ライフサイエンスコーパス: phosphatidylcholine

1 of the Kennedy pathway for the synthesis of phosphatidylcholine.

2 ture of cholesterol, phosphatidylserine, and phosphatidylcholine.

3 els at exchanging the human-like unsaturated phosphatidylcholine.

4 phatidylcholine can be semi-quantified using phosphatidylcholine.

5 idylation reaction of PLD's lipid substrate, phosphatidylcholine.

6 31 +/- 88 mg/d, of which 188 +/- 63 mg/d was phosphatidylcholine.

7 with equal amounts of phosphatidylserine and phosphatidylcholine.

8 ore desaturation of acyl groups occurring on phosphatidylcholine.

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

10 ynthesis of the essential membrane component phosphatidylcholine.

11 inds anionic phosphatidylserine over neutral phosphatidylcholine.

12 inal domain dimer with bound cholesterol and phosphatidylcholine.

13 ein) regulates the intermembrane transfer of phosphatidylcholine.

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

15 rial membranes, phosphatidylethanolamine and phosphatidylcholine.

16 o extracts PI4P from the PM, in exchange for phosphatidylcholine.

17 asmic leaf is rich in phosphatidylserine and phosphatidylcholine.

18 les and formation of the hydrogen bonds with phosphatidylcholine.

19 mimics made of natural, "neutron invisible" phosphatidylcholines.

20 ssociated lysophospholipids and ether linked phosphatidylcholines.

21 wo major lipid species, triacylglycerols and phosphatidylcholines.

22 changes to metabolism of sphingomyelins and phosphatidylcholines.

23 ylarginine, tyramine, 2-hydroxybutyric acid, phosphatidylcholine (32:1), and taurochenodesoxycholic a

24 D in PREDIMED, 1.28 [95% CI, 1.13-1.47]) and phosphatidylcholine 32_0 (RR per SD in PREDIMED, 1.23 [9

25 We identified an association with relative phosphatidylcholine 38:3 (%PC 38:3) concentration, which

26 xed micelles of STC and 1-palmitoyl, 2-oleyl phosphatidylcholine, a phospholipid present in high prop

27 In young mice, anti-phosphatidylcholine Abs, like anti-phosphorylcholine Abs

28 Acyl flux around the phosphatidylcholine acyl editing cycle was the largest a

29 rnitine (C3-OH, p-value = 2.6 x 10(-4)), and phosphatidylcholine acyl-alkyl C38:4 (PC ae C38:4, p-val

30 ant differences in lysophosphatidylcholines, phosphatidylcholines, acylcarnitine, amino acids and sph

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

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

33 (2 mM) Ca(2+) concentration on zwitterionic phosphatidylcholine and anionic phosphatidylserine lipid

34 icular lipid mixtures containing diphytanoyl-phosphatidylcholine and cholesterol plus different types

35 tory pathway that controls genes involved in phosphatidylcholine and fatty acid utilization and contr

36 sts and microsomal membranes, and hydrolyzes phosphatidylcholine and galactolipids to produce diacylg

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

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

39 Phosphatidylcholine and phosphatidylethanolamine are two

40 simulation of the whole TRPV1 embedded in a phosphatidylcholine and phosphatidylethanolamine membran

41 ynthesis of the most abundant phospholipids, phosphatidylcholine and phosphatidylethanolamine, respec

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

43 ed incorporations of arachidonate into liver phosphatidylcholine and phosphatidylethanolamine.

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

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

46 riacylglycerol, C54:9 triacylglycerol, C36:1 phosphatidylcholine and sucrose replicated in an indepen

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

48 ficant decrease in lysophosphatidylcholines, phosphatidylcholines and cholesterol esters and an incre

49 Phosphatidylcholines and cholesteryl esters were positiv

50 Pathway analysis showed that the three phosphatidylcholines and methionine are involved in homo

51 ve ion mode, MALDI spectra were dominated by phosphatidylcholines and phosphatidic acids.

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

53 rn representing higher levels of unsaturated phosphatidylcholines and phospholipid ethers, and lower

54 e outer leaf as consisting of sphingomyelin, phosphatidylcholine, and cholesterol and the inner leaf

55 hosphatidylethanolamine, phosphatidylserine, phosphatidylcholine, and cholesterol.

