ライフサイエンスコーパス: phosphatidylcholine

1 s, such as phosphatidylethanolamine (PE) and phosphatidylcholine.

2 egradation and remodeling of lung surfactant phosphatidylcholine.

3 hatidylethanolamine, phosphatidylserine, and phosphatidylcholine.

4 with membranes containing 2% PI(3)P and 98% phosphatidylcholine.

5 hospholipase D (PLD)-catalyzed hydrolysis of phosphatidylcholine.

6 ynthesis of the essential membrane component phosphatidylcholine.

7 inds anionic phosphatidylserine over neutral phosphatidylcholine.

8 inal domain dimer with bound cholesterol and phosphatidylcholine.

9 ore desaturation of acyl groups occurring on phosphatidylcholine.

10 ein) regulates the intermembrane transfer of phosphatidylcholine.

11 uires a fatty acid from the acyl-CoA pool or phosphatidylcholine.

12 rial membranes, phosphatidylethanolamine and phosphatidylcholine.

13 nt phospholipids; phosphatidylglycerols, and phosphatidylcholines.

14 ssociated lysophospholipids and ether linked phosphatidylcholines.

15 wo major lipid species, triacylglycerols and phosphatidylcholines.

16 changes to metabolism of sphingomyelins and phosphatidylcholines.

17 ritical behavior of mixtures of 1,2-dioleoyl-phosphatidylcholine/1,2-dipalmitoyl-phosphatidylcholine

18 Six biomarkers (ferritin, glycine, diacyl phosphatidylcholines 36:4 and 38:4, lysophosphatidylchol

19 orylated inositides), a phosphatidic acid, a phosphatidylcholine, a phosphatidylethanolamine, and a p

20 holipids and display a strong preference for phosphatidylcholines, a class of phospholipids whose exc

21 ed levels of alanine and decreased levels of phosphatidylcholine alkyl-acyl C42:5 and phosphatidylcho

22 of phosphatidylcholine alkyl-acyl C42:5 and phosphatidylcholine alkyl-acyl C44:4.

23 Thus, the mixture containing phosphatidylcholine and dihydrocaffeic acid amide is a p

24 d the incorporation of [(14)CH3]choline into phosphatidylcholine and observed similar effects.

25 Phosphocholine (pCho) is a precursor for phosphatidylcholine and osmoprotectants in plants.

26 palmitoyl phosphatidylcholine/egg 1,2-diacyl phosphatidylcholine and phenolic acids such as ferulic,

27 The enzymes responsible for the synthesis of phosphatidylcholine and phosphatidylethanolamine are att

28 harged lipids appears to be selective, since phosphatidylcholine and phosphatidylethanolamine promote

29 Measurements were made for neutral (phosphatidylcholine and phosphatidylethanolamine) and an

30 miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine.

31 ed incorporations of arachidonate into liver phosphatidylcholine and phosphatidylethanolamine.

32 hod has been tested on liposomes (containing phosphatidylcholine and phosphatidylglycerol) and four t

33 een of choline derivatives showed that total phosphatidylcholine and phosphatidylinositol (but not di

34 zwitterionic bicelle compositions involving phosphatidylcholine and sphingomyelin in which the acyl

35 We demonstrate that CARDS TX binds phosphatidylcholine and sphingomyelin specifically over

36 Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation

37 ed fatty acid level, but decreased saturated phosphatidylcholine and sphingomyelin within the T cells

38 , bradykinin and angiotensin II; two lipids, phosphatidylcholine and sphingomyelin; Irganox 1010 (a d

39 Phosphatidylcholine and sphingomyeline which have identi

40 almitate-enriched diacylglycerol between the phosphatidylcholine and triacylglycerol pathways, to the

41 mediate many metabolic functions, including phosphatidylcholine and triglyceride synthesis.

42 pid metabolism (reduced lyso- and acyl-alkyl-phosphatidylcholines and increased diacylphosphatidylcho

43 d changes in MIL-R promastigotes occurred to phosphatidylcholines and lysophosphatidylcholines and re

44 was characterized predominantly by saturated phosphatidylcholines and phosphatidylglycerols, which ar

45 mixed bilayers together with sphingomyelin, phosphatidylcholine, and cholesterol.

