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1 nation of molecular dynamics simulations and fluorescence correlation spectroscopy.
2 llular concentrations can be estimated using fluorescence correlation spectroscopy.
3 evel using both single-particle tracking and fluorescence correlation spectroscopy.
4 served by analytical ultracentrifugation and fluorescence correlation spectroscopy.
5 ion coefficients of two sliding clamps using fluorescence correlation spectroscopy.
6 on in black lipid membranes using dual-focus fluorescence correlation spectroscopy.
7 s well as 15-19 nm diameter probing areas in fluorescence correlation spectroscopy.
8  fluorescence microscopy in combination with fluorescence correlation spectroscopy.
9 hods, including single-particle tracking and fluorescence correlation spectroscopy.
10 h an automated spectroscopic system based on fluorescence correlation spectroscopy.
11 cterize complex protein assembly pathways by fluorescence correlation spectroscopy.
12 ding using circular dichroism and two-photon fluorescence correlation spectroscopy.
13 ent with DNA hybridization experiments using fluorescence correlation spectroscopy.
14 h background continues to be problematic for fluorescence correlation spectroscopy.
15 ase Abeta peptide with real-time imaging and fluorescence correlation spectroscopy.
16 ion peptide (pHLIP) in model membranes using fluorescence correlation spectroscopy.
17  per molecule than is achieved with confocal fluorescence correlation spectroscopy.
18 dback tracking microscopy and intramolecular fluorescence correlation spectroscopy.
19 ynamics within living cells using two-photon fluorescence correlation spectroscopy.
20 y or measured by alternative methods such as fluorescence correlation spectroscopy.
21 fusion coefficient and fitting parameters in fluorescence correlation spectroscopy.
22 of fibroblasts and epithelial cells by using fluorescence correlation spectroscopy.
23 d QDs in aqueous solution is confirmed using fluorescence correlation spectroscopy.
24 rs, and their mobilities were analyzed using fluorescence correlation spectroscopy.
25 tate at pH 6.3, are reported, as measured by fluorescence correlation spectroscopy.
26 HSF diffusibility, as shown here directly by fluorescence correlation spectroscopy.
27 s using an optical trap, and diffusion using fluorescence correlation spectroscopy.
28 Cherry-tagged beta1-integrins measured using fluorescence correlation spectroscopy.
29 O was exposed to HPS and was evaluated using fluorescence correlation spectroscopy.
30 ependently demonstrated and quantified using fluorescence correlation spectroscopy.
31 adient sedimentation and in HeLa cells using fluorescence correlation spectroscopy.
32 efty inhibitors in live zebrafish embryos by fluorescence correlation spectroscopy.
33 uorescence recovery after photobleaching and fluorescence correlation spectroscopy.
34 techniques, including confocal detection and fluorescence-correlation spectroscopy.
35 tegrated dual-color dual-focus line-scanning fluorescence correlation spectroscopy (2c2f lsFCS) techn
36 ynamic light scattering (DLS), and two-focus fluorescence correlation spectroscopy (2f-FCS) to charac
37 s inside the microgels by confocal two-focus fluorescence correlation spectroscopy (2fFCS).
38 efer methodology, was investigated by z-scan fluorescence correlation spectroscopy across a temperatu
39                                              Fluorescence correlation spectroscopy allowed us to coun
40                        FRET-based nanosecond fluorescence correlation spectroscopy allows long-range
41 opy XY-scans, photon counting histogram, and fluorescence correlation spectroscopy analyses.
