ライフサイエンスコーパス: yellow fluorescent protein

1 2+)-translocating channelrhodopsin linked to yellow fluorescent protein.

2 xpressing the viral core protein A4 fused to yellow fluorescent protein.

3 teins tagged with the C-terminal fragment of yellow fluorescent protein.

4 ng cortical slice via neuronal expression of yellow fluorescent protein.

5 ated lineage tracer mice, expressed enhanced yellow fluorescent protein.

6 fluorescence emission from halide-sensitive yellow fluorescent protein.

7 rexpression of human STIM1 conjugated to the yellow fluorescent protein.

8 sed the duct-specific lineage tracing marker yellow fluorescent protein.

9 IV-1 provirus and ROSA-26-regulated enhanced yellow fluorescent protein.

10 t protein mutant 3* (TorA-GFPmut3*) and TetR-yellow fluorescent protein.

11 in which subsets of pyramidal cells express yellow fluorescent protein.

12 ing certain point mutations or insertions of yellow fluorescent protein.

13 gion separating cyan fluorescent protein and yellow fluorescent protein.

14 ence (NES) within Htt exon and when fused to yellow fluorescent protein.

15 s using H1R-cyan fluorescent protein and H2R-yellow fluorescent protein.

16 cytosed BCR as compared with wild-type ezrin-yellow fluorescent protein.

17 gic and glutamatergic neurons labeled in the yellow fluorescent protein-16 (YFP-16) line (up to 500 H

18 y investigating the lateral mobility of GAT1-yellow fluorescent protein-8 (YFP8) expressed in neurobl

19 ed with cyan fluorescent protein (donor) and yellow fluorescent protein (acceptor).

20 Both MIR159 and APC8-yellow fluorescent protein accumulated in unicellular mi

21 ength, mutant human alpha-synuclein fused to yellow fluorescent protein (alpha-syn140*A53T-YFP) and T

22 The DII domain was fused to a yellow fluorescent protein and a nuclear localization se

23 auxin efflux transporter (ZmPIN1a) fused to yellow fluorescent protein and a synthetic auxin-respons

24 We used amyloid precursor protein (APP)-yellow fluorescent protein and brain-derived neurotrophi

25 pidermal leaf cells with fusions of OBAP1 to yellow fluorescent protein and immunogold labeling of em

26 to yeast expressing transporter fusions with yellow fluorescent protein and mCerulean triggered subst

27 We measure the FRET efficiencies between yellow fluorescent protein and mCherry-tagged versions o

28 We determined that ClpE-YFP (yellow fluorescent protein) and ClpC-YFP formed foci coi

29 ing calmodulin kinase II fused with enhanced yellow fluorescent protein, and b), time lapse FRET imag

30 most responsive to the ligand were fused to yellow fluorescent protein, and fluorescence levels in t

31 t and wild-type (WT) M2 regions, of cyan and yellow fluorescent protein, and of fluorescent and nonfl

32 collecting ducts were labeled with enhanced yellow fluorescent protein, and tracked the fate of thes

33 (CFP), emission intensities of CFP and YFP (yellow fluorescent protein) are captured before and afte

34 ce in the stem of the channel, we used Venus yellow fluorescent protein as a molecular stopper to tra

35 In this study, we observed that yellow fluorescent protein(+) ASCs in the medullary cord

36 with CFP (cyan fluorescent protein) and YFP (yellow fluorescent protein) at N-terminus and C-terminus

37 Yellow fluorescent protein-AtCDC48A, a fusion protein th

38 Time-lapse imaging of yellow fluorescent protein:ATK5 reveals colocalization w

39 ressing nonfluorescent halves (YN and YC) of yellow fluorescent protein attached to each receptor.

40 the human adenocarcinoma cell line HeLa with yellow fluorescent protein-Bap31 chimeras increased surf

41 Yellow fluorescent protein-based assay was performed to

42 ENSITIVE1-ETHYL METHANESULFONATE-SUPPRESSOR1-yellow fluorescent protein (BES1-YFP) transgenic line wa

43 is of cyan fluorescent protein (CFP)-arm-CTD-yellow fluorescent protein beta-catenin reveals that the

44 a2delta1)), and CACNA1C tagged with enhanced yellow fluorescent protein (Ca(v)1.2).

45 asis using a mitochondrial targeted enhanced yellow fluorescent protein-calmodulin construct.

