ライフサイエンスコーパス: fluorescence resonance energy transfer

1 ion between the proteins was confirmed using fluorescence resonance energy transfer.

2 es based on spectrally resolved, multiphoton fluorescence resonance energy transfer.

3 e cell-penetrating peptide and disruption of fluorescence resonance energy transfer.

4 between 40 and 200 bp using single-molecule Fluorescence Resonance Energy Transfer.

5 terized by gel-permeation chromatography and fluorescence resonance energy transfer.

6 y that is based on real-time measurements of fluorescence resonance energy transfer.

7 red EF-hand motif using transition-metal ion fluorescence resonance energy transfer.

8 Mammalian two-hybrid and fluorescence resonance energy transfer analyses confirme

9 ins using a co-immunoprecipitation assay and fluorescence resonance energy transfer analysis.

10 ion was confirmed in cancer cells in vivo by fluorescence resonance energy transfer analysis.

11 In this study, we use time-resolved fluorescence resonance energy transfer and a, to our kno

12 Moreover, single-molecule fluorescence resonance energy transfer and bulk biochemi

13 ed these mutants in cells with time-resolved fluorescence resonance energy transfer and death assays,

14 stin-3 receptor complexes in real time using fluorescence resonance energy transfer and fluorescence

15 Currently, biophysical methods like Fluorescence Resonance Energy Transfer and Fluorescence

16 Fluorescence resonance energy transfer and functionalize

17 uestioned the previous interpretation of the fluorescence resonance energy transfer and isothermal ti

18 n permeabilized cells, using single-molecule fluorescence resonance energy transfer and particle trac

19 mall-angle X-ray scattering, single-molecule fluorescence resonance energy transfer, and NMR) indicat

20 Additionally, using partition functions in a fluorescence resonance energy transfer approach, we foun

21 B1 sensors to monitor activation kinetics by fluorescence resonance energy transfer, Arg-389-ADRB1 ex

22 than 132 candidate protein complexes using a fluorescence resonance energy transfer assay confirmed t

23 Using a fluorescence resonance energy transfer assay in model me

24 l and atypical APDs in a novel time-resolved fluorescence resonance energy transfer assay, and correl

25 Using a fluorescence resonance energy transfer assay, we demonst

26 Using a cell-based fluorescence resonance energy transfer assay, we show th

27 FL-vinblastine-based human PXR time-resolved fluorescence resonance energy transfer assay, which was

28 ion between SHP2 and c-SRC was revealed by a fluorescence resonance energy transfer assay.

29 at, we developed a homogeneous time-resolved fluorescence resonance energy transfer assay.

30 (Sso) was investigated using presteady-state fluorescence resonance energy transfer assays coupled wi

31 Fluorescence resonance energy transfer assays showed tha

32 g yeast two-hybrid, pull-down, and in planta fluorescence resonance energy transfer assays, we conclu

33 e this issue using two novel and independent fluorescence resonance energy transfer assays.

34 he nTreg in a cognate fashion in Forster (or fluorescence) resonance energy transfer assays, and thes

35 hanges in protein and/or RNA components, and fluorescence resonance energy transfer-based assays demo

36 Immunoblotting, radioenzymatic- and fluorescence resonance energy transfer-based assays, vid

37 Cellular imaging experiments using fluorescence resonance energy transfer-based biosensors

38 PKD (wildtype or mutant S427E) and targeted fluorescence resonance energy transfer-based biosensors

39 To examine these, we used a set of fluorescence resonance energy transfer-based biosensors

40 Using transgenic mice expressing the fluorescence resonance energy transfer-based cGMP biosen

41 Novel fluorescence resonance energy transfer-based genetically

42 lexa488 to enable, to our knowledge, a novel fluorescence resonance energy transfer-based measurement

43 3G hotspots are defined, we used an in vitro fluorescence resonance energy transfer-based oligonucleo

44 ty of recombinant NSP4, we used an iterative fluorescence resonance energy transfer-based optimizatio

45 ty was examined in real-time mitosis using a fluorescence resonance energy transfer-based reporter an

46 Fluorescence resonance energy transfer-based reporters h

47 Here, using a fluorescence resonance energy transfer-based sensor for

48 ate (FLIPPi) sensors are genetically encoded fluorescence resonance energy transfer-based sensors tha

49 postmortem AD brain and added to a sensitive fluorescence resonance energy transfer-based tau uptake

50 rces across the LINC complex, we generated a fluorescence resonance energy transfer-based tension bio