42                                              Fluorescence correlation spectroscopy analysis of singly
43                                              Fluorescence correlation spectroscopy analysis revealed
44 e effect of varying three key parameters for Fluorescence Correlation Spectroscopy analysis, first in
45                             Here, we combine fluorescence correlation spectroscopy and acrylodan fluo
46 ion with lipid bilayers by means of scanning fluorescence correlation spectroscopy and all-atom molec
47 n live yeast, we developed a method coupling fluorescence correlation spectroscopy and calibrated ima
48    This dynamic evolution is monitored using fluorescence correlation spectroscopy and compared to a
49                                 We have used fluorescence correlation spectroscopy and cross-correlat
50                                        Using fluorescence correlation spectroscopy and cryogenic elec
51  fluorescence recovery after photobleaching, fluorescence correlation spectroscopy and electron micro
52 ement with previous literature reports using fluorescence correlation spectroscopy and fluorescence r
53  Wnt3 mobility at different length scales by fluorescence correlation spectroscopy and fluorescence r
54 bly expressed in CHO cells and studied using fluorescence correlation spectroscopy and fluorescent br
55               Here a technique that combines fluorescence correlation spectroscopy and homo-FRET anal
56                                      We used fluorescence correlation spectroscopy and mathematical m
57                           The combination of fluorescence correlation spectroscopy and nanodisc techn
58 echniques, namely cross-correlation scanning fluorescence correlation spectroscopy and number and bri
59 re widely used to analyze mobility data from fluorescence correlation spectroscopy and other experime
60  Forster resonance energy transfer (svFRET), fluorescence correlation spectroscopy and quartz-crystal
61                                      We used fluorescence correlation spectroscopy and quenching data
62 ntact cells by an established combination of fluorescence correlation spectroscopy and real-time trac
63                        Contrary to classical fluorescence correlation spectroscopy and related method
64 sion-based fluorescence techniques including fluorescence correlation spectroscopy and single particl
65  base subunit and alphaVbeta3 integrin using fluorescence correlation spectroscopy and single-particl
66                                        Using fluorescence correlation spectroscopy and three-dimensio
67                                        Using fluorescence correlation spectroscopy and vesicle cleara
68 IPBL, WAPL and sororin by mass spectrometry, fluorescence-correlation spectroscopy and fluorescence r
69 d imaging (Fluorescence Lifetime Imaging and Fluorescence Correlation Spectroscopy) and molecular mod
70      Next, using an RNA interference screen, fluorescence correlation spectroscopy, and confocal imag
71 tracentrifugation, dynamic light scattering, fluorescence correlation spectroscopy, and electron micr
72  fluorescence recovery after photobleaching, fluorescence correlation spectroscopy, and extraction ex
73 s two single-molecule sensitivity technique, fluorescence correlation spectroscopy, and fluorescence-
74 pid developments in fluorescence microscopy, fluorescence correlation spectroscopy, and fluorescent l
75            Here, using quantitative imaging, fluorescence correlation spectroscopy, and mathematical
76 orster resonance energy transfer, nanosecond fluorescence correlation spectroscopy, and microfluidic
77 tural studies using fluorescence anisotropy, fluorescence correlation spectroscopy, and size exclusio
78 ach that involves quantitative gel analysis, fluorescence correlation spectroscopy, and total interna
79 ity by Forster resonance energy transfer and fluorescence correlation spectroscopy; and segregation i
80 e fluorescence resonance energy transfer and fluorescence correlation spectroscopy are used to obtain
81 s in the plasma membrane of HEK293T cells by fluorescence correlation spectroscopy as well as fluores
82 ed tracer proteins were measured by means of fluorescence correlation spectroscopy at a total protein
83 correlation imaging, a multipoint version of fluorescence correlation spectroscopy, based upon a stat
84                                              Fluorescence correlation spectroscopy-based molecular br
85                                            A fluorescence-correlation-spectroscopy-based assay furthe
86 oves to be an order of magnitude faster than fluorescence-correlation-spectroscopy-based techniques f
87 an enhancement of the fluorescence signal in fluorescence correlation spectroscopy by a factor of two
88     Using a combination of X-ray scattering, fluorescence correlation spectroscopy, coarse-grained mo
89  of Tau using size exclusion chromatography, fluorescence correlation spectroscopy, cross-linking fol
90               Here we obtain single-molecule fluorescence correlation spectroscopy data and analyse t
91  (FRET) and molecular brightness analysis of fluorescence correlation spectroscopy data from live HeL
92         These observations combined with our fluorescence correlation spectroscopy data suggest that
93                                              Fluorescence correlation spectroscopy detects small inte
94                      In combination with the fluorescence correlation spectroscopy diffusion law, thi
