ライフサイエンスコーパス: correlation spectroscopy

1 p40Ap complex using two-dimensional infrared correlation spectroscopy.

2 monstrated and quantified using fluorescence correlation spectroscopy.

3 ntation and in HeLa cells using fluorescence correlation spectroscopy.

4 to HPS and was evaluated using fluorescence correlation spectroscopy.

5 rs in live zebrafish embryos by fluorescence correlation spectroscopy.

6 odal inhibitor, Lefty, by fluorescence cross-correlation spectroscopy.

7 covery after photobleaching and fluorescence correlation spectroscopy.

8 ectroscopy, and two-color fluorescence cross-correlation spectroscopy.

9 usions in living cells by fluorescence cross-correlation spectroscopy.

10 ecular dynamics simulations and fluorescence correlation spectroscopy.

11 trations can be estimated using fluorescence correlation spectroscopy.

12 th single-particle tracking and fluorescence correlation spectroscopy.

13 imerization by dual-color fluorescence cross-correlation spectroscopy.

14 in live yeast cells using fluorescence cross-correlation spectroscopy.

15 al time-lapse imaging and fluorescence cross-correlation spectroscopy.

16 nd Brightness analysis and Raster-scan Image Correlation Spectroscopy.

17 has been probed by through-space (13)C-(13)C correlation spectroscopy.

18 lytical ultracentrifugation and fluorescence correlation spectroscopy.

19 ipid membranes using dual-focus fluorescence correlation spectroscopy.

20 19 nm diameter probing areas in fluorescence correlation spectroscopy.

21 nts of two sliding clamps using fluorescence correlation spectroscopy.

22 NMR spectra and the use of statistical total correlation spectroscopy.

23 escence microscopy and spatio-temporal image correlation spectroscopy.

24 tical trap, and diffusion using fluorescence correlation spectroscopy.

25 beta1-integrins measured using fluorescence correlation spectroscopy.

26 be studied simultaneously by FT-IR and 2D IR correlation spectroscopies.

27 -color dual-focus line-scanning fluorescence correlation spectroscopy (2c2f lsFCS) technique that gre

28 sing COSY and heteronuclear multiple quantum correlation spectroscopy (2D NMR), we unequivocally demo

29 In this study, two-dimensional correlation spectroscopy (2D-COS) combined with mid-infr

30 Here, we introduce two-dimensional correlation spectroscopy (2DCOS) as a novel technique fo

31 scattering (DLS), and two-focus fluorescence correlation spectroscopy (2f-FCS) to characterize the de

32 ogy, was investigated by z-scan fluorescence correlation spectroscopy across a temperature range of 2

33 this study, we describe a generalized image correlation spectroscopy algorithm that accepts arbitrar

34 FRET-based nanosecond fluorescence correlation spectroscopy allows long-range distances and

35 photon counting histogram, and fluorescence correlation spectroscopy analyses.

36 Fluorescence cross-correlation spectroscopy analysis at the plasma membrane

37 Two-dimensional correlation spectroscopy analysis of the ATR-FTIR spectr

38 rgy transfer, and imaging fluorescence cross-correlation spectroscopy analysis revealed partial coloc

39 Here, we combine fluorescence correlation spectroscopy and acrylodan fluorescence scre

40 d bilayers by means of scanning fluorescence correlation spectroscopy and all-atom molecular dynamic

41 We have used fluorescence correlation spectroscopy and cross-correlation spectrosc

42 recovery after photobleaching, fluorescence correlation spectroscopy and electron microscopy in live

43 y at different length scales by fluorescence correlation spectroscopy and fluorescence recovery after

44 d sororin by mass spectrometry, fluorescence-correlation spectroscopy and fluorescence recovery after

45 evious literature reports using fluorescence correlation spectroscopy and fluorescence recovery after

