ライフサイエンスコーパス: YFP

1 YFP expression in roots transformed with pER8 was low ev

2 YFP fluorescence was normal in pOpOff2 transformed roots

3 YFP H-line and Thy1-GCaMP transgenic mice were used in t

4 YFP(+) BMCs in thy1-YFP mice have immunophenotypic featu

5 YFP(+) BMCs shared surface markers (CD11b+Gr1+Ly6C+Ly6G-

6 YFP(+) BMCs that infiltrated the cornea maintained their

7 YFP(+) BMCs, but not YFP(-) BMCs, significantly increase

8 The transgenic Thy-1-YFP mouse line, in which a small number of RGCs are labe

9 Using IL-12p40 YFP (Yet40) reporter mice, we show that CD103(+)CD11b(-)

10 e clamp region of RyR2(Ser-2367-CFP/Tyr-2801-YFP) induced by various ligands.

11 ual labeled RyR2 (RyR2(Ser-2367-CFP/Tyr-2801-YFP)).

12 cells expressing RyR2(Ser-2367-CFP/Tyr-2801-YFP).

13 ategy based on the bifunctional mCherry-2xCL-YFP-Vpr construct, in which 2xCL denotes a tandem cleava

14 Using a non-mobile version of STM (2xNLS-YFP-STM), we show that STM mobility is required to suppr

15 We analyzed a YFP-COP1-expressing transgenic line and endogenous COP1

16 inserting a CFP after residue Ser-2367 and a YFP after residue Tyr-2801 in the cardiac RyR (RyR2) to

17 Full-length NCX1 (FL-NCX1) and a YFP fusion protein of the NCX1 large intracellular loop

18 transport as determined by localization of a YFP-ATG8 reporter and its vacuolar cleavage during nitro

19 s also induced aggregation of alpha-syn*A53T-YFP in cultured cells, whereas none of six Parkinson's d

20 ellow fluorescent protein (alpha-syn140*A53T-YFP) and TgM83(+/-) mice expressing alpha-synuclein (A53

21 on the C-terminal side of Cys-739 abolished YFP-NCX1 palmitoylation.

22 rect visualization and measurement of alpha4-YFP expression and the effect of the presence (alpha5+/+

23 ying fusion genes for channelrhodopsin-2 and YFP, in either the rostral or caudal regions of the intr

24 ssion of tau or synuclein fusions to CFP and YFP, and confirmed its sensitivity and specificity to ta

25 fied biosensor enhanced FRET between CFP and YFP, consistent with heavy metal-induced folding of MT-I

26 n the cardiac RyR (RyR2) to yield a CFP- and YFP-dual labeled RyR2 (RyR2(Ser-2367-CFP/Tyr-2801-YFP)).

27 iciency was detected in mixtures of CFP- and YFP-tagged full-length Kir6.2 subunits and transmembrane

28 ) and dimeric (CD-28) receptors with GFP and YFP tags were used as controls to determine the molecula

29 Expression of the reporter genes (GFP and YFP) was also confirmed using reverse transcription-PCR

30 nked with CFP (cyan fluorescent protein) and YFP (yellow fluorescent protein) at N-terminus and C-ter

31 ndocrine cells expressing both serotonin and YFP, whereas single serotonin labeling was observed in 3

32 immunosuppressive action of BMCs (YFP(+) and YFP(-)) was evaluated in an allogenic mixed lymphocyte r

33 with wild-type, Y14D, or Y14F Cav1-CFP and -YFP constructs that FRET efficiency was greater with Y14

34 BRCA2-GFP and -YFP were compared to distinguish diffusion from fluoroph

35 and C-termini-tagged APP constructs: CFP-APP-YFP [containing the fluorescent tags, cyan fluorescent p

36 oducing free mCherry and the core-associated YFP-Vpr.

37 w and cyan fluorescent fusion proteins, AT1R-YFP and BK-CFP, displayed robust co-localized Forster re

38 relative abundance of cells expressing AUX1-YFP in the assayed population.

