ライフサイエンスコーパス: triacylglycerol

1 synthetic membranes, and the accumulation of triacylglycerol.

2 l role in the synthesis of the storage lipid triacylglycerol.

3 placement followed by a late accumulation of triacylglycerol.

4 the esterification of free fatty acids into triacylglycerol.

5 ids, accumulation of oligogalactolipids, and triacylglycerol.

6 tions of CPS on phosphatidylcholine (PC) and triacylglycerol.

7 tion, coincident with increased synthesis of triacylglycerol.

8 osphatidylcholine, and ultimately enter seed triacylglycerol.

9 cles fail to release fatty acids from stored triacylglycerol.

10 free sugars on total and LDL cholesterol and triacylglycerols.

11 thesis and its regulation to the assembly of triacylglycerols.

12 ounced reallocation of lipidome peak area to triacylglycerols.

13 the essentiality of major classes, including triacylglycerols.

14 cetylation required the conversion of FAs to triacylglycerols.

15 linolein/oleodilinolein represented the main triacylglycerols.

16 ydrolyze omega-3 fatty acids from structured triacylglycerols.

17 and the pattern in NEFAs echoed that of VLDL-triacylglycerols.

18 , respectively], only whey protein decreased triacylglycerol (-0.23 mmol/L; P = 0.025) compared with

19 ealthy controls was dominated by lipoprotein triacylglycerol (1)H NMR resonances and isoleucine.

20 s in the intensities of selected lipoprotein triacylglycerol (1)H NMR signals over those of healthy c

21 g and detecting lipids, namely, cholesterol, triacylglycerols, 1,2-diol diesters, wax esters, cholest

22 /- 3.6%; n = 13) exhibited a 45% higher VLDL-triacylglycerol 16:1n-7 molar percentage (P < 0.01), 16%

23 data provide support for the use of the VLDL-triacylglycerol 16:1n-7 molar percentage as a biomarker

24 In all subjects, VLDL-triacylglycerol 16:1n-7 was significantly (P < 0.01) rel

25 Phospholipids (40.2-43.6%) and triacylglycerols (31.8-34.7%) were the most represented

26 those of DHA supplementation (re-esterified triacylglycerol; 90% pure) on inflammation markers (prim

27 was modified with a decreased proportion of triacylglycerol accompanied by the increase of phospholi

28 The resultant purified triacylglycerols accomplished with the oxidative state (

29 te also inhibits v-ATPase function, yielding triacylglycerol accumulation but not insulin resistance.

30 mice exhibited a marked reduction in hepatic triacylglycerol accumulation compared with wild type obe

31 lipid-producing strain (45-fold increase in triacylglycerol accumulation) through the disruption of

32 AtGPAT9 is required for wild-type levels of triacylglycerol accumulation, and the transcript level i

33 OLEOSIN1 in Nicotiana benthamiana stimulates triacylglycerol accumulation, but their coexpression wit

34 es, potentially reduce the uptake of dietary triacylglycerol aiding in weight management.

35 ses in HDL cholesterol, LDL cholesterol, and triacylglycerols, although for LDL cholesterol and triac

36 ocytes incorporated 33% less fatty acid into triacylglycerol and 46% more into the pathway of beta-ox

37 sition of sn-1,2-diacylglyerol, thus forming triacylglycerol and a lysophospholipid.

38 terol biosynthesis, whereas SREBP-1 controls triacylglycerol and glycerophospholipid biosynthesis.

39 missing is an SREBP-1 analog that regulates triacylglycerol and glycerophospholipid homeostasis in r

40 blish Mga2 as a transcriptional regulator of triacylglycerol and glycerophospholipid homeostasis in S

41 genes, and mga2Delta cells showed disrupted triacylglycerol and glycerophospholipid homeostasis, mos

42 Mga2 and SREBP-1 regulate triacylglycerol and glycerophospholipid synthesis, where

43 he levels of PA and DAG for the synthesis of triacylglycerol and membrane phospholipids, the growth o

44 Triacylglycerol and phosphatidylcholine molecular specie

45 ER was able to incorporate fatty acids into triacylglycerol and phospholipids.

46 Later isolates displayed accumulation of triacylglycerol and reduced expression of fadD23, someti

47 the msn2Deltamsn4Delta strain had increased triacylglycerol and steryl ester levels.

