ライフサイエンスコーパス: dipalmitoyl

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

1 -14C]-phosphatidylcholine (PC), but not with dipalmitoyl-[1-14C]-PC, led to formation of covalent add

2 ays, and a triglyceride mimetic prodrug (1,3-dipalmitoyl-2-mycophenoloyl glycerol, 2-MPA-TG) to facil

3 l the blends had three main TGs; namely, 1,3-dipalmitoyl-2-oleoylglycerol (POP) (8.6-17.7%), 1-palmit

4 palmitic acid, glyceryl tripalmitate and 1,3-dipalmitoyl-2-oleoylglycerol irradiated over a range of

5 dIns(4,5)P(2) and much less by the synthetic dipalmitoyl analog, whereas IRK1 channels were activated

6 reas IRK1 channels were activated equally by dipalmitoyl and arachidonyl stearyl PtdIns(4,5)P(2).

7 diacylglyceryl moieties containing dioleoyl, dipalmitoyl, and dibutyryl chains.

8 ferent fatty acyl chain length (dimyristoyl, dipalmitoyl, and disteroyl phosphatidylcholine) in the a

9 y analysis to be a phosphodiester-linked 1,2-dipalmitoyl (C16:0) glycerol moiety and was identical in

10 , the PtdIns(3)P analogues with dioleoyl and dipalmitoyl chains were substrates for the 5-kinase enzy

11 t experiments with dibutyryl, dioctanoyl, or dipalmitoyl derivatives of PtdIns(4,5)P(2) suggested tha

12 n be either linear or branched, using sn-1,2 dipalmitoyl, dihexadecyl, diphytanoyl, and diphytanyl ph

13 l groups from radiolabeled [1-(14)C]-l-alpha-dipalmitoyl diphosphatidylcholine (DPPC) to RPE65.

14 or zwitterionic L-alpha-phosphatidylcholine, dipalmitoyl (DPPC) monolayers at a range of surface pres

15 The hydrolysis of different species of PC [dipalmitoyl (DPPC), dioleoyl(DOPC), palmitoylarachidonoy

16 ither acidic DL-alpha-phosphatidyl-L-serine, dipalmitoyl (DPPS) or zwitterionic L-alpha-phosphatidylc

17 Dipalmitoyl L-alpha-phosphatidyl-D-myo-inositol 3,4,5-tr

18 d with those obtained from liposomes made of dipalmitoyl-L-alpha-phosphatidylcholine (DPPC), a conven

19 c scheme, all-trans-retinal was reacted with dipalmitoyl-l-alpha-phosphatidylethanolamine to yield DP

20 Dipalmitoyl-PA (16:0) was comparable to PA from egg leci

21 polyphenolic molecules with egg PC (EPC) and dipalmitoyl PC (DPPC) bilayers.

22 respectively)) and phosphatidylcholine (PC; dipalmitoyl PC and 1-palmitoyl-2-stearoyl PC (DPPC and P

23 res of a saturated phosphatidylcholine (PC), dipalmitoyl-PC (DPPC), and cholesterol or 7-ketocholeste

24 s, whereas degradation of internalized [(3)H]dipalmitoyl-PC was significantly decreased.

25 s was also inhibited by the incorporation of dipalmitoyl-PC, but not by free cholesterol.

26 decrease Tmix in ternary GUVs of dioleoyl-PC/dipalmitoyl-PC/cholesterol, whereas 16 carbons increase

27 e hydrated ternary lamellar lipid mixture of dipalmitoyl-PC/dilauroyl-PC/cholesterol (DPPC/DLPC/Chol)

28 1-stearoyl-2-capryl-phosphatidylcholine/1,2-dipalmitoyl-phospha tid ylcholine (C18C10PC/DPPC).

29 PC), dipalmitoyl phosphoethanolamine (DPPE), dipalmitoyl phosphate (DPPA), dipalmitoyl phosphoglycero

30 almitoyl phosphatidylethanolamine (DPPE), or dipalmitoyl phosphatidic acid (DPPA).