39 was developed that showed BR-inducible BES1-YFP accumulation in the nucleus, which was decreased in

40 SUPPRESSOR1-yellow fluorescent protein (BES1-YFP) transgenic line was developed that showed BR-induci

41 Expression of the BES1-YFP reporter was strong in the auricle region of develop

42 erfere with incorporation of expressed beta2-YFP subunit into AP-2 or alter AP-2 deposition at surfac

43 rthermore, a drop in FRET efficiency between YFP and mCherry because of cleavage of the bifunctional

44 The immunosuppressive action of BMCs (YFP(+) and YFP(-)) was evaluated in an allogenic mixed l

45 ing prolines impaired palmitoylation of both YFP-NCX1 and FL-NCX1.

46 In dark-grown seedlings, both YFP-COP1 and endogenous COP1 accumulated in the nucleus

47 otein (YFP) is often used as an acceptor but YFP is prone to photobleaching and pH changes.

48 which sensory and motor axons are marked by YFP.

49 ans, we show that IL-10 production by CD4(+) YFP(+) T cells is controlled systemically during malaria

50 ite exhibiting comparable phenotypes, CD4(+) YFP(+) GFP(+) T cells from the liver and lung produced s

51 Mature splenic CD4(+) YFP(+) GFP(+) T cells, which preferentially expressed hi

52 ein (GFP) reporter mice, we show that CD4(+) YFP(+) T cells are the major source of IL-10 in both lym

53 plenic counterparts, showing that the CD4(+) YFP(+) GFP(+) T cells exert graded functions in distinct

54 CD4(+)YFP(+)GFP(+) T cells generally exhibited a short-lived e

55 In contrast, CD4(+)YFP(+)GFP(-) T cell-derived cells expanded rapidly and u

56 that primary malaria infection-induced CD4(+)YFP(+)GFP(+) T cells have limited memory potential, do n

57 Consistently, the surviving CD4(+)YFP(+)GFP(+) T cell-derived cells were unresponsive and

58 ness analysis confirmed actin-dependent CD44-YFP clusters on living cells.

59 characterized fluorescent bone marrow cells (YFP(+) BMCs) in the thy1-YFP mouse and determine if they

60 We produced dual CFP/YFP-tagged GluA2 subunit constructs that had normal acti

61 a Src-mediated conformational change in CFP/YFP-tagged WT-Cav1 pairs.

62 anced yellow fluorescence protein (VGAT-ChR2-YFP)-expressing mice and a novel fibreoptic 'laserspritz

63 firmed using a second reporter gene, Citrine YFP.

64 transgenic plants harboring CML38pro::CML38:YFP followed by liquid chromatography-tandem mass spectr

65 is end we used targeted expression of a COI1-YFP transgene in the coi1-1 mutant background.

66 We show that expression of COI1-YFP in the epidermis of the stamen filament and anther i

67 ith the anion efflux, CPK2/CPK20/CPK17/CPK34:YFP fluorescence was strictly localized at the tip plasm

68 blocks of spinal cord, we also assessed CST-YFP mice for 3D imaging and found that YFP fluorescence

69 aging and found that YFP fluorescence in CST-YFP mice is faint for clearing-based 3D imaging in compa

70 he nonspecific and faint YFP labeling in CST-YFP mice limits their utility for assessments of CST axo

71 We show here that in CST-YFP mice, some YFP-labeled axons are not from the CST.

72 al cord, and it was suggested that these CST-YFP mice would be useful for studies of CST regeneration

73 eta-glucuronidase (GUS) activity and DAO1pro:YFP-DAO1 signals, and transformation with DAO1pro:YFP-DA

74 AO1 signals, and transformation with DAO1pro:YFP-DAO1 complemented the mutant phenotypes.

75 Injection of diphtheria toxin deleted YFP(+) cells from Foxl1-Cre;Rosa(YFP/iDTR) mice and prev

76 ssing the first 126 amino acids, TAN1-DeltaI-YFP, failed to rescue the double mutant phenotype, while

77 sing a conserved middle region, TAN1-DeltaII-YFP, significantly rescued the mutant phenotype in terms

78 meristems and TIBA-pin apices activated DR5:YFP expression with similar kinetics; however, only lfs

79 f the auxin reporters pPIN1:PIN1:GFP and DR5:YFP Upon auxin microapplication, both lfs meristems and

80 revealed a similar distribution of all EphA2-YFP variants in cells.

