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

1 tical trap, and diffusion using fluorescence correlation spectroscopy.

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

3 ecular dynamics simulations and fluorescence correlation spectroscopy.

4 beta1-integrins measured using fluorescence correlation spectroscopy.

5 trations can be estimated using fluorescence correlation spectroscopy.

6 th single-particle tracking and fluorescence correlation spectroscopy.

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

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

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

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

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

12 lytical ultracentrifugation and fluorescence correlation spectroscopy.

13 ipid membranes using dual-focus fluorescence correlation spectroscopy.

14 19 nm diameter probing areas in fluorescence correlation spectroscopy.

15 microscopy in combination with fluorescence correlation spectroscopy.

16 p40Ap complex using two-dimensional infrared correlation spectroscopy.

17 ng single-particle tracking and fluorescence correlation spectroscopy.

18 d spectroscopic system based on fluorescence correlation spectroscopy.

19 ex protein assembly pathways by fluorescence correlation spectroscopy.

20 rcular dichroism and two-photon fluorescence correlation spectroscopy.

21 monstrated and quantified using fluorescence correlation spectroscopy.

22 ntation and in HeLa cells using fluorescence correlation spectroscopy.

23 rs in live zebrafish embryos by fluorescence correlation spectroscopy.

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

25 escence microscopy and spatio-temporal image correlation spectroscopy.

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

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

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

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

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

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

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

33 microgels by confocal two-focus fluorescence correlation spectroscopy (2fFCS).

34 Three-color fluorescence cross-correlation spectroscopy (3C-FCCS) has been shown to tra

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

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

37 Fluorescence correlation spectroscopy allowed us to count both the nu

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

39 photon counting histogram, and fluorescence correlation spectroscopy analyses.

40 Fluorescence cross-correlation spectroscopy analysis at the plasma membrane

41 Fluorescence correlation spectroscopy analysis revealed the relative

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

43 we developed a method coupling fluorescence correlation spectroscopy and calibrated imaging.

44 ic evolution is monitored using fluorescence correlation spectroscopy and compared to a computer simu

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

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

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

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

49 We used fluorescence correlation spectroscopy and mathematical modeling to me

50 The combination of fluorescence correlation spectroscopy and nanodisc technologies provi

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

52 Using raster image correlation spectroscopy and number and brightness analy

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

54 y an established combination of fluorescence correlation spectroscopy and real-time tracking of the c

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

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 ure is generally applicable to FCS and image correlation spectroscopy and therefore provides an impor

59 Using fluorescence correlation spectroscopy and three-dimensional stochasti

60 Using fluorescence correlation spectroscopy and vesicle clearance assays, w

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

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

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

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

65 uorescence imaging techniques (such as FRET, correlation spectroscopy, and fluorescence anisotropy) t

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

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

68 re, using quantitative imaging, fluorescence correlation spectroscopy, and mathematical modeling, we

69 nce energy transfer, nanosecond fluorescence correlation spectroscopy, and microfluidic mixing to det

70 nomeric as measured by fluorescence imaging, correlation spectroscopy, and photon counting histogram

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

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

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

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

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

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

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

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

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

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

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

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

83 Fluorescence correlation spectroscopy-based molecular brightness anal

84 theoretical approach named binding-unbinding correlation spectroscopy (BUCS), we describe the two-dim

85 t of the fluorescence signal in fluorescence correlation spectroscopy by a factor of two.

86 ombination of X-ray scattering, fluorescence correlation spectroscopy, coarse-grained molecular dynam

87 2D correlation spectroscopy (COSY) spectra are obtained in

88 Fast correlation spectroscopy (COSY) spectra are recorded eve

89 1D (1)HNMR and (1)H-(1)H correlation spectroscopy (COSY) spectra were acquired in

90 is of (1)H-, (31)P- and (13)C-NMR, (1)H-(1)H correlation spectroscopy (COSY), (1)H-(31)P heteronuclea

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

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

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

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

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

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

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

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

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

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

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

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

105 r concentration range from (13)C-(13)C total correlation spectroscopy experiments of complex mixtures

106 h 16S rRNA, we introduce Fluorescence Triple-Correlation Spectroscopy (F3CS).

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

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

109 Fluorescence cross-correlation spectroscopy (FCCS) is used to determine int

110 e energy transfer (SP-FRET) and fluorescence correlation spectroscopy (FCS) also reveal divalent meta

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 Fluorescence correlation spectroscopy (FCS) and photon counting histo

115 ry after photobleaching (FRAP), fluorescence correlation spectroscopy (FCS) and single-molecule track

116 Here fluorescence correlation spectroscopy (FCS) and transmission electron

117 We used Fluorescence Correlation Spectroscopy (FCS) and two photon excitation

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 e show, for the first time, how fluorescence correlation spectroscopy (FCS) can be used to study bind

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

122 Second, it can be combined with fluorescence correlation spectroscopy (FCS) for simultaneous analysis

123 In recent years fluorescence correlation spectroscopy (FCS) has become a routine meth

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

125 Fluorescence correlation spectroscopy (FCS) is a noninvasive techniqu

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

127 Fluorescence correlation spectroscopy (FCS) is a powerful approach to

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

129 Fluorescence correlation spectroscopy (FCS) is a powerful tool to inf

130 Fluorescence correlation spectroscopy (FCS) is a sensitive technique

131 Fluorescence correlation spectroscopy (FCS) methods are powerful tool

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

133 Imaging fluorescence correlation spectroscopy (FCS) performed using array det

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

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

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

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

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

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

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

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

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

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

144 , this issue was examined using fluorescence correlation spectroscopy (FCS) with photon counting hist

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

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

147 We have combined TR-FRET, fluorescence correlation spectroscopy (FCS), and biolayer interferome

148 Fluorescence correlation spectroscopy (FCS), dynamic light scattering

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

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

151 fter photobleaching (FRAP), and fluorescence correlation spectroscopy (FCS), to monitor the diverse b

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

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

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

155 address this controversy using fluorescence correlation spectroscopy (FCS), which enables us to moni

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

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

158 ound actin was characterized by fluorescence correlation spectroscopy (FCS).

