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1                                 Furthermore, uncaging of 1,5-(PP)(2)-InsP(4) but not 3,5-(PP)(2)-InsP
2 ngs, elevation of intracellular Ca(2+) by UV uncaging of 1-(4,5-dimethoxy-2-nitrophenyl)-EDTA-potenti
3                                        After uncaging of 2-AG, we monitored calcium levels, CB1-GIRK
4                On the other hand, two-photon uncaging of 4-methoxy-7-nitroindolinyl-caged L-glutamate
5 ty that kills cancer cells via photochemical uncaging of a cytotoxic drug.
6 ventricles of live zebrafish by means of the uncaging of a fluorescein derivative.
7  small groups of cells in this area by laser uncaging of a fluorescent dextran, and then tracked thei
8 membrane-associated dimeric protein with the uncaging of a powerful cytotoxic.
9 f techniques by demonstrating the mechanical uncaging of a reactive species within a single protein.
10 ances the templated reaction and enables the uncaging of a substrate.
11 ontrollable strategy via the photo-patterned uncaging of an o-nitrobenzyl-caged fluorescein conjugate
12 a rapid decrease in pH that accompanies the "uncaging" of an effector molecule from o-nitrobenzaldehy
13                                Photochemical uncaging of bio-active molecules was introduced in 1977,
14                       Photochemical release (uncaging) of bioactive messengers with three-dimensional
15                                              Uncaging of bis-CNB-GABA evokes inward GABAergic current
16                         Localized photolytic uncaging of Ca(2+) from o-nitrophenyl-EGTA in somatic ER
17 r NP-EGTA, the UV flash photolysis-catalysed uncaging of Ca(2+) generated CICR in only 9% of the beta
18 hondria were activated specifically by local uncaging of Ca(2+) in the nucleus.
19 c myocytes, where either one- and two-photon uncaging of Ca(2+) induced highly local or cell-wide phy
20                   Here, we utilize the photo-uncaging of Ca(2+) with CaV 2.1 channels fluxing Li(+) c
21 nd FAK inhibits repulsive turning from focal uncaging of Ca(2+) within filopodia.
22 thereby allowing CICR to be generated by the uncaging of Ca2+ (UV flash photolysis).
23                                  Because the uncaging of Ca2+ fails to stimulate CICR in the absence
24                  In the apical region, local uncaging of Ca2+ was able to trigger a CICR wave, which
25 glucose or high K+ stimulation or the global uncaging of Ca2+, we show granule fusion consistently fo
26 is retraction was prevented locally by focal uncaging of caged Ca(2+) that triggered Ca(2+) release f
27 f intact pancreatic acinar cells using local uncaging of caged Ca2+.
28 y carbacyclin-stimulated elevations in cAMP, uncaging of cAMP or exposure to a high concentration of
29                                        Rapid uncaging of Co(2+) ions by patterned UV light activates
30 eriments, primarily on M4-ipRGCs, with photo-uncaging of cyclic nucleotides and virally expressed CNG
31 an be patterned with dienophiles upon 365 nm uncaging of cyclopentadiene.
32 photon active at 720 nm, optically selective uncaging of DEAC450-caged biomolecules at 900 nm may all
33                                   Two-photon uncaging of DEAC450-Glu at 900 nm at spine heads on pyra
34                            The synthesis and uncaging of dendrimer- and polymeric bead-based model sy
35 t of nanobodies allows high-resolution photo-uncaging of different cell types in areas of interest.
36                                              Uncaging of DMn is considerably faster, but DMn has a si
37 ution using optically independent two-photon uncaging of each neurotransmitter.
38 exhibited direct (non-synaptic) responses to uncaging of excitatory and inhibitory transmitters.