81 The expression of EphA2-YFP variants and their kinase activity (phosphorylation

82 n labeling was observed in 36% and exclusive YFP labeling in 9%.

83 tif (GZ variant: G540I, G544I) and expressed YFP-tagged EphA2 (WT, HR, and GZ variants) in HEK293T ce

84 None of the tumor nodules expressed YFP, indicating that Foxl1-expressing cells are not the

85 ung carcinoma cell line H1299 that expresses YFP-tagged alpha1 from its normal genomic localization.

86 Overall, the nonspecific and faint YFP labeling in CST-YFP mice limits their utility for as

87 ts and join host vessels; subsequently a few YFP cells are shed into circulation.

88 pal gliogenesis (P2-P4), significantly fewer YFP+ cells were evident in the cortex, corpus callosum,

89 ealed the cortical decrease was due to fewer YFP+ astrocytes and oligodendrocytes, with a slightly ea

90 purified from brains of transgenic His6-FLAG-YFP-NL2 mice showed enrichment in the Gene Ontology term

91 We find the His6-FLAG-YFP-NL2 to be a suitable tag, with the unamplified YFP s

92 The non-fluorescent YFP variant sREACh is an efficient acceptor, which is us

93 dosomes in plants, resulted in enlarged FLY1-YFP bodies.

94 ural, two-protein system, with FtsA and FtsZ-YFP (having the FtsA-binding peptide instead of the mts)

95 mellar liposomes incorporating FtsA and FtsZ-YFP showed a variety of distributions, including foci an

96 in tubular multilamellar liposomes with FtsZ-YFP-mts, where mts is a membrane-targeting amphiphilic h

97 We also find that a functional YFP-QueE fusion localizes to the division septum in fila

98 Native expression of a functional YFP:FEA4 fusion recapitulated this pattern of expression

99 ansfer was observed from an N-terminal-fused YFP to a FRET acceptor, ReAsH (resorufin arsenical hairp

100 using Gag expression constructs (Gag or Gag-YFP, where YFP is yellow fluorescent protein) created fr

101 labeled cells in the spinal gray matter have YFP-labeled projections into the spinal cord white matte

102 ges from source cells expressing either hetN-YFP or hetN alone, despite a lack of intercellular excha

103 a lack of intercellular exchange of the HetN-YFP fusion protein.

104 In bigenic L126Z/WT-hSOD1:YFP mice, disease was not accelerated and WT-hSOD1:YFP r

105 ce, disease was not accelerated and WT-hSOD1:YFP remained diffusely distributed.

106 used to yellow fluorescent protein (WT-hSOD1:YFP) with G37R-hSOD1 produced earlier disease, and spina

107 Mitochondria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:Y

108 AGS3-Rluc-Galpha(i1)-YFP and AGS4-Rluc-G-Galpha(i1)-YFP BRET were observed in

109 AGS3-Rluc-Galpha(i1)-YFP and AGS4-Rluc-Galpha(i1)-YFP BRET were regulated by

110 uc-Galpha(i1)-YFP and AGS4-Rluc-G-Galpha(i1)-YFP BRET were observed in both pellet and supernatant su

111 Rluc-Galpha(i1)-YFP and AGS4-Rluc-Galpha(i1)-YFP BRET were regulated by Ric-8A but not by Galpha-inte

112 ent upon the amount of Ric-8A and Galpha(i1)-YFP.