46 Western diets (enriched in fat, phosphatidylcholine, and L-carnitine) promote inflammati

47 ining n-3 polyunsaturated species in the CL, phosphatidylcholine, and phosphatidylethanolamine profil

48 yl chains of cardiolipin (CL), mono-lyso CL, phosphatidylcholine, and phosphatidylethanolamine.

49 n lipid membranes, phosphatidylethanolamine, phosphatidylcholine, and phosphatidylinositol, and found

50 ed from the chloroplast, reincorporated into phosphatidylcholine, and ultimately enter seed triacylgl

51 in increased levels of specific oxysterols, phosphatidylcholines, and oxidized phospholipids, includ

52 for the small metabolites, diacylglycerides, phosphatidylcholines, and triacylglycerides, in the fly

53 unable to accumulate TAGs after heat stress, phosphatidylcholine appears to be the major fatty acid d

54 AsA) system mediated peroxidation of l-alpha-phosphatidylcholine aqueous dispersions stabilized by bi

55 Phosphatidylcholines are major myelin phospholipids, and

56 TgLCAT uses phosphatidylcholine as substrate to form lysophosphatidy

57 express autoantigen receptors, such as anti-phosphatidylcholine B1a cells, are virtually eliminated.

58 The interaction between PE and phosphatidylcholine-based liposomes was monitored by HAT

59 and Laurdan as fluorescent membrane probes, phosphatidylcholine-based unilamellar liposomes are harn

60 avior of capsaicin in a 1-palmitoyl-2-oleoyl phosphatidylcholine bilayer and with the target S1-S4 tr

61 In the specific case of PI/dimyristoyl phosphatidylcholine bilayers at 22 degrees C, DAG induce

62 al segregation into ceramide-rich domains in phosphatidylcholine bilayers, and the effect of choleste

63 increase in expression of enzymes mediating phosphatidylcholine biosynthesis and incorporation of po

64 al demonstrated that these compounds inhibit phosphatidylcholine biosynthesis from ethanolamine.

65 e-bound photosynthetic apparatus and one for phosphatidylcholine biosynthesis, that were not known to

66 ola LicCA-Cpt pathway in E. coli resulted in phosphatidylcholine biosynthesis.

67 ng histidine, phenylalanine, spermidine, and phosphatidylcholine C34:4, has a diagnostic value simila

68 Thus, phosphatidylcholine can be used as carrier vehicle of nu

69 ipids (cardiolipin, diacylglycerol, and lyso-phosphatidylcholine) can modulate the fusion process, sm

70 n cells, particularly specific subspecies of phosphatidylcholine carrying very long polyunsaturated f

71 ) composed of polymer-lipid/hydrogenated soy phosphatidylcholine/cholesterol/diD: 5.0/54.5/40/0.5.

72 is a glycerophospholipid that, together with phosphatidylcholine, constitutes more than half of the t

73 These data suggest that higher phosphatidylcholine consumption is associated with incre

74 e also find decreased photoreceptor-specific phosphatidylcholine containing very long-chain polyunsat

75 A set of 12 plasma phosphatidylcholines decreased (adjusted p < 0.01) post-

76 ocopherol's (aToc's) behavior in dimyristoyl phosphatidylcholine (di-14:0PC) bilayers.

77 Experiments were conducted with both phosphatidylcholine (dimyristoylphosphatidylcholine (DMP

78 either pure or in mixtures with dimyristoyl phosphatidylcholine, distearoyl phosphatidylcholine, sph

79 ased levels of steroids, sphingomyelins, and phosphatidylcholines distinguished patients from control

80 rane surface in 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine (DMPC)/1,2-dimyristoyl-sn-glycero-3-

81 Using 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC) nanoliposomes, we show that m

82 of the zwitterionic lipid (DMPC, dimyristoyl phosphatidylcholine; DOPC, dioleoyl phosphatidylcholine)

83 id (brain sphingomyelin (SM)) or dipalmitoyl phosphatidylcholine (DPPC)), low-Tm lipid (dioleoylphosp

84 pid bilayers of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC), 1,2-distearoyl-sn-glycero-3-

85 dioleoyl-phosphatidylcholine/1,2-dipalmitoyl-phosphatidylcholine (DPPC)/cholesterol in molar proporti

86 yl, dihexadecyl, diphytanoyl, and diphytanyl phosphatidylcholines (DPPC, DHPC, DPhoPC, and DPhPC, res

87 lcholine (DPPC), 1,2-distearoyl-sn-glycero-3-phosphatidylcholine (DSPC), isostearyl isostearate, and

