ライフサイエンスコーパス: embryonic stem cell

1 ctional interaction between BAP1 and PRC2 in embryonic stem cells.

2 and mediates its recruitment to chromatin in embryonic stem cells.

3 demethylation rates at 860,404 CpGs in mouse embryonic stem cells.

4 targeted TagRFP to the Myom2 locus in mouse embryonic stem cells.

5 tering and transcription activation in mouse embryonic stem cells.

6 some in preimplantation mouse embryos and in embryonic stem cells.

7 modeling to analyze Repli-BS data from human embryonic stem cells.

8 s gate exit from naive pluripotency of mouse embryonic stem cells.

9 HDR in multiple human cell types, including embryonic stem cells.

10 intrinsically covarying gene pairs in mouse embryonic stem cells.

11 on tRNA modifications change codon usage in embryonic stem cells.

12 constructs using neurons derived from human embryonic stem cells.

13 regulation of the totipotent state in mouse embryonic stem cells.

14 the proliferation and the survival of mouse embryonic stem cells.

15 data generated from S. cerevisiae and mouse embryonic stem cells.

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

17 envelope and plasma membrane fluctuations in embryonic stem cells.

18 mmalian stem cell types, such as pluripotent embryonic stem cells.

19 -joining maintains genome stability of human embryonic stem cells.

20 s to single cell clusters and differentiated embryonic stem cells.

21 ls of signalling pathway components in mouse Embryonic Stem Cells.

22 sine levels are highest in human pluripotent embryonic stem cells.

23 E ablates macrophage development from murine embryonic stem cells.

24 y affects gene expression in trophoblast and embryonic stem cells.

25 potency exit and germ layer specification of embryonic stem cells.

26 aptic function in neurons derived from human embryonic stem cells.

27 controlling chromatin accessibility of mouse embryonic stem cells.

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

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

30 hromatin at developmental gene loci in mouse embryonic stem cells.

31 iciency of homology-directed repair (HDR) in embryonic stem cells.

32 ive CME is essential for the pluripotency of embryonic stem cells.

33 e cytoplasm of neurons derived from human HD embryonic stem cells.

34 d for optimal maintenance of pluripotency in embryonic stem cells.

35 tionally complement the loss of Jpx in mouse embryonic stem cells.

36 Recent studies in 2-cell-like embryonic stem cells (2C-like cells) suggest that transc

37 sential for pluripotency and self-renewal of embryonic stem cells(3).

38 g efficiencies were low (<=6%), FA corrected embryonic stem cells acquired a strong proliferative adv

39 al cells and pericytes that are induced from embryonic stem cells also hinders these signaling cascad

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

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

42 C) is exclusively expressed in the placenta, embryonic stem cells and certain cancers however, its ro

43 In mammalian embryonic stem cells and cultured neurons, SRPK phosphor

44 ineage trees of human cancer cells and mouse embryonic stem cells and develop a statistical framework

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

46 es of heterozygous and homozygous Chd8 mouse embryonic stem cells and differentiated neural progenito

47 ll type-specific accessibility between mouse embryonic stem cells and embryonic stem cell-derived def

48 ers at the endogenous Sox2 and Mir290 SEs in embryonic stem cells and found that the allelic DNA meth

49 related with the pluripotency grade of mouse embryonic stem cells and human induced pluripotent stem

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

51 Under similar conditions, human embryonic stem cells and induced pluripotent stem cells

52 DNA demethylase TET1 is highly expressed in embryonic stem cells and is important both for lineage c

53 rectly predicted early data point sources as embryonic stem cells and late data point sources as hear

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

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

56 ing cells by stably expressing eCRs in mouse embryonic stem cells and measuring their subnuclear loca

57 on in three cellular models, including mouse embryonic stem cells and mouse myoblasts.

58 , DNMT3A, DNMT3A/3B and DNMT1 knockout human embryonic stem cells and observed a widespread increase

59 Studies from embryonic stem cells and other cell types have revealed

60 rmal cells from mouse and human Pax3-induced embryonic stem cells and Pax3-null embryonic day (E)9.5

61 hat SPOP suppresses stem cell traits of both embryonic stem cells and PrCa cells through promoting Na

62 hole-genome mapping of 5mC and 5hmC in mouse embryonic stem cells and show that, compared with bisulf

63 principle, we applied this strategy to mouse embryonic stem cells and successfully captured the expre

64 human colon carcinoma line HCT116, and mouse embryonic stem cells and their neural progenitor derivat

