ライフサイエンスコーパス: Drosophila embryo

1 (eve) stripe 2 expression in the precellular Drosophila embryo.

2 omplex epithelial folding event in the early Drosophila embryo.

3 controlling brinker (brk) expression in the Drosophila embryo.

4 ngement of the tissues on the surface of the Drosophila embryo.

5 nd microtubules in the epidermis of the late Drosophila embryo.

6 P) and dorsal-ventral (DV) axes of the early Drosophila embryo.

7 of a tubular epithelium resembling the early Drosophila embryo.

8 hibition dynamics within the geometry of the Drosophila embryo.

9 cific activation of the Toll receptor in the Drosophila embryo.

10 m development of vertebrates and that of the Drosophila embryo.

11 using the rapid division cycles in the early Drosophila embryo.

12 thering at Golgi membranes in the developing Drosophila embryo.

13 egulation of other Runt targets in the early Drosophila embryo.

14 apid and synchronous activation in the early Drosophila embryo.

15 the mesoderm and neuroectoderm in the early Drosophila embryo.

16 hat controls the dorsoventral pattern of the Drosophila embryo.

17 how periodic patterns are established in the Drosophila embryo.

18 pathway responsible for segmentation in the Drosophila embryo.

19 lopment and differentiation processes in the Drosophila embryo.

20 anterior-posterior axis along the developing Drosophila embryo.

21 n and activation of Torso at the ends of the Drosophila embryo.

22 elopmental control genes active in the early Drosophila embryo.

23 is pervasively used in the patterning of the Drosophila embryo.

24 long the anterior posterior (AP) axis of the Drosophila embryo.

25 axon guidance and target recognition in the Drosophila embryo.

26 ne how they come to bind Pol II in the early Drosophila embryo.

27 ss the dorsal-ventral (DV) axis of the early Drosophila embryo.

28 es cell-sheet fusion (dorsal closure) in the Drosophila embryo.

29 ut neural specific, glycan expression in the Drosophila embryo.

30 ong the midline in the ventral nerve cord of Drosophila embryo.

31 al segments and primordial germ cells in the Drosophila embryo.

32 lasma membrane growth of the mesoderm in the Drosophila embryo.

33 zed patterns of gene expression in the early Drosophila embryo.

34 organizes the anterior/posterior axis of the Drosophila embryo.

35 anscription factor Dorsal in the precellular Drosophila embryo.

36 ection of a proneural cell fate in the early Drosophila embryo.

37 e range of transcription factors in the live Drosophila embryo.

38 polarity during convergent extension in the Drosophila embryo.

39 myosin dynamics during dorsal closure in the Drosophila embryo.

40 identify interacting partners of Mst in the Drosophila embryo.

41 expression patterns in the blastoderm-stage Drosophila embryo.

42 rane cytoskeleton restraint in the syncytial Drosophila embryo.

43 200 spatiotemporal expression domains in the Drosophila embryo.

44 ated by its non-catalytic CUB domains in the Drosophila embryo.

45 ing the regulation of hunchback in the early Drosophila embryo.

46 es of epithelial cell junctions in the early Drosophila embryo.

47 uch as the development of the trachea of the Drosophila embryo.

48 rior-posterior patterning genes in the early Drosophila embryo.

49 essor of Hairless [Su(H)], in patterning the Drosophila embryo.

50 amics during single-cell wound repair in the Drosophila embryo.

51 behaviors, such as during dorsal closure in Drosophila embryos.

52 d cell motility across the segment border in Drosophila embryos.

53 sults in the formation of thinner muscles in Drosophila embryos.

54 nd repair in the epidermis of early and late Drosophila embryos.

55 ificities that are sequentially expressed in Drosophila embryos.

56 present high resolution Hi-C data from early Drosophila embryos.

57 cytoplasmic dynein-driven lipid droplets in Drosophila embryos.

58 for function in human colon cancer cells and Drosophila embryos.

59 both correct and off-target muscle fibers in Drosophila embryos.

60 intenance elements during DNA replication in Drosophila embryos.

61 modify the lifetime of Dronpa-Bcd in living Drosophila embryos.

