ライフサイエンスコーパス: mouse embryonic stem cell

1 4+ T cells, bone marrow dendritic cells, and mouse embryonic stem cells.

2 ising features of nucleosome organization in mouse embryonic stem cells.

3 omotes an elevated transcriptional output in mouse embryonic stem cells.

4 thod using gene expression measurements from mouse Embryonic Stem Cells.

5 regulation of the pluripotency gene Nanog in mouse embryonic stem cells.

6 ed protein 1 (KAP1; also known as TRIM28) in mouse embryonic stem cells.

7 in of any of the three Tet proteins and from mouse embryonic stem cells.

8 etic changes within the homeotic clusters of mouse embryonic stem cells.

9 ariants inserted at the same genomic site in mouse embryonic stem cells.

10 cept experiments in a human cell line and in mouse embryonic stem cells.

11 sms with methylated DNA, as we illustrate in mouse embryonic stem cells.

12 s to the ChIP-Seq data of 91 pairs of TFs in mouse embryonic stem cells.

13 nd gene expression during differentiation of mouse embryonic stem cells.

14 mic map of 5-methylcytosine, 5hmC and 5fC in mouse embryonic stem cells.

15 ble for the decay of uridylated pre-let-7 in mouse embryonic stem cells.

16 s demonstrated by culturing and transfecting mouse embryonic stem cells.

17 nce protein interaction partners of NANOG in mouse embryonic stem cells.

18 sing MNs from both wild-type and mutant SOD1 mouse embryonic stem cells.

19 zes haploidy in human HAP1 cells and haploid mouse embryonic stem cells.

20 nog gene expression was reported recently in mouse embryonic stem cells.

21 separate genomic loci and a plasmid donor in mouse embryonic stem cells.

22 unctional when integrated into the genome of mouse embryonic stem cells.

23 ximately 50 kb from the Hoxa gene cluster in mouse embryonic stem cells.

24 n identity when expressed in differentiating mouse embryonic stem cells.

25 ften in the context of bivalent chromatin in mouse embryonic stem cells.

26 chromosome transfer of Hsa21 into recipient mouse embryonic stem cells.

27 CR function in T cells derived in vitro from mouse embryonic stem cells.

28 rease mesoderm at the expense of endoderm in mouse embryonic stem cells.

29 -containing polycomb repressive complexes in mouse embryonic stem cells.

30 to relate these to gene expression levels in mouse embryonic stem cells.

31 it has a major effect on PRC2 recruitment in mouse embryonic stem cells.

32 lomere dynamics of respective chromosomes in mouse embryonic stem cells.

33 activation of bivalent gene transcription in mouse embryonic stem cells.

34 duce the expression of inflammatory genes in mouse embryonic stem cells.

35 f PRC2 to CpG island-containing promoters in mouse embryonic stem cells.

36 -binding, and regulatory element function in mouse embryonic stem cells.

37 otherwise microRNA-deficient Dgcr8 knockout mouse embryonic stem cells.

38 to the global chromatin affinity of BRG1 in mouse embryonic stem cells.

39 that is required for the differentiation of mouse embryonic stem cells.

40 itive DNA elements during differentiation of mouse embryonic stem cells.

41 emonstrate our approach on Oct4 and Nanog in mouse embryonic stem cells.

42 enine as another form of DNA modification in mouse embryonic stem cells.

43 constitutive heterochromatin organization in mouse embryonic stem cells.

44 that polycomb repressive complex 2-deficient mouse embryonic stem cells also release Bmp4 but retain

45 in repression at many developmental genes in mouse embryonic stem cells and are required for early de

46 lements at a defined chromosomal position in mouse embryonic stem cells and assessed their ability to

47 w approach for two typical qPCR datasets (of mouse embryonic stem cells and blood stem/progenitor cel

48 ands of endogenous RNA-RNA interactions from mouse embryonic stem cells and brain.