95  to VWF, using microscale thermophoresis and fluorescence correlation spectroscopy (dissociation cons
96 ence resonance energy transfer (SP-FRET) and fluorescence correlation spectroscopy (FCS) also reveal
97                    In this study, we combine fluorescence correlation spectroscopy (FCS) and a microf
98  vesicles can be studied with solution-based fluorescence correlation spectroscopy (FCS) and can be i
99                                      We used fluorescence correlation spectroscopy (FCS) and fluoresc
100                                              Fluorescence correlation spectroscopy (FCS) and fluoresc
101 scence recovery after photobleaching (FRAP), fluorescence correlation spectroscopy (FCS) and Forster
102                                        Using fluorescence correlation spectroscopy (FCS) and membrane
103  that have enabled these quantifications are fluorescence correlation spectroscopy (FCS) and photon c
104                                              Fluorescence correlation spectroscopy (FCS) and photon c
105 scence recovery after photobleaching (FRAP), fluorescence correlation spectroscopy (FCS) and single-m
106 ombined with spectroscopy techniques such as fluorescence correlation spectroscopy (FCS) and spectral
107                                         Here fluorescence correlation spectroscopy (FCS) and transmis
108                                      We used Fluorescence Correlation Spectroscopy (FCS) and two phot
109 Device characterization is carried out using fluorescence correlation spectroscopy (FCS) and two-phot
110 nce recovery after photobleaching (FRAP) and fluorescence correlation spectroscopy (FCS) are the two
111                                 Nuclease and fluorescence correlation spectroscopy (FCS) assays showe
112  about binding to an immobile substrate from fluorescence correlation spectroscopy (FCS) autocorrelat
113 icle, we obtain analytic expressions for the fluorescence correlation spectroscopy (FCS) autocorrelat
114                                In principle, fluorescence correlation spectroscopy (FCS) based method
115       Here, we show, for the first time, how fluorescence correlation spectroscopy (FCS) can be used
116                                              Fluorescence correlation spectroscopy (FCS) can resolve
117                     Here we demonstrate that fluorescence correlation spectroscopy (FCS) combined wit
118 performed (1)H pulsed-field gradient NMR and fluorescence correlation spectroscopy (FCS) experiments
119 f T4 ligase to dsDNA is also confirmed using fluorescence correlation spectroscopy (FCS) experiments,
120              Second, it can be combined with fluorescence correlation spectroscopy (FCS) for simultan
121                              In recent years fluorescence correlation spectroscopy (FCS) has become a
122                                              Fluorescence correlation spectroscopy (FCS) has permitte
123 ), in dissociating the Sp1-DNA complex using fluorescence correlation spectroscopy (FCS) in a microfl
124 ocyanine 540 (MC540), were first analyzed by fluorescence correlation spectroscopy (FCS) in different
125 cal temperature, pH and ionic strength using fluorescence correlation spectroscopy (FCS) in vitro.
126                                              Fluorescence correlation spectroscopy (FCS) is a noninva
127                                              Fluorescence Correlation Spectroscopy (FCS) is a popular
128                                              Fluorescence correlation spectroscopy (FCS) is a powerfu
129                                              Fluorescence correlation spectroscopy (FCS) is a powerfu
130                                              Fluorescence correlation spectroscopy (FCS) is a powerfu
131                                              Fluorescence correlation spectroscopy (FCS) is a sensiti
132 nce recovery after photobleaching (FRAP) and fluorescence correlation spectroscopy (FCS) measurements
133 Forster resonance energy transfer (FRET) and fluorescence correlation spectroscopy (FCS) measurements
134                                              Fluorescence correlation spectroscopy (FCS) methods are
135 d using either fluctuation-based techniques (fluorescence correlation spectroscopy (FCS) or raster-sc
136                                      Imaging fluorescence correlation spectroscopy (FCS) performed us
137 nuous fluorescence microphotolysis (CFM) and fluorescence correlation spectroscopy (FCS) permit measu
138 ividual lipids through a confocal volume via fluorescence correlation spectroscopy (FCS) provide a se
139                   When properly implemented, fluorescence correlation spectroscopy (FCS) reveals nume
140                                  In addition fluorescence correlation spectroscopy (FCS) showed that
141                             We established a fluorescence correlation spectroscopy (FCS) system to me
142                                      We used fluorescence correlation spectroscopy (FCS) to accuratel
143                                        Using fluorescence correlation spectroscopy (FCS) to distingui
144  agonist, ABEA-X-BY630, and the technique of fluorescence correlation spectroscopy (FCS) to investiga
145                                 Here, we use fluorescence correlation spectroscopy (FCS) to probe the
146                                  Here we use fluorescence correlation spectroscopy (FCS) to quantitat
