ライフサイエンスコーパス: embryonic

1 ned using a variety of TLR-transfected human embryonic 293 cell lines, while the PF-deficient mutants

2 s to define the steps required for the first embryonic abscission in Caenorhabditis elegans Our findi

3 of the E3 ubiquitin ligase Nedd4 Analysis of embryonic and adult fly heart revealed that the Nedd4 pr

4 deficient samples and single cells (at both embryonic and adult stage).

5 c stem cells (ESCs) but becomes activated in embryonic and adult tissues while TET1FL is expressed in

6 cific roles of PRC2 epigenetic regulators in embryonic and adult urothelial progenitors.

7 ows widespread chimeric contribution to both embryonic and extraembryonic lineages in vivo and permit

8 esis requires intricate interactions between embryonic and extraembryonic tissues to orchestrate and

9 enome expression in 67 first trimester human embryonic and fetal ovaries and testis and confirmed by

10 were robustly generated from multiple human embryonic and induced pluripotent stem cell lines and ha

11 tically dividing germ cells, and during late embryonic and larval development.

12 We find that UTF1 is expressed in embryonic and newborn gonocytes and in a subset of early

13 upernumerary mammary buds and normalizes the embryonic and postnatal hyperbranching phenotype of Eda

14 Nodal signaling during establishment of the embryonic axis.

15 egulators acting in the molecular control of embryonic bilateral symmetry.Retinoic acid (RA) regulate

16 development, during the integration of post-embryonic-born GABAergic neurons into the circuit, produ

17 genomic imprinting in the 12-day-old chicken embryonic brain and liver by examining ASE in F1 recipro

18 ators were identified in EML1 pulldowns from embryonic brain extracts.

19 th this, introduction of TRBP into the mouse embryonic brain in utero increased the fraction of cells

20 e damage in human cortical organoids and the embryonic brain of the ZIKV-induced mouse microcephaly m

21 (+/+) and Slc6a4 (+/-) mice and post-stress embryonic brains were assessed for whole genome level pr

22 mors arising from SS18-SSX expression in the embryonic, but not postnatal, Myf5 lineage share an anat

23 Embryonic carcinoma (EC) cells are malignant counterpart

24 Human embryonic carcinoma (EC) cells are shown to restrict the

25 e for GDF6 and BMP signaling in governing an embryonic cell gene signature to promote melanoma progre

26 stream cranial neural crest or from multiple embryonic cell populations evolving most quickly and int

27 vestigate the role of Utf1 (Undifferentiated embryonic cell transcription factor 1) in mouse germ cel

28 ion as a fundamental property of pluripotent embryonic cells in vivo.

29 itro expansion, and at ratios >1:3 postnatal:embryonic cells, they inhibit the ability of embryonic d

30 niotic primordium also serves as a source of embryonic cells, which may contribute to cardiovascular

31 rant egg morphology and a maternal-effect on embryonic chromosome segregation and survival, which was

32 At embryonic day (E) 12.5, the mesenchymal precursor pool b

33 ontrast, fetal steady-state hematopoiesis at embryonic day (E) 14.5 was not affected by homozygous Mo

34 inences (CGEs) between preterm-born [born on embryonic day (E) 29; examined on postnatal day (D) 3 an

35 o failed chorioallantoic fusion and death at embryonic day 10.5 (E10.5).

36 use RGCs shortly after they differentiate at embryonic day 12 and is essential for multiple aspects o

37 y, we isolated palatal mesenchyme cells from embryonic day 12.5 (E12.5) and E13.5 Osr2(RFP/+) and Osr

38 recipitation against Lmx1b in mouse limbs at embryonic day 12.5 followed by next-generation sequencin

39 oper exhibited severe anemia and died around embryonic day 14.5.

40 rebrain neuron cell body size is apparent in embryonic day 15.5 fetuses, and persists until postnatal

41 wn that the proliferation of late gestation (embryonic day 19) fetal rat hepatocytes is mitogen-indep

42 ryo serotonin levels and neurodevelopment at embryonic day E14.5, when peripheral sources of 5-HT pre

43 ect action of estrogens can be tested during embryonic days (E)14 to 19.

44 Here we show that embryonic deletion of Cacna1c in forebrain glutamatergic

45 Importantly, embryonic deletion of the same gene in astrocytes, or in

46 embryonic cells, they inhibit the ability of embryonic dental mesenchyme cells to induce tooth format

47 infiltration and loss of resident reparative embryonic-derived cardiac macrophages.