49 lied MCORE to map the chromatin landscape in mouse embryonic stem cells and differentiated neural cel

50 We also applied SingleSplice to data from mouse embryonic stem cells and discovered a set of genes

51 tate transition following differentiation of mouse embryonic stem cells and during reprogramming of s

52 ChIP-seq using mouse embryonic stem cells and enrichment levels of hist

53 o generate myelinating oligodendrocytes from mouse embryonic stem cells and established a myelin form

54 amily members in both human HCT116 cells and mouse embryonic stem cells and find that MLL4 is prefere

55 iation capacity of heparan sulfate-deficient mouse embryonic stem cells and functioning in concert wi

56 es, including Zscan4-expressing cells within mouse embryonic stem cells and hemoglobin-expressing cel

57 ssue fundamental to kidney development, from mouse embryonic stem cells and human induced pluripotent

58 evious approaches with the epigenome data in mouse embryonic stem cells and human lung fibroblast cel

59 he algorithm we present 3D architectures for mouse embryonic stem cells and human lymphoblastoid cell

60 We apply GAM to mouse embryonic stem cells and identify enrichment for s

61 g the transient G1 phase of rapidly dividing mouse embryonic stem cells and identifying a window for

62 , inhibited hematopoietic differentiation of mouse embryonic stem cells and impaired the formation of

63 ell blastomeres, and by direct conversion of mouse embryonic stem cells and induced pluripotent stem

64 on promoted precardiac mesoderm formation in mouse embryonic stem cells and involved endodermal produ

65 nvestigation to the inflammatory response in mouse embryonic stem cells and mouse embryonic stem cell

66 s of m5C in total and nuclear poly(A) RNA of mouse embryonic stem cells and murine brain.

67 sitivity, and the transcriptional profile of mouse embryonic stem cells and neural progenitors.

68 ast adenocarcinoma cell line MCF7 as well as mouse embryonic stem cells and observed similarly high c

69 in somatic cells based on work performed on mouse embryonic stem cells and oocytes.

70 ral resolution (6-hourly) in differentiating mouse embryonic stem cells and report new insight into m

71 Analysis of ChIP-Seq data in mouse embryonic stem cells and simulated data show that

72 duction and suppression of antiviral RNAi in mouse embryonic stem cells and suckling mice(10,11).

73 ogether on individual chromatin fragments in mouse embryonic stem cells and that half of the H3K9me3

74 H3K4 methylation genome-wide in human cells, mouse embryonic stem cells, and Drosophila Biochemical a

75 lling network that maintains pluripotency in mouse embryonic stem cells, and find an incoherent feedf

76 ammatory response mechanism is not active in mouse embryonic stem cells, and in vitro differentiation

77 vents TET2 downregulation in differentiating mouse embryonic stem cells, and short hairpin RNA agains

78 ny TFs remain associated with chromosomes in mouse embryonic stem cells, and that the exclusion previ

79 Using mouse embryonic stem cells as a model for complex mammal

80 direct differentiation of motor neurons from mouse embryonic stem cells as a tool to identify genes t

81 Using mouse embryonic stem cells as an in vitro model to study

82 2-, or 3-bp substitutions in MMR-proficient mouse embryonic stem cells as effectively as in MMR-defi

83 ity, we established synchronized cultures of mouse embryonic stem cells as they exit the ground state

84 Similarly, cardiomyocytes derived from mouse embryonic stem cells atrophied under pre-miR-29 co

85 rise Myst2/Kat7/Hbo1 protein interactions in mouse embryonic stem cells by affinity purification coup

86 introduced into the endogenous Msh2 gene of mouse embryonic stem cells by oligo targeting.

87 osine increased multipotent progenitors in a mouse embryonic stem cell colony-forming assay and in em

88 Profiling of 61 mouse embryonic stem cells confirmed known links between

89 nerating organized germ layers from a single mouse embryonic stem cell cultured in a soft fibrin matr

90 Mouse embryonic stem cells (D3 cell line) were different

91 centromeric chromatin-associated proteins in mouse embryonic stem cells deficient for either the meth

92 Mouse embryonic stem cells derived from the epiblast con

93 nction of engineered cardiac tissues made of mouse embryonic stem cell-derived cardiomyocytes (mESC-C

94 In this study we used mouse embryonic stem cell-derived embryoid bodies (EBs)

95 cess BMP2 signaling in zebrafish embryos and mouse embryonic stem cell-derived embryoid bodies substa

96 in correlation with dynamic cell movement in mouse embryonic stem cell-derived sprouting assays.