48 t on the NP-HPTLC plates, whereas individual triacylglycerol and wax ester species were separated on

49 Plasma levels of triacylglycerols and diacylglycerols, the lipoproteins t

50 High resolution (13)C NMR spectra of plasma triacylglycerols and glucose provided new insights into

51 n the endoplasmic reticulum in cells lacking triacylglycerols and localize exclusively to the endopla

52 For example, mixed cis and trans forms of triacylglycerols and phosphatidylcholines were identifie

53 ial distribution of two major lipid species, triacylglycerols and phosphatidylcholines.

54 Very-low-density lipoprotein (VLDL)-triacylglycerols and plasma free FA [nonesterified fatty

55 s are specific organelles for the storage of triacylglycerols and steryl esters.

56 hosphatidylethanolamine, phosphatidylserine, triacylglycerol, and cholesteryl ester.

57 erol, hypertension, high blood glucose, high triacylglycerol, and insulin resistance.

58 ral important lipids, including cholesterol, triacylglycerol, and phospholipids.

59 reduced plasma levels of apoC-II, apoC-III, triacylglycerols, and diacylglycerols, and increased apo

60 es from baseline in fasting and postprandial triacylglycerol, apolipoprotein B-48 (apoB-48; reflectin

61 high-density lipoprotein (HDL) cholesterol, triacylglycerols, apolipoproteins A-I and B, or very low

62 iogenesis and conversion of phospholipids to triacylglycerol are required for restoring some phosphol

63 itative data are reported on fatty acids and triacylglycerols as relative percentage of total fractio

64 algae that accumulate significant amounts of triacylglycerols as storage lipids when their growth is

65 ained oleosin and several other proteins and triacylglycerols as the main lipids.

66 Focusing on engineering the triacylglycerol assembly mechanisms led to modest increa

67 d polar compounds formation in sunflower oil triacylglycerols at 120 degrees C were investigated in t

68 he position of the omega-3 fatty acid on the triacylglycerol backbone influences how digestion occurs

69 incided with elevated gene expression of key triacylglycerol biosynthesis components.

70 Although the importance of PDAT in triacylglycerol biosynthesis has been illustrated in som

71 nging together gene expression levels of the triacylglycerol biosynthesis pathway and oil composition

72 th the others, including diacylglycerols and triacylglycerols, branched-chain amino acids, and marker

73 cing pancreatic lipase activity would reduce triacylglycerol breakdown resulting in lower amounts bei

74 Pancreatic lipase is important in dietary triacylglycerol breakdown; reducing pancreatic lipase ac

75 abolism and accumulate more intramyocellular triacylglycerol but have normal glucose and insulin tole

76 ns of the environment by the accumulation of triacylglycerol, but the relative changes occurring in m

77 either nutrient triggered an accumulation of triacylglycerol, but with different time scales and magn

78 adiposity index, whole body weight, glucose, triacylglycerol, cholesterol and blood pressure, without

79 production; stored within lipid droplets as triacylglycerol, cholesterol esters, and retinol esters;

80 Six lipid species (all belonging to the triacylglycerol class and containing palmitate at the fi

81 The HF+PO diet reduced the level of triacylglycerols compared with the control.

82 a more direct instrumental determination of triacylglycerol composition along with sn-2 positional i

83 erification process for their fatty acid and triacylglycerol composition, free fatty acid (FFA) conte

84 choline, leading to a proportional change in triacylglycerol composition.

85 on the quality parameters and fatty acid and triacylglycerol compositions of their oils.

86 Elevations in triacylglycerol concentration relative to baseline were

87 The lower serum triacylglycerol concentration was associated with reduce

88 Insulin, glucose, and triacylglycerol concentrations as well as blood pressure

89 ementation attenuated the increase in plasma triacylglycerol concentrations during the HFMM test that

90 acuoles suggested vacuolar storage of NO3(-) Triacylglycerol concentrations in the NR-KO cells increa

91 urces, which coincided with increased plasma triacylglycerol concentrations.