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

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

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

59 talk between these lysophosphatidylcholines, phosphatidylcholines, and coagulation and complement pro

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

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

62 Phosphatidylcholines are major myelin phospholipids, and

63 lations show a selective enrichment of ether phosphatidylcholine around p24 proteins, which are recep

64 TgLCAT uses phosphatidylcholine as substrate to form lysophosphatidy

65 Membranes are composed of bulk lipids (e.g., phosphatidylcholine), as well as regulatory lipids that

66 D simulations with 1.4 mol% PI(4,5)P(2) in a phosphatidylcholine bilayer identified 8 binding sites w

67 state, and an open state, each embedded in a phosphatidylcholine bilayer.

68 c diclofenac exerted distinct alterations in phosphatidylcholine bilayers, which are used in this wor

69 ctures revealed two evolutionarily conserved phosphatidylcholine-binding mechanisms and their roles i

70 Moreover, activation of phosphatidylcholine biosynthesis by phospholipase C trea

71 second and rate-limiting step of the de novo phosphatidylcholine biosynthesis is catalysed by CTP: ph

72 ing, we demonstrated that phosphocholine and phosphatidylcholine biosynthesis was markedly elevated i

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

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

75 ne (PE) biosynthesis; however, exogenous NBD-phosphatidylcholine, Bodipy-PE, and TopFluor-cholesterol

76 ipid N-methyltransferases (PLMTs) synthesize phosphatidylcholine by methylating phosphatidylethanolam

77 cholesterol-rich (SCOR) lipid mixtures with phosphatidylcholine can be cosolubilized by n-dodecyl-be

78 ts, for example indicating that ether-linked phosphatidylcholine can be semi-quantified using phospha

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

80 ne (PE)/phosphatidylglycerol) and mammalian (phosphatidylcholine/cholesterol (PC/Chol)) membranes.

81 art of the mechanism to preserve choline and phosphatidylcholine, choline transporter deficiency was

82 namic size increased with increasing l-alpha-phosphatidylcholine concentration (1.5-7.5 mM) for both

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

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

85 iminished choline transport yet the membrane phosphatidylcholine content remained unchanged.

86 cylglycerols, phosphatidylethanolamines, and phosphatidylcholines; decreases in abundance was observe

87 enzymes utilize a different and larger bulk phosphatidylcholine-derived DAG pool that is more slowly

88 AtDGAT1 produces TAG from a rapidly produced phosphatidylcholine-derived DAG pool.

89 Role of phosphatidylcholine-DHA in preventing APOE4-associated A

90 10(-5)), tyrosine (p-value = 2.1 x 10(-4)), phosphatidylcholine diacyl C32:1 (PC aa C32:1, p-value =

91 esis, interact with the acyl-editing enzymes phosphatidylcholine: diacylglycerol cholinephosphotransf

92 rol acyltransferase mutant dgat1-1 (in which phosphatidylcholine:diacylglycerol acyltransferase (AtPD

93 on in camelina (Camelina sativa) of a lychee PHOSPHATIDYLCHOLINE:DIACYLGLYCEROL CHOLINEPHOSPHOTRANSFE

94 ivity to relieve competition and knocked out phosphatidylcholine:diacylglycerol cholinephosphotransfe

95 AtROD1 encodes phosphatidylcholine:diacylglycerol cholinephosphotransfe

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

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

98 cerol (DOPG), and 1,2-dioleoyl-sn-glycerol-3-phosphatidylcholine (DOPC) structurally stabilize the co

99 eta) composition is dominated by dipalmitoyl phosphatidylcholine (DPPC), which is the most prevalent

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

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

102 estatic liver injury due to impaired biliary phosphatidylcholine excretion, resulted in cirrhosis and

103 The surfactant lipid class phosphatidylcholine expanded 17-fold, lysophosphatidylch

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

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

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

107 Twelve phosphatidylcholines, four lysophosphatidylcholines, and

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

109 wo of these phospholipids, sphingomyelin and phosphatidylcholine, have the highest GB of any small, m

110 ssing, stigmasterol (ST) and/or hydrogenated phosphatidylcholine (HPC) for the encapsulation lactofer

111 phospholipase D (PLD), which produces PA by phosphatidylcholine hydrolysis, and the CRY2-CIBN light-

112 es the exclusion of hydroxy fatty acids from phosphatidylcholine in developing transgenic Arabidopsis

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

114 and asymmetric chains in SMs and diphytanoyl-phosphatidylcholine in the lipid mixtures.

