ライフサイエンスコーパス: embryonic

1 identified a case of regeneration in Xenopus embryonic aggregates that restores a mucociliated epithe

2 2+)-sensitive promoter to express a secreted embryonic alkaline phosphatase (SEAP) reporter.

3 Here, we identify GORAB as a regulator of embryonic alveolar sac formation as genetically disrupti

4 Embryonic and adult stem cells possess the capability of

5 ells with distinct properties develop in the embryonic and adult thymus and have been identified as c

6 ng receptor, is expressed on myocytes during embryonic and fetal myogenesis and on nascent myofibers

7 development of the human brain occur in the embryonic and fetal stages-stages that are difficult to

8 e show that only 23 +/- 1% of neurons in the embryonic and larval CNS express para, while in the adul

9 vasive, in vivo time-lapse imaging of c1vpda embryonic and larval morphogenesis to reveal a sequence

10 tally, while its expression is restricted to embryonic and neo-natal beta-cells in mice.

11 It is essential for embryonic and postembryonic plant development and it aff

12 Furthermore, we found that both embryonic and postnatal CMs binucleate at a significantl

13 in cluster structures that protrude into the embryonic aortic lumen.

14 tissues at different sites within their post-embryonic body.

15 neuron activation, we identified a group of embryonic born dorsal DG (dDG) neurons, which were activ

16 er-mediated miRNA biogenesis is required for embryonic brain development and has been suggested to be

17 elopmental anoikis specifically protects the embryonic brain from the consequences of sporadic delami

18 nts of the metabolic adjustments to maintain embryonic carbon/nitrogen homeostasis.

19 The data show that H(2) S confers embryonic cardiac protection via opening of myocardial K

20 Past studies of embryonic cell division discovered that calcium concentr

21 During embryonic cell divisions, cell size changes rapidly in b

22 rapid genome duplication during synchronous embryonic cell divisions.

23 ol and steroid hormone metabolism with early embryonic cell movements.

24 he islet beta-like cells produced from human embryonic cell-derived beta-cell clusters.

25 Carbohydrates on embryonic cells are often highly expressed in cancer and

26 tered cell-to-cell positioning, we separated embryonic cells from the yolk and allowed them to develo

27 rest cells (NCCs) are migratory, multipotent embryonic cells that are unique to vertebrates and form

28 rs are overwhelmingly important in directing embryonic cells to a particular differentiation pathway,

29 hen Xist is deleted systemically in post-XCI embryonic cells using the Meox2-Cre driver, female pups

30 s or comparisons of multiple biopsies of few embryonic cells.

31 arkers associated with mesenchymal state and embryonic cellular phenotypes.

32 se a model in which uniquely large zebrafish embryonic centrosomes direct spindle placement within di

33 d on postnatal cFb-derived ECM compared with embryonic cFb-derived ECM.

34 The shift from maternal to embryonic control is a critical developmental milestone

35 dimensional collagen architecture of wounded embryonic corneas, whilst identifying temporal and spati

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

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

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

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

40 rogenitors labeled by tamoxifen induction at embryonic day 10.5.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 3 INs were organized into either early-born [embryonic day 9.5 (E9.5) to E10.5] or late-born (E11.5-E

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

60 n of the ppm1f gene in mice results in early embryonic death at day E10.5.

61 Embryonic deletion of integrin beta1 in the liver disrup

62 Cortical malformations arise during embryonic development and have been linked to childhood

63 tone variant function in the context of both embryonic development and human disease, specifically de

64 ms facilitate de novo DNA methylation during embryonic development and in somatic cells.

65 NAs and leads to severe defects during mouse embryonic development and skin morphogenesis.

66 tributions of individual cell populations to embryonic development and tissue regeneration.

67 fied via centriole rosette formation in both embryonic development and turnover of the olfactory epit

68 EMT is crucial to embryonic development and wound healing.

69 sions involved in vascular and hematopoietic embryonic development are still poorly understood.