92 P = 0.03) and postprandial (P = 0.01) serum triacylglycerol concentrations.

93 Natural sources of triacylglycerols containing omega-3 fatty acids are of p

94 38 lipases with a large number of structured triacylglycerols containing omega-3 fatty acids.

95 lation by Pho85-Pho80, caused an increase in triacylglycerol content and lipid droplet number in cell

96 All mutants analyzed had a higher triacylglycerol content and perturbed whole-cell fatty a

97 Although an elevated triacylglycerol content in non-adipose tissues is often

98 ted high liver glycogen content, lower liver triacylglycerol content, and lower serum concentrations

99 evidenced by the 2.25-fold increase in liver triacylglycerol content, but did not induce advanced liv

100 insulin resistance, and elevation in hepatic triacylglycerol content.

101 Variations in the triacylglycerol contents and melting and crystallization

102 Liver triacylglycerol contents were reduced by both protein so

103 t, the low amount of dietary 16:1n-7 in VLDL-triacylglycerols corresponded to a stronger signal of el

104 t the time evolution of the concentration of triacylglycerols, DAG, MAG and free fatty acids (FFA) an

105 roper neutral lipid compartmentalization and triacylglycerol degradation during postgerminative growt

106 striking, consisting of completely saturated triacylglycerol, diacylglycerol, and monoacylglycerol wi

107 concentrations, and decreased ectopic lipid (triacylglycerol/diacylglycerol) content in liver and mus

108 ly into the stomach, we show that inhibiting triacylglycerol digestion disrupts normal behaviour of s

109 In this study we examined the role of triacylglycerol digestion for intestinal fat sensing, an

110 fat sensing, and compared the effects of the triacylglycerol digestion products, fatty acids and 2-mo

111 monomers at IP, min/%; time reaching 10% of triacylglycerol dimers and polymers, min) in general bel

112 the cessation of growth and accumulation of triacylglycerols during nitrogen starvation, and the tem

113 io of 16:1n-7 to 16:0 [SCD1(1)(6)] in plasma triacylglycerol FA has been used as an index to reflect

114 We found no difference in postprandial triacylglycerol, FFA, insulin, glucose, glucagon, or GIP

115 nitrogen deprivation, were unable to degrade triacylglycerols following nitrogen resupply.

116 membrane separation produces products in the triacylglycerol form which possess better oxidative stab

117 HFA), only accumulates to high levels in the triacylglycerol fraction of castor (Ricinus communis) en

118 cyl-CoA synthetase LCS2 in the production of triacylglycerol from de novo-synthesized fatty acids.

119 Furthermore, triacylglycerols from HepG2-SMS1 cells are enriched in p

120 sterol, low-density lipoprotein cholesterol, triacylglycerol, glucose, insulin, C-peptide, homeostasi

121 ects on fasting or postprandial cholesterol, triacylglycerol, glucose, or hepatic insulin clearance i

122 Postprandial triacylglycerol, HDL-cholesterol, HDL(3)-cholesterol, an

123 acids up to 17% of total fatty acids in seed triacylglycerols; however, total seed oil is also reduce

124 No difference in effects was observed for triacylglycerol, hsCRP, insulin, and glucose concentrati

125 selective inhibitor of the key intracellular triacylglycerol hydrolase, adipose triglyceride lipase.

126 Lipases, a class of triacylglycerol hydrolases, have been extensively tested

127 zes the penultimate step in the synthesis of triacylglycerol (i.e. the production of diacylglycerol b

128 lgae oils have been studied in detail, their triacylglycerols identified and sn-2 positional arrangem

129 ntration was associated with reduced fasting triacylglycerol in chylomicrons and very-low-density lip

130 nd of major membrane lipids in seedlings and triacylglycerol in mature siliques.