97 We show that Lmo2-/- mouse embryonic stem cells differentiated to Flk-1+ haem

98 y response in mouse embryonic stem cells and mouse embryonic stem cell-differentiated cells.

99 l infection, but not to LPS, was observed in mouse embryonic stem cell-differentiated fibroblasts.

100 e applied PIQ to analyze DNase-seq data from mouse embryonic stem cells differentiating into prepancr

101 amming towards HC fate, both during in vitro mouse embryonic stem cell differentiation and following

102 We used the mouse embryonic stem cell differentiation system for in

103 an important role for DNA replication during mouse embryonic stem cell differentiation, which could s

104 Mouse embryonic stem cells do not differentiate into pla

105 We reported previously that mouse embryonic stem cells do not have a functional IFN-

106 Ablation of Jmjd3 in mouse embryonic stem cells does not affect the maintenan

107 ed histone 3 lysine 4 (substrate H3K4me2) in mouse embryonic stem cells (ES cells).

108 ions genome-wide across an isogenic panel of mouse embryonic stem cell (ESC) and neuronal progenitor

109 ion and early neurogenesis using an in vitro mouse embryonic stem cell (ESC) clonal assay system.

110 n single cells during the earliest stages of mouse embryonic stem cell (ESC) differentiation and duri

111 jd2 H3K9 demethylases cooperate in promoting mouse embryonic stem cell (ESC) identity.

112 To model X-SCID in vitro, we generated a mouse embryonic stem cell (ESC) line in which a disease-

113 To study TERT regulation, we generated mouse embryonic stem cell (ESC) lines containing single-

114 wever, hPSCs are unstable in classical naive mouse embryonic stem cell (ESC) WNT and MEK/ERK signal i

115 ere, using the self-organizing properties of mouse embryonic stem cell (ESC), we report that ESC-deri

116 Mouse embryonic stem cells (ESC) and epiblast stem cells

117 y using an RNA interference (RNAi) screen in mouse embryonic stem cells (ESC) with a Nanog reporter.

118 prepared from fresh OSPW on differentiating mouse embryonic stem cells (ESC).

119 g embryos of pregnant hyperglycemic mice and mouse embryonic stem cells (ESC).

120 r circuitry that governs the ground state of mouse embryonic stem cells (ESC).

121 , we performed comparative RNA sequencing of mouse embryonic stem cells (ESCs) and defined a pluripot

122 (3) The binding sites for SOX2 and POU5F1 in mouse embryonic stem cells (ESCs) and EpiSCs are diverge

123 ave generated Tet1/2/3 triple-knockout (TKO) mouse embryonic stem cells (ESCs) and examined their dev

124 Here, we combined mouse embryonic stem cells (ESCs) and extraembryonic tro

125 repression, we carried out an RNAi screen in mouse embryonic stem cells (ESCs) and identified a list

126 encing across multiple clonal populations of mouse embryonic stem cells (ESCs) and neural progenitor

127 ncing screen in clonal populations of hybrid mouse embryonic stem cells (ESCs) and neural progenitor

128 T1-(MOF)-containing MSL and NSL complexes in mouse embryonic stem cells (ESCs) and neuronal progenito

129 Mouse embryonic stem cells (ESCs) are maintained in a na

130 Factors that sustain self-renewal of mouse embryonic stem cells (ESCs) are well described.

131 hibition of Erk1/2 and Gsk3beta signaling in mouse embryonic stem cells (ESCs) by small-molecule inhi

