ライフサイエンスコーパス: glycerophospholipid

1 role for this plasmalogen molecular species glycerophospholipid.

2 small molecules biosynthesized from membrane glycerophospholipid.

3 ylserine and phosphatidylglycerol were minor glycerophospholipids.

4 between the two halophytes and the different glycerophospholipids.

5 ds from acyl-ACP to the 1-position of 2-acyl-glycerophospholipids.

6 abolite profiles with high levels of various glycerophospholipids.

7 nutrient-sensing pathways and regulation of glycerophospholipids.

8 lly metabolizes PAF and structurally related glycerophospholipids.

9 atalyzes a critical step in the synthesis of glycerophospholipids.

10 these AGPATs in remodeling of several of the glycerophospholipids.

11 developed for the rapid analyses of cellular glycerophospholipids.

12 the nonionic detergent NP-40, together with glycerophospholipids.

13 ion of the membrane, examined by doping with glycerophospholipids.

14 d fractional turnover of 16:0 in the choline glycerophospholipids.

15 ducing lysophosphatidic acid (LPA) from lyso-glycerophospholipids.

16 s required for the chlamydial uptake of host glycerophospholipids.

17 e in the biosynthesis of triacylglycerol and glycerophospholipids.

18 s at both the sn-1 and sn-2 positions of the glycerophospholipids.

19 minimal increase in activity with alkylacyl glycerophospholipids.

20 and certain other fatty acids into the major glycerophospholipids.

21 enoic acid and other isomers within platelet glycerophospholipids.

22 mallest and structurally simplest of all the glycerophospholipids.

23 gen atom into the arachidonate esterified to glycerophospholipids.

24 only 10.9 nmol/10(9) platelets from choline glycerophospholipids.

25 cum increases mycolate content and decreases glycerophospholipids.

26 increased plasma and BALF glycerolipids and glycerophospholipids.

27 lds near-complete structural information for glycerophospholipids.

28 rred tool for structural characterization of glycerophospholipids.

29 rs through hydrolysis of membrane-associated glycerophospholipids.

30 Since the oxidized glycerophospholipid 1-hexadecyl-2-azelaoyl glycerophosph

31 The glycerophospholipid 1-stearoyl-2-oleoyl-sn-glycero-3-pho

32 ons of 14 amino acids, 17 acylcarnitines, 81 glycerophospholipids, 14 sphingomyelins, and ferritin we

33 ylcarnitines, 25% for glycerolipids, 23% for glycerophospholipids, 16% for cholesteryl esters, 15% fo

34 for 3 h, tetra-acylated lipid A species and glycerophospholipids accumulate in the inner membrane.

35 All characterized P4-ATPases flip glycerophospholipids across the bilayer to the cytosolic

36 ensing pathways showed reciprocal changes in glycerophospholipid acyl chain lengths.

37 embranes acting as a hydrophobic support for glycerophospholipid acyl chains.

38 S. pombe that generates membranes where both glycerophospholipid acyl tails are predominantly 16-18 c

39 characteristics of fatty acid acyls matched glycerophospholipid acyls.

40 Compared to their parent glycerophospholipids, all lyso analogs had greater tempe

41 d a decrease in sphingolipids and acyl-alkyl-glycerophospholipids among women with incident T2D.

42 < 0.001) and pathways related to NF-kappaB, glycerophospholipid and ether lipid metabolism, as well

43 ipid A are nearly normal in MKV15, as is the glycerophospholipid and membrane protein composition.

44 ction) were 3- to 29-fold higher for choline glycerophospholipid and phosphatidylinositol than for et

45 d phosphatidylinositol than for ethanolamine glycerophospholipid and phosphatidylserine at each of th

46 Pathways including glycerophospholipid and sphingolipid metabolisms were si

47 f lipids: (i) mono/di/triacylglycerols, (ii) glycerophospholipids and (iii) cardiolipins.