88 olines were synthesized from 1,2-dipalmitoyl phosphatidylcholine/egg 1,2-diacyl phosphatidylcholine a

89 sruption, but not LPS, caused an increase of phosphatidylcholine ether and cholesteryl esters in CD11

90 her- vs lower-molecular-weight carnitine and phosphatidylcholine family members in specific cardiac r

91 T. denticola Cpt catalyzed in vitro phosphatidylcholine formation from CDP-choline and diacy

92 phodiesterase 6 (ENPP6)-act in sequence upon phosphatidylcholine found in MV membranes to produce pho

93 40 months, parent ratings of children in the phosphatidylcholine group (N=23) indicated fewer attenti

94 mposition; and plasma membrane outer leaflet phosphatidylcholine had a significantly lower level of u

95 O), a gut microbiota metabolite from dietary phosphatidylcholine, has mechanistic links to atheroscle

96 ic detergents that contain phosphocholine or phosphatidylcholine head groups and phospholipid vesicle

97 ion of choline released during PLD-catalyzed phosphatidylcholine hydrolysis, making its kinetic chara

98 choline, a critical step in the synthesis of phosphatidylcholine in a select number of eukaryotes inc

99 The abundance of polyunsaturated phosphatidylcholine in liver ER is selectively increased

100 gnificantly lower level of unsaturation than phosphatidylcholine in the remainder of the cell.

101 in diacylglycerol, 10:0 was not detected in phosphatidylcholine in these seeds.

102 c acids to produce corresponding phenoylated phosphatidylcholines in 48-56% yields.

103 phosphatidylcholines resulted in phenoylated phosphatidylcholines in 87-94% yields.

104 ocytes significantly reduced polyunsaturated phosphatidylcholines in the enterocyte plasma membrane a

105 s) comparing the top and bottom quintiles of phosphatidylcholine intake were 1.11 (1.06, 1.17; P-tren

106 atus, lifestyle, and dietary intakes, higher phosphatidylcholine intakes were associated with an incr

107 ds have very high activity of diacylglycerol-phosphatidylcholine interconversion.

108 is due to the channeling of fatty acids from phosphatidylcholine into TAG before being desaturated to

109 in mineralizing cells and data showing that phosphatidylcholine is broken down in MVs during mineral

110 The trimethylamine-containing nutrient phosphatidylcholine is the major dietary source for the

111 olipoprotein A-I (apoA-I) reconstituted with phosphatidylcholine, is known to cause a dramatic rise i

112 its both omega-6 and omega-3 desaturation in phosphatidylcholine, leading to a proportional change in

113 ation of phosphatidylethanolamine to produce phosphatidylcholine, leads to induction of the MET regul

114 ial-dependent metabolite of dietary choline, phosphatidylcholine (lecithin), and l-carnitine, is elev

115 h the smallest droplets being formed at high phosphatidylcholine levels and at surfactant-to-oil rati

116 g tetraoleoyl cardiolipin (TOCL) and several phosphatidylcholine lipid species.

117 -component mixtures of cholesterol and a PC (phosphatidylcholine) lipid, and we directly visualized t

118 olemia induces HDL lipidomic changes, losing phosphatidylcholine-lipid species and gaining cholestery

119 ronan molecules complex synergistically with phosphatidylcholine lipids present in joints to form a b

120 resonance (ESR) spectroscopy and in L-alpha-phosphatidylcholine liposome peroxidation assay measured

121 When small phosphatidylcholine liposomes are added to perforated ce

122 rimp lipid extract) were encapsulated in soy phosphatidylcholine liposomes with the addition of glyce

123 lation structures based on the entrapment of phosphatidylcholine liposomes, within a WPC matrix throu

124 omain (MPD) of ADAM17 binds to PS but not to phosphatidylcholine liposomes.

125 to phosphatidylserine-liposomes, but not to phosphatidylcholine-liposomes, has been reported, but th

126 3,4,5-triphosphate) but do not bind to 100% phosphatidylcholine-liposomes.

127 ne (LPE) and 2-4-fold higher amounts of lyso phosphatidylcholine (LPC) compared to SP2/0 and CHO cell

128 lood for several species of lipids including phosphatidylcholine, lyso-phosphatidylcholine, phosphati

129 e I), unfolded and bound to the surface of a phosphatidylcholine membrane at neutral pH (State II), a

130 ities, either in phosphatidylethanolamine or phosphatidylcholine membranes.