113 Using IFNbeta/YFP reporter mice, we identify these IFN-beta-producing

114 Il7(YFP+) TECs are sustained in Rag2(-/-) mice, even followi

115 t TECs coexpressing high levels of IL-7 (Il7(YFP+) TECs) reside within a subset of CD205(+)Ly51(+)CD4

116 ds, we explored the relationship between Il7(YFP+) TECs and mTECs.

117 ures, the thymocyte-induced reduction in Il7(YFP+) TECs dissociates from the receptor activator of NF

118 As the frequency of Il7(YFP+) TECs gradually declines as mTEC development unfold

119 eage moderately reduces the frequency of Il7(YFP+) TECs, whereas negative selection provokes a striki

120 ve selection provokes a striking loss of Il7(YFP+) TECs.

121 Still, Il7(YFP+) TECs can generate some CD80(+) mTECs in a stepwise

122 letions on the N-terminal side of Cys-739 in YFP-NCX1 did not affect NCX1 palmitoylation, with the ex

123 gliogenesis was accompanied by a decrease in YFP+ proliferative cells, but not increased cell death.

124 e and the absence of Vipp1, no difference in YFP expression was observed, which shows that Vipp1 is n

125 Control mice revealed an increase in YFP(+) neurons and dendrite formation over time.

126 e Mef2 KO mice also displayed an increase in YFP(+) neurons over time-but with significantly stunted

127 fraction of YFP-positive cortical neurons in YFP(J16) mice cortex were identified as callosal project

128 ter mice (messenger of IFN-beta) resulted in YFP(+) and eGFP(+) single-positive cells, whereas among

129 the C terminus of each protein, resulting in YFP complementation and a bright fluorescent signal.

130 In YFPs, the pi-stacking of the chromophore with Tyr203 red

131 n of an intact fluorescent protein including YFP when its two complementary, non-fluorescent N- and C

132 bryos, we recovered 616 verified independent YFP-positive lines representing protein traps in 374 gen

133 arized light to bleach and probe an internal YFP-FliN fusion, we show that the innermost components o

134 rrow cells transduced with a MSCV-HOXB4-ires-YFP vector.

135 Coupling of functional data from AtCruA ISD-YFP fusions with statistical analysis of the physiochemi

136 Following annular keratectomy, YFP(+) BMCs infiltrated the cornea.

137 beled within the helical domain (Galphai-L91-YFP) largely do not dissociate upon activation, yet stil

138 However, mitochondria in CFP-LGP2:YFP-LGP2 cells had lower FRET signal in the presence of

139 rotein of the NCX1 large intracellular loop (YFP-NCX1) were expressed in HEK cells.

140 (Myh11-CreERT2) were crossed with Rosa26-LSL-YFP mice for lineage tracing analysis.

141 plants expressing the mutant phyB(Lys996Arg)-YFP photoreceptor are hypersensitive to red light, (ii)

142 A maximum YFP/CFP FRET ratio of 2.8 was observed in the presence o

143 cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had higher FRET efficiencies in the prese

144 ndria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had higher F

145 llowing colitis in adult Sox2CreER:YFP mice, YFP initially expressed predominantly by glia becomes ex

146 e with anterogradely labeled CST axons, most YFP-labeled axons beyond established CST locations do no

147 reas among messenger of IFN-beta-BM-mDC most YFP(+) cells were also eGFP(+).

