryo derives from the entire anterior-posterior axis, and all segments are patterned

99 Wnt signaling controls regeneration of the anterior-posterior axis, and Bmp-Admp signaling controls

100 spects of neural crest maintenance along the anterior-posterior axis, and establish an unprecedented

101 hord development during the formation of the anterior-posterior axis, and its role in this process is

102 rgan-like structure that lengthens along its anterior-posterior axis as it grows.

103 leotides results in embryos with a truncated anterior-posterior axis, as well as elongated somites an

104 lineages in postmortem brain correlated with anterior-posterior axis, associating lineage history wit

105 observed in large cells scattered along the anterior-posterior axis at stage 13.

106 lumbosacral neural tube are reversed in the anterior-posterior axis at stage 15 (embryonic day 2.5),

107 ment cranial or caudal) were reversed in the anterior-posterior axis at stages 13 and 14 (embryonic d

108 ve rise to descendants that stream along the anterior-posterior axis at the ventral midline and contr

109 results suggest that interactions along the anterior-posterior axis between neighboring primary blas

110 ls exit the primitive streak and pattern the anterior-posterior axis, but how varying dosage informs

111 proteins regulate axonal outgrowth along the anterior-posterior axis, but the intracellular mechanism

112 , the spindle is aligned and centered on the anterior-posterior axis by a microtubule-dependent machi

113 tion and strength of Wnt signaling along the anterior-posterior axis by employing a Ror family Wnt re

114 isthmic organizer are partitioned along the anterior-posterior axis by lineage restriction boundarie

115 actors specify numerous cell fates along the anterior-posterior axis by regulating the expression of

116 nduction also directs a midbrain fate in the anterior-posterior axis by suppressing caudalization as

117 t subpopulations of follicle cells along the anterior/posterior axis can respond to Top/Egfr activati

118 apical ectodermal ridge and shortened in the anterior-posterior axis, consistent with the observed lo

119 th Wnts are expressed in gradients along the anterior-posterior axis, consistent with their role as d

120 In contrast, large errors along the anterior-posterior axis corresponding to nasal-temporal

121 The relative position of cells along the anterior-posterior axis could also be assigned using adu

122 l proliferation and tissue patterning during anterior-posterior axis, craniofacial and limb developme

123 y become polarized during stage 6 around the anterior-posterior axis defined by the polar cells, but

124 arization of the C. elegans zygote along the anterior-posterior axis depends on cortically enriched (

125 shape, suggesting that morphology along the anterior-posterior axis depends on neural ectoderm geome

126 ulatory mechanisms during distinct stages of anterior/posterior axis development, and uncover previou

127 tino/kreisler, a hox gene regulator, produce anterior-posterior axis disruptions of pharyngeal cartil

128 pression in the palatal epithelium along the anterior-posterior axis during early palate development.

129 nd patterning of the neuroectoderm along the anterior-posterior axis during gastrulation.

130 pr177 is essential for the patterning of the anterior-posterior axis during mammalian development.

131 the ancestral deuterostome embryo along its anterior-posterior axis during the late blastula and sub

132 ges as the body extends to form the complete anterior-posterior axis during the somite-forming stages

133 signaling is essential for establishing the anterior/posterior axis during regeneration by modulatin

134 Consistent with this, the rate of anterior-posterior axis elongation is reduced relative t

135 nd recapitulates phenotypic abnormalities of anterior-posterior axis extension.

136 sed to separate cellular fragments along the anterior-posterior axis, followed by comparative proteom

137 PCP proteins, polarize node cells along the anterior-posterior axis for breaking of left-right symme

138 alized at the posterior of young oocytes for anterior-posterior axis formation and later in the dorsa

139 Although the mechanisms of anterior-posterior axis formation are well understood in

140 we present evidence that Star is involved in anterior-posterior axis formation both in the female ger

141 ing a possible explanation for the defect in anterior-posterior axis formation caused by Notch and De

142 The Par-1 kinase is required for anterior-posterior axis formation in Drosophila.

143 Anterior-posterior axis formation in the Drosophila oocy

144 Anterior-posterior axis formation in the mouse embryo re

145 BPTF is required for anterior-posterior axis formation of the mouse embryo an

146 ut the precise role of the follicle cells in anterior-posterior axis formation remains enigmatic.

147 ng early in oogenesis and are independent of anterior-posterior axis formation.

