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1 membrane domain in a model membrane bilayer (dipalmitoylphosphatidylcholine).
2 nd high-T(m) lipids (either sphingomyelin or dipalmitoylphosphatidylcholine).
3 the hydrated liquid crystal bilayer phase of dipalmitoylphosphatidylcholine.
4 ompared to molecular dynamics simulations of dipalmitoylphosphatidylcholine.
5 on giant unilamellar vesicles (GUVs) of pure dipalmitoylphosphatidylcholine.
6 as attenuated if the hapten was coupled with dipalmitoylphosphatidylcholine.
7 atidylcholine vesicles containing trace [14C]dipalmitoylphosphatidylcholine.
8 proyldipalmitoylphosphatidylethanolamine and dipalmitoylphosphatidylcholine.
9 namely aspirin and ibuprofen, in bilayers of dipalmitoylphosphatidylcholine.
10 motion seem to be more hindered by SP-C than dipalmitoylphosphatidylcholine.
11 e axially symmetric even in the gel phase of dipalmitoylphosphatidylcholine.
12 iding the low surface tension in the lung is dipalmitoylphosphatidylcholine.
13 c lipids, and raft-like membranes containing dipalmitoylphosphatidylcholine(1,2-dipalmitoyl-sn-glycer
14 sembling an interdigitated state enriched in dipalmitoylphosphatidylcholine, a liquid-crystalline bil
15 to measure the transbilayer translocation of dipalmitoylphosphatidylcholine, a membrane-embedded phos
16 SPM, 1-alkyl-2-amidophosphatidylcholine, and dipalmitoylphosphatidylcholine, a popular model "raft li
17 d from our results and previous studies that dipalmitoylphosphatidylcholine alone is less likely to f
18 teraction of melittin with monolayers of 1,2-dipalmitoylphosphatidylcholine and 1,2-dipalmitoylphosph
19 roscopy in liposomes composed of mixtures of dipalmitoylphosphatidylcholine and cholesterol (0-40 mol
20 tions in a mixed bilayer membrane containing dipalmitoylphosphatidylcholine and dipalmitoylphosphatid
21 of multilamellar vesicles (MLVs) containing dipalmitoylphosphatidylcholine and dipalmitoylphosphatid
22 (19)F labeled) in multilamellar vesicles of dipalmitoylphosphatidylcholine and dipalmitoylphosphatid
24 atomistic molecular dynamics simulations of dipalmitoylphosphatidylcholine and dipalmitoylphosphatid
26 n B (SP-B), on the structure and collapse of dipalmitoylphosphatidylcholine and palmitoyl-oleoyl-phos
27 ed in spray-dried microparticles composed of dipalmitoylphosphatidylcholine and the pH-sensitive poly
28 menon was observed in monolayers formed with dipalmitoylphosphatidylcholine and with palmitic acid.
30 exes containing two molecules of protein and dipalmitoylphosphatidylcholine, and the complexes were u
31 PCAT1), required for synthesis of surfactant dipalmitoylphosphatidylcholine, and the proinflammatory
33 Apparent kinetic constants for PLA2 with dipalmitoylphosphatidylcholine as substrate were Km = 0.
34 escent probes and emerging contaminants with dipalmitoylphosphatidylcholine, as a minimalist model of
35 vesicles of L alpha phase lipid bilayers of dipalmitoylphosphatidylcholine at 50 degrees C under var
36 erence for dimyristoylphosphatidylcholine or dipalmitoylphosphatidylcholine bicelles relative to thos
37 cs simulations are performed on two hydrated dipalmitoylphosphatidylcholine bilayer systems: one with
38 asure the change in properties of a hydrated dipalmitoylphosphatidylcholine bilayer when solvated wit
39 molecular dynamics simulation of a gel-phase dipalmitoylphosphatidylcholine bilayer with nw = 11.8 wa
42 cular dynamics simulations of fully hydrated dipalmitoylphosphatidylcholine bilayers and monolayers a
44 on rates from 0.022 to 21.1 T of fluid phase dipalmitoylphosphatidylcholine bilayers are compared.
