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1 ts effect on the cubic mesophase of hydrated monoolein.
2 ystems at a 1:6 molar ratio entirely lacking monoolein.
3 sented supporting the fit of a porphyrin and monooleins.
4 ible that the hosting cubic phase created by monoolein alone, which itself is not a common membrane c
5 tudied cubic phase LLCs, which are formed of monoolein and water, are not useful in their intended ap
6                          Lipolysis products (monoolein) and fatty acid were also evaluated to simulat
7 d protein is dispersed with lipid, typically monoolein, and in so doing the cubic phase self-assemble
8 up, and provide the first demonstration that monoolein-based cubic lipid phase crystallization can su
9 ctroscopy demonstrates two molecules of sn-2 monoolein bound in the LFABP binding pocket in positions
10                       The L(3) phase was the monoolein/butanediol/water system; the addition of water
11 eference cubic-Pn3m phase formed by hydrated monoolein could be modified by other lipid types.
12 t a GpA-TM peptide readily crystallized in a monoolein cubic phase bilayer, yielding a dimeric alpha-
13 m transporter Na(+)/K(+)-ATPase (NKA) into a monoolein-derived LCP.
14                     Addition of lecithin and monoolein did not diminish the secretory effect of ricin
15                                     Hydrated monoolein forms the cubic-Pn3m mesophase that has been u
16 phosphatidylcholine (DPhPC) bilayers than in monoolein (GMO) bilayers (coupled for the four combinati
17        Bilayer thicknesses ranged from 25 A (monoolein in squalene) to 54 A (monoeicosenoin in decane
18 hat the density interpreted as porphyrin and monoolein is better fitted as polyethylene glycol.
19 dsorbed layers containing lysolecithin (LL), monoolein (MG), or glyceryl polyethyleneglycol ricinolea
20 at facilitate crystallization in cubic phase monoolein mixtures.
21 welling in bicontinuous structures formed by monoolein (MO) doped with both negatively charged dioley
22                                              Monoolein (MO) LCNPs, cubosomes with an internal nanostr
23 stigated the phase behavior of mesophases of monoolein (MO) mixed with additives commonly used for th
24 hat when mixed with monooleoyl-rac-glycerol (monoolein, MO) and water at appropriate proportions, the
25                             Thus, doping the monoolein of the monoolein/water liquid crystal with 1,2
26 pin, lyso-PC, a polyethylene glycol-lipid, 2-monoolein, oleamide, and cholesterol.
27 he low molecular weight peak of radiolabeled monoolein present in the fractions that contain LFABP in
28 ple lipolysis products including diolein and monoolein regioisomers were quantified within a single H
29  studies, we examined the metabolism of sn-2-monoolein (sn-2-18:1) by human intestinal Caco-2 cells.
30 ides, have on the phase behavior of hydrated monoolein, the lipid upon which the in meso method is ba
31 the enterocyte, the metabolism of [(3)H]sn-2-monoolein was examined by adding taurocholate-mixed sn-2
32                     The positional isomer, 2-monoolein, was tolerated to the highest level.
33 yl tail, are combined (from 10-30 wt %) into monoolein-water systems to create LLC phases.
34 fined diameters of approximately 5 nm in the monoolein/water cubic-phase liquid crystal.
35            Thus, doping the monoolein of the monoolein/water liquid crystal with 1,2-dioleoyl-sn-glyc
36 reases the shear strength of the cubic-phase monoolein/water lyotropic liquid crystal.
37  on the basis of the phase properties of the monoolein/water system.