ライフサイエンスコーパス: unsaturated fatty acid

1 Cu(2+)-mediated degradation of the liposomal unsaturated fatty acids).

2 tricted specificity toward hydroperoxides of unsaturated fatty acid.

3 and failed to accumulate LPs induced by this unsaturated fatty acid.

4 of human FZD5 CRD bound to C16:1 cis-Delta9 unsaturated fatty acid.

5 s was concentration-dependently inhibited by unsaturated fatty acid.

6 jor stimulatory factors as host-specific cis-unsaturated fatty acids.

7 esponses that upregulate the biosynthesis of unsaturated fatty acids.

8 t as Eci2, suggesting a role in oxidation of unsaturated fatty acids.

9 trients, such as proteins, carbohydrates and unsaturated fatty acids.

10 enin and is rescued by addition of exogenous unsaturated fatty acids.

11 r all macronutrients, were strongest for the unsaturated fatty acids.

12 structure-specific antimicrobial effects of unsaturated fatty acids.

13 fic proportion of anionic lipids, as well as unsaturated fatty acids.

14 ated sorbitan monoesters of saturated and/or unsaturated fatty acids.

15 auxiliary role in beta-oxidation of certain unsaturated fatty acids.

16 total to HDL cholesterol in comparison with unsaturated fatty acids.

17 ed with those of trans, other saturated, and unsaturated fatty acids.

18 s generated during beta-oxidation of certain unsaturated fatty acids.

19 ecific lysophospholipids preferentially with unsaturated fatty acids.

20 pid droplets and are strikingly sensitive to unsaturated fatty acids.

21 as was the repression of fabAB expression by unsaturated fatty acids.

22 hy analysis with substrate preference toward unsaturated fatty acids.

23 y enzymes required for the beta-oxidation of unsaturated fatty acids.

24 ymes which catalyze the hydroperoxidation of unsaturated fatty acids.

25 long-chain mostly polyunsaturated and highly unsaturated fatty acids.

26 m-dependent cysteine protease in response to unsaturated fatty acids.

27 the co-ordinated synthesis of saturated and unsaturated fatty acids.

28 n in membranes containing phospholipids with unsaturated fatty acids.

29 undant nitrated derivatives of all principal unsaturated fatty acids.

30 e mitochondrial beta-oxidation of long-chain unsaturated fatty acids.

31 tive starvation of cells for cholesterol and unsaturated fatty acids.

32 lizing function in cells that are exposed to unsaturated fatty acids.

33 cause they contain a much larger fraction of unsaturated fatty acids.

34 iacylglycerol molecular species that contain unsaturated fatty acids.

35 sterol efflux appear insensitive to dietary unsaturated fatty acids.

36 so differentially modulated by saturated and unsaturated fatty acids.

37 ASQD molecular species carried predominantly unsaturated fatty acids.

38 ular synthesis and uptake of cholesterol and unsaturated fatty acids.

39 medium- to long-chain, saturated and omega-3 unsaturated fatty acids.

40 t in breakdown of fatty acids especially for unsaturated fatty acids.

41 gen species derived of nitric oxide (NO) and unsaturated fatty acids.

42 ears to be dependent on the concentration of unsaturated fatty acids.

43 the ER membrane to control the production of unsaturated fatty acids.

44 nfers resistance to tetracycline and certain unsaturated fatty acids.

45 lysocardiolipin to generate cardiolipin with unsaturated fatty acids.

46 attenuated by supplementing the medium with unsaturated fatty acids.

47 attenuated by supplementing the medium with unsaturated fatty acids.

48 as disordered domains contain high levels of unsaturated fatty acids.

49 aturated fatty acids whereas FakB2 preferred unsaturated fatty acids.

50 take of fruit, vegetables, whole grains, and unsaturated fatty acids.

51 mutations that reduce inhibition by bile and unsaturated fatty acids.

