ライフサイエンスコーパス: EGFP

1 EGFP expression correlated well with the presence of Nav

2 EGFP messenger RNA (mRNA) and GFP plasmid DNA (pDNA) wer

3 EGFP(Vglut2) neurons were not TH-ir.

4 EGFP-CETN2, a centrosome and transition zone marker, ide

5 EGFP-N782 binds to chromatin together with the XRCC5/6 c

6 EGFP-tagged Myo18Agamma expressed in ventricular myocyte

7 fluorescence from the brain slices of Thy-1 EGFP transgenic mice, we show that there is an inherent,

8 enous administration of AAV9-gfaABC1D-Kir4.1-EGFP.

9 ression of the oxytocin exon 1-intron-exon 2-EGFP construct was also identified in SF3B3 and MCM7 kno

10 us EGF increased S100A4 mRNA levels in 231BR-EGFP cells (1.40+/-0.02-fold, P<0.01 compared with vehic

11 irpin RNA-mediated S100A4 silencing in 231BR-EGFP cells decreased their migration and invasion in res

12 oliferation, migration and invasion of 231BR-EGFP cells in an ER-dependent manner.

13 Co-culture of 231BR-EGFP cells with E2-treated astrocytes led to the upregul

14 alidated on a screening platform with a T-2A-EGFP knock-in reporter engineered by CRISPR/Cas9.

15 enerating an attP-FRT-SA-T2A-GAL4-polyA-3XP3-EGFP-FRT-attP transgenic library for multiple uses (Lee

16 high transfection efficiency (63.6 +/- 3.44% EGFP + viable cells) with high cell viability (77.3 +/-

17 ations of EGFP+ vagal brainstem neurons: (a) EGFP+ neurons in the nAmb projecting to the esophagus or

18 s from C57BL/6 (control), LysM-EGFP, B6 ACTb-EGFP, CCR2(-/-), CD11c-EYFP, CD11c-EYFP-DTR, germ-free m

19 Cas9-mediated approach was used to attach an EGFP coding module to the C-terminus of the endogenous N

20 akpoint sequences, and another to deliver an EGFP-HSV1-tk construct flanked by sequences homologous t

21 The insertion of an EGFP cassette replacing the reading frames for two neigh

22 cell lines with variable copy numbers of an EGFP transgene, we discovered that CRISPR knockout is re

23 Using an EGFP-nanobody interaction as a model, this protocol desc

24 Utilizing an EGFP reporter system for observing ASFV replication and

25 pattern of colocalization between TH-ir and EGFP(Vgat) , we first performed Nissl-based parcellation

26 ctrally compatible with the ATeam sensor and EGFP for simultaneous dual-color measurements of intrace

27 During study of both the SOD1FP and EGFP chimeras, we observed fluorescence also in small ce

28 with external mitochondria during uptake and EGFP-labelled mitochondria are found within early macrop

29 rough HfQ mediated silencing of EGFP by anti-EGFP synthetic small regulatory RNAs.

30 for luminal and nuclear membrane-associated EGFP-tagged proteins.

31 We confirmed that average EGFP lifetimes consistently decreased (3 to 2 ns) with i

32 edial DMV projecting to the stomach, and (b) EGFP+ neurons in the lateral DMV projecting to the cecum

33 g to the esophagus or laryngeal muscles, (b) EGFP+ neurons in the medial DMV projecting to the stomac

34 er EGFP-Rab5 as well as the PI(3)P biosensor EGFP-2xFYVE.

35 ibility with GFP filter sets, recognition by EGFP antibodies, and excellent performance in mouse, hum

36 icant increase or decrease of the N-cadherin-EGFP clustering, respectively.

37 icant increase or decrease in the N-cadherin-EGFP clustering, respectively.

38 highly efficient doxycycline-inducible Cas9-EGFP vector.

