ライフサイエンスコーパス: embryogenesis

1 in preparation for rapid cell cycles during embryogenesis.

2 ficantly to developmental studies, including embryogenesis.

3 rain development simultaneously occur during embryogenesis.

4 nal factors and/or extraembryonic tissues in embryogenesis.

5 mmation, Ripk1(D325A/D325A) mice died during embryogenesis.

6 at control the highly coordinated process of embryogenesis.

7 sponge regeneration is as equally dynamic as embryogenesis.

8 housands of genes during spermatogenesis and embryogenesis.

9 heir use as a tractable model of early human embryogenesis.

10 s that act through this pathway to influence embryogenesis.

11 targeted knockdowns that can last throughout embryogenesis.

12 s had already emerged at this early stage of embryogenesis.

13 every 2 minutes during Phallusia mammillata embryogenesis.

14 iogenesis of the primary cilium during mouse embryogenesis.

15 w this process is modified during nonzygotic embryogenesis.

16 rliest hemato-endothelial progenitors during embryogenesis.

17 ometry in shaping morphogen signaling during embryogenesis.

18 ncomplete separation of the forebrain during embryogenesis.

19 of miRNAs and associated targets throughout embryogenesis.

20 as a platform to study the energy budget of embryogenesis.

21 al YDA-dependent signaling events, including embryogenesis.

22 to zygotic transition (MZT) during zebrafish embryogenesis.

23 fate specification and cell behavior during embryogenesis.

24 and as a transcriptional repressor in mouse embryogenesis.

25 identified many genes that are essential for embryogenesis.

26 , an essential gene for stomach formation in embryogenesis.

27 rgets or how binding affects Bicc1-dependent embryogenesis.

28 AH5 deficiency at the molecular level during embryogenesis.

29 essential for cell fate specification during embryogenesis.

30 city in the heat dissipated during zebrafish embryogenesis.

31 osomal components, are capable of completing embryogenesis.

32 disrupt male fertility and potentially early embryogenesis.

33 ng to the establishment of the blueprint for embryogenesis.

34 lipoprotein (LDL)-like particles to promote embryogenesis.

35 Arpp19, but not Ensa, is essential for mouse embryogenesis.

36 he regulation of the cell cycle during early embryogenesis.

37 tion, proliferation and cell survival during embryogenesis.

38 crease in mitophagy levels during Drosophila embryogenesis.

39 ritical roles in mammalian gametogenesis and embryogenesis.

40 cells, whereas H3K27 was essential for late embryogenesis.

41 is determined by ambient temperature during embryogenesis.

42 tion, occurring in XX cells outside of early embryogenesis.

43 ges were similar between somatic and zygotic embryogenesis.

44 ation regulator in orchestrating early mouse embryogenesis.

45 eam transcriptional regulator of Yes1 during embryogenesis.

46 transcriptional cis regulators during early embryogenesis.

47 ow proliferation and growth are timed during embryogenesis.

48 functioning nervous system to develop during embryogenesis.

49 rlying two-segment-wide prepattern directing embryogenesis.

50 cess recapitulating aspects of early in vivo embryogenesis.

51 d in the parental bias of mutations in early embryogenesis.

52 nd thus creates a powerful approach to study embryogenesis.

53 e precluded assessment of Crk's full role in embryogenesis.

54 cting how functioning circuits emerge during embryogenesis.

55 to scRNA-seq data from early stages of mouse embryogenesis.

56 xpression of maternal histones in Drosophila embryogenesis.

57 amics during an inaccessible period of human embryogenesis.

58 verns mesodermal fate decisions early during embryogenesis.

59 ochromatin formation during early Drosophila embryogenesis.

60 e undergoes reprogramming in preparation for embryogenesis.

61 rovides a powerful model system for studying embryogenesis.

62 er NSCs enter G(0) or G(2) quiescence during embryogenesis.

63 on the spatiotemporal resolution of cells in embryogenesis.

64 ogenetic event that occurs during C. elegans embryogenesis.