131 iposomes to nearly background levels of pure phosphatidylcholine membranes.

132 ts bioavailability by encapsulation in mixed phosphatidylcholine micelles.

133 esamol could be solubilised and entrapped in phosphatidylcholine mixed micelles (PCS) with 96.8% effi

134 Triacylglycerol and phosphatidylcholine molecular species distribution was a

135 t the A/W interface and penetration into egg phosphatidylcholine monolayer compared to lysozyme.

136 Humans had higher contents of phosphatidylcholines, oleic acid, and carnitine in plasm

137 eable than pure 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine or DSPC bilayers.

138 I was reconstituted in membranes composed of phosphatidylcholine or plant thylakoid lipids, indicatin

139 centrations of fatty acids, cholesterol, and phosphatidylcholine (p < 0.01 at 72 h; 100 muM MPA) whic

140 changes in hydrodynamic radius of detergent/phosphatidylcholine particles during the micelle-vesicle

141 ositional isomers, such as the regioisomeric phosphatidylcholines PC 16:0/18:1(n-9) and PC 18:1(n-9)/

142 sed to localize double bond positions within phosphatidylcholine (PC) acyl chains.

143 lates biosynthesis of the major phospholipid phosphatidylcholine (PC) and causes expansion of the end

144 es convert nascent to mature HDL, comprising phosphatidylcholine (PC) and cholesterol, which are sele

145 se C (BtPI-PLC), which specifically binds to phosphatidylcholine (PC) and cleaves GPI-anchored protei

146 re the basis of a niosomal system containing phosphatidylcholine (PC) and distearoylphosphatidylethan

147 quired for the synthesis of the phospholipid phosphatidylcholine (PC) and for betaine, an important o

148 mitochondrial phospholipids, bilayer-forming phosphatidylcholine (PC) and non-bilayer-forming phospha

149 spray ionization of the glycerophospholipids phosphatidylcholine (PC) and phosphatidylethanolamine (P

150 decreased levels of cortical and cerebellar phosphatidylcholine (PC) and phosphatidylethanolamine (P

151 ignals from the most abundant phospholipids (phosphatidylcholine (PC) and phosphatidylethanolamine (P

152 In phosphatidylcholine (PC) and phosphatidylglycerol (PG) m

153 ransferase (AAPT) catalyzes the synthesis of phosphatidylcholine (PC) and phosphotidylethanolamine (P

154 y, for example, ether and diacyl species and phosphatidylcholine (PC) and sphingomyelin (SM) lipids.

155 nvestigate the preferred positions of CPS on phosphatidylcholine (PC) and triacylglycerol.

156 ), monogalactosyl diacyglycerol (MGalD), and phosphatidylcholine (PC) and/or their mixtures were stud

157 sity using gramicidin A channels embedded in phosphatidylcholine (PC) bilayers composed of equimolar

158 virulence factor that binds specifically to phosphatidylcholine (PC) bilayers containing negatively

159 ilayers containing 70 mol % PE than for pure phosphatidylcholine (PC) bilayers upon exposure of both

160 Phosphatidylcholine (PC) bilayers were demethylated eith

161 PHOHYDROLASE1 (PAH1) and PAH2 stimulates net phosphatidylcholine (PC) biosynthesis and proliferation

162 The immediate responses to inhibition of phosphatidylcholine (PC) biosynthesis in yeast are alter

163 ants partitioned more dietary choline toward phosphatidylcholine (PC) biosynthesis via the cytidine d

164 he 1950s established the choline pathway for phosphatidylcholine (PC) biosynthesis.

165 de novo and by the remodeling of unsaturated phosphatidylcholine (PC) by lyso-PC acyltransferase 1 (L

166 a) with membranes regulates the synthesis of phosphatidylcholine (PC) by the CDP-choline (Kennedy) pa

167 ns in de novo choline synthesis and produces phosphatidylcholine (PC) enriched in docosahexaenoic aci

168 There it flops the phospholipids of the phosphatidylcholine (PC) family from the inner to the ou

169 and modification of ALA10 expression affects phosphatidylcholine (PC) fatty acyl desaturation by dist

170 ough it is synthesized on the membrane lipid phosphatidylcholine (PC) from an oleoyl ester.