62 ession (stripes 3 and 7) in blastoderm stage Drosophila embryos.

63 mechanical response of motor neurons in live Drosophila embryos.

64 cluster spatial gene expression patterns in Drosophila embryos.

65 pared gene expression in haploid and diploid Drosophila embryos.

66 ia its phosphatase domain with N-cadherin in Drosophila embryos.

67 rom RNA in situ hybridization experiments of Drosophila embryos.

68 sets up the anterior-posterior axis in early Drosophila embryos.

69 culturing of primary cells dissociated from Drosophila embryos.

70 es of the Hunchback (Hb) protein gradient in Drosophila embryos.

71 ity and emergence of coordinated movement in Drosophila embryos.

72 of heterochromatin domain formation in early Drosophila embryos.

73 y test these notions using lipid droplets in Drosophila embryos.

74 osaminoglycan, O-linked glycans expressed in Drosophila embryos.

75 ibutions to the rapid syncytial divisions of Drosophila embryos.

76 ch to analyze transport of lipid droplets in Drosophila embryos.

77 r of primordial germ cell (PGC) formation in Drosophila embryos.

78 d insulator activity in human K562 cells and Drosophila embryos.

79 muli: anoxia-induced developmental arrest in Drosophila embryos.

80 contraction and tissue folding in developing Drosophila embryos.

81 opy (RLSM) to image highly opaque late-stage Drosophila embryos.

82 he three-dimensional epidermal structures of Drosophila embryos.

83 e examine transcriptional bursting in living Drosophila embryos.

84 ve mesoderm and neurogenic ectoderm of early Drosophila embryos.

85 int segmentation and cell tracking in entire Drosophila embryos.

86 a new regulator of beta-catenin abundance in Drosophila embryos.

87 alyzing histone marks and gene expression in Drosophila embryos.

88 hat mediates rapid furrow formation in early Drosophila embryos.

89 ndle elongation using experimental data from Drosophila embryos.

90 f fast cellular dynamics across gastrulating Drosophila embryos.

91 s-knirps, hunchback, and snail-in developing Drosophila embryos.

92 rtex, maintain genome integrity in syncytial Drosophila embryos.

93 tudy scaled anterior-posterior patterning in Drosophila embryos.

94 using light sheet microscopy to image whole Drosophila embryos.

95 ablishment of the anterior-posterior axis in Drosophila embryos.

96 detect and map genome methylation in stage 5 Drosophila embryos.

97 these insertions, called the CPTI lines, in Drosophila embryos.

98 and influence the resolution of infection in Drosophila embryos.

99 thway is essential for wound closure in late Drosophila embryos.

100 y the segmentation gene cascade in the early Drosophila embryo [1].

101 ling of morphogen gradients in the syncytial Drosophila embryo, a single cell with multiple dividing

102 In Drosophila embryos, a concentration gradient of nuclear

103 In Drosophila embryos, a nuclear gradient of the Dorsal (Dl

104 ng cellularization, the first cytokinesis in Drosophila embryos, a reservoir of microvilli unfolds to

105 ation of chromatin remodeling factor CHD1 in Drosophila embryos abolishes incorporation of H3.3 into

106 et, including published RNAi screening using Drosophila embryos [Additional files 1, 2], dataset for

107 required for cell-autonomous Hh response in Drosophila embryos, alone suffices to rescue embryonic H

108 ndent inductive signaling event in the early Drosophila embryo, an experimental system that offers un

109 k that contributes to regionalization of the Drosophila embryo and establishes the domains of Hox pro

110 the onset of ventral furrow formation in the Drosophila embryo and in the process of hair-cell determ

111 precursors cover the ventral surface of the Drosophila embryo and larva and provide templates for cu

112 Dpp and regulate its signalling in both the Drosophila embryo and ovary.

113 s a chemoattractant for PGC migration in the Drosophila embryo and that downstream signaling proteins

114 on the Bicoid/Hunchback system in the early Drosophila embryo and that this system achieves approxim

115 the specification of the mesectoderm in the Drosophila embryo and the endomesoderm in the sea urchin

116 be protocols for labeling apoptotic cells in Drosophila embryos and adult male gonads.

