ライフサイエンスコーパス: fatty acid metabolism

1 ice through physiologic functions apart from fatty acid metabolism.

2 s well as SCD1, the rate-limiting enzyme for fatty acid metabolism.

3 of the hepatic genes involved in glucose and fatty acid metabolism.

4 ) is an essential facet in the regulation of fatty acid metabolism.

5 he tricarboxylic acid cycle (TCA) cycle, and fatty acid metabolism.

6 neogenesis, glyoxylate cycle, and long-chain fatty acid metabolism.

7 ys important roles in whole-body glucose and fatty acid metabolism.

8 evidence that CTRP1 is a novel regulator of fatty acid metabolism.

9 d the relation between GIP, 11beta-HSD1, and fatty acid metabolism.

10 d its application to (13)C-tracer studies of fatty acid metabolism.

11 novel and complex connection between PD and fatty acid metabolism.

12 luding the citric acid cycle, polyamine, and fatty acid metabolism.

13 hould be broadly applicable to investigating fatty acid metabolism.

14 rial DNA depletion, mutation, or a defect of fatty acid metabolism.

15 that serve as key determinants of myocardial fatty acid metabolism.

16 ay major roles in regulating cholesterol and fatty acid metabolism.

17 reflect tissue-specific aspects of lipid and fatty acid metabolism.

18 ty acids to acyl-CoAs in the initial step of fatty acid metabolism.

19 it altered expression of genes that regulate fatty acid metabolism.

20 ynthesis and for A2B receptors in decreasing fatty acid metabolism.

21 poptosis, reactive oxygen species (ROS), and fatty acid metabolism.

22 strating diabetes-induced changes in retinal fatty acid metabolism.

23 ll development after infection by modulating fatty acid metabolism.

24 ion levels of representative marker genes in fatty acid metabolism.

25 ivation of genes involved in cholesterol and fatty acid metabolism.

26 Bile acid (BA) signaling regulates fatty acid metabolism.

27 dentified fadR, which encodes a regulator of fatty acid metabolism.

28 in addition to possessing fas genes used in fatty acid metabolism.

29 the natriuretic peptides influence lipid and fatty acid metabolism.

30 s, gene silencing, life-span regulation, and fatty acid metabolism.

31 potentially other functions associated with fatty acid metabolism.

32 a gene that is central to the regulation of fatty acid metabolism.

33 terium tracing studies of redox cofactor and fatty acid metabolism.

34 variety of biosynthetic pathways, including fatty acid metabolism.

35 A carboxylases (ACCs) have crucial roles in fatty acid metabolism.

36 hat may play crucial roles in adipose tissue fatty acid metabolism.

37 their CoA derivatives play a central role in fatty acid metabolism.

38 at plays a pivotal role in the regulation of fatty acid metabolism.

39 SL) catalyzes the initial step in long chain fatty acid metabolism.

40 nd that ACC1 and ACC2 have distinct roles in fatty acid metabolism.

41 e in transcription of the genes of bacterial fatty acid metabolism.

42 dative stress generated from polyunsaturated fatty acid metabolism.

43 e acyltransferases have crucial functions in fatty acid metabolism.

44 A carboxylases (ACCs) have crucial roles in fatty acid metabolism.

45 the ELO family of genes that are involved in fatty acid metabolism.

46 ) is essential for the regulation of hepatic fatty acid metabolism.

47 ce entails dysregulation of both glucose and fatty acid metabolism.

48 ressed >1.5-fold, including many involved in fatty acid metabolism.

49 c phenotypes associated with perturbation in fatty acid metabolism.

50 ates well with their downregulated amino and fatty acid metabolism.

51 zation, extracellular matrix attachment, and fatty acid metabolism.

52 ) regulate genes involved in cholesterol and fatty acid metabolism.

53 AMPK in turn promotes glycolysis and alters fatty acid metabolism.

54 CoA synthetase 1 (ACSL1) plays a key role in fatty acid metabolism.

55 luding glycerophospholipid, glycerolipid and fatty acid metabolism.

56 esters and triglycerides, SCD is pivotal in fatty acid metabolism.

57 tion factor that regulates genes involved in fatty acid metabolism.

58 ofiles, consistent with severe disruption of fatty acid metabolism.

59 e enzyme stearoyl-CoA desaturase-1 (SCD1) in fatty acid metabolism.

60 nase/insulin pathway and an up-regulation of fatty acid metabolism.

61 fatty acid transport protein, CD36, altering fatty acid metabolism.

