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1 ence (NES) within Htt exon and when fused to yellow fluorescent protein.
2 s using H1R-cyan fluorescent protein and H2R-yellow fluorescent protein.
3 cytosed BCR as compared with wild-type ezrin-yellow fluorescent protein.
4 2+)-translocating channelrhodopsin linked to yellow fluorescent protein.
5 xpressing the viral core protein A4 fused to yellow fluorescent protein.
6 teins tagged with the C-terminal fragment of yellow fluorescent protein.
7 ng cortical slice via neuronal expression of yellow fluorescent protein.
8 ated lineage tracer mice, expressed enhanced yellow fluorescent protein.
9 sed the duct-specific lineage tracing marker yellow fluorescent protein.
10 rexpression of human STIM1 conjugated to the yellow fluorescent protein.
11 IV-1 provirus and ROSA-26-regulated enhanced yellow fluorescent protein.
12 t protein mutant 3* (TorA-GFPmut3*) and TetR-yellow fluorescent protein.
13 in which subsets of pyramidal cells express yellow fluorescent protein.
14 fluorescence emission from halide-sensitive yellow fluorescent protein.
15 gion separating cyan fluorescent protein and yellow fluorescent protein.
16 gic and glutamatergic neurons labeled in the yellow fluorescent protein-16 (YFP-16) line (up to 500 H
17 y investigating the lateral mobility of GAT1-yellow fluorescent protein-8 (YFP8) expressed in neurobl
20 ength, mutant human alpha-synuclein fused to yellow fluorescent protein (alpha-syn140*A53T-YFP) and T
22 auxin efflux transporter (ZmPIN1a) fused to yellow fluorescent protein and a synthetic auxin-respons
24 pidermal leaf cells with fusions of OBAP1 to yellow fluorescent protein and immunogold labeling of em
25 to yeast expressing transporter fusions with yellow fluorescent protein and mCerulean triggered subst
26 We measure the FRET efficiencies between yellow fluorescent protein and mCherry-tagged versions o
27 li to accumulate variation in populations of yellow fluorescent proteins and then evolved these prote
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
36 with CFP (cyan fluorescent protein) and YFP (yellow fluorescent protein) at N-terminus and C-terminus
39 udy, we constructed a FRET probe composed of yellow fluorescent protein attached at the N-terminus of
40 ressing nonfluorescent halves (YN and YC) of yellow fluorescent protein attached to each receptor.
41 the human adenocarcinoma cell line HeLa with yellow fluorescent protein-Bap31 chimeras increased surf
43 ENSITIVE1-ETHYL METHANESULFONATE-SUPPRESSOR1-yellow fluorescent protein (BES1-YFP) transgenic line wa
44 is of cyan fluorescent protein (CFP)-arm-CTD-yellow fluorescent protein beta-catenin reveals that the
47 n transfectants, we now demonstrate that AID-yellow fluorescent protein can stably localize to the nu
48 loss of mu2 led to increased accumulation of YELLOW FLUORESCENT PROTEIN-CESA6 particles at the plasma
49 ziflam caused a reduction in the velocity of YELLOW FLUORESCENT PROTEIN:CESA6 particles at the plasma
50 chimeric proteins fused to enhanced cyan or yellow fluorescent protein (CFP or YFP, respectively).