148 FS cell microenvironment, we injected murine YFP(+) embryonic stem cells (ESC) into the amniotic flui

149 , we use two unique mouse strains--an Ndfip1-YFP reporter and an Ndfip1-deficient strain--to show tha

150 h a partner kinase juxtaposes nonfluorescent YFP fragments fused to the C terminus of each protein, r

151 nifested as a marked shift in the normalized YFP/mCherry fluorescence ratio, reliably predicted viral

152 YFP(+) BMCs, but not YFP(-) BMCs, significantly increased growth of TG neurit

153 al system; however, high-level ChR2 (but not YFP) expression was associated with substantial cytotoxi

154 , via piggyBac transposition, over 600 novel YFP-trap proteins tagging just under 400 Drosophila loci

155 FRET experiments conducted using Nox1-YFP and NOXA1-CFP illustrate that NoxA1ds disrupts the b

156 Site-specific protein cleavage of YFP-TRF1 by tobacco etch virus protease resolves telomer

157 CD4 and AP-2 resulted in complementation of YFP and a bright fluorescent signal by confocal microcop

158 Deletion of YFP(+) cells did not alter levels of markers of liver in

159 We further demonstrate that the density of YFP-labeled axon arbors hinders tracing of single axons

160 and spectral overlap between the emission of YFP and the visible-region (QX) absorption bands of the

161 (Pet-1) to drive 5-HT neuronal expression of YFP, we identified 5-HT neurons in live acute slices.

162 Accordingly, a significant fraction of YFP-positive cortical neurons in YFP(J16) mice cortex we

163 o complementary non-fluorescent fragments of YFP and co-expressed in 293T cells.

164 internal reflection fluorescence imaging of YFP-MotB (part of a stator force-generating unit) confir

165 itive; though cells expressing low levels of YFP were also positive for benzidine, a hemoglobin stain

166 Importantly, the midcell localization of YFP-p1 was disrupted in a strain that does not express F

167 lls promoted plasma membrane localization of YFP-PLCbeta3.

168 elling along the length of the axon, loss of YFP signal, and transected appearance.

169 Loss of YFP(+) NSCs following Hif1a gene inactivation in vivo wa

170 e deletion resulted in a significant loss of YFP(+) NSCs within the SVZ by 45 d post recombination, w

171 In vitro measurements of YFP/CFP fluorescence emission ratios indicated that the

172 esting 1 (LH1) complex shows the position of YFP attachment to the RC-H subunit, on the cytoplasmic s

173 epletion of PARP3 impairs the recruitment of YFP-Ku80 to laser-induced DNA damage sites and induces a

174 Nuclear magnetic resonance studies of YFP 10C confirm halide binding occurs on a slow time sca

175 ia, and the expression of surface markers on YFP(+) BMCs was analyzed by flow cytometry.

176 to express cyan fluorescent protein (CFP) or YFP fused to either biologically active HCV helicase or

177 infected with lentivirus containing ChR2 or YFP gene and subjected to cytotoxicity analysis.

178 d constructs to be imaged with either GFP or YFP filter cubes.

179 tricular viral injections to express VAPB or YFP throughout the brain and spinal cord of superoxide d

180 h reduced compared with that of the original YFP 10C construct, primarily through a reduced associati

181 At the cellular level, pCkx3::YFP reporter-gene studies revealed that the Ckx3 promote

182 r, mitochondria-targeted circularly permuted YFP (mt-cpYFP).

183 ines expressing the biologically active phyA-YFP photoreceptor in different tissues, and analyzed the

184 is drastically decreased compared with phyB-YFP, and (iii) SUMOylation of phyB inhibits binding of P

185 tage of yellow fluorescent protein-positive (YFP(+)) hepatocytes contained markers of oxidative stres

186 that is prone to aggregation, with prominent YFP-fluorescent aggregates observed in the motor neurons

187 ne encoding the Yellow Fluorescence Protein (YFP) into the dexamethasone inducible vector pOpOff2 and

188 en CD44 fused to yellow fluorescent protein (YFP) and CD44 fused to cyan fluorescent protein on K562

189 AtCruA fusion to yellow fluorescent protein (YFP) and expression in developing embryos of A. thaliana

190 lizing IFN-gamma-yellow fluorescent protein (YFP) and IL-10-GFP dual reporter mice, we show that prim

191 eron (IFN-gamma)-yellow fluorescent protein (YFP) and IL-10-green fluorescent protein (GFP) reporter

192 al exon encoding yellow fluorescent protein (YFP) and protein affinity tags.