62 liver is a major metabolic organ involved in fatty acid metabolism.

63 0) T antigens and oncogenic Ras(12V), affect fatty acid metabolism.

64 1(-/-) mice was associated with altered free fatty acid metabolism.

65 r in lipotoxic diseases due to modulation of fatty acid metabolism.

66 acking its DNA-binding-dependent activity on fatty acid metabolism.

67 artners of ABCD2 involved in polyunsaturated fatty-acid metabolism.

68 cardiolipin, phosphonolipid, amino acid, and fatty acid metabolism; a partial Kreb's cycle; a reduced

69 and skeletal muscle, an accelerated rate of fatty acid metabolism, abnormal glucose metabolism, cons

70 Loss of Acbp also results in fatty acid metabolism abnormalities, with hair lipid pro

71 phy (X-ALD) is a disorder of very-long-chain fatty acid metabolism, adrenal insufficiency, and cerebr

72 s, some of which include sucrose metabolism, fatty acid metabolism, amino acid metabolism, carbon fix

73 in pathways of branched-chain amino acid and fatty acid metabolism and (b) increased maximal capacity

74 ich plays a critical role in polyunsaturated fatty acid metabolism and (like another important target

75 is of IL-6 in males may inadvertently affect fatty acid metabolism and augment aging-related neuroinf

76 hospholipase C-delta1, a protein involved in fatty acid metabolism and calcium regulation.

77 s involved in vesicle trafficking transport, fatty acid metabolism and cellular component biogenesis.

78 This increase in fatty acid metabolism and decrease in efficiency is conc

79 erall, this work demonstrates a link between fatty acid metabolism and E3 ligase activities in plants

80 dy, we tested the hypothesis that myocardial fatty acid metabolism and efficiency are abnormal in obe

81 udies suggest that alterations in myocardial fatty acid metabolism and efficiency in obesity can caus

82 d obesity and exhibit enhanced mitochondrial fatty acid metabolism and elevated oxidative capacity of

83 Palmitate induced fatty acid metabolism and endoplasmic reticulum (ER) str

84 gs identify an intimate relationship between fatty acid metabolism and ER proteostasis that influence

85 P) functions both intracellularly as part of fatty acid metabolism and extracellularly as diazepam bi

86 t cycle, the diet-induced effects on growth, fatty acid metabolism and final eating quality were asse

87 We therefore examined glucose and fatty acid metabolism and hepatic glucose production in

88 We review new developments in adipose tissue fatty acid metabolism and how that might relate to cardi

89 FadR is a master regulator of fatty acid metabolism and influences virulence in certai

90 tial for the expression of genes involved in fatty acid metabolism and ingestion-associated stress re

91 R-33a and -b also regulate genes involved in fatty acid metabolism and insulin signaling.

92 l-CoA carboxylase (ACC) has crucial roles in fatty acid metabolism and is an attractive target for dr

93 like acetyl-CoA, is a high energy product of fatty acid metabolism and is produced through a similar

94 T liver biopsies, intrahepatic expression of fatty acid metabolism and lipid transport genes was lowe

95 cated in regulating cholesterol homeostasis, fatty acid metabolism and lipogenesis.

96 tional signature without normal increases in fatty acid metabolism and mitochondrial biogenesis genes

97 reases in expression of proteins involved in fatty acid metabolism and of mitochondrial chaperones.

98 regulates metabolic pathways in glucose and fatty acid metabolism and protein synthesis.

99 ide hydrolase (sEH), opening a new branch of fatty acid metabolism and providing an additional site f

100 These genes are associated with fatty acid metabolism and represent mechanistic targets

101 Consequently, fatty acid metabolism and ROS production were enhanced,

102 e compatible with a multilevel impairment of fatty acid metabolism and significant mitochondrial dysf

103 Altered fatty acid metabolism and the accumulation of triacylgly

104 receptor (GPCR) pathways control glucose and fatty acid metabolism and the onset of obesity and diabe

105 Regulation of fatty acid metabolism and the physiological effects of f

106 acid uptake should consider the influence of fatty acid metabolism and the possible interactions betw

107 e, mitochondrial capacity around glucose and fatty acid metabolism and thermogenesis is found to decl

108 , and echium oil affects the biochemistry of fatty acid metabolism and thus the balance of proinflamm

109 nvestigated the role of FABP4 in endothelial fatty acid metabolism and tumour angiogenesis.