132 Mouse embryonic stem cells (ESCs) can differentiate into

133 Mouse embryonic stem cells (ESCs) cultured in serum are

134 Using CRISPR/Cas9 technology, we generated mouse embryonic stem cells (ESCs) deficient for all thre

135 ons that maintain an undifferentiated state, mouse embryonic stem cells (ESCs) differentiate into var

136 Populations of cultured mouse embryonic stem cells (ESCs) exhibit a subfraction

137 stream of LIF, WNT and MAPK-ERK to stabilize mouse embryonic stem cells (ESCs) in their naive state h

138 ntiation of inner ear sensory epithelia from mouse embryonic stem cells (ESCs) in three-dimensional c

139 e found that 30% of the genome in interphase mouse embryonic stem cells (ESCs) is marked with H3S10ph

140 Naive pluripotent mouse embryonic stem cells (ESCs) resemble the preimplan

141 Here, we show in mouse embryonic stem cells (ESCs) that MLL4 associates w

142 ression from the naive status represented by mouse embryonic stem cells (ESCs) to a state capacitated

143 rformed a large-scale pooled shRNA screen in mouse embryonic stem cells (ESCs) to discover genes asso

144 Here, we used mouse embryonic stem cells (ESCs) to identify an endosiR

145 and GSK3beta can be selectively inhibited in mouse embryonic stem cells (ESCs) using a chemical-genet

146 We found that mouse embryonic stem cells (ESCs) with critically short

147 In a functional genomics screen of mouse embryonic stem cells (ESCs) with nested hemizygous

148 In mouse embryonic stem cells (ESCs), CBX6 and CBX7 are the

149 Here, we show that, in mouse embryonic stem cells (ESCs), H3.3 is required for

150 -range chromatin interactions genome-wide in mouse embryonic stem cells (ESCs), iPSCs, and fibroblast

151 Mouse embryonic stem cells (ESCs), like the blastocyst f

152 s at four developmental stages in the mouse [mouse embryonic stem cells (ESCs), mesoderm (MES), cardi

153 959-972) report that, in naive mouse embryonic stem cells (ESCs), p53 controls DNA meth

154 tion of DNA methylation at imprinted loci in mouse embryonic stem cells (ESCs), suggesting that epige

155 he human hematopoietic stem cells (HSCs) and mouse embryonic stem cells (ESCs), we demonstrated that

156 rtoire of GSK-3-dependent phosphorylation in mouse embryonic stem cells (ESCs), we found that approxi

157 n-coding transcripts (lincRNAs) expressed in mouse embryonic stem cells (ESCs), which might be incomp

158 e of TET enzymes in the regulation of TEs in mouse embryonic stem cells (ESCs).

159 that encode a module of TF-binding sites in mouse embryonic stem cells (ESCs).

160 a specific regulator of genomic stability in mouse embryonic stem cells (ESCs).

161 s enzyme to specific regions of chromatin in mouse embryonic stem cells (ESCs).

162 eural genes differentially between human and mouse embryonic stem cells (ESCs).

163 eted regions (NDRs) throughout the genome of mouse embryonic stem cells (ESCs).

164 introduce genome-wide targeted mutations in mouse embryonic stem cells (ESCs).

165 ical to the maintenance and reprogramming of mouse embryonic stem cells (ESCs).

166 higher-order chromatin compaction in vivo in mouse embryonic stem cells (ESCs).

167 ic antibodies in wild-type and Tdg-deficient mouse embryonic stem cells (ESCs).

168 EC fate from neural progenitors derived from mouse embryonic stem cells (ESCs).

169 al lung and thyroid progenitors derived from mouse embryonic stem cells (ESCs).

170 osons and the murine leukemia virus (MLV) in mouse embryonic stem cells (ESCs).

171 enes during the RA-driven differentiation of mouse embryonic stem cells (ESCs).