193 Both SIS8-yellow fluorescent protein (YFP) and UGT72E1-YFP fusion proteins localize to the nuc

194 tion centre (RC)/yellow fluorescent protein (YFP) complex accelerates photosynthetic growth in the ba

195 nd quantified by yellow fluorescent protein (YFP) expression.

196 We expressed yellow fluorescent protein (YFP) from a yeast promoter and selected for a regular al

197 hat a functional yellow fluorescent protein (YFP) fusion of BdCSLF6 is localized to the Golgi apparat

198 However, FLY1-yellow fluorescent protein (YFP) fusions are localized in punctae that are predomina

199 Yellow fluorescent protein (YFP) is often used as an acceptor but YFP is prone to ph

200 rossing "H-line" yellow fluorescent protein (YFP) mice with the 5xFAD mouse model, which we call the

201 ed from IFN-beta yellow fluorescent protein (YFP) reporter mice (messenger of IFN-beta) resulted in Y

202 reported to have yellow fluorescent protein (YFP) selectively expressed in forebrain neurons leading

203 Yellow fluorescent protein (YFP) tagging of a homolog of SLOW ANION CHANNEL-ASSOCIAT

204 By using yellow fluorescent protein (YFP) translational fusions, CML38 protein was found to b

205 Yellow fluorescent protein (YFP) was present in >96% of hepatocytes before exposure

206 ll when Galphai2 yellow fluorescent protein (YFP) was tethered to the carboxyl terminus of the alpha2

207 are labeled with yellow fluorescent protein (YFP), permitted investigation of whether subtypes of RGC

208 1 particles with yellow fluorescent protein (YFP)-tagged APOBEC3 proteins and examined their associat

209 c interaction of yellow fluorescent protein (YFP)-tagged beta3 integrin with c(RGDfK) peptide.

210 ssion of TRF1 or yellow fluorescent protein (YFP)-TRF1 fusion protein above endogenous levels prevent

211 rotein (CFP) and yellow fluorescent protein (YFP).

212 axons expressing yellow fluorescent protein (YFP).

213 II (MT-II), and yellow fluorescent protein (YFP).

214 rotein (CFP) and yellow fluorescent protein (YFP).

215 rotein (CFP) and yellow fluorescent protein (YFP)] and FLAG-APP-Myc.

216 functional fluorescent PUB13 fusion protein (YFP-PUB13) localizes to TGN and Golgi compartments and t

217 ed Medicago truncatula roots, and quantified YFP fluorescence and mRNA levels.

218 ddition, we use SiMPull to directly quantify YFP and mCherry maturation probabilities, showing these

219 al cells (Sox9CreER(T2);Pten(flox/flox);R26R(YFP) or Pten(DeltaDuct/DeltaDuct) mice) and used Pten(De

220 giving transgenic mice (nestin-CreERT2/R26R-YFP/CDK5(flox/flox) [iCdk5] and nestin-CreERT2/R26R-YFP/

221 5(flox/flox) [iCdk5] and nestin-CreERT2/R26R-YFP/CDK5(wt/wt) [WT]) tamoxifen during postnatal (P) day

222 We generated nestin-CreER(T2)/R26R-YFP/Hif1a(fl/fl) triple transgenic mice, to enable tamox

223 sient absorption spectroscopy of purified RC/YFP complexes show that the YFP-RC intermolecular distan

224 The structure of the RC/YFP-light-harvesting 1 (LH1) complex shows the position

225 9, and quantified and phenotyped recombined (YFP+) cells at P14 and P21.

226 Lengths of profiles of regenerating YFP(+) axons were measured 2 wk later from confocal imag

227 luorescent protein (RelA-FP) construct: RelA-YFP, RelA-mEos2 and RelA-Dendra2.

228 ingly, dexamethasone removal did not reverse YFP inhibition.