131 mmonly is used to induce the accumulation of triacylglycerol in microalgae, leads to a state of cellu

132 yzes the committed step for the synthesis of triacylglycerol in Saccharomyces cerevisiae, exerts a ne

133 Sensing of dietary triacylglycerol in the proximal small intestine results

134 we report that resting levels of long-chain triacylglycerols in mitochondrial myopathy correlate wit

135 ch is known about the role of LDs in storing triacylglycerols in seeds, their biogenesis and function

136 es of cholesterol esters, phospholipids, and triacylglycerols in the context of lesion characteristic

137 all plant membrane phospholipids and storage triacylglycerols is catalyzed by a glycerol-3-phosphate

138 Arabidopsis SEIPINs increased triacylglycerol levels and altered composition.

139 hese mice had reductions in both circulating triacylglycerol levels and the mRNA levels of lipogenic

140 Reduced plasma and liver triacylglycerol levels in E1 and E4-mice were linked to

141 ol promotes the reduction of cholesterol and triacylglycerol levels.

142 associated with decreased serum glucose and triacylglycerol levels.

143 s on ECHIDNA (ECH), a plant homolog of yeast Triacylglycerol lipase (TLG2/SYP4) interacting protein T

144 we studied the topology of Tgl3p, the major triacylglycerol lipase of the yeast Saccharomyces cerevi

145 mutants defective in SUGAR-DEPENDENT1 (SDP1) triacylglycerol lipase or PEROXISOMAL ABC TRANSPORTER 1

146 differentially expressed bacterial proteins (triacylglycerol lipase, N-acetylmuramoyl-L-alanine amida

147 investigate the regulatory network of yeast triacylglycerol lipases in more detail, we also examined

148 Tgl3p, Tgl4p, and Tgl5p are the major triacylglycerol lipases of the yeast Saccharomyces cerev

149 showed increased expression of mRNAs for the triacylglycerol lipases PPA2105 and PPA1796 and the hyal

150 these investigations to the two other yeast triacylglycerol lipases, Tgl4p and Tgl5p.

151 Total cholesterol (TC), LDL cholesterol, triacylglycerol, lipoprotein(a), and apolipoprotein B we

152 ls contain subcellular lipid droplets with a triacylglycerol matrix enclosed by a layer of phospholip

153 wed that Ime4 epitranscriptionally regulates triacylglycerol metabolism and vacuolar morphology throu

154 A number of individual genes involved in triacylglycerol metabolism have previously been reported

155 exposure are the phospholipid and fatty acid triacylglycerol metabolism pathways.

156 dentified here between m(6)A methylation and triacylglycerol metabolism via the Ime4 protein provides

157 get for the engineering of high-biomass/high-triacylglycerol microalgae.

158 basis of their structure or position in the triacylglycerol molecule.

159 ant performance (the ratio of IP to oxidized triacylglycerol monomers at IP, min/%; time reaching 10%

160 zation of phosphatidate for the synthesis of triacylglycerol or membrane phospholipids.

161 e any systematic effect on fatty acids (FA), triacylglycerols or nutritional fat subclasses but signi

162 er that DDHD2 regulates brain triglycerides (triacylglycerols, or TAGs).

163 s or any secondary outcomes including plasma triacylglycerols, oxidized LDL, and LDL cholesterol.

164 c9,t11-CLA lowered triacylglycerol (P </= 0.01) and had no effect on other

165 0(-7)), fasting insulin (P=5.4x10(-32)), and triacylglycerols (P=1.4x10(-29)).

166 , blood pressure (P=7.7x10(-5)), and fasting triacylglycerols (P=9.0x10(-5)), and PC14:1/0:0 was posi

167 As a percentage of triacylglycerol palmitate, de novo lipogenesis was 2-fol

168 glycerol between the phosphatidylcholine and triacylglycerol pathways, to the benefit of the former.

169 ains across lipid species, including di- and triacylglycerols, phospholipids, cholesteryl esters, and

170 mmon Kilka (Clupeonella cultiventris caspia) triacylglycerols (PKO) as affected by 1-1.5% (w/w) of un

171 the highly regulated storage and release of triacylglycerol primarily in adipose tissue, and excessi

172 to gain a basic mechanistic understanding of triacylglycerol production in photosynthetic cells.

