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1 hrough the evanescent wave contribute to the fluorescence fluctuations.
2 ent Dronpa can nevertheless enhance TagRFP-T fluorescence fluctuations.
3 scopes, acquiring videos in which we analyze fluorescence fluctuations.
4 eatly depend on the characteristics of these fluorescence fluctuations.
5 ng correlation analysis of extrinsic oxazine fluorescence fluctuations.
6  separations, we find significant long-lived fluorescence fluctuations among discrete levels originat
7 (PCH) analysis describes the distribution of fluorescence fluctuation amplitudes due to populations o
8                                Here, we used fluorescence fluctuation analyses to quantitatively expl
9  Our approach is based on the application of fluorescence fluctuation analysis (FFA) and multiangle l
10 atography for the isolation and a model-free fluorescence fluctuation analysis for the investigation
11                Moreover, individual-eisosome fluorescence fluctuation analysis shows that eisosomes i
12 le RNA and protein detection with two-photon fluorescence fluctuation analysis to measure the average
13                            Here we show that fluorescence-fluctuation analysis of raster scans at var
14                         In this work we used fluorescence fluctuation analytical methods to determine
15 dsorbed on a semiconductor NP surface showed fluorescence fluctuations and blinking, with time consta
16 ugmented iFCS with an analysis of moments of fluorescence fluctuations and used it to measure stages
17 hrough the evanescent wave contribute to the fluorescence fluctuations, and when fluorescent and nonf
18 ions microscopy, and we also briefly address fluorescence fluctuation approaches, notably raster imag
19                              Using different fluorescence fluctuation approaches, we established that
20       Fluorophores with stochastic and rapid fluorescence fluctuations are favorable for improving SO
21 e fluorescence observation volume from which fluorescence fluctuations are measured, even at relative
22 eo microscopy experiments allow detection of fluorescence fluctuations at the timescales approaching
23 mpose a brief (few-second-long) trace of the fluorescence fluctuations, at each point in a cell, into
24                                          The fluorescence fluctuation autocorrelation function depend
25                        An expression for the fluorescence fluctuation autocorrelation function in the
26              Theoretical expressions for the fluorescence fluctuation autocorrelation function when b
27                                              Fluorescence fluctuation autocorrelation functions were
28    Here, we present an analysis of resonance fluorescence fluctuations based on photon counting stati
29         Through these quantities, we build a fluorescence-fluctuation-based diffusion tensor that con
30  a novel tool for extracting quantities from fluorescence fluctuation data, i.e., the measured photon
31                              Using simulated fluorescence fluctuation data, we find the BCa method to
32    We introduce a new analysis technique for fluorescence fluctuation data.
33 onstrate that the theory successfully models fluorescence fluctuation data.
34  a DNA hairpin in gels, we directly observed fluorescence fluctuations due to conformational intercon
35                                          The fluorescence fluctuation dynamics were found to be inhom
36 milarly, the autocorrelation function of the fluorescence fluctuations exhibited unexpected changes w
37                              Most dual-color fluorescence fluctuation experiments are performed on fl
38                       Brightness analysis of fluorescence fluctuation experiments has been used to su
39 alysis and identify the optimal position for fluorescence fluctuation experiments in the capillary.
40        A novel technique for the analysis of fluorescence fluctuation experiments is introduced.
41 that the contribution of autofluorescence to fluorescence fluctuation experiments is negligible at EG
42                         Lastly, we performed fluorescence fluctuation experiments on cells expressing
43             The photon counting histogram of fluorescence fluctuation experiments, in which few molec
44  analyzing the fluctuation amplitude g(0) of fluorescence fluctuation experiments.
45 at describes the effects of sampling time on fluorescence fluctuation experiments.
46 ross-correlation function was applied to the fluorescence fluctuation from these two positions to cap
47 t of an approach in which the pixel-to-pixel fluorescence fluctuations from a single fluorescence ima
48 xes based on the analysis of single molecule fluorescence fluctuations from laser scanning confocal i
49 technique is based on brightness analysis of fluorescence fluctuations from three fluorescent protein
50                                              Fluorescence fluctuations, generated by trans-cis isomer
51 nescent wave, in solution, contribute to the fluorescence fluctuations have been published previously
52                 Here we describe an enhanced fluorescence fluctuation imaging analysis, which employs
53                                              Fluorescence fluctuation imaging is a powerful means to
54 ight's behavior, including millisecond-scale fluorescence fluctuations in single molecules as well as
55                              Building on the fluorescence fluctuation increase by contact (FLINC) pri
56          The intensity distribution of these fluorescence fluctuations is experimentally captured by
57                                    We report fluorescence fluctuation measurements of enhanced GFP (E
58 opy with advanced image-processing tools and fluorescence fluctuation methods and distinguished three
59                                 We introduce fluorescence fluctuation methods to determine, at high s
60    We used a unique method based on 2-photon fluorescence fluctuation microscopy to measure directly,
61 ng coimmunoprecipitation, cross-linking, and fluorescence fluctuation microscopy, we show that HS doe
62 ctional GFP-Mrr fusion protein using in vivo fluorescence fluctuation microscopy.
