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1 tricular myocytes by using a light-sensitive caged compound.
2 tinuous irradiation of cells loaded with the caged compound.
3 gh the photolytic release of substrates from caged compounds.
4 ents and the loading with indicator dyes and caged compounds.
5 rategy for spatially localized photolysis of caged compounds.
6 hange and a pulsed laser system for uncaging caged compounds.
7 th sufficient sensitivity to 2PE for use in "caged" compounds.
8 m laser light, the glycine released from the caged compound activates glycine-mediated whole-cell cur
9 mooth muscle cells using local photolysis of caged compounds and Ca2+ imaging.
10                The increased availability of caged compounds and of the technologies required to expl
11  patch clamp technique was used to introduce caged compounds and to record the activity of a Ca(2+)-a
12 mit UV light locally, for photoactivation of caged compounds and, in particular, used for photo-contr
13                                              Caged compounds are a valuable tool to photocontrol the
14                                              Caged compounds are biologically inert signaling molecul
15                                              Caged compounds are light-sensitive probes that function
16                                              Caged compounds are molecules rendered functionally iner
17                                              Caged compounds are molecules that release a protective
18                     Since many nitroaromatic caged compounds are two-photon active at 720 nm, optical
19 or-channels on neurons equilibrated with the caged compound, as detected by whole-cell current record
20              Owing to the success of several caged compounds based on ruthenium complexes, we synthes
21 we synthesized a family of light-activatable caged compounds by attaching o-nitrobenzyl (o-NB) or cou
22                                     Although caged compounds continue to be used primarily for mechan
23 photolysis of many widely used nitroaromatic caged compounds (e.g., 4-carboxymethoxy-5,7-dinitroindol
24 337 or 360 nm light, were performed with the caged compound equilibrated with HEK 293 cells transient
25 oscopy, showing that the 2'-phosphate of the caged compound exhibits an altered chemical shift of -2.
26  basic properties required to make effective caged compounds for the biological sciences.
27        To test this hypothesis without using caged compounds, force responses and individual sarcomer
28                                          The caged compound has a major absorption band with a maximu
29                                          The caged compound has a major absorption band with a maximu
30                               Photosensitive caged compounds have enhanced our ability to address the
31 f formation of the photolysis product from a caged compound in the microsecond time scale.
32 zed excitation can be used for photolysis of caged compounds in femtoliter volumes and for diffusion
33 otic response induced by flash photolysis of caged compounds in isolated mast cells and chromaffin ce
34 sue through nonlinear scattering, or release caged compounds in sub-femtoliter volumes.
35                                   We compare caged-compound-induced reactions monitored by FTIR and d
36 validate that the inhibitory activity of the caged compound is dependent on exposure to light.
37                                   This novel caged compound is synthesized efficiently, is stable in
38                                Photolysis of caged compounds is a powerful tool for studying subcellu
39 o probe the photolysis mechanism of one such caged compound, namely gamma-(alpha-carboxy-2-nitrobenzy
40 me the in situ electrochemical monitoring of caged compound photochemistry in brain tissue with FSCV,
41                                         Such caged compounds play an important role in transient kine
42 have recently utilized a new ruthenium-based caged compound, ruthenium-bipyridine-triphenylphosphine-
43                                          All caged compounds showed the expected decrease in binding
44  not need a standard and can be used for any caged compounds that present different emission properti
45 ient than photolysis of the most widely used caged compounds (the quantum yield of photolysis is 0.7
46 I describe important examples of widely used caged compounds, their design features and synthesis, as
47                     Importantly, the cloaked caged compound was biologically inert at the high concen
48                            The catalytically caged compound was synthesized in a two-step process, st
49 ince the first example of a light-activated (caged) compound was described.
50 ed to striatal cholinergic interneurons, the caged compounds were photolyzed in an chromatically orth
51 of nonrepetitive reactions, e.g., induced by caged compounds, were limited to the millisecond time do
52 ultiple pathways, use of (thio)-coumarin-102 caged compounds will enable arbitrarily timed flashes of
53                                 Such cloaked caged compounds will enable the study of the signaling o
54              We combined local photolysis of caged compounds with fluorescence imaging to visualize m