46 n transfectants, we now demonstrate that AID-yellow fluorescent protein can stably localize to the nu

47 loss of mu2 led to increased accumulation of YELLOW FLUORESCENT PROTEIN-CESA6 particles at the plasma

48 ziflam caused a reduction in the velocity of YELLOW FLUORESCENT PROTEIN:CESA6 particles at the plasma

49 chimeric proteins fused to enhanced cyan or yellow fluorescent protein (CFP or YFP, respectively).

50 cells coexpressing IL-17RA fused to cyan or yellow fluorescent proteins (CFP or YFP) were used to ev

51 s, we constructed a unique set of 125 kinase-yellow fluorescent protein chimeras in the filamentous S

52 ns with channelrhodopsin-2 fused to enhanced yellow fluorescent protein (ChR2-EYFP) and used DAT(IRES

53 ruct for channelrhodopsin2 fused to enhanced yellow fluorescent protein (ChR2-eYFP) was virally deliv

54 e-induced structural changes in the Aequorea yellow fluorescent protein Citrine reveals the structura

55 Substitution of the enhanced yellow fluorescent protein component of a FLIPPi sensor

56 s with the vascular marker maize PINFORMED1a-yellow fluorescent protein confirmed that Tdy2 was expre

57 t resonance energy transfer between cyan and yellow fluorescent proteins conjugated at its N and C te

58 ts of transgenic mice expressing a G85R SOD1-yellow fluorescent protein construct.

59 nstructed by inserting a circularly permuted yellow fluorescent protein (cpYFP) into a region of the

60 y developed by inserting circularly permuted yellow fluorescent protein (cpYFP) into the NADH-binding

61 ion constructs (Gag or Gag-YFP, where YFP is yellow fluorescent protein) created from all representat

62 delta-subunits, with one (delta1YFP) or two yellow fluorescent protein (delta2YFP) molecules fused a

63 dwiched between cyan fluorescent protein and yellow fluorescent protein, demonstrated a basal level o

64 We prepared fusion proteins comprising yellow fluorescent protein-Dictyostelium myosin II motor

65 lls were labeled by transgenic expression of yellow fluorescent protein, DiOlistics or diffusion of D

66 Galpha(i1) tagged with Renilla luciferase or yellow fluorescent protein expressed in mammalian cells

67 nt truncated and point mutants of hENT1-YFP (yellow fluorescent protein) expressed in Madin-Darby can

68 ced cyan fluorescent protein and/or enhanced yellow fluorescent protein, expressed in COS1 cells, and

69 ortex was used to monitor via optical window yellow fluorescent protein expressing neurons, enhanced

70 led to a decrease in the number of enhanced yellow fluorescent protein-expressing cells and down-reg

71 We established and used a stable yellow fluorescent protein-expressing STIM1 cell line (Y

72 g of HIV-1 Tat into the lateral ventricle of yellow fluorescent protein-expressing transgenic mice pr

73 s injections inducing Cre-dependent enhanced yellow fluorescent protein expression in ChAT-IRES-Cre m

74 tivity was assessed by beta-galactosidase or yellow fluorescent protein expression in the pancreas an

75 green fluorescent protein (EGFP) > enhanced yellow fluorescent protein (EYFP) > enhanced cyan fluore

76 ize the mechanical stability of the enhanced yellow fluorescent protein (EYFP) (a mutant form of the

77 t hyperpolarizability (beta) of the enhanced yellow fluorescent protein (eYFP) could be explained by

78 Whereas a composite containing an enhanced yellow fluorescent protein (eYFP) exhibited hypsochromic

79 usion protein colocalized with FtsZ-enhanced yellow fluorescent protein (EYFP) in M. smegmatis.

80 red fluorescent protein (DsRed) and enhanced yellow fluorescent protein (EYFP) linked by a 19-amino-a

81 Expression of the enhanced yellow fluorescent protein (EYFP) reporter gene in PPEPs

82 We used CD11c promoter-enhanced yellow fluorescent protein (EYFP) transgenic mice to vis

83 The CD11c enhanced yellow fluorescent protein (EYFP) transgenic mouse was c

84 The authors used mice expressing enhanced yellow fluorescent protein (eYFP) under control of the C

85 d population of PG cells expressing enhanced yellow fluorescent protein (EYFP) under the control of t

86 e appearance of a reporter protein, enhanced yellow fluorescent protein (EYFP), in cells.

