ライフサイエンスコーパス: embryonic day

1 or 2-3 cell layers after Dox induction from embryonic day 0 (E0) to P21 and from E9 to P21, respecti

2 water (1 g/kg) of the treatment cohorts from embryonic day 0.5 until the end of lactation.

3 Here, we show that knockout of p75(NTR) from embryonic day 10 (E10) in neural progenitors using a con

4 across 12 developmental time points between embryonic day 10 and postnatal day 45.

5 inally, we found that deletion of HuR before embryonic day 10 disrupts both neocortical lamination an

6 The five populations analyzed were embryonic day 10.5 (E10.5) endothelium and hemogenic end

7 s were assessed for developmental defects at embryonic day 10.5 (E10.5).

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

9 drivers that are activated at early [Nestin; embryonic day 10.5 (E10.5)] and late [human glial fibril

10 ed that Cdh5(-/-)GFP(+/+) HSCs emerging from embryonic day 10.5 and 11.5 (E10.5 and E11.5) AGM or der

11 os, yolk sacs and placentas, and die between embryonic day 10.5 and 11.5.

12 arly mouse embryos but begins to increase at embryonic day 10.5 and remains elevated through birth.

13 ryonic stem cell colony-forming assay and in embryonic day 10.5 aorta-gonad-mesonephros explants.

14 y penetrant NT defects, while excision after embryonic day 10.5 did not result in NT defects.

15 This panel was then applied against single embryonic day 10.5 heart cells to demonstrate its abilit

16 In the CNS of embryonic day 10.5 mouse embryos, CD31(+)F4/80(+) hemato

17 We found that in embryonic day 10.5 mouse hearts, CD166 and HCN4, markers

18 ic cultures, named pancreatoids, composed of embryonic day 10.5 murine epithelial progenitors and nat

19 een both cell lines and resemblance to mouse embryonic day 10.5 otocyst cells implied reasonable robu

20 Geminin mutant versus wild-type siblings at embryonic day 10.5 revealed decreased expression of key

21 FBP is embryo lethal from embryonic day 10.5 to birth.

22 uired for development as null embryos die by embryonic day 10.5 with cardiovascular phenotypes.

23 beta at Ser-9 starting early in development (embryonic day 10.5), leading to enhanced GSK3beta activi

24 racerebroventricular macrophages arrive from embryonic day 10.5, and can traverse ventricular walls i

25 se embryos, is important for survival before embryonic day 10.5, but its function in embryos is unkno

26 use NP with in utero microelectroporation at embryonic day 10.5, close to the estimated peak of area

27 rogenitors labeled by tamoxifen induction at embryonic day 10.5.

28 Between embryonic days 10.5 and 14.5, active proliferation drive

29 merge from neuroepithelial stem cells around embryonic day 11 and produce excitatory cortical neurons

30 r chimerism that continuously increases from embryonic day 11 onward, sometimes even taking over enti

31 placental vulnerability is pronounced before embryonic day 11, when even mild immune challenge result

32 sequenced more than 52,500 single cells from embryonic day 11.5 (E11.5) postembryonic day 5 (P5) gona

33 At embryonic day 11.5 (E11.5), the majority of Pax6-positiv

34 xtrastriolar (MES) regions of the utricle at embryonic day 11.5 (E11.5), while cells in the lateral e

35 rise in the aorta-gonad-mesonephros (AGM) on embryonic day 11.5 (E11.5).

36 VGluT2 was detectable in most DA neurons at embryonic day 11.5 and was localized in developing axons

37 lts in congestive heart failure and death by embryonic day 11.5 as a result of hypoproliferation of t

38 sors in the mouse dentate neuroepithelium at embryonic day 11.5 give rise to proliferative Hopx(+) ne

39 axon tracts require Fz3 function as early as embryonic day 11.5, and that Fz3 is required for pathfin

40 pulse into Connexin30(-/-) mouse otocysts at embryonic day 11.5, is able to prevent putative hearing

41 hat ventricular injection of FGF2 protein at embryonic day 11.5-before neurogenesis and before the fo

42 eatures upon loss of Lhx2 in the cortex from embryonic day 11.5.

