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1 utively active formin constructs tagged with fluorescent protein.
2 rect the separate expression of NSP3 and the fluorescent protein.
3 cetyl H3K9-specific scFv, tethered to a cyan fluorescent protein.
4 al subunit protein fused with enhanced green fluorescent protein.
5 coding enhanced firefly luciferase and green fluorescent protein.
6 e tumor niche) by transferring a liposoluble fluorescent protein.
7 and expressing another subunit tagged with a fluorescent protein.
8  ability to reliably visualize low-abundance fluorescent proteins.
9 RET assays and FRET imaging, especially with fluorescent proteins.
10 ratio of fluorescence intensities of the two fluorescent proteins.
11 ticidin resistance genes as well as mScarlet fluorescent proteins.
12 egans and Drosophila melanogaster expressing fluorescent proteins.
13 mited due to a lack of bright and stable red fluorescent proteins.
14 een Renilla luciferase8-tagged D2R and green fluorescent protein 2 (GFP2)-tagged K-Ras (plasma membra
15    The sensor is composed of yellow and blue fluorescent proteins, a phosphopeptide binding domain, a
16 gon promoter (700 bp) driving enhanced green fluorescent protein (AAV GCG-EGFP), to specifically iden
17 that overexpressed CRF (AAV2/5-CRF) or green fluorescent protein (AAV2/5-GFP).
18   The carcinoma cells express enhanced green fluorescent protein after internalization and cell viabi
19 nd iterative ExCel, which enables imaging of fluorescent proteins after 20x linear expansion.
20 ssing TBX18 (or the reporter construct green fluorescent protein) after AV node ablation, and observe
21       Based on the chromophore core of green fluorescent proteins, AggFluor is comprised of a series
22 stinct variants of the Entacmaea quadricolor fluorescent protein-an opportunity to examine epistasis
23                 The T-DNA also carried a red fluorescent protein and a hygromycin resistance (hptII)
24 f genetically-encoded proteins such as green fluorescent protein and externally added fluorogens that
25 put/output relation in the live fish using a fluorescent protein and find that different hair cells v
26 ent heterodimers labeled with enhanced green fluorescent protein and mApple to quantify the effects o
27 TCRalpha cells, we generated mice with green fluorescent protein and red fluorescent protein reporter
28 a recombinant HAZV expressing enhanced green fluorescent protein and used live-cell fluorescent imagi
29 fluorescent signals from bacteria expressing fluorescent proteins and demonstrate label-free readout
30 nce of crosstalk with a number of orange/red fluorescent proteins and dyes.
31               We compared four different red fluorescent proteins and found that mKate2 yields the hi
32 e micrometric imaging of spectrally distinct fluorescent proteins and label-free nonlinear signals wi
33 ited by the brightness and photostability of fluorescent proteins and rhodopsins.
34                                              Fluorescent proteins and silk proteins serve as edible p
35 onformational dynamics of phototransformable fluorescent proteins and their correlation with the obse
36 ccumulate variation in populations of yellow fluorescent proteins and then evolved these proteins tow
37 d DFHBI, a mimic of the chromophore in green fluorescent protein, and activate its fluorescence.
38 cted from HEK293T cell lines expressing blue fluorescent protein, and clinical samples of DNA with tw
39 nsitive to blue light used to activate green fluorescent protein, and thus, light exposure during bra
40 naptic compartments in adult C. elegans with fluorescent proteins, and isolated synaptic and somatic
41                                              Fluorescent proteins are a powerful experimental tool, a
42                                              Fluorescent proteins are limited in number, while DNA ba
43                                              Fluorescent proteins are used extensively in transgenic
44 ropy is a popular tool to study homo-FRET of fluorescent proteins as an indicator of dimerization, in
45 25, pUL17, and pUL36 fused with green or red fluorescent proteins as well as viruses with specific de
46 resolved amino-terminus and cerulean, a cyan fluorescent protein, as a tag at the carboxyl-terminus o
47 interaction was obtained using a split-green fluorescent protein assay.