171 Pulsed field gradient NMR of the phosphatidylcholine (PC) head group analogs, dimethyl ph

172 e role of bilayer-forming phospholipids like phosphatidylcholine (PC) in protein transport into the i

173 he ratio of phosphatidylethanolamine (PE) to phosphatidylcholine (PC) is inverted (4 times higher in

174 Phosphatidylcholine (PC) is the major site for PUFA synt

175 anolamine (PE), phosphatidylserine (PS), and phosphatidylcholine (PC) lipids extracted from HeLa cell

176 lcholine receptor (nAChR) reconstituted into phosphatidylcholine (PC) membranes lacking cholesterol a

177 h stabilize the protein, and polyunsaturated phosphatidylcholine (PC) or phosphatidylethanolamine (PE

178 The ABCB4 transporter mediates phosphatidylcholine (PC) secretion at the canalicular me

179 r membrane of hepatocytes, where it mediates phosphatidylcholine (PC) secretion.

180 bind phosphatidylglycerol (PG) acid but not phosphatidylcholine (PC) vesicles in a pH-dependent mann

181 Phosphatidylcholine (PC) was used as an edible encapsula

182 cated that phosphatidylethanolamine (PE) and phosphatidylcholine (PC) were the major lipid components

183 lethanolamine (PE), phosphatidylserine (PS), phosphatidylcholine (PC), and sphingomyelin (SM) cations

184 l attachment were inhibited by PS but not by phosphatidylcholine (PC), demonstrating that TIM-1-media

185 s, namely, phosphatidylethanolamine (PE) and phosphatidylcholine (PC), enhance RdRp activation in vit

186 composed of lipids containing head groups of phosphatidylcholine (PC), phosphatidylethanolamine (PE),

187 patial distribution of phospholipid classes, phosphatidylcholine (PC), phosphatidylethanolamines (PE)

188 Beyond its function for the synthesis of phosphatidylcholine (PC), the methylation of PE facilita

189 The synthesis of phosphatidylcholine (PC), the most abundant cellular pho

190 hether bilayer-forming phospholipids such as phosphatidylcholine (PC), the most abundant phospholipid

191 , the product of the complete deacylation of phosphatidylcholine (PC), was long thought to not be a s

192 We demonstrate that cell-membrane-mimicking phosphatidylcholine (PC)-terminated monolayers improve t

193 ts role in the metabolism of lung surfactant phosphatidylcholine (PC).

194 acts the turnover of the major phospholipid, phosphatidylcholine (PC).

195 in nanoliposomes made of partially purified phosphatidylcholine (PC).

196 limiting enzyme involved in the synthesis of phosphatidylcholine (PC).

197 he most abundant mitochondrial phospholipid, phosphatidylcholine (PC).

198 The phosphatidylcholine (PC)/BA ratio in treated mice correc

199 The effect of the phosphatidylcholine (PC):EA molar ratio on the physicoch

200 cylglycerol species, unmodified and oxidized phosphatidylcholine (PC/Ox-PC), and diacylglycerol (DG)

201 stearoyl SM (PSM and SSM, respectively)) and phosphatidylcholine (PC; dipalmitoyl PC and 1-palmitoyl-

202 e in phosphatidylethanolamine (PE) and ether phosphatidylcholine (PCe) and increase in lysophosphatid

203 rt the direct CCS measurement of a series of phosphatidylcholines (PCs) and phosphatidylethanolamines

204 Phosphatidylcholines (PCs) and phosphatidylethanolamines

205 ation mode, for example, this can occur with phosphatidylcholines (PCs) and phosphatidylserines (PSs)

206 Multiple saturated and unsaturated phosphatidylcholines (PCs) and their fragments are detec

207 ylglycerol (PGs), glycerophospholipids (PI), phosphatidylcholines (PCs) and tripeptides.

208 In particular, the presence of abundant phosphatidylcholines (PCs) can reduce the ion yields for

209 d for the quantitative determination of four phosphatidylcholines (PCs) in human exhaled breath parti

210 ee major PL classes found in living systems: phosphatidylcholines (PCs), phosphatidylethanolamine (PE

211 labile methyl groups is in the production of phosphatidylcholines (PCs), which are ligands for the nu

212 s of LCFAs, especially between PEs, PIs, and phosphatidylcholines (PCs; P </= 3.5 x 10(-6)).