46 In addition, scanning fluorescence cross-correlation spectroscopy and FRET measurements revealed

47 Here a technique that combines fluorescence correlation spectroscopy and homo-FRET analysis was used

48 We used fluorescence correlation spectroscopy and mathematical modeling to me

49 The combination of fluorescence correlation spectroscopy and nanodisc technologies provi

50 Using raster image correlation spectroscopy and number and brightness analy

51 mely cross-correlation scanning fluorescence correlation spectroscopy and number and brightness analy

52 nance energy transfer (svFRET), fluorescence correlation spectroscopy and quartz-crystal microbalance

53 We used fluorescence correlation spectroscopy and quenching data to monitor t

54 Contrary to classical fluorescence correlation spectroscopy and related methods, this combi

55 , Frizzled1 (Fzd1), using fluorescence cross-correlation spectroscopy and show that the co-receptor,

56 uorescence techniques including fluorescence correlation spectroscopy and single particle tracking, a

57 and alphaVbeta3 integrin using fluorescence correlation spectroscopy and single-particle electron mi

58 The general picture concluded from photon correlation spectroscopy and small angle X-ray scatterin

59 Using fluorescence correlation spectroscopy and three-dimensional stochasti

60 Using fluorescence correlation spectroscopy and vesicle clearance assays, w

61 uorescence Lifetime Imaging and Fluorescence Correlation Spectroscopy) and molecular modelling, we sh

62 erence spectroscopy), (1)H-(1)H TOCSY (total correlation spectroscopy), and (13)C-(1)H HSQC-TOCSY, fo

63 imity index measurements, fluorescence cross-correlation spectroscopy, and biochemical experiments de

64 ing an RNA interference screen, fluorescence correlation spectroscopy, and confocal imaging, we ident

65 tion, dynamic light scattering, fluorescence correlation spectroscopy, and electron microscopy.

66 recovery after photobleaching, fluorescence correlation spectroscopy, and extraction experiments to

67 nts in fluorescence microscopy, fluorescence correlation spectroscopy, and fluorescent labeling techn

68 We used live-cell imaging, spatial image correlation spectroscopy, and k-space image correlation

69 using fluorescence anisotropy, fluorescence correlation spectroscopy, and size exclusion chromatogra

70 lves quantitative gel analysis, fluorescence correlation spectroscopy, and total internal reflection

71 on-counting histogram analysis, raster image correlation spectroscopy, and two-color fluorescence cro

72 r resonance energy transfer and fluorescence correlation spectroscopy; and segregation into larger do

73 ifferent from the original raster-scan image correlation spectroscopy approach, where data are acquir

74 gh lipofection using image-based fluctuation correlation spectroscopy approaches.

75 nergy transfer (FRET) and fluorescence cross-correlation spectroscopy are noninvasive, optical method

76 Number and Brightness and Raster-scan Image Correlation Spectroscopy as methods to monitor kinetics

77 ma membrane of HEK293T cells by fluorescence correlation spectroscopy as well as fluorescence recover

78 Combining imaging with correlation spectroscopy, as in raster image correlation

79 fluctuation approaches, notably raster image correlation spectroscopy, as tools to record fast diffus

80 a homogeneous dual-color fluorescence cross-correlation spectroscopy assay for saturation- and compe

81 The fluorescence cross-correlation spectroscopy assay has the advantage that it

82 teins were measured by means of fluorescence correlation spectroscopy at a total protein concentratio

83 We developed an approach, displacement correlation spectroscopy based on time-resolved image co

84 Fluorescence correlation spectroscopy-based molecular brightness anal

85 order of magnitude faster than fluorescence-correlation-spectroscopy-based techniques for such measu

86 ed methods like two-color fluorescence cross-correlation spectroscopy can provide this information, b

87 Fast correlation spectroscopy (COSY) spectra are recorded eve

88 1D (1)HNMR and (1)H-(1)H correlation spectroscopy (COSY) spectra were acquired in

89 i enhanced by polarization transfer (INEPT), correlation spectroscopy (COSY), and heteronuclear singl

90 elective 1D NOESY, selective 2D NOESY, NOESY-correlation spectroscopy (COSY), NOESY-total correlation

