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1 sterol, dipalmitoyl phosphatidylcholine, and dioleoylphosphatidylcholine.
2 lesterol, distearoylphosphatidylcholine, and dioleoylphosphatidylcholine.
3 s within model membrane vesicles composed of dioleoylphosphatidylcholine.
5 ynamic averaging in bilayer membranes of 1,2-dioleoylphosphatidylcholine, 1,2-dimyristoylphosphatidyl
7 vesicles in a limiting volume of water [D2O:dioleoylphosphatidylcholine:alamethicin; 220:1:0.05; (M:
8 ees C and 37 degrees C DSMs were enriched in dioleoylphosphatidylcholine and DRMs were enriched in SM
9 We show that bilayers composed of equimolar dioleoylphosphatidylcholine and sphingomyelin spontaneou
10 s (P-23, P-29) into bilayers composed of SM, dioleoylphosphatidylcholine, and cholesterol, separated
11 aft stability in vesicles containing sterol, dioleoylphosphatidylcholine, and one of the following or
13 nosecond molecular dynamics simulations of a dioleoylphosphatidylcholine bilayer at 66% RH (5.4 water
14 r determining the structure of a fluid-phase dioleoylphosphatidylcholine bilayer from x-ray and neutr
15 ynamics of the lipid and water components of dioleoylphosphatidylcholine bilayers at various levels o
17 from mixtures of various molar fractions of dioleoylphosphatidylcholine, cholesterol, and egg sphing
18 was found that when the T domain is added to dioleoylphosphatidylcholine-containing vesicles, all thr
19 ectrum of Dauda bound to KcsA in bilayers of dioleoylphosphatidylcholine contains three components, w
21 ift in the fluorescence emission spectrum in dioleoylphosphatidylcholine [di(C18:1)PC] but smaller sh
23 PEG-mediated fusion of SUVs composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
24 25 nm small unilamellar vesicles composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
25 ilinoleoylphosphatidylcholine), a mixture of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
26 on of small unilamellar vesicles composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
27 on of small unilamellar vesicles composed of dioleoylphosphatidylcholine/dioleoylphosphatidylethanola
29 were incorporated into vesicles composed of dioleoylphosphatidylcholine (DOPC) adopted a topography
30 lly labeled M2-TMPs were studied in hydrated dioleoylphosphatidylcholine (DOPC) and dimyristoylphosph
31 s was investigated using a mixture either of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphati
32 er, previous investigations on the system of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphati
33 ogenous cardiolipin added in the presence of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphati
35 The importance of helper lipids, including dioleoylphosphatidylcholine (DOPC) and phosphatidylethan
36 he peptide in lipid compositions formed from dioleoylphosphatidylcholine (DOPC) and varied percentage
37 uid argon system, and then applied to a neat dioleoylphosphatidylcholine (DOPC) bilayer at 66% relati
39 ers with a biologically relevant width, i.e. dioleoylphosphatidylcholine (DOPC) bilayers), while poly
40 y the kinetics of folding and insertion into dioleoylphosphatidylcholine (DOPC) bilayers, as a functi
44 brain sphingomyelin (bSM) was exchanged into dioleoylphosphatidylcholine (DOPC) GUVs, lateral diffusi
45 y the oligomeric structure of PLB in SDS and dioleoylphosphatidylcholine (DOPC) lipid bilayers recons
48 l phosphatidylcholine (DPPC)), low-Tm lipid (dioleoylphosphatidylcholine (DOPC) or 1-palmitoyl 2-oleo
49 4 carbons, were incorporated separately into dioleoylphosphatidylcholine (DOPC) or dioleoylphosphatid
50 ared using binary mixtures of bis-SorbPC and dioleoylphosphatidylcholine (DOPC) revealed a similar NM
51 ifferent vesicle systems have been compared: dioleoylphosphatidylcholine (DOPC) small unilamellar ves
52 tely 6:4 POPC:cholesterol<POPC approximately dioleoylphosphatidylcholine (DOPC)<1,2-dioleoyl-sn-glyce
54 em consisting of NADPH-P450 reductase (CPR), dioleoylphosphatidylcholine (DOPC), an ionic detergent,
55 LPC), dimyristoylphosphatidylcholine (DMPC), dioleoylphosphatidylcholine (DOPC), and 1-palmitoyl-2-ol
56 e lipids with different physical properties, dioleoylphosphatidylcholine (DOPC), dioleoylphosphatidyl
57 method was applied to a system consisting of dioleoylphosphatidylcholine (DOPC), egg sphingomyelin (e
58 tion of SP with bilayers, composed of either dioleoylphosphatidylcholine (DOPC), or a 50:50 mixture o
59 solid-supported lipid bilayers consisting of dioleoylphosphatidylcholine (DOPC), palmitoyloleoylphosp
60 predominant lipids in the outer leaflet and dioleoylphosphatidylcholine (DOPC), POPC, 1-palmitoyl-2-
61 dioleoylphosphatidylethanolamine (DOPE) and dioleoylphosphatidylcholine (DOPC), the proteins produce
62 osphatidylethanolamine (DOPE), together with dioleoylphosphatidylcholine (DOPC), to the photochemistr
68 gg yolk phosphatidylcholine (egg PC) or from dioleoylphosphatidylcholine (DOPC)/dilinolenoylphosphati
69 n, we studied the lipid mixing kinetics with dioleoylphosphatidylcholine (DOPC)/ganglioside GD1a (GD1
70 defined tilted transmembrane orientations in dioleoylphosphatidylcholine (DOPC)and dilauroylphosphati
73 regated, compacted DNA were formed by adding dioleoylphosphatidylcholine followed by removing the cho
74 ), a mixture of SM (sphingomyelin) and DOPC (dioleoylphosphatidylcholine) in their outer leaflets, an
75 oriented stacks and unilamellar vesicles of dioleoylphosphatidylcholine lipid bilayers to obtain the
76 Here, we describe melittin partitioning into dioleoylphosphatidylcholine lipids using CHARMM and OPLS
77 ace charge density of supported zwitterionic dioleoylphosphatidylcholine membranes with a variable fr
78 ds, dioleoylphosphatidylethanolamine (DOPE), dioleoylphosphatidylcholine, monooleoylglycerol, and cho
79 structure with binding constants relative to dioleoylphosphatidylcholine of 0.67 +/- 0.04 and 0.87 +/
80 ent when the receptor was reconstituted into dioleoylphosphatidylcholine or into a mixture of that li
81 with dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylcholine, or a 1:1 mixture of these p
82 cholesterol, dipalmitoylphosphatidylcholine, dioleoylphosphatidylcholine, palmitoyloleoylphosphatidyl
83 when MscL is reconstituted into bilayers of dioleoylphosphatidylcholine runs from Leu-69 to Leu-92,
84 em of giant unilamellar vesicles composed of dioleoylphosphatidylcholine, sphingomyelin, and choleste
85 azole (IANBD) reconstituted into bilayers of dioleoylphosphatidylcholine varied with position, sugges
86 kbone amides of alamethicin reconstituted in dioleoylphosphatidylcholine vesicles by an exchange-trap
87 ystal structure of rat PITPbeta complexed to dioleoylphosphatidylcholine was determined to 2.18 A res
88 choline, dimyristoylphosphatidylcholine, and dioleoylphosphatidylcholine), we have modeled and simula
89 , composed of O-ethylphosphatidylcholine and dioleoylphosphatidylcholine, were labeled with a carbocy
90 composed of dioleoylphosphatidylglycerol and dioleoylphosphatidylcholine, were labeled with a rhodami
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