43 l deletion of ZO-1 in the mouse is lethal by embryonic day 11.5.

44 and non-ENS gut cells of mice, collected at embryonic days 11.5 and 15.5, when different subtypes of

45 led a localized domain of Zic1 expression at embryonic days 11.5-12.5 in a region overlapping the sup

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

47 transcriptome analyses of 14,441 cells from embryonic day 12 submandibular and parotid salivary glan

48 ted, consistent with partial lethality after embryonic day 12.

49 of the first epithelial stalk at early-stage embryonic day 12.5 (E12.5) according to both TUNEL stain

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

51 resence by acetylcholinesterase staining and embryonic day 12.5 (E12.5) intestine transcriptome by RN

52 ivity for mouse liver tissues collected from embryonic day 12.5 (E12.5) to postnatal week 8 (W8), enc

53 ls results in the cessation of myogenesis by embryonic day 12.5 (E12.5), as assayed by myosin heavy c

54 Reduced pericyte coverage was observed at embryonic day 12.5 and persisted throughout development,

55 were isolated from Shh-cre;ROSA:YFP mice at embryonic day 12.5 and postnatal day 0, representing opp

56 s, mouse cochlear cultures were initiated at embryonic day 12.5 and subjected to pharmacological trea

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

58 However, at embryonic day 12.5 in the mouse brainstem, trains of spo

59 Mechanistically, loss of Nf1 increased embryonic day 12.5 Runx1(+)/Blbp(+) progenitors that ena

60 y continued to receive these chemicals until embryonic day 12.5, whereupon placental samples were col

61 e small guanosine triphosphatase RSG1 die at embryonic day 12.5, with developmental abnormalities cha

62 This wave occurred by embryonic day 12.5, with MCs disappearing from the corne

63 cytes resulted in embryonic lethality before embryonic day 12.5.

64 eral developmental delay and death at around embryonic day 12.5.

65 nic-polycytidylic acid (PIC) injected during embryonic days 12 to 16.

66 ation of this pathway in Foxg1(-/-) nulls at embryonic days 12.5 and 14.5.

67 at the onset of gonadal sex determination at embryonic day 13 (E13) and after cord formation in the t

68 s as they develop in the mouse brain between embryonic day 13 and postnatal day 5 in order to identif

69 ular function of this factor was examined in embryonic day 13 hepatoblast culture with maturation fac

70 ient Area X-CB+ domain became discernable at embryonic day 13 in the Islet1-ventral striatal field.

71 1 and JM-a CYT-2 was first detectable around embryonic day 13 in the mouse, mainly in the collecting

72 etion of Pou4f1 in SGNs beginning in mice at embryonic day 13 rescues the early path-finding and apop

73 ka virus at embryonic day 6 and evaluated at embryonic day 13 show markedly diminished levels of vira

74 The pregnant rats were injected with BrdU at embryonic day 13, and their fetuses were sacrificed from

75 cavity immediately surrounding the embryo on embryonic day 13-13.5 (E13-13.5) corrected pre-mRNA spli

76 oinjection into the mouse amniotic cavity at embryonic day 13-13.5, reduces target RNA expression for

77 zyme for the de novo production of dNTPs, at embryonic day 13.

78 this master regulatory locus is activated at embryonic day 13.5 (E13.5) by an early enhancer (EE), wh

79 that PACAP was an anti-mitogenic signal from embryonic day 13.5 (E13.5) onward both in culture and in

80 ssion was inhibited during erythropoiesis in embryonic day 13.5 and embryonic day 18.5 fetal liver an

81 tablished primary mesenchymal cultures of WT embryonic day 13.5 diaphragmatic cells.

82 of the lateral ganglionic eminence (LGE) at embryonic day 13.5 may underlie such deficits by inducin

83 served DNA regulatory enhancer (Dlx5/6ei) in embryonic day 13.5 medial ganglionic eminence (E13.5 MGE

84 posterior regions of the palatal shelves in embryonic day 13.5 Pax9-deficent embryos in comparison w

85 Genome-wide DNA methylation analysis of embryonic day 13.5 PGCs and sperm of Tet1 knockout mice

86 Bash bursts disappear by embryonic day 13.5 via alteration of the looping circuit

87 genitor niche at a higher rate than younger (embryonic day 13.5) NPCs do.