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

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

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

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

163 random motility (RAMOT) assay based on image correlation spectroscopy for the automated, label-free,

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

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

166 Fluorescence correlation spectroscopy has been previously used to inv

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

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

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

170 Hyperfine sublevel correlation spectroscopy (HYSCORE) spectra exhibit stron

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

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

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

179 Image correlation spectroscopy is a well-established analysis

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

181 Since correlation spectroscopy is one of the most important ap

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

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

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

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

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

187 Accordingly, fluorescence correlation spectroscopy measurements in dividing cells

188 Parallel fluorescence correlation spectroscopy measurements show that this con

189 We have applied the fluorescence correlation spectroscopy methodology to study surfactant

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

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

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

193 en as an example, we show that k-space image correlation spectroscopy of quantum dots blinking detect

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

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

196 with fructose was analyzed with fluorescence correlation spectroscopy on the level of a few molecules

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

198 copy, dynamic light scattering, fluorescence correlation spectroscopy, optical spectroscopy, nuclear

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

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

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

202 tryptophan in combination with fluorescence correlation spectroscopy (PET-FCS).

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

204 ed-interleaved excitation fluorescence cross-correlation spectroscopy (PIE-FCCS) and fluorescence lif

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

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

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

208 More importantly, 2D IR correlation spectroscopy provides unique information abo

209 as well as spatially resolved FCS from image correlation spectroscopy, providing an important theoret

210 nance energy transfer and fluorescence cross-correlation spectroscopy, respectively) as well as bioch

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

212 was monitored using Two Photon Fluorescence Correlation Spectroscopy, revealing concentration and si

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

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

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

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

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

218 own to <30 pM with PIE-raster lifetime image correlation spectroscopy (RLICS).

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

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

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

222 have developed a multiconfocal fluorescence correlation spectroscopy setup to measure the dynamics o

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

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

225 Fluorescent correlation spectroscopy showed effective complexation w

226 he technique, termed scattering interference correlation spectroscopy (SICS), autocorrelates the sign

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

228 d four-color single-laser fluorescence cross-correlation spectroscopy, solely based on FPs.

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

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

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

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

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

234 Two-color spatio-temporal image cross-correlation spectroscopy (STICCS) is a new, to our knowl

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

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

237 The method is based on statistical total correlation spectroscopy (STOCSY) and partial least squa

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

239 We previously showed that statistical total correlation spectroscopy (STOCSY) can be used to edit NM

240 eviously published method (statistical total correlation spectroscopy, STOCSY).

241 In comparison to a recent fluorescence correlation spectroscopy study, we suggest the microseco

242 on, thanks to the multiconfocal fluorescence correlation spectroscopy system, up to five spots could

243 As revealed by fluorescence correlation spectroscopy, the binding constant of purifi

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

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

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

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

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

249 we apply an extended version of raster image correlation spectroscopy to determine directional anisot

250 cule fluorescence spectroscopy and two-focus correlation spectroscopy to determine the theta points f

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 d surface plasmon resonance and fluorescence correlation spectroscopy to examine the interaction of S

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

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

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

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

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

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

260 In this study, we used fluorescence correlation spectroscopy to monitor the binding properti

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

262 ernating laser excitation fluorescence cross-correlation spectroscopy to observe the single molecule

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

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

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

266 By applying fluorescence cross-correlation spectroscopy to VDAC reconstituted into gian

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

268 ectroscopy, in combination with fluorescence correlation spectroscopy, to follow the population dynam

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

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

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

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

273 2D) NMR (13)C-(13)C constant-time (CT) total correlation spectroscopy (TOCSY) experiments.

274 2D total correlation spectroscopy (TOCSY) provides unique spin co

275 complement to existing methods such as total correlation spectroscopy (TOCSY) to expand the range of

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

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

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

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

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

281 or the liposome, as measured by fluorescence correlation spectroscopy, was also increased when pH is

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

283 Using solid-state NMR correlation spectroscopy we find detailed evidence for a

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

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

286 Using fluorescence correlation spectroscopy, we determined that cytosolic s

287 Using fluorescence correlation spectroscopy, we measure the diffusion coeff

288 Using fluorescence correlation spectroscopy, we measured a dissociation con

289 Using fluorescence correlation spectroscopy, we monitor the formation of mo

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

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

292 Using fluorescence correlation spectroscopy, we show that the diffusive mov

293 By means of two-color z-scan fluorescence correlation spectroscopy, we show that the nanosized dom

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

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

296 Fluorescence cross-correlation spectroscopy within the zebrafish paraxial m

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

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

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

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