70 further improved by removing females during embryonic development as larval diet costs are significa

71 The variants affect normal embryonic development by disrupting the synthesis of NAD

72 lia of the left-right organizer during early embryonic development can lead to laterality defects suc

73 Moreover, naive pluripotency during embryonic development coincides with a reduction in CDK8

74 how the axial tissues that are formed during embryonic development give rise to the adult spine and s

75 Early post-implantation human embryonic development has been challenging to study due

76 ranscription factor gene Prdm16 during mouse embryonic development has been shown to cause a severe l

77 C. elegans, the roles of the PAR proteins in embryonic development have been extensively studied, yet

78 ons in most aspects of cellular function and embryonic development in both animals and plants.

79 he cell-cycle timing asynchrony of the early embryonic development in C. elegans is determined indepe

80 of action during eye formation in vertebrate embryonic development is still unknown.

81 Here, we show that embryonic development of cartilage in the skate (Leucora

82 Embryonic development of the alveolar sac of the lung is

83 can transfer from parents to progeny during embryonic development or accumulate through Se-enriched

84 site were treated with estradiol (E2) during embryonic development prior to gonadal differentiation.

85 The mechanisms of pattern formation during embryonic development remain poorly understood.

86 Axonal connectivity is largely built during embryonic development through highly constrained process

87 quantified mouse polyA-RNA from day 10.5 of embryonic development to birth, sampling 17 tissues and

88 iological processes such as wound repair and embryonic development where cell spreading and migration

89 n body, from the early stages of life (i.e., embryonic development) to life-threatening diseases (e.g

90 During embryonic development, a simple ball of cells re-shapes

91 ntum in the study of cell differentiation in embryonic development, adult stem cells, and cancer path

92 During embryonic development, GATA transcription factors GATA2

93 Almost all animals undergo embryonic development, going from a single-celled zygote

94 proutys have been extensively studied during embryonic development, their role and mode of action dur

95 ng system plays multiple, essential roles in embryonic development, tissue homeostasis, and human dis

96 the surrounding extracellular matrix during embryonic development, wound repair, and tumor invasion.

97 n fatty acid synthesis to critically support embryonic development.

98 fficient and senescent placenta that impairs embryonic development.

99 nexpected role of this pathway in vertebrate embryonic development.

100 ediated gene silencing that is essential for embryonic development.

101 nvironments at the expense of retarding post-embryonic development.

102 of how it affects cellular processes during embryonic development.

103 failure of neural tube closure during early embryonic development.

104 sitions during stem cell differentiation and embryonic development.

105 uctures and large chromatin domains in early embryonic development.

106 g RING E3-ubiquitin ligase with functions in embryonic development.

107 tion that primes transcriptional program for embryonic development.

108 nal modification involved in oncogenesis and embryonic development.

109 nct waves at various anatomical sites during embryonic development.

110 The potent impact of FGF-FGFR in multiple embryonic developmental processes makes it challenging t

111 This embryo enters embryonic diapause until the newborn leaves the pouch 9

112 Subclustering of these major embryonic domains revealed over 50 cell states with dist

113 ances pSmad1/5 activation, we used zebrafish embryonic dorsoventral (DV) patterning as an assay for B

114 inesis and uncovered novel functions for the embryonic ECM proteins SLIT2 and NPNT (nephronectin) in

115 These data demonstrate that embryonic ECM undergoes constant replacement, which is l

116 e core subunits, enhancer of zeste 2 (EZH2), embryonic ectoderm development (EED), and suppressor of

117 We found that HDAC3 is expressed broadly in embryonic epidermis and is required for its orderly step

118 This double face is evident in the embryonic epidermis of zebrafish loss-of-function mutant

119 Embryonic exposure to CAR significantly increased levels

120 polyunsaturated fatty acids (PUFAs) in their embryonic fatty acid pool.

121 f the HSC state in the adult bone marrow and embryonic fetal liver, the mechanism of HSC self-renewal

122 o profile human skeletal muscle tissues from embryonic, fetal, and postnatal stages.