148 we observed putative HSN homologs along the anterior-posterior axis from the head to the tail, but t

149 pI cell in the epithelium oriented along the anterior-posterior axis, giving rise to pIIa and pIIb, w

150 a segmental form of cardiac defect along the anterior-posterior axis in all homozygous mice identifie

151 id (Bcd) is key for the establishment of the anterior-posterior axis in Drosophila embryos.

152 Bicoid is a morphogen that sets up the anterior-posterior axis in early Drosophila embryos.

153 exposure and extended posteriorly along the anterior-posterior axis in hemizygous mice.

154 the paraxial mesoderm is patterned along the anterior-posterior axis in metameric units, or somites,

155 gap and pair-rule gene expression along the anterior-posterior axis in relation to embryo length.

156 ed a subtle morphological gradient along the anterior-posterior axis in stem members of amniote clade

157 tive in distinct spatial registers along the anterior-posterior axis in the CNS.

158 secreted factor regulating patterning of the anterior-posterior axis in the developing limb.

159 Initiation of the development of the anterior-posterior axis in the mouse embryo has been tho

160 ce of genetic programs helping establish the anterior-posterior axis in visceral endoderm.

161 serves an essential role in formation of the anterior-posterior axis in Xenopus laevis embryos, and t

162 regulation of the component genes along the anterior/posterior axis in a manner that correlates with

163 HOM-C/Hox genes pattern cell fate along the anterior/posterior axis in many animals.

164 function during gastrulation to generate the anterior/posterior axis in Xenopus.

165 ng regulates fine scale cell fates along the anterior-posterior axis, in part by creating an adhesion

166 he Mullerian duct actively migrate along the anterior-posterior axis independent of the proliferative

167 vertebrate hindbrain is subdivided along the anterior-posterior axis into a series of seven segments,

168 cortex of the cerebellum is folded along the anterior-posterior axis into lobules separated by fissur

169 e hindbrain is transiently divided along the anterior-posterior axis into seven morphologically and m

170 a common mechanism for patterning along the anterior/posterior axis involving a posterior signaling

171 The anterior-posterior axis is a key feature of the bilateri

172 results suggest that the orientation of the anterior-posterior axis is already anticipated before AV

173 The medial-to-lateral Dpp gradient along the anterior-posterior axis is complemented by a lateral-to-

174 n Drosophila, embryonic patterning along the anterior-posterior axis is controlled by the morphogen g

175 Patterning of the vertebrate limb along the anterior-posterior axis is controlled by the zone of pol

176 in all deuterostomes, but, in chordates, the anterior-posterior axis is established at right angles t

177 The Drosophila melanogaster anterior-posterior axis is established during oogenesis

178 ential RA responsiveness along the hindbrain anterior-posterior axis is shaped primarily by the dynam

179 The Drosophila anterior-posterior axis is specified when the posterior

180 The anterior-posterior axis is therefore established by a re

181 mbryos the spindle failed to align along the anterior/posterior axis, leading to abnormal cleavage co

182 rm and ectoderm contribute to the autonomous anterior-posterior axis lengthening of ventral explants

183 differences in integrin regulation along the anterior-posterior axis may contribute to differences in

184 d endoderm formation, the positioning of the anterior-posterior axis, neural patterning and left-righ

185 anscription (JAK/STAT) pathway regulates the anterior posterior axis of the Drosophila follicle cells

186 HOX genes specify cell fate in the anterior-posterior axis of animal embryos.

187 Hox genes pattern the anterior-posterior axis of animals and are posited to dr

188 le (or Pbx1) to affect development along the anterior-posterior axis of animals.

189 The Hox gene cluster patterns the anterior-posterior axis of bilaterians.

190 The anterior-posterior axis of Drosophila becomes polarized

191 The anterior-posterior axis of Drosophila originates from tw

192 ntial to reorient mitotic spindles along the anterior-posterior axis of elongation, and orthogonal to

193 started to use distinct landmarks along the anterior-posterior axis of HF to allow segmentation into

194 We show that cell position along the anterior-posterior axis of hindbrain rhombomere 8 determ

195 l patterns of Hox gene expression across the anterior-posterior axis of metazoan embryos.

196 egulate the identity of structures along the anterior-posterior axis of most animals.