229 We treated AAV-TBG-Cre; Rosa(YFP) mice with diethylnitrosamine (DEN), followed by mul

230 xin deleted YFP(+) cells from Foxl1-Cre;Rosa(YFP/iDTR) mice and prevented the resolution of hepatic s

231 Based on studies of Foxl1-Cre;Rosa(YFP/iDTR) mice, Foxl1(+) HPCs and/or their descendants a

232 g HPCs and their descendants (Foxl1-Cre;Rosa(YFP/iDTR)-inducible diphtheria toxin receptor [iDTR] mic

233 causes recombination (AAV-TBG-Cre) into Rosa(YFP) mice.

234 ing experiments based on Sox18Cre(ERt2)/Rosa-YFP mice.

235 Lineage tracing by using Cdh5cre(ERt2)/Rosa-YFP reporter strategy demonstrated that the CD31-/loVEGF

236 NDCs were isolated from Shh-cre;ROSA:YFP mice at embryonic day 12.5 and postnatal day 0, repr

237 +) and Pdx1Cre;Kras(G12D/+);p53(fl/+);Rosa26(YFP) mice (PDAC), and Pdx1Cre;Kras(G12D/+);p53(fl/+);Spa

238 mice (Pdx1Cre;Kras(G12D/+);p53(fl/+);Rosa26(YFP);Cre;Etv1(fl/fl)) reduced levels of SPARC and hyalur

239 ied out on double-transgenic Wnt1-Cre/ROSA26-YFP mice showing stable YFP expression in all neural cre

240 esence of tau in dendritic spines of rTg4510-YFP mouse brain by array tomography.

241 he coupled protonation reaction, for several YFP variants and detect slow kinetics (dissociation rate

242 pinal cords of paralyzed bigenic mice showed YFP fluorescent inclusion-like structures.

243 ct consequence of vascular regression, since YFP(+) neurosphere formation over serial passage was una

244 log of SLOW ANION CHANNEL-ASSOCIATED1 (SLAH3:YFP) was widespread along PTs, but, in accordance with t

245 Transient expression of a SlCAT9-YFP fusion in tobacco confirmed a tonoplast localisation

246 pinal neurons are labeled with YFP, and some YFP-labeled cells in the spinal gray matter have YFP-lab

247 We show here that in CST-YFP mice, some YFP-labeled axons are not from the CST.

248 Sox2CreER:YFP and PLP1creER:tdT mice were used to determine the fa

249 Following colitis in adult Sox2CreER:YFP mice, YFP initially expressed predominantly by glia

250 Specifically, YFP-labeled axons are present in regions beyond those wi

251 crossover nanostructure that recruits split YFP when properly assembled.

252 lementation (BiFC; also referred to as split-YFP assays) are applicable to the analysis of protein-pr

253 has been shown to be co-localized with SR33-YFP, a protein involved in pre-mRNA splicing, suggesting

254 dogenous SRDs-containing proteins and an SRD-YFP fusion localize with AAL to the nuclear membrane.

255 enic Wnt1-Cre/ROSA26-YFP mice showing stable YFP expression in all neural crest-derived cell populati

256 Emx1-Cre x Thy1-STOP-YFP mice have been reported to have yellow fluorescent p

257 all such constructs, including double-tagged YFP-Kir6.2-CFP (Y6.2C), formed functional K(ATP) channel

258 TAN1-YFP expressed in tan1 air9 significantly rescued the dou

259 N1 fused to yellow fluorescent protein, TAN1-YFP, and several deletion constructs were transformed in

260 of cortical division site localized TANGLED1-YFP.