172 We show that Wt1-deficient mouse embryonic stem cells exhibit reduced hematopoietic

173 Here we study the differentiation of mouse embryonic stem cells expressing an inducible RUNX1

174 kle-like and filament structures occurred in mouse embryonic stem cells expressing little or no NEAT1

175 ilobases (kb) of mouse and human sequence in mouse embryonic stem cells for enhancer activity we iden

176 f RUNX1 in the transition of differentiating mouse embryonic stem cells from hemogenic to hematopoiet

177 In mouse embryonic stem cells, genomic deletion of the 11-b

178 that hundreds of (lowly expressed) genes in mouse embryonic stem cells have reduced noise due to sub

179 bly in the formation of induced neurons from mouse embryonic stem cells, human fibroblasts, and norma

180 1p levels and L1 mobilization in pluripotent mouse embryonic stem cells, implying that Tex19.1 preven

181 to generate mechanosensitive hair cells from mouse embryonic stem cells in a three-dimensional (3D) c

182 to a consensus DNA sequence in vitro and in mouse embryonic stem cells in vivo.

183 asure the dynamics of the chromatin fiber in mouse embryonic stem cells, in combination with dynamica

184 out single-molecule imaging of CHD4 in live mouse embryonic stem cells, in the presence and absence

185 ly, we show that in vitro differentiation of mouse embryonic stem cells into alpha motor neurons reca

186 Here the authors differentiate mouse embryonic stem cells into neurons, and analyze the

187 A to restore Galpha expression in Ric8A(-/-) mouse embryonic stem cells, involved two helical domains

188 e deficiency in the inflammatory response in mouse embryonic stem cells is also attributed to the lac

189 ng present initially in both male and female mouse embryonic stem cells is lost from the active X dur

190 in A2-deletion-induced cellular apoptosis in mouse embryonic stem cells is partly rescued by S477D/T4

191 The mouse embryonic stem cell knockout resource provides a b

192 The differentiation potential of mouse embryonic stem cells lacking both NDST1 and NDST2

193 ring at the euchromatic ROSA26 locus between mouse embryonic stem cells lacking either ATM, H2AX, or

194 ration of an Rsx transgene on an autosome in mouse embryonic stem cells leads to gene silencing in ci

195 ctivity in vitro, and knockdown of Dis3l2 in mouse embryonic stem cells leads to the stabilization of

196 Consistent with this, a mutant mouse embryonic stem cell line with a deletion in the FB

197 Furthermore, genetically modified Dnmt2-only mouse embryonic stem cells lost the DNA methylation patt

198 that CTCF binds thousands of transcripts in mouse embryonic stem cells, many in close proximity to C

199 c retinoic acid (RA) signaling and modulates mouse embryonic stem cell (mESC) differentiation in part

200 In this study, we used mouse embryonic stem cell (mESC) differentiation to unco

201 more than 3700 compounds in three syngeneic mouse embryonic stem cell (mESC) lines: htt(-/-), extend

202 the H1 triple isoform knockout (H1DeltaTKO) mouse embryonic stem cell (mESC) model system.

203 acetyltransferase (HAT) Mof is essential for mouse embryonic stem cell (mESC) pluripotency and early

204 ere, we clarify the molecular foundations of mouse embryonic stem cell (mESC) self-renewal by applyin

205 Mouse embryonic stem cell (mESC) self-renewal can be mai

206 ry networks of 18 TFs/chromatin modifiers in mouse embryonic stem cell (mESC).

207 whether ERbeta influences differentiation of mouse embryonic stem cells (mESC) into neural lineages,

208 t2 have distinct roles in regulating 5hmC in mouse embryonic stem cells (mESC).

209 vator of transcription3 (STAT3) signaling in mouse embryonic stem cells (mESC).

210 Tet1 is robustly expressed in mouse embryonic stem cells (mESCs) and has been implicat

211 formed an unbiased loss-of-function study in mouse embryonic stem cells (mESCs) and identified 20 lin

212 Naive mouse embryonic stem cells (mESCs) and primed epiblast s

213 metabolism, thereby impacting maintenance of mouse embryonic stem cells (mESCs) and subsequent embryo

214 Mouse embryonic stem cells (mESCs) are clonal population

215 We have recently reported that mouse embryonic stem cells (mESCs) are deficient in expr

216 Mouse embryonic stem cells (mESCs) are key tools for gen

217 that amongst different developmental stages, mouse embryonic stem cells (mESCs) are resistant to cell