48 In contrast, more than 50% of glycerophospholipids and 30% of cholesterol were found i

49 rease in amino acids (AAs) as well as diacyl-glycerophospholipids and a decrease in sphingolipids and

50 While the bundle glycerophospholipids and acyl chains resemble those of o

51 sed widespread perturbation in metabolism of glycerophospholipids and amino acids (Trp, Met, and Cys,

52 n-cell line specific changes in fatty acids, glycerophospholipids and carbohydrates over time, induce

53 induced by Etf-1, and they provide host-cell glycerophospholipids and cholesterol that are necessary

54 es we have spectrally resolved more than 130 glycerophospholipids and determined changes initiated by

55 ell wall, as demonstrated by perturbation of glycerophospholipids and fatty acids.

56 he blockade of the chlamydial uptake of host glycerophospholipids and impairment in chlamydial growth

57 s that is esterified to the sn-2-position of glycerophospholipids and is released from selected lipid

58 s that is esterified to the sn-2 position of glycerophospholipids and is released from selected phosp

59 containing rafts contained more ethanolamine glycerophospholipids and less sphingomyelin than did the

60 s revealed the buildup of several species of glycerophospholipids and other storage lipids in selecti

61 lipids were observed for multiple classes of glycerophospholipids and polyphosphatidylinositides betw

62 We observed temporal regulation of glycerophospholipids and production of pro-inflammatory

63 al structures and differential abundances of glycerophospholipids and saccharides in females and male

64 lyzed plasmenylcholine > phosphatidylcholine glycerophospholipids and selectively cleaved phospholipi

65 Numerous interactions between glycerophospholipids and sphingolipids are observed in t

66 abundance and determine the turnover rate of glycerophospholipids and sphingolipids by direct analysi

67 nly explained by the lower concentrations of glycerophospholipids and sphingolipids in vegans.

68 The glycerophospholipids and sphingolipids that appear as in

69 Serum concentrations of most acylcarnitines, glycerophospholipids and sphingolipids were altered in s

70 ibution and localization of major classes of glycerophospholipids and sphingolipids.

71 oups because of lower concentrations of some glycerophospholipids and sphingolipids.

72 olome coverage, especially for low-abundance glycerophospholipids and sphingolipids.

73 generated by enzymatic cleavage of stores of glycerophospholipids and sphingomyelin, respectively, in

74 chromofuscus PLD is known to hydrolyze both glycerophospholipids and sphingomyelin.

75 e tentative identification of markers showed glycerophospholipids and their oxidized lipids were sign

76 tive intensities for at least five different glycerophospholipids and three free fatty acids in the n

77 uilding blocks of more complex lipids (e.g., glycerophospholipids and triacylglycerols).

78 T2 generates precursors for the synthesis of glycerophospholipids and triacylglycerols.

79 an, serotonin, taurine, 8 acylcarnitines, 13 glycerophospholipids, and 3 sphingolipids) exhibited sig

80 eks, and mitigated alterations of glutamate, glycerophospholipids, and carnitine levels in released m

81 132 lipid species, including sphingolipids, glycerophospholipids, and glycerolipids, that differed s

82 Because ATX hydrolyzes nucleotides, lyso-glycerophospholipids, and phosphosphingolipids into bioa

83 Lipid remodeling of glycerolipids, glycerophospholipids, and prenols also take place, indic

84 Glycerolipids, glycerophospholipids, and sphingolipids exhibited diurna

85 ighest concentrations of the acylcarnitines, glycerophospholipids, and sphingolipids, and fish eaters

86 ed polyunsaturated fatty acids, deprotonated glycerophospholipids, and sphingolipids.

87 Networks associated with inositol phosphate, glycerophospholipids, and sterol metabolism are tightly

88 ization of 29 sulfoglycosphingolipids and 45 glycerophospholipids, and we confirmed lipid identities

89 unsaturated fatty acid (VLC-PUFA)-containing glycerophospholipids are highly enriched in the retina;

90 and function of these highly unusual retinal glycerophospholipids are lacking.