39 By analyzing the localization of a Cdh2-EGFP fusion protein expressed under the control of the z

40 Delaminating cardiomyocytes accumulate Cdh2-EGFP on the surface facing the basal side of compact lay

41 In addition, Cdh2-EGFP molecules also appear on the basal side of cardiomy

42 volves into a clear punctate pattern as Cdh2-EGFP molecules outside the punctae cluster to increase t

43 Within a few hours, Cdh2-EGFP distribution on the lateral sides of cardiomyocytes

44 sh cdh2 promoter, we initially observed Cdh2-EGFP expression along the lateral sides of embryonic car

45 transition from an even distribution of Cdh2-EGFP to the formation of punctae.

46 timer transgenic line, we observed that Cdh2-EGFP molecules appear to move from the lateral to the ba

47 junction with the Th(2A-CreER) and CGRPalpha-EGFP lines described previously for labeling type II fib

48 ations from 3-week- to 2-month-old CGRPalpha-EGFP (GENSAT) mice showed expression of Cgrpalpha in a s

49 ures were prepared from male and female ChAT-EGFP mice, and current-clamp recordings obtained from BF

50 green stroma, whereas we could not find COL-EGFP(+) cells in tumors developing in the parabiotic par

51 econstituted with bone marrow cells from COL-EGFP mice very rarely showed stromal fibroblasts express

52 ors was confirmed in parabiotic pairs of COL-EGFP mice and transgenic mice developing autochthonous i

53 Lack of incorporation of COL-EGFP(+) cells from the circulation into tumors was confi

54 of the type I collagen (Col-I) promoter (COL-EGFP) had green stroma, whereas we could not find COL-EG

55 ncer cells injected under full-thickness COL-EGFP skin grafts transplanted in nonreporter mice develo

56 Compared with wild type MOG1 or control EGFP, mutant MOG1 with mutation E83D associated with Bru

57 the ventricular zone of the cerebral cortex, EGFP is mostly expressed in developing neurons in the tr

58 Using CX(3)CR1-EGFP/TRAP tdTomato mice, we found CX(3)CR1 expression in

59 al crest development, as read out by crestin:EGFP expression.

60 CRY1::EGFP appropriately lengthened the behavioral period in C

61 At the circuit level, CRY1::EGFP induced the spatiotemporal wave of PER2 expression

62 Phase of CRY1::EGFP expression was critical, however, because constitut

63 Expression of CRY1::EGFP or CRY2::EGFP under a minimal Cry1 promoter was cir

64 Expression of CRY1::EGFP or CRY2::EGFP under a minimal Cry1 promoter was circadian and rap

65 We have created Csf1r-EGFP transgenic sheep via lentiviral transgenesis of a c

66 ssues in mice with combined CSF1R-FRed/Csf1r-EGFP confirmed the restriction of CSF1R expression to MP

67 commitment to the macrophage lineage, Csf1r-EGFP bone marrow provides a tool for studying the earlie

68 Macrophages of Jax C57BL/6-Tg (Csf1r-EGFP-NGFR/FKBP1A/TNFRSF6) 2Bck/J mice express enhanced g

69 of ferumoxytol, and 18 Jax C57BL/6-Tg (Csf1r-EGFP-NGFR/FKBP1A/TNFRSF6) 2Bck/J mice received rhodamine

70 onstrated that CyclinA2-betagal and CyclinA2-EGFP were expressed from mid-G1 to mid-M phase.

71 from CyclinA2-LacZ-floxed-EGFP, or CyclinA2-EGFP mice, demonstrated that CyclinA2-betagal and Cyclin

72 Measurements of DBP-EGFP extravasation in plvapb mutants provided direct pro

73 of the genetically tagged plasma protein DBP-EGFP, we show that the developmental acquisition of vasc

74 of cells coexpressing UNC5B-mCherry and DCC-EGFP revealed a netrin-1-induced increase in colocalizat

75 olocalization of coexpressed full-length DCC-EGFP with DCC-T-mCherry, a putative DCC dominant negativ