173 Apart from these methods, the specificity of triacylglycerol profiles has previously been detected in

174 s the effect of irradiation treatment in the triacylglycerol profiles of chestnut.

175 ds, liposoluble antioxidants, fatty acid and triacylglycerol profiles, and oxidative status of oil ob

176 ly associated with the level of intrahepatic triacylglycerol (r = 0.53; P = .007).

177 2% and approximately 14% variance for FA and triacylglycerols, respectively) to processing.

178 ol (vitamin A), esterified and packaged into triacylglycerol-rich chylomicrons for bodily distributio

179 ation rewires cellular metabolism to adopt a triacylglycerol-rich lifestyle reliant on the Kennedy pa

180 Blood was collected hourly for 10 h, and the triacylglycerol-rich lipoprotein (TRL) fraction was isol

181 ApoC-II is provided as a component of triacylglycerol-rich lipoproteins and is the co-factor f

182 l community support the concept of targeting triacylglycerol-rich lipoproteins to reduce risk of CVD.

183 r lipoprotein lipase (LPL) at the surface of triacylglycerol-rich lipoproteins.

184 lar diacylglycerol acyltransferase activity, triacylglycerol secretion, and mitochondrial function.

185 ining linoleic acid (LA), and more saturated triacylglycerol species than control eggs.

186 tes within holobionts featured predominantly triacylglycerols, sterol esters, and free fatty acids.

187 generation, insulin resistance, and reduced triacylglycerol storage.

188 PL) activity and stimulates the lipolysis of triacylglycerol stored by adipocytes in the white adipos

189 tinued to run, liver and muscle glycogen and triacylglycerol stores were similar in both genotypes; h

190 We found that the uptake of triacylglycerol substrates via the scavenger receptor CD

191 atase that catalyzes the penultimate step in triacylglycerol synthesis and plays a role in the transc

192 rsion of phosphatidate to diacylglycerol for triacylglycerol synthesis and simultaneously controls ph

193 These include transcripts for starch and triacylglycerol synthesis but also transcripts for photo

194 Intriguingly, the coexpression of triacylglycerol synthesis isozymes from castor along wit

195 te that these unusual structures recruit the triacylglycerol synthesis machinery and grow by expansio

196 f Pah1 and its physiological functions (e.g. triacylglycerol synthesis).

197 arker of pentose phosphate pathway activity, triacylglycerol synthesis, and flux through anaplerotic

198 hatases and catalyze the penultimate step of triacylglycerol synthesis.

199 h is the penultimate step in one pathway for triacylglycerol synthesis.

200 iates in the glycerol-3-phosphate pathway of triacylglycerol synthesis: diacylglycerol (DAG), which m

201 green alga C. reinhardtii showed substantial triacylglycerol (TAG) accumulation and up-regulation of

202 actylum NO inhibits cell growth and triggers triacylglycerol (TAG) accumulation.

203 (66% of 1,3-DAG, 18% of 1,2-DAG) and 16% of triacylglycerol (TAG) along with micro nutrients like ga

204 WD-induced accumulation of hepatic triacylglycerol (TAG) and diacylglycerol (DAG) content w

205 the accumulation of high cellular levels of triacylglycerol (TAG) and starch are variants of what ma

206 Neutral lipids, predominantly triacylglycerol (TAG) and sterol ester, are stored withi

207 The neutral lipids steryl ester and triacylglycerol (TAG) are stored in the membrane-bound o

208 ses (DGATs) catalyze a rate-limiting step of triacylglycerol (TAG) biosynthesis in higher plants and

209 s between milk FA composition and genes from triacylglycerol (TAG) biosynthesis pathway.