88 Adar1(E861A/E861A) embryos died at ~E13.5 (embryonic day 13.5), with activated interferon and doubl

89 tal, and acinar cells but become bipotent by embryonic day 13.5, giving rise to endocrine cells and d

90 al cerebellar cells from the mouse embryo at embryonic day 13.5.

91 Trpm7 deletion late in cardiogenesis (about embryonic day 13; alphaMHC-Cre) produces viable mice wit

92 ds on a transcriptional switch between mouse embryonic days 13 and 14.5.

93 L/6J mice were intraperitoneally injected on embryonic days 13 and 17 each with 240mug of human monoc

94 Fetal mice were injected with ACK2 on embryonic days 13.5 to 14.5 and surviving pups were tran

95 xpressed during mouse brain development from embryonic day 14 (E14), peaked around the time of birth,

96 uire action potential-generating capacity at embryonic day 14 (E14), the earliest age tested, and act

97 and intellectual disability risk factors at embryonic day 14 and adult PSD in mice.

98 Despite efficient gene knockout in embryonic day 14.5 (E14.5) dermal condensates, morphogen

99 We compared the gene expression profiles of embryonic day 14.5 (E14.5) Yap conditional knockout and

100 cantly decreased in Cln5-/- mouse embryos at embryonic day 14.5 (E14.5), and expression of Tuj1, an i

101 Fetal tissue was harvested at embryonic day 14.5 (E14.5), when the early adipogenic co

102 Although En2 promoter was active in Embryonic day 14.5 -: 15.5 LC neurons, expression dimini

103 ding mice mating, two-cell embryo injection, embryonic day 14.5 embryo digestion, fluorescence-activa

104 Homozygous mice die at embryonic day 14.5 in cardiac failure, exhibiting abnorm

105 cells of edited and nonedited blastomeres at embryonic day 14.5 showed that off-target single-nucleot

106 erebral cortex at a progenitor driven phase (embryonic day 14.5) and at birth-after neurons from all

107 deletion at the onset of differentiation, at embryonic day 14.5, disrupted Hensen's cell formation.

108 ssels and follicle progenitor cells began by embryonic day 14.5, when nascent hair placodes had blood

109 tbp4, Matn1, Matn3, and Tpo-was decreased at embryonic day 14.5, while levels of apoptotic proteins w

110 wall, which gives rise to the neocortex, at embryonic day 14.5.

111 etal liver but are decreased in frequency by embryonic day 14.5.

112 th 100% penetrance in embryos examined after embryonic day 14.5.

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

114 ng rat development, which take place between embryonic days 14 and 18 (E14-E18) and E20-E21, have bee

115 y, whereas subcutaneous fat develops between embryonic days 14 and 18.

116 pses from late prenatal mouse embryo stages (embryonic days 14-18) into adulthood [postnatal day (P)4

117 ce were analyzed with MR imaging at 9.4 T on embryonic days 14.5 (eight dams and 58 fetuses; imprinti

118 Gene expression profiling on embryonic day 15 suggested the dysregulation of mammalia

119 in retinal ganglion cells (RGCs) as early as embryonic day 15.

120 mutant fetal testes of 129Sv and B6 mice at embryonic day 15.5 (E15.5), prior to overt tumorigenesis

121 ice, lymphatic valve morphogenesis begins at embryonic day 15.5 (E15.5).

122 ind that the mouse BBB becomes functional at embryonic day 15.5 (E15.5).

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

124 1, age and sex-matched euploid controls, and embryonic day 15.5 forebrains from Ts1Cje, Ts65Dn, and D

125 2 is expressed broadly by progenitors in the embryonic day 15.5 subventricular zone, during the peak

126 ransgenic mice during a critical period from embryonic day 15.5 to postnatal day 14 was accompanied b

127 By embryonic day 15.5, kidneys of nephron progenitor cell-s

128 On embryonic day 15.5, mutant Mullerian ducts and Wolffian

129 e palates of these miR transgenic embryos at embryonic day 15.5.

