戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 st to Laurdan and its carboxylate analogue C-Laurdan.
2 fectants was measured by labeling cells with Laurdan.
3 roscopy with an environment-sensitive probe, laurdan.
4 ne physical state detected by bis-pyrene and laurdan.
5  giant plasma membrane vesicles (GPMVs) than Laurdan.
6 lipids that forces water molecules away from laurdan.
7 nd shows higher fluorescence brightness than Laurdan.
8 ow, as tracked with the fluorescent marker C-laurdan.
9  that membrane raft accumulation assessed by Laurdan (6-dodecanoyl-2-dimethyl aminonaphthalene) label
10               As a fluorescent probe we used LAURDAN (6-dodecanoyl-2-dimethylaminonaphthalene), a dye
11         The effects of temperature and pH on Laurdan (6-lauroyl-2-(dimethylamino)naphthalene) fluores
12    6-Dodecanoyl-2-dimethylamino-naphthalene (LAURDAN), 6-propionyl-2-dimethylamino-naphthalene (PRODA
13 the emission intensity at two wavelengths of Laurdan, a membrane fluorescent dye sensitive to local m
14 erived from the exogenous fluorescent probes laurdan, acridine orange, propidium iodide, and Snarf ar
15 ence emission spectra of Prodan, Patman, and Laurdan all showed spectral changes consistent with an i
16 ce polarization of the phase-sensitive probe Laurdan and FRET between phase-partitioning probes in mo
17 ctroscopic data, generalized polarization of Laurdan and infrared carbonyl and phosphate stretching f
18 ly the cell plasma membranes, in contrast to Laurdan and its carboxylate analogue C-Laurdan.
19 axation in response to the excited states of Laurdan and Prodan.
20 opy using the membrane probes bis-pyrene and laurdan) and compared with sPLA(2) activity.
21 of 6-dodecanoyl-2-dimethylamino-naphthalene (Laurdan) and Lissamine rhodamine B 1,2-dihexadecanoyl-sn
22 scanning microscopy using the membrane probe laurdan argued that susceptibility to sPLA(2) is a conse
23 onstrate this analysis in NIH3T3 cells using Laurdan as a biosensor to monitor changes in the membran
24 embrane interactions were investigated using Laurdan as a membrane-anchored fluorescent dye.
25                             Using Prodan and Laurdan as fluorescent membrane probes, phosphatidylchol
26  we investigate the fluorescence lifetime of Laurdan at two different emission wavelengths and find t
27 -sensitive probes Laurdan, carboxyl-modified Laurdan (C-Laurdan), Di-4-ANEPPDHQ, and Di-4-AN(F)EPPTEA
28 ubbles with environmentally-sensitive probes Laurdan, carboxyl-modified Laurdan (C-Laurdan), Di-4-ANE
29 P values lead us to further propose that the Laurdan chromophore resides in the polar headgroup regio
30 eriments utilizing the phase-sensitive probe Laurdan confirmed gel-phase characteristics at pH 2, exp
31                                          The Laurdan-derived LogD values at pH 7.4 were found to be 2
32                                      Second, laurdan detected increased solvation of the lower headgr
33 probes Laurdan, carboxyl-modified Laurdan (C-Laurdan), Di-4-ANEPPDHQ, and Di-4-AN(F)EPPTEA (FE), for
34 ical scheme based on the use of a lipophilic Laurdan dye for examining MIN6 cell membranes upon expos
35 omics and membrane fluidity assays (FRAP and Laurdan dye staining) we further show that the human ACS
36      Analysis of the spatial distribution of laurdan fluorescence at several temperatures indicated t
37                Interestingly, the two-photon Laurdan fluorescence images showed snowflake-like lipid
38 ted with light polarized in the y direction, Laurdan fluorescence in the center cross section of the
39         The generalized polarization (GP) of Laurdan fluorescence in the center cross section of the
40 ied from the areas of deconvoluted lognormal laurdan fluorescence peaks.