123 ation, redox state and migration using mouse embryonic fibroblast Balb/3T3, human dermal fibroblast N

124 eomes extracted from Escherichia coli, mouse embryonic fibroblast cell cultures, and Arabidopsis thal

125 cell-based complementation studies in mouse embryonic fibroblast deficient for Esco1 and Esco2, as a

126 we analyze de novo DNA methylation in mouse embryonic fibroblasts (2i-MEFs) derived from DNA-hypomet

127 Moreover, PGAM5 deficient mouse embryonic fibroblasts (MEFs) exhibited decreased phospho

128 mouse bone marrow-derived macrophages, mouse embryonic fibroblasts (MEFs), and human HeLa cells upon

129 -2 can be cell surface-biotinylated on mouse embryonic fibroblasts (mEFs), revealing that endogenous

130 ripotent stem cells in comparison with mouse embryonic fibroblasts (MEFs).

131 lls, we deleted ELMOD2 in immortalized mouse embryonic fibroblasts and discovered a number of cellula

132 n immortalization of Rb1 (-/-) primary mouse embryonic fibroblasts and in aggressive tumor growth in

133 Experiments carried out in mouse embryonic fibroblasts corroborated these findings.

134 I gene from lambda phage in transgenic mouse embryonic fibroblasts during the transition from primary

135 h1, Pou4f3, and Gfi1) that can convert mouse embryonic fibroblasts, adult tail-tip fibroblasts and po

136 opy were performed in prkar1 knock-out mouse embryonic fibroblasts, neonatal myocytes, or adult LV my

137 rogramming potential of Tet2-deficient mouse embryonic fibroblasts.

138 d initiation of inflammation in Mus musculus embryonic fibroblasts.

139 rious cultured human cell lines and in mouse embryonic fibroblasts.

140 tor forces in live human platelets and mouse embryonic fibroblasts.

141 D2, and increased caveolar mobility in mouse embryonic fibroblasts.

142 core components and the accessory proteins, EMBRYONIC FLOWER 1 (EMF1), LIKE HETEROCHROMATIN PROTEIN1

143 In contrast, embryonic geometry is highly predictive of individual pa

144 hat AP patterning is robust to variations in embryonic geometry; segmentation gene expression remains

145 r transcriptomes of human extraembryonic and embryonic germ layers differentiated in a stereotyped ar

146 Among the three embryonic germ layers, the mesoderm plays a central role

147 imordial germ cells (PGCs) in the C. elegans embryonic gonad primordium.

148 lement protein subcomponents C1r/C1s, urchin embryonic growth factor, and bone morphogenetic protein

149 em, endogenous electric field (EF) influence embryonic growth.

150 ncluding human fetal echocardiography, chick embryonic heart ultrasound images, and zebrafish embryon

151 Embryonic hearts (19 out of 21 days of incubation) mount

152 lize the coronary microvasculature in intact embryonic hearts and quantify vessel organization.

153 We profiled 7 histone modifications in embryonic hearts from each of 9 distinct Carnegie stages

154 Formation of de novo HFs recapitulated embryonic HF development, and mature follicles produced

155 Embryonic interneuron development underlies cortical fun

156 the D melanogaster skeletal muscle myosin II embryonic isoform (EMB).

157 ordings from 20 sensors in parallel in human embryonic kidney (HEK293) cells and in human induced plu

158 av1.9 in heterologous systems (e.g. in human embryonic kidney 293 (HEK293) cells) has hampered studie

159 phosphate-buffered saline (SCI + PBS), human embryonic kidney 293 (HEK293) cells, and hAFSCs transpla

160 yanodine receptor isoform 2-expressing human embryonic kidney 293 cells) cells, biochemistry, dual Ca

161 As control cell lines HEK 293 from embryonic kidney and RC 124 from adult kidney tissue as

162 cleotide polymorphism was expressed in human embryonic kidney cells, and its effect on phospholemman

163 o partially mimic the branch geometry of the embryonic kidney epithelial network.