87 sensory neurons and live imaging of enhanced yellow fluorescent protein (eYFP)-actin dynamics, we rep

88 n a pollen-specific manner and that enhanced yellow fluorescent protein (EYFP)-RabA4d-labeled membran

89 geny by indelibly marking them with enhanced yellow fluorescent protein (EYFP).

90 tion and micropatterning of ferrocene-tagged yellow fluorescent proteins (Fc-YFPs) onto beta-cyclodex

91 ive of this class (cyan fluorescence protein/yellow fluorescent protein-fluorescence resonance energy

92 HSP-FRET consists of the cyan and yellow fluorescent protein fluorophores linked by the cy

93 While pairs of cyan and yellow fluorescent proteins (FPs) are most commonly used

94 Fragments of yellow fluorescent protein fused to FKBP and FRB produce

95 We generated mice that express yellow fluorescent protein fused to the N terminus of th

96 We expressed a chimera of yellow fluorescent protein fused to the N-terminal regio

97 nt of recombinant WNV NS2B-NS3, and cyan and yellow fluorescent proteins fused by a dodecamer peptide

98 In wild type, enhanced yellow fluorescent protein-fused AGG1 and AGG2 are assoc

99 Using cyan and yellow fluorescent protein fusion constructs, we show th

100 lar localization using a C-terminal enhanced yellow fluorescent protein fusion indicated that UKL1 an

101 lecule sensitivity using a newly constructed yellow fluorescent protein fusion library for Escherichi

102 A MAR1:yellow fluorescent protein fusion localizes to the chlor

103 ntly expressed in Nicotiana tabacum, an ECA3-yellow fluorescent protein fusion protein showed overlap

104 ting duct cells expressing an IFT88-enhanced yellow fluorescent protein fusion recapitulated the aln-

105 Analysis of an RPS5-super Yellow Fluorescent Protein fusion revealed that RPS5 loc

106 Microscopic analysis of a Mnx::yellow fluorescent protein fusion showed that the protei

107 A PDIL2-1-yellow fluorescent protein fusion was mainly localized i

108 e we show that the foci are due to OmpR-YFP (yellow fluorescent protein) fusion binding to specific s

109 versions of IAA1 localized to the nucleus as Yellow Fluorescent Protein fusions and interacted with b

110 equently tested the subcellular targeting of yellow fluorescent protein fusions for selected proteins

111 hanced cyan fluorescent protein and enhanced yellow fluorescent protein fusions of the proteins were

112 ana Sieve-Element-Occlusion-Related1 (SEOR1)-yellow fluorescent protein fusions show that At SEOR1 me

113 g ALS-associated human G85R SOD1 joined with yellow fluorescent protein (G85R SOD1YFP), which produce

114 ow fluorescent protein-SlGGB1/amino-terminal yellow fluorescent protein-Gbeta heterodimer were locali

115 sts in which an internal ribosome entry site/yellow fluorescent protein gene was inserted downstream

116 proteins, maize PROTEIN DISULFIDE ISOMERASE-Yellow Fluorescent Protein, GLOSSY8a-monomeric Red Fluor

117 d cells expressing CFTR and a halide-sensing yellow fluorescent protein (H148Q/I152L) were transfecte

118 ) mouse liver, PK11195 translocated enhanced yellow fluorescent protein-hCAR into the nucleus.

119 His tag (His6), His-tagged enhanced yellow fluorescent protein (His6-eYFP), and His6-tagged

120 n 16-18 month-old transgenic mice expressing yellow fluorescent protein in layer V pyramidal neurons.

121 yan fluorescent protein and DDR1 tagged with yellow fluorescent protein in live cells.

122 YFP mice, which selectively express enhanced yellow fluorescent protein in serontonergic neurons, the

123 Expression of ACA-yellow fluorescent protein in the ctxI/ctxII-null cells

124 Fusion of AtRGGA with yellow fluorescent protein indicated that AtRGGA is loca

125 itioned mice with cells labelled by enhanced yellow fluorescent protein instead of ChR2.

126 ation of GSK3beta and is sufficient to drive yellow fluorescent protein into the nucleus.

127 ce resonance energy transfer between cyan or yellow fluorescent protein-labeled G protein subunits an

128 ells by photophysical analysis of individual yellow fluorescent protein-labeled TatA complexes.