130 explants from control and mutant embryos at embryonic day 15.5.

131 nd shape of supernumerary cusps in molars at embryonic day 15.5.

132 p patterns of mice lacking Sostdc1 or Shh at embryonic day 15.5.

133 stematic comparisons between different ages (embryonic days 15 and 18, postnatal day 8, and adult), w

134 stologic sections of the vertebral column at embryonic days 15.5 and 17.5 revealed an abnormal organi

135 However, analysis between embryonic days 15.5-17.5 reveals that, in BMPER(-/-) emb

136 GPR88 protein was initially detected at embryonic day 16 (E16) in the striatal primordium.

137 3) and after cord formation in the testis at embryonic day 16 (E16).

138 is pathway occurs in late gestation at about embryonic day 16 and requires the photopigment in the fe

139 -guided IUCT was conducted in rat fetuses on embryonic day 16.

140 yonic lethal as a result of severe anemia by embryonic day 16.5 (E16.5).

141 the Ets transcription factor Erg die between embryonic day 16.5 and 3 months of age as a result of pu

142 using hematopoietic progenitors from either embryonic day 16.5 Cdk5(+/+) or Cdk5(-/-) embryos to ena

143 Wild-type, embryonic day 16.5 mouse hearts (n=6 per zone) were harv

144 size of the pancreas in Ucp2(-/-) fetuses at embryonic day 16.5, associated with a higher number of a

145 ing occurs and is down-regulated starting at embryonic day 16.5, concurrent with the onset of termina

146 t ventricular dilatation in mouse embryos at embryonic day 16.5.

147 ation in dental epithelium and mesenchyme at embryonic day 16.5; however, the cell apoptosis is unaff

148 d to synchronized gilts and analyzed between embryonic day 17 and embryonic day 18.

149 tion of the left uterine vascular pedicle at embryonic day 17 of gestation was validated by weighing

150 Alcian blue staining at embryonic day 17.5 showed abnormal fusion of the posteri

151 In fetal testes at embryonic day 17.5, endogenous DNMT3L also enhanced the

152 increase in gene expression occurred between embryonic days 17 and 19.

153 bited decreased somatic and cortical size at embryonic day 18 (E18) and as adults.

154 bral cortex, waves of activity occur between embryonic day 18 and postnatal day 8 and originate in pa

155 cle cell (VSMC) layer, which are apparent at embryonic day 18 and the first postnatal week.

156 Depletion of Nup62 from cultured embryonic day 18 rat hippocampal and cortical neurons re

157 ts and analyzed between embryonic day 17 and embryonic day 18.

158 7 in MLKL-deficient mouse intestines around embryonic day 18.

159 artially blocks thymocyte differentiation at embryonic day 18.5 (E18.5).

160 maturation of mesenteric lymphatic valves at embryonic day 18.5 and at postnatal days 0 and 4.

161 or basal and starvation-induced autophagy in embryonic day 18.5 BAT3(-/-) mouse embryos and in mouse

162 ing erythropoiesis in embryonic day 13.5 and embryonic day 18.5 fetal liver and adult spleen and bone

163 were significantly less growth restricted at embryonic day 18.5 than their female counterparts.

164 is a critical perinatal window, ranging from embryonic day 18.5 to postnatal day 14 in mice, in which

165 naive female mice, the weight of fetuses at embryonic day 18.5 was significantly reduced compared wi

166 mbryos obtained through Caesarean section at embryonic day 18.5 were cyanotic, suffered from respirat

167 At embryonic day 18.5, GSK3beta activity decreased to level

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

169 ho time msec, 800/1.8-49.8) was performed at embryonic day 19.

170 were administered into the amniotic space at Embryonic Day 20 or after birth by intraperitoneal injec

171 sly, we showed ethanol treatment of cultured embryonic day 20 septal neurons distorts the maturation

172 ed into the amniotic sac of pregnant rats at Embryonic Day 20 to simulate antenatal models of chorioa

173 pregnant rats by intraamniotic injection at Embryonic Day 20, and pups were delivered by cesarean se

174 The intrauterine phase (embryonic day 21) is earmarked by a reduction of endothe

175 Pups were delivered by cesarean section at Embryonic Day 22 and treated with rhIGF-1/BP3 (0.02-20 m

176 d pups were delivered by cesarean section at Embryonic Day 22.

