ライフサイエンスコーパス: uncaging of

1 ngs, elevation of intracellular Ca(2+) by UV uncaging of 1-(4,5-dimethoxy-2-nitrophenyl)-EDTA-potenti

2 On the other hand, two-photon uncaging of 4-methoxy-7-nitroindolinyl-caged L-glutamate

3 ventricles of live zebrafish by means of the uncaging of a fluorescein derivative.

4 small groups of cells in this area by laser uncaging of a fluorescent dextran, and then tracked thei

5 f techniques by demonstrating the mechanical uncaging of a reactive species within a single protein.

6 a rapid decrease in pH that accompanies the "uncaging" of an effector molecule from o-nitrobenzaldehy

7 Photochemical uncaging of bio-active molecules was introduced in 1977,

8 Photochemical release (uncaging) of bioactive messengers with three-dimensional

9 Uncaging of bis-CNB-GABA evokes inward GABAergic current

10 Localized photolytic uncaging of Ca(2+) from o-nitrophenyl-EGTA in somatic ER

11 r NP-EGTA, the UV flash photolysis-catalysed uncaging of Ca(2+) generated CICR in only 9% of the beta

12 hondria were activated specifically by local uncaging of Ca(2+) in the nucleus.

13 c myocytes, where either one- and two-photon uncaging of Ca(2+) induced highly local or cell-wide phy

14 Here, we utilize the photo-uncaging of Ca(2+) with CaV 2.1 channels fluxing Li(+) c

15 nd FAK inhibits repulsive turning from focal uncaging of Ca(2+) within filopodia.

16 thereby allowing CICR to be generated by the uncaging of Ca2+ (UV flash photolysis).

17 Because the uncaging of Ca2+ fails to stimulate CICR in the absence

18 In the apical region, local uncaging of Ca2+ was able to trigger a CICR wave, which

19 is retraction was prevented locally by focal uncaging of caged Ca(2+) that triggered Ca(2+) release f

20 f intact pancreatic acinar cells using local uncaging of caged Ca2+.

21 y carbacyclin-stimulated elevations in cAMP, uncaging of cAMP or exposure to a high concentration of

22 photon active at 720 nm, optically selective uncaging of DEAC450-caged biomolecules at 900 nm may all

23 Two-photon uncaging of DEAC450-Glu at 900 nm at spine heads on pyra

24 The synthesis and uncaging of dendrimer- and polymeric bead-based model sy

25 Uncaging of DMn is considerably faster, but DMn has a si

26 ution using optically independent two-photon uncaging of each neurotransmitter.

27 exhibited direct (non-synaptic) responses to uncaging of excitatory and inhibitory transmitters.

28 Two-photon uncaging of fluorescein near nonsuperfused gastric surfa

29 Using uncaging of GABA, there is a decreasing GABAergic influe

30 his electrical filtering, we used two-photon uncaging of glutamate and compared the integration of el

31 photon imaging, optogenetics, and dual-color uncaging of glutamate and GABA, we demonstrate that plat

32 t is accomplished using UV laser-based photo-uncaging of glutamate and imaging neuronal activation by

33 Laser-scanning photo-uncaging of glutamate focally activated neurons in layer

34 d two recently developed methods, two-photon uncaging of glutamate for determining the EPSC of indivi

35 Moreover, activation of MOPP cells by focal uncaging of glutamate induced strong inhibition of granu

36 Using two-photon uncaging of glutamate on spine heads from mouse layer-5

37 ) on depolarizations generated by two-photon uncaging of glutamate on spines from mouse neocortical p

38 ut screening method exploiting laser-induced uncaging of glutamate to construct excitatory input maps

39 Here, we use two-photon laser uncaging of glutamate to directly activate glutamate rec

40 Focal uncaging of glutamate, accomplished by switching a pulse

41 hoton laser scanning microscopy and 2-photon uncaging of glutamate, Carter and Sabatini (this issue o

42 ation of EPSPs, generated through two-photon uncaging of glutamate, this action was largely shunted b

43 ser scanning microscopy and two-photon laser uncaging of glutamate, we show that SK channels regulate

44 ser-scanning microscopy and two-photon laser uncaging of glutamate.

45 g iontophoresis of l-aspartate or two-photon uncaging of glutamate.

46 Uncaging of glycerophosphoryl-myo-inositol 4,5-bisphosph

47 ereas postsynaptic stores (activated by spot-uncaging of inositol 1,4,5-trisphosphate) remain unaffec

48 ith UDP-GlcNAc had an attenuated response to uncaging of InsP3.

49 eover, the Ca(2+) responses to melatonin and uncaging of IP(3) were mutually exclusive in infected RB

50 Photo-uncaging of IP3 in neurons expressing PI3K* elicits a ma

51 ow-intensity tetanic synaptic stimulation or uncaging of IP3 increased the decay time of spontaneous

52 On uncaging of IP3, astrocyte Ca2+ responses reliably propa

53 Furthermore, uncaging of MNI glutamate reveals that thalamocortical n

54 Two-photon (2P) uncaging of MNI-glutamate onto individual spines suggest

55 ary spatiotemporal pattern, using two-photon uncaging of MNI-glutamate with beam multiplexing.

56 Photolytic uncaging of p-hydroxyphenacyl (pHP) GABA demonstrates ba

57 of presynaptic GABA receptors by photolytic uncaging of RuBi-GABA has a biphasic effect on EPSC ampl

58 (520 mum) by excitability testing and focal uncaging of RuBi-GABA on the axon at varying distances f

59 le-cell patch-clamp recording and photolytic uncaging of RuBi-GABA.

60 nitrodibenzofuran (NDBF) for ultra-efficient uncaging of second messengers inside cells.

61 Thus, optical uncaging of signaling lipids can uncover their rapid eff

62 Further, uncaging of Sph leads to the translocation of the autoph

63 micropatterns by means of photolithographic uncaging of surface amines.

64 on as well as pinpoint the location at which uncaging of the molecules occurred.

65 aling lipids sphingosine and diacylglycerol; uncaging of the probe for these two species triggered ca

66 In addition, through uncaging of the same compound, gene expression is contro