ライフサイエンスコーパス: embryonic day

1 ups generated from the p1 domain (where E is embryonic day).

2 s expressed in the retina and lens by murine embryonic day 10 (E10) and tumors are observed by E12.5.

3 lacking both epsins 1 and 2 (Epn1/2) die at embryonic day 10 and exhibit an abnormal vascular phenot

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

5 KLF2(-/-) double knockout mice are anemic at embryonic day 10.5 (E10.5) and die by E11.5, in contrast

6 y expressing Blimp-1Deltaexon7 die at around embryonic day 10.5 (E10.5) due to placental defects.

7 est of Blimp1/Prdm1 mutant embryos at around embryonic day 10.5 (E10.5) has been attributed to placen

8 ll become inhibitory (GAD67(+)) in mice from embryonic day 10.5 (E10.5) to postnatal day 28 (P28).

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

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

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

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

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

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

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

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

17 ate disruption of brain-specific Trpm7 after embryonic day 10.5 does not alter normal brain developme

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

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

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

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

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

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

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

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

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

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

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

29 Homozygous R702C mice die at embryonic day 10.5-11.5, whereas homozygous D1424N and E

30 kg choline chloride in AIN76A) prenatally on embryonic days 10-22, on postnatal days (PD) 25-50, or a

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

32 pendent RGC precursors in the earliest born (embryonic day 11) retinal cohort, but these precursors r

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

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

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

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

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

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

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

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

41 he UTY gene, show embryonic lethality before embryonic day 11.5.

42 arch, otic vesicle, forebrain and/or limb at embryonic day 11.5.

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

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

45 ermal desmosomes are calcium-dependent until embryonic day 12 (E12) and become hyper-adhesive by E14.

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

47 viruses (AAV) for their ability to transduce embryonic day 12 or 13 SMGs.

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 associated with endocrine cells) as early as embryonic day 12.5 (E12.5) and increased dramatically by

52 In embryonic day 12.5 (e12.5) embryos, where Meg3 is matern

53 Bright(-/-) embryonic day 12.5 (E12.5) fetal livers showed an increa

54 es severe deficits in surface area growth by embryonic day 12.5 (E12.5) in the mouse.

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

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

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

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

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

60 f elevated apoptosis observed transiently at embryonic day 12.5 in the developing retina.

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

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

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

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

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

66 cytes resulted in embryonic lethality before embryonic day 12.5.

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

68 S) speciation of developing chick corneas at embryonic days 12, 14, and 16 were investigated using sy

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

70 les from 14 distinct epithelial locations at embryonic days 12.5, 13.5, 14, and 15, and characterized

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

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

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

74 1 and JM-a CYT-2 was first detectable around embryonic day 13 in the mouse, mainly in the collecting

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

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

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

78 anced Pdgfrbeta-dependent proliferation from embryonic day 13.5 (E13.5) of mouse development.

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

80 Pial collaterals begin forming between embryonic day 13.5 and 14.5 as sprout-like extensions fr

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

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

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

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

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

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

87 ral-to-dorsal fashion in a tight window from embryonic day 13.5 until postnatal day 3, which correlat

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

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

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

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

92 Mouse embryos lacking Bag1 die at embryonic day 13.5, with reduced erythroid colony formin

93 lated from wild-type and Tlr4(Lps-d) mice at embryonic day 13.5.

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

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

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

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

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

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

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

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

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

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

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

105 ing results from gene expression profiles of embryonic day 14.5 palates from Tgfbr2(fl/fl);Wnt1-Cre m

106 were isolated from adult (6-8 wk) and fetal (embryonic day 14.5) livers of mice and reprogrammed to b

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

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

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

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

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

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

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

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

115 l mast cells in scarless wounds generated at embryonic day 15 (E15) are fewer in number, less mature,

116 ith saline or methylazoxymethanol acetate at embryonic Day 15 or 17 to induce differing malformation

117 we found that neural stem cells (NSCs) from embryonic day 15 rat cortex increased their rate of prol

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

119 ts exposed to methylazoxymethanol acetate at embryonic Day 15.

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

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

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

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

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

125 1, age and sex-matched euploid controls, and embryonic day 15.5 forebrains from Ts1Cje, Ts65Dn, and D

126 2 is expressed broadly by progenitors in the embryonic day 15.5 subventricular zone, during the peak

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

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 pocampal area was similar in rats exposed at embryonic Days 15 and 17 but was smaller compared with c

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

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

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

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

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

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

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

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

140 Endochondral ossification in embryos from embryonic day 16.5 was assessed by histologic and immuno

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

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

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

144 ve terminals and axons at the nascent NMJ on embryonic days 16.5-18.5.

145 g agent methylazoxymethanol acetate (MAM) on embryonic day 17 (E17) produces behavioral and anatomica

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

147 ts exposed to methylazoxymethanol acetate at embryonic Day 17, which was greater than rats exposed to

148 the cortex of Sprague-Dawley rat fetuses on embryonic day 17.