48 y via in vitro experiments of enhanced green fluorescent protein at different buffer viscosities.
49  constructed a FRET probe composed of yellow fluorescent protein attached at the N-terminus of an ace
50           In contrast, an SSB variant with a fluorescent protein attached directly to the C-terminus
51 nces highly divergent from A. victoria green fluorescent protein (avGFP).
52 al crosstalk between the opto-RTKs and green fluorescent protein-based biosensors enables simultaneou
53  in imaging protein-protein interactions and fluorescent protein-based biosensors.
54  improved two-color calcium imaging with red fluorescent protein-based indicators.
55 tic screen in mammalian cells by combining a fluorescent protein-based MYC abundance sensor, CRISPR/C
56                                              Fluorescent protein-based pH sensors have gained widespr
57 the range of the current genetically encoded fluorescent protein-based sensors.
58 he response and brightness achieved by green fluorescent protein-based sensors.
59            In this study, we utilized a blue fluorescent protein (BFP) that converts to green fluores
60                                By developing fluorescent protein biosensing in intact seeds, we obser
61 eveloped beta-cell-selective virally-encoded fluorescent protein biosensors that can be rapidly and e
62 laterals are labeled by synaptophysin-tagged fluorescent proteins, but not PSD95, consistent with the
63 labeling technology to enhance the signal of fluorescent proteins by up to two orders of magnitude.
64  We show that supercharged variants of green fluorescent protein can assemble into a variety of archi
65                       Nucleic acid mimics of fluorescent proteins can be valuable tools to locate and
66 ased single and paired eGFP+ (enhanced green fluorescent protein)+ cardiomyocytes predominantly in th
67 (rAAV2) vectors encoding CIP fused with cyan-fluorescent-protein (CFP), with or without nuclear local
68 ed the electrostatic properties of the green fluorescent protein chromophore in a photoswitchable var
69           Using a photoswitchable rsFastLime fluorescent protein combined with a simple illumination
70 ive experiments in yeast using 37 synonymous fluorescent proteins confirmed that an exogenous gene wi
71                      The expression of green fluorescent protein-conjugated (PR)(50) (a 50-repeat PR
72                                A Cupid-Green Fluorescent Protein (Cupid-GFP) fusion protein was teste
73 sion of the luciferase NanoLuc to the orange fluorescent protein CyOFP, has emerged as a bright biolu
74 , the topology of the structural link to the fluorescent protein demonstrably affects the internal dy
75 in Gag and tagged at its C-terminus with the fluorescent protein Dendra2 have the same morphology and
76 able, and they expressed NSP3 and a separate fluorescent protein detectable by live cell imaging.
77 unctional energy transfer from a cytoplasmic fluorescent protein domain to the retinal chromophore bo
78  reporter strain of mice with enhanced green fluorescent protein driven by the endogenous promotor fo
79 differences in expression of enhanced yellow fluorescent protein driven from the tyrosine hydroxylase
80 orter 1 (MCT1) tagged with an enhanced green fluorescent protein (EGFP) at the N-terminal.
81 in a transgenic line in which enhanced green fluorescent protein (eGFP) is expressed under control of
82 tificial chromosome (BAC) and enhanced green fluorescent protein (eGFP) reporter mouse, combined with
83 p a reporter virus expressing enhanced green fluorescent protein (eGFP), which we then used to screen
84 aster S2 cells expressing the enhanced green fluorescent protein (EGFP)-tagged regulatory light chain
85 F mice) whose B-cells express enhanced green fluorescent protein (EGFP).
86 fetal-derived Cdx2 cells with enhanced green fluorescent protein (eGFP).
87 gical studies, the enhanced green and yellow fluorescent proteins (EGFP and EYFP) were not specifical
88                            Recent efforts in fluorescent protein engineering have succeeded in develo
89 an tumor suppressor, p53, fused to a far-red fluorescent protein, eqFP650.