129 GALLS-FL tagged with yellow fluorescent protein localized to the nucleus of t

130 ytosis of cargos at the plasma membrane, mu2-YELLOW FLUORESCENT PROTEIN localized to transient foci a

131 LRE fused to citrine yellow fluorescent protein (LRE-cYFP) remains functional

132 Somewhat surprisingly, VirE2-yellow fluorescent protein mainly localized to the cytop

133 ough adulthood that bear a nuclear-localized yellow fluorescent protein marker directly driven by dfd

134 ed a nitrate-inducible promoter fused to the yellow fluorescent protein marker gene YFP.

135 od anatomical data are critical, a monomeric yellow fluorescent protein (mCitrine) was N-terminally f

136 Using affinity chromatography and split-Yellow Fluorescent Protein methods, a nuclear transcript

137 The recent development of transgenic mGLU-yellow fluorescent protein mice that express a genetic r

138 into the transient blue-shifting of isolated yellow fluorescent protein molecules under ambient condi

139 glutamine sensors based on improved cyan and yellow fluorescent proteins, monomeric Teal Fluorescent

140 sing the reporter transgenic twitcher-Thy1.1-yellow fluorescent protein mouse.

141 ssisted capture, the subcellular location of yellow fluorescent protein-NCX1 fusion proteins, and NCX

142 ansferring and activating B cells expressing yellow fluorescent protein only in the ASC compartment.

143 hannelrhodopsin 2 (ChR2) fused with enhanced yellow fluorescent protein or mCherry was injected into

144 concept, we used the N-terminal fragment of yellow fluorescent protein- or nVenus-tagged Agrobacteri

145 RET between cyan fluorescent protein-PLB and yellow fluorescent protein-PLB in AAV-293 cells showed h

146 T between cyan fluorescent protein-SERCA and yellow fluorescent protein-PLB, was increased by the I40

147 A smaller percentage of yellow fluorescent protein-positive (YFP(+)) hepatocytes

148 Following UUO, enhanced yellow fluorescent protein-positive cells were confined

149 fragment containing residues from Venus and yellow fluorescent protein produced either constitutive

150 was also inserted into a live organism, the yellow fluorescent protein producing nematode Caenorhabd

151 A yellow fluorescent protein:PttSUT3 fusion localized to p

152 Interestingly, the movement of yellow fluorescent protein-RabA4d-labeled vesicles and t

153 n of D(1)-green fluorescent protein and D(2)-yellow fluorescent protein receptors within internal sto

154 ddition, ZML2 activated transcription of the yellow fluorescent protein reporter gene driven by the C

155 iption affects the permanent expression of a yellow fluorescent protein reporter in post-germinal cen

156 hanced cyan fluorescent protein and enhanced yellow fluorescent protein, respectively, C-terminally t

157 onal Ctr1 monomers fused with either cyan or yellow fluorescent protein resulted in fluorescence reso

158 o protein vesicular stomatitis virus protein-yellow fluorescent protein revealed that vesicles from b

159 Overexpression of yellow fluorescent protein-ROP2 is associated with its d

160 endogenous SERT and heterologously expressed yellow fluorescent protein-SERT from axons to the somato

161 ion protein as well as the carboxyl-terminal yellow fluorescent protein-SlGGB1/amino-terminal yellow

162 ies from ChAT-eGFP or superoxide dismutase 1-yellow fluorescent protein (SOD1YFP) transgenic animals

163 Here we show that secreted A5 fused to yellow fluorescent protein specifically labels apoptotic

164 Interestingly, coexpression of the YFP (yellow fluorescent protein)-tagged KIF5B assists dendrit

165 used Renilla luciferase-tagged receptors and yellow fluorescent protein-tagged beta-arrestin2, Rab5,

166 nes, as well as live cell imaging studies of yellow fluorescent protein-tagged C1 domains, reveal tha

167 ng assay based on transgenic mice expressing yellow fluorescent protein-tagged EB3 to study microtubu

168 (FRET) between cyan fluorescent protein- and yellow fluorescent protein-tagged KCNQ subunits expresse

169 In epidermal cells, the yellow fluorescent protein-tagged MyoB1/2 localize to ve

170 also induced expression of exogenous RyR1 or yellow fluorescent protein-tagged RyR1 in muscles of adu