164 acycline-inducible APOL1 expression in human embryonic kidney HEK293 cells and examined the effects o

165 datasets of pubertal mammary gland tips and embryonic kidney tips, as well as homeostatic intestinal

166 ms' tumor (WT) morphologically resembles the embryonic kidney, consisting of blastema, epithelial and

167 criptomes of 544 individual cells from mouse embryonic kidneys.

168 Embryonic large molecule derived from yolk sac (ELYS) is

169 is and in situ hybridization assays of maize embryonic leaves suggested that maize ANT1 (ZmANT1) regu

170 Loss of SMN entirely is embryonic lethal in mammals.

171 like in rodents, where the grin1 knockout is embryonic lethal, grin1 double-mutant fish (grin1a (-/-)

172 e F0 and F1 domains (R35E,R118E), which were embryonic lethal.

173 ast, homozygous Kcnt1(R455H/R455H) mice were embryonic lethal.

174 Mice lacking Ankmy2 are mid-embryonic lethal.

175 ementation of selected n-6 PUFAs rescued the embryonic lethality and defective permeability barrier.

176 s the mir-35-42 mutant phenotype by inducing embryonic lethality and low fecundity.

177 ors result in CED-3-dependent suppression of embryonic lethality and meiotic chromosome non-disjuncti

178 A lipodystrophy allele of seip-1 resulted in embryonic lethality as well and could be rescued by PUFA

179 TSPCs impairs their self-renewal, leading to embryonic lethality before embryonic day 9.0, a developm

180 pathy, and homozygous expression resulted in embryonic lethality by midgestation.

181 The D325A mutation in mouse RIPK1 leads to embryonic lethality during mouse development(2,3).

182 n a weak ced-3(-) mutant, and suppresses the embryonic lethality of a mutant defective for the apopto

183 described, and murine Nmnat1 knockouts show embryonic lethality, indicating that complete absence of

184 ac trabeculation, cause cardiomyopathies and embryonic lethality, yet how tissue symmetry is broken t

185 xpression can cause developmental defects or embryonic lethality.

186 vation of developmental genes and subsequent embryonic lethality.

187 d Sax, and elevated Dpp signaling results in embryonic lethality.

188 iotropic developmental phenotypes, including embryonic lethality.

189 nockout of Specc1l in mouse results in early embryonic lethality.

190 m-line elimination of the Ubiad1 gene caused embryonic lethality.

191 Vitamin E (VitE) deficiency results in embryonic lethality.

192 The Ser/Thr protein kinase MELK (maternal embryonic leucine zipper kinase) has been considered an

193 acquire metastatic capability by adopting an embryonic-like phenotype, and that a lineage approach wo

194 nt, MCs enter the skin from the yolk sac and embryonic liver and are later mixed with cells originati

195 The embryonic liver is the main site of erythropoietin synth

196 verexpressing or suppressing Vcan in primary embryonic lung fibroblasts could, respectively, mimic or

197 od availability and whether it recapitulates embryonic mechanisms remain poorly understood.

198 We find that embryonic meningeal fibroblasts are transcriptionally di

199 yonic heart ultrasound images, and zebrafish embryonic microscope images, with the average Dice coeff

200 M) and programmed cell death (PCD) along the embryonic midline.

201 elopmental and stem cell biologists studying embryonic morphogenesis and adult tissue renewal.

202 1 that direct MHB-specific expression in the embryonic mouse brain.

203 Using conditional inactivation in the embryonic mouse eye, our data indicate that loss of Nf2

204 at laminin 211 increases BP proliferation in embryonic mouse neocortex.

205 Myosin heavy chain-embryonic (MyHC-emb) is a skeletal muscle-specific contr

206 o regulate spatiotemporal gene expression in embryonic neural development and uncover a crucial epige

207 onditions that more closely recapitulate the embryonic niche.

208 the number of active replication origins in embryonic nuclei is higher than in somatic ones, ensurin

209 r, Cep55 is dispensable for cell division in embryonic or adult tissues.

210 use models correlates AM function with their embryonic or monocyte origin.