65 o sequence difficult-to-map regions in mouse embryonic stem cells and to identify distinct methylatio

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

67 reased retinoic acid signaling in both human embryonic stem cells and zebrafish mutant models, as wel

68 ith the use of adult renal progenitor cells, embryonic stem cells, and induced pluripotent stem cells

69 en characterized in certain cancerous cells, embryonic stem cells, and other rapidly proliferative ce

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

71 In the 20 years since human embryonic stem cells, and subsequently induced pluripote

72 me integrity, maintenance of pluripotency of embryonic stem cells, antibody-gene diversification, coo

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

74 election of variants was analyzed in a mouse embryonic stem cell-based functional assay.

75 to cumbersome and time-consuming traditional embryonic stem cell-based methods.

76 ell fate decisions during development and in embryonic stem cells by maintaining pluripotency or by r

77 rmined that Sox2 directly binds RNA in mouse embryonic stem cells by UV-cross-linked immunoprecipitat

78 Mouse embryonic stem cells can be differentiated into ureteric

79 Here we show that human embryonic stem cells can be used to generate gastruloids

80 Embryonic stem cells can propagate indefinitely in a plu

81 3K9me3)-marked heterochromatin is reduced in embryonic stem cells compared to differentiated cells.

82 Primed mouse embryonic stem cells contain a rare subset of "2C-like"

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

84 seq is sensitive enough to distinguish mouse embryonic stem cells cultured under different conditions

85 Here, we show that mouse embryonic stem cells cultured under extended pluripotent

86 Human embryonic stem cells, cultured with BMP4 on extracellula

87 e neural network previously trained in mouse embryonic stem cell cultures (InDelphi-mESC) is able to

88 Embryonic stem cell cultures are thought to self-organiz

89 Embryonic stem cell cycle miRs are a class of microRNAs

90 we investigate chromatin boundaries in mouse embryonic stem cells, defined by the regions with decrea

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

92 lysis were recovered from transplanted human embryonic stem cell-derived beta cells.

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

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

95 Genome-editing in human embryonic stem cell-derived cardiomyocytes confirms the

96 ssessed in isolated cardiomyocytes and human embryonic stem cell-derived cardiomyocytes, and function

97 oblastoma cell lines, primary astrocytes and embryonic stem cell-derived cortical interneurons.

98 ility between mouse embryonic stem cells and embryonic stem cell-derived definitive endoderm cells, s

99 Overexpression of NLGN4 in human embryonic stem cell-derived neurons resulted in an incre

100 lity and sensitivity of this method in mouse embryonic stem cells, developing embryos, adult tissues,

101 al role in the DNA damage response (DDR) and embryonic stem cell development.

102 ass cytometry time course dataset from mouse embryonic stem cells differentiating into the three germ

103 ed several TFs across a time course of human embryonic stem cell differentiation and studied their in

104 ng literature and new experimental data from embryonic stem cell differentiation reporter assays.

105 ed to neurons transdifferentiated from human embryonic stem cells, directly increased dendritic arbor

106 ted YY1 binding sites were hypomethylated in embryonic stem cells, during neurodifferentiation, and i

107 In mouse embryonic stem cells, Dux drives a small percentage of c

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

109 ) signalling drives differentiation of mouse embryonic stem cells (ES cells) and pre-implantation emb

110 Embryonic stem cell (ESC) derived tissue is a promising

111 tenance of distinct chromatin domains during embryonic stem cell (ESC) differentiation are crucial fo

112 Embryonic Stem Cell (ESC) differentiation requires compl

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

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

115 developmental pathways and study effects on embryonic stem cell (ESC) germ layer specification and m

116 he RNA-associated protein Srrt/Ars2 sustains embryonic stem cell (ESC) identity by preventing prematu

117 progenitor cell (NPC) development from mouse embryonic stem cell (ESC) lines deficient for XRCC4 plus

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

119 fibroblasts, accompanied by induction of an embryonic stem cell (ESC) phenotype.