115 The second kind of domain is rich in phosphatidylcholine in the outer leaf and in cholesterol

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

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

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

119 istribution of Delta9 and Delta11 isomers of phosphatidylcholines in mouse brain and in human colon s

120 thanolamines elevated in astrocytes and nine phosphatidylcholines in neurons.

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

122 e to the rich content of choline, especially phosphatidylcholine, in eggs because choline has been su

123 sion of genes important for the formation of phosphatidylcholine, including LYSOPHOSPHATIDYLCHOLINE A

124 t content; milk phosphatidylethanolamine and phosphatidylcholine increased by 22 and 26%, respectivel

125 In addition, PG, but not phosphatidylcholine, inhibited downstream S100A9-elicite

126 hose in the highest compared with the lowest phosphatidylcholine intake quartile had 28% (95% CI: 1%,

127 Higher phosphatidylcholine intake was associated with lower ris

128 However, both total choline and phosphatidylcholine intakes were associated with better

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

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

131 P-binding cassette transporter that extrudes phosphatidylcholine into the bile canaliculi of the live

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

133 The mostly extraplastidial lipid phosphatidylcholine is found only in the outer envelope.

134 ynthesis of the major membrane phospholipid, phosphatidylcholine, is catalyzed by CTP:phosphocholine

135 1-(Palmitoyl)-2-(5-keto-6-octene-dioyl) phosphatidylcholine (KOdiA-PC), a major type of oxidized

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

137 ular ions of the EGFR inhibitor erlotinib, a phosphatidylcholine lipid, and cholesterol, which were r

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

139 hese results indicate that sphingomyelin and phosphatidylcholine lipids can act as charge-reducing ag

140 sphatidylserine lipids than for zwitterionic phosphatidylcholine lipids in the same membrane.

141 e activate B-cells via supported bilayers of phosphatidylcholine lipids, a natural ligand for the IgM

142 ity in extruded vesicles composed of neutral phosphatidylcholine lipids, including for the common cas

143 lipids overall but has a minor affinity for phosphatidylcholine lipids.

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

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

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

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

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

149 diacylglycerol, phosphatidic acid, and lyso-phosphatidylcholine (LPC) have all been implicated in ER

150 cytosolic phospholipase A2 activity and lyso-phosphatidylcholine (Lyso-PC) levels in ALS patients sug

151 iposomes to nearly background levels of pure phosphatidylcholine membranes.

152 to negatively charged (phosphatidylserine or phosphatidylcholine) membranes than purely zwitterionic

153 Phosphatidylcholine metabolites were associated with hig

154 ts bioavailability by encapsulation in mixed phosphatidylcholine micelles.

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

156 n toward the inner leaf by the sphingomyelin phosphatidylcholine mixture.

157 Triacylglycerol and phosphatidylcholine molecular species distribution was a

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

159 ipids, lysophosphatidylcholines (n = 11) and phosphatidylcholines (n = 61), and the protein members o

160 (NES = -1.77, P = 0.005, FDR P = 0.02), and phosphatidylcholines (NES = -1.72, P = 0.01, P = 0.03) w

161 E. chaffeensis cannot synthesize phosphatidylcholine or cholesterol but encodes enzymes f

162 resulted in defective bacterial growth when phosphatidylcholine or palmitic acid was used as the sol

163 choline) membranes than purely zwitterionic (phosphatidylcholine or phosphatidylethanolamine) ones.

164 he biosynthesis of phosphatidylethanolamine, phosphatidylcholine, or cardiolipin (CL).

165 S and oxidized 1-palmitoyl-2-arachidonoyl-sn-phosphatidylcholine (oxPAPC) dependent pro-inflammatory

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

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

168 Yields of phosphatidylcholine (PC) acidolysis with CLA use to be l

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

170 In oilseed crops, PUFAs are synthesized on phosphatidylcholine (PC) and accumulated in triacylglyce

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

172 an opposite leaflet composed of unsaturated phosphatidylcholine (PC) and cholesterol.

173 The aim was to characterize phosphatidylcholine (PC) and choline metabolism in prete

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

175 HH group showed significantly lower serum phosphatidylcholine (PC) and significantly higher phosph

176 atidylethanolamine (PE), sphingomyelin (SM), phosphatidylcholine (PC) and their molecular species wer

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

178 De novo phosphatidylcholine (PC) biosynthesis via the Kennedy pa

179 exhibit markers of increased rate of de novo phosphatidylcholine (PC) biosynthesis.