211 able part of the brain owing to their common embryonic origin.

212 hPGCLCs are aggregated with mouse embryonic ovarian somatic cells to form xenogeneic recon

213 The mesenchyme is the main component of the embryonic pancreatic microenvironment, yet its cellular

214 dentified risk loci in periderm development, embryonic patterning, and/or regulation of cellular proc

215 mmachc mutants survived the embryonic period but perished in early juvenile life.

216 s, thus allowing the specific disturbance of embryonic photosynthesis.

217 and pharmacological approaches to show that embryonic photosynthetic activity is necessary for norma

218 Selective ablation of Prdm12 in embryonic POMC neurons led to significantly reduced Pomc

219 g the CNS, but originate primarily from late embryonic precursors and become replaced by bone-marrow-

220 how that snMacs do not derive from the early embryonic precursors colonizing the CNS, but originate p

221 C2 activity and lack silenced chromatin like embryonic progenitors.

222 we transplanted serotonergic neuron enriched embryonic raphe nucleus-derived neural stem cells/progen

223 ecimens still remain the only unquestionable embryonic remains of a sauropod dinosaur providing an in

224 stages and RGCs differentiated in vitro from embryonic retinal progenitors for the effects of aging a

225 e that Smyhc1 is essential for myogenesis in embryonic slow muscles, and loss of Smyhc1 results in de

226 In birds and mammals the embryonic somites generate a linear series of impenetrab

227 onstrated that Hox expression continues from embryonic stages through postnatal and adult stages excl

228 for telomere protection in mouse pluripotent embryonic stem (ES) and epiblast stem cells.

229 histone methyltransferase SUV420H2 regulates embryonic stem (ES) cell fate by patterning the epigenet

230 PADI4 was recently implicated in regulating embryonic stem and hematopoietic progenitor cells.

231 ws: maternal reprogramming at fertilization, embryonic stem cell (ESC) differentiation, and the conti

232 f various developmental programs and also of embryonic stem cell (ESC) differentiation.

233 on landscape using a panel of knockout human embryonic stem cell (ESC) lines.

234 ntify drugs that reduce ACE2 levels in human embryonic stem cell (hESC)-derived cardiac cells and lun

235 The membrane fraction from MYL4-/- human embryonic stem cell derived atrial cells demonstrated in

236 f MLH3 eliminates expansions in an FXD mouse embryonic stem cell model.

237 enotoxicity or phenotypic changes in a human embryonic stem cell reporter assay.

238 In vitro experiments showed that human embryonic stem cell-derived cardiomyocytes (hESC-CMs) co

239 n of neonatal mouse cardiomyocytes and human embryonic stem cell-derived cardiomyocytes are considera

240 Mouse embryonic stem cells (ESCs) and epiblast-derived stem ce

241 h POLR3G expression being highly enriched in embryonic stem cells (ESCs) and tumor cells relative to

242 anscription elongation-associated factors in embryonic stem cells (ESCs) compared to somatic cells.

243 Pluripotent embryonic stem cells (ESCs) contain the potential to for

244 We used Chd7 null embryonic stem cells (ESCs) derived from Chd7 mutant mou

245 D carriers via injection of mdx (murine DMD) embryonic stem cells (ESCs) into wild-type (WT) blastocy

246 Human embryonic stem cells (ESCs) offer a promising therapeuti

247 In our study, we focused on embryonic stem cells (ESCs), because this cell type disp

248 on self-renewal and differentiation of mouse embryonic stem cells (ESCs).

249 d by distinctive CpG methylation dynamics in embryonic stem cells (ESCs).

250 culture human cerebral organoids from human embryonic stem cells (hESC) to investigate the effect of

251 e transplanted DA neurons derived from human embryonic stem cells (hESCs) into the striatum and asses

252 When and how human embryonic stem cells (hESCs) irreversibly commit to diff

253 Mouse embryonic stem cells (mESCs) cultured with MEK/ERK and G

254 data from a retinoic acid (RA)-induced mouse embryonic stem cells (mESCs) differentiation experiment.