31 iPLA2 does have a marked preference for 1,2-dipalmitoyl phosphatidic acid presented in a vesicle, ge

32 For comparison, data for a mixture of dipalmitoyl phosphatidyl choline (DPPC), cholesterol, an

33 lar dynamics simulation data for bilayers of dipalmitoyl phosphatidyl choline and cholesterol for dip

34 oyl phosphatidyl choline and cholesterol for dipalmitoyl phosphatidyl choline:cholesterol ratios of 2

35 ar vesicles of dilauroyl phosphatidylcholine/dipalmitoyl phosphatidylcholine (DLPC/DPPC)/cholesterol

36 unilamellar vesicles made of dimyristoyl or dipalmitoyl phosphatidylcholine (DMPC or DPPC), the latt

37 rated lipid bilayer to systems consisting of dipalmitoyl phosphatidylcholine (DPPC) and cholesterol,

38 nic phospholipids were removed; a mixture of dipalmitoyl phosphatidylcholine (DPPC) and dipalmitoyl p

39 The model membranes consisted of dipalmitoyl phosphatidylcholine (DPPC) and mixtures of d

40 ith experimental data and with properties of dipalmitoyl phosphatidylcholine (DPPC) bilayers.

41 properties of triolein-rich, low-cholesterol dipalmitoyl phosphatidylcholine (DPPC) emulsion particle

42 de GM1 alone and in a binary system with 1,2-dipalmitoyl phosphatidylcholine (DPPC) have been investi

43 e stable than analogous liposomes containing dipalmitoyl phosphatidylcholine (DPPC) instead of DSPC.

44 ons with recent results of a simulation of a dipalmitoyl phosphatidylcholine (DPPC) lipid bilayer sho

45 ded fibrillar networks after adsorption to a dipalmitoyl phosphatidylcholine (DPPC) monolayer in cont

46 ecreased alpha-helical content in films with dipalmitoyl phosphatidylcholine (DPPC) of 52 versus 70%,

47 Lipid was extracted, and [3H]dipalmitoyl phosphatidylcholine (DPPC) secretion was cal

48 on produced surface pressure-area curves for dipalmitoyl phosphatidylcholine (DPPC) that were indisti

49 dylethanolamine (DPPE), and the phospholipid dipalmitoyl phosphatidylcholine (DPPC) were studied in t

50 high-Tm lipid (brain sphingomyelin (SM)) or dipalmitoyl phosphatidylcholine (DPPC)), low-Tm lipid (d

51 he behavior of its most prevalent component, dipalmitoyl phosphatidylcholine (DPPC), although the dom

52 n erythrocytes were modified by insertion of dipalmitoyl phosphatidylcholine (DPPC), dipalmitoyl phos

53 re similar to the liquid condensed phase for dipalmitoyl phosphatidylcholine (DPPC), the most abundan

54 res 6-8 mN/m higher than values observed for dipalmitoyl phosphatidylcholine (DPPC), the most prevale

55 ed peptides that were reconstituted into 1,2-dipalmitoyl phosphatidylcholine (DPPC)-enriched liposome

56 iquid-condensed (LC) and greatly enriched in dipalmitoyl phosphatidylcholine (DPPC).

57 either with palmitoyl sphingomyelin or with dipalmitoyl phosphatidylcholine and present intermediate

58 containing dioleoyl phosphatidylcholine and dipalmitoyl phosphatidylcholine first tested the predict

59 fects local membrane structure by attracting dipalmitoyl phosphatidylcholine headgroups, curving the

60 sn-2 over sn-1 fatty acid by 5-fold for 1,2-dipalmitoyl phosphatidylcholine in a mixed micelle.