110 I an association of downregulated genes with fatty acid metabolism and upregulated genes with inflamm

111 hich acts as a molecular brake that inhibits fatty acid metabolism and WAT browning.Histone deacetyla

112 cate that (i) MUC1 regulates cholesterol and fatty acid metabolism, and (ii) activation of these path

113 in cholesterol metabolism, 3 participate in fatty acid metabolism, and 4 have no known connection to

114 he effects of ethanol on SREBP-1 activation, fatty acid metabolism, and development of alcoholic fatt

115 thway, related to oxidative phosphorylation, fatty acid metabolism, and glycolysis.

116 oxidative phosphorylation, drug metabolism, fatty acid metabolism, and intestinal maturation, events

117 its of respiratory complexes, ATP machinery, fatty acid metabolism, and Krebs cycle, which further de

118 nsferase, a mitochondrial enzyme involved in fatty acid metabolism, and MED13, a component of the Med

119 EBP target genes, selective reprogramming of fatty acid metabolism, and suppression of inflammatory-r

120 gamma coactivator 1alpha, a key regulator of fatty acid metabolism, and that proliferator-activated r

121 luding amino acid, iron, and polyunsaturated fatty acid metabolism, and the biosynthesis of glutathio

122 ode connecting carbohydrate, amino acid, and fatty acid metabolism, and the regulation of pyruvate fl

123 indicate that variants in genes important in fatty acid metabolism are associated with SCA survival i

124 We conclude that fadR and regulation of fatty acid metabolism are essential for V. vulnificus to

125 trophic acetate, propionate and longer chain fatty acid metabolism are mostly understood, but key ste

126 lved in lipid metabolism, especially omega-6 fatty acid metabolism, are up-regulated in livers of mic

127 his review is to highlight the importance of fatty acid metabolism as a major determinant in fatty ac

128 Our results indicate fatty acid metabolism as a target for tumour-specific ap

129 derivative, which is an essential factor in fatty acid metabolism as acyltransferase cofactor and in

130 A switch to fatty acid metabolism as an energy source and an enhance

131 ogether, our studies identify HIF control of fatty acid metabolism as essential for ccRCC tumorigenes

132 e Hippo pathway in lung cancer, and point to fatty acids metabolism as a key regulator of lung cancer

133 iferator-activated receptor signalling' and 'fatty acid metabolism' as the three most enriched pathwa

134 ive and respiratory capacities, nitrogen and fatty acid metabolism, as well as the first complete ele

135 ly suppressed TCA cycle, altered glucose and fatty acids metabolism, as well as nucleic acids metabol

136 implications in the chronic abnormalities of fatty acid metabolism associated with obesity and diabet

137 dge of the complex mechanisms of peroxisomal fatty acid metabolism at a molecular level and elucidate

138 al DOCK gene, regulates postprandial TAG and fatty acid metabolism by controlling activation of its p

139 urrent knowledge regarding the regulation of fatty acid metabolism by distinct cell autonomous circad

140 In contrast, restoring fatty acid metabolism by genetic or pharmacological meth

141 diator co-activator subunit in regulation of fatty acid metabolism by nuclear receptor-like transcrip

142 new potential probe for assessing myocardial fatty acid metabolism by PET.

143 DT-15 plays a critical role in regulation of fatty acid metabolism by the nematode PPAR-like nuclear

144 cyclic and acyclic products generated during fatty acid metabolism can also function as important che

145 Genetic disorders of amino acid and fatty acid metabolism can be detected with tandem mass s

146 with type 1 diabetes, myocardial glucose and fatty acid metabolism can be manipulated by altering pla

147 lestatic disease progression because altered fatty acid metabolism can enhance reactive oxygen specie

148 including gene silencing, regulation of p53, fatty acid metabolism, cell cycle regulation, and life s

149 odds ratio, 2.04; P = 1.24 x 10(-7)) with a fatty acid metabolism; confirmation of PDE4DIP was obser

150 lved in cholesterol efflux (ABCA1 and NPC1), fatty acid metabolism (CROT and CPT1a), and insulin sign

151 riants of genes that control polyunsaturated fatty acid metabolism (CYP4F3, FADS1, and FADS2), along

152 rohumoral activation, increased adverse free fatty acid metabolism, decreased protective glucose meta

153 nimals have shown that, with age, myocardial fatty acid metabolism decreases, and glucose metabolism

154 thways for steroid biosynthesis, cell cycle, fatty acid metabolism, DNA replication, and biosynthesis

155 where they have been postulated to regulate fatty acid metabolism due to their ability to form stabl

156 in muscle during contracture, alterations in fatty acid metabolism during cardiac ischemia and postis

157 in coordinately regulating carbohydrate and fatty acid metabolism during the progression from fastin

158 centrations was not clear because of complex fatty acid metabolism dynamics in soil.

