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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
18 The carcinoma cells express enhanced green fluorescent protein after internalization and cell viabi
20 ssing TBX18 (or the reporter construct green fluorescent protein) after AV node ablation, and observe
22 stinct variants of the Entacmaea quadricolor fluorescent protein-an opportunity to examine epistasis
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
32 e micrometric imaging of spectrally distinct fluorescent proteins and label-free nonlinear signals wi
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
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
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
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
52 al crosstalk between the opto-RTKs and green fluorescent protein-based biosensors enables simultaneou
55 tic screen in mammalian cells by combining a fluorescent protein-based MYC abundance sensor, CRISPR/C
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
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
70 ive experiments in yeast using 37 synonymous fluorescent proteins confirmed that an exogenous gene wi
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
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
87 gical studies, the enhanced green and yellow fluorescent proteins (EGFP and EYFP) were not specifical
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
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
102 a heterologous system, ELF3 fused with green fluorescent protein forms speckles within minutes in res
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
108 lar details down to the molecular level with fluorescent proteins (FPs) currently the main tool for z
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
119 s a diphtheria toxin receptor-enhanced green fluorescent protein fusion protein under the control of
121 chondrial echoforms using current GFP (Green Fluorescent Protein) fusion microscopy approaches is ext
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.
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
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
145 defect in laccase targeting of a Lac1-green fluorescent protein (GFP) fusion to the cell wall with t
147 , we utilized mouse lines that express green fluorescent protein (GFP) in cells that contain the 67 k
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
163 hich GABAergic SC interneurons express green fluorescent protein (GFP), few GFP-labeled cells (11%) r
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
173 Wild-type muscle fibers overexpressing green fluorescent protein (GFP)-tubb6 (but not GFP-tubb5) have
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
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
189 slices from mice expressing enhanced yellow fluorescent protein in MC3R neurons to test how alpha-MS
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
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.
203 efficiency for homo- and hetero-oligomers of fluorescent protein-labeled forms of EGFR and its paralo
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
208 uorescent dyes, such as labeling efficiency, fluorescent protein maturation, photostability, bleachin
210 (Tregs) in WT forkhead box P3 (Foxp3)-green fluorescent protein mice, few in either site became Treg
212 ial suspension of Vibrio cholerae, where the fluorescent protein (mKO; monomeric Kusabira Orange) and
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
227 dvantageous properties of primed convertible fluorescent proteins (pr-pcFPs) to simultaneously visual
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
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
242 esign highly efficient reversibly switchable fluorescent proteins (RSFPs) amenable to various nanosco
244 fluorescent protein expression pattern, the fluorescent protein's molecular ion could be used to ide
248 , but reliable imaging and quantification of fluorescent protein signals deep inside the tissues has
250 nsferrin receptor) coupled to a pH-sensitive fluorescent protein, such as superecliptic pHluorin (SEP
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
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
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
266 , transfected via TALEN constructs for green fluorescent protein, that mimic development of VF epithe
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
272 l new method that enables cells expressing a fluorescent protein to label their surrounding cells, fa
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
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
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
293 ere, we generated variants of enhanced green fluorescent protein with different COs using circular pe
296 fetime differences as a mean to discriminate fluorescent proteins with similar spectral properties an
298 ainstem slices of male and female SST-yellow fluorescent protein (YFP) and SST-channelrhodopsin 2 (Ch
300 Using a recombinant Nipah virus expressing a fluorescent protein (ZsG), we visualized virus tropism i