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1 iffer to a large extent in their mixing with dimyristoylphosphatidylcholine.
2 oriented and nonoriented samples in hydrated dimyristoylphosphatidylcholine.
4 to viscosities of 2.2 poise for bilayers of dimyristoylphosphatidylcholine (28 degrees C) and 3.0 po
5 te of association of apolipoprotein A-I with dimyristoylphosphatidylcholine, a process that occurs th
6 is technique was applied here to mixtures of dimyristoylphosphatidylcholine and a shorter-tail lipid,
8 n of A54145 with model membranes composed of dimyristoylphosphatidylcholine and dimyristoylphosphatid
9 holipid bilayers, prepared from a mixture of dimyristoylphosphatidylcholine and dimyristoylphosphatid
10 lamellar vesicles of an equimolar mixture of dimyristoylphosphatidylcholine and distearoylphosphatidy
12 hanol crosspeaks in dispersions of saturated dimyristoylphosphatidylcholine and monounsaturated stear
13 fluid phases in binary mixtures composed of dimyristoylphosphatidylcholine and one of two totally sy
14 anes of 1,2-dioleoylphosphatidylcholine, 1,2-dimyristoylphosphatidylcholine, and 1,2-dilauroylphospha
15 t lipid types (dilauroylphosphatidylcholine, dimyristoylphosphatidylcholine, and dioleoylphosphatidyl
16 nfluenza A virus M2 transmembrane channel in dimyristoylphosphatidylcholine bilayer for each of the f
17 molecular dynamics simulations of a solvated dimyristoylphosphatidylcholine bilayer using this polari
18 s of harzianin HK VI (HZ) interacting with a dimyristoylphosphatidylcholine bilayer were performed at
21 coelastic properties of planar phospholipid (dimyristoylphosphatidylcholine) bilayer membranes at 308
23 vidual bacteriorhodopsin helices in explicit dimyristoylphosphatidylcholine bilayers to examine the a
26 te of association of apolipoprotein A-I with dimyristoylphosphatidylcholine by inserting into defects
27 prepared at a 100:5:1 molar ratio of L-alpha-dimyristoylphosphatidylcholine:cholesterol:wild-type or
28 display similar lipid-binding activities in dimyristoylphosphatidylcholine clearance assays and form
30 ystalline medium, DMPC/DHPC bicelles (DMPC = dimyristoylphosphatidylcholine; DHPC = dihexanoylphospha
31 city of approximately 45% in the presence of dimyristoylphosphatidylcholine/dimyristoylphosphatidylse
32 omponents and gel/fluid state acyl chains in dimyristoylphosphatidylcholine/distearoylphosphatidylcho
33 rties of gel and fluid clusters of equimolar dimyristoylphosphatidylcholine/distearoylphosphatidylcho
34 0, and a fusion-inactive mutant DeltaG1 with dimyristoylphosphatidylcholine (DMPC) and 1-palmitoyl-2-
35 ic lanthanide ions to a bicellar solution of dimyristoylphosphatidylcholine (DMPC) and dihexanoylphos
36 ctures of the fully hydrated fluid phases of dimyristoylphosphatidylcholine (DMPC) and dilauroylphosp
37 ractions exhibited by gramicidin embedded in dimyristoylphosphatidylcholine (DMPC) and dilauroylphosp
38 alpha-helical structure able to permeabilize dimyristoylphosphatidylcholine (DMPC) and dimyristoylpho
39 gned model membranes composed of mixtures of dimyristoylphosphatidylcholine (DMPC) and dimyristoylpho
40 al a well-structured VDAC1 in 2D crystals of dimyristoylphosphatidylcholine (DMPC) and diphytanoylpho
41 t probes in two model lipid bilayer systems, dimyristoylphosphatidylcholine (DMPC) and DMPC/cholester
42 ed discoidal lipoproteins reconstituted from dimyristoylphosphatidylcholine (DMPC) and human apolipop
43 ere conducted with both phosphatidylcholine (dimyristoylphosphatidylcholine (DMPC) and palmitoyloleoy
44 using model lipoproteins reconstituted from dimyristoylphosphatidylcholine (DMPC) and selected mutan
46 dged to a corresponding atomistic model of a dimyristoylphosphatidylcholine (DMPC) bilayer at various
47 binding of Abeta monomers to a zwitterionic dimyristoylphosphatidylcholine (DMPC) bilayer coincubate
50 performed molecular dynamics simulations of dimyristoylphosphatidylcholine (DMPC) bilayers to model
51 spectra of acyl- and nonacyl-gA in hydrated dimyristoylphosphatidylcholine (DMPC) bilayers were comp
52 dium dodecyl sulfate (SDS) micelles and into dimyristoylphosphatidylcholine (DMPC) bilayers, respecti
55 this region on the conformation, stability, dimyristoylphosphatidylcholine (DMPC) binding kinetics,