120 Using a mouse embryonic stem cell (ESC) system to mimic this period, w

121 Activating Wnt, Bmp signaling in mouse embryonic stem cell (ESC)-derived lateral plate mesoderm

122 Profilin2 (PFN2) is a target of the embryonic stem cell (ESC)-enriched miR-290 family of mic

123 escribe the development and validation of an embryonic stem cell (ESC)-GEMM platform for rapid modeli

124 cture defined for maintenance of naive state embryonic stem cells (ESC) also explains transcription f

125 Deletion analyses in B, T, and embryonic stem cells (ESC) identified a core of essentia

126 nd efficient protocol to differentiate mouse embryonic stem cells (ESC) to SpMNs and CrMNs, we now re

127 ranscriptional factor for the maintenance of embryonic stem cells (ESCs) and cancer stem cells (CSCs)

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

129 Human embryonic stem cells (ESCs) and human induced pluripoten

130 Human pluripotent stem cells such as embryonic stem cells (ESCs) and induced pluripotent stem

131 rved in virtually all cell types, except for embryonic stem cells (ESCs) and oocytes which are intrin

132 ive screening in lineage-related mouse naive embryonic stem cells (ESCs) and primed epiblast stem cel

133 roblems inherent in the use of controversial embryonic stem cells (ESCs) and somehow problematic indu

134 generated combinations of Tet knockout (KO) embryonic stem cells (ESCs) and systematically measured

135 Remarkably, coculturing embryonic stem cells (ESCs) and trophoblast stem cells (

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

137 Embryonic stem cells (ESCs) can be used to derive differ

138 erturbed DNA modification landscape in mouse embryonic stem cells (ESCs) carrying a double knockout (

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

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

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

142 Pluripotency progression of mouse embryonic stem cells (ESCs) from naive to formative and

143 .3 and showed that the K4A mutation in mouse embryonic stem cells (ESCs) impaired differentiation and

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

145 Here, we generated mouse embryonic stem cells (ESCs) knocked in for a slow elonga

146 gene regulatory network (GRN) of naive mouse embryonic stem cells (ESCs) must be reconfigured to enab

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

148 n vitro NMP populations produced either from embryonic stem cells (ESCs) or epiblast stem cells (EpiS

149 Self-renewing embryonic stem cells (ESCs) respond to environmental cue

150 Mouse embryonic stem cells (ESCs) sporadically express preimpl

151 ion between 'serum' and '2i' states of mouse embryonic stem cells (ESCs) takes place with minimal enh

152 response to replication stress (RS) in mouse embryonic stem cells (ESCs) that induces genes expressed

153 we use a CRISPR mutagenesis screen in mouse embryonic stem cells (ESCs) to identify unexpected roles

154 ting forebrain structures in vivo from mouse embryonic stem cells (ESCs) via neural blastocyst comple

155 In embryonic stem cells (ESCs), a core transcription factor

156 In embryonic stem cells (ESCs), a subset of silent developm

157 YAP is expressed in self-renewing embryonic stem cells (ESCs), although it is still debate

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

159 f the most highly transcribed genes in mouse embryonic stem cells (ESCs), by recruiting the transcrip

160 c acid (RA) induces rapid differentiation of embryonic stem cells (ESCs), partly by activating expres

161 can be partially recapitulated by combining embryonic stem cells (ESCs), trophoblast stem cells (TS)

162 Here, we show that exposure of embryonic stem cells (ESCs), which are the in vitro equi

163 een shape, mechanics, and fate, we use mouse embryonic stem cells (ESCs), which change shape as they

164 on neuronal differentiation of normal mouse embryonic stem cells (ESCs), with outcomes being compare

165 r localization of lncRNAs in human and mouse embryonic stem cells (ESCs).

166 n of worms and maintains the pluripotency of embryonic stem cells (ESCs).

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

168 role of DOT1L and its catalytic activity in embryonic stem cells (ESCs).

169 tosines in DNA plays a crucial role in mouse embryonic stem cells (ESCs).

170 ring the transition of naive-to-primed mouse embryonic stem cells (ESCs).

171 ochondria after growth factor stimulation in embryonic stem cells (ESCs).

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

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

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

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

176 BAP1 inactivation causes apoptosis in mouse embryonic stem cells, fibroblasts, liver, and pancreatic

177 a genome editing at two nucleotides in human embryonic stem cells, followed by differentiation into a

178 wild-type or DNA methylation-deficient mouse embryonic stem cells following HDAC inhibition.