90 oyed an ER-targeted, redox-responsive, green fluorescent protein-eroGFP-that reports on ambient chang
91 on @ 980/540 nm, green channel), and mOrange fluorescent protein (excitation/emission @ 548/566 nm, r
92 al axons can be simultaneously observed with fluorescent proteins expressed in a combinatorial manner
93  intracellular delivery of an enhanced green fluorescent protein-expressing plasmid to cells at a sca
94 ls from a panel of transgenic mice, in which fluorescent protein expression identifies cells at diffe
95 esized that, in MSI from mice with a defined fluorescent protein expression pattern, the fluorescent
96 oped for the purification of enhanced yellow fluorescent protein (EYFP) from mice.
97                                  Using green fluorescent protein-FKBP-MCAK CRISPR cells we found that
98 ally explored for plasmid DNA encoding green fluorescent protein following electroporation of 3T3 fib
99 ondrial turnover as analyzed by MitoTimer, a fluorescent protein for which the emission is regulated
100 ultiple green fluorescent protein (GFP)-like fluorescent proteins for their suitability.
101 w that both mCardinal and iRFP670 are useful fluorescent proteins for zebrafish expression.
102 a heterologous system, ELF3 fused with green fluorescent protein forms speckles within minutes in res
103                                    Cnidarian fluorescent protein (FP) derivatives such as GFP, mCherr
104  and characterized 9 previously undiscovered fluorescent protein (FP) homologs from Aequorea victoria
105 NS-1E cells expressing proinsulin fused to a fluorescent protein (FP) under basal culture conditions
106 itory rhodopsin, with mScarlet, a bright red fluorescent protein (FP).
107         Bright monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as protein
108 lar details down to the molecular level with fluorescent proteins (FPs) currently the main tool for z
109                Recently, near-infrared (NIR) fluorescent proteins (FPs) engineered from bacterial phy
110                          Genetically encoded fluorescent proteins (FPs) have been used for metal ion
111                                              Fluorescent proteins (FPs) have revolutionized cell biol
112  important fluorescent molecules in biology, fluorescent proteins (FPs), absorb and emit light are ge
113      Using two monomeric near-infrared (NIR) fluorescent proteins (FPs), we engineered an NIR Forster
114 ated target cell-killing, and monomeric teal fluorescent protein from the endogenous Gzmb locus.
115 al clone engineered to express two different fluorescent proteins from spliced and unspliced transcri
116 s and nucleosides, and when fused with a red fluorescent protein function as ratiometric indicators.
117 ter resonance energy transfer (FRET) between fluorescent proteins fused to the C-termini of LRRC8 sub
118             This assay monitors FRET between fluorescent proteins fused to the mutant ABD and the act
119 s a diphtheria toxin receptor-enhanced green fluorescent protein fusion protein under the control of
120                                        Using fluorescent protein fusion to cytosolic proteins with kn
121 chondrial echoforms using current GFP (Green Fluorescent Protein) fusion microscopy approaches is ext
122                                              Fluorescent protein fusions of BdXFUC1 localized to the
123                                        Using fluorescent protein fusions, we show that the Arabidopsi
124 d by intracellular localization studies with fluorescent protein fusions.
125 ging Nu1 and a 730-bp insertion of the green fluorescent protein gene downstream of enolase (23%).
126  which conditional expression of the ZsGreen fluorescent protein gene requires the presence of exogen
127 ed VSV-EBOV with no MLD that expressed green fluorescent protein (GFP) (VSV-EBOVDeltaMLD-GFP), VSV-EB
128 ) fixation in individual nodules using green fluorescent protein (GFP) and barcode strain identificat
129  inhibitory peptide [AIP], is fused to green fluorescent protein (GFP) and expressed from a cardiomyo
130     Fluorescence proteins, such as the green fluorescent protein (GFP) and its derivatives, are coexp
131 ecreted alkaline phosphatase (SEAP) or green fluorescent protein (GFP) and subjected to shear stress.