147                                 Here, we use fluorescence correlation spectroscopy (FCS) to show that
148 le photon counting (TCSPC) was combined with fluorescence correlation spectroscopy (FCS) to study the
149 er a commercial instrument could be used for fluorescence correlation spectroscopy (FCS) under pulsed
150                   We develop an extension of fluorescence correlation spectroscopy (FCS) using a spin
151  serum albumin (BSA) into the nanoslits; and fluorescence correlation spectroscopy (FCS) was further
152                                              Fluorescence correlation spectroscopy (FCS) was used to
153                                              Fluorescence correlation spectroscopy (FCS) was used to
154                                              Fluorescence correlation spectroscopy (FCS) was used to
155 ing (high-speed) atomic force microscopy and fluorescence correlation spectroscopy (FCS) we found out
156 present study, this issue was examined using fluorescence correlation spectroscopy (FCS) with photon
157 plexus epithelial cells were evaluated using fluorescence correlation spectroscopy (FCS) with photon
158  to obtain by ensemble measurements, we used fluorescence correlation spectroscopy (FCS), a method th
159  diffusion have relied almost exclusively on fluorescence correlation spectroscopy (FCS), a technique
160 c locations in the nucleus can be studied by fluorescence correlation spectroscopy (FCS), a well-esta
161 aster image correlation spectroscopy (RICS), fluorescence correlation spectroscopy (FCS), and atomic
162                    We have combined TR-FRET, fluorescence correlation spectroscopy (FCS), and biolaye
163 s, with thermophoresis, gel electrophoresis, fluorescence correlation spectroscopy (FCS), and microfl
164                                              Fluorescence correlation spectroscopy (FCS), dynamic lig
165                                              Fluorescence correlation spectroscopy (FCS), fluorescenc
166                                        Using fluorescence correlation spectroscopy (FCS), intermolecu
167                                              Fluorescence correlation spectroscopy (FCS), is a widely
168 nce Recovery After Photobleaching (FRAP) and Fluorescence Correlation Spectroscopy (FCS), obtaining e
169 etic data for several such assays, including Fluorescence Correlation Spectroscopy (FCS), ribosome Ru
170                                        Using fluorescence correlation spectroscopy (FCS), RR1 was sho
171 ce recovery after photobleaching (FRAP), and fluorescence correlation spectroscopy (FCS), to monitor
172 ent adenosine-A3 receptor (A3AR) agonist and fluorescence correlation spectroscopy (FCS), we demonstr
173                                        Using Fluorescence Correlation Spectroscopy (FCS), we have cha
174 thioflavin T (ThT) fluorescence, NMR, EM and fluorescence correlation spectroscopy (FCS), we show tha
175            We address this controversy using fluorescence correlation spectroscopy (FCS), which enabl
176 employed a unique analytical system based on fluorescence correlation spectroscopy (FCS), which measu
177 ce spectroscopy, Circular Dichroism (CD) and Fluorescence Correlation Spectroscopy (FCS).
178 action with chromatin, by spatially resolved fluorescence correlation spectroscopy (FCS).
179 of membrane-bound actin was characterized by fluorescence correlation spectroscopy (FCS).
180 ptides were studied by using single-molecule fluorescence correlation spectroscopy (FCS).
181 bilities in the nucleoplasm as determined by fluorescence correlation spectroscopy (FCS).
182 rophobic anchors and glycan structures using fluorescence correlation spectroscopy (FCS).
183 ated data constitutes a significant issue in fluorescence correlation spectroscopy (FCS).
184 ochelatin-related peptides and studied using fluorescence correlation spectroscopy (FCS).
185 cessible by spectroscopic techniques such as fluorescence correlation spectroscopy (FCS).
186 tive fluorophores at the membrane surface by fluorescence correlation spectroscopy (FCS).
187 gh faster time resolution can be achieved by fluorescence-correlation spectroscopy (FCS), where inten
188               A theory is presented to study fluorescence correlation spectroscopy for particles with
189                                Here we apply fluorescence correlation spectroscopy for quantitative a
190 will find use in the application of FRET and fluorescence correlation spectroscopy for the analysis o
191 ion of Forster Resonance Energy Transfer and Fluorescence Correlation Spectroscopy (FRET-FCS) has a u
192 n of several spectroscopic techniques (e.g., fluorescence correlation spectroscopy, FRET, lifetime qu
193                                              Fluorescence correlation spectroscopy further excluded t
194                                              Fluorescence correlation spectroscopy has been previousl
195                                   Multicolor fluorescence correlation spectroscopy has been recently
196 h as single-particle tracking and nanoscopic fluorescence correlation spectroscopy, has been applied
197 uorescence anisotropy, light scattering, and fluorescence correlation spectroscopy, have not provided
198                     We have extended inverse fluorescence correlation spectroscopy (iFCS) to endow it
199 ane (TM) probes in RBL mast cells by imaging fluorescence correlation spectroscopy (ImFCS).