52 Remodeled CL contains mostly unsaturated fatty acids.

53 sed to physiological levels of saturated and unsaturated fatty acids.

54 ounds and endogenous modulators, such as cis-unsaturated fatty acids, 24(S)-hydroxycholesterol, and v

55 Highly unsaturated fatty acids accelerate sterol regulatory-ele

56 Highly unsaturated fatty acid activation of peroxisome prolifer

57 were less likely to meet Adequate Intakes of unsaturated fatty acids (all P-trend < 0.001), despite h

58 of PPARalpha activators (i.e. nonesterified unsaturated fatty acids and chylomicron remnants) that i

59 Defective acylation of CL with unsaturated fatty acids and decreased total CL are assoc

60 Unsaturated fatty acids and esters can be oxidized in si

61 produced by nonenzymatic reaction of NO with unsaturated fatty acids and exert anti-inflammatory acti

62 Among 96 of the unsaturated fatty acids and glycerophospholipids identif

63 ceptor, these proteins sense the presence of unsaturated fatty acids and initiate reactions preventin

64 urated fatty acids levels, (ii) retention of unsaturated fatty acids and low levels of cyclopropane f

65 -deficient seeds exhibited a smaller loss of unsaturated fatty acids and lower accumulation of lipid

66 Unsaturated fatty acids and mastoparan increased phospho

67 ynuclein has been shown to have affinity for unsaturated fatty acids and membranes enriched in polyun

68 f formation of many long chain saturated and unsaturated fatty acids and of dicarboxylic acids are ei

69 s LNO2 and OA-NO2, derived from reactions of unsaturated fatty acids and oxides of nitrogen, are a cl

70 ses, reduced the moisture, and preserved the unsaturated fatty acids and proteins.

71 on oleic acid/linoleic acid ratio, levels of unsaturated fatty acids and specific polyphenols, some s

72 idopsis thaliana) contain elevated levels of unsaturated fatty acids and strongly express two fatty a

73 ys even when formulas had an high content of unsaturated fatty acids and valuable Long Chain Polyunsa

74 the fabAB operon was repressed by exogenous unsaturated fatty acids, and DNA sequences upstream of t

75 e enzyme required for the generation of mono-unsaturated fatty acids, and fatty acid-binding protein

76 e of vitamins C, E, B6, and B12, and folate, unsaturated fatty acids, and fish are related to a low r

77 DM polarization in response to saturated and unsaturated fatty acids, and identify the potential to r

78 om hexane extraction of the flour is rich in unsaturated fatty acids, and polyphenols (resulting from

79 Unsaturated fatty acids are metabolized to reactive prod

80 Unsaturated fatty acids are preferentially esterified in

81 In bacteria, unsaturated fatty acids are produced by the de novo fatt

82 Because both saturated and unsaturated fatty acids are required for growth when fat

83 ular signaling mechanisms employed by highly unsaturated fatty acids are unknown, this review present

84 olvins (RvE1 and RvD1), derived from omega-3 unsaturated fatty acids, are potent inhibitors for infla

85 evealed significant accumulation of Delta(5)-unsaturated fatty acids as acyl-CoAs compared to the acc

86 enerated a fabM strain that does not produce unsaturated fatty acids as determined by gas chromatogra

87 y of the emerging knowledge regarding highly unsaturated fatty acids as kinase cascade activators.

88 The amount of unsaturated fatty acids (as a percentage of total fatty

89 mposition of the diet by replacing SFAs with unsaturated fatty acids, as well as lean protein and car

90 ene product and shows that it can repair the unsaturated fatty acid auxotrophy when it is expressed i

91 work, a connection between the regulator of unsaturated fatty acid biosynthesis in E. coli, FabR, th

92 Unsaturated fatty acids block the binding between Ubxd8

93 Therefore, saturated and unsaturated fatty acids bring about opposite macrophage

94 dizes lyso-PE containing either saturated or unsaturated fatty acids but exhibits poor activity on l-

95 ffinity ligands (long chain fatty acyl-CoAs, unsaturated fatty acids), but not weak affinity ligands

96 cSpt23p and scMga2p control the formation of unsaturated fatty acids by a mechanism that involves the

97 n the conversion of saturated fatty acids to unsaturated fatty acids by Delta9 desaturases.