76 ted by diptheria toxin treatment of Lgr5-DTR-EGFP mice at E16.5 while first wave follicles developed

77 Using mice carrying a DTR/EGFP transgene under the control of the Foxp3 promoter (

78 ons and in hippocampal slices expressing EB3-EGFP and vGlut1-mCherry, we found that dynamic MTs prefe

79 n extracts of mammalian cells expressing Eg5-EGFP, moved processively toward the microtubule plus-end

80 owed that co-delivery of adenovirus encoding EGFP-tagged Cas9 and lentivirus encoding a single guide

81 studies in vivo, a transgenic mouse encoding EGFP under the control of this putative sensory neuron s

82 at marks wild-type cells with the endogenous EGFP-tagged protein, whereas mutant cells are marked wit

83 dothelial cells with an EFNB2-tdTomato/EPHB4-EGFP dual reporter human embryonic stem cell line to ide

84 ERbeta-EGFP cells expressed oxytocin more abundantly in the ros

85 oendocrine (presumably pre-autonomic) ERbeta-EGFP neurons predominated in the posterior PVN.

86 control of the mouse ERbeta promoter (ERbeta-EGFP) to examine the chemical architecture of PVN ERbeta

87 orogold revealed that the rostral PVN ERbeta-EGFP cells are neuroendocrine neurons whereas non-neuroe

88 en receptor alpha-ir colocalized with ERbeta-EGFP at low levels (15 +/- 3%).

89 it possible to utilize hundreds of existing EGFP-expressing mice, tumors, pathogens and other tools,

90 ytes drive the aggregation of Htt103Q(Exon1)-EGFP from a diffuse ensemble into inclusion bodies (IBs)

91 phage precursors and blood monocytes express EGFP in these animals.

92 n animals, the rbRosa26-EGFP rabbits express EGFP, and the rbRosa26-Cre-reporter rabbits express tdTo

93 Using transgenic mice that express EGFP in response to activation of the senescence-associa

94 All expressed EGFP, with increased levels in the nonclassical subset.

95 me (HAC) carrying a constitutively expressed EGFP transgene.

96 n the ARA-where every TH-ir neuron expressed EGFP(Vgat) .

97 not all Nav1.8-expressing neurons expressed EGFP.

98 We expressed EGFP- and mCherry-tagged receptor chains in HeLa cells t

99 rarely showed stromal fibroblasts expressing EGFP.

100 ngle cell analysis in macrophages expressing EGFP-tagged p65 and a TNFalpha promoter-driven mCherry.

101 ncluding the use of reporter mice expressing EGFP from the Ret locus, and whole-mount cytokeratin sta

102 d male and female transgenic mice expressing EGFP under the control of the mouse ERbeta promoter (ERb

103 rMV(EZ)EGFP(1) and rMV(EZ)EGFP(6) did not induce satisfactory s

104 y growth curves, which indicated that rMV(EZ)EGFP(1) was overattenuated.

105 es, whereas both in vitro and in vivo rMV(EZ)EGFP(3) was functionally equivalent to the commercial MV

106 rMV(EZ)EGFP(1) and rMV(EZ)EGFP(6) did not induce satisfactory serum antibody respo

107 -post-fertilization (dpf) embryo of Tg (fli1:EGFP or kdrl:mCherry) zebrafish, TRCs are much more effi

108 hibits developmental angiogenesis in Tg(fli1:EGFP) zebrafish and inhibits human microvascular endothe

109 on of hyaloid vessel angiogenesis in Tg(fli1:EGFP) zebrafish.

110 ryonic fibroblasts from CyclinA2-LacZ-floxed-EGFP, or CyclinA2-EGFP mice, demonstrated that CyclinA2-

111 by an intraperitoneal route into BALB/cJ(Fms-EGFP/-) mice, which express enhanced green fluorescent p

112 imentin network, which was rescued following EGFP-Hic-5 expression.

113 ation, dispersion and separation by FACS for EGFP resulted in an 86% pure population of alpha-cells.