91 Molecular species of glycerophospholipids are typically quantified using carb

92 Ethanolamine glycerophospholipids are ubiquitous cell membrane compon

93 ular lipids, and identified the accumulating glycerophospholipid as acylphosphatidylglycerol (acyl-PG

94 ynthesize the majority of their ethanolamine glycerophospholipids as 1-O-alk-1'-enyl-2-acyl-sn-glycer

95 Glycerophospholipids as well as other family lipids, suc

96 ATG2A can bind tens of glycerophospholipids at once and transfers lipids robust

97 ases A2 (sPLA2's) are enzymes that hydrolyze glycerophospholipids at the sn-2 position, which leads t

98 phospholipase A(2) (iPLA(2)beta) hydrolyzes glycerophospholipids at the sn-2-position to yield a fre

99 proteins, we discovered that E-Syts transfer glycerophospholipids between membrane bilayers in the pr

100 ng, and hydrogen-bonding behaviors of SM and glycerophospholipid bilayers found remarkable difference

101 with tryptophan derivatives interacting with glycerophospholipid bilayers in vesicles, tryptophan par

102 h differential abundance included those from glycerophospholipid, bile acid and acylcarnitine metabol

103 Phosphatidylserine (PS), another anionic glycerophospholipid, binds to mCD14 with lower apparent

104 whereas SREBP-1 controls triacylglycerol and glycerophospholipid biosynthesis.

105 nvolved in both membrane ornithine lipid and glycerophospholipid biosynthesis.

106 intermediates from sphingolipid pathways to glycerophospholipid biosynthesis.

107 ellular bacterium, partially lacks genes for glycerophospholipid biosynthesis.

108 Such lipids included glycerophospholipids (both diacyl and aryl-acyl), sphing

109 hidonoyl-containing choline and ethanolamine glycerophospholipids by other phospholipases to generate

110 lung tissue and P. carinii differed from the glycerophospholipids by the presence of high levels of s

111 characterization of complex lipids, such as glycerophospholipids, by tandem mass spectrometry (MS/MS

112 imulated sphingolipid (glucosylceramide) and glycerophospholipid (cardiolipin) synthesis.

113 The mitochondrial signature glycerophospholipid, cardiolipin (CL), binds to transpor

114 in esophageal adenocarcinoma cells shortened glycerophospholipid chains, linking de novo lipogenesis

115 the level of incorporation into the choline glycerophospholipids (ChoGpl).

116 protein that is homologous to enzymes called glycerophospholipid-cholesterol acyltransferases and, fo

117 enterica serovar typhimurium translocates a glycerophospholipid:cholesterol acyltransferase (SseJ) i

118 mophila, such as phospholipases A (PLAs) and glycerophospholipid:cholesterol acyltransferases (GCATs)

119 ometry was used to separate and quantify the glycerophospholipid classes as well as molecular species

120 ction of molecular species within particular glycerophospholipid classes.

121 results illustrate that large differences in glycerophospholipid composition may exist, even in close

122 rometry (FTICR-MS) to measure changes in the glycerophospholipid composition of total lipid extracts

123 iator biosynthesis in the context of overall glycerophospholipid composition.

124 l metabolites were significantly altered and glycerophospholipids comprised a significant fraction of

125 al-based mechanism of oxidation of pulmonary glycerophospholipids containing arachidonate.

126 Glycerophospholipids containing arachidonic acid (20:4)

127 ice showed a significant decrease in retinal glycerophospholipids containing VLC-PUFAs, specifically

128 Mass spectrometry of total glycerophospholipids demonstrated a marked difference in

129 olipids, sphingosine 1-phosphate, and diacyl-glycerophospholipids did not activate FUS1::lacZ.

130 LDI-TOF MS approach for analysis of cellular glycerophospholipids directly from extracts of mammalian

131 a compound structurally dissimilar to acidic glycerophospholipids, efficiently releases the nucleotid

132 ial metabolites were closely associated with glycerophospholipid, fatty acid and amino acid metabolis

133 of 219 molecular ions, including CLs, other glycerophospholipids, fatty acids, and metabolites, were

134 tely 5-fold and resolved it from both the ER glycerophospholipid flippase activity and the geneticall

135 ane proteins in the Triton extract; and (iv) glycerophospholipid flippase activity in the ER can be a

136 sing an activity-enriched fraction devoid of glycerophospholipid flippase activity, we now report tha

137 Cardiolipin is a glycerophospholipid found predominantly in the mitochond

138 membrane, but how these enzymes distinguish glycerophospholipids from sphingolipids is not known.