98 Aspergilli oxidize C18 unsaturated fatty acids by dioxygenase-cytochrome P450 f

99 The oxygenation of unsaturated fatty acids by dioxygenases occurs in all ki

100 The oxidation and nitration of unsaturated fatty acids by oxides of nitrogen yield elec

101 Some of the identified AsPL contained unsaturated fatty acids (C16:1, C18:1 to C18:3), but sat

102 lipid breakdown products, primarily from the unsaturated fatty acids C18:1 and C18:2.

103 (C16:0 and C18:0) were released faster than unsaturated fatty acids (C18:1n9, C18:2n6 and C18:3n3) f

104 Linoleic acid (unsaturated fatty acid, C18:2) accelerated the spontaneo

105 o have a unique role in generating very long unsaturated fatty acids (C26:1) that cannot be salvaged

106 ia supplemented with different saturated and unsaturated fatty acids can be detected using CARS hyper

107 ings indicate that increased availability of unsaturated fatty acids can compromise the stress-induce

108 dopamine indicated the requirement of a long unsaturated fatty acid chain for an optimal functional i

109 Interestingly, only PA species with unsaturated fatty acid chains, such as those produced by

110 nities of PPAR alpha for fatty acyl-CoAs and unsaturated fatty acids, CoA thioesters of peroxisome pr

111 cing FRS compared with other oils varying in unsaturated fatty acid composition.

112 ent repression of fabB and fabA by exogenous unsaturated fatty acids confirmed the role for FabR in r

113 nt in flaxseed level provided an increase in unsaturated fatty acid content namely omega-3 fatty acid

114 cteristics, while production area influenced unsaturated fatty acids, content of vanillic acid and so

115 Blends with unsaturated fatty acid contents between 60 and 70% were

116 s influence showed higher (p<0.05) sugar and unsaturated fatty acid contents, which could be attribut

117 The incorporated cis-unsaturated fatty acids decrease Saureus membrane fluidi

118 These studies show that dietary trans unsaturated fatty acids decrease the rate of lipid perox

119 bolism, DNA replication, and biosynthesis of unsaturated fatty acids; decreases occurred in the amino

120 The results suggest that unsaturated fatty acids differentially affect concentrat

121 Unsaturated fatty acids (e.g., oleic and palmitoleic aci

122 It is well known that the unsaturated fatty acids easily undergo oxidation reactio

123 tion, for example during the biosynthesis of unsaturated fatty acids, eicosanoids, gibberellins and c

124 Oxidation of unsaturated fatty acids--either nonenzymatic or enzymati

125 Storage of unsaturated fatty acid emulsions at 25 degrees C for 3 d

126 Decreases in unsaturated fatty acids, especially eicosapentaenoic aci

127 hotochemistry of mycolactone A/B and related unsaturated fatty acid esters is reported.

128 Feeding also increases the levels of other unsaturated fatty acid ethanolamides (FAEs) (e.g. linole

129 Identification and quantification of unsaturated fatty acid (FA) isomers in a biological syst

130 is the key step that regulates the levels of unsaturated fatty acids (FAs) in cells.

131 n tissue is selectively enriched with highly unsaturated fatty acids (FAs).

132 the most severe defect in the production of unsaturated fatty acids, fat-6;fat-7, exhibits slow grow

133 uding alkanols, saturated and cis- and trans-unsaturated fatty acids, fatty acid methyl esters, sphin

134 st strain (designated OLE1 KO) that required unsaturated fatty acids for growth but not saturated fat

135 abH deletion mutant requires only long-chain unsaturated fatty acids for growth, a source of long-cha

136 ta9 desaturases, in addition to synthesizing unsaturated fatty acids for properly functioning membran

137 Oil analysis showed that the major unsaturated fatty acids for the four species were linole

138 and fabB genes are responsible for anaerobic unsaturated fatty acid formation in Pseudomonas aerugino

139 activity is negatively modulated by bile and unsaturated fatty acids found in the upper small intesti

140 linoleic and linolenic acids were the major unsaturated fatty acids found.