114 TTX-R INa recorded from EGFP-positive hypothalamic neurons demonstrate the usefu

115 (vy)/MIP-TF mice, Th1 reactivity spread from EGFP to other B-cell antigens.

116 ary for T cell autoreactivity to spread from EGFP to other B-cell autoantigens.

117 Here we demonstrate that functional EGFP-Mnk expressed from a transgene localizes to the nuc

118 Furthermore, EGFP is predominantly expressed in GABAergic neurons, wh

119 bel with EGFP expression in neurons of GAD67-EGFP mice.

120 de in the DCN of CBA/Ca and transgenic GAD67-EGFP mice to investigate the cells giving rise to these

121 Furthermore, the administration of AAV GCG-EGFP at various doses to adult wild type mice did not si

122 The administration of AAV GCG-EGFP by intraperitoneal or intraductal injection led to

123 AAV GCG-EGFP delivery to mice followed by islet isolation, dispe

124 enhanced green fluorescent protein (AAV GCG-EGFP), to specifically identify alpha-cells.

125 of a target enhanced green fluorescent gene (EGFP).

126 iple successful devices, where target genes (EGFP, TdTomato, and FtsZ) and the promoters (inducible a

127 /loxP recombination to express enhanced GFP (EGFP) in neurons expressing the vesicular glutamate (vGL

128 Here, we incorporated a Gli2-EGFP allele into 2 different genetic mouse models of Hh-

129 uorescence anisotropy imaging of histone H2B-EGFP to interrogate global chromatin compaction changes

130 Using HDC-EGFP bacterial artificial chromosome (BAC) transgenic mi

131 histamine in heart failure post-MI using HDC-EGFP transgenic mice and HDC-knockout (HDC(-/-)) mice.

132 the delivery of siRNA into human cells (HeLa-EGFP).

133 3(Gq)-mCherry) and control virus (rAAV5-hSyn-EGFP) were stereotactically administered to the hypoglos

134 y is predictive of the subsets, with the ID4-EGFP(Bright) population being mostly, if not purely, SSC

135 mostly, if not purely, SSCs, whereas the ID4-EGFP(Dim) population is in transition to the progenitor

136 The probe design exploits a lysyl residue in EGFP that is essential for chromophore maturation, and i

137 as used to examine the temporal variation in EGFP expression in cells transfected with CRISPR-Cas9 co

138 o enhanced green fluorescent protein (MLV-IN-EGFP).

139 the four gamma-secretase subunits including EGFP-tagged nicastrin.

140 ect for spectrum-shifted variants, including EGFP.

141 s, and then mapped the distribution of TH-ir EGFP(Vgat) neurons onto atlas templates from the Allen R

142 TH-ir EGFP(Vgat) neurons were distributed throughout the rostr

143 th these mechanistic findings, hRASGRP1-ires-EGFP enhances fitness of stem- and progenitor- cells, bu

144 ); beta-catenin(exon3); Rosa26(LSL-rtta-ires-EGFP); TRE-Spdef mice, which express an oncogenic form o

145 oncogenic roles of miR-211, we generated K14-EGFP-miR-211 transgenic mice tagged with GFP.

146 Using Troponin T-Cre;CyclinA2-LacZ-EGFP mice, we examined cardiac myocyte cell cycle activi

147 Using intravital microscopy in Lgr5(EGFP-Ires-CreERT2) mice, we monitored individual crypt d

148 ith only Cre alleles (Villin-Cre(ERT2), Lgr5-EGFP-IRES-Cre(ERT2), Hnf4alpha(+/+), and Hnf4gamma(+/+))

149 performed studies with Villin-Cre(ERT2);Lgr5-EGFP-IRES-Cre(ERT2);Hnf4alpha(f/f);Hnf4gamma(Crispr/Cris