139 l activation of the host cPLA2 and uptake of glycerophospholipids from the host cells.

140 ay has been proposed to extract mislocalized glycerophospholipids from the outer leaflet of the OM an

141 ediated retrograde lipid transport (removing glycerophospholipids from the outer membrane and returni

142 disrupted lipid metabolism in AIS, including glycerophospholipid, glycerolipid and fatty acid metabol

143 es in relative abundances of >600 individual glycerophospholipid, glycerolipid, sphingolipid and ster

144 compositions of a series of fatty acids and glycerophospholipid (GP) species between the normal and

145 andem mass spectrometry (ESI-MS/MS) provides glycerophospholipid (GPL) class (i.e., headgroup composi

146 ype phospholipases (PLAs) are key players in glycerophospholipid (GPL) homeostasis and in mammalian c

147 complete structural information for a given glycerophospholipid (GPL) species.

148 ide (LPS) and the inner leaflet is formed by glycerophospholipid (GPL).

149 igosaccharides (LOS) and an inner leaflet of glycerophospholipids (GPL).

150 In this context, different lipoforms of glycerophospholipids (GPLs) are among the prime targets

151 Glycerophospholipids (GPLs) constitute a chemical family

152 for detailed structural characterization of glycerophospholipids (GPLs) for many types of biological

153 Glycerophospholipids (GPLs), one of the main components

154 olysaccharide (LPS), and an inner leaflet of glycerophospholipids (GPLs).

155 es of this free fatty acid as well as of the glycerophospholipids harboring it.

156 t the most prominent components of all major glycerophospholipid headgroup classes in islets are arac

157 cylcarnitines, amino acids, biogenic amines, glycerophospholipids, hexose, and sphingolipids related

158 -1 analog that regulates triacylglycerol and glycerophospholipid homeostasis in response to low oxyge

159 scriptional regulator of triacylglycerol and glycerophospholipid homeostasis in S. pombe, analogous t

160 a cells showed disrupted triacylglycerol and glycerophospholipid homeostasis, most notably with an in

161 31.8 nmol/10(9) platelets from ethanolamine glycerophospholipids (hydrolysis of plasmenylethanolamin

162 Among 96 of the unsaturated fatty acids and glycerophospholipids identified from rat brain tissue, 5

163 dylcholine was found to be the most abundant glycerophospholipid in both seed oils whereas phosphatid

164 Phosphatidylcholine (PC) is the major glycerophospholipid in eukaryotic cells and is an essent

165 ass spectrometry (MS/MS), several classes of glycerophospholipids in A. pallida.

166 C=C locations for more than 200 unsaturated glycerophospholipids in bovine liver among which we iden

167 (LC) for LC/UVPD-MS analysis of cyclopropyl glycerophospholipids in Escherichia coli ( E. coli) and

168 y expressed and metabolically interconnected glycerophospholipids in eukaryotes and prokaryotes.

169 Roles for glycerophospholipids in exocytosis have been proposed, b

170 aturated and polyunsaturated fatty acids and glycerophospholipids in human serum, where uncommon isom

171 We used mass spectrometry to quantify glycerophospholipids in mock-infected and virus-infected

172 tectable changes in specific 20:4-containing glycerophospholipids in peritoneal cells, but not in RAW

173 Transbilayer flipping of glycerophospholipids in the endoplasmic reticulum (ER) i

174 A significant fraction of the glycerophospholipids in the human body is composed of pl

175 no acids, acylcarnitines, sphingolipids, and glycerophospholipids in the liver and blood.

176 of PLA2 catalyzed hydrolysis of zwitterionic glycerophospholipids in the presence of bile salts.

177 egreesC accumulate hexa-acylated lipid A and glycerophospholipids in their inner membranes.