197 Polarization of node cells along the anterior-posterior axis of mouse embryos is responsible

198 distinct profiles of responsivity across the anterior-posterior axis of PVT during conflict, includin

199 The anterior-posterior axis of RIalpha mutants is well devel

200 roteins distribute asymmetrically across the anterior-posterior axis of the 1-cell-stage C. elegans e

201 determination of pattern formation along the anterior-posterior axis of the animal embryo.

202 are regionally specified with respect to the anterior-posterior axis of the avian embryo.

203 Furthermore, slow wave propagation along the anterior-posterior axis of the brain is largely mediated

204 entry of the sperm centrosome polarizes the anterior-posterior axis of the C. elegans zygote by indu

205 The anterior-posterior axis of the Caenorhabditis elegans em

206 The anterior-posterior axis of the Caenorhabditis elegans zy

207 ng a stable concentration gradient along the anterior-posterior axis of the cell.

208 ly, we show a gradient of s-ShhNp across the anterior-posterior axis of the chick limb, demonstrating

209 d in the guidance of retinal axons along the anterior-posterior axis of the chick optic tectum.

210 the polarizing signal for patterning of the anterior-posterior axis of the developing limb bud.

211 a morphogen to regulate patterning along the anterior-posterior axis of the developing wing.

212 FGF activity occurs as a gradient along the anterior-posterior axis of the dorsal midbrain and direc

213 protein in establishing a pattern along the anterior-posterior axis of the early Drosophila embryo.

214 ity of the cytoplasm does not vary along the anterior-posterior axis of the embryo during the first c

215 The anterior-posterior axis of the embryo is positioned late

216 mimic cytokine gradient polarization in the anterior-posterior axis of the embryo led to differentia

217 here morphogen gradients spanning the entire anterior-posterior axis of the embryo provide positional

218 he Bicoid protein gradient that patterns the anterior-posterior axis of the embryo.

219 which form in a metameric pattern along the anterior-posterior axis of the embryo.

220 ribution of HOX protein expression along the anterior-posterior axis of the embryo.

221 in turn are required to establish the future anterior-posterior axis of the embryo.

222 rphogen gradient, a signal that patterns the anterior-posterior axis of the embryo.

223 the regionalized identity of cells along the anterior-posterior axis of the emergent gut tube, which

224 rupt the transitions between zones along the anterior-posterior axis of the eye disc that express dif

225 mulated by the Unpaired ligand, patterns the anterior-posterior axis of the follicular epithelium.

226 nduce posterior fate, thereby polarising the anterior-posterior axis of the future embryo and then to

227 shows that Odz4 is required to establish the anterior-posterior axis of the gastrulating mouse embryo

228 rained in tissue fate and position along the anterior-posterior axis of the gut, the medial gut endod

229 al-cortical interactions that vary along the anterior-posterior axis of the hippocampus (HPC) to supp

230 ce for dissociable memory networks along the anterior-posterior axis of the hippocampus suggests that

231 fferentially interact with regions along the anterior-posterior axis of the hippocampus.

232 of the trochal lineages with respect to the anterior-posterior axis of the larva.

233 terior prestalk compartments lying along the anterior-posterior axis of the migrating slug.

234 The anterior-posterior axis of the mouse embryo is establish

235 trate that cell-fate determination along the anterior-posterior axis of the Mullerian duct occurs pri

236 fragments derived from several levels of the anterior-posterior axis of the neural tube at E14.5 and

237 Embryonic cellular position along the anterior-posterior axis of the neural tube was shown to

238 wn to specify cerebellar territory along the anterior-posterior axis of the neural tube, the mechanis

239 hus, Slmb may induce the polarisation of the anterior-posterior axis of the oocyte by targeting the P

240 monolayer organization and disruption of the anterior-posterior axis of the oocyte.

241 lls at later stages leads to a defect in the anterior-posterior axis of the oocyte.

242 aphic positioning of retinal axons along the anterior-posterior axis of the optic tectum in both Xeno

243 orting during apical tip formation, when the anterior-posterior axis of the organism is formed, by co

244 that exhibit a defined patterning along the anterior-posterior axis of the organism.

245 cked in that fewer sensory axons crossed the anterior-posterior axis of the plexus.

246 as recently been shown to correlate with the anterior-posterior axis of the postimplantation embryo.

247 show that chemogenetic inhibition across the anterior-posterior axis of the PVT, but not anterior or

248 signaling guides commissural axons along the anterior-posterior axis of the spinal cord.