141 Total unsaturated fatty acid fraction was higher than total sa

142 t step followed by the loss of an alpha,beta-unsaturated fatty acid from the sn-2 position in the sec

143 transacylase that transfers acyl chains with unsaturated fatty acids from phospholipids to monolysoca

144 tween nitric oxide (NO), nitrite (NO2-), and unsaturated fatty acids give rise to electrophilic nitro

145 os of n-3 to n-6 fatty acids for both highly unsaturated fatty acids (>/=20 carbon atoms) (HUFAs) and

146 inding domain, indicate that a wide array of unsaturated fatty acids had little effect on LXRalpha ac

147 We found that unsaturated fatty acid has preferential uptake into lipi

148 Dietary fish oil containing omega 3 highly unsaturated fatty acids has cardioprotective and anti-in

149 lular surface expression of ABCA1 protein by unsaturated fatty acids have been identified.

150 Expression levels of genes of the highly unsaturated fatty acid (HUFA) and cholesterol biosynthet

151 rated C22 fatty acid and the limiting highly unsaturated fatty acid (HUFA) in neural tissue.

152 Focusing on n-3 highly unsaturated fatty acids (HUFAs), a subgroup analysis ass

153 ses are required for the synthesis of highly unsaturated fatty acids (HUFAs), which are mainly esteri

154 bditis elegans can add a double bond into an unsaturated fatty-acid hydrocarbon chain and convert n-6

155 Presence of one saturated and one unsaturated fatty acid in the asymmetric TAG favoured th

156 esis was blocked in the absence of exogenous unsaturated fatty acids in a DeltafadR strain and found

157 :1) is a key step, which regulates levels of unsaturated fatty acids in cells.

158 ogether with FAD3 it increases the levels of unsaturated fatty acids in crown galls under hypoxia and

159 the FabR repressor, control biosynthesis of unsaturated fatty acids in Escherichia coli.

160 ntial source of new natural antioxidants and unsaturated fatty acids in food industry, cosmetics and

161 Our work establishes a novel function for unsaturated fatty acids in HCV replication.

162 Significant correlations between BMI and unsaturated fatty acids in intramyocellular lipids, and

163 rprinting of deuterium-labeled saturated and unsaturated fatty acids in living C. elegans revealed th

164 Such findings suggest that unsaturated fatty acids in milled rice contribute to ric

165 detection of a broad range of saturated and unsaturated fatty acids in negative mode showing lineari

166 Oleic acid dominated among unsaturated fatty acids in nutmeg and anise seed oils wh

167 missible 5% for calcium content in milks and unsaturated fatty acids in oil.

168 serines and phosphatidylinositols increased; unsaturated fatty acids in phosphatidylserine increased;

169 e additive with the effects of nonesterified unsaturated fatty acids in regulating FGF21 expression.

170 was shown to have highly elevated levels of unsaturated fatty acids in the cell membrane.

171 ptional repressor controls the proportion of unsaturated fatty acids in the membrane by regulating th

172 The levels of unsaturated fatty acids in the pah1Delta mutant were una

173 We showed previously that cis-unsaturated fatty acids, including arachidonic acid and

174 th deleterious intakes of saturated or trans-unsaturated fatty acids inconsistent with the recommenda

175 the fad3-2 fad7-2 fad8 mutant that lacks tri-unsaturated fatty acids incorporated (14)C-MDA into 18:2

176 demiological data suggest that dietary trans unsaturated fatty acids increase the risk of heart disea