150 Using lineage tracing in Lgr5-EGFP-CreERT2/Rosa26-Tomato and Lgr6-EGFP-CreERT2/Rosa26-

151 Studies were performed in Lgr5-EGFP-IRESCreERT2, Bmi1-CreERT2, Hopx-CreERT2, and TRE-H2

152 b double knockout (Cbl/Cbl-b DKO) using Lgr5-EGFP-IRES-CreERT2, to demonstrate a mammary epithelial c

153 in Lgr5-EGFP-CreERT2/Rosa26-Tomato and Lgr6-EGFP-CreERT2/Rosa26-Tomato reporter mice, we demonstrate

154 We used Lhx6-EGFP and Npas1-tdTm mice strains to identify low-frequen

155 reduced mobility of the actin probe Lifeact-EGFP in OXT synapses.

156 ilopodial dynamics in mouse resident Lifeact-EGFP macrophages, we show that filopodia, or filopodia-l

157 ransfer (FRET) between a protein fusion LuxP-EGFP and 7-diethylamino-3-[N-(2-maleimidoethyl)carbamoyl

158 d liver tissues from C57BL/6 (control), LysM-EGFP, B6 ACTb-EGFP, CCR2(-/-), CD11c-EYFP, CD11c-EYFP-DT

159 D colocalized with the early endosome marker EGFP-Rab5 as well as the PI(3)P biosensor EGFP-2xFYVE.

160 mera of ChAT promoter-EGFP and mito-mCherry, EGFP efficiently transferred to mito-mCherry(+) cells.

161 Bafilomycin-A1 treatment and tandem mCherry-EGFP-LC3B reporter transfection demonstrated that the au

162 and clearing, or retrograde tracing in a MET(EGFP) transgenic mouse, we identify three novel subpopul

163 The amacrine cells labeled in Tg(mglur6b:EGFP)zh1 constitute a novel cholinergic, non-GABAergic,

164 Here we present Tg(mglur6b:EGFP)zh1, a new transgenic zebrafish line recapitulating

165 MHV68-EGFP infection induced a more pronounced intra-insulitis

166 GFP-expressing murine herpes virus-68 (MHV68-EGFP) caused occasional transient elevation in their blo

167 Moreover, in MHV68-EGFP-infected A(vy)/MIP-TF mice, Th1 reactivity spread f

168 Unlike their MIP-TF littermates, MHV68-EGFP-infected A(vy)/MIP-TF mice developed moderate intra

169 and B-cell stress could exacerbate the MHV68-EGFP-induced B-cell autoreactivity.

170 hether TH-ir neurons colocalized with native EGFP(Vglut2) - or EGFP(Vgat) -fluorescence, respectively

171 ties of Layer VI cortical neurons from Ntsr1-EGFP; Foxp2(+/R552H) male and female mice.

172 Here, we used Ntsr1-EGFP mice to identify Foxp2+ neurons in the mouse audito

173 Cellular colocalization of EGFP with neuropeptides, transcription modulators, and n

174 The selective expression of EGFP in dSPNs of Sox8-EGFP BAC mice is maintained at pos

175 x1-EGFP BAC enabled a reliable expression of EGFP in Prox1-expressing cells of the transgenic rats an

176 her shown to drive a circadian expression of EGFP protein.

177 sulted in breakpoint-dependent expression of EGFP-tk and ganciclovir-mediated apoptosis.

178 y in HEK293T cells with an mCherry fusion of EGFP-K85AcK, and showed that this approach can be extend

179 During progressive internalization of EGFP-E. coli, fluorescence lifetimes were acquired and c

180 ection efficiencies by quantifying levels of EGFP protein expression.

181 ied and the average fluorescence lifetime of EGFP is known to be affected by pH.

