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 fluorescence diminished substantially in the acidic

3 EGFP was also detected in discrete brain regions of tran

4 EGFP was expressed throughout the length of the sciatic

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

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

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

8 ally verified the technique, using myosin-1C-EGFP as a model system and fit its binding curve.

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

16 Using a cell model expressing an ABCD2-EGFP fusion protein, we first demonstrated by proximity

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

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

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

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

21 n CRE recombinase-dependent activation of an EGFP-tagged L10a ribosomal protein subunit, which allows

22 ed cultures of P. putida KT2440 producing an EGFP-fused model protein by means of the plasmid pA-EGFP

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

24 Utilizing an EGFP reporter system for observing ASFV replication and

25 ECFP and EGFP transgenic reporters based upon Csf1r and Cx3cr1 di

26 We demonstrated that signals of NowGFP and EGFP can be clearly distinguished by fluorescence lifeti

27 incorporation of (15)N-labelled protein and EGFP-beta-actin into nascent stereocilia.

28 inhibition of mTOR complex 1 induced RFP and EGFP expression and decreased cell proliferation.

29 l tubules, with increased numbers of RFP and EGFP puncta that peaked at 1 day after IRI.

30 oduce autophagic vacuoles expressing RFP and EGFP puncta.

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

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

33 carcinoma cells, gene-edited to express AP2-EGFP.

34 tagged with enhanced green fluorescence (AP2-EGFP) and on lateral protrusions from immobile SUM159 br

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

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

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

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

39 ition 5) of the genome to generate rHRSV(B05)EGFP(5).

40 red a dissociation constant of 20 nM between EGFP-labeled LcrV from Yersinia pestis and its cognate m

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

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

43 highly efficient doxycycline-inducible Cas9-EGFP vector.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 at Debio0719 reduced the retention of CX3CR1-EGFP(+) osteoclast precursors in bone by increasing thei

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

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

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

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

75 in cells that were enriched for pPAN-driven EGFP(high) and pK8.1-driven blue fluorescent protein-pos

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

77 sing gene-edited cells that express dynamin2-EGFP instead of dynamin2 and live-cell TIRF imaging with

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

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

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

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

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

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

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

85 sified immunogold (SIG) was mainly in ERbeta-EGFP dendrites.

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 phage precursors and blood monocytes express EGFP in these animals.

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

92 nine kidney (MDCK) cells that stably express EGFP-EAAT2a or EGFP-EAAT2b and found robust basolateral

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

94 ch as the nodose ganglion, failed to express EGFP, suggesting that additional regulatory elements dic

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

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

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

98 We expressed EGFP-tagged Mnk deletion or point mutation variants and

99 the ensuing beading of dendrites expressing EGFP by 2PLSM.

100 rarely showed stromal fibroblasts expressing EGFP.

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

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 rMV(EZ)EGFP(1), rMV(EZ)EGFP(3), and rMV(EZ)EGFP(6) contained th

106 muscular vaccination of macaques with rMV(EZ)EGFP(3) resulted in the identification of EGFP(+) cells

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

108 rMV(EZ)EGFP(1), rMV(EZ)EGFP(3), and rMV(EZ)EGFP(6) contained the ATU upstream o

109 rMV(EZ)EGFP(1), rMV(EZ)EGFP(3), and rMV(EZ)EGFP(6) contained the ATU upstream of the N gene, follow

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

111 inistration stimulated adipogenesis from FAP-EGFP.

112 er normal conditions, nephrons expressed few EGFP and RFP puncta, but ischemia-reperfusion injury (IR

113 lucose increased MG concentrations in tg(fli:EGFP) zebrafish embryos and rapidly induced several addi

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

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

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

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

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

119 the phosphate-binding pocket is required for EGFP-XRCC1 accumulation at DNA damage induced by UVA las

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

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

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

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

124 llowing transfection, mortalin-enhanced GFP (EGFP) is located primarily in mitochondria, whereas mort

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

126 luorescence cell sorting and RNA-seq in hcrt:EGFP zebrafish.

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

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

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

130 3(Gq)-mCherry) and control virus (rAAV5-hSyn-EGFP) were stereotactically administered to the hypoglos

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

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

133 Live-imaging EGFP-beta-actin or dendra2-beta-actin reveal stable F-ac

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

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

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

137 opular fluorescent proteins (FPs), including EGFP, can be unreliable for quantitative imaging, result

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

139 ect for spectrum-shifted variants, including EGFP.

140 Transfer of the T cells into EGFP reporter animals can be used to kill EGFP-expressin

141 ) in p48Cre; TetO-KrasG12D; Rosa26(rtTa-IRES-EGFP) (iKras*) mice and LSL-KrasG12D mice bred with p48C

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

143 The just EGFP death-inducing (Jedi) T cells enable visualization

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

145 to EGFP reporter animals can be used to kill EGFP-expressing cells, allowing selective depletion of d

146 an affinity toward double-strand breaks (Ku-EGFP) that DNA damage induces a transient decrease in ch

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 cal microscopy calibrated by single-molecule EGFP detection to determine the number of dynamins recru

163 live-cell TIRF imaging with single-molecule EGFP sensitivity and high temporal resolution, we detect

164 the motor, four of the tags (EGFP, monomeric EGFP, tagRFPt, and mApple) cause aberrantly long motor r

165 ily in mitochondria, whereas mortalinDelta51-EGFP lacking the mitochondrial targeting sequence is dis

166 By pair correlation analysis of EGFP molecular flow into chromatin before and after dama

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

168 We find from comparison of EGFP molecular flow with a molecule that has an affinity

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

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

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

172 Expression of EGFP-rab11a fusion proteins in Xenopus laevis photorecep

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

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

175 EZ)EGFP(3) resulted in the identification of EGFP(+) cells in the muscle at days 3, 5, and 7 postvacc

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

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

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

179 vivo tracking of infected cells by means of EGFP fluorescence in the absence of cytopathic changes i

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

181 The number of EGFP puncta returned to control levels at 3 days after I

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

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

184 In addition, we detect recruitment of EGFP-Ras, MEK, and phosphorylated Erk to patterned EGF i

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

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

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

188 CK) cells that stably express EGFP-EAAT2a or EGFP-EAAT2b and found robust basolateral membrane expres

189 spiral limbus (mimicking the cochlea of Otoa(EGFP/EGFP) mutant mice).