200 als the number of SecYEG channels counted by fluorescence correlation spectroscopy in a single proteo
201 orescence recovery after photobleaching, and fluorescence correlation spectroscopy in Drosophila mela
202 ter resonance energy transfer and dual-color fluorescence correlation spectroscopy in studies with eG
203              Urease diffusion measured using fluorescence correlation spectroscopy increased by 16-28
204                                    Line-scan fluorescence correlation spectroscopy indicated an essen
205 contain inclusions of HTT, and analysis by a fluorescence correlation spectroscopy indicated that kno
206                 Our results demonstrate that fluorescence correlation spectroscopy is a convenient to
207                       In this paper, imaging-fluorescence-correlation spectroscopy is used to measure
208 n coefficient of Bdp-Chol, as measured using fluorescence correlation spectroscopy, is (7.4 +/- 0.3)
209 ystems by imaging total internal reflection- fluorescence correlation spectroscopy (ITIR-FCS) and mol
210            Imaging total internal reflection fluorescence correlation spectroscopy (ITIR-FCS) is a we
211 tudy using imaging total internal reflection-fluorescence correlation spectroscopy (ITIR-FCS) showed
212 ion depletion microscopy in combination with fluorescence correlation spectroscopy, LYVE-1 diffusion
213 e, independent techniques in parallel (e.g., fluorescence correlation spectroscopy, MALDI-MS, and flu
214  problem by using a combination of live-cell fluorescence correlation spectroscopy, mass spectrometry
215                                              Fluorescence correlation spectroscopy measurements demon
216 nal diffusion coefficients are determined by fluorescence correlation spectroscopy measurements for p
217                                 Accordingly, fluorescence correlation spectroscopy measurements in di
218                                     Parallel fluorescence correlation spectroscopy measurements show
219                    Single point and scanning fluorescence correlation spectroscopy measurements show
220                                 We have used fluorescence correlation spectroscopy measurements to qu
221                                Complementary fluorescence correlation spectroscopy measurements were
222 ents using both ensemble and single-molecule fluorescence correlation spectroscopy measurements.
223                          We have applied the fluorescence correlation spectroscopy methodology to stu
224 study, we addressed these questions by using fluorescence correlation spectroscopy, molecular dynamic
225 s in living cells via multiphoton excitation fluorescence correlation spectroscopy (MPE-FCS).
226                                    Numerical fluorescence correlation spectroscopy (NFCS) involves qu
227                                        Using fluorescence correlation spectroscopy of dye-labeled FTA
228 gyration and hydrodynamic radii estimated by fluorescence correlation spectroscopy of the two coexist
229 of individual HIV-1 particles using scanning fluorescence correlation spectroscopy on a super-resolut
230 and recovery with fructose was analyzed with fluorescence correlation spectroscopy on the level of a
231 ectron microscopy, dynamic light scattering, fluorescence correlation spectroscopy, optical spectrosc
232 ways can be distinguished in single-molecule fluorescence correlation spectroscopy or bulk time-resol
233                                Combined with fluorescence correlation spectroscopy, our probe can sen
234 ow that coupling this dilution strategy with fluorescence correlation spectroscopy permits quantitati
235 ysis (FPA) and photo-induced energy-transfer fluorescence correlation spectroscopy (PET-FCS) to show
236 nsic label by tryptophan in combination with fluorescence correlation spectroscopy (PET-FCS).
237 ng photoinduced electron transfer coupled to fluorescence correlation spectroscopy (PET-FCS).
238 n supported membranes using a combination of fluorescence correlation spectroscopy, photon counting h
239 e Fluorescence Resonance Energy Transfer and Fluorescence Correlation Spectroscopy provide quantitati
240 uorescence recovery after photobleaching and fluorescence correlation spectroscopy provided further e
241  +/- 123 nM by microscale thermophoresis and fluorescence correlation spectroscopy, respectively).