117 Septin complex was purified from Drosophila embryos and also reconstituted from recombina

118 n epidermal cells surrounding wounds in late Drosophila embryos and early larvae.

119 l analysis on endogenous Notch purified from Drosophila embryos and found that the glycosylation stat

120 ecipitation microarray (ChIP-chip) assays in Drosophila embryos and identified three distinct Pol II

121 ctopic expression of the spider Antp gene in Drosophila embryos and imaginal tissue that this unique

122 thermore, LC8 decorates microtubules both in Drosophila embryos and in HeLa cells, increases the micr

123 In Drosophila embryos and larvae, a small number of identif

124 olymerase (Pol II) is a pervasive feature of Drosophila embryos and mammalian stem cells, but its rol

125 ion tissue anisotropy maps across developing Drosophila embryos and quantified differences in cell-sh

126 ormed ChIP-seq experiments on tightly staged Drosophila embryos and show that massive recruitment of

127 thologs could substitute for Shrub in mutant Drosophila embryos and that loss of Shrub function cause

128 ease recognition site into I-SceI expressing Drosophila embryos and used Illumina amplicon sequencing

129 entified as the earliest wound attractant in Drosophila embryos and zebrafish larvae.

130 gulating spatial gene expression patterns in Drosophila embryo, and show that DNA shape-based models

131 ila eggs, duplication of free centrosomes in Drosophila embryos, and centrosome amplification in cult

132 A loss of LC8 function causes apoptosis in Drosophila embryos, and its overexpression induces malig

133 idate MEDUSA by quantifying wound closure in Drosophila embryos, and we show that the results of our

134 Terminal regions of the Drosophila embryo are patterned by the localized activat

135 tion and cytoskeletal planar polarity in the Drosophila embryo are regulated by a common signal provi

136 Drosophila embryos are highly sensitive to gamma-ray-ind

137 Fixed Drosophila embryos are hybridized in solution with a mix

138 segments in Drosophila melanogaster Whereas Drosophila embryos are long-germ, with segments specifie

139 rmation, in bits, using the gap genes in the Drosophila embryo as an example.

140 ls migrate from posterior to anterior of the Drosophila embryo as two bilateral streams of cells to s

141 te synchronously towards the anterior of the Drosophila embryo as two distinct groups located on each

142 inant of epithelial apical-basal polarity in Drosophila embryos, as an upstream component of the Hipp

143 The Drosophila embryo at the mid-blastula transition (MBT) c

144 rentially with one of the two centrosomes in Drosophila embryos at cellular blastoderm stage.

145 Segmentation of the Drosophila embryo begins with the establishment of spati

146 ted to reconstitute Galileo transposition in Drosophila embryos but no events were detected.

147 s are not required for axon extension in the Drosophila embryo, but rather are specifically required

148 ional during the rapid mitotic cycles of the Drosophila embryo; but its genetic inactivation had no c

149 nes contribute to the regionalization of the Drosophila embryo by establishing fields in which specif

150 ogy of epithelial cells in the cellularizing Drosophila embryo by injecting magnetic particles and st

151 Knirps has essential roles in patterning the Drosophila embryo by means of short-range repression, an

152 boundaries of gene expression emerge in the Drosophila embryo by measuring the absolute number of ac

153 pathway specifies neuronal identities in the Drosophila embryo by regulating developmental patterning

154 believed to be established in pre-blastoderm Drosophila embryos by the diffusion of Bcd protein after

155 genous cargoes, lipid droplets purified from Drosophila embryos, can be used to perform high-precisio

156 Loss and gain of pbl function in Drosophila embryos cause pattern defects that indicate a

157 Our findings show that in Drosophila embryos, Cdk1 positive feedback serves primar

158 fered considerably from analogous studies in Drosophila embryo cells that did not exhibit a similar a

159 om several systems including mouse liver and Drosophila embryos characterizing over 5,500 and 13,000

160 For Drosophila embryo cleavage, this growth is rapid but reg

161 H2a and H2b are stored in lipid droplets in Drosophila embryos complexed with the protein Jabba.

162 event accumulation of excess histones, early Drosophila embryos contain massive extranuclear histone