65 file, and magnitude of p53 activation during embryogenesis.

66 rbon, and this appears to be critical during embryogenesis.

67 own about its role in colon formation during embryogenesis.

68 nt opposes cell differentiation during early embryogenesis.

69 animals do not sequester a germ line during embryogenesis.

70 ial cellular organization is fundamental for embryogenesis.

71 laminin also preserves PGC quiescence during embryogenesis.

72 lation in vertebrates, is a critical step in embryogenesis.

73 Rs) in gametes or their maintenance in early embryogenesis.

74 y regulation in cell formation in Drosophila embryogenesis.

75 n understanding developmental patterning and embryogenesis.

76 ell fate and tissue shape during early human embryogenesis.

77 common evolutionary mechanism for changes in embryogenesis.

78 fficient to rescue the tps1-1 mutant through embryogenesis.

79 -associated protein, Hedgehog signaling, and embryogenesis.

80 h small and canonical ORFs from mRNAs across embryogenesis.

81 which may reflect the requirements of early embryogenesis.

82 t cells at a late post-implantation stage of embryogenesis.

83 y differences exist between regeneration and embryogenesis.

84 bility barrier for eggshell synthesis during embryogenesis.

85 n (smFISH) studies in Caenorhabditis elegans embryogenesis.

86 biology including crucial cellular events in embryogenesis.

87 ESC-TSC pairing, and consequently synthetic embryogenesis.

88 egans embryos at different stages throughout embryogenesis.

89 in a RIPK3- and MLKL-dependent manner during embryogenesis(1-3).

90 essenger RNA processing, cell signalling and embryogenesis(1-4).

91 d to maternal immune activation (MIA) during embryogenesis(3,4) with mouse models that are geneticall

92 ion catalogue of wild-type mice during early embryogenesis (4-36 somites).

93 Late Embryogenesis Abundant (LEA) proteins are mostly predict

94 Late embryogenesis abundant (LEA) proteins containing seed ma

95 uding type 2C protein phosphatases, the LATE EMBRYOGENESIS ABUNDANT PROTEIN4-5 genes, and homologs of

96 on-tolerant (DT) taxa, including, e.g., late embryogenesis abundant proteins (LEA) and reactive oxyge

97 t, and to feminizing temperatures where most embryogenesis accrues.

98 49%, respectively) affecting the sea urchin embryogenesis activity.

99 ehog signaling governs critical processes in embryogenesis, adult stem cell maintenance, and tumorige

100 ular pathways that trigger the initiation of embryogenesis after fertilization in flowering plants, a

101 essed throughout plant development including embryogenesis and AtBUD13 proteins is localized in the n

102 ributions to enhancer commissioning in early embryogenesis and bookmarking enhancers to enable rapid

103 and crucial for the cellular dynamics during embryogenesis and cancer progression.

104 iginating from pluripotent stem cells during embryogenesis and continuing even as matured lymphocytes

105 factor) complex and plays a crucial role in embryogenesis and corticogenesis.

106 As billions of cells die during mammalian embryogenesis and daily in adult organisms, clearing dea

107 DNA methylation is essential for normal embryogenesis and development in mammals and can be capt

108 xtending the rejuvenation phase during early embryogenesis and editing the genome, it may be possible

109 pression mechanism is not operational during embryogenesis and emerges when the heart begins to matur

110 GPs are known to promote PGC survival during embryogenesis and exit from quiescence after hatching, a

111 ERBB4 signaling is involved in embryogenesis and homeostasis of healthy adult tissues,

112 ily of serpentine receptors is essential for embryogenesis and homeostasis, and stringent control of

113 gnaling systems that plays many roles during embryogenesis and in adults; abnormal HH signaling can l

114 The zebrafish is ideal for studying embryogenesis and is increasingly applied to model human

115 2 (ROR2), is normally expressed only during embryogenesis and is tightly down-regulated in postnatal

116 sympathetic innervation of the heart during embryogenesis and its importance for cardiac development

