ライフサイエンスコーパス: caged compound

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

1 tricular myocytes by using a light-sensitive caged compound.

2 tinuous irradiation of cells loaded with the caged compound.

3 ents and the loading with indicator dyes and caged compounds.

4 gh the photolytic release of substrates from caged compounds.

5 hange and a pulsed laser system for uncaging caged compounds.

6 rategy for spatially localized photolysis of 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 light-sensitive probes that function

14 Caged compounds are molecules rendered functionally iner

15 Since many nitroaromatic caged compounds are two-photon active at 720 nm, optical

16 or-channels on neurons equilibrated with the caged compound, as detected by whole-cell current record

17 Although caged compounds continue to be used primarily for mechan

18 photolysis of many widely used nitroaromatic caged compounds (e.g., 4-carboxymethoxy-5,7-dinitroindol

19 337 or 360 nm light, were performed with the caged compound equilibrated with HEK 293 cells transient

20 oscopy, showing that the 2'-phosphate of the caged compound exhibits an altered chemical shift of -2.

21 To test this hypothesis without using caged compounds, force responses and individual sarcomer

22 The caged compound has a major absorption band with a maximu

23 The caged compound has a major absorption band with a maximu

24 Photosensitive caged compounds have enhanced our ability to address the

25 f formation of the photolysis product from a caged compound in the microsecond time scale.

26 zed excitation can be used for photolysis of caged compounds in femtoliter volumes and for diffusion

27 otic response induced by flash photolysis of caged compounds in isolated mast cells and chromaffin ce

28 sue through nonlinear scattering, or release caged compounds in sub-femtoliter volumes.

29 validate that the inhibitory activity of the caged compound is dependent on exposure to light.

30 Photolysis of caged compounds is a powerful tool for studying subcellu

31 o probe the photolysis mechanism of one such caged compound, namely gamma-(alpha-carboxy-2-nitrobenzy

32 Such caged compounds play an important role in transient kine

33 have recently utilized a new ruthenium-based caged compound, ruthenium-bipyridine-triphenylphosphine-

34 ient than photolysis of the most widely used caged compounds (the quantum yield of photolysis is 0.7

35 I describe important examples of widely used caged compounds, their design features and synthesis, as

36 The catalytically caged compound was synthesized in a two-step process, st

37 ed to striatal cholinergic interneurons, the caged compounds were photolyzed in an chromatically orth

38 Such cloaked caged compounds will enable the study of the signaling o

39 We combined local photolysis of caged compounds with fluorescence imaging to visualize m

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。