182 The majority of EGFP-positive neurons bound isolectin B4, although a sma

183 Confocal micrographs of EGFP fusion proteins localized at key cell organelles in

184 and was necessary for the proper mobility of EGFP-mini-nesprin-2G, a functional TAN line reporter con

185 Indatraline increased the number of EGFP-LC3 cells expressing autophagosomes in the cytoplas

186 gmodon hispidus) resulted in high numbers of EGFP(+) cells in epithelia of the nasal septum and conch

187 There was a strong presence of EGFP(Vgat) fluorescence in TH-ir neurons across all brai

188 e directly observe the exocytotic release of EGFP-CD63 ILVs as discrete particles from individual WPB

189 translated through HfQ mediated silencing of EGFP by anti-EGFP synthetic small regulatory RNAs.

190 e, we identify three novel subpopulations of EGFP+ vagal brainstem neurons: (a) EGFP+ neurons in the

191 nt endocytic pathways suggest that uptake of EGFP-labelled mitochondria occurs via an actin-dependent

192 Switches based on EGFP, glucose dehydrogenase, NanoLuciferase, and dehydro

193 e cells in TH-RFP mice and M1 ipRGCs in OPN4-EGFP mice.

194 ns colocalized with native EGFP(Vglut2) - or EGFP(Vgat) -fluorescence, respectively.

195 Suppression of the overlapping EGFP signal provided a means to perform multiplexed imag

196 everal markers of senescence, including p16, EGFP, senescence-associated beta-galactosidase, and the

197 he example of HeLa cells expressing paxillin-EGFP to visualize focal adhesions.

198 2',3'-cyclic-nucleotide 3'-phosphodiesterase-EGFP(+) mice were treated with cuprizone, and OPCs were

199 rse genetics, we engineered recombinant PIV5-EGFP viruses with mutations in the head-stalk linker reg

200 Prdm8(EGFP/EGFP) mice showed nonprogressive b-wave deficits on

201 BP cell specification was normal in Prdm8(EGFP/EGFP) retina as determined by VSX2(+) cell numbers

202 novel genetically encoded fluorescent probe (EGFP-K85AcK) that responds to sirtuins in living cells.

203 In a chimera of ChAT promoter-EGFP and mito-mCherry, EGFP efficiently transferred to m

204 Enhanced green fluorescence protein (EGFP) and tandem dimer Tomato (tdTomato) were fused at N

205 a novel enhanced green fluorescence protein (EGFP)-based reporter assay system that allows us to perf

206 encoding enhanced green fluorescent protein (EGFP) and assessed transfection efficiencies by quantify

207 Using enhanced green fluorescent protein (EGFP) as a model protein, we carry out an experimental o

208 with an enhanced green fluorescent protein (EGFP) at the N-terminal.

209 Using enhanced green fluorescent protein (EGFP) fluorescence from the brain slices of Thy-1 EGFP t

210 t of DCC-enhanced green fluorescent protein (EGFP) from intracellular vesicles to the plasma membrane

211 on of an enhanced green fluorescent protein (EGFP) gene fused to a target promoter.

212 pressing enhanced green fluorescent protein (EGFP) into the dLGN.

213 cadherin-enhanced green fluorescent protein (EGFP) on the plasma membrane of isolated VSMCs, whereas

214 cadherin-enhanced green fluorescent protein (EGFP) on the VSMC surface.

215 specific enhanced green fluorescent protein (EGFP) reporter fused to the L10a large ribosomal subunit

216 rying an enhanced green fluorescent protein (EGFP) reporter gene in a panel of 12 organs after IP inj

217 encoding enhanced green fluorescent protein (EGFP) within an additional transcriptional unit (ATU) at

218 led with enhanced green fluorescent protein (EGFP), whereas CN neurons were from postnatal mouse prim

219 ted with enhanced green fluorescent protein (EGFP)-expressing E. coli.

220 bearing enhanced green fluorescent protein (EGFP)-specific CD8(+) T cells.

221 s study, enhanced green fluorescent protein (EGFP)-tagged L- and P-protein expression was coupled wit

222 sing the enhanced green fluorescent protein (EGFP)-tagged regulatory light chain (RLC) of NMII and mC

223 with an enhanced green fluorescent protein (EGFP)-tagged transgene inserted near the male-determinin

224 d by the enhanced green fluorescent protein (EGFP).