178 he rapid loss of phosphocholine from choline glycerophospholipids, in conjunction with neutral-loss s

179 alterations in both choline and ethanolamine glycerophospholipids, including a decreased plasmenyleth

180 he side chains of biological lipids, such as glycerophospholipids, is also essential.

181 : (i) fatty acyls, (ii) glycerolipids, (iii) glycerophospholipids, (iv) cardiolipins, (v) sphingolipi

182 ) catalyzes release of arachidonic acid from glycerophospholipids, leading to thromboxane A(2) (TxA(2

183 metabolite profile, which featured elevated glycerophospholipid levels compared with those without H

184 Glycerophospholipid levels inCerS5-deficient mice were n

185 a metabolite profile, featured with elevated glycerophospholipid levels, compared to HIV-uninfected w

186 howed positive correlations with host plasma glycerophospholipid levels.

187 howed positive correlations with host plasma glycerophospholipid levels.

188 ted at similar rates to lipid IV(A), whereas glycerophospholipids like phosphatidic acid or phosphati

189 confirm that selected TCL1 clones react with glycerophospholipid, lipoprotein, and polysaccharides th

190 combining the sphingolipid SM C22:3 and the glycerophospholipid lysoPCaC24:0 was discovered for seps

191 The glycerophospholipid lysoPCaC26:1 identified patients wit

192 We discover three additional pathways viz., Glycerophospholipid metablism, h-Efp pathway and CARM1 a

193 ine and proline metabolism (P=1.12x10(-7) ), glycerophospholipid metabolism (P=1.3x10(-10) ), and the

194 ntheses and down-regulated those involved in glycerophospholipid metabolism [including cardiolipin (C

195 osphatidic acid (LPA) is a common product of glycerophospholipid metabolism and an important mediator

196 other things-to a concentration decrease in glycerophospholipid metabolism and endocannabinoid signa

197 ing two prominent lipid metabolism pathways: glycerophospholipid metabolism and fatty acid biosynthes

198 etween renal tubulointerstitial fibrosis and glycerophospholipid metabolism and L-carnitine metabolis

199 etabolites related to amino acid metabolism, glycerophospholipid metabolism and mitochondrial beta-ox

200 significant perturbations in amino acid and glycerophospholipid metabolism associated with prenatal

201 nique defects in nucleotide, one-carbon, and glycerophospholipid metabolism at the transcript and pro

202 ites were mainly mapped into the hippocampal glycerophospholipid metabolism in a region-specific mann

203 riptome suggests the possible involvement of glycerophospholipid metabolism in the development of res

204 top bacterial genera contributing to the GMB glycerophospholipid metabolism pathway and showed positi

205 bacterial genera that contribute to the GMB glycerophospholipid metabolism pathway and showed positi

206 Via TEAK we identified a nonlinear glycerophospholipid metabolism subpathway involving the

207 linked to lipid metabolism, inflammation and glycerophospholipid metabolism that were associated with

208 of metabolites involved in the processes of glycerophospholipid metabolism, arachidonic acid metabol

209 and phenylalanine metabolism (BH(4) cycle), glycerophospholipid metabolism, energy metabolism, and a

210 AMD RPE as compared to normal RPE, including glycerophospholipid metabolism, involved in autophagy, l

211 Twenty three metabolites related to glycerophospholipid metabolism, oxidation and antioxidat

212 tty acid, eicosanoid, and fatty acid-derived glycerophospholipid metabolism, resulting in an overall

213 votal role in regulation of triglyceride and glycerophospholipid metabolism.

214 haviors by modulating peripheral and central glycerophospholipid metabolism.

215 ly enriched in fatty acyl, sphingolipid, and glycerophospholipid metabolism.

216 easily integrated into the lipid bilayer of glycerophospholipid model membranes.