91 ar ((13)C-(1)H) single quantum correlations (correlation spectroscopy, COSY, and heteronuclear single

92 work we show that the use of two-dimensional correlation spectroscopy coupled to IR absorption spectr

93 size exclusion chromatography, fluorescence correlation spectroscopy, cross-linking followed by West

94 Here we obtain single-molecule fluorescence correlation spectroscopy data and analyse them within th

95 o analyze single molecule fluorescence cross-correlation spectroscopy data for intracellular membrane

96 olecular brightness analysis of fluorescence correlation spectroscopy data from live HeLa cells trans

97 es and perform dual-color fluorescence cross-correlation spectroscopy (dcFCCS).

98 diffuse optical system consisting of diffuse correlation spectroscopy (DCS) and frequency-domain near

99 Diffuse correlation spectroscopy (DCS) is emerging as a powerful

100 -infrared spectroscopy (FD-NIRS) and diffuse correlation spectroscopy (DCS).

101 sicles presented spherical shapes and photon correlation spectroscopy detected that their hydrodynami

102 In combination with the fluorescence correlation spectroscopy diffusion law, this provides in

103 g microscale thermophoresis and fluorescence correlation spectroscopy (dissociation constants KD = 23

104 ing 2D MRS method of double quantum filtered correlation spectroscopy (DQF-COSY).

105 ry was benchmarked against (1)H diffusion-T2 correlation spectroscopy (DRCOSY), which has a stronger

106 lecular (co)mobility by fluorescence (cross-)correlation spectroscopy (F(C)CS) in a SPIM has been int

107 Using fluorescence cross-correlation spectroscopy (FCCS) and fluorescence recover

108 Characterization by fluorescence cross-correlation spectroscopy (FCCS) confirmed lateral mobili

109 OLIG2 dimerization using fluorescence cross-correlation spectroscopy (FCCS) of live HEK cells transf

110 fetime imaging (FLIM) and fluorescence cross-correlation spectroscopy (FCCS) to structurally and quan

111 In this study, we combine fluorescence correlation spectroscopy (FCS) and a microfluidic shear

112 be studied with solution-based fluorescence correlation spectroscopy (FCS) and can be isolated on a

113 Fluorescence correlation spectroscopy (FCS) and fluorescence recovery

114 ry after photobleaching (FRAP), fluorescence correlation spectroscopy (FCS) and Forster resonance ene

115 Using fluorescence correlation spectroscopy (FCS) and membrane-binding kine

116 abled these quantifications are fluorescence correlation spectroscopy (FCS) and photon counting histo

117 spectroscopy techniques such as fluorescence correlation spectroscopy (FCS) and spectral imaging.

118 after photobleaching (FRAP) and fluorescence correlation spectroscopy (FCS) are the two most direct m

119 In principle, fluorescence correlation spectroscopy (FCS) based methods can provide

120 H pulsed-field gradient NMR and fluorescence correlation spectroscopy (FCS) experiments combined with

121 (MC540), were first analyzed by fluorescence correlation spectroscopy (FCS) in different alcohol solu

122 Fluorescence correlation spectroscopy (FCS) is a noninvasive techniqu

123 Fluorescence Correlation Spectroscopy (FCS) is a popular tool for mea

124 Fluorescence correlation spectroscopy (FCS) is a powerful technique t

125 Fluorescence correlation spectroscopy (FCS) is a sensitive technique

126 ance energy transfer (FRET) and fluorescence correlation spectroscopy (FCS) measurements on single gi

127 Fluorescence correlation spectroscopy (FCS) methods are powerful tool

128 r fluctuation-based techniques (fluorescence correlation spectroscopy (FCS) or raster-scan image corr

129 In addition fluorescence correlation spectroscopy (FCS) showed that cytosolic Bax

130 We established a fluorescence correlation spectroscopy (FCS) system to measure the per

131 with SCR using a combination of Fluorescent Correlation Spectroscopy (FCS) techniques.

