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1 isolated perfused lungs by a pleural surface fluorescence method.
2 tion coupling was investigated using a novel fluorescence method.
3 newborn rabbit lungs using a pleural surface fluorescence method.
4 icroscopy and by a total internal reflection fluorescence method.
5  excellent correlation with a referee CRISPR fluorescence method.
6 obe technique, and by the two-photon excited fluorescence method.
7 he performance is comparable to the benchtop fluorescence method.
8 uction was measured with an ethidium bromide fluorescence method.
9 ycline uptake was assayed at 37 degrees by a fluorescence method.
10 e ligands could be characterized directly by fluorescence methods.
11 estigated using rapid mixing and equilibrium fluorescence methods.
12 rying solvent conditions, using stopped-flow fluorescence methods.
13 membranes of varying lipid composition using fluorescence methods.
14 zation by leveraging the high sensitivity of fluorescence methods.
15 instrument or even the best super-resolution fluorescence methods.
16 ens of seconds) approaching those of speckle fluorescence methods.
17 in vapor, solution, and solid states through fluorescence methods.
18  with a lag phase, as observed previously by fluorescence methods.
19 well as for the metrological traceability of fluorescence methods.
20 troscopy (XPS), atomic force microscopy, and fluorescence methods.
21 osomal conformation during translation using fluorescence methods.
22 a using stopped-flow, circular dichroism and fluorescence methods.
23 noglycosides to be characterized directly by fluorescence methods.
24  the red cell membrane by centrifugation and fluorescence methods.
25                          By using the fura-2 fluorescence method, a difference in the kinetics of Ca2
26    The present work proposes a new UHPLC-PDA-fluorescence method able to identify and quantify the ma
27                                    Using the fluorescence method, accelerated TPT release was observe
28  to be consistent with previous results from fluorescence methods, although new features are found.
29                 We have used two independent fluorescence methods and confocal microscopy to show tha
30                    Here, combining live-cell fluorescence methods and kinetic modeling, we demonstrat
31 ariety of solution conditions using in vitro fluorescence methods and molecular dynamics (MD) simulat
32 (JATP; derived with a low oxygen/chlorophyll fluorescence method), and carbon isotope discrimination
33 n molecular reactions relies increasingly on fluorescence methods, and there is a demand for more sen
34              In contrast, recently developed fluorescence methods are continuous and convenient.
35                         In particular, burst fluorescence methods are exploited to observe metal-ion
36                     Optical sensors based on fluorescence methods are used in numerous areas of socie
37                                              Fluorescence methods are versatile tools for obtaining d
38 antitative conventional and super-resolution fluorescence methods, as well as mathematical modeling,
39                                            A fluorescence method based on changes in an extrinsic pro
40                               We developed a fluorescence method based on the oxymercuration of vinyl
41                                      Using a fluorescence method called colocalization single-molecul
42                Here, we improve and extend a fluorescence method called transition metal ion FRET tha
43 ck pairing, suggesting that this homogeneous fluorescence method can be used for all single-base mism
44                                         This fluorescence method can be used to determine pK(a)'s for
45 f a two-wavelength total internal reflection fluorescence method capable of real-time imaging of cell
46 < 0.01) suggesting that our novel microplate fluorescence method could be applied for the fast live/d
47                                              Fluorescence methods demonstrate that the N-terminal, bu
48                     Several well-established fluorescence methods depend on environment-sensitive pro
49         The results were consistent with the fluorescence method described above.
50                                          The fluorescence methods employed the single tryptophan resi
51  5-HT3AB receptors on the plasma membrane by fluorescence methods, employing meCFP- and meYFP-labeled
52 y applicable to any sensitive, laser-induced fluorescence method for detection of nucleic acids.
53                                      A novel fluorescence method for determining the depth of Trp res
54                                            A fluorescence method for measuring the effective concentr
55      We previously developed and validated a fluorescence method for monitoring the cis-trans isomeri
56             Here, we report a kinetics-based fluorescence method for quantitative tracking of peroxyn
57 n vitro, enabled by the development of a new fluorescence method for studying substrate transport kin
58                This work presents an on-line fluorescence method for the allura red (AR) determinatio
59                                     Previous fluorescence methods for assaying DNA glycosylases are o
60 interactions in these LUVs were monitored by fluorescence methods for content leakage, and contents m
61 ustrates the effectiveness of confocal X-ray fluorescence methods for investigating trace element dis
62                                   We use two fluorescence methods, Forster Resonance Energy Transfer
63                                  However, no fluorescence method has been developed for single-strand
64                         Single-molecule (SM) fluorescence methods have been increasingly instrumental
65                                Time-resolved fluorescence methods have been used to show that 8-hydro
66 uction two decades ago, single-molecule (SM) fluorescence methods have matured and branched out to ad
67 lular lead uptake were characterized using a fluorescence method in cells loaded with indo-1.