41 model cell membranes, using a combination of laurdan fluorescence spectroscopy and coarse-grained mol
42                                              Laurdan fluorescence, novel spectral fitting, and dynami
43 ative evaluation of the phase behavior using Laurdan generalized polarization, and of enzyme binding
44 ere used to assess merocyanine 540 emission, laurdan generalized polarization, phosphatidylserine exp
45                      Binding experiments and Laurdan generalized-polarization measurements suggest th
46 xistence temperature regime and based on the Laurdan GP data, we observe that when the hydrophobic mi
47                             As judged by the LAURDAN GP histogram, we concluded that the lipid phase
48   Detection of the fluorescent properties of Laurdan has been proven to be an efficient tool to inves
49     Among the dyes used in membrane studies, LAURDAN has the advantage to be sensitive to the lipid c
50 isruption of lipid order was consistent with Laurdan imaging results indicating that POVPC and PGPC d
51 ution of polarity and dipolar relaxations of LAURDAN in each pixel of an image.
52 his result indicates that the chromophore of Laurdan in PLFE GUVs is aligned parallel to the membrane
53 of the excitation-emission matrices (EEM) of LAURDAN in several lipid structures.
54                                     From the LAURDAN intensity images the excitation generalized pola
55                                     From the Laurdan intensity images the generalized polarization fu
56                                              LAURDAN is a fluorescence probe widely used for characte
57         The generalized polarization (GP) of Laurdan-labeled cells contains useful information about
58 ated and unconjugated BSs as determined with Laurdan-labeled liposomes.
59            Optical microspectrophotometry of Laurdan-labeled neutrophils revealed a large blue shift
60                 To address a key drawback of Laurdan linked to its rapid internalization and subseque
61 arse-grained molecular dynamics simulations, Laurdan multiphoton imaging, and atomic force microscopy
62 ous fluorescence study using dipyrenylPC and Laurdan probes and thus support the proposition that 1)
63 lly sensitive solvatochromic probes, such as Laurdan, provides information about the organization of
64          Various fluorescent probes (Prodan, Laurdan, pyrene-labeled fatty acid, and dansyl-labeled p
65 emission of the environment-sensitive probe, laurdan, revealed that erythrocyte membrane order decrea
66          Traditionally the spectral shift of Laurdan's emission from blue in the ordered lipid phase
67 and find that when the dipolar relaxation of Laurdan's emission is spectrally isolated, analysis of t
68  phasor representation to analyze changes in Laurdan's fluorescence lifetime we obtain two different
69                               A reduction of Laurdan's generalized polarization in relation to change
70 m to construct EEM data based on a model for LAURDAN's photophysics.
71 the phasors, allowing a better assessment of LAURDAN's surroundings in terms of hydration, water mobi
72 of approximately 3.9), no differences in the Laurdan spectra of the respective BS were found at pH 6.
73                                          The LAURDAN spectrum is sensitive to the lipid composition a
74     We use the lipophilic fluorescence probe Laurdan to study cell membranes.
75                     The emission spectrum of LAURDAN was examined by two-photon fluorescence microsco
76  natural lipid mixtures, in which the probe, LAURDAN, was incorporated.
77 chemical sensitive dyes, Di-4-ANEPPDHQ and C-laurdan, we demonstrated that AdipoRon decreased the rig
78 of 6-dodecanoyl-2-dimethylamine-naphthalene (LAURDAN), which is sensitive to the changes in water con
79  the gel-like and fluid fluorescent peaks of laurdan, which is embedded in the liposome membranes, ar
80 ore sensitive to cholesterol extraction than Laurdan, which is redistributed within both plasma membr
81 e use of the fluorescent fatty acid analogue Laurdan, whose emission spectrum is sensitive to structu
82 e order (assessed with the fluorescent probe laurdan) with hydrolysis rate revealed that sPLA(2) acti