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