132                            Here we use green fluorescent protein (GFP) as a model cargo to compare de
133  G proteins, and Axin reduced gammaTub-green fluorescent protein (GFP) at branch points, and two func
134     Herein, we report two photostable, green fluorescent protein (GFP) based indicators, ZIBG1 and ZI
135 ells engineered to contain an inverted green fluorescent protein (GFP) cassette flanked by recombinat
136 isomerization in molecules such as the green fluorescent protein (GFP) chromophore can occur either v
137          The neutral or A state of the green fluorescent protein (GFP) chromophore is a remarkable ex
138                  A structurally locked green fluorescent protein (GFP) chromophore with a phenyl grou
139 ally encoded dopamine sensors based on green fluorescent protein (GFP) enable high-resolution imaging
140 y and gene delivery efficacy using the green fluorescent protein (GFP) encoded DNA plasmid (pGFP) as
141 ter cells, as assessed by retention of green fluorescent protein (GFP) expression from a replication-
142  and sgRNA using BAMEA-O16B knocks out green fluorescent protein (GFP) expression of human embryonic
143                                        Green fluorescent protein (GFP) fusion constructs with the por
144 ve transcription unit and expressing a green fluorescent protein (GFP) fusion of ER.
145  defect in laccase targeting of a Lac1-green fluorescent protein (GFP) fusion to the cell wall with t
146      Among these FPs are the brightest green fluorescent protein (GFP) homolog yet characterized and
147 , we utilized mouse lines that express green fluorescent protein (GFP) in cells that contain the 67 k
148                         Regarding TuMV-green fluorescent protein (GFP) infection, bZIP60 and bZIP28 s
149         The fluorescence emission from green fluorescent protein (GFP) is known to be heavily influen
150                               We use a green fluorescent protein (GFP) mapping strategy to identify t
151                Using a validated CRFR1-green fluorescent protein (GFP) reporter mouse, our laboratory
152  in both KO cell lines by a PR8 (H1N1) green fluorescent protein (GFP) reporter virus.
153 tent HIV provirus encoding an enhanced green fluorescent protein (GFP) reporter, into irradiated adul
154 ification of variant-positive cells by green fluorescent protein (GFP) staining in chimeric Proteus s
155 luorescence intensities of recombinant green fluorescent protein (GFP) standards (ranging from 1.5-25
156 sive promoter of sdsA1 gene along with Green Fluorescent Protein (GFP) to construct a novel SDS biose
157 fic, high-affinity RNA aptamer against Green Fluorescent Protein (GFP) to identify interactors of a G
158 ter generating a strain that expresses green fluorescent protein (GFP) under an interferon-stimulated
159 tablished a T. cruzi strain expressing green fluorescent protein (GFP) under the control of dihydrofo
160 rescent protein (BFP) that converts to green fluorescent protein (GFP) upon a C-to-T substitution as
161 joining wild type (WT) mice expressing green fluorescent protein (GFP) with mdx mice.
162         We show that an inert protein, green fluorescent protein (GFP), can form a detectable diffusi
163 hich GABAergic SC interneurons express green fluorescent protein (GFP), few GFP-labeled cells (11%) r
164                            We selected green fluorescent protein (GFP), siderocalin (Scn), and retino
165 of 3CL(pro) Our reporter is based on a green fluorescent protein (GFP)-derived protein that fluoresce
166 ts with mCherry-labeled capsids and/or green fluorescent protein (GFP)-labeled envelopes and infected
167 e first engineered and tested multiple green fluorescent protein (GFP)-like fluorescent proteins for
168 ese colors derive from photoprotective green fluorescent protein (GFP)-like pigments produced by the
169  treatment led to rapid disassembly of green fluorescent protein (GFP)-MxA structures; FRAP revealed
170 assessed for nGD using wild-type mouse green fluorescent protein (GFP)-positive multipotent induced p
171 redox) conditions impact the fate of a Green fluorescent protein (Gfp)-tagged AR plasmid (pRP4-gfp) w
172                                        Green fluorescent protein (GFP)-tagging is the prevalent strat
173 Wild-type muscle fibers overexpressing green fluorescent protein (GFP)-tubb6 (but not GFP-tubb5) have
174 nfocal laser scanning microscopy using green fluorescent protein (GFP).