39                                   Two-photon uncaging of fluorescein near nonsuperfused gastric surfa
40 recordings, activation of GABAARs, either by uncaging of GABA or by optogenetic stimulation of GABAer
41                                        Using uncaging of GABA, there is a decreasing GABAergic influe
42 his electrical filtering, we used two-photon uncaging of glutamate and compared the integration of el
43 photon imaging, optogenetics, and dual-color uncaging of glutamate and GABA, we demonstrate that plat
44 t is accomplished using UV laser-based photo-uncaging of glutamate and imaging neuronal activation by
45 rat brain (both sexes) by pairing two-photon uncaging of glutamate at spines and APs evoked by somati
46  that unitary-like activation via two-photon uncaging of glutamate causes GC spines to release GABA b
47                         Laser-scanning photo-uncaging of glutamate focally activated neurons in layer
48 d two recently developed methods, two-photon uncaging of glutamate for determining the EPSC of indivi
49 ly different methods: (i) UV light-triggered uncaging of glutamate in intact cells or (ii) piezo-driv
50  Moreover, activation of MOPP cells by focal uncaging of glutamate induced strong inhibition of granu
51 dings of somatic depolarizations elicited by uncaging of glutamate on dendritic fragments, and, in ne
52                             Using two-photon uncaging of glutamate on spine heads from mouse layer-5
53 ) on depolarizations generated by two-photon uncaging of glutamate on spines from mouse neocortical p
54 ut screening method exploiting laser-induced uncaging of glutamate to construct excitatory input maps
55                Here, we use two-photon laser uncaging of glutamate to directly activate glutamate rec
56                     Here we employed optical uncaging of glutamate to mimic synaptic excitation of di
57                                        Focal uncaging of glutamate, accomplished by switching a pulse
58 hoton laser scanning microscopy and 2-photon uncaging of glutamate, Carter and Sabatini (this issue o
59 ation of EPSPs, generated through two-photon uncaging of glutamate, this action was largely shunted b
60 ser scanning microscopy and two-photon laser uncaging of glutamate, we show that SK channels regulate
61 ser-scanning microscopy and two-photon laser uncaging of glutamate.
62 g iontophoresis of l-aspartate or two-photon uncaging of glutamate.
63                                              Uncaging of glycerophosphoryl-myo-inositol 4,5-bisphosph
64  lipo-Pd@Au nanorods is able to catalyze the uncaging of inactive drug precursors and release heat to
65 ereas postsynaptic stores (activated by spot-uncaging of inositol 1,4,5-trisphosphate) remain unaffec
66 ith UDP-GlcNAc had an attenuated response to uncaging of InsP3.
67 eover, the Ca(2+) responses to melatonin and uncaging of IP(3) were mutually exclusive in infected RB
68                                        Photo-uncaging of IP3 in neurons expressing PI3K* elicits a ma
69 ow-intensity tetanic synaptic stimulation or uncaging of IP3 increased the decay time of spontaneous
70                                           On uncaging of IP3, astrocyte Ca2+ responses reliably propa
71                                 Furthermore, uncaging of MNI glutamate reveals that thalamocortical n
72                              Two-photon (2P) uncaging of MNI-glutamate onto individual spines suggest
73 ary spatiotemporal pattern, using two-photon uncaging of MNI-glutamate with beam multiplexing.
74                                  Local photo-uncaging of oxymorphone in the DRN produced conditioned
75                                   Photolytic uncaging of p-hydroxyphenacyl (pHP) GABA demonstrates ba
76  of presynaptic GABA receptors by photolytic uncaging of RuBi-GABA has a biphasic effect on EPSC ampl
77  (520 mum) by excitability testing and focal uncaging of RuBi-GABA on the axon at varying distances f
78 patch clamp electrophysiology and photolytic uncaging of RuBi-GABA we show that GABA(B) receptors are
79 le-cell patch-clamp recording and photolytic uncaging of RuBi-GABA.
80 nitrodibenzofuran (NDBF) for ultra-efficient uncaging of second messengers inside cells.
81                                Thus, optical uncaging of signaling lipids can uncover their rapid eff
82 ne include the bioluminescence-induced photo-uncaging of small-molecules, bioluminescence based photo
83                                     Further, uncaging of Sph leads to the translocation of the autoph
84  micropatterns by means of photolithographic uncaging of surface amines.
85 on of the lipid derivatives before and after uncaging of the lipids.
86 on as well as pinpoint the location at which uncaging of the molecules occurred.
87                                 Light-driven uncaging of the photolabile calcium chelator DMNP-EDTA s
88 aling lipids sphingosine and diacylglycerol; uncaging of the probe for these two species triggered ca
89                         In addition, through uncaging of the same compound, gene expression is contro
90                                     Finally, uncaging of these protected peptides by either UV or two