177 we used a rabbit model and compared preterm [embryonic day 29 (E29), 3 d old] and term (E32, <2 h old

178 pluripotent state of the inner cell mass at embryonic day 3.5 (E3.5) and the induction of let-7 upon

179 cells from eight-cell embryos and individual embryonic day 3.5 blastocysts showed unexpectedly variab

180 Et, increases daily for heart to 1-2 kPa by embryonic day 4 (E4), and although this is ~10-fold soft

181 vian auditory organ, the basilar papilla, by embryonic day 5 (E5).

182 r emerges at the distal tip of the embryo at embryonic day 5.5 and translocates to the prospective an

183 Whereas ZIKV infection at embryonic day 6 (E6) resulted in placental insufficiency

184 pregnant mice challenged with Zika virus at embryonic day 6 and evaluated at embryonic day 13 show m

185 en shown to result in embryonic lethality at embryonic day 6.5 (E6.5) before blood vessel formation.

186 rs in ectoderm are already pre-accessible in embryonic day 6.5 (E6.5) Epi when cells enter a primed p

187 Maternal inoculation at embryonic day 6.5 (E6.5) or E7.5 resulted in fetal demis

188 In the mouse embryo at embryonic day 6.5, cells located at the junction between

189 itive streak and migrating mesoderm cells on embryonic day 6.5.

190 or stroma were generated in chick corneas on embryonic day 7.

191 ults in embryonic lethality at approximately embryonic day 7.

192 n mice results in embryonic lethality before embryonic day 7.

193 Deletion of Vegfc in embryonic day 7.5 (E7.5) embryos in the C57BL6 mouse gen

194 In embryonic day 7.5 (E7.5) mutants, the domain of expressi

195 +)Flk1(+) mesodermal precursor population at embryonic day 7.5 (E7.5), a cell fraction also endowed w

196 ppa2 and Dppa4, which remain expressed until embryonic day 7.5 (E7.5), when their promoters are remet

197 When Fgf8-cre expression is induced at embryonic day 7.5 (T-E7.5), in the adult the entire DR a

198 of up to 60% of cardiac progenitor cells at embryonic day 7.5 was well tolerated and permitted embry

199 l allocation of definitive endoderm cells on embryonic day 7.5.

200 elay and failure to initiate gastrulation by embryonic day 7.5.

201 Tet1/2/3-deficient embryos (embryonic day 8.0-8.5) showed hyperactivated Wnt signali

202 949, and 1,166 single murine heart cells at embryonic day 8.5 (e8.5), e9.5, and e10.5, respectively.

203 he 45 analyzed litters, assessed as early as embryonic day 8.5 (e8.5).

204 otein is depleted from muscle progenitors at embryonic day 8.5 (Myf5-Lap1CKO mice).

205 active specifically in the cardiac inflow at embryonic day 8.5 and throughout later SAN development a

206 tently, many mutant embryos that survived to embryonic day 8.5 displayed defects in ventral closure o

207 From as early as embryonic day 8.5 onwards, Axin2(+) cells can give rise

208 in the telencephalon and anterior retina at embryonic day 8.5 triggered upregulation of the p53 effe

209 within a critical developmental time window (embryonic day 8.5-10.5), when NT patterning and closure

210 that P3H2-null mice are embryonic-lethal by embryonic day 8.5.

211 ics" or "lower dose plastics" mixture during embryonic days 8 to 14 of gonadal sex determination and

212 uterine MDSCs, significantly increased from embryonic days 8.5 to 9.5.

213 rat, and human cells and microinjected into embryonic-day-8.5 embryos.