225 express enhanced green fluorescent protein (EGFP).

226 pressing green fluorescent reporter protein (EGFP) under control of the type I collagen (Col-I) promo

227 anced green and yellow fluorescent proteins (EGFP and EYFP) were not specifically optimized for neuro

228 espite the species mismatch, the mouse Prox1-EGFP BAC enabled a reliable expression of EGFP in Prox1-

229 lymphatic reporter rat using the mouse Prox1-EGFP BAC.

230 1-enhanced green fluorescent protein (Prox1-EGFP) transgenic mice with telomere dysfunction.

231 Together, Prox1-EGFP rat model will contribute to the advancement of lym

232 When N-myristoylation-defective rapsyn-EGFP mutant (G2A) and RING-H2 domain truncated rapsyn-EG

233 The targeting of rapsyn-EGFP (WT and mutants) is independent of synaptic activit

234 nt (G2A) and RING-H2 domain truncated rapsyn-EGFP were electroporated into sternomastoid muscles, a s

235 electively at synapses, similar to WT rapsyn-EGFP.

236 RARE-EGFP reporter axolotls showed divergent reporter activit

237 uced two lines of knock-in rabbits (rbRosa26-EGFP, and rbRosa26-Cre-reporter).

238 In F1 generation animals, the rbRosa26-EGFP rabbits express EGFP, and the rbRosa26-Cre-reporter

239 mGreenLantern can directly replace EGFP/EYFP in diverse systems due to its compatibility wi

240 Cal-Light drives expression of the reporter EGFP with high spatiotemporal resolution only in the pre

241 alpha-tTA;Teto-Cre;Dnmt3a(fl/fl); Rosa26LOXP(EGFP/EGFP) (Dnmt3a(Delta/Delta)) mice.

242 ng ATAC-seq in sorted prosensory cells (Sox2-EGFP(+)) and surrounding cells (Sox2-EGFP(-)) from E12,

243 s (Sox2-EGFP(+)) and surrounding cells (Sox2-EGFP(-)) from E12, E14.5 and E16 cochlear ducts.

244 Open chromatin regions detected in Sox2-EGFP(+) cells map to over 48,000 orthologous regions in

245 ccessibility with developmental time in Sox2-EGFP(+) cells, with most changes in the E12-14.5 window.

246 In Sox2-EGFP(+), we find greater accessibility in and near genes

247 ress Sox8 in the embryonic striatum and Sox8-EGFP BAC transgenic mice specifically reveal the direct

248 elective expression of EGFP in dSPNs of Sox8-EGFP BAC mice is maintained at postnatal timepoints.

249 Finally, we show that Sox8-EGFP BAC mice can be used to interrogate the altered dSP

250 cific marker of embryonic dSPNs and the Sox8-EGFP BAC transgenic mice are an excellent tool to study

251 Here, we have used a Sox9(EGFP) reporter to examine chromatin across ISC different

252 n and 5-hydroxymethylcytosine (5hmC) in Sox9(EGFP) populations, which reveals 5hmC enrichment in abso

253 on factor (TF) motifs in the context of Sox9(EGFP) populations, we classify broadly permissive and dy

254 nct gene expression signatures in the 2 Sox9-EGFP ISC populations.

255 tro IGF1 enhanced enteroid formation by Sox9-EGFP(High) facultative ISCs but not Sox9-EGFP(Low) activ

256 ox9-EGFP(High) facultative ISCs but not Sox9-EGFP(Low) actively cycling ISCs.

257 expression of a dominant negative Stat3Cbeta-EGFP gene in myotubes and in mouse muscle blocked the at

258 on of the ROSA26-CAG-(LoxP)tdTomato(StopLoxP)EGFP (ROSA-TG) Cre-reporter was confirmed in primary cel

259 r, C type 1 (mrc1a) promoter to drive strong EGFP expression in lymphatic vessels at all stages of de

260 to sixfold greater brightness in cells than EGFP.