163 AP polarity of the Drosophila embryo depends on bicoid, which is necessary

164 ning of the dorsal-ventral axis in the early Drosophila embryo depends on the nuclear distribution of

165 The dorsoventral (DV) patterning of the Drosophila embryo depends on the nuclear localization gr

166 hment of dorsal-ventral (DV) polarity in the Drosophila embryo depends upon a localized signal that i

167 ch to our understanding of these events: the Drosophila embryo; developing and regenerating mouse mus

168 hat exhibit highly dynamic behavior in early Drosophila embryo development.

169 In Drosophila embryos, disco and the paralogous disco-relat

170 ion in embryo size affects patterning of the Drosophila embryo dorsal-ventral (DV) axis is not known.

171 Drosophila embryo dorsoventral (DV) polarity is defined

172 itch-like entry into mitosis observed in the Drosophila embryo during the 14(th) mitotic cycle is tim

173 phosphatase (GTPase) remains inactive within Drosophila embryos during the first two-thirds of embryo

174 Here, we show that laser wounding of the Drosophila embryo epidermis triggers an instantaneous ca

175 Using whole-mount in situ hybridization in Drosophila embryos exposed to constitutively active RTK

176 Here we demonstrate that Drosophila embryos expressing catalytically deficient Tr

177 In early Drosophila embryos, forks starting from closely spaced o

178 In the Drosophila embryo, formation of a bone morphogenetic pro

179 which cell-surface proteins are expressed in Drosophila embryos from GAL4-dependent insertion lines a

180 In the Drosophila embryo, germ plasm is anchored to the posteri

181 Recent work in the Drosophila embryo has begun to shed light on this proble

182 The Drosophila embryo has recently emerged as a powerful mod

183 fic group of enhancers that act in the early Drosophila embryo have a highly conserved arrangement of

184 uter simulations and quantitative imaging of Drosophila embryos have been used to recreate the dynami

185 ing human embryonic stem cells and the early Drosophila embryo, have begun to challenge this view.

186 n of microtubule alignment within developing Drosophila embryos, here we demonstrate that microtubule

187 ith those of the corresponding system in the Drosophila embryo, highlighting distinct and common path

188 Here, we find that in early Drosophila embryos, histone balance in the nuclei is reg

189 r (SOP) cells within distinct regions of the Drosophila embryo in an epidermal growth factor-dependen

190 probes are hybridized to fixed, mixed-staged Drosophila embryos in 96-well plates.

191 tocol for RNA in situ hybridization (ISH) to Drosophila embryos in a 96-well format.

192 a microfluidic device to rapidly orient >700 Drosophila embryos in parallel for end-on imaging.

193 approach to annotate developmental stage for Drosophila embryos in the gene expression images.

194 nce of a second mechanism that polarizes the Drosophila embryo, in addition to the ventrally restrict

195 We examined dNTP metabolism in the early Drosophila embryo, in which gastrulation is preceded by

196 lled RNA Polymerase II (Pol II) in the early Drosophila embryo, including four of the eight Hox genes

197 oundaries that separate every segment of the Drosophila embryo into anterior and posterior compartmen

198 De novo formation of cells in the Drosophila embryo is achieved when each nucleus is surro

199 The development of the precellular Drosophila embryo is characterized by exceptionally rapi

200 Dorsoventral (DV) patterning of the Drosophila embryo is controlled by a concentration gradi

201 The dorsal-ventral patterning of the Drosophila embryo is controlled by a well-defined gene r

202 Gene expression in the Drosophila embryo is controlled by functional interactio

203 pical secretion from epithelial tubes of the Drosophila embryo is mediated by apical F-actin cables g

204 Gastrulation of the Drosophila embryo is one of the most intensively studied

205 The early Drosophila embryo is patterned by graded distributions o

206 The anterior region of the Drosophila embryo is patterned by the concentration grad

207 Dorsoventral patterning of the Drosophila embryo is regulated by graded distribution of

208 Cellularization of the Drosophila embryo is the process by which a syncytium of

209 Furrow formation in early syncytial Drosophila embryos is exceptionally rapid, with furrows

210 Anaphase B in Drosophila embryos is initiated by the inhibition of mic

211 dies of dorsal-ventral polarity in the early Drosophila embryo, is well known for its role in the inn