214 (+) cKit(-) endothelial cells harvested from embryonic day 9 (E9) aorta-gonad-mesonephros (AGM) regio

215 myocytes to a similar degree (50% to 60%) at embryonic day 9.0 could be fully rescued by residual myo

216 newal, leading to embryonic lethality before embryonic day 9.0, a developmental stage equivalent to t

217 3 INs were organized into either early-born [embryonic day 9.5 (E9.5) to E10.5] or late-born (E11.5-E

218 d that V3 INs are organized into early-born [embryonic day 9.5 (E9.5) to E10.5] or late-born (E11.5-E

219 y cilia on the developing neuroepithelium at embryonic day 9.5 (E9.5).

220 cells isolated at seven time points spanning embryonic day 9.5 (primordial heart tube) to postnatal d

221 ry MKs and directly microdissected TGCs from embryonic day 9.5 implantation sites.

222 imultaneously colonize the whole embryo from embryonic day 9.5 in a chemokine-receptor-dependent mann

223 d to arterial endothelium and endocardium by embryonic day 9.5 in transgenic mouse embryos.

224 erus to visualize the developing embryo from embryonic day 9.5 to birth.

225 icular zone and neural progenitor cells from embryonic day 9.5 to postnatal day 7.

226 enitor cells of the SNS, isolated from mouse embryonic day 9.5 trunk neural tube explants.

227 otential upon early hematopoietic tissues at embryonic day 9.5, an embryonic stage not previously des

228 the yolk sac and enter the CNS quite early (embryonic day 9.5-10 in mice).

229 Etv2 and that it has embryonic lethality by embryonic day 9.5.

230 l patterning, they succumb to apoptosis from embryonic day 9.75 onwards.

231 Early cardiac Trpm7 deletion (before embryonic day 9; TnT/Isl1-Cre) results in congestive hea

232 of the developing mouse neural tube between embryonic days 9.5-13.5.

233 ngiogenesis and cardiac defects beginning at embryonic day approximately 10.5.

234 ctivated by WNK1, died in utero beginning at embryonic day approximately 11.

235 enX (0, 2, or 10 mg/kg) via oral gavage from embryonic day (E) 1.5 to 11.5 or 17.5 to evaluate exposu

236 Intrauterine inoculation at embryonic day (E) 10, but not E14, with African, Asian o

237 leted in this tissue in Fgfr2(ST-/-) mice at embryonic day (E) 10.5.

238 As early as embryonic day (E) 11, pioneering axons tipped with large

239 os were examined for the presence of NTDs at embryonic day (E) 11.5 or E12.5.

240 Tsc1 deletion within thalamic precursors at embryonic day (E) 12.5 disrupts thalamic circuitry and a

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

242 on followed by high-throughput sequencing of embryonic day (e) 13.5 and 15.5 mouse pancreata.

243 r cells (NPCs), the cell cycle slows between embryonic day (E) 13.5 and E15.5 while other embryonic N

244 These cells populate the intestine by embryonic day (E) 13.5 and, before PP organogenesis (E14

245 on into the myocardium were impaired between embryonic day (E) 13.5 to 15.5 in mutant hearts because

246 type 5% w/w ethanol consumption regimen from embryonic day (E) 13.5-16.5, spanning the peak of cortic

247 Whole-genome RNA-sequencing analysis of embryonic day (E) 14.5 cap stage molars revealed reducti

248 pseudostratified epithelium prior to murine embryonic day (E) 14.5 to an exquisitely folded columnar

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

250 Rb1(-/-) embryos die on embryonic day (E) 14.5-15.5.

251 pparent late in development, but that before embryonic day (E) 15, fetal blood neutrophils display li

252 rain regions across nine perinatal ages from embryonic day (E) 17 to postnatal day (P) 11 and found t

253 While embryonic day (E) 18.5 Six2Frs2alphaKO kidneys were hypo

254 utamate) K(mf) ) was significantly higher at embryonic day (E) 18.5, in line with increased expressio

255 de, and reduced high-molecular-weight ADN at embryonic day (E) 18.5.

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

257 s lineage markers such as Nanog and Gata6 at embryonic day (E) 3.25, and the EPI and PrE precursor ce

258 express the Sry-type HMG box gene Sox17 from embryonic day (E) 7.5 to E8.5 specifically differentiate

259 We demonstrate that from embryonic day (E) 8.5 all megakaryocyte (MK) colony-form

260 EMPs develop in the yolk sac at embryonic day (E) 8.5, migrate and colonize the nascent

261 is highly expressed in the placenta between embryonic day (E) 9.5 and E12.5.