242 transfection, was monitored using Two Photon Fluorescence Correlation Spectroscopy, revealing concent
243 per-resolution STED microscopy with scanning fluorescence correlation spectroscopy (scanning STED-FCS
244                                              Fluorescence correlation spectroscopy served to assess (
245            We have developed a multiconfocal fluorescence correlation spectroscopy setup to measure t
246 n using single plane illumination microscopy-fluorescence correlation spectroscopy (SPIM-FCS), a mult
247 uperresolution STED microscopy combined with fluorescence correlation spectroscopy (STED-FCS) to acce
248 g optical STED nanoscopy in combination with fluorescence correlation spectroscopy (STED-FCS), a tech
249                                      Indeed, fluorescence correlation spectroscopy studies showed bin
250                    In comparison to a recent fluorescence correlation spectroscopy study, we suggest
251 imultaneously performing tens or hundreds of fluorescence correlation spectroscopy-style measurements
252              Rate information (determined by fluorescence correlation spectroscopy) suggests that the
253     In addition, thanks to the multiconfocal fluorescence correlation spectroscopy system, up to five
254      Consistent with this, we found by using fluorescence correlation spectroscopy that a third of di
255 noprecipitation, in vitro cross-linking, and fluorescence correlation spectroscopy that hnRNP E1 bind
256                           We show using FRET-fluorescence correlation spectroscopy that purified T4 g
257                               As revealed by fluorescence correlation spectroscopy, the binding const
258 s at the level of individual molecules using fluorescence correlation spectroscopy, thereby avoiding
259 n, which is not observed at the experimental fluorescence correlation spectroscopy timescales (>100 m
260                    Total internal reflection-fluorescence correlation spectroscopy (TIR-FCS) is an em
261 er-resolution microscopy in combination with fluorescence correlation spectroscopy to assess the char
262 fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy to assess the form
263                                 We performed fluorescence correlation spectroscopy to demonstrate the
264 the overall sizes of large RNAs, we employed fluorescence correlation spectroscopy to examine the hyd
265        We used surface plasmon resonance and fluorescence correlation spectroscopy to examine the int
266 asis for this PC-dependent behavior, we used fluorescence correlation spectroscopy to explore enzyme
267                                       We use fluorescence correlation spectroscopy to investigate bin
268 e, we used imaging total internal reflection-fluorescence correlation spectroscopy to investigate EGF
269 ence resonance energy transfer (SM-FRET) and fluorescence correlation spectroscopy to investigate the
270 n order to explain these effects, we applied fluorescence correlation spectroscopy to investigate the
271 y of the Ran-RCC1 complex in living cells by fluorescence correlation spectroscopy to investigate whe
272                       In this study, we used fluorescence correlation spectroscopy to monitor the bin
273 fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy to study functiona
274 uorescence recovery after photobleaching and fluorescence correlation spectroscopy, to examine the dy
275 t analysis spectroscopy, in combination with fluorescence correlation spectroscopy, to follow the pop
276 tilize a novel technique, ultrafast-scanning fluorescence correlation spectroscopy, to measure the mo
277  we use a single-molecule optical technique--fluorescence correlation spectroscopy--to probe the dena
278    We show that in comparison to traditional fluorescence correlation spectroscopy, tracking provides
279 ics of PLC-beta3 binding to Galphaq FRET and fluorescence correlation spectroscopy, two physically di
280    Time-resolved absorption spectroscopy and fluorescence correlation spectroscopy verify that, unlik
281  developed a method of performing near-field fluorescence correlation spectroscopy via an array of pl
282 l approach combining photon antibunching and fluorescence correlation spectroscopy was used to confir
283                   Simultaneous homo-FRET and fluorescence correlation spectroscopy was used to detect
284                                              Fluorescence correlation spectroscopy was used to quanti
285 stem region for the liposome, as measured by fluorescence correlation spectroscopy, was also increase
286 ion magic angle spinning NMR as well as with fluorescence correlation spectroscopy we demonstrate tha
287                    By pairing split-GFP with fluorescence correlation spectroscopy, we compared the c
288                                        Using fluorescence correlation spectroscopy, we determined tha
289              Using total internal reflection-fluorescence correlation spectroscopy, we examined the v
290                                        Using fluorescence correlation spectroscopy, we measure the di
291                                        Using fluorescence correlation spectroscopy, we measured a dis
292               Using fluorescence imaging and fluorescence correlation spectroscopy, we measured the C
293                                        Using fluorescence correlation spectroscopy, we monitor the fo
294            Using static light scattering and fluorescence correlation spectroscopy, we monitored the
295                                        Using fluorescence correlation spectroscopy, we observed that
296 roscopy, biochemical interaction studies and fluorescence correlation spectroscopy, we show that in l
297                                        Using fluorescence correlation spectroscopy, we show that the
298                 By means of two-color z-scan fluorescence correlation spectroscopy, we show that the
299 alphaS bound to planar membranes measured by fluorescence correlation spectroscopy were correlated.
300  Here, we present a robust approach based on fluorescence correlation spectroscopy with ultra-high sp

 
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