171 ted cyan fluorescent protein and an enhanced yellow fluorescent protein-tagged synaptophysin or posts

172 r the N or C termini, and a pair of cyan and yellow fluorescent protein-tagged tau were co-transfecte

173 transfectants with wild-type (WT) or mutant yellow fluorescent protein-tagged TLR4 variants revealed

174 The yellow fluorescent protein-tagged Y353F mutant displayed

175 ation studies of several GATL proteins using yellow fluorescent protein tagging provide evidence supp

176 Full-length TAN1 fused to yellow fluorescent protein, TAN1-YFP, and several deleti

177 Venus is a yellow fluorescent protein that has been developed for i

178 eric ephrin-A1 (mEA1) and enhanced monomeric yellow fluorescent protein that is linked to a supported

179 ign is inspired by the red shift seen in the yellow fluorescent protein that results from pi-pi stack

180 gent-Insoluble Membranes lipids, and targets yellow fluorescent protein to Detergent-Insoluble Membra

181 expressing mitochondrially targeted enhanced yellow fluorescent protein to excitotoxic glutamate resu

182 of RPS5 were sufficient for directing super Yellow Fluorescent Protein to the PM.

183 Parasites were tagged with yellow fluorescent protein to verify infection.

184 By single-cell imaging of stable AID-yellow fluorescent protein transfectants, we now demonst

185 We measured the pH-sensitive fluorescence of Yellow Fluorescent Protein transgenically expressed in m

186 visualized as chimeric proteins tagged with yellow fluorescent protein, transiently associate with a

187 A VviCCC-yellow fluorescent protein translational fusion protein

188 in protein atypical-1 (CPNA-1), as well as a yellow fluorescent protein translational fusion, are loc

189 t of the pattern of constitutively expressed yellow fluorescent protein-TSPO in Arabidopsis.

190 We used enhanced yellow fluorescent protein under control of the Pet-1 en

191 gic neurons specifically labeled by enhanced yellow fluorescent protein under control of the Pet-1 pr

192 f proteins tagged with Renilla luciferase or yellow fluorescent protein under transient assay conditi

193 s coding for channelrhodopsin-2 and enhanced yellow fluorescent protein unilaterally into the unlesio

194 (vascular endothelial-cadherin-Cre-enhanced yellow fluorescent protein [VE-Cad-Cre-EYFP]).

195 energy transfer) proteins, where variants of yellow fluorescent protein (Venus) and cyan fluorescent

196 Transgenic mice expressing yellow fluorescent protein (Venus) under the control of

197 ype and impa-4 Arabidopsis plants expressing yellow fluorescent protein-VirD2 displayed nuclear local

198 In Nicotiana benthamiana leaves, SYMRK-yellow fluorescent protein was localized at the plasma m

199 degradation tag to Venus, a rapidly folding yellow fluorescent protein, we obtained both fluorescenc

200 ich the PKD2L1 promoter drives expression of yellow fluorescent protein, we previously reported that

201 (NLS) and either cyan fluorescent protein or yellow fluorescent protein, we show that each of the wil

202 etized transgenic mice expressing axoplasmic yellow fluorescent protein were stimulated electrically

203 The cyan and yellow fluorescent proteins were attached to full-length

204 orresponding to the N termini of the cyan or yellow fluorescent proteins were fused to the ends of th

205 lecules (mannosidase I and sialyltransferase-yellow fluorescent protein) were identified by immunogol

206 tochondrial-surface associated BTPC-enhanced yellow fluorescent protein when both fusion proteins wer

207 onditionally expressed the reporter enhanced yellow fluorescent protein while concomitantly deleting

208 Co-expression of WT-hSOD1 fused to yellow fluorescent protein (WT-hSOD1:YFP) with G37R-hSOD

209 eonGreen is the brightest monomeric green or yellow fluorescent protein yet described to our knowledg

210 cyan fluorescent protein donor and B2-fused yellow fluorescent protein (YFP) acceptor, we registered

211 ich CD8 T cells are irreversibly tagged with yellow fluorescent protein (YFP) after activation.