117 decompaction is initially established during embryogenesis and maintained throughout larval developme

118 Tgifs are essential for embryogenesis and may function in tumor progression.

119 clade transcriptional repressor WOX genes in embryogenesis and meristems maintenance, but the mechani

120 enerate an integrated understanding of early embryogenesis and new strategies for therapeutic interve

121 ose 6-phosphate (Tre6P) and is essential for embryogenesis and normal postembryonic growth and develo

122 lar events that build the human brain during embryogenesis and of how abnormalities in this process l

123 provide a unique platform for studying early embryogenesis and pave the way to creating viable synthe

124 in, Drp1 (dynamin-related protein 1), die in embryogenesis and show an accumulation of clustered mito

125 morphogens direct cell fate decisions during embryogenesis and signal to maintain tissue homeostasis

126 enhancers are active during early Drosophila embryogenesis and that by focusing on a single, relative

127 tial to a range of processes associated with embryogenesis and tissue homeostasis.

128 naling is one of the key cascades regulating embryogenesis and tissue homeostasis; it has also been i

129 ption factor that has essential roles during embryogenesis and tumorigenesis.

130 erochromatin establishment during vertebrate embryogenesis and uncover functions for Smarca2 in prote

131 In humans this process only occurs during embryogenesis and viable strategies to induce new HFs in

132 nerally expressed in plants as a response to embryogenesis and water-related stress.

133 ation of cell junctions in processes such as embryogenesis and wound healing and also explain the piv

134 sses associated with cell migration, such as embryogenesis and wound healing.

135 orm a single-cell RNA-sequencing analysis of embryogenesis and X chromosome inactivation in a marsupi

136 ide insights into the evolution of mammalian embryogenesis and X dosage compensation.

137 Fam20C orthologue, contributes to fertility, embryogenesis, and development.

138 ional gene required for NAD synthesis during embryogenesis, and NADSYN1 has bi-allelic missense varia

139 demethylation during early zygote formation, embryogenesis, and neuronal differentiation and is intol

140 model for disease, drug discovery, toxicity, embryogenesis, and neuroscience.

141 d system models primate-specific features of embryogenesis, and that gastruloid cells exhibit evoluti

142 ogical processes including neurodevelopment, embryogenesis, and tumorigenesis.

143 dynamic behaviors during tissue development, embryogenesis, and wound healing.

144 ion, particularly during differentiation and embryogenesis; and (c) mitonuclear coregulation adapted

145 SCs in vertebrate ears stop dividing during embryogenesis; and soon after birth, vestibular SCs in m

146 th angiogenesis), and SALL4 (associated with embryogenesis/angiogenesis), for ubiquitin-mediated degr

147 ram and the appearance of PAX7+ cells during embryogenesis are poorly understood.

148 Here we used auxin-dependent suspensor embryogenesis as a model to determine transcriptome chan

149 nd cRGCs arise as early as E14, not later in embryogenesis as reported.

150 nase II (CaMKII) activation are required for embryogenesis, as well as neuronal, immunological, and c

151 Fgf8 is expressed transiently during embryogenesis at the midbrain-hindbrain border, an area

152 , which starts, in Arabidopsis thaliana, mid-embryogenesis, at about the same time and developmental

153 e coproduced in most pancreatic cells during embryogenesis but become much more enriched in endocrine

154 rians, axial patterning is not restricted to embryogenesis but continues throughout a prolonged life

155 Embryonic stem cells can reintegrate into embryogenesis but contribute primarily to epiblast linea

156 phila, we find that Vps29 is dispensable for embryogenesis but required for retromer function in agin

157 ct of a retinoic acid-responsive gene during embryogenesis, but currently viewed as a multifaceted fa

158 ct patterns of gene expression to coordinate embryogenesis, but how spatiotemporal expression diversi

159 ts to be expressed in mammalian cells during embryogenesis, but its role in cellular fitness has long

160 gene silencing is incompletely set early in embryogenesis, but nevertheless is repeatedly lost and g

161 n of the pancreatic endocrine lineage during embryogenesis, but the role of Notch in mature beta cell

162 domains were essential for the regulation of embryogenesis by Bicc1.