218 We have measured mouse embryonic stem cells (mESCs) at different states d

219 rin regulates the naive pluripotent state of mouse embryonic stem cells (mESCs) by enabling LIF-depen

220 Here, we show that depletion of Nup153 in mouse embryonic stem cells (mESCs) causes the derepressi

221 Female mouse embryonic stem cells (mESCs) contain two active X

222 Mouse embryonic stem cells (mESCs) cultured under serum/

223 Mouse embryonic stem cells (mESCs) deficient for DGCR8,

224 Studies with mouse embryonic stem cells (mESCs) demonstrated an incre

225 ist in a state of primed pluripotency, while mouse embryonic stem cells (mESCs) display a naive or pr

226 he catalytic SET domains of MLL3 and MLL4 in mouse embryonic stem cells (mESCs) does not disrupt self

227 g during adherent culture differentiation of mouse embryonic stem cells (mESCs) generates a populatio

228 on heterogeneity in the pluripotent state of mouse embryonic stem cells (mESCs) has been increasingly

229 c cells derived from murine embryos and from mouse embryonic stem cells (mESCs) have primarily been s

230 is both necessary and sufficient to convert mouse embryonic stem cells (mESCs) into 2-cell-embryo-li

231 Serum-to-2i interconversion of mouse embryonic stem cells (mESCs) is a valuable in vitr

232 to widespread erasure of DNA methylation in mouse embryonic stem cells (mESCs) lacking the de novo D

233 anscriptional activity of Oct3/4 (Pou5f1) in mouse embryonic stem cells (mESCs) maintained under stan

234 The maintenance of pluripotency in mouse embryonic stem cells (mESCs) relies on the activit

235 The metabolic function of Cited2 in mouse embryonic stem cells (mESCs) remains elusive.

236 Mouse embryonic stem cells (mESCs) represent a valuable

237 The maintenance of mouse embryonic stem cells (mESCs) requires LIF and seru

238 Genome-wide mapping of 5fC in mouse embryonic stem cells (mESCs) reveals that 5fC pref

239 or nuclease (TALEN)-mediated gene editing in mouse embryonic stem cells (mESCs) to produce mice with

240 The ability of mouse embryonic stem cells (mESCs) to self-renew or diff

241 romosomal translocations can be generated in mouse embryonic stem cells (mESCs) via CRISPR/Cas9.

242 onsible for self-renewal and pluripotency of mouse embryonic stem cells (mESCs) was extracted from se

243 increases globally during differentiation of mouse embryonic stem cells (mESCs), and is particularly

244 the temporal dynamics of NANOG expression in mouse embryonic stem cells (mESCs), and to dissect the l

245 critically required for the pluripotency of mouse embryonic stem cells (mESCs), but the detailed mec

246 own or Parp1 heterozygosity of Brca2(cko/ko) mouse embryonic stem cells (mESCs), carrying a null (ko)

247 Here, we show that mouse embryonic stem cells (mESCs), either lacking Tet3

248 types considered hard to transduce, such as mouse embryonic stem cells (mESCs), human ESCs (hESCs),

249 ogen synthase kinase-3 (GSK-3) substrates in mouse embryonic stem cells (mESCs), providing a broad pr

250 In mouse embryonic stem cells (mESCs), the transcriptional

251 In mouse embryonic stem cells (mESCs), Wnt proteins stimula

252 e we describe a transcriptional regulator of mouse embryonic stem cells (mESCs), Yin-yang 2 (YY2), th

253 sophila adult follicle stem cells (FSCs) and mouse embryonic stem cells (mESCs).

254 toestrogen molecule enhances self-renewal of mouse embryonic stem cells (mESCs).

255 , -green (G), -blue (B), and -purple (P), in mouse embryonic stem cells (mESCs).

256 knockdown of over 100 lncRNA transcripts in mouse embryonic stem cells (mESCs).