213 inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphing

214 particularly fatty acids, diacylglycerides, phosphatidylcholine, phosphatidylethanolamine, and phosp

215 f lipids including phosphatidylcholine, lyso-phosphatidylcholine, phosphatidylethanolamine, phosphati

216 In young leaves of phosphate-limited plants, phosphatidylcholine/phosphatidylethanolamine and associa

217 erol esters (CEs), lysophosphatidylcholines, phosphatidylcholines, phosphatidylethanolamines (PEs), s

218 Here, we use model lipid membranes (made of phosphatidylcholine, phosphatidylserine, and ceramide) a

219 Disruption of phosphatidylcholine, phosphatidylserine, and/or phosphat

220 spholipid classes in the exosomes, including phosphatidylcholine, phosphatidylserine, phosphatidyleth

221 with factor Xa (FXa) and phospholipids (FXa/phosphatidylcholine-phosphatidylserine [PCPS]) vs LD100

222 size or molecular species composition of the phosphatidylcholine pool in infected HeLa cells.

223 atidylcholine (DOPC) or 1-palmitoyl 2-oleoyl phosphatidylcholine (POPC)), and a lower (28 mol %) or h

224 (DMPG) and 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine (POPC)/1-palmitoyl-2-oleoyl-sn-glyce

225 ayers consisting of: 1) 1-palmitoyl 2-oleoyl-phosphatidylcholine (POPC); 2) 1-palmitoyl 2-oleoyl-phos

226 s increase dependence on dietary choline for phosphatidylcholine production at the expense of betaine

227 mulations of the mammalian StART-like PtdIns/phosphatidylcholine (PtdCho) transfer protein PITPalpha,

228 phospholipids, phosphatidylethanolamine and phosphatidylcholine (PtdCho), are synthesized by the tra

229 both its phosphatidylinositol (PtdIns)- and phosphatidylcholine (PtdCho)-binding properties to stimu

230 At 26-28 wk of gestation, plasma phosphatidylcholine PUFA concentrations were measured an

231 proportion of sphingomyelin and ceramide to phosphatidylcholine (q=0.008), suggesting a pleiotropic

232 hasic behavior with respect to the detergent/phosphatidylcholine ratio.

233 Here we studied different detergent/phosphatidylcholine reconstitution media and tested thei

234 he mechanism of conversion of CDP-choline to phosphatidylcholine remained unclear.

235 ne acyltransferase 3 (Lpcat3) is involved in phosphatidylcholine remodeling in the small intestine an

236 Deprotection of protected phenoylated phosphatidylcholines resulted in phenoylated phosphatidy

237 The experiments with fluorescent phosphatidylcholine reveal a low level of phospholipase

238 Saturated phosphatidylcholine (SatPC), the major component of surf

239 fibrate treatment further stimulates biliary phosphatidylcholine secretion in rat hepatocytes, thereb

240 d vectorial bile salt transport and specific phosphatidylcholine secretion into the apical compartmen

241 954S) or almost absence (S346I and P726L) of phosphatidylcholine secretion.

242 azole, significantly inhibited MDR3-mediated phosphatidylcholine secretion.

243 Using a binary mixture of citrem and soy phosphatidylcholine (SPC) at different weight ratios, we

244 cholesteryl esters and a surface depleted of phosphatidylcholine species containing polyunsaturated a

245 entify in which complex lipid species (i.e., phosphatidylcholine, sphingolipids, etc) these FA differ

246 dimyristoyl phosphatidylcholine, distearoyl phosphatidylcholine, sphingomyelin, or galactosylceramid

247 ally significant changes in plasma levels of phosphatidylcholines, sphingomyelins and others in just

248 creased; and most phosphatidylethanolamines, phosphatidylcholines, sphingomyelins, and lysophosphatid

249 lating metabolites that included lower serum phosphatidylcholines, sphingomyelins, tryptophan, ornith

250 e ternary lipid mixture, 2:1:2 POPC/SM/chol (phosphatidylcholine/sphyngomyelin/cholesterol), showing

251 olled trial to assess whether high-dose oral phosphatidylcholine supplementation during pregnancy to

252 of the highly conserved Kennedy pathway for phosphatidylcholine synthesis in eukaryotes.

253 gs show that T. denticola possesses a unique phosphatidylcholine synthesis pathway combining conserve

254 fects on Cho metabolism, including increased phosphatidylcholine synthesis.