48 conditions, including tumor suppression [2], embryonic development [3, 4], tissue repair [5-8], and o

49 romatin factors that have essential roles in embryonic development and cell fate decisions.

50 rupting properties, may pose a risk to early embryonic development and cellular homeostasis during ad

51 ional coactivator with critical functions in embryonic development and emerging roles in cancer.

52 g of how heart formation is initiated during embryonic development and for applying stem cell biology

53 l species and are frequently associated with embryonic development and growth.

54 regulator of WNT signaling, involved in both embryonic development and homeostasis of adult organs.

55 The expression of survivin proceeds during embryonic development and in addition has already been d

56 mooth muscle progenitor cells emerges during embryonic development and is maintained postnatally at a

57 esults demonstrate that UTF1 is required for embryonic development and regulates male germ cell devel

58 te the pathway, plays critical roles both in embryonic development and the maintenance of homeostasis

59 by the down-regulation of genes involved in embryonic development and vasculogenesis, and up-regulat

60 mesenchymal transition (EMT) is critical for embryonic development and wound healing, and occurs in f

61 Here, we report that abnormal embryonic development in aged female mice is associated

62 nery, and that Donson is essential for early embryonic development in mice as well, suggesting an ess

63 t is essential for differentiation and early embryonic development in mice.

64 Early embryonic development is characterized by rapid cleavage

65 Although during embryonic development much evidence indicates that both

66 f temperature for interspecific variation in embryonic development time remains unclear.

67 icate a much stronger role of temperature in embryonic development time than currently thought.

68 diameter, density/growth, and branching from embryonic development to three months, spanning the dura

69 rter for Cu acquisition and is essential for embryonic development, a homologous protein, Ctr2, has b

70 ignaling pathway plays a central role during embryonic development, and its aberrant activation has b

71 In embryonic development, cells differentiate through stere

72 of several key biological processes, such as embryonic development, disease progression and aging.

73 ygotic expression of gdf3 is dispensable for embryonic development, while maternally deposited gdf3 i

74 wever, the SASP has also been shown to favor embryonic development, wound healing, and even tumor gro

75 th, and transdifferentiation throughout post-embryonic development.

76 ms regulating X chromosome activity in early embryonic development.

77 al signaling at multiple stages in zebrafish embryonic development.

78 ects of increased temperatures on successful embryonic development.

79 g modulates phenotypes during Xenopus laevis embryonic development.

80 ) neurons, which may contribute to a delayed embryonic development.

81 transition from morula to blastocyst during embryonic development.

82 Armc5 plays an important role in early mouse embryonic development.

83 per morphogenesis and organ formation during embryonic development.

84 l mRNA during maternal zygotic transition in embryonic development.

85 differentiation and survival of mDANs during embryonic developmental stages.

86 erentiation in direct programming relates to embryonic differentiation is unclear.

87 expression profiles of NDCs at key stages of embryonic disc formation.

88 Over half of embryonic DNase I hypersensitive sites (DHSs) were annot

89 Activity-dependent pruning also occurs at embryonic Drosophila neuromuscular junctions (NMJs), whe

90 8 represents an early and specific marker of embryonic dSPNs and the Sox8-EGFP BAC transgenic mice ar

91 we present the molecular characterization of embryonic duck bill, which we show contains a high densi

92 so-ventral epidermis are critical in driving embryonic elongation.

93 ers during differentiation of Neurogenin3(+) embryonic endocrine progenitors, regardless of the speci

94 nscription of Wt1 as the master regulator of embryonic EPDCs.

95 r embryo delaminate as single cells from the embryonic epidermis to give rise to the nervous system.

96 t cells, the HBBP1-BGLT3 region contacts the embryonic epsilon-globin gene, physically separating the

97 Altogether, maternal and/or ancestral embryonic exposure to BPA affects liver metabolism leadi

98 Dmrt1 exhibited early male-specific embryonic expression, preceding the onset of gonadal sex

99 l structures of a mitochondrion from a mouse embryonic fibroblast cell line (NIH3T3) were visualized

100 nor fraction (30-40%) of the 26S in WT mouse embryonic fibroblast cells.