51 eviously demonstrated that the efficiency of fluorescence resonance energy transfer between cyanine 3

52 hod to image molecular proximity in terms of fluorescence resonance energy transfer between donor and

53 Binding of aptamers to GO-nS guarantees the fluorescence resonance energy transfer between fluoropho

54 For the first time, we show time-resolved fluorescence resonance energy transfer between receptor

55 , alpha-SNAP depletion significantly reduces fluorescence resonance energy transfer between Stim1 and

56 etitor from the binding protein and disrupts fluorescence resonance energy transfer between the two f

57 leaching, and to a lesser extent Forster (or fluorescence) resonance energy transfer between the labe

58 staining procedure to the chromosome, FRET (fluorescence resonance energy transfer) between G-quadru

59 combination of functional, radioligand, and fluorescence resonance energy transfer binding experimen

60 Using a fluorescence resonance energy transfer biosensor in comb

61 ts in endothelial microdomains using a novel fluorescence resonance energy transfer biosensor reveale

62 ion, AC141 and VP39 were previously shown by fluorescence resonance energy transfer by fluorescence l

63 ptide, and C-type natriuretic peptide evoked fluorescence resonance energy transfer changes correspon

64 The single molecule fluorescence resonance energy transfer data show that th

65 ophores is critical to the interpretation of fluorescence resonance energy transfer data.

66 on C16 of hVELC, we performed time-resolved fluorescence resonance energy transfer, directly detecti

67 liposome-polymer hybrid NPs, as evidenced by fluorescence resonance energy transfer, dynamic light sc

68 ooth muscle cells as evidenced by changes in fluorescence resonance energy transfer efficiency of an

69 Here we performed single molecule fluorescence resonance energy transfer experiments and u

70 ent, double electron-electron resonance, and fluorescence resonance energy transfer experiments appli

71 Gel electrophoresis and single-molecule fluorescence resonance energy transfer experiments have

72 contaminating ADP is a confounding factor in fluorescence resonance energy transfer experiments measu

73 Recent fluorescence resonance energy transfer experiments revea

74 ar dynamics simulations with single-molecule fluorescence resonance energy transfer experiments to ex

75 We used transition metal ion fluorescence resonance energy transfer experiments to mo

76 zation of the receptors, sensitized emission fluorescence resonance energy transfer experiments were

77 extensively used as donor-acceptor pairs in fluorescence resonance energy transfer experiments, espe

78 ng, respectively, in good agreement with the fluorescence resonance energy transfer experiments.

79 Here we show, using multisite fluorescence resonance energy transfer, far-UV CD, and k

80 A fluorescence lifetime imaging microscopy-fluorescence resonance energy transfer (FLIM-FRET) Src b

81 Fluorescence resonance energy transfer-fluorescence life

82 Yeast two-hybrid, coimmunoprecipitation, and fluorescence resonance energy transfer-fluorescence life

83 nd 14-3-3a was confirmed in planta using the fluorescence resonance energy transfer-fluorescence life

84 Mechanistically, fluorescence-resonance energy transfer-fluorescence-life

85 Here, using a fluorescence resonance energy transfer/fluorescence life

86 superresolution imaging and is an excellent fluorescence resonance energy transfer (FRET) acceptor f

87 Fluorescence resonance energy transfer (FRET) analyses e

88 surface was seen by confocal microscopy and fluorescence resonance energy transfer (FRET) analysis a

89 By combining fluorescence resonance energy transfer (FRET) and chemil

90 Using fluorescence resonance energy transfer (FRET) and coimmu

91 interactions among the HAS isoenzymes using fluorescence resonance energy transfer (FRET) and flow c

92 In the present study, we used fluorescence resonance energy transfer (FRET) and fluore

93 tructure of the 12RSS in the SC and PC using fluorescence resonance energy transfer (FRET) and molecu

94 Using fluorescence resonance energy transfer (FRET) and novel

95 ecular tension probes are primarily based on fluorescence resonance energy transfer (FRET) and report

96 Single molecule fluorescence resonance energy transfer (FRET) and small-

97 Fluorescence resonance energy transfer (FRET) apta-immun

98 Genetically encoded sensors based on fluorescence resonance energy transfer (FRET) are powerf

99 nt improvement in comparison to an analogous fluorescence resonance energy transfer (FRET) assay base