179 ular properties, and we also find that mouse embryonic stem cells have a global translation speed of

180 ng of PcG proteins to ectopic sites in mouse embryonic stem cells, here we show that PRC1 can trigger

181 Using a human embryonic stem cell (hESC)-based pancreatic differentiat

182 entiation and proliferation markers in human embryonic stem cell (hESC)-derived beta-cells and human

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

184 DA-approved chemotherapy drugs against human embryonic stem cells (hESC) in which we engineered TP53

185 Our analysis on ChIP-seq experiment in human embryonic stem cells (hESC) revealed that DNMT3B, mCA an

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

187 Human embryonic stem cells (hESCs) and induced pluripotent ste

188 Human embryonic stem cells (hESCs) exhibit an intrinsic capaci

189 ism and cognitive function in mice and human embryonic stem cells (hESCs) expressing mutant fatty aci

190 zonation during the differentiation of human embryonic stem cells (hESCs) from endoderm toward termin

191 protocol for the derivation of mouse haploid embryonic stem cells (hESCs) from female gametes that al

192 ed genome editing to generate isogenic human embryonic stem cells (hESCs) harboring clinically releva

193 Here, we found that single human embryonic stem cells (hESCs) have different and biased d

194 cosphingolipid (GSL) profiles in naive human embryonic stem cells (hESCs) have not been systematicall

195 ment and during the differentiation of human embryonic stem cells (HESCs) into insulin-producing cell

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

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

198 used CRISPR/Cas9 to generate isogenic human embryonic stem cells (hESCs) that lack the individual pr

199 th neurogenesis and cardiogenesis from human embryonic stem cells (hESCs) through distinct mechanisms

200 We engineered human embryonic stem cells (hESCs) to carry NCBRS-associated h

201 we describe a method to differentiate human embryonic stem cells (hESCs) to thalamic organoids (hThO

202 We used human embryonic stem cells (hESCs) with a common dyskerin muta

203 Maintenance of human embryonic stem cells (hESCs) with stable genome is impor

204 itical role in regulating behaviors of human embryonic stem cells (hESCs), affecting their proliferat

205 ortical organoids (hCOs), derived from human embryonic stem cells (hESCs), provide a platform to stud

206 cells (hPGCLCs) obtained in vitro from human embryonic stem cells (hESCs).

207 PR, we inactivated the TET1 gene in H9 human embryonic stem cells (hESCs).

208 ffects were observed in WRN(-/-) or BLM(-/-) embryonic stem cells, however upon their differentiation

209 Single-cell CRISPR screening on mouse embryonic stem cells identifies key genes associated wit

210 C2 thus plays essential roles in maintaining embryonic stem cell identity and in controlling cellular

211 suggested as being critical for maintaining embryonic stem cells in a pluripotent state.

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

213 ssfully engraft human microglia derived from embryonic stem cells in the mouse brain.

214 uripotent factor transcripts and traps mouse embryonic stem cells in the pluripotent state.

215 tain uncommitted cells of the blastocyst and embryonic stem cells in the pluripotent state.

216 engineered ureteric buds differentiated from embryonic stem cells in three-dimensional culture and gr

217 ontrasts with the profiling data of HeLa and embryonic stem cells in which distinct down-regulation o

218 Es) are shared between MBNL1-low cancers and embryonic stem cells including a MAP2K7Deltaexon2 splice

219 are often described as sharing features with embryonic stem cells, including the expression of OCT4A,

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

221 We focus on embryonic stem cells, induced pluripotent stem cells and

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

223 ges in the O-GlcNAc proteome, while in mouse embryonic stem cells it leads to loss of O-GlcNAcase and

224 alter gene transcription in hepatocytes and embryonic stem cells lacking both REV-ERBalpha and -beta

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

226 After reprogramming, embryonic stem cell-like colonies emerged in culture, wh

227 ] to [Formula: see text] measured in a mouse embryonic stem cell line.

228 we show that the mutation rate in two human embryonic stem cell lines derived and banked for clinica

229 precedented temporal resolution in two human embryonic stem cell lines, human colon carcinoma line HC

230 Here, we report on the embryonic stem cell marker, reduced expression 1 (REX1;

231 cing assays, patients' RNA analyses, a mouse embryonic stem cell (mESC) complementation assay and ret

232 Channelrhodopsin-2 (ChR2) transfected mouse embryonic stem cell (mESC) derived motor neurons to expl

233 , using loss-of-function approaches in mouse embryonic stem cells (mESCs) and deep sequencing of rRNA

234 d sequenced TET2-crosslinked RNAs from mouse embryonic stem cells (mESCs) and found a high enrichment

235 applied CAP-C to formaldehyde prefixed mouse embryonic stem cells (mESCs) and investigated loop domai

236 Here, we show that mouse embryonic stem cells (mESCs) can be coaxed to robustly u

237 Mouse embryonic stem cells (mESCs) cultured in the presence of

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

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

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

241 We found that pluripotent mouse embryonic stem cells (mESCs) form aggregates that upon e

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

243 in Xenopus embryos and differentiating mouse embryonic stem cells (mESCs) leads to a surprisingly res

244 2) We report that absence of Mettl5 in mouse embryonic stem cells (mESCs) results in a decrease in gl

245 in Dnmt3a/3b/3l triple-knockout (TKO) mouse embryonic stem cells (mESCs) reveal that Dnmt3b3 prefers

246 ead to differentiation instability in murine embryonic stem cells (mESCs) via DNA hypomethylation at

247 uch as telomeres and retroelements, in mouse embryonic stem cells (mESCs)(1-3).