61 alproic acid interacting with fully hydrated dipalmitoyl phosphatidylcholine lipid bilayers are studi

62 We find that monolayers containing dipalmitoyl phosphatidylcholine mixed with membrane-acti

63 thermore, we find unusual phase behavior for dipalmitoyl phosphatidylcholine monolayers containing 25

64 ed well experimental heat-capacity curves of dipalmitoyl phosphatidylcholine small unilamellar vesicl

65 omes transfer phosphorylcholine from L-alpha-dipalmitoyl phosphatidylcholine to hybrid and complex ty

66 LSE-cholesterol (20%), or binary mixtures of dipalmitoyl phosphatidylcholine(DPPC)-dihydrocholesterol

67 was significantly reduced in the presence of dipalmitoyl phosphatidylcholine, a known inhibitor of he

68 f a bilayer membrane containing cholesterol, dipalmitoyl phosphatidylcholine, and dioleoylphosphatidy

69 the anticancer drug doxorubicin (DOX) and a dipalmitoyl phosphatidylcholine/Chol lipid bilayer.

70 osphatidylcholines were synthesized from 1,2-dipalmitoyl phosphatidylcholine/egg 1,2-diacyl phosphati

71 l bilayer mixtures of cholesterol (Chol) and dipalmitoyl-phosphatidylcholine (DPPC).

72 ures of 1,2-dioleoyl-phosphatidylcholine/1,2-dipalmitoyl-phosphatidylcholine (DPPC)/cholesterol in mo

73 arlo simulations of ErbB homodimerization in dipalmitoyl-phosphatidylcholine lipid bilayers.

74 reases in the major surfactant phospholipid, dipalmitoyl-phosphatidylcholine.

75 0 mol % ganglioside GT(1b), the phospholipid dipalmitoyl phosphatidylethanolamine (DPPE), and the pho

76 PPC), dipalmitoyl phosphatidylserine (DPPS), dipalmitoyl phosphatidylethanolamine (DPPE), or dipalmit

77 palmitoyl oleoyl phosphatidylethanolamine or dipalmitoyl phosphatidylethanolamine (HAn-PE) were incor

78 f dipalmitoyl phosphatidylcholine (DPPC) and dipalmitoyl phosphatidylglycerol (DPPG) (9:1, mol:mol);

79 Using melittin and a dipalmitoyl phosphatidylglycerol bilayer as a model syst

80 ls from isotopically symmetric or asymmetric dipalmitoyl phosphatidylglycerol bilayers during their i

81 n of dipalmitoyl phosphatidylcholine (DPPC), dipalmitoyl phosphatidylserine (DPPS), dipalmitoyl phosp

82 GUVs containing PI(4,5)P2, cholesterol, and dipalmitoyl phosphatidylserine separated into two coexis

83 ruitment of Gag, but not PHPLCdelta1, to the dipalmitoyl-phosphatidylserine-enriched gel phase of the

84 PA), dipalmitoyl phosphoglycerol (DPPG), and dipalmitoyl phospho-l-serine (DPPS).

85 holipid tails for all phospholipids studied, dipalmitoyl phosphocholine (DPPC), dipalmitoyl phosphoet

86 t of the hydrolysis of the natural substrate dipalmitoyl phosphocholine.

87 studied, dipalmitoyl phosphocholine (DPPC), dipalmitoyl phosphoethanolamine (DPPE), dipalmitoyl phos

88 lamine (DPPE), dipalmitoyl phosphate (DPPA), dipalmitoyl phosphoglycerol (DPPG), and dipalmitoyl phos

89 by the preferential conversion of synthetic dipalmitoyl PI-5-P to PI-4,5-P(2), lack of effect of pho

90 leoyl-PI(4,5)P2 [DO-PI(4,5)P2] and saturated dipalmitoyl-PI(4,5)P2 [DP-PI(4,5)P2] successfully recrui

91 esolution of mouse CD1d bound to a synthetic dipalmitoyl-PIM2.