212 ecifically labeled using genetically encoded yellow fluorescent protein (YFP) and a chemically attach

213 ytosis, mutagenesis of human DAT tagged with yellow fluorescent protein (YFP) and an extracellular HA

214 ed tight co-clustering between CD44 fused to yellow fluorescent protein (YFP) and CD44 fused to cyan

215 lasma membrane, as shown by imaging of CPK17-yellow fluorescent protein (YFP) and CPK34-YFP in growin

216 ction was measured by FRET between M(3)-AChR-yellow fluorescent protein (YFP) and cyan fluorescent pr

217 eled with green fluorescent protein (GFP) or yellow fluorescent protein (YFP) and expressed in human

218 ab27bN133I) forms of Rab27b were tagged with yellow fluorescent protein (YFP) and expressed in pariet

219 These were verified by AtCruA fusion to yellow fluorescent protein (YFP) and expression in devel

220 In this study, utilizing IFN-gamma-yellow fluorescent protein (YFP) and IL-10-GFP dual repo

221 udy, using dual gamma interferon (IFN-gamma)-yellow fluorescent protein (YFP) and IL-10-green fluores

222 Changes in cap-dependent yellow fluorescent protein (YFP) and internal ribosome e

223 vector carrying an artificial exon encoding yellow fluorescent protein (YFP) and protein affinity ta

224 We destabilized the reporter yellow fluorescent protein (YFP) and the P. falciparum p

225 Both SIS8-yellow fluorescent protein (YFP) and UGT72E1-YFP fusion

226 muscles (1-4) in transgenic mice expressing yellow fluorescent protein (YFP) as a reporter.

227 te phagosome formation, the distributions of yellow fluorescent protein (YFP) chimeras of enzymes and

228 , we show that a hybrid reaction centre (RC)/yellow fluorescent protein (YFP) complex accelerates pho

229 f the UPS, such as the ubiquitin (Ub)-fusion yellow fluorescent protein (YFP) degradation substrate,

230 ged with either Renilla luciferase (RLuc) or yellow fluorescent protein (YFP) demonstrated saturable,

231 in the corneas of transgenic mice expressing yellow fluorescent protein (YFP) driven by the thy1 prom

232 An RNAi-insensitive beta2-yellow fluorescent protein (YFP) expressed in the beta1

233 Pdgfra-CreER(T2):Rosa26R-YFP mice to induce yellow fluorescent protein (YFP) expression in PDGFRA/NG

234 cell layer were visualized and quantified by yellow fluorescent protein (YFP) expression.

235 Expression of yellow fluorescent protein (YFP) followed by preembeddin

236 We expressed yellow fluorescent protein (YFP) from a yeast promoter a

237 Yellow fluorescent protein (YFP) fused to the transit pe

238 Here, we generated an HSV expressing a gD-yellow fluorescent protein (YFP) fusion and found that g

239 ng BdCSLF6, we demonstrate that a functional yellow fluorescent protein (YFP) fusion of BdCSLF6 is lo

240 n be complemented by re-expression of an Arg-yellow fluorescent protein (YFP) fusion, but not by an N

241 However, FLY1-yellow fluorescent protein (YFP) fusions are localized i

242 g phospho-mimic and nonphosphorylatable phyB-yellow fluorescent protein (YFP) fusions demonstrated th

243 e stable murine DC line XS106 to express the yellow fluorescent protein (YFP) gene under the control

244 in basic protein (shiverer), also expressing yellow fluorescent protein (YFP) in a subset of axons.

245 tion of Notch1 and concomitant expression of yellow fluorescent protein (YFP) in nestin-expressing Ty

246 ng EAE by using transgenic mice that express yellow fluorescent protein (YFP) in neurons.

247 lices and filaments in Escherichia coli when yellow fluorescent protein (YFP) is fused to its N termi

248 Yellow fluorescent protein (YFP) is often used as an acc

249 Yellow fluorescent protein (YFP) is widely used as a gen

250 coronal brain slices were prepared from thy1-yellow fluorescent protein (YFP) mice at postnatal day 3

251 genic mouse model of AD by crossing "H-line" yellow fluorescent protein (YFP) mice with the 5xFAD mou

252 We generated a nestin-CreER(T2)/R26R-yellow fluorescent protein (YFP) mouse to inducibly labe

253 Using an inducible nestin-CreER(T2)/R26R-yellow fluorescent protein (YFP) mouse, we investigated

254 individual cell types by placing the foreign yellow fluorescent protein (YFP) on their outer surface,

255 expressed cyan fluorescent protein (CFP) or yellow fluorescent protein (YFP) reporter genes under th