132 We used fluorescence correlation spectroscopy (FCS) to accurately and precise

133 Using fluorescence correlation spectroscopy (FCS) to distinguish between di

134 Here we use fluorescence correlation spectroscopy (FCS) to quantitatively and acc

135 al instrument could be used for fluorescence correlation spectroscopy (FCS) under pulsed stimulated e

136 n (BSA) into the nanoslits; and fluorescence correlation spectroscopy (FCS) was further used to inves

137 Fluorescence correlation spectroscopy (FCS) was used to determine the

138 ed) atomic force microscopy and fluorescence correlation spectroscopy (FCS) we found out that, upon c

139 lial cells were evaluated using fluorescence correlation spectroscopy (FCS) with photon counting hist

140 ensemble measurements, we used fluorescence correlation spectroscopy (FCS), a method that offers sin

141 ve relied almost exclusively on fluorescence correlation spectroscopy (FCS), a technique that provide

142 n the nucleus can be studied by fluorescence correlation spectroscopy (FCS), a well-established techn

143 orrelation spectroscopy (RICS), fluorescence correlation spectroscopy (FCS), and atomic force microsc

144 ophoresis, gel electrophoresis, fluorescence correlation spectroscopy (FCS), and microfluidic experim

145 Fluorescence correlation spectroscopy (FCS), is a widely used tool ro

146 After Photobleaching (FRAP) and Fluorescence Correlation Spectroscopy (FCS), obtaining estimates in w

147 several such assays, including Fluorescence Correlation Spectroscopy (FCS), ribosome Run-Off Assays

148 Using fluorescence correlation spectroscopy (FCS), RR1 was shown to detect

149 -A3 receptor (A3AR) agonist and fluorescence correlation spectroscopy (FCS), we demonstrated high-aff

150 Using Fluorescence Correlation Spectroscopy (FCS), we have characterized th

151 (ThT) fluorescence, NMR, EM and fluorescence correlation spectroscopy (FCS), we show that fibril disa

152 e resolution can be achieved by fluorescence-correlation spectroscopy (FCS), where intensity fluctuat

153 ique analytical system based on fluorescence correlation spectroscopy (FCS), which measures antibody-

154 py, Circular Dichroism (CD) and Fluorescence Correlation Spectroscopy (FCS).

155 ores at the membrane surface by fluorescence correlation spectroscopy (FCS).

156 hromatin, by spatially resolved fluorescence correlation spectroscopy (FCS).

157 pectroscopic techniques such as fluorescence correlation spectroscopy (FCS).

158 omain near infrared spectroscopy and diffuse correlation spectroscopy (FDNIRS-DCS) to measure cerebra

159 Fluorescence lifetime correlation spectroscopy (FLCS) and photon counting hist

160 We report a novel noncontact diffuse correlation spectroscopy flow-oximeter for simultaneous

161 in the application of FRET and fluorescence correlation spectroscopy for the analysis of oligomeriza

162 r Resonance Energy Transfer and Fluorescence Correlation Spectroscopy (FRET-FCS) has a unique ability

163 nent analysis (PCA) and two-dimensional (2D) correlation spectroscopy has assisted us to explore in v

164 Fluorescence correlation spectroscopy has been previously used to inv

165 article tracking and nanoscopic fluorescence correlation spectroscopy, has been applied to characteri

166 peckle microscopy and spatial temporal image correlation spectroscopy have been used to capture high-

167 riments, and 2D heteronuclear single-quantum correlation spectroscopy (HSQC)-NOESY.

168 nformation from 2D-HSQC spectra, termed HSQC correlation spectroscopy (HSQCcos), is reported.

169 lization from multicolor images, image cross-correlation spectroscopy (ICCS) offers several advantage

170 scanning confocal microscopy images by image correlation spectroscopy (ICS) or fluctuation moments me

171 We have extended inverse fluorescence correlation spectroscopy (iFCS) to endow it with unique

172 es in RBL mast cells by imaging fluorescence correlation spectroscopy (ImFCS).

173 r of SecYEG channels counted by fluorescence correlation spectroscopy in a single proteoliposome.