163 thematically model basal ECM turnover during embryogenesis by exploiting our ability to live image de

164 vement of nuclear pore complex components in embryogenesis, cell differentiation and tissue-specific

165 During embryogenesis cells make fate decisions within complex t

166 During embryogenesis, chromatin accessibility profiles control

167 ive studies of pancreatic islet cells, mouse embryogenesis datasets and the integration of scRNA-seq

168 During mammalian embryogenesis, de novo hematopoiesis occurs transiently

169 iological functions and processes, including embryogenesis, development, and homeostasis.

170 During embryogenesis, different signaling pathways are repeated

171 During mammalian embryogenesis, differential gene expression gradually bu

172 S, die with identical phenotypes during late embryogenesis due to perturbations in gene expression th

173 150 participants seeking to reverse-engineer embryogenesis, emphasizing quantitative simulation and t

174 ular and nervous systems that begin early in embryogenesis establishing their future interactions and

175 D1 prod double mutants die during embryogenesis, exhibiting enhanced phenotypes associated

176 During mammalian embryogenesis, extensive cellular remodeling is needed f

177 During embryogenesis, FAMK-1 maintains intercellular partitions

178 IN) is a common phenomenon in cleavage-stage embryogenesis following in vitro fertilization (IVF)(1-3

179 are required to uncover critical aspects of embryogenesis, for example, subtle phenotypic difference

180 misprocessing mutations that mediate viable embryogenesis furthers our understanding of LCC molecula

181 spos-LGR4 signaling plays important roles in embryogenesis, gastrointestinal homeostasis, and food in

182 that Tnt1 actively transposed during somatic embryogenesis, generating an average of 6.37 insertions

183 Although the development of BAT during embryogenesis has been well addressed in rodents, how BA

184 on in morphogenetic events in early metazoan embryogenesis has not been carried out.

185 eating the cellular foundations of mammalian embryogenesis have emerged recently.

186 n, and how the endocardium segregates during embryogenesis have remained largely unknown, however.

187 ompact chromatin near its target loci during embryogenesis (hours prior to major transcriptional acti

188 tical for dramatic cellular movements during embryogenesis; however, tumor cells can reactivate EMT p

189 PRM analysis of zebrafish embryogenesis identified developmental stage-specific ce

190 platform for investigating post-implantation embryogenesis in a dish.

191 of proliferating progenitors persisting post embryogenesis in a newly identified retinociliary juncti

192 Large numbers of genes essential for embryogenesis in Arabidopsis encode enzymes of plastidia

193 required for male sex determination in early embryogenesis in B. dorsalis as an intermediate male det

194 studies that quantified the energy budget of embryogenesis in Drosophila and started to untangle the

195 omozygous TBX4 inactivating mutations during embryogenesis in humans.

196 racks the progression of the epiblast during embryogenesis in Macaca fascicularis, but shows greater

197 cular mechanisms underlying nonhuman primate embryogenesis in the early postimplantation period, with

198 0/125 (16.0%) living female worms had normal embryogenesis in the IVM annual, IVM semiannual, IVM+ALB

199 0/125 (16.0%) living female worms had normal embryogenesis in the IVM annual, IVM semiannual, IVM+ALB

200 by females did not affect their fecundity or embryogenesis in their progeny.

201 We find embryogenesis in V. tsujii ranges from 25-38 days, and t

202 gment in the eyes, has been recruited during embryogenesis in various extraocular tissues including a

203 derived stem cells can be generated to mimic embryogenesis in vitro.

204 equired for chromatin accessibility in early embryogenesis, in contrast to its essential functions la

205 ound that rpl15 null mutants do not complete embryogenesis, indicating that RPL15 is an essential gen

206 Early embryogenesis is a conserved and self-organized process.

207 Post-implantation embryogenesis is a highly dynamic process comprising mul

208 Early embryogenesis is accompanied by reductive cell divisions

209 Somatic embryogenesis is an important tissue culture technique t

210 n disaggregation and animal ABCF proteins in embryogenesis is consistent with the possibility that me

211 Heterogeneity of lymphatic vessels during embryogenesis is critical for organ-specific lymphatic f

212 incipal determinant of ZGA during vertebrate embryogenesis is debated.