45 l sampling with the membrane model mimicking dipalmitoylphosphatidylcholine bilayers is in good agree
46 cts on domain formation by sphingomyelin and dipalmitoylphosphatidylcholine but only a weak influence
48 of a phospholipid molecule in an ergosterol-dipalmitoylphosphatidylcholine complex is estimated to b
50 osahexaenoylphosphatidylcholine (di22:6-PC), dipalmitoylphosphatidylcholine (di16:0-PC), sn-1-palmito
51 osed for the hydrated lamellar lipid mixture dipalmitoylphosphatidylcholine/dilauroylphosphatidylchol
52 le yeast membranes, composed of cholesterol, dipalmitoylphosphatidylcholine, dioleoylphosphatidylchol
53 CG MD simulation is carried out for a 1:1 dipalmitoylphosphatidylcholine/dipalmitoylphosphatidylet
54 ansfer of monolayers of either dilauroyl- or dipalmitoylphosphatidylcholine (DLPC and DPPC, respectiv
56 formation in mixtures of the saturated lipid dipalmitoylphosphatidylcholine (DPPC) and a fluorescence
57 hanges occurring in membranes constructed of dipalmitoylphosphatidylcholine (DPPC) and cholesterol at
58 choline (DPPTC), in macroscopically oriented dipalmitoylphosphatidylcholine (DPPC) and dimyristoylpho
59 ively charged liposomal bilayers composed of dipalmitoylphosphatidylcholine (DPPC) and dipalmitoylpho
60 f human surfactant protein-B (SP-B(1-25)) in dipalmitoylphosphatidylcholine (DPPC) and dipalmitoylpho
62 io of dioleoylphosphatidylcholine (DOPC) and dipalmitoylphosphatidylcholine (DPPC) and various amount
63 al and simulated pressure-area isotherms for dipalmitoylphosphatidylcholine (DPPC) at temperatures ra
64 simulation of cholesterol at 12.5 mol% in a dipalmitoylphosphatidylcholine (DPPC) bilayer at 50 degr
65 , termed Nanodiscs, in which the fragment of dipalmitoylphosphatidylcholine (DPPC) bilayer is surroun
66 o dipalmitoylphosphatidylserines (DPPS) in a dipalmitoylphosphatidylcholine (DPPC) bilayer membrane.
67 mulated the interaction of salicylate with a dipalmitoylphosphatidylcholine (DPPC) bilayer via atomic
68 n investigated in gel and liquid crystalline dipalmitoylphosphatidylcholine (DPPC) bilayers by a comb
69 r nanodomains dispersed throughout primarily dipalmitoylphosphatidylcholine (DPPC) domains in mixed D
70 phosphocholine ion from deuterated forms of dipalmitoylphosphatidylcholine (DPPC) have been examined
71 SM) and its interaction with cholesterol and dipalmitoylphosphatidylcholine (DPPC) have been studied
72 from addition of GA to membrane vesicles of dipalmitoylphosphatidylcholine (DPPC) in excess water co
73 different vesicle systems has been examined: dipalmitoylphosphatidylcholine (DPPC) large unilamellar
75 structure of hybrid bilayers (HB) formed by dipalmitoylphosphatidylcholine (DPPC) lipid monolayers a
76 a peptide and model bilayers of zwitterionic dipalmitoylphosphatidylcholine (DPPC) lipids and anionic
77 s of the phosphate headgroup of freeze-dried dipalmitoylphosphatidylcholine (DPPC) liposomes was stud
79 gramicidin A' (GA) on the phase structure of dipalmitoylphosphatidylcholine (DPPC) multilamellar vesi
80 -C13(palm)(2)] of SP-C, in mixtures with 1,2-dipalmitoylphosphatidylcholine (DPPC) or 1,2-dipalmitoyl
81 ation was found in binary mixtures of either dipalmitoylphosphatidylcholine (DPPC) or sphingomyelin (
82 d-decorated NP in model membranes containing dipalmitoylphosphatidylcholine (DPPC) phospholipids and
83 ion of influenza A M2 (M2) incorporated in a dipalmitoylphosphatidylcholine (DPPC) supported planar b
84 effect in a 1:10 mixture of haloperidol and dipalmitoylphosphatidylcholine (DPPC) that suppresses th
85 ical forces on the structure of unilamellar, dipalmitoylphosphatidylcholine (DPPC) vesicles, both opt
87 hment of noncomplement activating liposomes [dipalmitoylphosphatidylcholine (DPPC) vesicles] with pho
88 arge, unilamellar vesicles (LUV) composed of dipalmitoylphosphatidylcholine (DPPC) were made asymmetr
89 the bulk-phase interaction between SP-A, 1,2-dipalmitoylphosphatidylcholine (DPPC), and Ca2+ ions alo
90 oylphosphatidylglycerol (DPPG), zwitterionic dipalmitoylphosphatidylcholine (DPPC), and cationic dipa
91 mixtures of diphytanoylphosphatidylcholine, dipalmitoylphosphatidylcholine (DPPC), and cholesterol p
92 composed of ternary mixtures of cholesterol, dipalmitoylphosphatidylcholine (DPPC), and dioleoylphosp
93 pids dipalmitoylphosphatidylglycerol (DPPG), dipalmitoylphosphatidylcholine (DPPC), and dipalmitoylph