174 overy after photobleaching, and fluorescence correlation spectroscopy in Drosophila melanogaster S2 c

175 alytic domain (CD)-GFP to DNA by Fluorescent Correlation Spectroscopy in live cells and detected the

176 erhauser Effects and double-quantum-filtered correlation spectroscopy in nuclear magnetic resonance (

177 energy transfer and dual-color fluorescence correlation spectroscopy in studies with eGFP- and mCher

178 oated surface investigated with X-ray Photon Correlation Spectroscopy in surface-sensitive conditions

179 sions of HTT, and analysis by a fluorescence correlation spectroscopy indicated that knockdown of PFD

180 Sensitivity-enhanced 2D proton correlation spectroscopy is a useful and straightforward

181 Image correlation spectroscopy is a well-established analysis

182 However, when image correlation spectroscopy is applied to a highly heteroge

183 Since correlation spectroscopy is one of the most important ap

184 In this paper, imaging-fluorescence-correlation spectroscopy is used to measure diffusion ra

185 ging total internal reflection- fluorescence correlation spectroscopy (ITIR-FCS) and molecular dynami

186 aging total internal reflection fluorescence correlation spectroscopy (ITIR-FCS) is a well-establishe

187 aging total internal reflection-fluorescence correlation spectroscopy (ITIR-FCS) showed that monomeri

188 heoretical framework for Fourier-space image correlation spectroscopy (kICS).

189 microscopy in combination with fluorescence correlation spectroscopy, LYVE-1 diffusion is restricted

190 sing a combination of live-cell fluorescence correlation spectroscopy, mass spectrometry, and hydrody

191 coefficients are determined by fluorescence correlation spectroscopy measurements for probe molecule

192 Accordingly, fluorescence correlation spectroscopy measurements in dividing cells

193 Here, we report x-ray photon correlation spectroscopy measurements of dynamics at the

194 Parallel fluorescence correlation spectroscopy measurements show that this con

195 r conventional dual-color fluorescence cross-correlation spectroscopy measurements.

196 We therefore developed multimodal Image Correlation Spectroscopy (mICS) to measure anisotropic m

197 ressed these questions by using fluorescence correlation spectroscopy, molecular dynamics simulations

198 ells via multiphoton excitation fluorescence correlation spectroscopy (MPE-FCS).

199 The method is based on phasor image-correlation spectroscopy of histone fluorescence lifetim

200 hydrodynamic radii estimated by fluorescence correlation spectroscopy of the two coexisting conformat

201 HIV-1 particles using scanning fluorescence correlation spectroscopy on a super-resolution STED micr

202 vealed by temporal and spatio-temporal image correlation spectroscopy on the tens-of-seconds timescal

203 istinguished in single-molecule fluorescence correlation spectroscopy or bulk time-resolved small-ang

204 tion spectroscopy (FCS) or raster-scan image correlation spectroscopy) or particle tracking.

205 Combined with fluorescence correlation spectroscopy, our probe can sensitively dete

206 ing this dilution strategy with fluorescence correlation spectroscopy permits quantitative assessment

207 d photo-induced energy-transfer fluorescence correlation spectroscopy (PET-FCS) to show how a small a

208 ed electron transfer coupled to fluorescence correlation spectroscopy (PET-FCS).

209 embranes using a combination of fluorescence correlation spectroscopy, photon counting histogram anal

210 ed interleaved excitation fluorescence cross-correlation spectroscopy (PIE-FCCS).

211 ed-interleaved excitation fluorescence cross-correlation spectroscopy (PIE-FCCS).

212 e Resonance Energy Transfer and Fluorescence Correlation Spectroscopy provide quantitative measuremen

213 covery after photobleaching and fluorescence correlation spectroscopy provided further evidence for a

214 nance energy transfer and fluorescence cross-correlation spectroscopy quantitative imaging.

215 y microscale thermophoresis and fluorescence correlation spectroscopy, respectively).