213 Embryogenesis is directed by morphogens that induce diff

214 Human embryogenesis is hallmarked by two phases of yolk sac de

215 A long-standing question in the field of embryogenesis is how the zygotic genome is precisely act

216 st that the requirement for fertilization in embryogenesis is mediated by male-genome transmission of

217 patterned and functionally assembled during embryogenesis is poorly understood.

218 Although chemical signaling during embryogenesis is readily addressed by a plethora of avai

219 Thus, degradation of RA during embryogenesis is required for formation of highly specia

220 A defining feature of early embryogenesis is the transition from maternal to zygotic

221 on reprogramming, as occurs during mammalian embryogenesis, is a major hindrance for the transmission

222 is present within neurogenic regions during embryogenesis, is found in cultured neurons and can modu

223 the ECM can undergo acute remodeling during embryogenesis, it is experimentally difficult to determi

224 ing dispensable for SAN morphogenesis during embryogenesis, its deletion hampers atrial activation by

225 ing the transcriptional impact of TEs during embryogenesis, KZFPs facilitate their genome-wide incorp

226 During zebrafish embryogenesis, large muscle segments, called myotomes, a

227 hat induces epiboly defects during zebrafish embryogenesis, leading to the disruption of dorsoventral

228 During embryogenesis, morphogens form a concentration gradient

229 egulatory networks (GRNs) that direct animal embryogenesis must respond to varying environmental and

230 tol (GPI)-anchored proteins are critical for embryogenesis, neurogenesis, and cell signaling.

231 ring various biological processes, including embryogenesis, neuronal pathfinding, and tumor formation

232 During embryogenesis, newly differentiated endothelial cells re

233 a role for the C-terminal region of NKAP in embryogenesis, nkap mutant zebrafish with a C-terminally

234 genital malformations syndrome affecting the embryogenesis of the brain and genitourinary systems and

235 blastomeres and epithelial cells during the embryogenesis of the ctenophore Mnemiopsis leidyi.

236 ew summarizes current evidence regarding the embryogenesis of the human meninges in the context of me

237 We also describe the late-stage embryogenesis of Vargula tsujii and discuss the size cla

238 logical differences within the same stage of embryogenesis or gametogenesis.

239 of genes, we identified 52 genes involved in embryogenesis, out of which 22 are involved in nucleic a

240 Early in embryogenesis, P1 is silent, while P2 is strongly activa

241 l of nuclear growth by live imaging of early embryogenesis, perturbations of blastomere dimensions, a

242 During mouse embryogenesis, progenitors within the liver known as hep

243 cell and nuclear sizes during Xenopus laevis embryogenesis provide a robust scaling system to study m

244 ociated receptor kinase 1 (BAK1) and somatic embryogenesis receptor kinase 4 (SERK4) redundantly and

245 teraction with a shape complementary SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) coreceptor kin

246 leucine-rich repeat (LRR) domain of SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) family protein

247 dy, we show that loss of function of SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) genes results

248 lobulin G (IgG) antibodies against T. gondii embryogenesis-related protein (TgERP).

249 port our hypothesis: (a) Differentiation and embryogenesis rely on mitochondrial function; (b) mitoch

250 lying euchromatin establishment during early embryogenesis remain poorly understood.

251 f the basement membrane in post-implantation embryogenesis remains unknown.

252 yet whether they fully recapitulate in vivo embryogenesis remains unsolved.