249 out mice, MSN axons fail to extend along the anterior-posterior axis of the striatum, and many do not

250 ost, along a consistent gradient running the anterior-posterior axis of the symbiotic organ.

251 c acid (RA) is a morphogen that patterns the anterior-posterior axis of the vertebrate hindbrain.

252 establishing different digit fates along the anterior-posterior axis of the vertebrate limb bud.

253 to organize growth and patterning along the anterior-posterior axis of the wing primordium.

254 s orthogonal to a 'backbone' that models the anterior-posterior axis of the worm.

255 rminants are partitioned unequally along the anterior-posterior axis of the zygote, ensuring the daug

256 total influx under anesthesia, or across the anterior/posterior axis of the brain.

257 nt of regional commitments along most of the anterior/posterior axis of the developing embryo depends

258 a concentration gradient that organizes the anterior/posterior axis of the Drosophila embryo.

259 was induced in follicle cells all along the anterior/posterior axis of the egg chamber.

260 s location with an error bar of ~1 along the anterior/posterior axis of the embryo.

261 ionally, little data is available on how the anterior/posterior axis of the heart tube is determined

262 tablishes the cerebellar territory along the anterior/posterior axis of the neural tube.

263 hancer display variably penetrant defects in anterior-posterior axis orientation and DE formation.

264 nes lead to defects in germ-layer formation, anterior-posterior axis orientation and left-right axis

265 e demonstrate that Rumpelstiltskin regulates anterior-posterior axis patterning by functioning as a d

266 Drosophila hnRNP F/H homolog, contributes to anterior-posterior axis patterning by regulating transla

267 lso suggest that homeobox gene regulation of anterior-posterior axis patterning may have evolved prio

268 Anterior-posterior axis patterning of the Drosophila emb

269 Mouse anterior-posterior axis polarization is preceded by form

270 als that restriction of clonal spread in the anterior-posterior axis precedes restriction in the dors

271 es of cells and tissues along the developing anterior-posterior axis, probably in all bilaterian meta

272 eletal differentiation is reversed along the anterior-posterior axis relative to that of other tetrap

273 the formation of these projections along the anterior-posterior axis remain unknown.

274 Establishment of the anterior-posterior axis requires posterior localization

275 Along the anterior-posterior axis, several segment polarity genes

276 connect to the hippocampus along its longer anterior-posterior axis, shedding light on the way this

277 As stimulation sites were sampled along the anterior-posterior axis, small amplitude, nasally direct

278 During anterior-posterior axis specification in the Drosophila

279 is elegans zygotes, symmetry breaking during anterior-posterior axis specification is guided by centr

280 lopmental processes, including gastrulation, anterior-posterior axis specification, organ and tissue

281 d that Oncopeltus hunchback has two roles in anterior-posterior axis specification.

282 ells are asymmetrically positioned along the anterior-posterior axis such that more cilia are placed

283 rk in the Drosophila oocyte that defines the anterior-posterior axis, suggesting that microtubule org

284 split along the midline and fused across the anterior-posterior axis, suggesting that these defects m

285 Along the anterior-posterior axis, the posteriorly expressed prote

286 fferentiation of neuronal subtypes along the anterior-posterior axis, their mode of action is not ent

287 The Drosophila anterior-posterior axis therefore becomes polarised by a

288 lar with its two processes growing along the anterior-posterior axis under the guidance of Wnt signal

289 influences on cortical surface area along an anterior-posterior axis using neuroimaging data of adult

290 a-aminobutyric acid (GABAA) system along its anterior-posterior axis, using localized microinfusions

291 Dictyostelium establishes an anterior/posterior axis utilizing seven-transmembrane cA

292 entation genes patterns the embryo along its anterior-posterior axis via subdivision of the blastoder

293 nal organisation in both species followed an anterior-posterior axis, we observed a marked reconfigur

294 RXR caused striking malformations along the anterior-posterior axis, whereas in zebrafish only ligan

295 t signaling participates in establishing the anterior/posterior axis, whereas HOM-C genes confer regi

296 y embryo into reiterative segments along the anterior-posterior axis, while Hox genes assign segments

297 gions organized along the dorsal-ventral and anterior-posterior axis with distinct functional network

298 Loss of circular fibres led to a bifurcated anterior-posterior axis with fused heads forming in sing

299 ing activity appears as a gradient along the anterior-posterior axis with two- to threefold higher le

300 ng discs are expanded specifically along the anterior-posterior axis, with increased proliferation in