101 thylation (H3K27me3) in both Pten null mouse embryonic fibroblasts (MEFs) and Pten null mouse prostat

102 Mechanistically, Tmem30a-mutant mouse embryonic fibroblasts (MEFs) exhibited diminished PS fli

103 of PDAC cancer cells and SerpinB2(-/-) mouse embryonic fibroblasts (MEFs) resulted in increased tumou

104 n initiation factor 2alpha (eIF2alpha) mouse embryonic fibroblasts (MEFs); moreover, ECD mRNA levels

105 ontin and other FN-type matrix in both mouse embryonic fibroblasts and human melanoma.

106 G12V))-induced premature senescence in mouse embryonic fibroblasts and normal human bronchial epithel

107 ogen-driven immortalization of primary mouse embryonic fibroblasts and recapitulates early steps of c

108 ratio was rescued in FKBP65-deficient murine embryonic fibroblasts by reconstitution with wild-type b

109 WT KRAS to rescue the growth defect of mouse embryonic fibroblasts deficient in all Ras genes.

110 -related GTPase (IRGM1) was overexpressed in embryonic fibroblasts from dynamin1 like (DNM1L) protein

111 epithelial tissues from patients with CD and embryonic fibroblasts from mice, along with enteroids an

112 ysis of cultured mesoderm explants and mouse embryonic fibroblasts from null mutants shows that the m

113 vestigate integrin beta3 and paxillin in rat embryonic fibroblasts growing on two different extracell

114 c-Myc) or Oct4 during reprogramming of mouse embryonic fibroblasts into iPSCs.

115 s are abrogated in lamin A/C-deficient mouse embryonic fibroblasts that recapitulate the defective nu

116 hance copper accumulation in Ctr1(-/-) mouse embryonic fibroblasts.

117 12, or 14 in tetraploid immortalized murine embryonic fibroblasts.

118 key components in mRNP architectures, in the embryonic function of lsy-6 miRNA.

119 poptotic signaling pathways and formation of embryonic gene clusters, whereas the NS5A TCR activation

120 l genome loss disrupts the normal pattern of embryonic gene expression blocking development at the mo

121 ent and types of genetic variation impacting embryonic gene expression, and their interactions with d

122 lineage-inappropriate genes, including extra-embryonic genes, are aberrantly expressed.

123 ckdown decreased Kdr transcripts in cultured embryonic gonads at multiple developmental stages.

124 The expression of Dmrt1 was induced in ZW embryonic gonads that were masculinized by aromatase inh

125 To elucidate Grh functions we identified embryonic Grh targets by ChIP-seq and gene expression an

126 miR-1 produces defects in somatic muscle and embryonic heart development, which have been partly attr

127 concomitant with specific cell ablation and embryonic heart transplantation studies, we identified a

128 ong these lincRNAs, 564 are expressed in the embryonic heart, and 730 are expressed in the adult hear

129 ular endothelial growth factor in Hyal2(-/-) embryonic hearts, suggest that HYAL2 is important to inh

130 w that Erf is required in all three waves of embryonic hematopoiesis.

131 signaling is not required for engraftment of embryonic HSCs.

132 t DONSON is expressed in progenitor cells of embryonic human brain and other proliferating tissues, i

133 stems analysis revealed similarities between embryonic implantation and cancer cell adhesion, which s

134 enoside Ro was the most potent in inhibiting embryonic implantation within non-cytotoxic concentratio

135 esults in substantially higher activity than embryonic injection.

136 mouse development is the segregation of the embryonic inner cell mass and the extra-embryonic trophe

137 ium imaging shows that the beta-cells in the embryonic islet become functional during early zebrafish

138 l system using adenovirus infection of human embryonic kidney (293) cells.

139 expression of Mac-1 on the surface of human embryonic kidney (HEK) 293 cells induced their adhesion

140 Human embryonic kidney (HEK) cells and ovine mesenchymal stem

141 human embryonic stem cells (ESCs) and human embryonic kidney (HEK) cells.

142 CpG methylation at the HOXA5 locus in human embryonic kidney (HEK293T) cells.

143 tivation and arrestin-3 recruitment in human embryonic kidney 293 cells confirmed that norbuprenorphi

144 Transient transfection of human embryonic kidney 293 cells with this reporter vector inc

145 However, by utilizing the human embryonic kidney cell line HEK293T, it was possible to d

146 ochrome c from mitochondria in lysates human embryonic kidney cells HEK293T.

147 ctions and dynamics directly in living human embryonic kidney cells using fluorescence fluctuation sp

148 ated neutrophils and 5-LOX-transfected human embryonic kidney cells, propofol attenuated the producti

149 el is highly degraded by proteasome in human embryonic kidney cells.