92 lly available bovine PI and PS and synthetic dipalmitoyl-PS but not to other phospholipid standards,

93 d PT PtdIns(5)P analogues were equivalent to dipalmitoyl PtdIns(5)P in augmenting cell death induced

94 mbinant ING2 similar to liposomes containing dipalmitoyl PtdIns(5)P, indicating that the replacement

95 Fully saturated dipalmitoyl-PtdIns4P was a poor substrate for all three

96 in D peptides conjugated to the TLR2 agonist dipalmitoyl-S-glyceryl cysteine stimulated CD4 T lymphoc

97 hanol (AEE) and a 60:40 molar mixture of 1,2-dipalmitoyl- sn-glycero-3-phosphocholine and 1,2-dipalmi

98 lmitoyl- sn-glycero-3-phosphocholine and 1,2-dipalmitoyl- sn-glycero-3-phosphoethanolamine- N-[methox

99 yl-sn-glycero-3-phospho-RAC-(1-glycerol)/1,2-dipalmitoyl-sn-g lycero-3-phosphocholine and involved fo

100 f 1,2-dipalmitoyl-sn-glycero-3-phosphate/1,2-dipalmitoyl-sn-glycero-3-phosph ocholine and 1,2-dipalmi

101 alpha-synuclein and vesicles composed of 1,2-dipalmitoyl-sn-glycero-3-phosphate/1,2-dipalmitoyl-sn-gl

102 -glycero-3-phosphatidyl-choline (DMPC), 1, 2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and

103 he interdigitated gel phase (LbetaI) of 1, 2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) bila

104 ate of flip-flop in a liquid crystalline 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) bila

105 le- and multicomponent lipid bilayers of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC), 1,2

106 icles of L alpha phase lipid bilayers of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine at 50 degre

107 tadecanoate are less permeable than pure 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine or DSPC bil

108 the (2)H spectra of headgroup-deuterated 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine.

109 ivalent cation-mediated interaction with 1,2-dipalmitoyl-sn-glycero-3-phosphatidylglycerol (DPPG) lip

110 hrough its preferential interaction with 1,2-dipalmitoyl-sn-glycero-3-phosphatidylinositol 4,5-bispho

111 exadecanoyl-sn-glycero-3-phosphocholine, 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol)] unit

112 lmitoyl-sn-glycero-3-phosph ocholine and 1,2-dipalmitoyl-sn-glycero-3-phospho-RAC-(1-glycerol)/1,2-di

113 1,2-dioleoyl-sn-glycero-3-phosphocholine/1,2-dipalmitoyl-sn-glycero-3-phosphochol ine/cholesterol (DO

114 2-dilauroyl-sn-glycero-3-phosphocholine/1, 2-dipalmitoyl-sn-glycero-3-phosphocholine (DLPC/DPPC), 1,

115 ne (DOPC) (fluid at room temperature) or 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) (gel at r

116 additives in a liquid bilayer made from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and 1,2-d

117 namic properties of fully hydrated mixed 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and 1,2-d

118 ported lipid bilayers (SLBs) composed of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and a syn

119 Monolayers of binary mixtures of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and asial

120 exchangeable, disulfide-based mimics of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and chole

121 altered the thermodynamic properties of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayers,

122 le sterol (B) in host bilayers made from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) containin

123 The dependence of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) flip-flop

124 acting with analogues of cholesterol and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in the li

125 ites in supported bilayers consisting of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) lipid dom

126 ze and quantify solute partitioning into 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) lipid ves

127 trol experiments with stiffer, gel-phase 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) liposomes

128 Lipid vesicles having either a 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) or mixed-

129 stoyl-sn-glycero-3-phosphocholine (DMPC)/1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) phospholi

130 in liquid-ordered bilayers derived from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) plus chol

131 rough vesicle membranes composed of pure 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) was measu

132 ur different phosphatidylcholine lipids, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dimy

133 The molecular ion intensities of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dipa

134 -palmitoyl-2-oleoyl-phosphatidylcholine, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and 1,2-

135 ycero-3-phosphocholine (DOPC):DSPC, DOPC:1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and 1,2-

136 toyl-sn-glycero-3-phosphocholine (DMPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and 1,2-

137 toyl-sn-glycero-3-phosphocholine (DMPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and 1-pa

138 ported lipid bilayers composed of gel phase, dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and flui

139 ontaining dipalmitoylphosphatidylcholine(1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), choleste

140 we measured the insertion of Abeta into 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)-gangliosi

141 -disordered (l(d)) bilayers derived from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC).