217 mice exhibited normal hemodynamic function, glycerophospholipid molecular species composition, and n

218 he quantity of other classes of lipid (e.g., glycerophospholipid) molecular species present, thereby

219 s in clinical cohort studies demand detailed glycerophospholipid molecule information and the applica

220 ansmembrane protein, which binds cardiolipin glycerophospholipids near the inner membrane and promote

221 In addition, glycerophospholipids occurred differentially abundant in

222 hingolipids exhibiting 2-6% larger CCSs than glycerophospholipids of similar mass, likely a result of

223 bacterial cells by integrating extraction of glycerophospholipids on a microchip with a nanoelectrosp

224 n the acyl chain composition of any class of glycerophospholipid or diacylglycerol between lipid extr

225 dentified a novel family of oxidized choline glycerophospholipid (oxPC) molecular species enriched in

226 turally conserved family of oxidized choline glycerophospholipids (oxPC(CD36)) that serve as novel hi

227 the most significant metabolites map to the glycerophospholipid pathway.

228 A significant enrichment of the glycerophospholipids pathway was identified (P = 4.7 x 1

229 nalyses further highlighted dysregulation of glycerophospholipid pathways in melanoma tumor nodules,

230 [fatty acids (341.2100 and 382.3736 m/z) and glycerophospholipids (PE (P-16:0/22:6, m/z 746.5099, and

231 s fatty acyl information, in the case of the glycerophospholipids (PE, PS, and PC), via ester bond cl

232 ivity of PAF-AH in bile toward byproducts of glycerophospholipid peroxidation.

233 s formed upon electrospray ionization of the glycerophospholipids phosphatidylcholine (PC) and phosph

234 no acids (tryptophan and phenylalanine), and glycerophospholipids (phosphatidylcholine [PC] aa C36:1

235 lace Cer-1-P in a class more akin to certain glycerophospholipids (phosphatidylethanolamine, phosphat

236 is number to 10 molecules, with the membrane glycerophospholipid, phosphatidylinositol 24:4, emerging

237 idic acid (PAs), phosphatidylglycerol (PGs), glycerophospholipids (PI), phosphatidylcholines (PCs) an

238 phosphatidylcholine, and the proinflammatory glycerophospholipid platelet-activating factor (PAF) wer

239 (DGKalpha) knockout mice were determined for glycerophospholipids, polyphosphatidylinositides (GPInsP

240 d 63% of the mass lost from the ethanolamine glycerophospholipid pool) but only 10.9 nmol/10(9) plate

241 ses occurred in the choline and ethanolamine glycerophospholipid pools in murine myocardium (collecti

242 Furthermore, 19606R exhibited a shift in its glycerophospholipid profile towards increased abundance

243 1 deficiency significantly modulates hepatic glycerophospholipid profile.

244 that Rv1692 is the final enzyme involved in glycerophospholipid recycling/catabolism, a pathway not

245 pplication of this method to the analysis of glycerophospholipid remodeling in murine primary residen

246 ct on the overall pattern of zymosan-induced glycerophospholipid remodeling.

247 By number and measured intensity, glycerophospholipids represent the largest lipid class,

248 e presence of overlapping peaks from choline glycerophospholipids requiring chromatographic separatio

249 rsity, complex lipids such as glycerolipids, glycerophospholipids, saccharolipids, etc. are construct

250 t transmembrane segment is a key enforcer of glycerophospholipid selection, and specific substitution

251 In more complex bilayers composed of a fluid glycerophospholipid, SM analog, and PCer, the thermal st

252 We synthesized a family of sterol-modified glycerophospholipids (SML) in which the sn-1 or sn-2 pos

253 gnificantly enhances the signal intensity of glycerophospholipid species in mass spectrometry (MS) an

254 unbiased absolute (molar) quantification of glycerophospholipid species independent of instrument se

255 ion patterns for four subclasses of modified glycerophospholipid species.

256 ion cross sections (CCS) of sphingolipid and glycerophospholipid species.

257 f the two fractions contained various diacyl-glycerophospholipids species, where the majority of them

258 A third cluster solely comprised of glycerophospholipids (specifically ether-linked phosphat

259 ized by a distinctive enrichment in hexoses, glycerophospholipids, sphingolipids, and acylcarnitines,

260 ntified hundreds of lipid species, including glycerophospholipids, sphingolipids, and sterols, from a

261 dentification of fatty acids, glycerolipids, glycerophospholipids, sphingolipids, and sterols.