100 Here we used site-specific fluorescence resonance energy transfer (FRET) assay to i

101 ave developed a primosomal protein-dependent fluorescence resonance energy transfer (FRET) assay usin

102 Using an acceptor photobleaching fluorescence resonance energy transfer (FRET) assay, we

103 experimentally for inhibitory activity using fluorescence resonance energy transfer (FRET) assays aga

104 Using coimmunoprecipitation and fluorescence resonance energy transfer (FRET) assays, we

105 f bacterial enzymes using a highly sensitive Fluorescence Resonance Energy Transfer (FRET) based assa

106 rotein based biosensing system employing the Fluorescence Resonance Energy Transfer (FRET) between a

107 igned for the analysis of adenosine based on fluorescence resonance energy transfer (FRET) between Cd

108 antigen Troponin I (cTnI) in blood based on fluorescence resonance energy transfer (FRET) between co

109 Fluorescence resonance energy transfer (FRET) between fl

110 We measured intramolecular fluorescence resonance energy transfer (FRET) between fl

111 -induced conformational dynamics we measured fluorescence resonance energy transfer (FRET) between fl

112 We used fluorescence resonance energy transfer (FRET) between ge

113 doxorubicin (DOX, an antileukemic agent) via fluorescence resonance energy transfer (FRET) between PE

114 ids) and content mixing (from development of fluorescence resonance energy transfer (FRET) between ph

115 Using a fluorescence resonance energy transfer (FRET) biosensor,

116 pared with a 10% increase with an equivalent fluorescence resonance energy transfer (FRET) biosensor.

117 anosensors allowed in vitro determination of fluorescence resonance energy transfer (FRET) changes in

118 In the framework of this algorithm, absolute fluorescence resonance energy transfer (FRET) efficiency

119 Fluorescence resonance energy transfer (FRET) enables ph

120 Based on dose-response curves from in vivo fluorescence resonance energy transfer (FRET) experiment

121 r Aura virus capsid protease (AVCP) based on fluorescence resonance energy transfer (FRET) for screen

122 ed and synthesized novel substrates based on Fluorescence Resonance Energy Transfer (FRET) for the MP

123 contact between QDs and Zn(2+) but affording fluorescence resonance energy transfer (FRET) from dual-

124 We quantified fluorescence resonance energy transfer (FRET) from GFP t

125 LB C-terminal residues significantly altered fluorescence resonance energy transfer (FRET) from PLB t

126 this study, a novel sensing system based on fluorescence resonance energy transfer (FRET) from quant

127 red peroxide cleavage leads to a decrease in fluorescence resonance energy transfer (FRET) from the f

128 ensor enables the energy transfer based on a fluorescence resonance energy transfer (FRET) from the Q

129 olor from green to orange via intramolecular fluorescence resonance energy transfer (FRET) from the Z

130 llergen Lup an 1 (beta-conglutin) exploiting fluorescence resonance energy transfer (FRET) has been d

131 Fluorescence resonance energy transfer (FRET) in combina

132 measurements of conformational changes using fluorescence resonance energy transfer (FRET) in live ce

133 Fluorescence resonance energy transfer (FRET) is a power

134 sonance (EPR) membrane docking geometry, and fluorescence resonance energy transfer (FRET) kinetic st

135 of the type 1 ryanodine receptor (RyR1) and fluorescence resonance energy transfer (FRET) measuremen

136 Fluorescence resonance energy transfer (FRET) melting st

137 Additionally, by the fluorescence resonance energy transfer (FRET) method, we

138 have employed both bulk and single-molecule fluorescence resonance energy transfer (FRET) methods to

139 protocol describes procedures for performing fluorescence resonance energy transfer (FRET) microscopy

140 anges in SNAP25 by total internal reflection fluorescence resonance energy transfer (FRET) microscopy

141 the developed quantum dots-based (QDs-based) fluorescence resonance energy transfer (FRET) nanosensor

142 We describe a red-shifted fluorescence resonance energy transfer (FRET) pair optim

143 Using fluorescence resonance energy transfer (FRET) peptides r

144 release, using our Syx-based intramolecular fluorescence resonance energy transfer (FRET) probe, whi

145 developed to detect glucose in tear by using fluorescence resonance energy transfer (FRET) quenching

146 photoinduced electron transfer (PET)-coupled fluorescence resonance energy transfer (FRET) response.

