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1 reases in the major surfactant phospholipid, dipalmitoyl-phosphatidylcholine.
2 was significantly reduced in the presence of dipalmitoyl phosphatidylcholine, a known inhibitor of he
3 either with palmitoyl sphingomyelin or with dipalmitoyl phosphatidylcholine and present intermediate
4 f a bilayer membrane containing cholesterol, dipalmitoyl phosphatidylcholine, and dioleoylphosphatidy
6 ar vesicles of dilauroyl phosphatidylcholine/dipalmitoyl phosphatidylcholine (DLPC/DPPC)/cholesterol
7 unilamellar vesicles made of dimyristoyl or dipalmitoyl phosphatidylcholine (DMPC or DPPC), the latt
8 rated lipid bilayer to systems consisting of dipalmitoyl phosphatidylcholine (DPPC) and cholesterol,
9 nic phospholipids were removed; a mixture of dipalmitoyl phosphatidylcholine (DPPC) and dipalmitoyl p
12 properties of triolein-rich, low-cholesterol dipalmitoyl phosphatidylcholine (DPPC) emulsion particle
13 de GM1 alone and in a binary system with 1,2-dipalmitoyl phosphatidylcholine (DPPC) have been investi
14 e stable than analogous liposomes containing dipalmitoyl phosphatidylcholine (DPPC) instead of DSPC.
15 ons with recent results of a simulation of a dipalmitoyl phosphatidylcholine (DPPC) lipid bilayer sho
16 ded fibrillar networks after adsorption to a dipalmitoyl phosphatidylcholine (DPPC) monolayer in cont
17 ecreased alpha-helical content in films with dipalmitoyl phosphatidylcholine (DPPC) of 52 versus 70%,
18 oncentration, the surface tension, gamma, of dipalmitoyl phosphatidylcholine (DPPC) or Curosurf monol
20 on produced surface pressure-area curves for dipalmitoyl phosphatidylcholine (DPPC) that were indisti
21 dylethanolamine (DPPE), and the phospholipid dipalmitoyl phosphatidylcholine (DPPC) were studied in t
22 high-Tm lipid (brain sphingomyelin (SM)) or dipalmitoyl phosphatidylcholine (DPPC)), low-Tm lipid (d
23 he behavior of its most prevalent component, dipalmitoyl phosphatidylcholine (DPPC), although the dom
24 n erythrocytes were modified by insertion of dipalmitoyl phosphatidylcholine (DPPC), dipalmitoyl phos
25 re similar to the liquid condensed phase for dipalmitoyl phosphatidylcholine (DPPC), the most abundan
26 res 6-8 mN/m higher than values observed for dipalmitoyl phosphatidylcholine (DPPC), the most prevale
27 that the L(beta) composition is dominated by dipalmitoyl phosphatidylcholine (DPPC), which is the mos
28 ed peptides that were reconstituted into 1,2-dipalmitoyl phosphatidylcholine (DPPC)-enriched liposome
31 ures of 1,2-dioleoyl-phosphatidylcholine/1,2-dipalmitoyl-phosphatidylcholine (DPPC)/cholesterol in mo
32 LSE-cholesterol (20%), or binary mixtures of dipalmitoyl phosphatidylcholine(DPPC)-dihydrocholesterol
33 osphatidylcholines were synthesized from 1,2-dipalmitoyl phosphatidylcholine/egg 1,2-diacyl phosphati
34 containing dioleoyl phosphatidylcholine and dipalmitoyl phosphatidylcholine first tested the predict
35 fects local membrane structure by attracting dipalmitoyl phosphatidylcholine headgroups, curving the
37 alproic acid interacting with fully hydrated dipalmitoyl phosphatidylcholine lipid bilayers are studi
40 thermore, we find unusual phase behavior for dipalmitoyl phosphatidylcholine monolayers containing 25
41 ed well experimental heat-capacity curves of dipalmitoyl phosphatidylcholine small unilamellar vesicl
42 omes transfer phosphorylcholine from L-alpha-dipalmitoyl phosphatidylcholine to hybrid and complex ty