253 mental events that build these organs during embryogenesis, remodel them during metamorphosis, and re

254 The synchronous cleavage divisions of early embryogenesis require coordination of the cell-cycle osc

255 t formation of striolar/central zones during embryogenesis requires Cytochrome P450 26b1 (Cyp26b1)-me

256 ramming cell fate during the first stages of embryogenesis requires that transcriptional activators g

257 er pulses of ERK activation during zebrafish embryogenesis, revealing rheostat-like responses of an E

258 Maize somatic embryogenesis (SE) requires the induction of embryogenic

259 sident macrophage populations develop during embryogenesis, self-renew in the steady state and expand

260 Control of metazoan embryogenesis shifts from maternal to zygotic gene produ

261 centromeres and chromosome healing in early embryogenesis show that, once established, these centrom

262 hey all exhibit a very similar mode of early embryogenesis: spiral cleavage.

263 that represses a network of mRNAs to control embryogenesis, stem cell fate, fertility and neurologica

264 Thus, Crk regulates diverse events in embryogenesis that require orchestrated cytoskeletal dyn

265 We conclude that, during mouse embryogenesis, the Arpp19 and Ensa paralog genes display

266 During vertebrate embryogenesis, the cranial neural crest (CNC) forms at t

267 As in embryogenesis, the development of structure inside a cel

268 During early embryogenesis, the ectoderm is rapidly subdivided into n

269 During Drosophila embryogenesis, the germband first extends to curl around

270 During embryogenesis, the size of HLBs is controlled in a preci

271 During embryogenesis, the suppressing mechanism dominated in en

272 ing and location of the GNAS mutation during embryogenesis, the tissues involved, and the role of G(s

273 ayside with the advent of genetic studies of embryogenesis, they demonstrated that embryos provide co

274 data demonstrate Sec22b contributes to early embryogenesis through activity both in hematopoietic/end

275 chromosomes are paired in somatic cells from embryogenesis through adulthood.

276 ues or organs at 9 developmental stages from embryogenesis to adulthood.

277 ther, these co-receptors are required during embryogenesis to mediate proper HH signaling.

278 ompartmentalized degradation of oskar during embryogenesis to minimize its inheritance by pole cells.

279 etaboly, and occurred by profoundly altering embryogenesis to produce a larval stage, the nymph becom

280 Here, we study mouse skin embryogenesis to tackle m6A's functions and physiologica

281 l to development-from the earliest stages of embryogenesis to the construction and differentiation of

282 emical assays - that Drosophila melanogaster embryogenesis utilizes 10 mJ of energy generated by the

283 s, but none of the lncRNAs were required for embryogenesis, viability or fertility.

284 As a major portion of embryogenesis was deferred to postembryonic life with th

285 he genomic and epigenomic impacts of somatic embryogenesis, we characterized soybean (Glycine max) ep

286 nteractome undergoes from oogenesis to early embryogenesis, we characterized the early embryo Me31B i

287 fects of ethanol on early transcripts during embryogenesis, we treated zebrafish embryos with ethanol

288 ished single-cell EMT datasets in cancer and embryogenesis, we uncover the roles of ICS on adaptation

289 s in the developmental context of C. elegans embryogenesis, we undertook chromosome tracing to map th

290 essential genes for the cell development and embryogenesis were overexpressed in ovaries.

291 lts therefore pinpoint the time during early embryogenesis when cells acquire the ability to sense ch

292 mosomes can functionally interact outside of embryogenesis when X inactivation is initiated and sugge

293 the vertebral column is established early in embryogenesis, when pairs of somites are rhythmically pr

294 regulate processes such as wound healing and embryogenesis where cell differentiation must coordinate

295 a significant fraction is present throughout embryogenesis, where it is dynamically recruited to the

296 nockouts of either gene were lethal in early embryogenesis, whereas PPIL1 patient mutation knockin mi

297 s dispensable for de novo methylation during embryogenesis, which is mainly mediated by DNMT3B.

298 human brain can occur outside the context of embryogenesis with a degree of reproducibility that is c

299 ith a null allele of Bmp2 or Bmp4 die during embryogenesis with defects in ventral body wall closure

300 c process of high cell plasticity underlying embryogenesis, wound healing, cancer metastasis and drug