190 ring TTS on the basilar membrane of the Otoa(EGFP/EGFP) mice to improve our understanding of the fund

191 confirmed by monitoring the movement of Oxtr-EGFP as well as by immunogold labeling.

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

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

194 minantly suppresses mouse SCN Period1 (Per1)-EGFP-expressing clock cells.

195 and potentiates NPY's inhibition of SCN Per1-EGFP cells.

196 2',3'-cyclic-nucleotide 3'-phosphodiesterase-EGFP(+) mice were treated with cuprizone, and OPCs were

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

198 We crossed PLP-EGFP reporter mice into a Plp1-null background to invest

199 As development progressed, most PLP-EGFP-expressing cells gave rise to oligodendrocyte proge

200 The expression of PLP-EGFP in the spinal cord was quite dynamic during develop

201 e found that, at very early time points, PLP-EGFP was expressed in Sox2+ undifferentiated precursors

202 Using PLP-EGFP mice to investigate Plp1 promoter activity, we foun

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

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

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

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

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

208 ce; the enhanced green fluorescence protein (EGFP) was inserted into the Bex2 locus.

209 ter than enhanced green fluorescent protein (EGFP) and exhibits a fluorescence lifetime of 5.1 ns.

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

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

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

213 pressing enhanced green fluorescent protein (EGFP) in ERbeta-containing cells were implanted with osm

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

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

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

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

218 Enhanced green fluorescent protein (EGFP) reporter gene expression was quantified and Cx32 e

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

220 sed Sox9-enhanced green fluorescent protein (EGFP) reporter mice that permit analyses of both activel

221 encoding enhanced green fluorescent protein (EGFP) was introduced between the phosphoprotein and matr

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

223 r (pPAN)-enhanced green fluorescent protein (EGFP), and pK8.1-monomeric blue fluorescent protein (tag

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

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

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

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

228 rminally enhanced green fluorescent protein (EGFP)-tagged pUL51 supported normal virus replication an

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

230 istry in enhanced green fluorescent protein (EGFP)-TH mice revealed colocalization of DA, l-amino aci

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

232 4.5) and enhanced green fluorescent protein (EGFP; pKa 5.9), we generated CAG-RFP-EGFP-LC3 mice to di

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

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

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

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

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

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

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

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

241 Using this system, we eliminate a rare EGFP-expressing cell type in the heart and demonstrate i

242 RARE-EGFP reporter axolotls showed divergent reporter activit

243 perimentally verify the technique with H-Ras-EGFP as a model system and determine its oligomeric stat

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

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

246 In cells transfected with CMV-regulated EGFP-VP-peptide plasmid, C(292)-->A mutant did not stimu

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

248 ced with a retrovirus encoding Tet-repressor-EGFP.

249 privation, renal epithelial cells in CAG-RFP-EGFP-LC3 mice produce autophagic vacuoles expressing RFP

250 rotein (EGFP; pKa 5.9), we generated CAG-RFP-EGFP-LC3 mice to distinguish early autophagic vacuoles f

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

252 Overall, Scn10a-EGFP transgenic mice recapitulate the majority of the Na

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

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

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

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

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

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

259 GFP(Low)) and reserve/facultative ISCs (Sox9-EGFP(High)) to study IGF1 action on ISCs in normal intes

260 analyses of both actively cycling ISCs (Sox9-EGFP(Low)) and reserve/facultative ISCs (Sox9-EGFP(High)

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

262 CAM(-) cells from DDC-injured livers of Sox9-EGFP mice.

263 IGF1 increased percentages of Sox9-EGFP(High) ISCs in S-phase but did not expand this popul

264 stines, IGF1 increased total numbers of Sox9-EGFP(Low) ISCs and percentage of these cells in M-phase.

265 nce analysis in human cells, using the split-EGFP system.

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

267 Optogenetic activation of striatal EGFP-TH interneurons produced strong GABAergic inhibitio

268 ergic neurons but not in any of the striatal EGFP-TH interneurons.

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

270 y transfer assay showing disruption of SUR1(-EGFP)/Syn-1A(-mCherry) interaction along with increased

271 c properties of the motor, four of the tags (EGFP, monomeric EGFP, tagRFPt, and mApple) cause aberran

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

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

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

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

276 used HiTS-RAP to analyze interactions of the EGFP and negative elongation factor subunit E (NELF-E) p

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

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

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

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

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

282 transplanted purified FAPs from transgenic, EGFP mice into the injured muscles of C57/BL6 mice and f

283 cytometry-based approach, we observed unique EGFP reporter expression patterns in endocrine and stem/

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

285 identified as possessing temporally varying EGFP-expression.

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

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

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

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

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

291 , and vesicular monoamine transporter-2 with EGFP in midbrain dopaminergic neurons but not in any of

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

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

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

295 of bacteriophage MS2 coat protein fused with EGFP.

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

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

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

299 h 2-photon microscopy and 3D imaging, of Wt1-EGFP transgenic mice.

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