147 Fluorescence resonance energy transfer (FRET) revealed t

148 Here, we describe a novel fluorescence resonance energy transfer (FRET) sensor tha

149 Genetically-encoded fluorescence resonance energy transfer (FRET) sensors re

150 eptors with PP2C-type phosphatases to send a fluorescence resonance energy transfer (FRET) signal in

151 report receptor activation by changes in the fluorescence resonance energy transfer (FRET) signal.

152 By measuring of fluorescence resonance energy transfer (FRET) signals be

153 We used single-molecule fluorescence resonance energy transfer (FRET) spectrosco

154 ptic vesicle-bilayer junction, combined with fluorescence resonance energy transfer (FRET) spectrosco

155 Here, we used fluorescence resonance energy transfer (FRET) spectrosco

156 Fluorescence Resonance Energy Transfer (FRET) spectrosco

157 Immunoprecipitation and fluorescence resonance energy transfer (FRET) studies sh

158 re, we show using chemical cross-linking and fluorescence resonance energy transfer (FRET) that alpha

159 Here we describe sensors that use fluorescence resonance energy transfer (FRET) to combine

160 Here we have used fluorescence resonance energy transfer (FRET) to demonst

161 Here, we combined zero-mode waveguides with fluorescence resonance energy transfer (FRET) to directl

162 Here we use single-molecule fluorescence resonance energy transfer (FRET) to observe

163 anophotonic zero-mode waveguides (ZMWs) with fluorescence resonance energy transfer (FRET) to resolve

164 Fluorescence resonance energy transfer (FRET) was also o

165 Two-step coimmunoprecipitation (co-IP) and fluorescence resonance energy transfer (FRET) were used

166 Here fluorescence resonance energy transfer (FRET) with new L

167 al pulldown assays, fluorescence microscopy, fluorescence resonance energy transfer (FRET), and fluor

168 transient kinetics, nanosecond time-resolved fluorescence resonance energy transfer (FRET), and kinet

169 chosen as the appropriate model receptor of fluorescence resonance energy transfer (FRET), and loade

170 nitored at the single-molecule (SM) level by fluorescence resonance energy transfer (FRET), one elect

171 nels, we developed an approach that combines fluorescence resonance energy transfer (FRET), simulated

172 egrative structure modeling based on in vivo fluorescence resonance energy transfer (FRET), small-ang

173 Here we show, using single-molecule fluorescence resonance energy transfer (FRET), that homo

174 Also, by using fluorescence resonance energy transfer (FRET), we demons

175 e developed a novel PDGFR biosensor based on fluorescence resonance energy transfer (FRET), which can

176 o DNA bending by HMGB1 using single-molecule fluorescence resonance energy transfer (FRET), which ena

177 In this study, using a fluorescence resonance energy transfer (FRET)-based acti

178 the development and optimization of a novel fluorescence resonance energy transfer (FRET)-based add-

179 Studies with a fluorescence resonance energy transfer (FRET)-based alph

180 ce, proteomics, qRT-PCR, immunofluorescence, fluorescence resonance energy transfer (FRET)-based and

181 and in living human cells, using a series of fluorescence resonance energy transfer (FRET)-based beta

182 Here, we employed fluorescence resonance energy transfer (FRET)-based bios

183 Therefore, we targeted fluorescence resonance energy transfer (FRET)-based bios

184 Here we describe a series of fluorescence resonance energy transfer (FRET)-based calc

185 etween maltose and glucose and over existing fluorescence resonance energy transfer (FRET)-based dete

186 We have developed a fluorescence resonance energy transfer (FRET)-based heav

187 Here we constructed a fluorescence resonance energy transfer (FRET)-based prob

188 and green fluorescent protein (GFP) create a fluorescence resonance energy transfer (FRET)-based rati

189 we develop two separate genetically encoded fluorescence resonance energy transfer (FRET)-based sens

190 Here we present a fluorescence resonance energy transfer (FRET)-based sens

191 While fluorescence resonance energy transfer (FRET)-based sens

192 This protocol describes our fluorescence resonance energy transfer (FRET)-based sing

193 By fluorescence resonance energy transfer (FRET)-based spec

194 insight into nucleotide selection, we use a fluorescence resonance energy transfer (FRET)-based syst

195 d for one-step pan-IAV reverse-transcription fluorescence resonance energy transfer (FRET)-PCR.

196 d alpha-catenin conformation sensor based on fluorescence resonance energy transfer (FRET).

197 f the drug and of the polymer backbone using fluorescence resonance energy transfer (FRET).

198 immobilized quantum dots (QDs) as donors in fluorescence resonance energy transfer (FRET).