255 pt in T. denticola resulted in abrogation of phosphatidylcholine synthesis.

256 y to separate and uniquely identify isomeric phosphatidylcholines that differ only in their position(

257 lamine also contributes to the production of phosphatidylcholine, the most abundant class of lipids i

258 mediated hydrolysis of arachidonic acid from phosphatidylcholine, thereby integrating the production

259 Treponema denticola synthesizes phosphatidylcholine through a licCA-dependent CDP-cholin

260 transport by transferring an acyl group from phosphatidylcholine to cholesterol, promoting the matura

261 ina sativa to test whether the conversion of phosphatidylcholine to DAG impacts TAG levels in seeds.

262 ynthesis of ladderane lipid tails and a full phosphatidylcholine to enable biophysical studies on che

263 Exogenous delivery of polyunsaturated phosphatidylcholine to ER accelerated SREBP-1c processin

264 are enzymes that catalyze the hydrolysis of phosphatidylcholine to generate an important signaling l

265 . the transfer of different acyl groups from phosphatidylcholine to monolysocardiolipin by yeast tafa

266 by lubricin molecules, complexes with joint phosphatidylcholines to provide the extreme lubrication

267 yristoyl phosphatidylcholine; DOPC, dioleoyl phosphatidylcholine) to the negatively charged lipid (DO

268 in vitro is increased when it interacts with phosphatidylcholine transfer protein (PC-TP), a cytosoli

269 thioesterase that is activated upon binding phosphatidylcholine transfer protein (PC-TP).

270 PCTP (phosphatidylcholine transfer protein) regulates the inte

271 al complex formed between a PC and the human phosphatidylcholine transfer protein.

272 se in expression of Stard7, an intracellular phosphatidylcholine transport protein.

273 ors previously reported that newborns in the phosphatidylcholine treatment group have increased suppr

274 Maternal phosphatidylcholine treatment may, by increasing activat

275 The concentrations of two phosphatidylcholines, two diglycerides and two acyl-carn

276 In two-component phosphatidylcholine unilamellar vesicles [1,2-dioleoyl-s

277 te variant, are essentially inactive against phosphatidylcholine vesicles and multiple types of eukar

278 from ATP-loaded lipid (1-palmitoyl-2-oleoyl-phosphatidylcholine) vesicles devoid of any erythrocyte

279 yso phosphatidylcholine was synthesized from phosphatidylcholine via regioselective enzymatic hydroly

280 ine, choline, and female sex, whereas plasma phosphatidylcholine was a negative determinant.

281 Phosphatidylcholine was found to be the most abundant gl

282 1-(Palmitoyl)-2-(5-keto-6-octene-dioyl) phosphatidylcholine was incorporated on their surface to

283 2-acyl-1-lyso phosphatidylcholine was synthesized from phosphatidylcho

284 Phosphatidylcholine was the most common phospholipid, ac

285 Soy phosphatidylcholine was used to synthesize liposome-like

286 Higher concentrations of plasma phosphatidylcholine were associated with characteristics

287 concentrations of free choline, betaine, and phosphatidylcholine were measured with the use of liquid

288 factors: increases in 5 different acyl-alkyl phosphatidylcholines were associated with lower alcohol

289 The structures of phenoylated phosphatidylcholines were confirmed by spectral analysis

290 cis and trans forms of triacylglycerols and phosphatidylcholines were identified by this DMS-EIEIO w

291 Novel phenoylated phosphatidylcholines were synthesized from 1,2-dipalmito

292 Choline metabolites, including phosphatidylcholine, were reduced due to genotype and/or

293 esters, triglycerides, free fatty acids, and phosphatidylcholine, which is blocked by inhibitors of f

294 ed to examine whether dietary consumption of phosphatidylcholine, which is mainly derived from eggs,

295 use of their function in the biosynthesis of phosphatidylcholine, which is unique to eukaryotic membr

296 The associations of phosphatidylcholine with all-cause and CVD mortality wer

297 , the evidence for an association of dietary phosphatidylcholine with CVD and mortality is limited.

298 n of liposomal membranes composed of soybean phosphatidylcholine with the bile salts (BSs) cholate (C

299 ultiple testing; within these compounds, the phosphatidylcholine with the greatest decrease in abunda

300 elles of lysophosphatidylcholines and diacyl phosphatidylcholines with different chain lengths conver