159 seases known for abnormalities in long-chain fatty acid metabolism, e.g., the Sjogren-Larsson syndrom

160 R)alpha is known primarily as a regulator of fatty acid metabolism, energy balance, and inflammation,

161 ease in gene expression of mitochondrial and fatty acid metabolism enzymes in hepatocytes with reduce

162 It was demonstrated that, by impacting fatty acid metabolism, ETF and ETFDH mutations led to se

163 tionship between iron, oxidative injury, and fatty acid metabolism exists, but transduction mechanism

164 gulation (ZMIZ1), genome maintenance (FEN1), fatty acid metabolism (FADS1 and FADS2), cancer cell mot

165 1 diabetes, the myocardium relies heavily on fatty acid metabolism for energy.

166 in in inflammation, insulin sensitivity, and fatty acid metabolism, future studies should examine mil

167 translocation, DNA binding, and induction of fatty acid metabolism genes acyl coenzyme A oxidase and

168 Transcripts of fatty acid metabolism genes, motility and chemotaxis gen

169 Fatty acid metabolism governs multiple intracellular sig

170 Fatty acid metabolism has received significant attention

171 Hypothalamic fatty acid metabolism has recently been implicated in th

172 oA carboxylases (ACCs), a crucial enzyme for fatty acid metabolism, has been shown to promote fatty a

173 Changes in fatty acid metabolism have been implicated as causal in

174 pharmacologic manipulation of the enzymes of fatty acid metabolism have led to the hypothesis that ne

175 alities such as metabolic acidosis, abnormal fatty acid metabolism, hyperlipidemia, and hyperglycemia

176 , depressed myocardial contractile function, fatty acid metabolism, hypertrophic remodeling, and redu

177 ependent mechanisms that result in increased fatty acid metabolism: (i) elevated levels of Fiaf, whic

178 creen of the genes that regulate glucose and fatty acid metabolism identified an ACC necessary for sa

179 The results indicate that alterations in fatty-acid metabolism, impaired Akt activation by insuli

180 Thus, FAS and fatty acid metabolism in cancer has become a focus for t

181 This study determined retinal-specific fatty acid metabolism in control and diabetic animals.

182 r, there are no experimental data on retinal fatty acid metabolism in diabetes.

183 determine the functional effects of altered fatty acid metabolism in experimental models.

184 This proliferative barrier imposed by fatty acid metabolism in hCOs could be rescued by simult

185 eficiency did not alter hepatic ceramide and fatty acid metabolism in high cholesterol atherogenic di

186 ipoxygenase (12/15-LOX)-mediated unsaturated fatty acid metabolism in HSC function.

187 ted to analyze the role of PPAR-alpha-linked fatty acid metabolism in islet function in health and in

188 etabolic syndrome due to positive effects on fatty acid metabolism in liver and white adipose tissue.

189 In light of these findings, we have studied fatty acid metabolism in MCF7 human breast cancer cells

190 al expression of genes involved in lipid and fatty acid metabolism in men with insulin resistance.

191 FGF21 also regulates fatty acid metabolism in mice consuming a diet that prom

192 licated in the regulation of cholesterol and fatty acid metabolism in multiple tissues, including liv

193 dies demonstrate a pivotal role of essential fatty acid metabolism in myocardial phospholipid remodel

194 ynthetases are necessary for very long-chain fatty acid metabolism in Neuro2a cells.

195 These data show that ACOT7 counterregulates fatty acid metabolism in neurons and protects against ne

196 ism; however, the basic metabolic control of fatty acid metabolism in neurons remains enigmatic.

197 ences of C75 treatment and the alteration of fatty acid metabolism in neurons.

198 al oxygen consumption (MVo(2)), glucose, and fatty acid metabolism in nondiabetic subjects and three

199 ide evidence for the importance of lipid and fatty acid metabolism in OC and serve as the foundation

200 We discuss the role of fatty acid metabolism in Plasmodium and why we believe t

201 ceptor (PR) signaling and 12/15-LOX-mediated fatty acid metabolism in preimplantation mouse uterus.

202 aerobic desaturases to the enzymes used for fatty acid metabolism in proteobacteria: DesA, a 2-posit

203 chanism parallels a phenotypic disruption in fatty acid metabolism in SIRT6 null mice as revealed by

204 d body composition, glucose homeostasis, and fatty acid metabolism in Sost(-/-) mice as well as mice

205 me functional prediction supported decreased fatty acid metabolism in the gut microbiome of subjects

206 ctional intracellular protein that regulates fatty acid metabolism in the nucleus via interactions wi

207 -regulated genes involved in the glucose and fatty acid metabolism in the primary hepatocytes.