142 sphoethanolamine (DPPE) and subsequently 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC).

143 -3-phosphocholine (DOPC)/cholesterol and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)/cholester

144 leoyl-sn-glycero-3-phosphocholine (DOPC)/1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)], we repo

145 mitoyl-sn-glycero-3-phosphoethanolamine/1, 2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPE/DPPC), 7:3

146 a')) states and with its ester analogue 1, 2-dipalmitoyl-sn-glycero-3-phosphocholine (Pam(2)PtdCho) i

147 dy of the in-plane phonon excitations in 1,2-dipalmitoyl-sn-glycero-3-phosphocholine above and below

148 olesterol-containing bilayers, made from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine and 1,2-distearo

149 erol (B) in host membranes derived from 1, 2-dipalmitoyl-sn-glycero-3-phosphocholine and varying conc

150 2-oleoyl-sn-glycero-3-phosphocholine and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine in the liquid-or

151 fluid PAPC membranes, but not into solid 1,2-dipalmitoyl-sn-glycero-3-phosphocholine membranes.

152 the laser focus through surface-adhered 1,2-dipalmitoyl-sn-glycero-3-phosphocholine vesicles, produc

153 1,2-dipalmitoyl-sn-glycero-3-phosphocholine was selectively

154 d of different molecular ratios of DPPC (1,2-dipalmitoyl-sn-glycero-3-phosphocholine) and POPC (1-pal

155 l-3-TrimethylAmmonium-Propane) and DPPC (1,2-DiPalmitoyl-sn-glycero-3-PhosphoCholine) surfaces are fu

156 imyristoyl-sn-glycero-3-phosphocholine, 1, 2-dipalmitoyl-sn-glycero-3-phosphocholine, and 1, 2-distea

157 ecanoyl-sn-glycero-3-phosphocholine, and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine.

158 lations on giant unilamellar vesicles of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine.

159 rmed by different phospholipid mixtures (1,2-dipalmitoyl-sn-glycero-3-phosphocholine/1, 2-dilauroyl-s

160 ture lipid multilayers consisting of 1:1 1,2-dipalmitoyl-sn-glycero-3-phosphocholine/1,2-dioleoyl-sn-

161 fect was found from vesicles composed of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine/1-palmitoyl-2-ol

162 st supported a lipid bilayer composed of 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) and

163 l-sn-glycero-3-phosphocholine (DPPC) and 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) bila

164 toyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE), cho

165 l-sn-glycero-3-phosphocholine (DSPC) and 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE), wer

166 exchangeable phospholipids, derived from 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine and 1,2-dis

167 nvestigated by measuring the exchange of 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-n,n-Dimethy

168 at anti-biotin antibodies for biotin-cap-1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(7-nitro-

169 idylethanolamine-PEO conjugates (i.e. , 1, 2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[methoxyp

170 (e thylen e glycol)2000]carboxamide and 1, 2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[methoxyp

171 hocholine (DPPC/DLPC) 1:1 (mol/mol), and 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine/1, 2-dipalm

172 tation when interacting with a supported 1,2-dipalmitoyl-sn-glycero-3-phosphoglycerol (DPPG) bilayer

173 d the stereoisomers of another analogue, 1,2-dipalmitoyl-sn-glycero-3-thiophospho-1-myo-inositol (DPP

174 e mimics of Chol (cholesterol) and Phos (1,2-dipalmitoyl-sn-glycerol-3-phospho-(1'rac-glycerol)) via

175 earoyl-sn-glycero-3-phosphocholine) and 1, 2-dipalmitoyl-sn-glycerophosphatidylethanolamine-PEO conju

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。