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

181 d CCTbeta catalyze the rate-limiting step in phosphatidylcholine (PC) biosynthesis.

182 rporation of ferulic acid (FA) into egg-yolk phosphatidylcholine (PC) in a lipase-catalyzed acidolysi

183 in the chloroplast, followed by assembly of phosphatidylcholine (PC) in the endoplasmic reticulum (E

184 Phosphatidylcholine (PC) is a major cell membrane consti

185 Phosphatidylcholine (PC) is a primary class of membrane

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

187 strated via the charge inversion reaction of phosphatidylcholine (PC) lipid cations generated from ra

188 f diacylglyceryltrimethylhomo-Ser (DGTS) and phosphatidylcholine (PC) lipids measured in each cell.

189 The proportion of EPA in serum phosphatidylcholine (PC) mirrors dietary EPA intake duri

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

191 Phospholipase B-mediated hydrolysis of phosphatidylcholine (PC) results in the formation of fre

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

193 ferase (CCT) is the key regulatory enzyme in phosphatidylcholine (PC) synthesis and is activated by b

194 ansferase (CCT), the rate-limiting enzyme in phosphatidylcholine (PC) synthesis, is an amphitropic en

195 ynthesis of phosphatidylethanolamine (PE) or phosphatidylcholine (PC) via the Kennedy pathway.

196 h combinations of sodium caseinate (CAS) and phosphatidylcholine (PC) was optimized.

197 Phosphatidylcholine (PC) was used as an edible encapsula

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

199 s study investigated the effects of modified phosphatidylcholine (PC) with different alkyl chain leng

200 ologic effect of phosphatidylserine (PS) and phosphatidylcholine (PC), 2 phospholipids highly abundan

201 s a rate-limiting enzyme in the synthesis of phosphatidylcholine (PC), a predominant mitochondrial me

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

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

204 rous diacylglyceryltrimethylhomo-Ser (DGTS), phosphatidylcholine (PC), monogalactosyldiacylglycerol (

205 T and 0.2 mM at 2 T, while the headgroups of phosphatidylcholine (PC), phosphatidyl-ethanolamine (PE)

206 1p co-isolates with phosphatidylserine (PS), phosphatidylcholine (PC), phosphatidylethanolamine (PE),

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

208 Phosphatidylcholine (PC), phosphatidylethanolamine (PE),

209 der AT and HT, the lipidome was dominated by phosphatidylcholine (PC), phosphatidylethanolamine (PE),

210 nDi allows complete and rapid methylation of phosphatidylcholine (PC), phosphatidylethanolamine (PE),

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

212 Plants use several pathways to synthesize phosphatidylcholine (PC), the major phospholipid of euka

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

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

215 ts identified a metabolic bottleneck between phosphatidylcholine (PC), the site of CPA biosynthesis,

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

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

218 high proportion of the HFAs are retained in phosphatidylcholine (PC).

219 into larger metabolites, including the lipid phosphatidylcholine (PC).

220 removal of HFA from the site of synthesis on phosphatidylcholine (PC).

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

222 ilamellar vesicles made of PDMS-g-PEO and/or phosphatidylcholine (PC).

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

224 , fatty acid desaturation, and generation of phosphatidylcholine (PC).

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

226 es of Dnf2 are glucosylceramide (GlcCer) and phosphatidylcholine (PC, or their lyso-lipid derivatives

227 Phosphatidylcholines (PC) and sphingomyelins (SM) were t

228 choline (KOdiA-PC), a major type of oxidized phosphatidylcholines (PC) found on oxLDL, has a high bin

229 nd phenylalanine), and glycerophospholipids (phosphatidylcholine [PC] aa C36:1 and Lyso-PC a C18:1).

230 ansfer of HFAs from their site of synthesis (phosphatidylcholine; PC) to triacylglycerol (TAG), espec

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

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

233 rides decreased in mixed field exposures and phosphatidylcholines (PCs) remained largely unchanged.

234 chromatography-tandem mass spectrometry (21 phosphatidylcholines (PCs), 7 lysophosphatidylethanolami

235 e of fish from polluted and reference sites; phosphatidylcholines (PCs), phosphatidylethanolamines (P

236 ctive fractions led to the identification of phosphatidylcholines (PCs).