208 hetase (ACSL) family that plays key roles in fatty acid metabolism in various tissues in an isozyme-s

209 been documented to play an important role in fatty acid metabolism in vivo and subsequently may be in

210 the importance of Clk2 in the regulation of fatty acid metabolism in vivo and suggest that inhibitio

211 yrate is used to measure carbohydrate versus fatty acid metabolism in vivo.

212 ncoding genes, emphasizing the importance of fatty-acid metabolism in neurological diseases.

213 multiple P450s and suppression of genes for fatty acid metabolism) in response to CPR loss in the tw

214 It is likely that abnormalities in fatty acid metabolism, in conjunction with adipose tissu

215 nase plays a central role in polyunsaturated fatty acid metabolism, inaugurating the biosynthesis of

216 n of expression of numerous genes modulating fatty acid metabolism, including ADIPOR1 (adiponectin re

217 was strongly associated with markers of n-3 fatty acid metabolism, including degree of unsaturation

218 e used (13)C tracers and lipidomics to probe fatty acid metabolism, including desaturation, as a func

219 display features indicative of altered lipid/fatty acid metabolism, including differential adiposity

220 rular gene expression of enzymes involved in fatty acid metabolism, including induction of stearoyl-C

221 olic disorders characterized by dysregulated fatty acid metabolism, including nonalcoholic steatohepa

222 gested that enhanced capacity for energy and fatty acid metabolism, increased protein degradation, re

223 CD36 is a scavenger receptor involved in fatty acid metabolism, innate immunity and angiogenesis.

224 ly represented categories included lipid and fatty acid metabolism, insulin action, and cell-cycle re

225 Proper fatty acid metabolism is critical for hair and skin deve

226 However, interference with adipose tissue fatty acid metabolism is not to be undertaken lightly an

227 Fatty acid metabolism is perturbed in atherosclerotic le

228 etic heart, glycolysis is suppressed whereas fatty acid metabolism is promoted.

229 dings of this study suggest that unsaturated fatty acid metabolism is significantly dysregulated in t

230 transcription factor involved in sustaining fatty acid metabolism, is upregulated in Salmonella-infe

231 associated with glycolysis (Warburg effect), fatty acid metabolism (lipogenesis, oxidation, lipolysis

232 ased, and that this dependence on myocardial fatty acid metabolism may be detrimental to cardiac func

233 yocardial ischemia, prolonged suppression of fatty acid metabolism may persist despite restoration of

234 eficiency primarily affected very long chain fatty acid metabolism, mutant fibroblasts also showed re

235 nvolved in amino sugar, nucleotide sugar and fatty acid metabolism, one carbon pool for folate metabo

236 ments in our understanding of adipose tissue fatty acid metabolism open up the possibility of new pha

237 bolism and the possible interactions between fatty acid metabolism or metabolites and fatty acid tran

238 rting 7 of the 26 genes as being involved in fatty acid metabolism or PPARgamma interaction.

239 the acetyl-proteins are enzymes involved in fatty acid metabolism, oxidative phosphorylation or the

240 mechanism of D/SD include Malassezia-induced fatty acid metabolism, particularly lipase-mediated brea

241 We investigated whether genetic variation in fatty acid metabolism pathways was associated with SCA s

242 , oxidative response and protein, carbon and fatty acid metabolism pathways.

243 ed involvement of amino acid and short-chain fatty acid metabolism pathways.

244 uding protein-glycosylation, polyunsaturated fatty acid metabolism, phospholipid modeling, and glucos

245 Given that deregulated fatty acid metabolism plays a key role in kidney fibrosi

246 t in branched-chain amino acid catabolism or fatty acid metabolism possessed altered susceptibility t

247 iated with dysregulation of intramyocellular fatty acid metabolism, possibly because of an inherited

248 iated with dysregulation of intramyocellular fatty acid metabolism, possibly because of an inherited

249 target of azole antifungals) and a putative fatty acid metabolism protein (and a potential azole dru

250 with lipid metabolism, sterol biosynthesis, fatty acid metabolism, protein transport, oxidoreductase

251 Acyl-CoA synthetases play a pivotal role in fatty acid metabolism, providing activated substrates fo

252 in gene expression consistent with preserved fatty acid metabolism, reduced endogenous DNA damage, de

253 lpha), a transcription factor that modulates fatty acid metabolism, regulates substrate preference in

254 ntified oxidative stress and polyunsaturated fatty acid metabolism-related pathways, as well as tryps

255 pression of cardiac Ppara and its downstream fatty acid metabolism-related targets.