257 es loaded with single guide RNAs (sgRNAs) in mouse embryonic stem cells (mESCs).

258 luripotency and cell fate decision making in mouse embryonic stem cells (mESCs).

259 osaic neuralized embryoid bodies (nEBs) from mouse embryonic stem cells (mESCs).

260 Both HeLa and mouse embryonic stem cell mRNAs harboring m(6)As have sh

261 Using Sm-ChIPi, we demonstrated that within mouse embryonic stem cells, one polycomb repressive comp

262 ated using 2D methods or MLOs generated from mouse embryonic stem cells, our human MLOs produced neur

263 ntal route of hemangiogenic progenitors from mouse embryonic stem cells, perform genome-wide CRISPR s

264 of RXR for these functions was validated in mouse embryonic stem cells, primary neurons, and APOE3 a

265 lysis of published genome-wide datasets from mouse embryonic stem cells revealed that the Ring1b subu

266 We analyzed mouse embryonic stem cells, revealing in detail the popu

267 Here we show that in mouse embryonic stem cells, Rif1 coats late-replicating

268 m the GAPDH housekeeping gene (5.45 ng total mouse embryonic stem cell RNA) and measured associated s

269 In mouse embryonic stem cells, RYBP plays a central role in

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

271 mRtel1-deficient mouse embryonic stem cells showed sensitivity to a range

272 ificial chromosome (BAC) transgenic HeLa and mouse embryonic stem cells stably expressing enhanced gr

273 motor neurons in both chick neural tube and mouse embryonic stem cells, suggesting that miR-218 play

274 ly assess Ago-bound small RNAs, we adapted a mouse embryonic stem cell system to express a single epi

275 e drug (D-penicillamine) in the conventional mouse embryonic stem cell test.

276 Here we show in mouse embryonic stem cells that asymmetric sequence dete

277 With this approach, we show in mouse embryonic stem cells that endogenous Dnmt1 gene tr

278 rovide genomic evidence in budding yeast and mouse embryonic stem cells that the efficiency-accuracy

279 The LIF network was used to encapsulate mouse embryonic stem cells; the encapsulated cells remai

280 When TDP-43 was depleted from mouse embryonic stem cells, these cryptic exons were spl

281 y the method to an experiment on pluripotent mouse embryonic stem cells to classify a set of previous

282 EMOIR as a proof of principle, we engineered mouse embryonic stem cells to contain multiple scratchpa

283 nd Hi-Cap data as well as ChIA-PET data from mouse embryonic stem cells to investigate promoter-cente

284 In mouse embryonic stem cells, transcriptional silencing of

285 icSHAPE of the mouse embryonic stem cell transcriptome versus purified

286 Here, using a de novo targeting assay in mouse embryonic stem cells we unexpectedly discover that

287 Using neurons differentiated from mouse embryonic stem cells, we analyze protein and RNA e

288 Using CRISPR/Cas9-mediated editing of mouse embryonic stem cells, we find that deletion of 11

289 high resolution Hi-C dataset generated from mouse embryonic stem cells, we found that most local gen

290 Applying the method to mouse embryonic stem cells, we identified promoter-ancho

291 Using conventional gene targeting in mouse embryonic stem cells, we report here the generatio

292 Using embryoid body cultures of mouse embryonic stem cells, we reveal that FGF signaling

293 Using the auxin-inducible degron system in mouse embryonic stem cells, we show that CTCF is absolut

294 On publicly available Hi-C data from mouse embryonic stem cells, we show that the Poisson met

295 Embryoid bodies, formed from mouse embryonic stem cells, were used as a model to stud

296 In mouse embryonic stem cells where TRIM28 plays a major ro

297 h1 as regulating FLK1+ mesoderm formation in mouse embryonic stem cells, which in turn specifies hema

298 roduce a targeted autosome loss in aneuploid mouse embryonic stem cells with an extra human chromosom

299 tiated motile fibroblast cells from isogenic mouse embryonic stem cells with or without disruption of

300 Treatment of differentiating mouse embryonic stem cells with Wnt3a resulted in enhanc