149 genes, we performed mRNA-seq experiments on embryonic day 17.5 (E17.5) mouse placenta cDNA samples f

150 Col10a1-TAP63alpha transgenic mice at either embryonic day 17.5 (E17.5) or postnatal day 1 (P1) obser

151 sed in gamma-MNs in the mouse spinal cord by embryonic day 17.5 and continues to molecularly distingu

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

153 stnatally, En2 expression is extinguished by embryonic day 17.5.

154 ction and severe hydronephrosis beginning at embryonic day 17.5.

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

156 ct developmental stages of the mouse cortex, embryonic day 18 (E18) and postnatal day 7 (P7), we esta

157 ely as mast cells of fibrotic wounds made at embryonic day 18 (E18).

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

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

160 The diffusion of RF across embryonic day 18 chick corneal epithelium ex vivo was mo

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

162 bone development is inhibited in gestational embryonic day 18.5 (E18.5) embryos from rat dams made ob

163 VEGF-A expression was detected at embryonic day 18.5 (E18.5), the onset of ciliary process

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

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

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

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

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

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

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

171 oinjection of amniotic fluid into the fetal (embryonic day 18.5) gastrointestinal tract reduced LPS-m

172 At embryonic day 18.5, GSK3beta activity decreased to level

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

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

175 RGCs were isolated from embryonic day 20 (E20) or postnatal days 5 to 7 (P5-7) S

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

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 esis, showing that p53 is active as early as embryonic day 3.5 and that p53 activity becomes restrict

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

181 poration techniques in chick embryos between embryonic days 3 and 6, we demonstrate that organiser pr

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

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

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

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

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

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

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

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

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

191 ty becomes restricted to embryonic tissue by embryonic day 6.5.

192 ults in embryonic lethality at approximately embryonic day 7.

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

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

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

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

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

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

199 949, and 1,166 single murine heart cells at embryonic day 8.5 (e8.5), e9.5, and e10.5, respectively.

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

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

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

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

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

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

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

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

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

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

210 velopment of inhibitory inputs to NL between embryonic day 9 (E9) and E17.

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

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

213 ng differentiation of cardiac progenitors at embryonic day 9.0.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 ta-gonado-mesonephros region of the fetus on embryonic day (E) 10.5-11.

230 showed an anterior-to-posterior gradient at embryonic day (E) 10.5-11.5.

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

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

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

234 rted to be expressed in the retina at around embryonic day (E) 11.5.

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

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

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

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

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

240 d strains of mice, teratomas initiate around embryonic day (E) 13.5 during the same developmental per

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

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

243 gnant C57BL/6 mice were treated beginning at embryonic day (E) 14 and quantitative reverse-transcript

244 Villi first emerge at embryonic day (E) 14.5 from a previously flat luminal su

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

246 Starting at embryonic day (E) 14.5, fADN (0.62 +/- 0.02 mug (g body

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

248 reased expression of Bmp10 and pSmad1/5/8 at embryonic day (E) 14.5.

249 ild-type mouse whole eyes or retinas between embryonic day (E) 15 and post-natal day (P) 30.

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

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

252 e we demonstrate that Ucn 3 first appears at embryonic day (E) 17.5 and, from approximately postnatal

253 ntly established a new myelin coculture from embryonic day (E) 18 rat embryos consisting of hippocamp

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

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 At embryonic day (E) 6.5, we find that the X/X(Xist-) ExE l

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 S, and CSA/C was performed on eyefronts from embryonic day (E) 9 to E14 and staining visualized by co

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 ental time points in the transition from the embryonic day (E)10.5 stage of lens placode invagination

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

266 laser captured embryonic mouse diaphragms at embryonic day (E)11.5 and E12.5 when experimental pertur

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

268 ound that endothelial cells of lymph sacs at embryonic day (E)12.5 and tracheal lymphatics at E16.5 w

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 FB tissue from wildtype and FGF-2-deficient embryonic day (E)14.5 embryos, respectively.

273 hair cell differentiation in mice starts at embryonic day (E)14.5, beginning with the inner hair cel

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

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

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

277 orneal morphogenesis of the Er/Er embryos at embryonic day (E)18.5.

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

279 AChE+ cells were first detectable in an embryonic day (E)4 retina, while ChAT appeared 1 day lat

280 erve growth cones reach the cornea margin at embryonic day (E)5, where they are initially repelled fo

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

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

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

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

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

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

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

288 filtered air (FA) or diesel exhaust (DE) on embryonic days (E) 9-17.

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

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

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

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

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

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

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

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 x--into the cerebral ventricles of chicks at embryonic day (ED) 4.

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

300 FP-Cre mouse to trace the fate of EPDCs from embryonic day (ED)10 until birth.