261 CLIN1B destruction box was fused to TANGLED1-YFP to generate a line that mostly rescued the division

262 We then cloned a hpRNA targeting YFP under the regulation of the inducible promoters, tra

263 In vivo analysis using a TatA-YFP fusion showed that the TatB F13Y substitution result

264 Under these conditions the TatA-YFP fusion supports full physiological Tat transport act

265 ative stress, DNA damage, or cell death than YFP-negative hepatocytes, indicating that YFP(+) hepatoc

266 roduced changes in cell adhesion rather than YFP expression: clonal populations oscillated between si

267 d CST-YFP mice for 3D imaging and found that YFP fluorescence in CST-YFP mice is faint for clearing-b

268 our days after transplantation we found that YFP(+) sorted cells maintained the expression of pluripo

269 an YFP-negative hepatocytes, indicating that YFP(+) hepatocytes are newly formed cells.

270 y of purified RC/YFP complexes show that the YFP-RC intermolecular distance and spectral overlap betw

271 mbranes as demonstrated by the fact that the YFP-tagged SYP72 localized to the ER in wild-type plants

272 Many of these YFP mutants bind halides with affinities in the millimol

273 YFP(+) BMCs in thy1-YFP mice have immunophenotypic features of MDSCs.

274 ging in comparison with fluorescence in Thy1-YFP-H mice and fluorescence of mini-ruby biotinylated de

275 voxel-based morphometry (VBM) study of Thy1-YFP mice following auditory fear conditioning complement

276 ted into the vitreous humor of B6.Cg-Tg(Thy1-YFP)HJrs/J mice.

277 bone marrow cells (YFP(+) BMCs) in the thy1-YFP mouse and determine if they promote trigeminal gangl

278 -smear counts of circulating cells from Tie1-YFP embryos showed that up to 30% of blood-borne cells a

279 -lapse imaging of germ-line transformed Tie1-YFP reporter quail embryos combined with the endothelial

280 When Tie1-YFP positive cells and tissues are transplanted to wild

281 133(+)) generate intermediate astrocyte (Tnc(YFP-low) CD15(+)) precursors and GABAergic transient amp

282 ehog (Shh), and blockade of reception in TNC(YFP-low) cells attenuates proliferation in the PWM, redu

283 ural stem-cell-like primary progenitors (Tnc(YFP-low) CD133(+)) generate intermediate astrocyte (Tnc(

284 the catalytic domain of E3 ligase, CHIP, to YFP-tagged KCNQ1 +/- KCNE1 subunits with a GFP-nanobody

285 nalysis of Sr33 and Sr50 CC domains fused to YFP and either nuclear localization or nuclear export si

286 d plastid localization using AtRBSK fused to YFP.

287 Full-length Kir6.2 subunits were linked to YFP or cyan fluorescent protein (CFP) at N or C termini,

288 he context of HD in vivo, we bred transgenic YFP(J16) with R6/2 mice, a widely used HD model.

289 yellow fluorescent protein (YFP) and UGT72E1-YFP fusion proteins localize to the nucleus when transie

290 2 to be a suitable tag, with the unamplified YFP signal localizing appropriately to inhibitory synaps

291 changes occur in the anal depressor, we used YFP:actin to monitor, and mutant analysis, laser-ablatio

292 nsfer-based assay (CAMYEL, cAMP sensor using YFP-Epac-Rluc), we assessed the predicted compounds for

293 Cs in a stepwise differentiation process via YFP(-)Ly51(low)CD80(low) intermediates.

294 osis and found that HCA and HCC nodules were YFP(+) lineage-labeled; positive for osteopontin, SRY (s

295 expression constructs (Gag or Gag-YFP, where YFP is yellow fluorescent protein) created from all repr

296 hese neurons are transgenically labeled with YFP in the 5XY mouse, which enable longitudinal imaging

297 and reticulospinal neurons are labeled with YFP, and some YFP-labeled cells in the spinal gray matte

298 We tagged all 27 Drosophila Rabs with YFP(MYC) at their endogenous chromosomal loci, determine

299 nohistochemical double labeling studies with YFP and serotonin antisera combined with electron micros

300 notion, HEK293 cells stably transfected with YFP-tagged R753Q TLR2 displayed reduced recruitment of M