261 sgene positive alpha-cells demonstrated that EGFP expression did not alter the intracellular Ca(2+) p

262 an Id4-eGfp reporter mouse to discover that EGFP intensity is predictive of the subsets, with the ID

263 We hypothesized that EGFP's low solubility in mammalian systems must limit th

264 n within the zebrafish retina indicates that EGFP and mglur6b mRNA are not only expressed in bipolar

265 nally, we used confocal imaging to show that EGFP-labelled mitochondria colocalise with a macropinocy

266 ion vector with a CAG promoter to detect the EGFP fluorescence only when skipping of mdx-type exon 23

267 g, which is particularly conspicuous for the EGFP-tagged variant, resulting in a massive accumulation

268 o genome editing, a 3-fold repression in the EGFP expression was observed when MCF-7 were transfected

269 IF(MCF) compared to 1-fold repression in the EGFP expression when MCF-7 were transfected with C(3)-ZI

270 the insertion of IRAlu at the 3'-UTR of the EGFP cDNA led to a rhythmic circadian nuclear retention

271 ulted a reduced silencing (~28 times) of the EGFP in microgravity.

272 other SoxE factors and we show here that the EGFP signal co-localizes with the OPC markers throughout

273 Finally, we confirmed that the EGFP-mdx23 Tg provided a highly sensitive platform to ch

274 Treating the EGFP-ataxin-3-84Q zebrafish with the calpain inhibitor c

275 These EGFP(+) axons are first observed to reach their midbrain

276 ted a novel transgenic mouse model with this EGFP expression vector (EGFP-mdx23 Tg).

277 eatment in ovariectomized (OVX) female Thy1M-EGFP mice.

278 ment in NSG mice and, upon administration to EGFP(+) /SCLtTA/TRE-BCR-ABL mice, the combination enhanc

279 raperitoneal or intraductal injection led to EGFP expression selectively in the alpha-cell population

280 lucose, peri-insulitis, and Th1 responses to EGFP which did not spread to other B-cell antigens.

281 nce or overexpressed cytosolic unmodulatable EGFP.

282 Using EGFP-HDAC11 transgenic reporter mice, we found that HDAC

283 identified as possessing temporally varying EGFP-expression.

284 ouse model with this EGFP expression vector (EGFP-mdx23 Tg).

285 Incorporation of VHHASC-EGFP into these structures allowed the visualization of

286 structural-activity-based screen of in vitro EGFP-silencing was used to select optimal siRNA designs

287 oot ganglion neurons of transgenic mice were EGFP-positive (mean diameter = 26.5 mum).

288 (BAC)-based lymphatic reporter mouse, where EGFP is expressed under the regulation of the Prox1 prom

289 al chromosome (BAC) transgenic mice in which EGFP expression is controlled by the HDC promoter, we id

290 enerated a transgenic marmoset line in which EGFP is expressed under the control of the human minimal

291 gradely labeled neurons did not colabel with EGFP expression in neurons of GAD67-EGFP mice.

292 Arginine vasopressin colocalized with EGFP more often in females (18 +/- 3%) than males (4 +/-

293 ver, discrete TH-ir signals colocalized with EGFP(Vgat) neurons, which we validated by in situ hybrid

294 beta-immunoreactivity (-ir) colocalized with EGFP.

295 of bacteriophage MS2 coat protein fused with EGFP.

296 Infecting these mice with EGFP-expressing murine herpes virus-68 (MHV68-EGFP) caus

297 imaging of end-binding protein 3 tagged with EGFP (EB3-GFP) in primary external granule layer cells s

298 When used together with EGFP-based biosensors, the new pair enables simultaneous

299 ane organization of functionally active Wnt3-EGFP in cerebellar cells of live transgenic zebrafish em

300 reased levels of the ER stress reporter Xbp1-EGFP.