175 in of interest is genetically fused to green fluorescent protein (GFP).
176 y 12 copies of a small 26 kDa protein, green fluorescent protein (GFP).
177 reporter gene used in the study is the green fluorescent protein (GFP).
178 FST1) at the plasmalemma when fused to green fluorescent protein (GFP).
179                                        Green fluorescent proteins (GFPs) have become indispensable im
180                              For split green fluorescent proteins (GFPs), fragment reassembly leads t
181 d female GFP-M line (n = 24) and male yellow fluorescent protein-H line (n = 5) mice undergoing RT in
182 ent stem cell (iPSC) reporter lines in which fluorescent proteins have been introduced into the PAX7
183  conventional metabolite sensors composed of fluorescent proteins have been made to detect some metab
184                                              Fluorescent proteins have revolutionized biomedical rese
185 Cubes' that are similar in size to the green fluorescent protein, have single-point attachment to pro
186 n human cells, we developed mGreenLantern, a fluorescent protein having up to sixfold greater brightn
187 tagged at its N terminus with enhanced green fluorescent protein; (ii) mutations D63A and Y248A, bloc
188 ed transgenes expressing different colors of fluorescent protein in Arabidopsis pollen tetrads.
189  slices from mice expressing enhanced yellow fluorescent protein in MC3R neurons to test how alpha-MS
190 to obtain Chx10-Cre;Ai9 mice, expressing red fluorescent protein in retinal Cre-positive cells.
191 xygen for the maturation of oxygen-requiring fluorescent proteins in Bacteroides species.
192  photoconversion and photobleaching rates of fluorescent proteins in cells.
193 e difficulties of expressing measurements of fluorescent proteins in numbers of molecules.
194  systems, and readout of multiple orthogonal fluorescent proteins in situ.
195 S5S (short) was studied by tagging them with fluorescent proteins in their cytosolic loops.
196 cable and suggests that greater potential of fluorescent proteins, including biosensors, could be unl
197 sing LLT and SLT transcript leaders to green fluorescent protein indicated that for five genes, the s
198 e-mutation trajectories between the parental fluorescent proteins, informative about the protein's ev
199 signaling targets, biosensor components, and fluorescent proteins involved.
200 show that stable expression of near-infrared fluorescent protein (iRFP) in patient-derived glioblasto
201 sgenic mouse line in which the expression of fluorescent protein is driven by the galanin promoter.
202 c mouse expressing the mitochondria-targeted fluorescent protein Keima (mt-Keima).
203 efficiency for homo- and hetero-oligomers of fluorescent protein-labeled forms of EGFR and its paralo
204                 A fusion of COX19 to the red fluorescent protein localized to mitochondria in vivo, s
205 ansgenic mouse, in which expression of a red fluorescent protein (mApple) is driven by the GLP-1R pro
206 uorophores that are compatible with standard fluorescent protein markers and applicable to cells, tis
207 ni-white(+) or polyubiquitin-regulated DsRed fluorescent protein markers.
208 uorescent dyes, such as labeling efficiency, fluorescent protein maturation, photostability, bleachin
209                      We directly compare our fluorescent protein measurement with the commonly used m
210  (Tregs) in WT forkhead box P3 (Foxp3)-green fluorescent protein mice, few in either site became Treg
211  suppressor activity in DAF(-/-) Foxp3-green fluorescent protein mice.