177 Thus, unsaturated fatty acids induce a non-canonical, phylogen

178 y, the PLD inhibitor 1-butanol prevented the unsaturated fatty acid-induced reduction in ABCA1 levels

179 Instead unsaturated fatty acids inhibit extraction of ubiquitina

180 Highly unsaturated fatty acids inhibit the proteolytic release

181 man embryonic kidney 293 cells indicate that unsaturated fatty acids interfere with oxysterols bindin

182 found that inclusion of oleic acid (OA), an unsaturated fatty acid, into the LNP formulation signifi

183 Interplay between saturated and unsaturated fatty acids is also observed.

184 X 'trapping' may explain how dietary highly unsaturated fatty acids lead to a repartitioning of fatt

185 ccelerate (an)aerobic thermal degradation of unsaturated fatty acids leading to the formation of alip

186 acids to primary hepatocytes, nonesterified unsaturated fatty acid levels are very low, representing

187 Roasting treatment increased levels of unsaturated fatty acids (linoleic, oleic and elaidic aci

188 A GPI anchor bearing unsaturated fatty acid lipid chains (1) was synthesized

189 omolar range, long chain fatty acyl-CoAs and unsaturated fatty acids may both represent endogenous PP

190 In this way highly unsaturated fatty acids may function as nutritional fact

191 nic epithelial cells HCT116 by saturated and unsaturated fatty acids mediated through Nods proteins.

192 Unsaturated fatty acid-mediated stabilization of Insig-1

193 for 12/15-lipoxygenase (12/15-LOX)-mediated unsaturated fatty acid metabolism in HSC function.

194 The findings of this study suggest that unsaturated fatty acid metabolism is significantly dysre

195 C26:0 N-acyl chain of KRN7000 with shorter, unsaturated fatty acids modifies the outcome of Valpha14

196 rations of saturated fatty acids (SFA), mono-unsaturated fatty acids (MUFA), gamma-oryzanol, gamma-to

197 in worms with a specific enrichment of mono-unsaturated fatty acids (MUFAs).

198 has shown the regulating effect of n-3 poly-unsaturated fatty acid (n-3 PUFA) on cell signaling tran

199 for speciated mercury, serum omega-3 highly unsaturated fatty acids (n-3 HUFAs), and selenium.

200 In contrast, nitro derivatives of unsaturated fatty acids (NO(2)-FA) are endogenous produc

201 Palmitoleate, the other main unsaturated fatty acid of Saccharomyces, fails to inhibi

202 amma-oryzanol, saturated fatty acid and mono-unsaturated fatty acid of the glutinous rice showed an i

203 of docosahexaenoic acid (22:6), a principal unsaturated fatty acid of the photoreceptor membrane, to

204 FAR1 preferred saturated and unsaturated fatty acids of 16 or 18 carbons as substrate

205 Supplementation of broth with the unsaturated fatty acid oleate restored wild-type growth

206 Conversely,the unsaturated fatty acid oleate triggered autophagic respo

207 almitic acid (PA) and stearic acid (SA)) and unsaturated fatty acid (oleic acid (OA)) were used.

208 In this report, we evaluated the effects of unsaturated fatty acids on LXR-regulated hepatic gene ex

209 via the incorporation of proportionally more unsaturated fatty acids (or fatty acids with analogous p

210 ranched-chain alpha-ketoacids, saturated and unsaturated fatty acids, or 5-aminoimidazole-4-carboxami

211 rrent perspective summarizes our research on unsaturated fatty acid oxidation in the context of infla

212 Thereby (poly)unsaturated fatty acid oxidation products were demonstra

213 ed fatty acids (p<0.001) and decrease in cis-unsaturated fatty acids (p<0.001).

214 A significantly lower amount of unsaturated fatty acids, particularly linolenic acid in

215 Unsaturated fatty acids play an important role in the pr

216 Unsaturated fatty acids play key roles in membrane curva

217 taenoates and tetraenoates, representing the unsaturated fatty acid portion of mycolactone A/B, were

218 total lipid contents and the fruits' mainly unsaturated fatty acid profiles are reported.