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
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
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 lls were labeled by transgenic expression of yellow fluorescent protein, DiOlistics or diffusion of D
65 using differences in expression of enhanced yellow fluorescent protein driven from the tyrosine hydr
66 n biological studies, the enhanced green and yellow fluorescent proteins (EGFP and EYFP) were not spe
67 Galpha(i1) tagged with Renilla luciferase or yellow fluorescent protein expressed in mammalian cells
68 ortex was used to monitor via optical window yellow fluorescent protein expressing neurons, enhanced
69 led to a decrease in the number of enhanced yellow fluorescent protein-expressing cells and down-reg
71 g of HIV-1 Tat into the lateral ventricle of yellow fluorescent protein-expressing transgenic mice pr
72 s injections inducing Cre-dependent enhanced yellow fluorescent protein expression in ChAT-IRES-Cre m
73 tivity was assessed by beta-galactosidase or yellow fluorescent protein expression in the pancreas an
74 green fluorescent protein (EGFP) > enhanced yellow fluorescent protein (EYFP) > enhanced cyan fluore
75 t hyperpolarizability (beta) of the enhanced yellow fluorescent protein (eYFP) could be explained by
76 Whereas a composite containing an enhanced yellow fluorescent protein (eYFP) exhibited hypsochromic
79 red fluorescent protein (DsRed) and enhanced yellow fluorescent protein (EYFP) linked by a 19-amino-a
83 The authors used mice expressing enhanced yellow fluorescent protein (eYFP) under control of the C
84 d population of PG cells expressing enhanced yellow fluorescent protein (EYFP) under the control of t
86 sensory neurons and live imaging of enhanced yellow fluorescent protein (eYFP)-actin dynamics, we rep
87 n a pollen-specific manner and that enhanced yellow fluorescent protein (EYFP)-RabA4d-labeled membran
89 tion and micropatterning of ferrocene-tagged yellow fluorescent proteins (Fc-YFPs) onto beta-cyclodex
90 ive of this class (cyan fluorescence protein/yellow fluorescent protein-fluorescence resonance energy
95 nt of recombinant WNV NS2B-NS3, and cyan and yellow fluorescent proteins fused by a dodecamer peptide
98 lar localization using a C-terminal enhanced yellow fluorescent protein fusion indicated that UKL1 an
99 lecule sensitivity using a newly constructed yellow fluorescent protein fusion library for Escherichi
101 ntly expressed in Nicotiana tabacum, an ECA3-yellow fluorescent protein fusion protein showed overlap
102 ting duct cells expressing an IFT88-enhanced yellow fluorescent protein fusion recapitulated the aln-
106 e we show that the foci are due to OmpR-YFP (yellow fluorescent protein) fusion binding to specific s
107 versions of IAA1 localized to the nucleus as Yellow Fluorescent Protein fusions and interacted with b
108 equently tested the subcellular targeting of yellow fluorescent protein fusions for selected proteins
109 hanced cyan fluorescent protein and enhanced yellow fluorescent protein fusions of the proteins were
110 ana Sieve-Element-Occlusion-Related1 (SEOR1)-yellow fluorescent protein fusions show that At SEOR1 me
111 g ALS-associated human G85R SOD1 joined with yellow fluorescent protein (G85R SOD1YFP), which produce
112 ow fluorescent protein-SlGGB1/amino-terminal yellow fluorescent protein-Gbeta heterodimer were locali
113 sts in which an internal ribosome entry site/yellow fluorescent protein gene was inserted downstream
114 proteins, maize PROTEIN DISULFIDE ISOMERASE-Yellow Fluorescent Protein, GLOSSY8a-monomeric Red Fluor
115 male and female GFP-M line (n = 24) and male yellow fluorescent protein-H line (n = 5) mice undergoin
116 d cells expressing CFTR and a halide-sensing yellow fluorescent protein (H148Q/I152L) were transfecte
120 n 16-18 month-old transgenic mice expressing yellow fluorescent protein in layer V pyramidal neurons.
122 e brain slices from mice expressing enhanced yellow fluorescent protein in MC3R neurons to test how a
123 YFP mice, which selectively express enhanced yellow fluorescent protein in serontonergic neurons, the
128 ce resonance energy transfer between cyan or yellow fluorescent protein-labeled G protein subunits an
131 ytosis of cargos at the plasma membrane, mu2-YELLOW FLUORESCENT PROTEIN localized to transient foci a
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
141 ssisted capture, the subcellular location of yellow fluorescent protein-NCX1 fusion proteins, and NCX
143 ansferring and activating B cells expressing yellow fluorescent protein only in the ASC compartment.