150 fidelity of DNA replication in HEK293T human embryonic kidney cells.

151 man airway epithelia (HAE) in vitro In human embryonic kidney HEK293 cells, the transfection of a dup

152 In explant cultures of embryonic kidney rudiments, retinoic acid stimulated Nri

153 hown to be transcriptionally active in 293T (embryonic kidney), Vero (African-green monkey kidney epi

154 whole-body deletion of the p32 results in an embryonic lethal phenotype, mice heterozygous for p32 ar

155 ctivated kinase 4 (PAK4) in the mouse causes embryonic lethality associated with heart and brain defe

156 ated thin filament length, were the cause of embryonic lethality in HSPB7 KOs.

157 p53 deletion prevents the embryonic lethality of normal tissues lacking Mdm2, sugg

158 use model and found that loss of Fdxr led to embryonic lethality potentially due to iron overload in

159 h GATA genes, but not either alone, leads to embryonic lethality prior to the onset of their expressi

160 To bypass embryonic lethality we used Tie2CRE-mediated recombinati

161 es viability of the individual (for example, embryonic lethality) or results in profound loss of fitn

162 at disruption of both CRTC2 and CRTC3 causes embryonic lethality, and that a single allele of either

163 Ssb1/Ssb2 double knockout (DKO) caused early embryonic lethality, whereas conditional Ssb1/Ssb2 doubl

164 ut of both paralogs in mice results in early embryonic lethality.

165 olyploid giant cancer cells (PGCCs) acquired embryonic-like stemness and were capable of tumor initia

166 uman embryo culture and in the derivation of embryonic-like structures from human pluripotent stem ce

167 that causes widespread cell death within the embryonic limb bud.

168 duced changes in prenatal movement influence embryonic limb growth to alter proportions.

169 e hepatocyte and cholangiocyte lineages from embryonic liver progenitor cells and their subsequent ma

170 Data were acquired from the embryonic liver, heart and umbilical cord.

171 in from forming chromosomes during the first embryonic mitosis, leading to its loss.

172 We previously reported that embryonic motor cortical neurons transplanted immediatel

173 euronal differentiation and migration in the embryonic mouse cerebellum.

174 -cycle deficits of radial glial cells in the embryonic mouse cortex and human forebrain organoids.

175 m(6)A sequencing of embryonic mouse cortex reveals enrichment of mRNAs relat

176 individual proteins encoded by ZIKV into the embryonic mouse cortex, we show that expression of ZIKV-

177 ferentiated progenitor cells in vitro and in embryonic mouse livers.

178 The embryonic mouse lung is a widely used substitute for hum

179 Real-time imaging of the embryonic murine cardiovascular system is challenging du

180 Ascl2 knockout in embryonic myoblasts decreases both the number of Pax7(+)

181 a signaling, revealing a regulatory role for embryonic myosin in the TGFbeta signaling pathway.

182 nts the first transcriptome-wide analysis of embryonic NDCs.

183 cal-basal spindle orientation in delaminated embryonic neuroblasts.

184 CTCF deficiency in embryonic neurons is lethal in mice, but mice with postn

185 turation and OR expression in the developing embryonic OE.

186 of temporal factor expression in Drosophila embryonic or larval neural progenitors.

187 l surface markers for GSC are developed from embryonic or neural stem cell systems; however, currentl

188 cy in mice resulted in a partially penetrant embryonic or perinatal lethal phenotype, with the produc

189 ted the major CLP gene Irf6 only in the late embryonic oral epithelium ( Irf6 cKO), bypassing the rol

190 pithelial cells' (NECs) of fish gills, whose embryonic origin is unknown.

191 This in turn diminished the embryonic origin of postnatal NSCs, resulting in loss of

192 ally regarded as nonskeletogenic, and so the embryonic origin of trunk denticle odontoblasts remains

193 s of UCP2 observed on beta-cell mass have an embryonic origin.

194 udal domains but little is known about their embryonic origins.

195 onstrate distinct expression patterns in the embryonic ovary and interact with each other and other o

196 a has been challenging due to the absence of embryonic phenotypes in murine loss-of-function studies.