255 Mouse embryonic stem cells (mESCs) display unique mechanical p

256 ere significantly decreased in Tet2 KO mouse embryonic stem cells (mESCs) in comparison with wild-typ

257 ) in shaping 3D genome organization in mouse embryonic stem cells (mESCs).

258 cal interaction between TET1 and NANOG using embryonic stem cells and bacterial expression systems.

259 By generating ETS1-deficient human embryonic stem cells and by expressing the dominant-nega

260 KDM6A is important for differentiation of embryonic stem cells and development of various tissues.

261 ylation (mCH) has been reported in mammalian embryonic stem cells and in the brain.

262 ch is expressed on the cell surface of human embryonic stem cells and many cancer types.

263 ousands of individual regulatory elements in embryonic stem cells and measure cis and trans effects b

264 me-wide RNAi screen in BRCA2-deficient mouse embryonic stem cells and validation in KB2P1.21 mouse ma

265 Activation of Hoxb1 in embryonic stem cells arrests cardiac differentiation, wh

266 Mouse embryonic stem cells can be differentiated into ureteric

267 and found that the organoids developed from embryonic stem cells contained a diverse array of glial

268 In the absence of Vimentin, pluripotent embryonic stem cells fail to differentiate properly, wit

269 ys reveal that Dppa2/4 double knockout mouse embryonic stem cells fail to exit pluripotency and diffe

270 Embryonic stem cells in culture self-organise to form sp

271 Mettl3 or the nuclear reader Ythdc1 in mouse embryonic stem cells increases chromatin accessibility a

272 ddressed this by injecting labeled wild-type embryonic stem cells into blastocysts derived from lipod

273 in mammals, we used CRISPR to generate mouse embryonic stem cells lacking one or both of the two muri

274 e transplantation of DA neurons derived from embryonic stem cells or induced pluripotent stem cells (

275 Gene disruption in mouse embryonic stem cells or zygotes is a conventional geneti

276 Moreover, endogenous tagging of Nanog in embryonic stem cells reveals that ERK inhibition promote

277 time course dataset from differentiation of embryonic stem cells to cardiomyocytes.

278 bine induced neurons (iNeurons) derived from embryonic stem cells with quantitative proteomics to rev

279 ells, YIPF5 knockout and mutation knockin in embryonic stem cells, and patient-derived induced plurip

280 Here we show that in mouse embryonic stem cells, EloA localizes to both thousands o

281 We report that in mouse embryonic stem cells, expression of a transgene comprisi

282 Here, we map circRNA inventories of mouse embryonic stem cells, neuronal progenitor cells and diff

283 Using Drosophila and mouse embryonic stem cells, we characterise a recruitment hier

284 nal repression, and at CAG trinucleotides in embryonic stem cells, where it positively correlates wit

285 intrinsically covarying gene pairs in mouse embryonic stem cells.

286 es in silencing repetitive elements in mouse embryonic stem cells.

287 e maintenance and genomic stability of mouse embryonic stem cells.

288 n MLL2-dependent gene as a reporter in mouse embryonic stem cells.

289 Embryonic stem-cell-related transcription factors are ce

290 ulations, culminating in defects to anterior embryonic structures, including the pharyngeal arches, h

291 a zebrafish model, we genetically ablate all embryonic tendon cells and find complete regeneration of

292 olarized growth is observed in polyp but not embryonic tentacle primordia.

293 Here, we show that zebrafish embryonic tissue explants, prepared prior to germ layer

294 plex organ systems are assembled from simple embryonic tissues is a major challenge.

295 pped hPSC-derived myogenic progenitors to an embryonic-to-fetal transition period.

296 rome (CdLS), thought to arise from defective embryonic transcription.

297 binding becomes more prevalent and requires embryonic transcription.

298 r and mother, but not of the zygote, affects embryonic viability and growth during gestation.

299 ion during the implantation stages to confer embryonic viability.

300 ng both postnatal and adult mice, as well as embryonic zebrafish, we demonstrate that endothelial-spe