256 idome and demonstrate immediate responses in fatty acid metabolism represented by increases in eicosa

257 Cellular imbalances of cholesterol and fatty acid metabolism result in pathological processes,

258 BMIPP SPECT detects abnormalities in fatty acid metabolism resulting from myocardial ischemia

259 ndrial dysfunction is linked to dysregulated fatty acid metabolism, resulting in increased levels of

260 othesis that TNT exposure affected lipid and fatty acid metabolism, showing that hormetic effects cou

261 However, its myocardial glucose and fatty acid metabolism still responds to changes in plasm

262 eir toxic levels in peroxisomal disorders of fatty acid metabolism, such as adrenoleukodystrophy and

263 Pctp(-/-) mice exhibit altered fatty acid metabolism that is accompanied by reduced hep

264 Endogenous fatty acid metabolism that results in elongation and des

265 eotide-dependent deacetylase SIRT1 regulates fatty acid metabolism through multiple nutrient sensors.

266 The response of fatty acid metabolism to administration of bifidobacteri

267 ase, which together convert intermediates of fatty acid metabolism to alkanes and alkenes.

268 ndicate a role for GPR84 in directly linking fatty acid metabolism to immunological regulation.

269 pha coordinately regulates mitochondrial and fatty acid metabolism to promote tumor growth.

270 hysiological processes including glucose and fatty acid metabolism, transcription, cell growth, mitoc

271 lant infection in M. oryzae by regulation of fatty acid metabolism, turgor establishment and inductio

272 etabolism as well as a possible regulator of fatty acid metabolism, UCP3.

273 about how LRH-1 controls hepatic glucose and fatty acid metabolism under physiological conditions.

274 decrease in expression of enzymes related to fatty acid metabolism, urea cycle, cell replication, and

275 However, blocking fatty acid metabolism using inhibitors to prevent acyl-a

276 in human umbilical vein endothelial cells on fatty acid metabolism, viability and angiogenesis.

277 r characterization revealed that a switch to fatty acid metabolism was a central driver of cardiac ma

278 ssure has affected the genetic regulation of fatty acid metabolism, we assessed 233 serum metabolic p

279 action of nuclear receptors, in glucose and fatty acid metabolism, we generated skeletal muscle-spec

280 To elucidate the specific roles of ACSL5 in fatty acid metabolism, we used adenoviral-mediated overe

281 The alterations in brain fatty acid metabolism were concomitant with a loss of le

282 Several genes involved in lipid droplet and fatty acid metabolism were differentially expressed in I

283 wn to have a central role in regulating free fatty acid metabolism were downregulated in the livers,

284 itric acid cycle, amino acid metabolism, and fatty acid metabolism were found to be highly enriched h

285 l known PPARalpha target genes involved with fatty acid metabolism were observed, reflecting the expe

286 c glycolysis, oxidative phosphorylation, and fatty acid metabolism, were also reduced in T cells lack

287 ression of genes involved with oogenesis and fatty acid metabolism when on its host.

288 itine O-octanoyltransferase, are involved in fatty acid metabolism, whereas down-regulated proteins,

289 sis by coordinated regulation of glucose and fatty acid metabolism, which provide a molecular basis f

290 nd decreased expression of genes involved in fatty acid metabolism, which was prevented by blockade o

291 by increasing protein and RNA synthesis and fatty acid metabolism, while decreasing autophagy.

292 Therefore, V. cholerae co-ordinates fatty acid metabolism with 1-acyl G3P synthesis.

293 To examine the association of endogenous fatty acid metabolism with future development of metabol

294 These cells exhibited altered fatty acid metabolism with increased rates of beta-oxida

295 tyl-CoA carboxylase (ACC) is a key enzyme of fatty acid metabolism with multiple isozymes often expre

296 ain, which would represent a novel branch of fatty acid metabolism with potential signaling functions

297 proteins are clearly important in regulating fatty acid metabolism, with striking protection against

298 and more effective methods to interfere with fatty-acid metabolism, with insulin resistance, hyperlip

299 is growing evidence supporting the idea that fatty acid metabolism within discrete hypothalamic regio

300 remodeling resulted in profound increases in fatty acid metabolism within this tissue.