262 5hmC initiates asynchronously among PGCs at embryonic day (E) 9.5 to E10.5 and accounts for the uniq

263 At embryonic day (E) 9.5, when neural crest-derived cells w

264 gh-frequency sounds) born early around mouse embryonic day (E) 9.5-10.5, and those in the apex (respo

265 After the completion of neurogenesis around embryonic day (E) 90, when the cerebrum is still lissenc

266 ls (PGCs) that enter the fetal testis around embryonic day (E)10.5.

267 As a result of a low choline supply between embryonic day (E)11 and E17 of gestation, the number of

268 nergic (YFP+) neurons were first detected at embryonic day (E)11.5, and the proportion of cholinergic

269 nitors were delayed in forming two layers at embryonic day (E)13.5 when embryonic skin begins to stra

270 We found evidence of axon degradation at embryonic day (E)13.5.

271 s from heterozygous (Hsd11b(+/-)) matings at embryonic day (E)14.5 and E17.5, where all three genotyp

272 uced preterm birth in timed pregnant C57BL/6 embryonic day (E)15.5 mice and rescues their pups from s

273 oietic progenitors, anemia, and lethality by embryonic day (E)15.5.

274 function in both SMGRKO and GR(-/-) mice at embryonic day (E)17.5, associated with generalized oedem

275 The current study used an ex vivo [embryonic day (E)18] chick femur defect model to examine

276 eoxyuridine (BrdU) at various stages between embryonic day (E)3 and E16 and killing animals at postna

277 Expression and localization of polySia in embryonic day (E)5-14 chick eyefronts and E9 trigeminal

278 n the chicken (Gallus gallus) inner ear from embryonic day (E)5-E10.

279 lyzed 45,334 single-cell transcriptomes from embryonic day (E)7.5, when endoderm progenitors are spec

280 d the miRNA and gene expression profiles for embryonic day (E)8.5 endoderm, E14.5 Dlk1(+) liver cells

281 NCAM and ST8SiaII mRNA transcripts peaked by embryonic day (E)9, remained steady between E10 and E14

282 -gonad-mesonephros region, and visualized at embryonic day (E)9.0 in the yolk sac and neuroectoderm;

283 3-induced embryonic stem cells and Pax3-null embryonic day (E)9.5 mouse embryos, we identified conser

284 alysis of post-implantation conceptuses from embryonic day (E)9.5 to E13.5 revealed poorly developed

285 r hemorrhage and embryonic mortality between embryonic days (E) 12.5 and E13.5.

286 ouse B1 cell precursors are produced between embryonic days (E) 13.5 and 15.5 and remain largely quie

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

288 at is developing ventral to the pituitary at embryonic days (e)14.5, e16.5, and e18.5.

289 de neurons (peak cell cycle exit for both at embryonic day [E]12.5-E13.5), tyrosine hydroxylase neuro

290 The early phase (sampled at embryonic day [E]27-E35 following E24-E28 (3) H-thymidin

291 ue fetuses to x-rays during early gestation (embryonic day [E]30-E42), i.e., before the onset of cort

292 cells during the period of RGC neurogenesis (embryonic day, E, 12.5 to 18.5) when the RPE is closely

293 genetrap allele was embryonic lethal before embryonic day E10.5, whereas the heterozygous condition

294 ops (FFLs) using genomic data covering mouse embryonic days E10.5 to E14.5.

295 unctions occurs over a prolonged time during embryonic days E10.5-E14.5 in the mouse.

296 n mice results in embryonic lethality before embryonic day E11.5.

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

298 the 32- to 64-cell mouse embryo transition, Embryonic day (E3.25), whose study in literature is conc

299 landscapes in mouse forebrain precursors at embryonic days E8.5 and E10.5 (before and after neural t

300 x groups and treatment initiated orally from embryonic day (ED) 6 to postnatal day (PND) 15.