219 and IRMPD of Ag-adducted phospholipids with unsaturated fatty acids (R(x)COOH, x = 1 or 2) provided

220 ive signaling mediators that are formed when unsaturated fatty acids react with nitric oxide or nitri

221 fat diets containing long chain saturated or unsaturated fatty acids, reasoning that providing an abu

222 of this review is to demonstrate that highly unsaturated fatty acids regulate lipid metabolism by mod

223 es highly unstable when cells are exposed to unsaturated fatty acids (regulated stability).

224 s to 2 +/- 1.5 min when cells are exposed to unsaturated fatty acids (regulated stability).

225 e only a single pathway for synthesis of the unsaturated fatty acids required to make functional memb

226 um Bacillus subtilis to adjust the levels of unsaturated fatty acids required to optimize membrane li

227 Oxidation of unsaturated fatty acids requires the action of auxiliary

228 Unsaturated fatty acids rescue palmitate-induced apoptos

229 In a second experiment, different sources of unsaturated fatty acids (rich in oleic, linoleic and alp

230 roteins formed after saturated compared with unsaturated fatty acid-rich meals may explain difference

231 model of cellular lipid metabolism in which unsaturated fatty acids serve a protective function agai

232 Here we show that unsaturated fatty acids stabilize Insig-1 without affect

233 nges included declines in tissue n--3 highly unsaturated fatty acid status (36.81%, 1909-T; 31.28%, 1

234 The liver appears to use the highly unsaturated fatty acid status as a nutrient sensor to de

235 here is little direct evidence about how the unsaturated fatty acid substrates enter and move within

236 acid had a positive effect, while long chain unsaturated fatty acids such as arachidic (20:0) and lig

237 unds found in the ethyl acetate fraction are unsaturated fatty acids such as linoleic acid, linolenic

238 Both saturated and unsaturated fatty acids such as palmitate and oleate, re

239 The results from this study showed that unsaturated fatty acids, such as oleic acid (18:1-n9), h

240 saturase 1 (SCD-1) halts the biosynthesis of unsaturated fatty acids, such as oleic acid, and negativ

241 Highly unsaturated fatty acids suppress lipogenic gene transcri

242 f the two genes, fabA and fabB, required for unsaturated fatty acid synthesis and has been reported t

243 Anaerobic unsaturated fatty acid synthesis in bacteria occurs thro

244 In marked contrast, unsaturated fatty acid synthesis in Pseudomonas aerugino

245 Delta9-Desaturases are central enzymes in unsaturated fatty acid synthesis regulated at the transc

246 We report in vivo experiments in which unsaturated fatty acid synthesis was blocked in the abse

247 codes a 3-ketoacyl-ACP synthase required for unsaturated fatty acid synthesis, and it seemed possible

248 report that this defect is due to deficient unsaturated fatty acid synthesis, resulting in aberrant

249 re found to target genes for cholesterol and unsaturated fatty acid synthesis.

250 cholerae FabR was a functional repressor of unsaturated fatty acid synthesis.

251 bic (fabAB) and aerobic (desCB) pathways for unsaturated fatty acid synthesis.

252 ressor of beta-oxidation and an activator of unsaturated fatty acid synthesis.

253 bZ, a protein that plays no specific role in unsaturated fatty acid synthesis.