56 spontaneous interaction of the mutants with dimyristoylphosphatidylcholine (DMPC) indicated that all
57 ately 8.5 nm disks formed spontaneously when dimyristoylphosphatidylcholine (DMPC) large unilamellar
58 rated dioleoylphosphatidylcholine (DOPC) and dimyristoylphosphatidylcholine (DMPC) lipid bilayers ori
59 omeric and tetrameric peptide can solubilize dimyristoylphosphatidylcholine (DMPC) liposomes and fold
62 ed dipalmitoylphosphatidylcholine (DPPC) and dimyristoylphosphatidylcholine (DMPC) membranes, which w
63 of dihexanoylphosphatidylcholine (DHPC) and dimyristoylphosphatidylcholine (DMPC) mixtures, where th
65 he edges of bilayer ribbons composed of pure dimyristoylphosphatidylcholine (DMPC) or palmitoyl-oleoy
66 emonstrated that [1-44]apoA-I interacts with dimyristoylphosphatidylcholine (DMPC) over a wide range
68 tein E (apoE) in binding to the phospholipid dimyristoylphosphatidylcholine (DMPC) to form discoidal
69 the in vitro binding of apoE complexed with dimyristoylphosphatidylcholine (DMPC) to human aortic Bg
70 aracterize the association of Lp-PLA(2) with dimyristoylphosphatidylcholine (DMPC) vesicles and found
71 ow that the conformation of each analogue in dimyristoylphosphatidylcholine (DMPC) vesicles is simila
72 nstructed by adsorption of small unilamellar dimyristoylphosphatidylcholine (DMPC) vesicles onto poly
74 xplicit dilauroylphosphatidylcholine (DLPC), dimyristoylphosphatidylcholine (DMPC), dioleoylphosphati
75 te structures formed in solutions containing dimyristoylphosphatidylcholine (DMPC)/dihexanoylphosphat
76 ropic phase behavior of the ternary mixtures dimyristoylphosphatidylcholine (DMPC)/dimyristoylphospha
77 bilayer, the thermotropic phase behavior of dimyristoylphosphatidylcholine (DMPC)/dimyristoylphospha
78 s heat capacity versus temperature curves of dimyristoylphosphatidylcholine (DMPC)/distearoylphosphat
79 r ribbons and perforated bilayers containing dimyristoylphosphatidylcholine (DMPC, di-C(14) tails) an
83 n peaks were observed for native PS I in the dimyristoylphosphatidylcholine films, and were assigned
87 n 60 min following the addition of inositol, dimyristoylphosphatidylcholine levels had decreased from
88 The structure of fully hydrated gel phase dimyristoylphosphatidylcholine lipid bilayers was obtain
89 Furthermore, combined treatment with l-alpha-dimyristoylphosphatidylcholine liposome and the glucosyl
90 ramicidin A (gA) channel in a fully hydrated dimyristoylphosphatidylcholine membrane in the presence
92 ity of GRP1 in a reaction mixture containing dimyristoylphosphatidylcholine micelles, 3-[(3-cholamido
95 or, were successfully incorporated into SapA-dimyristoylphosphatidylcholine nanoparticles and studied
96 choline.DAGK also exhibited a preference for dimyristoylphosphatidylcholine or dipalmitoylphosphatidy
97 an attenuated ability to solubilize l-alpha-dimyristoylphosphatidylcholine phospholipid vesicles com
98 ptide was unstructured in aqueous buffer and dimyristoylphosphatidylcholine-polymerized diacetylene v
100 Six different anesthetic (halothane)/lipid (dimyristoylphosphatidylcholine) ratios have been investi
101 resence of choline exhibited lower levels of dimyristoylphosphatidylcholine than wild type cells grow
102 We conclude that HD forms complexes with dimyristoylphosphatidylcholine that are surprisingly sim
104 is applied to NMR order parameter data from dimyristoylphosphatidylcholine, the resulting <A> is 10%
105 ApoA-V interacts with bilayer vesicles of dimyristoylphosphatidylcholine to form discoidal complex
106 e we use small and large unilamellar L-alpha-dimyristoylphosphatidylcholine vesicles (SUVs and LUVs)
107 ApoA-I-(44-186) induced solubilization of dimyristoylphosphatidylcholine vesicles at a rate compar
108 The ability of apoA-V(1-146) to solubilize dimyristoylphosphatidylcholine vesicles at a rate faster
109 n erythrocytes were incubated with sonicated dimyristoylphosphatidylcholine vesicles containing trace
110 ing studies indicated that apoA-V transforms dimyristoylphosphatidylcholine vesicles into discoidal c
114 s), composed of human apolipoprotein A-I and dimyristoylphosphatidylcholine, were investigated by phy
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