197 ctus and shown to play a role in controlling embryonic polarity and regulating the NF-kappaB signalin

198 The neural crest is an embryonic population of multipotent stem cells that form

199 tro into cardiac-lineage cells; and test the embryonic potency of iCPCs via injection into the cardia

200 Transplanting embryonic precursors of GABAergic neurons from the media

201 The embryonic precursors of these cortical neurons were in u

202 he islet following differentiation from post-embryonic progenitors.

203 developmentally regulated manner in chicken embryonic retinal pigment epithelium (RPE)/choroid in th

204 other during embryogenesis to establish the embryonic SAM and to specify cotyledon boundaries, and S

205 ain transcription factor signatures of their embryonic site of origin, the pallium and subpallium.

206 Transcriptional profiling of Ctip1 (-/-) embryonic skin identified altered expression of genes en

207 ly human embryos, our understanding of early embryonic somatic mutations is very limited.

208 germline genes, not directly associated with embryonic somatic tissue genesis, is the one that encode

209 4 is expressed in the axonal growth cones of embryonic spinal commissural neurons, motoneurons, dorsa

210 n of alternative codon-derived DPRs in chick embryonic spinal cord confirmed in vitro data, revealing

211 nal state rather than following the expected embryonic spinal intermediates.

212 dence of thermal local adaptation during the embryonic stage for developmental rate or survival.

213 At the embryonic stage, we found that PSD-95 puncta outnumber g

214 g in the distal limb primes the ZRS at early embryonic stages maintaining a poised, but inactive stat

215 hereas comparative transcriptomic studies of embryonic stages of hemimetabolous insects are completel

216 aracterized its neuroanatomical profile from embryonic stages to adulthood.

217 Embryonic stem (ES) cell pluripotency is governed by OCT

218 romatin plays a critical role in controlling embryonic stem (ES) cell self-renewal and pluripotency.

219 Utf1 is expressed in pluripotent embryonic stem (ES) cells and regulates ES cell differen

220 oma (EC) cells are malignant counterparts of embryonic stem (ES) cells and serve as useful models for

221 40 ortholog, BRD1, at bivalent loci in human embryonic stem (ES) cells.

222 the gene expression dynamics of early mouse embryonic stem (mES) cell differentiation, uncovering di

223 ank of over 100,000 individual haploid mouse embryonic stem (mES) cell lines targeting 16,970 genes w

224 Our data add to recent evidence in embryonic stem and neural progenitor cells, suggesting a

225 mide is a staurosporine analog that promotes embryonic stem cell (ESC) differentiation by inhibiting

226 blished several human stem cell lines: human embryonic stem cell (hESC) line carrying the common T158

227 We find that during embryonic stem cell differentiation loss of HMGNs leads

228 y-state and nascent RNA levels and perturbed embryonic stem cell differentiation.

229 pping to predicted fetal brain promoters and embryonic stem cell enhancers.

230 ce-dependent activation of expression of the embryonic stem cell markers OCT4, NANOG, SOX2 and SSEA1

231 directly determines the efficiency of mouse embryonic stem cell self-renewal.

232 Sal-like protein 4 (SALL4), an embryonic stem cell transcriptional regulator, is re-exp

233 Here, we combined mouse embryonic stem cells (ESCs) and extraembryonic trophobla

234 oduced RNA-genome interaction maps for human embryonic stem cells (ESCs) and human embryonic kidney (

235 TET1ALT is repressed in embryonic stem cells (ESCs) but becomes activated in emb

236 of chimeras created by injecting tetraploid embryonic stem cells (ESCs) expressing green fluorescent

237 Here, we used mouse embryonic stem cells (ESCs) to identify an endosiRNA-bas

238 ene promoters upon differentiation of murine embryonic stem cells (ESCs) to neural progenitor cells (

239 of induction of differentiation of mammalian embryonic stem cells (ESCs), accumulation of the repress

240 959-972) report that, in naive mouse embryonic stem cells (ESCs), p53 controls DNA methylatio

241 ich reflect aberrant differences relative to embryonic stem cells (ESCs).

242 superior chromosomal stability compared with embryonic stem cells (ESCs).

243 We then found CX45 was expressed in human embryonic stem cells (hESCs) and human dermal fibroblast

244 Naive human embryonic stem cells (hESCs) can be derived from primed

245 ic organoids (COs) from differentiated human embryonic stem cells (hESCs) or induced pluripotent stem

246 uired for self-renewal and survival of human embryonic stem cells (hESCs).

247 ed pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs).

248 ogen molecule enhances self-renewal of mouse embryonic stem cells (mESCs).