248 In mouse embryonic stem cells (mESCs), chemical blockade of Gsk3a

249 In mouse embryonic stem cells (mESCs), CpG-rich developmental reg

250 t for PRDM10 in pre-implantation embryos and embryonic stem cells (mESCs), where loss of PRDM10 resul

251 sessment of Wnt signal transduction in mouse embryonic stem cells (mESCs).

252 marks, and DNase hypersensitivity) in mouse embryonic stem cells (mESCs).

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

254 role during cell stage transitions of mouse embryonic stem cells (mESCs).

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

256 been studied previously in mouse embryos and embryonic stem cell models.

257 strong core-periphery mesoscale structure in embryonic stem cells, neural progenitor cells, and corti

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

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

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

261 y monocytes, cerebral organoids derived from embryonic stem cells, organotypic mouse cerebellar slice

262 They are associated with embryonic stem cell pathways, including BMP and Wnt sign

263 In mouse embryonic stem cells, phenocopying METTL14 knockdown, H3

264 The neural crest, an embryonic stem-cell population, is a vertebrate innovati

265 erexpression of NEUROG2 and NEUROG1 in human embryonic stem cells produces a network of excitatory an

266 nced the expression of genes associated with embryonic stem cell programs.

267 Embryonic stem-cell-related transcription factors are ce

268 ferentiation, a proportion of Whsc1-depleted embryonic stem cells remain entrapped in a pluripotent s

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

270 of whole transcriptome data from nup155(+/-) embryonic stem cells revealed changes in a variety of no

271 CRISPR interference of RLTR13D6 elements in embryonic stem cells revealed that only a minority play

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

273 Low CMA activity promotes embryonic stem cell self-renewal, whereas its up-regulat

274 periments in Dnmt3a/3b double knockout mouse embryonic stem cells show that the corresponding Arg878H

275 PEMT-deficient embryonic stem cells showed a dramatic decrease in adipo

276 taining nucleosomes at desired loci in mouse embryonic stem cells so that their fate after DNA replic

277 Embryonic stem cell-specific 5-hydroxymethylcytosine-bin

278 HMCES (5hmC binding, embryonic stem cell-specific-protein), originally identi

279 we develop a conditional mutation system in embryonic stem cells that completely removes PRC1 cataly

280 truloids are three-dimensional aggregates of embryonic stem cells that display key features of mammal

281 iation of insulin-producing cells from human embryonic stem cells, the generation of mature functiona

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

283 te differentiation stages derived from human embryonic stem cells to construct different types of RT

284 of growth factors and drugs to induce mouse embryonic stem cells to differentiate into ureteric bud

285 Using in vitro directed differentiation of embryonic stem cells to motor neurons, we show that the

286 its enhancers during the differentiation of embryonic stem cells to neural progenitors.

287 al work describing how the innate ability of embryonic stem cells to self-organize into layers and gr

288 middle-down analyses of histones from mouse embryonic stem cells via online chromatography to fracti

289 We cultured H1 human embryonic stem cells (WA-01, passage 27-40) and induced

290 n during neuronal lineage induction of human embryonic stem cells we identified miR-934, a primate-sp

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

292 methods to data from S. cerevisiae and mouse embryonic stem cells, we find that the extracted rates r

293 Using direct neuronal programming of embryonic stem cells, we found that two main vertebrate

294 Here, using both P19 cells and mouse embryonic stem cells, we resolve this paradox, demonstra

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

296 pagation and long-term self-renewal of human embryonic stem cells while preserving their pluripotency

297 12a system can eliminate the Y chromosome in embryonic stem cells with high efficiency (c.

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

299 and differentiated cells obtained from human embryonic stem cells with relatively long telomeres have

300 ndogenous retroviral (ERV) elements in mouse embryonic stem cells, with gain of chromatin accessibili