216 Here the bioimaging approaches Raster Image Correlation Spectroscopy (RICS) and image-Means Square D

217 two fluorescence-based methods: raster image correlation spectroscopy (RICS) and single particle trac

218 the same experiment by using a raster image correlation spectroscopy (RICS) based analysis.

219 Raster image correlation spectroscopy (RICS) is a fluorescence image

220 maging methods (PIE-FI) such as raster image correlation spectroscopy (RICS) or number and brightness

221 s by employing a combination of raster image correlation spectroscopy (RICS), fluorescence correlatio

222 correlation spectroscopy, as in raster image correlation spectroscopy (RICS), makes it possible to ex

223 lapping time series analysis to raster image correlation spectroscopy (RICS), we observed time-depend

224 for single-color fluorescence lifetime cross-correlation spectroscopy (sc-FLCCS).

225 n STED microscopy with scanning fluorescence correlation spectroscopy (scanning STED-FCS, sSTED-FCS)

226 Surface enhanced Raman correlation spectroscopy (SERCS) is shown as a label-fre

227 Fluorescence correlation spectroscopy served to assess (i) SGLT1 abun

228 er were investigated by both second-harmonic correlation spectroscopy (SHCS) and a traditional equili

229 scribe the implementation of second harmonic correlation spectroscopy (SHCS) to measure the adsorptio

230 Fluorescent correlation spectroscopy showed effective complexation w

231 nation of dilution experiments, X-ray photon correlation spectroscopy, small angle X-ray scattering,

232 Imaging fluorescence cross-correlation spectroscopy (SPIM-FCCS) and molecular dynam

233 e plane illumination microscopy-fluorescence correlation spectroscopy (SPIM-FCS), a multiplexed modal

234 Here, we develop the simulated Raman correlation spectroscopy (SRCS) process to determine whi

235 n STED microscopy combined with fluorescence correlation spectroscopy (STED-FCS) to access and compar

236 D nanoscopy in combination with fluorescence correlation spectroscopy (STED-FCS), a technique which a

237 Spatiotemporal image correlation spectroscopy (STICS) is a simple and powerfu

238 ngle-molecule data with spatiotemporal image correlation spectroscopy (STICS) with a focus on measure

239 ta and the introduction of statistical total correlation spectroscopy (STOCSY) as a tool for biomarke

240 Statistical total correlation spectroscopy (STOCSY) yielded information on

241 pectroscopic tools such as Statistical Total Correlation Spectroscopy (STOCSY), Subset Optimization b

242 carried out by computing a statistical total correlation spectroscopy (STOCY) analysis of the (1)H NM

243 Indeed, fluorescence correlation spectroscopy studies showed binding of 324.6

244 Here, we demonstrate a WM-enhanced correlation spectroscopy technique capable of narrowing

245 r and brightness and raster scanning imaging correlation spectroscopy) the effect of pressure on the

246 centrins by two-dimensional infrared (2D IR) correlation spectroscopy, the change in heat capacity an

247 ot observed at the experimental fluorescence correlation spectroscopy timescales (>100 mus), appears

248 microscopy in combination with fluorescence correlation spectroscopy to assess the characteristics o

249 lifetime imaging microscopy and fluorescence correlation spectroscopy to assess the formation of Pou5

250 By using fluorescence cross-correlation spectroscopy to characterize the Mtrm::Polo

251 correlation spectroscopy, and k-space image correlation spectroscopy to examine the aggregation stat

252 izes of large RNAs, we employed fluorescence correlation spectroscopy to examine the hydrodynamic rad

253 The first use of statistical correlation spectroscopy to extract chemical information

254 Application of temporal image cross correlation spectroscopy to image series of cells coexpr

255 aging total internal reflection-fluorescence correlation spectroscopy to investigate EGFR dynamics on

256 ching and fluorescence correlation and cross-correlation spectroscopy to investigate in vivo chromati

257 plain these effects, we applied fluorescence correlation spectroscopy to investigate the lateral mole