249 evelopment, applications of IDP-ASE to human embryonic stem cells and breast cancer cells indicate th

250 rs show that ablation of PRC2 genes in human embryonic stem cells and in mice results in changes in p

251 astomeres, and by direct conversion of mouse embryonic stem cells and induced pluripotent stem cells.

252 ing the earliest stages of X inactivation in embryonic stem cells and is dependent on the C-terminal

253 e established synchronized cultures of mouse embryonic stem cells as they exit the ground state of pl

254 yst2/Kat7/Hbo1 protein interactions in mouse embryonic stem cells by affinity purification coupled to

255 e in response to regenerative demands, while embryonic stem cells continuously replicate, suggesting

256 human fibroblasts as well as mesenchymal and embryonic stem cells for both two- and three-dimensional

257 liferation in somatic cells, but its role in embryonic stem cells is unknown.

258 aneous deletion of these shadow enhancers in embryonic stem cells leads to impaired activation of Hox

259 This study confirms that in embryonic stem cells Myst2 is part of H3 and H4 histone

260 plantable insulin-producing cells from human embryonic stem cells or induced pluripotent stem cells i

261 The capacity of pluripotent embryonic stem cells to differentiate into any cell type

262 a targeted autosome loss in aneuploid mouse embryonic stem cells with an extra human chromosome and

263 Moreover, human embryonic stem cells with deletion of EZH1 or EZH2 fail

264 ethylation genome-wide in human cells, mouse embryonic stem cells, and Drosophila Biochemical analysi

265 o interrogate the 2-Mb POU5F1 locus in human embryonic stem cells, and identified 45 cis-regulatory e

266 ry response mechanism is not active in mouse embryonic stem cells, and in vitro differentiation promo

267 mesoderm formation in frog embryos and human embryonic stem cells.

268 ays that had alphaKG-sensitive expression in embryonic stem cells.

269 wise microRNA-deficient Dgcr8 knockout mouse embryonic stem cells.

270 ctive RAS protein normally expressed only in embryonic stem cells.

271 as "preborder"; its transcriptome resembles embryonic stem cells.

272 dy marked as potential regulatory domains in embryonic stem cells.

273 printed genes in Naa10p-knockout embryos and embryonic stem cells.

274 Foxa2+ population during differentiation of embryonic stem cells.

275 eted from select subsets of ribosomes within embryonic stem cells.

276 progenitors (NMPs) within the posteriormost embryonic structure, the tailbud.

277 Furthermore, IFIH1(T946) mice manifested an embryonic survival defect consistent with enhanced respo

278 s severe consequences for egg production and embryonic survival, with important broader relevance to

279 es, provide one of the best illustrations of embryonic symmetry.

280 We experimentally increased embryonic temperature in free-living tropical and north

281 nd Zeb2 plays a fundamental role in defining embryonic territories in the mouse, as E-cadherin needs

282 in normal physiological processes, including embryonic tissue boundary formation and directional guid

283 as meiotic factors are not a feature of most embryonic tissue development.

284 formed in situ hybridisation utilising human embryonic tissue, and observed expression in the develop

285 known to histologically resemble developing embryonic tissue.

286 ra expression occurs in the absence of extra-embryonic tissues or localised sources of signals.

287 thought to play a central role in sculpting embryonic tissues, maintaining organ architecture and co

288 es convey positional information to organize embryonic tissues.

289 ing the demarcation between intra- and extra-embryonic tissues.

290 to identify transcriptome changes from late embryonic to adult mouse muscle and demonstrate that alt

291 the embryonic inner cell mass and the extra-embryonic trophectoderm.

292 Without Eed, the obligatory subunit of PRC2, embryonic urothelial progenitors demonstrate reduced pro

293 nomously and noncell-autonomously to control embryonic vascular tissue formation and root initiation,

294 ough they lacked apparent deformities in the embryonic vasculature and heart, the placental labyrinth

295 niscent of local activation of Toll in early embryonic ventral hypoderm, consistent with the hypothes

296 transcriptional activity is dispensable for embryonic viability in the first hour after fertilizatio

297 e, the chicken W chromosome is essential for embryonic viability of the heterogametic sex.

298 rdingly we suggest that for each nucleus the embryonic volume arises from a structural element contai

299 activity in a mouse atrial cell line and in embryonic zebrafish and differentially regulates PRRX1 e

300 Thus, ExM of the larval and embryonic zebrafish may enable systematic studies of how