199 ), intrinsic 2-aminopurine fluorescence, and fluorescence resonance energy transfer (FRET).

200 e-targeted Src biosensor (Kras-Src) based on fluorescence resonance energy transfer (FRET).

201 immobilized quantum dots (QDs) as donors in fluorescence resonance energy transfer (FRET).

202 immobilized quantum dots (QDs) as donors in fluorescence resonance energy transfer (FRET).

203 lotillin organization in human T-cells using fluorescence resonance energy transfer (FRET).

204 properties and are well suited as donors in fluorescence resonance energy transfer (FRET).

205 quenched by gold nanoparticles (Au NPs) via fluorescence resonance energy transfer (FRET).

206 eadout in our sensor was monitored by either fluorescence resonance energy transfer (FRET, switch-on)

207 Moreover, the Forster (or fluorescence) resonance energy transfer (FRET) between t

208 [Ca(2+)] changes in real-time using Forster (Fluorescence) resonance energy transfer (FRET).

209 yacrylamide gel electrophoresis, after which fluorescence-resonance energy transfer (FRET) reports on

210 ion of DNA sequences related to HIV based on fluorescence resonance energy transfer(FRET) between car

211 e absence of SERCA but also by time-resolved fluorescence resonance energy transfer from SERCA to PLB

212 se X-ray crystallography and single-molecule fluorescence resonance energy transfer imaging to elucid

213 Here, we used single-molecule fluorescence resonance energy transfer imaging to probe

214 Here, using single-molecule fluorescence resonance energy transfer imaging, we exami

215 Using various approaches, including fluorescence resonance energy transfer imaging, we found

216 Finally, using fluorescence resonance energy transfer imaging, we found

217 tivated localization microscopy imaging, and fluorescence resonance energy transfer imaging.

218 me distance distributions from time-resolved fluorescence resonance energy transfer in bimane-labeled

219 Using fluorescence resonance energy transfer in permeabilized

220 hymena group I ribozyme, via single-molecule fluorescence resonance energy transfer in solutions with

221 The proximity of TRPV4 tails, analyzed by fluorescence resonance energy transfer, increased by dep

222 Distance constraints derived by fluorescence resonance energy transfer independently ver

223 We also examine fluorescence resonance energy transfer indicators and id

224 of dye-labeled peptides to QD surfaces using fluorescence resonance energy transfer interactions in Q

225 ng the translating ribosome, single-molecule fluorescence resonance energy transfer investigations re

226 Fluorescence resonance energy transfer measurements in c

227 Fluorescence resonance energy transfer measurements indi

228 R, optical and vibrational spectroscopy, and fluorescence resonance energy transfer measurements of s

229 Intersubunit fluorescence resonance energy transfer measurements reve

230 Fluorescence resonance energy transfer measurements show

231 Anisotropy and fluorescence resonance energy transfer measurements were

232 Fluorescence resonance energy transfer measurements, com

233 By using photo-cross-linking and fluorescence resonance energy transfer measurements, we

234 ral to the interpretation of single-molecule fluorescence resonance energy transfer measurements, whe

235 nhancement, small-angle X-ray scattering and fluorescence resonance energy transfer measurements, whi

236 processes observed found to be based on the fluorescence resonance energy transfer mechanism from Hb

237 A fluorescence resonance energy transfer mechanism was use

238 orsal skinfold chamber model and multiphoton fluorescence resonance energy transfer microscopy, nitri

239 serum albumin (BSA)) can be employed to gate fluorescence resonance energy transfer occurring from a

240 Based on the intra-molecular fluorescence resonance energy transfer of OPA-tryptophan

241 atants, and C3 cleavage sites were mapped by fluorescence resonance energy transfer peptides.

242 Consistently, fluorescence resonance energy transfer probes revealed a

243 e expressing a modified form of the Cameleon fluorescence resonance energy transfer reporter for intr

244 Fluorescence resonance energy transfer sensor-based cAMP

245 ye-to-heme distances P(r) from time-resolved fluorescence resonance energy transfer show that ATP dec

246 othesis, we have developed a single-molecule fluorescence resonance energy transfer signal between IF

247 ooth muscle cells as evidenced by changes in fluorescence resonance energy transfer signal of a Plk1