212 ial suspension of Vibrio cholerae, where the fluorescent protein (mKO; monomeric Kusabira Orange) and
213 P, SNAP-tag, HaloTag or the photoconvertible fluorescent protein mMaple.
214 gonal chemistry, and optogenetics, we tether fluorescent proteins, model enzymes, and growth factors
215 lasmic MuSK effector protein) fused to green fluorescent protein (MuSK-GFP and rapsyn-GFP, respective
216  binding protein with either an endogenously fluorescent protein or a synthetic fluorophore as the in
217 ked whether arbitrary molecules (e.g., green fluorescent protein or mCherry) could be converted into
218 rthermore, the nature and properties of used fluorescent proteins or fluorescent dyes, such as labeli
219 rters of enzyme activity are based on either fluorescent proteins or small molecules.
220                Green-to-red photoconvertible fluorescent proteins (PCFPs) are key players in advanced
221                             Photoconvertible fluorescent proteins (PCFPs) are widely used in super-re
222                              Photoswitchable fluorescent proteins (PFPs) that can change fluorescence
223                   Collagen1alpha1-GFP (green fluorescent protein)-positive CFs were characterized aft
224  transplanted with transgenic enhanced green fluorescent protein-positive BM.
225                                        Green-fluorescent protein-positive hypnozoites turned red-fluo
226                                        Green fluorescent protein-positive prostate carcinoma cells in
227 dvantageous properties of primed convertible fluorescent proteins (pr-pcFPs) to simultaneously visual
228                                        Green fluorescent protein, previously expressed in vitro with
229 coexpression of a second, distinctly colored fluorescent protein provides a soluble reference species
230 ic lattice at ambient conditions: We utilize fluorescent proteins providing ultra-stable Frenkel exci
231  lungs of prospero homeobox 1-enhanced green fluorescent protein (Prox1-EGFP) transgenic mice with te
232 eporter mice (a knockin allele with tdTomato fluorescent protein regulated by the endogenous p16Ink4a
233 ecular mechanisms for the photoconversion of fluorescent proteins remain elusive owing to the challen
234 mammals, a hu.32 vector expressing the green fluorescent protein reporter gene was evaluated in the c
235  mice with green fluorescent protein and red fluorescent protein reporters linked to TCRalpha, reveal
236 enomic imaging systems predominantly rely on fluorescent protein reporters, which lack the optical pr
237 psin domains and various fluorescent dye and fluorescent protein reporters.
238 ever, determining the lifetimes of different fluorescent proteins requires the detection of a relativ
239   Including a custom-tailored NMR toolbox in fluorescent protein research provides new opportunities
240 of a recombinant HSV-1 that encodes a yellow-fluorescent-protein (rHSV48Y; MOI = 1).
241        ExCel enables simultaneous readout of fluorescent proteins, RNA, DNA location, and anatomical
242 esign highly efficient reversibly switchable fluorescent proteins (RSFPs) amenable to various nanosco
243                        Reversibly switchable fluorescent proteins (RSFPs) serve as markers in advance
244  fluorescent protein expression pattern, the fluorescent protein's molecular ion could be used to ide
245 neural activity to different properties of a fluorescent protein scaffold.
246                         Calcium imaging with fluorescent protein sensors is widely used to record act
247 fused to the C-terminus of superfolder green fluorescent protein (sfGFP).
248 , but reliable imaging and quantification of fluorescent protein signals deep inside the tissues has
249              SL4-cancer cells expressing red fluorescent protein (SL4-RFP) (1 x 10(6)) were injected
250 nsferrin receptor) coupled to a pH-sensitive fluorescent protein, such as superecliptic pHluorin (SEP
251                   Multicolor combinations of fluorescent proteins, such as Brainbow, have expanded th
252 rturbed color vision caused by intrinsic red-fluorescent protein, suggesting that color vision may no
253 bacteria have been hindered by the lack of a fluorescent protein system to track and visualize protei
254 d thermostabilities of detergent-solubilized fluorescent protein-tagged CLR.RAMP complexes expressed
255  striatum of female and male mice with green fluorescent protein-tagged D1 or D2.
256 atory studies using endogenous expression of fluorescent protein-tagged genes.