94 s shown, by comparison to dispersions of SM, dipalmitoylphosphatidylcholine (DPPC), and DPPC/choleste
95 perties of the zwitterionic phospholipid 1,2-dipalmitoylphosphatidylcholine (DPPC), and the anionic f
96 mportant pulmonary surfactant phospholipids, dipalmitoylphosphatidylcholine (DPPC), bound to SPLUNC1
98 domain formations in mixed lipid bilayers of dipalmitoylphosphatidylcholine (DPPC), dilauroylphosphat
99 layers composed of sterol/steroid mixed with dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphati
100 gett (LB) monolayers and bilayers of L-alpha-dipalmitoylphosphatidylcholine (DPPC), fluorescently dop
101 rdered domain-forming lipids/lipid mixtures: dipalmitoylphosphatidylcholine (DPPC), sphingomyelin (SM
102 ensed Gibbs monolayer, which is the case for dipalmitoylphosphatidylcholine (DPPC), the C2F5-labeled
103 In this work, the stability of AgNPs in dipalmitoylphosphatidylcholine (DPPC), the major compone
104 comparison of the interactions of Chol with dipalmitoylphosphatidylcholine (DPPC), which has a simil
105 olecular dynamics simulations performed on a dipalmitoylphosphatidylcholine (DPPC)-cholesterol bilaye
112 performed molecular dynamics simulations on dipalmitoylphosphatidylcholine (DPPC)/dimethylsulfoxide
113 e of bovine liver phosphatidylcholine (BLPC)/dipalmitoylphosphatidylcholine (DPPC)/dipalmitoylphospha
114 nique, we studied the changes occurring in a dipalmitoylphosphatidylcholine (DPPC):cholesterol (CH) m
115 ng the permeation of chain perdeuterated 1,2-dipalmitoylphosphatidylcholine (DPPC-d62) and 1-palmitoy
116 enous injection of saline (n=16), 1080 mg/kg dipalmitoylphosphatidylcholine (DPPC; n=14), or 400 mg/k
119 the collagen-like domain, was incubated with dipalmitoylphosphatidylcholine:egg phosphatidylcholine (
120 rol, dielaidoylphosphatidylethanolamine, and dipalmitoylphosphatidylcholine further elucidate the val
121 oylphosphatidylserines in the environment of dipalmitoylphosphatidylcholines has been calculated by u
122 ugated phosphatidylethanolamine and 75 mol % dipalmitoylphosphatidylcholine have been examined by usi
123 play significant roles in the lung, such as dipalmitoylphosphatidylcholine in pulmonary surfactant;
126 The newborn baboons were treated with [14C]dipalmitoylphosphatidylcholine-labeled surfactant and ve
128 X-ray data are presented for the benchmark dipalmitoylphosphatidylcholine lipid bilayer in the most
130 all-atom molecular dynamics simulations of a dipalmitoylphosphatidylcholine lipid bilayer, we observe
132 urface forces measurements between gel-phase dipalmitoylphosphatidylcholine membranes in DMSO-water m
133 arins, but not warfarin, intercalate between dipalmitoylphosphatidylcholine molecules, whereas grazin
134 The pulmonary surfactant is modeled as a dipalmitoylphosphatidylcholine monolayer with a peptide
135 full pulmonary surfactant protein SP-B, with dipalmitoylphosphatidylcholine monolayers, which are the
136 ation, location, and dynamic properties in a dipalmitoylphosphatidylcholine multilamellar model membr
137 ellar phase transition temperature of either dipalmitoylphosphatidylcholine or dioleoylphosphatidylch
138 inding of apoA-II to apoA-I-rHDL, containing dipalmitoylphosphatidylcholine or palmitoyloleoylphospha
139 E on a lipoprotein particle, we crystallized dipalmitoylphosphatidylcholine particles containing two
140 dministered synthetic surfactant (13.5 mg of dipalmitoylphosphatidylcholine per milliliter, 364 patie
141 palmitoyl-2-oleoyl phosphatidylethanolamine, dipalmitoylphosphatidylcholine, phosphatidylinositol 4,5
142 teracted with zwitterionic monolayers of 1,2-dipalmitoylphosphatidylcholine, revealing the important
144 into the molecular envelope of apoE bound to dipalmitoylphosphatidylcholine that had been determined
146 responsible for degradation of internalized dipalmitoylphosphatidylcholine, the major phospholipid c
147 ophages, as CD36 knockdown reduces uptake of dipalmitoylphosphatidylcholine, the most prevalent surfa
149 compared with previous simulations for pure dipalmitoylphosphatidylcholine under the same conditions
150 n and palmitic acid to the susceptibility of dipalmitoylphosphatidylcholine vesicles and to rationali
151 s of dilauroylphosphatidylcholine (DLPC) and dipalmitoylphosphatidylcholine vesicles with 70, 90, and
153 out on the liquid crystal (Lalpha) phase of dipalmitoylphosphatidylcholine with a mole fraction of 6
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