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1 ts effect on the cubic mesophase of hydrated monoolein.
2 sented supporting the fit of a porphyrin and monooleins.
3 ible that the hosting cubic phase created by monoolein alone, which itself is not a common membrane c
4 tudied cubic phase LLCs, which are formed of monoolein and water, are not useful in their intended ap
6 d protein is dispersed with lipid, typically monoolein, and in so doing the cubic phase self-assemble
7 up, and provide the first demonstration that monoolein-based cubic lipid phase crystallization can su
8 ctroscopy demonstrates two molecules of sn-2 monoolein bound in the LFABP binding pocket in positions
11 t a GpA-TM peptide readily crystallized in a monoolein cubic phase bilayer, yielding a dimeric alpha-
15 phosphatidylcholine (DPhPC) bilayers than in monoolein (GMO) bilayers (coupled for the four combinati
19 welling in bicontinuous structures formed by monoolein (MO) doped with both negatively charged dioley
20 stigated the phase behavior of mesophases of monoolein (MO) mixed with additives commonly used for th
21 hat when mixed with monooleoyl-rac-glycerol (monoolein, MO) and water at appropriate proportions, the
24 he low molecular weight peak of radiolabeled monoolein present in the fractions that contain LFABP in
25 studies, we examined the metabolism of sn-2-monoolein (sn-2-18:1) by human intestinal Caco-2 cells.
26 ides, have on the phase behavior of hydrated monoolein, the lipid upon which the in meso method is ba
27 the enterocyte, the metabolism of [(3)H]sn-2-monoolein was examined by adding taurocholate-mixed sn-2
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