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

238 es in triglycerides (TG), diglycerides (DG), phosphatidylcholine, phosphatidylethanolamine, ceramide

239 protein particles, we incorporated ApoE into phosphatidylcholine/phosphatidylethanolamine liposomes a

240 esters, diacylglycerides, triacylglycerides, phosphatidylcholines, phosphatidylethanolamines, and sph

241 tive towards diverse phospholipids including phosphatidylcholine, phosphatidylinositol and phosphatid

242 xture of phospholipids, with high amounts of phosphatidylcholines, phosphatidylinositols (PI) and cho

243 broside, ceramide, phosphatidylethanolamine, phosphatidylcholine, phosphatidylserine, and phosphatidi

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

245 ation of the oncogenic G12V-KRAS mutant in a phosphatidylcholine/phosphatidylserine bilayer, we first

246 mors (n = 34 cases), pseudouridine and C36:2 phosphatidylcholine plasmalogen had the strongest statis

247 n of fatty acyl chains into the sn-2 site of phosphatidylcholine, play important roles in pathophysio

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

249 uctures of ELIC embedded in palmitoyl-oleoyl-phosphatidylcholine- (POPC-) only nanodiscs in both the

250 hesis was not detected, as acyl flux through phosphatidylcholine preceded the incorporation into TAG.

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

252 ucture of a representative TCR bound to CD1b-phosphatidylcholine provides a molecular mechanism for t

253 redominately reactive to self antigens, like phosphatidylcholine (PtC), or antigens expressed by the

254 , we demonstrate the germline-like status of phosphatidylcholine (PtC)-specific (PtC(+)) peritoneal B

255 omoting genes such as CHPT1, which catalyzes phosphatidylcholine (PtdCho) synthesis and regulates cho

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

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

258 ment, as well as the lysophosphatidylcholine/phosphatidylcholine ratio.

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

260 Deprotection of protected phenoylated phosphatidylcholines resulted in phenoylated phosphatidy

261 were loaded into liposomes prepared from soy phosphatidylcholine (SPC) with various stabilizers (chol

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

263 plex mixture of phospholipids with different phosphatidylcholine species present in large amounts.

264 e middle of the tail core, regardless of the phosphatidylcholine species.

265 phocholine (ChoP), a reaction product of the phosphatidylcholine-specific phospholipase C (PC-PLC) of

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

267 uded advanced glycation end products (AGEs), phosphatidylcholines, sphingolipids, saturated/unsaturat

268 Unsaturated phosphatidylcholines, sphingomyelins, phosphatidylethano

269 lates lipid sensing by GCalpha and find that phosphatidylcholine stimulates PfPP1-dependent egress.

270 the incorporation of cholesterol in various phosphatidylcholine supported lipid bilayers by neutron

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

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

273 ts indicate that enhanced phosphocholine and phosphatidylcholine synthesis supports the prolonged sur

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

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

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

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

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

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

280 Hydrolysis of phosphatidylcholine to choline was found to be catalysed

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

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

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

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

285 PCTP (phosphatidylcholine transfer protein) regulates the inte

286 They point to a higher accumulation of phosphatidylcholines, triacylglycerols, and diacylglycer

287 line or cholesterol, phosphatidylserine, and phosphatidylcholine, two low-affinity MPP(+) binding sit

288 at PvrA directly regulates genes involved in phosphatidylcholine utilization and fatty acid catabolis

289 flagella-dependent adhesion of Salmonella to phosphatidylcholine vesicles and epithelial cells.

290 Using phosphatidylcholine vesicles containing the membrane pro

291 rent residue at an experimental pH of 9.5 in phosphatidylcholine vesicles.

292 yso phosphatidylcholine was synthesized from phosphatidylcholine via regioselective enzymatic hydroly

293 2-acyl-1-lyso phosphatidylcholine was synthesized from phosphatidylcho

294 The differential abundance of phosphatidylcholines we found can be attributed at least

295 Higher concentrations of plasma phosphatidylcholine were associated with characteristics

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

297 The structures of phenoylated phosphatidylcholines were confirmed by spectral analysis

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

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

300 thyl group-dependent endogenous synthesis of phosphatidylcholine, which is needed for lipoprotein syn