258 RCC1 complex in living cells by fluorescence correlation spectroscopy to investigate whether binding

259 reflection fluorescence microscopy and image correlation spectroscopy to monitor and map diffusion of

260 esults expand the application range of image correlation spectroscopy to multicellular systems and de

261 orescence correlation spectroscopy and cross-correlation spectroscopy to quantify the diffusion, phot

262 ination microscopy with spatiotemporal image correlation spectroscopy to quantify the flow velocities

263 lifetime imaging microscopy and fluorescence correlation spectroscopy to study functional and structu

264 covery after photobleaching and fluorescence correlation spectroscopy, to examine the dynamic interpl

265 l technique, ultrafast-scanning fluorescence correlation spectroscopy, to measure the molecular inter

266 opy, and sliding window temporal image cross correlation spectroscopy, to measure time profiles of th

267 By using 2D (1)H-(31)P total correlation spectroscopy (TOCSY) correlation experiments

268 correlation spectroscopy (COSY), NOESY-total correlation spectroscopy (TOCSY) experiments, and 2D het

269 2D) NMR (13)C-(13)C constant-time (CT) total correlation spectroscopy (TOCSY) experiments.

270 2D total correlation spectroscopy (TOCSY) provides unique spin co

271 diffusion-ordered spectroscopy (DOSY), total correlation spectroscopy (TOCSY), and T2 relaxometry to

272 are completed through carbon-detected, total correlation spectroscopy (TOCSY)-based side chain chemic

273 ta3 binding to Galphaq FRET and fluorescence correlation spectroscopy, two physically distinct method

274 ved absorption spectroscopy and fluorescence correlation spectroscopy verify that, unlike the corresp

275 Finally, 2D IR correlation spectroscopy was used for the determination

276 mbining photon antibunching and fluorescence correlation spectroscopy was used to confirm that the tw

277 Simultaneous homo-FRET and fluorescence correlation spectroscopy was used to detect structural c

278 le spinning NMR as well as with fluorescence correlation spectroscopy we demonstrate that these nanod

279 By pairing split-GFP with fluorescence correlation spectroscopy, we compared the composition of

280 g two-color, live-cell superresolution cross-correlation spectroscopy, we demonstrate that the two fl

281 Using fluorescence correlation spectroscopy, we determined that cytosolic s

282 Here, using FRET and fluorescence cross-correlation spectroscopy, we introduce a method to measu

283 Using fluorescence correlation spectroscopy, we measure the diffusion coeff

284 Using fluorescence correlation spectroscopy, we measured a dissociation con

285 Using fluorescence imaging and fluorescence correlation spectroscopy, we measured the Ca(2+) concent

286 nts within a single cell with temporal image correlation spectroscopy, we measured the mechanosensiti

287 ing static light scattering and fluorescence correlation spectroscopy, we monitored the changes in hy

288 hemical interaction studies and fluorescence correlation spectroscopy, we show that in live Yersinia

289 f previously published fluorescence lifetime correlation spectroscopy which relies on lifetime differ

290 e application of traditional two-dimensional correlation spectroscopy, which relies on regeneration o

291 ARICS is a powerful expansion of image correlation spectroscopy with the potential of becoming

292 sent a robust approach based on fluorescence correlation spectroscopy with ultra-high speed axial lin

293 Fluorescence cross-correlation spectroscopy within the zebrafish paraxial m

294 Using in-situ x-ray photon correlation spectroscopy (XPCS) experiments, we show tha

295 le X-ray scattering (WAXS) with X-ray photon-correlation spectroscopy (XPCS) in the small-angle X-ray

296 established techniques such as X-ray photon correlation spectroscopy (XPCS) is challenging.

297 The technique of X-ray Photon Correlation Spectroscopy (XPCS) is reviewed as a method

298 Here, we demonstrate X-ray photon correlation spectroscopy (XPCS) with submicrosecond time

299 uspended in polymer melts using X-ray photon correlation spectroscopy (XPCS), while also monitoring e

300 Co-distribution and two-dimensional infrared correlation spectroscopies yielded the mechanism of aggr