ライフサイエンスコーパス: dioleoylphosphatidylethanolamine

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1 ffinity for di(C18:1)PC is equal to that for dioleoylphosphatidylethanolamine.

2 -dioleoyloxy-3-trimethylammonium-propane and dioleoylphosphatidylethanolamine (1:1 mol/mol).

3 L-C(12)-sphingomyelin, Lissamine rhodamine B dioleoylphosphatidylethanolamine and BODIPY-TR-C(12)-sph

4 hexagonal II phase transition temperature of dioleoylphosphatidylethanolamine and promotes formation

5 ), a mixture of dioleoylphosphatidylcholine, dioleoylphosphatidylethanolamine, and free sterols (1:1:

6 nsferase (CAT)-DNA/lipid 67 (cationic lipid)/dioleoylphosphatidylethanolamine complex (4:1:2 in a fin

7 3-bis(tetradecyloxy)-1-propanaminium bromide/dioleoylphosphatidylethanolamine (DMRIE/DOPE).

8 In multilamellar vesicles of dioleoylphosphatidylethanolamine:DOPC (1:1, mol:mol) pre

9 amellar domains--was observed in mixtures of dioleoylphosphatidylethanolamine:DOPC that were dehydrat

10 -hydroxyethyl)imidazolinium chloride (DOTIM)/dioleoylphosphatidylethanolamine (DOPE) (1:1) liposomes

11 mes (LUV) composed of a 3:1 molar mixture of dioleoylphosphatidylethanolamine (DOPE) and 1,2-bis[10-(

12 With binary mixtures of dioleoylphosphatidylethanolamine (DOPE) and dioleoylphos

13 llar liposomes containing defined amounts of dioleoylphosphatidylethanolamine (DOPE) and dioleoylphos

14 -2 position were investigated in a matrix of dioleoylphosphatidylethanolamine (DOPE) by 2H and 31P NM

15 sed of cholesteryl hemisuccinate (CHEMS) and dioleoylphosphatidylethanolamine (DOPE) confers steric s

16 em of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphatidylethanolamine (DOPE) did not reveal i

17 bromide (GAP-DLRIE) plus the neutral colipid dioleoylphosphatidylethanolamine (DOPE) enhanced CAT exp

18 and increases with the increasing content of dioleoylphosphatidylethanolamine (DOPE) in dioleoylphosp

19 y into dioleoylphosphatidylcholine (DOPC) or dioleoylphosphatidylethanolamine (DOPE) lipid membranes

20 spontaneous curvature, and bending moduli of dioleoylphosphatidylethanolamine (DOPE) monolayers doped

21 les composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanolamine (DOPE), bovine brain sp

22 ce of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphatidylethanolamine (DOPE), but not by card

23 perties, dioleoylphosphatidylcholine (DOPC), dioleoylphosphatidylethanolamine (DOPE), dioleoylphospha

24 idylcholine (DOPC) and varied percentages of dioleoylphosphatidylethanolamine (DOPE), dioleoylphospha

25 ds or their mixtures with the helper lipids, dioleoylphosphatidylethanolamine (DOPE), dioleoylphospha

26 ation of nonlamellar-forming lipids, such as dioleoylphosphatidylethanolamine (DOPE), together with d

27 cles composed of dioleoylphosphatidylcholine/dioleoylphosphatidylethanolamine (DOPE)/sphingomyelin/ch

28 ids, were incorporated into N-monomethylated dioleoylphosphatidylethanolamine (DOPE-Me) at concentrat

29 s of the phase behavior of N-mono-methylated dioleoylphosphatidylethanolamine (DOPE-Me) to determine

30 ous mixtures of a nonlamellar-forming lipid (dioleoylphosphatidylethanolamine; DOPE) together with a

31 The binding constants for dioleoylphosphatidylethanolamine for both TbMscL and EcM

32 Choosing model parameters appropriate to dioleoylphosphatidylethanolamine in water, we obtain pha

33 to 8, were synthesized and incorporated with dioleoylphosphatidylethanolamine into liposomes.

34 sphatidylethanolamine-N-methyl (DOPE-Me), or dioleoylphosphatidylethanolamine-N,N-dimethyl (DOPE-Me2)

35 of dioleoylphosphatidylethanolamine (DOPE), dioleoylphosphatidylethanolamine-N-methyl (DOPE-Me), or

36 orating the neutral colipids cholesterol and dioleoylphosphatidylethanolamine on this interaction was

37 les composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanolamine, sphingomyelin, and cho

38 UVs composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanolamine, sphingomyelin, cholest

39 phosphatidylethanolamine or N-monomethylated dioleoylphosphatidylethanolamine systems.

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