257 i to intact animals and large, immobile, and fluorescent protein-tagged mitochondria as fiducial mark
258 perature-dependent photobody localization of fluorescent protein-tagged phyB (phyB-FP) in the epiderm
259   To address these limitations, we developed fluorescent-protein-tagged actin nanobodies, termed 'act
260 (histone or tubulin) proteins were marked by fluorescent protein-tagging.
261 hysical characteristics of the coral-derived fluorescent protein TagRFP-T.
262                         Using photopatterned fluorescent protein targets and a single-cell immunoassa
263 rker engineered from a reversibly switchable fluorescent protein that enables spatiotemporally precis
264 oteins of rOCT1 and rOCT1 mutants with green fluorescent protein that had been reconstituted into nan
265 e expressing alpha-smooth muscle actin-green fluorescent protein that labels MECs.
266 , transfected via TALEN constructs for green fluorescent protein, that mimic development of VF epithe
267            Based on engineered AMPK fused to fluorescent proteins, the sensor allows direct, real-tim
268                                 Transport of fluorescent proteins through single pores is kinetically
269  its class I Q344ter mutant fused to Dendra2 fluorescent protein to characterize a novel light-indepe
270 vability, we subjected populations of yellow fluorescent protein to directed evolution under differen
271 ession of channelrhodopsin 2-enhanced yellow fluorescent protein to GAD1(+) GABAergic neurons.
272 l new method that enables cells expressing a fluorescent protein to label their surrounding cells, fa
273  monomers functionalized with a mutant green fluorescent protein to prepare protein oligomers.
274 rter mice in which glial cells express DsRed fluorescent protein to study the cellular constituents o
275 y unexploited class of reversibly switchable fluorescent proteins to engineer a new type of calcium s
276  photophysical dark state populations within fluorescent proteins to modulate and selectively detect
277 g the ribosome to restrict the expression of fluorescent proteins to the neuronal soma.
278 etic screen based on a virus-inducible green fluorescent protein transcriptional reporter to identify
279 G-baToN) which relies upon nanobody-directed fluorescent protein transfer to enable sensitive and spe
280  targeting messenger RNAs (mRNAs) of a green fluorescent protein transgene, and CD46, CD55 and CD71 c
281  as well as a derivative encoding tomato red fluorescent protein (tRFP) in place of ORF3.
282 dometrial stromal cell line that uses yellow fluorescent protein under the control of the prolactin p
283 roblasts were labeled postnatally with green fluorescent protein using mice expressing a tamoxifen-de
284 d of photoconvertible probes is dominated by fluorescent protein variants, which can introduce pertur
285 the VHA B subunit tagged with enhanced green fluorescent protein (VHA(B) -eGFP) enabled subcellular p
286 the Glbs tagged at the C-terminus with green fluorescent protein was used to determine their subcellu
287 23-339) was expressed as a fusion with green fluorescent protein, we found that we were able to elici
288 th additional promoters and the use of other fluorescent proteins, we aim to contribute towards enhan
289 9 editing to endogenously tag receptors with fluorescent proteins, we demonstrate that the method del
290 toring anisotropy changes in photoswitchable fluorescent proteins while photoswitching to the off sta
291 ration of recombinant rotaviruses expressing fluorescent proteins will be valuable for the study of r
292        Now, we have the first structure of a fluorescent protein with a successfully matured chromoph
293 ere, we generated variants of enhanced green fluorescent protein with different COs using circular pe
294           A tFT is a fusion of two different fluorescent proteins with distinct fluorophore maturatio
295                          The availability of fluorescent proteins with distinct phototransformation p
296 fetime differences as a mean to discriminate fluorescent proteins with similar spectral properties an
297                      Both 25/26KT Gag-yellow fluorescent protein (YFP) and 29/31KT Gag-YFP bound nons
298 ainstem slices of male and female SST-yellow fluorescent protein (YFP) and SST-channelrhodopsin 2 (Ch
299                     The expression of Yellow Fluorescent Protein (YFP) in these animals is restricted
300 Using a recombinant Nipah virus expressing a fluorescent protein (ZsG), we visualized virus tropism i

 
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