210 Inhibition of triacylglycerol (TAG) biosynthetic enzymes has been sugg

211 oleaginous plant species is the formation of triacylglycerol (TAG) by the acyl-CoA-dependent acylatio

212 and K270, purity properties; fatty acid and triacylglycerol (TAG) composition and antioxidant compou

213 dy demonstrates a strong interaction between triacylglycerol (TAG) composition and effects of shear r

214 tudy was to gain knowledge about the role of triacylglycerol (TAG) composition in fatty acids (FA) of

215 ncomitantly with MGDG decrease, the level of triacylglycerol (TAG) containing medium chain FAs increa

216 The triacylglycerol (TAG) crystal structures and morphologie

217 on of desnutrin/ATGL at S406 to decrease its triacylglycerol (TAG) hydrolase activity, lowering basal

218 triglyceride lipase (ATGL), a major hepatic triacylglycerol (TAG) hydrolase, were inversely regulate

219 ty, lipid synthesis, and the accumulation of triacylglycerol (TAG) in leaf tissue.

220 ycerolipid synthesis and the accumulation of triacylglycerol (TAG) in response to nutrient starvation

221 Triacylglycerol (TAG) is a storage lipid used for food p

222 Triacylglycerol (TAG) is the main storage lipid in plant

223 lorella and resulted in close agreement with triacylglycerol (TAG) levels determined by thin layer ch

224 triglyceride lipase (ATGL) serves as a major triacylglycerol (TAG) lipase and controls the bulk of in

225 vation in yeast and mammals, but the role of triacylglycerol (TAG) metabolism in plant stress respons

226 Triacylglycerol (TAG) metabolism is a key aspect of intr

227 Enantiomers of racemic triacylglycerol (TAG) mixtures were separated using two

228 1MS2 used for (1)D allowed quantification of triacylglycerol (TAG) molecular species of Parinari cura

229 f how these PUFAs are channeled from PC into triacylglycerol (TAG) needs to be further explored.

230 tudied how pHo influences the stimulation of triacylglycerol (TAG) storage by low pO2 and LPS.

231 of PC that is required for LD biogenesis and triacylglycerol (TAG) storage.

232 in rapid proliferation but are redirected to triacylglycerol (TAG) stored in lipid droplets during st

233 The anabolism and catabolism of myocardial triacylglycerol (TAG) stores are important processes for

234 Liver triacylglycerol (TAG) synthesis and secretion are closel

235 Acyltransferases are key contributors to triacylglycerol (TAG) synthesis and, thus, are of great

236 omitantly, increased conversion of MGDG into triacylglycerol (TAG) was observed.

237 ned 69% PL, 9% diacylglycerol (DAG), and 23% triacylglycerol (TAG) with a stoichiometry of 46 PL, 6 D

238 Microalgal triacylglycerol (TAG), a promising source of biofuel, is

239 thogen accumulates lipid droplets containing triacylglycerol (TAG).

240 er 75% of fatty acids in white adipose (WAT) triacylglycerol (TAG).

241 l-coenzyme A (CoA)-dependent biosynthesis of triacylglycerol (TAG).

242 underlie a rigid SFA:MUFA:PUFA hierarchy in triacylglycerol (TAG).

243 xpressed in tissues that predominantly store triacylglycerol (TAG).

244 to the diacylglycerol (DAG, 17 species) and triacylglycerol (TAG, 17 species) classes.

245 Plant seeds are the primary source of triacylglycerols (TAG) for food, feed, fuel, and industr

246 two-steps enzymatic esterification and (iv) triacylglycerols (TAG) purification (liquid column chrom

247 (PL), diacylglycerols, free fatty acids and triacylglycerols (TAG) using thin layer chromatography.

248 store excess lipids as two major compounds, triacylglycerols (TAGs) and cholesteryl esters (CEs), in

249 Triacylglycerols (TAGs) and steryl esters, which are sto

250 ether relative concentrations of circulating triacylglycerols (TAGs) between carriers compared with n

251 Triacylglycerols (TAGs) displayed the complete panel of

252 o be a power combination for the analysis of triacylglycerols (TAGs) from tissue sections by laser de

253 mutants also constitutively over-accumulated triacylglycerols (TAGs) in a manner that was synergistic

254 validated to analyze ratios of regioisomeric triacylglycerols (TAGs) in fats and oils.

255 resulting in an accumulation of unsaturated triacylglycerols (TAGs) in the cytosol.