144 hannelrhodopsin 2 (ChR2) fused with enhanced yellow fluorescent protein or mCherry was injected into
145 concept, we used the N-terminal fragment of yellow fluorescent protein- or nVenus-tagged Agrobacteri
146 RET between cyan fluorescent protein-PLB and yellow fluorescent protein-PLB in AAV-293 cells showed h
147 T between cyan fluorescent protein-SERCA and yellow fluorescent protein-PLB, was increased by the I40
150 fragment containing residues from Venus and yellow fluorescent protein produced either constitutive
151 was also inserted into a live organism, the yellow fluorescent protein producing nematode Caenorhabd
154 n of D(1)-green fluorescent protein and D(2)-yellow fluorescent protein receptors within internal sto
155 ddition, ZML2 activated transcription of the yellow fluorescent protein reporter gene driven by the C
156 iption affects the permanent expression of a yellow fluorescent protein reporter in post-germinal cen
157 hanced cyan fluorescent protein and enhanced yellow fluorescent protein, respectively, C-terminally t
158 onal Ctr1 monomers fused with either cyan or yellow fluorescent protein resulted in fluorescence reso
159 o protein vesicular stomatitis virus protein-yellow fluorescent protein revealed that vesicles from b
162 endogenous SERT and heterologously expressed yellow fluorescent protein-SERT from axons to the somato
163 ion protein as well as the carboxyl-terminal yellow fluorescent protein-SlGGB1/amino-terminal yellow
164 ies from ChAT-eGFP or superoxide dismutase 1-yellow fluorescent protein (SOD1YFP) transgenic animals
166 Interestingly, coexpression of the YFP (yellow fluorescent protein)-tagged KIF5B assists dendrit
167 used Renilla luciferase-tagged receptors and yellow fluorescent protein-tagged beta-arrestin2, Rab5,
168 ng assay based on transgenic mice expressing yellow fluorescent protein-tagged EB3 to study microtubu
169 (FRET) between cyan fluorescent protein- and yellow fluorescent protein-tagged KCNQ subunits expresse
171 also induced expression of exogenous RyR1 or yellow fluorescent protein-tagged RyR1 in muscles of adu
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
175 ation studies of several GATL proteins using yellow fluorescent protein tagging provide evidence supp
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 ts evolvability, we subjected populations of yellow fluorescent protein to directed evolution under d
182 he expression of channelrhodopsin 2-enhanced yellow fluorescent protein to GAD1(+) GABAergic neurons.
186 We measured the pH-sensitive fluorescence of Yellow Fluorescent Protein transgenically expressed in m
187 visualized as chimeric proteins tagged with yellow fluorescent protein, transiently associate with a
189 in protein atypical-1 (CPNA-1), as well as a yellow fluorescent protein translational fusion, are loc
192 gic neurons specifically labeled by enhanced yellow fluorescent protein under control of the Pet-1 pr
193 uman endometrial stromal cell line that uses yellow fluorescent protein under the control of the prol
194 s coding for channelrhodopsin-2 and enhanced yellow fluorescent protein unilaterally into the unlesio
196 energy transfer) proteins, where variants of yellow fluorescent protein (Venus) and cyan fluorescent
198 ype and impa-4 Arabidopsis plants expressing yellow fluorescent protein-VirD2 displayed nuclear local
200 degradation tag to Venus, a rapidly folding yellow fluorescent protein, we obtained both fluorescenc
201 ich the PKD2L1 promoter drives expression of yellow fluorescent protein, we previously reported that
202 (NLS) and either cyan fluorescent protein or yellow fluorescent protein, we show that each of the wil
203 etized transgenic mice expressing axoplasmic yellow fluorescent protein were stimulated electrically
205 tochondrial-surface associated BTPC-enhanced yellow fluorescent protein when both fusion proteins wer
206 onditionally expressed the reporter enhanced yellow fluorescent protein while concomitantly deleting