254 The anaerobic unsaturated fatty acid synthetic pathway of Escherichia

255 LH-butter contained higher health beneficial unsaturated fatty acids than the control and thus render

256 arachidonic acid (AA), a biologically active unsaturated fatty acid that can be further metabolized t

257 acids were characterized by higher level of unsaturated fatty acid that decreased with time (glass j

258 lay a role in the turnover of lipid membrane unsaturated fatty acids that are essential for membrane

259 dehydes that are generated from oxidation of unsaturated fatty acids that are synthesized as a result

260 has been identified as a specific sensor for unsaturated fatty acids that regulates lipogenic activit

261 biophysical characteristics of saturated and unsaturated fatty acids, the increased 16:0 in fab1 fad5

262 desaturase, whose expression is regulated by unsaturated fatty acids through both transcriptional and

263 all interfering RNA abolished the ability of unsaturated fatty acids to inhibit lipid transport activ

264 ates, using a diverse chain of saturated and unsaturated fatty acids to study the efficiency of this

265 ed herein in the context of the oxidation of unsaturated fatty acids to vascular and inflammatory sig

266 chemical ionization conditions, reacts with unsaturated fatty acids to yield an [M + 54]+ ion, which

267 s formed under these conditions, reacts with unsaturated fatty acids to yield nitroalkene derivatives

268 gher levels of carbohydrates, organic acids, unsaturated fatty acids, tocopherols and phenolic acids.

269 coupled to GM1-ceramides with short- or cis-unsaturated fatty acids trafficked efficiently across th

270 embrane associated fatty acids, particularly unsaturated fatty acids, trans-isomers, and specific rel

271 rvation that feeding cells with saturated or unsaturated fatty acids triggers mechanistically distinc

272 tion of the gene encoding FabI results in an unsaturated fatty acid (UFA) auxotroph despite the prese

273 The double bond in anaerobic unsaturated fatty acid (UFA) biosynthesis is introduced

274 Although the unsaturated fatty acid (UFA) synthetic pathway of Escher

275 Unsaturated fatty acids (UFA) are essential components o

276 utant was restored upon supplementation with unsaturated fatty acids (UFA), but not with the saturate

277 titis necrotic collections were analyzed for unsaturated fatty acids (UFAs) and saturated fatty acids

278 Unsaturated fatty acids (UFAs) have profound effects on

279 ity is essential for production of the major unsaturated fatty acids (UFAs) in plant lipids.

280 77 ligand-binding domain (Nur77LBD) enriches unsaturated fatty acids (UFAs) in tissue lipid mixtures.

281 alyze the formation of cyclopropane rings on unsaturated fatty acids (UFAs) that are natural componen

282 d cerulein AP to SAP with greater cytokines, unsaturated fatty acids (UFAs), and multisystem organ fa

283 acement of saturated fatty acids (SFAs) with unsaturated fatty acids (UFAs), especially polyunsaturat

284 the conversion of the cis to trans isomer of unsaturated fatty acid upon short-term nZVI exposure, re

285 Unsaturated fatty acid (USFA) and saturated fatty acid (

286 jor fatty acid in the seed oil and the total unsaturated fatty acid was 62.38%.

287 The protective effect of unsaturated fatty acids was significantly better in the

288 An alternative pathway of beta-oxidation for unsaturated fatty acids was studied in Escherichia coli.

289 tein ratios of most phospholipids containing unsaturated fatty acids were higher in ISG than in whole

290 cell wall components including ferulate and unsaturated fatty acids were identified in TEs by thioac

291 Multiple unsaturated fatty acids were observed to form a terminal

292 (PC) vesicles containing the aforementioned unsaturated fatty acids were oxidized, we were able to d

293 Unsaturated fatty acids were predominant compounds, with

294 , which can be derived from the oxidation of unsaturated fatty acids, were more abundant in the fragr

295 alian olive oils were richer in squalene and unsaturated fatty acids, whereas Tunisian olive oils sho

296 cally, signals from the DSF family are cis-2-unsaturated fatty acids which regulate diverse biologica

297 Unsaturated fatty acids, which are elevated in diabetes,

298 ned, with a good ratio between saturated and unsaturated fatty acids, which indicates a healthy conte

299 r flavoenzyme required for the metabolism of unsaturated fatty acids with double bonds at even carbon

300 ide ((*)NO)-derived reactive species nitrate unsaturated fatty acids, yielding nitroalkene derivative