256 dation is achieved by lipases that hydrolyze triacylglycerols (TAGs) into free fatty acids and glycer

257 de values (PVs) were determined and oxidised triacylglycerols (TAGs) measured by UHPLC-ESI/MS at 0, 7

258 o fingerprint the primary crystallisation of triacylglycerols (TAGs) molecules and their transition b

259 This CSO contained twelve triacylglycerols (TAGs) out of which trilinolenin (alpha

260 rated and unsaturated FA distribution of the triacylglycerols (TAGs) present in high oleic sunflower

261 idylethanolamines (PEs), sphingomyelins, and triacylglycerols (TAGs) were associated with cardiovascu

262 LC-MS was employed for the identification of triacylglycerols (TAGs), carotenoids and phospholipids;

263 s lose their lipid droplets (LDs) containing triacylglycerols (TAGs), cholesteryl esters, and retinyl

264 Plant triacylglycerols (TAGs), or vegetable oils, provide appr

265 Here, we show that triacylglycerols (TAGs), present in Arabidopsis guard ce

266 NPs that are mainly composed of high melting triacylglycerols (TAGs).

267 ic acid precursor of polar glycerolipids and triacylglycerols (TAGs).

268 ets (LDs) coincides with the accumulation of triacylglycerols (TAGs).

269 sterol and campesterol was incorporated into triacylglycerols (TAGs).

270 acids in the sn-2 and sn-3 positions of seed triacylglycerols (TAGs).

271 sion are redirected toward carbohydrates and triacylglycerols (TAGs).

272 smic lipid droplets (LDs) of neutral lipids (triacylglycerols [TAGs], sterylesters, etc.) are reserve

273 an integral membrane protein that catalyzes triacylglycerol (TG) synthesis using diacylglycerol and

274 rganelles that store neutral lipids, such as triacylglycerol (TG), as reservoirs of metabolic energy

275 to and is stabilized by droplets containing triacylglycerol (TG).

276 r laboratory has shown that the breakdown of triacylglycerols (TGs) is regulated in a cell-cycle-depe

277 Triacylglycerols (TGs) stored in lipid droplets (LDs) ar

278 Although mostly non-polar lipids (triacylglycerols, TGs) were present in the fish tissue,

279 HepG2-SMS1 cells have fewer triacylglycerols than controls but similar diacylglycero

280 els of mycolic acid wax ester and long-chain triacylglycerols than those for wild-type bacteria.

281 the diacylglycerol used for the synthesis of triacylglycerol that accumulates in the stationary phase

282 lglycerols, although for LDL cholesterol and triacylglycerols there was significant heterogeneity bet

283 us quantifying individual fatty acids within triacylglycerols through multivariate linear regression

284 facilitate the movement of CPA from PC into triacylglycerol to produce viable seeds with additional

285 f diacylglyceryl-N,N,N-trimethylhomo-Ser and triacylglycerols, together with the up-regulation of gen

286 oisomer characterisation of fatty acids in a triacylglycerol usually requires the use of stereospecif

287 The release of the first fatty acid from the triacylglycerol was independent on the unsaturation degr

288 The increase of triacylglycerols was no longer significant when studies

289 fferential localization of phospholipids and triacylglycerols was observed within the embryo and radi

290 ApoC-II adsorption to a triacylglycerol/water interface resulted in large increa

291 We characterized apoC-II at phospholipid/triacylglycerol/water interfaces, which more closely mim

292 tions between eicosanoids, phospholipids and triacylglycerols, we provide evidence that these lipids

293 e, diacylglycerol (DAG) and intramyocellular triacylglycerol were increased.

294 otal cholesterol, LDL cholesterol, apoB, and triacylglycerol were similar with the 3 diets.

295 Interestingly, triacylglycerols were found in areas surrounding neovess

296 Polymers of triacylglycerols were found only in the polar fraction o

297 e hydrolyzed to free DHA and are absorbed as triacylglycerol, whereas the transporter at blood brain

298 hingolipids, and nonpolar lipids (diacyl and triacylglycerols), which are the main lipid classes dete

299 LPL hydrolyzes triacylglycerol, which increases local surface pressure

300 etween the theoretical and actual amounts of triacylglycerols with partition number 42 (DeltaECN42 |0