248 Here, using an IF2-tRNA single-molecule fluorescence resonance energy transfer signal, we direct

249 Single-molecule fluorescence resonance energy transfer (smFRET) analyses

250 Single molecule fluorescence resonance energy transfer (smFRET) analysis

251 Here, we have combined single-molecule fluorescence resonance energy transfer (smFRET) and bulk

252 Here, we use single molecule fluorescence resonance energy transfer (smFRET) and two

253 Using single-molecule fluorescence resonance energy transfer (smFRET) between

254 ing tasks in the analysis of single-molecule fluorescence resonance energy transfer (smFRET) experime

255 sed this approach to perform single-molecule fluorescence resonance energy transfer (smFRET) experime

256 Using single-molecule fluorescence resonance energy transfer (smFRET) imaging,

257 ological ion gradients using single-molecule fluorescence resonance energy transfer (smFRET) imaging.

258 e application of three-color single-molecule fluorescence resonance energy transfer (smFRET) methods

259 Single-molecule fluorescence resonance energy transfer (smFRET) methods

260 Previous single-molecule fluorescence resonance energy transfer (smFRET) studies

261 To this end, single-molecule fluorescence resonance energy transfer (smFRET) techniqu

262 Concomitantly, we have used single-molecule fluorescence resonance energy transfer (smFRET) to chara

263 Here we have used single molecule fluorescence resonance energy transfer (smFRET) to inves

264 We used single-molecule fluorescence resonance energy transfer (smFRET) to study

265 Here we used single-molecule fluorescence resonance energy transfer (smFRET) to study

266 idden Markov modeling-fitted single-molecule fluorescence resonance energy transfer (smFRET) trajecto

267 Single-molecule Forster or fluorescence resonance energy transfer (smFRET) was used

268 Using single-molecule fluorescence resonance energy transfer (smFRET), we have

269 se detection reaction (LDR) with single-pair fluorescence resonance energy transfer (spFRET) to provi

270 ftening' is explored here by single-molecule fluorescence resonance energy transfer studies of single

271 Single-molecule fluorescence resonance energy transfer studies reveal th

272 ted mutagenesis and homogenous time-resolved fluorescence resonance energy transfer studies that asse

273 Using live-cell fluorescence resonance energy transfer studies, we demon

274 and fluorescence lifetime imaging microscopy-fluorescence resonance energy transfer studies.

275 ve co-localization analysis, and a new FRET (fluorescence resonance energy transfer) technique to dem

276 have been investigated using single-molecule fluorescence resonance energy transfer techniques.

277 a genetically encoded FAK biosensor based on fluorescence resonance energy transfer, that FN-mediated

278 We have used site-directed time-resolved fluorescence resonance energy transfer to determine the

279 Here, we have used single-molecule fluorescence resonance energy transfer to directly obser

280 Here, we use fluorescence resonance energy transfer to investigate th

281 For this, we used fluorescence resonance energy transfer to monitor positi

282 Here, we have used single-molecule fluorescence resonance energy transfer to monitor tertia

283 Here, we use single-molecule fluorescence resonance energy transfer to monitor the in

284 Here we use single-molecule fluorescence resonance energy transfer to probe the acti

285 We have used fluorescence resonance energy transfer to study the mech

286 s are brought together using single-molecule fluorescence resonance energy transfer together with col

287 ite-directed spectroscopies of time-resolved fluorescence resonance energy transfer (TR-FRET) and dou

288 centration (EC50) value of the time-resolved fluorescence resonance energy transfer (TR-FRET) assay w

289 Using a novel Time-resolved Fluorescence Resonance Energy Transfer (TR-FRET) assay,

290 nstrate the combination of the time-resolved fluorescence resonance energy transfer (tr-FRET) measure

291 ormed on KDM1A/CoREST, using a time-resolved fluorescence resonance energy transfer (TR-FRET) technol

292 We have used time-resolved fluorescence resonance energy transfer (TR-FRET) to dete

293 C2 for phospholipid membranes as measured by fluorescence resonance energy transfer was modestly lowe

294 stance constraints obtained by time-resolved fluorescence resonance energy transfer, we define the re

295 Employing single-pair fluorescence resonance energy transfer, we monitored DNA

296 Using time-resolved fluorescence resonance energy transfer, we provide, to o

297 y to monitor their formation and decay using fluorescence resonance energy transfer, we reveal the ge

298 Using fluorescence resonance energy transfer, we studied cotra

299 scent protein, demonstrated a basal level of fluorescence resonance energy transfer, which increased

300 n gp120 subunit and measured single-molecule fluorescence resonance energy transfer within the contex