256 FP treatment of BM-pDC derived from IFN-beta yellow fluorescent protein (YFP) reporter mice (messenge

257 hy1-STOP-YFP mice have been reported to have yellow fluorescent protein (YFP) selectively expressed i

258 Recombinant viruses with a yellow fluorescent protein (YFP) tag on the N or C termi

259 Yellow fluorescent protein (YFP) tagging of a homolog of

260 escribed for the site-specific attachment of yellow fluorescent protein (YFP) to glass surfaces on le

261 To address these questions, we fused yellow fluorescent protein (YFP) to mature IGFBP-3 lacki

262 olarity is detected in this system, we fused yellow fluorescent protein (YFP) to the C terminus of th

263 By using yellow fluorescent protein (YFP) translational fusions,

264 n into fat, we rendered FVBN mice expressing yellow fluorescent protein (YFP) under control of a mono

265 cence complementation, where one fragment of yellow fluorescent protein (YFP) was fused to receptors

266 Yellow fluorescent protein (YFP) was present in >96% of

267 f GalphaGPR in the intact cell when Galphai2 yellow fluorescent protein (YFP) was tethered to the car

268 Fragments of yellow fluorescent protein (YFP) were fused to the NH2 o

269 between two nonfluorescent fragments of the yellow fluorescent protein (YFP) when they are united by

270 transgenic virus that expresses the enhanced yellow fluorescent protein (YFP), driven by the human cy

271 hich a small number of RGCs are labeled with yellow fluorescent protein (YFP), permitted investigatio

272 CSM 14.1 cell lines stably expressed yellow fluorescent protein (YFP), YFP-Bcl-x(L,) YFP-Bcl-

273 rgy transfer (FRET) analysis using expressed yellow fluorescent protein (YFP)-CAR and CFP-R16A fusion

274 between cyan fluorescent protein (CFP)- and yellow fluorescent protein (YFP)-fused RRs in vitro.

275 Surprisingly, yellow fluorescent protein (YFP)-hGRbeta was predominant

276 Yellow fluorescent protein (YFP)-labeled C2J ES cells we

277 eletion of these three parS1 sites abrogated yellow fluorescent protein (YFP)-ParB1 focus formation i

278 amban (PLB), we expressed Cerulean-SERCA and yellow fluorescent protein (YFP)-PLB in adult rabbit ven

279 I throughout layer V of the neocortex within yellow fluorescent protein (YFP)-positive axons.

280 Yellow fluorescent protein (YFP)-positive cells signific

281 We labeled HIV-1 particles with yellow fluorescent protein (YFP)-tagged APOBEC3 proteins

282 lls, we demonstrated specific interaction of yellow fluorescent protein (YFP)-tagged beta3 integrin w

283 val of extracellular potassium (K(+)) caused yellow fluorescent protein (YFP)-tagged NCX1 to redistri

284 egenerating system and cytosol, release of a yellow fluorescent protein (YFP)-tagged raft-independent

285 imaging, we show that expression of TRF1 or yellow fluorescent protein (YFP)-TRF1 fusion protein abo

286 mission to yield a class of mutants known as yellow fluorescent protein (YFP).

287 re heritably labeled at high efficiency with yellow fluorescent protein (YFP).

288 ally labeled K19(+) cholangiocytes expressed yellow fluorescent protein (YFP).

289 GFP as well as to some GFP variants such as yellow fluorescent protein (YFP).

290 se NIH3T3 cells expressing H3.3 fused to the yellow fluorescent protein (YFP).

291 pair, the cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP).

292 tein (CFP) and coexpressed with PLB fused to yellow fluorescent protein (YFP).

293 apparatus in vivo, SKu2 protein was fused to yellow fluorescent protein (YFP).

294 d between cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP).

295 protein (GFP) with damaged axons expressing yellow fluorescent protein (YFP).

296 FP), chicken metallothionein II (MT-II), and yellow fluorescent protein (YFP).

297 ent tags, cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP)] and FLAG-APP-Myc.

298 B sites in living cells using 53BP1 fused to yellow fluorescent protein (YFP-53BP1) as a surrogate ma

299 myotubes expressing Rem tagged with enhanced yellow fluorescent protein (YFP-Rem), as assayed by elec

300 A mu-opioid receptor fused to yellow fluorescent protein (YMOR) was constructed and ex