208 eonGreen is the brightest monomeric green or yellow fluorescent protein yet described to our knowledg
211 ytosis, mutagenesis of human DAT tagged with yellow fluorescent protein (YFP) and an extracellular HA
212 ed tight co-clustering between CD44 fused to yellow fluorescent protein (YFP) and CD44 fused to cyan
213 lasma membrane, as shown by imaging of CPK17-yellow fluorescent protein (YFP) and CPK34-YFP in growin
214 ction was measured by FRET between M(3)-AChR-yellow fluorescent protein (YFP) and cyan fluorescent pr
215 eled with green fluorescent protein (GFP) or yellow fluorescent protein (YFP) and expressed in human
216 ab27bN133I) forms of Rab27b were tagged with yellow fluorescent protein (YFP) and expressed in pariet
217 These were verified by AtCruA fusion to yellow fluorescent protein (YFP) and expression in devel
219 udy, using dual gamma interferon (IFN-gamma)-yellow fluorescent protein (YFP) and IL-10-green fluores
220 vector carrying an artificial exon encoding yellow fluorescent protein (YFP) and protein affinity ta
221 ntal brainstem slices of male and female SST-yellow fluorescent protein (YFP) and SST-channelrhodopsi
225 te phagosome formation, the distributions of yellow fluorescent protein (YFP) chimeras of enzymes and
226 , we show that a hybrid reaction centre (RC)/yellow fluorescent protein (YFP) complex accelerates pho
227 sleep expression beyond what T(a) warming in yellow fluorescent protein (YFP) control mice achieved.
228 f the UPS, such as the ubiquitin (Ub)-fusion yellow fluorescent protein (YFP) degradation substrate,
229 ged with either Renilla luciferase (RLuc) or yellow fluorescent protein (YFP) demonstrated saturable,
230 in the corneas of transgenic mice expressing yellow fluorescent protein (YFP) driven by the thy1 prom
232 Pdgfra-CreER(T2):Rosa26R-YFP mice to induce yellow fluorescent protein (YFP) expression in PDGFRA/NG
237 Here, we generated an HSV expressing a gD-yellow fluorescent protein (YFP) fusion and found that g
238 ng BdCSLF6, we demonstrate that a functional yellow fluorescent protein (YFP) fusion of BdCSLF6 is lo
239 n be complemented by re-expression of an Arg-yellow fluorescent protein (YFP) fusion, but not by an N
241 g phospho-mimic and nonphosphorylatable phyB-yellow fluorescent protein (YFP) fusions demonstrated th
242 protein (CFP)-tagged Fpn in conjunction with yellow fluorescent protein (YFP) fusions of Heph and APP
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
248 lices and filaments in Escherichia coli when yellow fluorescent protein (YFP) is fused to its N termi
251 coronal brain slices were prepared from thy1-yellow fluorescent protein (YFP) mice at postnatal day 3
252 genic mouse model of AD by crossing "H-line" yellow fluorescent protein (YFP) mice with the 5xFAD mou
254 Using an inducible nestin-CreER(T2)/R26R-yellow fluorescent protein (YFP) mouse, we investigated
255 individual cell types by placing the foreign yellow fluorescent protein (YFP) on their outer surface,
256 expressed cyan fluorescent protein (CFP) or yellow fluorescent protein (YFP) reporter genes under th
257 FP treatment of BM-pDC derived from IFN-beta yellow fluorescent protein (YFP) reporter mice (messenge
258 hy1-STOP-YFP mice have been reported to have yellow fluorescent protein (YFP) selectively expressed i
261 escribed for the site-specific attachment of yellow fluorescent protein (YFP) to glass surfaces on le
262 olarity is detected in this system, we fused yellow fluorescent protein (YFP) to the C terminus of th
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
267 f GalphaGPR in the intact cell when Galphai2 yellow fluorescent protein (YFP) was tethered to the car
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
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.
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
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
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