212 es also function in vivo: when injected into Drosophila embryos lacking droplet-bound histones, bacte

213 In Drosophila embryos lacking the alpha(2)delta-3 subunit o

214 We propose that in Drosophila embryos, lipid droplets serve as a histone bu

215 cules via RNA strand exchange in a cell-free Drosophila embryo lysate, a step beyond simple buffered

216 In the early Drosophila embryo, measurements of the morphogen Dorsal,

217 ell wound repair in the genetically amenable Drosophila embryo model.

218 In Drosophila, embryos mutant for giant show a gap in the a

219 In the Drosophila embryo, Nanos and Pumilio collaborate to repr

220 In the early Drosophila embryo, Nuclear-fallout (Nuf), a Rab11 effect

221 In many cell types, including early Drosophila embryos, Nuf/FIP3, a Rab11 effector, mediates

222 er cells, and most restore Wnt regulation in Drosophila embryos null for both fly APCs.

223 fects of the geometry of the early syncytial Drosophila embryo on the effective diffusivity of cytopl

224 hereas the preparation of primary cells from Drosophila embryos only requires 2-4 h.

225 imaging of developmental gene expression in Drosophila embryos opens up exciting new prospects for u

226 lls and internalized mesodermal cells within Drosophila embryos over 2 hours during gastrulation.

227 nuclear concentration gradient in the early Drosophila embryo, patterning the dorsal-ventral (DV) ax

228 repressor complexes have been purified from Drosophila embryos: PRC1, PRC2, Pcl-PRC2 and PhoRC.

229 LC8 decorates microtubules in vitro and in Drosophila embryos, promotes microtubule assembly, and s

230 prior to nuclear envelope breakdown (NEB) in Drosophila embryos, proper centrosome separation does no

231 Drosophila embryos provide a superb model.

232 The Bicoid gradient in the Drosophila embryo provided the first example of a morpho

233 Patterning of the terminal regions of the Drosophila embryo relies on the gradient of phosphorylat

234 Patterning in the Drosophila embryo requires local activation and dynamics

235 Anterior-posterior axis patterning of the Drosophila embryo requires Nanos activity selectively in

236 TRIP and NOPO E3 ligases in human cells and Drosophila embryos, respectively, and show that TRIP pro

237 tent with this, removal of the ASAD from the Drosophila embryo results in beta-cat/Arm accumulation a

238 functions of both Forkhead genes in the same Drosophila embryo results in defective hearts with missi

239 ing DNA and an increase in S-phase length in Drosophila embryos, revealing an unexpected role for Cdk

240 In early Drosophila embryos, several mitotic cycles proceed with

241 nd the activation of the morphogen dorsal in Drosophila embryos show striking structural and function

242 nts of the Hunchback transcription factor in Drosophila embryos show that its target genes can respon

243 -5, KLP61F, in astral, centrosome-controlled Drosophila embryo spindles and to test the hypothesis th

244 In early Drosophila embryos, ST also caused increased microtubule

245 In this issue, Song et al. (2017) show that Drosophila embryos synthesize a large fraction of nucleo

246 singly, despite the breakneck speed at which Drosophila embryos synthesize DNA, maternally deposited

247 esolution dataset of a genetically perturbed Drosophila embryo that captures all cells in 3D.