63                                              Fluorescence fluctuations occurring between two FRET sta
64 novel sensing strategy using aptamer-induced fluorescence fluctuation of graphene quantum dots (GQDs)
65 ) at equilibrium on a local scale, analyzing fluorescence fluctuations of individual pH-sensitive flu
66 y enhances the image resolution by analyzing fluorescence fluctuations over time.
67                                         Such fluorescence fluctuation patterns may contain informatio
68 f particle brightness and concentration from fluorescence-fluctuation photon-counting statistics usin
69                            The brightness of fluorescence fluctuations provides information about pro
70 al volume changes that produce an additional fluorescence fluctuation signal for luminal, but not for
71            This work investigates the use of fluorescence fluctuation spectroscopy (FFS) as a tool fo
72 rom immobile sources present a challenge for fluorescence fluctuation spectroscopy (FFS) because the
73                                              Fluorescence fluctuation spectroscopy (FFS) has recently
74 of bright particles at low concentrations by fluorescence fluctuation spectroscopy (FFS) is challengi
75 ubtypes and their G-proteins using two-color fluorescence fluctuation spectroscopy (FFS) of mouse MIN
76                                              Fluorescence fluctuation spectroscopy (FFS) quantifies i
77                                              Fluorescence fluctuation spectroscopy (FFS) quantifies t
78 RF) microscopy and a series of complementary Fluorescence Fluctuation Spectroscopy (FFS) techniques.
79                       In this study, we used fluorescence fluctuation spectroscopy (FFS) to evaluate
80 tein mCherry is of considerable interest for fluorescence fluctuation spectroscopy (FFS), because the
81                  Here, we present results of fluorescence fluctuation spectroscopy analyses indicatin
82 ess-transit statistics (BTS) method based on fluorescence fluctuation spectroscopy and combine inform
83                                              Fluorescence fluctuation spectroscopy can be used to mea
84 escence cumulant analysis (TIFCA) to analyze fluorescence fluctuation spectroscopy data.
85                                              Fluorescence fluctuation spectroscopy determines the bri
86                                              Fluorescence fluctuation spectroscopy experiments were c
87                                              Fluorescence fluctuation spectroscopy has become an impo
88            In particular, dual-color, z-scan fluorescence fluctuation spectroscopy in conjunction wit
89  of protein heterointeractions by dual-color fluorescence fluctuation spectroscopy in living cells.
90                           In addition, using fluorescence fluctuation spectroscopy in single living c
91                                     Although fluorescence fluctuation spectroscopy is a powerful tool
92 nsity scan through the sample, followed by a fluorescence fluctuation spectroscopy measurement at eac
93                           Here, we develop a fluorescence fluctuation spectroscopy method using self-
94  was recently demonstrated that conventional fluorescence fluctuation spectroscopy methods are not su
95                                   Dual-color fluorescence fluctuation spectroscopy provides a general
96                                              Fluorescence fluctuation spectroscopy provides a powerfu
97                                              Fluorescence fluctuation spectroscopy provides informati
98    Here, we use a newly developed multipoint fluorescence fluctuation spectroscopy technique to study
99 internal reflection fluorescence microscopy, fluorescence fluctuation spectroscopy techniques, and th
100 in living human embryonic kidney cells using fluorescence fluctuation spectroscopy techniques, namely
101 ultipoint moment analysis (TIMMA), a form of fluorescence fluctuation spectroscopy that is capable of
102 ) Gag protein expressed in COS-1 cells using fluorescence fluctuation spectroscopy to determine the s
103                                Here, we used fluorescence fluctuation spectroscopy to directly detect
104                             Here, we applied fluorescence fluctuation spectroscopy to quantitatively
105 report the first experimental realization of fluorescence fluctuation spectroscopy under high pressur
106                                              Fluorescence fluctuation spectroscopy utilizes the signa
107 NE proteins in their native environment with fluorescence fluctuation spectroscopy, these studies rai
108 ocorrelation function, traditionally used in fluorescence fluctuation spectroscopy, which separates a
109 ion-dependent dimerization of p85alpha using fluorescence fluctuation spectroscopy.
110 ging environment for brightness studies with fluorescence fluctuation spectroscopy.
111 otropy, and in living cells using two-photon fluorescence fluctuation spectroscopy.
112 ed phenomena may be of broader importance in fluorescence fluctuation spectroscopy.
113 n-dependent number and brightness (cdN&B), a fluorescence fluctuation technique that can be implement
114               In contrast, three established fluorescence fluctuation techniques (FCS, FCCS, and PCH)
115                                        Using fluorescence fluctuation techniques (photon-counting his
116 of a tBid monomer, measured separately using fluorescence fluctuation techniques.
117                                 We attribute fluorescence fluctuations to the interfacial ET reaction
118      Correlation analysis of single-molecule fluorescence fluctuations uncovered site-dependent nanos
119     We argue that spatiotemporal analysis of fluorescence fluctuations using multiple detection chann
120 protein-protein interactions into changes in fluorescence fluctuations, which are quantifiable throug
121                          Finally, we observe fluorescence fluctuations with a correlation time of ove
122 ume and analyze the temporal behavior of the fluorescence fluctuations within the stationary observat

 
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