68                              Using the novel fluorescence method in the beating heart, we have shown
69  aequorin luminescence method and the fura-2 fluorescence method in two transfected mammalian cell sy
70 ility, measured by a related pleural surface fluorescence method in which the airspace was filled wit
71 in permeability, measured using a dual-label fluorescence method, in skin and skeletal muscle compare
72                             With ratiometric fluorescence methods (indo-5F as the Ca2+ probe), the mi
73              In this work, a single-molecule fluorescence method is developed for measuring the kinet
74                                      Here, a fluorescence method is displayed using an energy-dispers
75 tion of nanomaterials in complex matrices by fluorescence methods is complicated by photodegradation,
76          Using stopped-flow and steady-state fluorescence methods, kinetic substrate isotope effects,
77                                  A real-time fluorescence method measured the time required by molecu
78                                   The simple fluorescence method of determining clonality of metastas
79                                         This fluorescence method potentially provides a rapid, easy t
80                                       Unlike fluorescence methods, Raman detection benefits from the
81 were quantified by absorption (NanoDrop) and fluorescence methods (RiboGreen) prior to dilution in bu
82                                              Fluorescence methods showed that hairpin-disrupting Gly
83  we provide an overview of a single molecule fluorescence method, termed "protein induced fluorescenc
84                 We describe a solution-based fluorescence method that discriminates between wild-type
85  hybrids were examined by chromatography and fluorescence methods that attested to the integrity of h
86 cribe bulk steady state and pre-steady state fluorescence methods that enabled us to quantitatively e
87 eavy meromyosin was investigated using three fluorescence methods that monitor the number of heavy me
88 tudies, we find, using real time equilibrium fluorescence methods, that alpha-synuclein binds strongl
89 uences derived from the DIS(Mal) variant and fluorescence methods, the two DIS dimer isoforms have be
90           We describe a simple but sensitive fluorescence method to accurately detect the esterificat
91                                Using a novel fluorescence method to assay NKCC1 activity in single ce
92          Herein, we employ a single-molecule fluorescence method to assess the dynamics of the inter-
93 apparatus, we implement a recently described fluorescence method to characterize the adsorption/desor
94                          We have developed a fluorescence method to examine how membrane sterol later
95     We previously reported a pleural surface fluorescence method to measure net capillary-to-airspace
96                                 We present a fluorescence method to selectively image mitochondrial d
97 n covalently tethered hexamers together with fluorescence methods to assay the conformations and nucl
98  mouse collecting ducts with biochemical and fluorescence methods to demonstrate an acute stimulation
99 easured using sequential-mixing stopped-flow fluorescence methods to determine the contribution of ea
100                           Here, we have used fluorescence methods to determine the effect of caveolae
101                           Here, we have used fluorescence methods to directly test this idea by asses
102 e, we combine structural and single molecule fluorescence methods to examine how PRC1, the human MAP6
103                  Here we use single-molecule fluorescence methods to guide the capture of structures
104 rpose of this study was to establish in situ fluorescence methods to measure tear film ionic concentr
105 neous conclusions and in part by the lack of fluorescence methods to monitor each individual step.
106                  We employed single-molecule fluorescence methods to probe the dynamic relation of th
107 sue by applying ensemble and single-molecule fluorescence methods to study the process of kinesin ste
108 l capabilities of the total-reflection X-ray fluorescence method (TXRF) were considered for the analy
109 nic phosphate (Pi) release was measured by a fluorescence method using a coumarin-labelled phosphate
110 ns were determined by the two-photon induced fluorescence method using both femtosecond and nanosecon
111                By comparison, solution-based fluorescence methods using sequence-specific probes are
112 idation products was confirmed that the DPPP fluorescence method was accurate and reliable at differe
113                             Thus, "turn-off" fluorescence method was applied for ultrasensitive detec
114                                   An in situ fluorescence method was applied to measure the ionic com
115                               A non-invasive fluorescence method was developed to monitor liposomal r
116 e device for the detection of NO(2)(-) via a fluorescence method was developed.
117 fluid-filled rat lung by the pleural surface fluorescence method was high (0.019 +/- 0.004 cm/s at 12
118                     A sensitive quantitative fluorescence method was used to explore the time course
119                               A quantitative fluorescence method was used to test the hypothesis that
120                   Thus, we conclude that the fluorescence method we developed provides a reliable det
121                                Using a novel fluorescence method, we detected target-directed release
122          In this study, using a stopped-flow fluorescence method, we examined the kinetic impact of D
123                 Here, using the stopped-flow fluorescence method, we measured the target search kinet
124                 Using cell fractionation and fluorescence methods, we demonstrate that the early endo
125                                        Using fluorescence methods, we determined that apoA-II binding
126                        Using single-molecule fluorescence methods, we found complex structural dynami
127                          Specifically, using fluorescence methods, we have determined the interaction
128         Using steady-state and time-resolved fluorescence methods, we now show that these excitation
129 analytical sedimentation and single molecule fluorescence methods, we show that a PriC dimer activate
130  combination of ensemble and single-molecule fluorescence methods, we show that the MuA tetramer can
131                           Using quantitative fluorescence methods, we studied the assembly and dynami
132 anate and DPPP (diphenyl-1-pyrenylphosphine) fluorescence methods were comparatively examined to dete
133                                              Fluorescence methods were developed to quantify membrane
134         Temperature-jump and continuous-flow fluorescence methods were used to measure the folding ki
135                                              Fluorescence methods were utilized to study dynamic aspe
136 es, including circular dichroism and various fluorescence methods, were used to examine the propertie
137 illisecond time resolution suggest that this fluorescence method will be useful for following the kin
138 sing laser temperature jump and stopped-flow fluorescence methods with U1A proteins labeled with the
139 t can then be readily monitored by sensitive fluorescence methods without the need to add exogenous f

 
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