248 tability of the Bicoid morphogen gradient in Drosophila embryos that express a Bicoid-eGFP fusion pro

249 We show that the centrioles in Drosophila embryos that lack the centrosomal protein Cen

250 . show through analysis of the oskar mRNA in Drosophila embryos that regulatory elements within mRNAs

251 We show that in Drosophila embryos the MPM-2 monoclonal antibody, raised

252 les concern the Bicoid gradient in the early Drosophila embryo, the dorsoventral patterning of a frog

253 l processes, including the patterning of the Drosophila embryo, the establishment of diverse neuronal

254 For the Drosophila embryo, the following two functional classes

255 anterior-posterior axis specification in the Drosophila embryo, the Hunchback (Hb) protein forms a sh

256 We propose that in Drosophila embryos, the latter process (anaphase B) depe

257 In Drosophila embryos, the midblastula transition (MBT) dra

258 In early Drosophila embryos, the transcription factor Dorsal regu

259 of precision for the Bicoid morphogen in the Drosophila embryo: the concentration differences that di

260 In the Drosophila embryo, these cells have been termed founder

261 In the Drosophila embryo, this process occurs asymmetrically be

262 tes a highly ordered square cell grid in the Drosophila embryo through sequential and spatially regul

263 larization in the anterior pole of the early Drosophila embryo to explore how cells compete for space

264 Here we use the Drosophila embryo to investigate how hemocytes (Drosophi

265 BMPs changed the steep BMP gradient found in Drosophila embryos to a shallower profile, analogous to

266 article tracking velocimetry in gastrulating Drosophila embryos to measure the movement of cytoplasm

267 erate abundant neurons were established from Drosophila embryos to study silencing of genes by RNA in

268 ion, the first complete cytokinetic event in Drosophila embryos, to show that cleavage furrow ingress

269 In the Drosophila embryo, Toll is required to establish gene ex

270 The Drosophila embryo transiently exhibits a double-segment

271 The Drosophila embryo undergoes several cycles of rapid furr

272 determinants Dorsal, Twist, and Snail in the Drosophila embryo using chromatin immunoprecipitation co

273 irst wave of de novo transcription in living Drosophila embryos using dual-fluorescence detection of

274 id from three dipteran species in transgenic Drosophila embryos using the Drosophila bicoid cis-regul

275 ws for the quantification of single mRNAs in Drosophila embryos, using commercially available smFISH

276 Cell rearrangements shape the Drosophila embryo via spatially regulated changes in cel

277 ts within single cells of fixed, whole-mount Drosophila embryos via a combination of FISH, immunohist

278 by studies of pattern formation in the early Drosophila embryo, we analyze cascades of 2-state reacti

279 genetic and imaging experiments in the early Drosophila embryo, we describe a signal integration mech

280 ng dorsal-ventral (DV) axis formation in the Drosophila embryo, we find that the poised enhancer sign

281 specific transcription factors active in the Drosophila embryo, we found that binding of all factors

282 on genetic and imaging studies in the early Drosophila embryo, we found that Torso RTK signaling can

283 To address this issue in the early Drosophila embryo, we sought to count individual materna

284 Using single-molecule mRNA quantification in Drosophila embryos, we determine the magnitude of fluctu

285 tivation approaches and live-cell imaging in Drosophila embryos, we dissect the role of condensin I i

286 programs that ultimately lead to patterns in Drosophila embryos, we manipulate maternally supplied pa

287 By monitoring transcription in living Drosophila embryos, we provide the first evidence for tr

288 Here we address this question using early Drosophila embryos where the maternal gradient Bicoid (B

289 ty in these mutants is evident in developing Drosophila embryos where tissue recoil following laser a

290 in the first mitotic divisions of the early Drosophila embryo, where groups of epithelial cells sync

291 Zelda (Zld) plays such a role in the Drosophila embryo, where it has been shown to control th

292 eloping a barbed end incorporation assay for Drosophila embryos, which revealed barbed end enrichment

293 tial for it to direct myoblast fusion in the Drosophila embryo, while the conserved DCrk-binding prol

294 along the dorsal-ventral (DV) axis of early Drosophila embryos, while repressors establish ventral b

295 of defined mRNA structures was monitored in Drosophila embryo whole-cell lysates.

296 Bicoid-dependent transcription in the early Drosophila embryo with high temporal resolution, allowin

297 ets, performing ChIP-seq for the TF Twist in Drosophila embryos with different experimental fragment

298 e amnioserosa cells during dorsal closure in Drosophila embryos with in vivo imaging of green-fluores

299 Drosophila embryos with mutations in the JAK/Stat ligand

300 Drosophila embryos with trr alleles encoding catalytic m