262 gories including fatty acyls, glycerolipids, glycerophospholipids, sphingolipids, sterols, and prenol

263 tion and the positions of chain-branching in glycerophospholipids, sphingomyelins and triacylglycerol

264 gh degree of specificity for LPA; other lyso-glycerophospholipids, sphingosine 1-phosphate, and diacy

265 wing the spatial distributions of particular glycerophospholipids, sphinoglipids, and free fatty acid

266 ommon in all 4 sample types; fatty acyls and glycerophospholipids strongly overlapped between groups.

267 d lipid profiling technology to evaluate the glycerophospholipid structure and composition of two mac

268 congested with monoanions from more abundant glycerophospholipid subclasses.

269 Expression of fatty acid and glycerophospholipid synthesis genes was significantly up

270 plsC316 encodes the main AGPAT required for glycerophospholipid synthesis in R. capsulatus, while ol

271 ga2 and SREBP-1 regulate triacylglycerol and glycerophospholipid synthesis, whereas Sre1 and SREBP-2

272 s required for ether bond formation in ether glycerophospholipid synthesis.

273 mal zymosan-dependent PG synthesis, the only glycerophospholipid that exhibited a significant change

274 Phosphatidylethanolamine is a glycerophospholipid that, together with phosphatidylchol

275 Plasmalogens are a subclass of glycerophospholipids that are enriched in the plasma mem

276 mines) are a biologically important class of glycerophospholipids that have been difficult to synthes

277 r segments with structurally defined choline glycerophospholipids that may serve as a physiological s

278 Structurally defined oxidized choline glycerophospholipids that serve as high-affinity ligands

279 to form EET-CoAs that are incorporated into glycerophospholipids, thereby sequestering EETs.

280 (MS)-based lipidomics strategy that exposes glycerophospholipids to an ethereal solution of diazomet

281 Phospholipase A(2) (PLA(2)) hydrolyzes glycerophospholipids to free fatty acid and lyso-phospho

282 GDPD) catalyzes the hydrolysis of deacylated glycerophospholipids to glycerol phosphate and alcohol.

283 tory phospholipase A(2)s (sPLA(2)) hydrolyze glycerophospholipids to liberate lysophospholipids and f

284 D inhibitors (which block the conversion of glycerophospholipids to phosphatidic acid) to deplete ce

285 e A2 beta enzyme that selectively hydrolyses glycerophospholipids to release free fatty acids.

286 at MsbA plays a role in lipid A and possibly glycerophospholipid transport.

287 Conventionally, shotgun analysis of glycerophospholipids via direct electrospray ionization

288 The best on-chip extraction efficiency for glycerophospholipids was as high as 83.3% by integrating

289 on flux across membranes composed of choline glycerophospholipids was primarily due to entropic effec

290 A total of 156 unique circulating glycerophospholipids were identified, of which 52 (1 LPG

291 hen the levels of high-energy phosphates and glycerophospholipids were lowered.

292 sphingolipids (SPs) and cholesterol, whereas glycerophospholipids were reduced, and storage lipids we

293 expression patterns and a similar number of glycerophospholipids were simultaneously visualized from

294 n-regulation of sphingolipids and acyl-alkyl-glycerophospholipids were sustained or strengthened.

295 japonicus synthesizes unusual "asymmetrical" glycerophospholipids where the tails differ in length by

296 6:0 was targeted to choline and ethanolamine glycerophospholipids, whereas more [1-(14)C]20:4n-6 was

297 bstantially enriched in sphingomyelin and in glycerophospholipids with a higher degree of saturation

298 oyl-2-oleoyl-sn-glycero- and 1,2-dioleoyl-sn-glycerophospholipids with phosphocholine (PC) or phospho

299 a on the relative distribution of individual glycerophospholipids within each of the major classes.

300 of this conformational motif for peroxidized glycerophospholipids within membranes.