ライフサイエンスコーパス: citrate

1 synthesizing rhizoferrin from putrescine and citrate.

2 hours after a 100 mg oral dose of sildenafil citrate.

3 lts for the pulmonary delivery of sildenafil citrate.

4 r sustained pulmonary delivery of sildenafil citrate.

5 density lipoprotein (VLDL), amino acids, and citrate.

6 ake and sperm production through gut-derived citrate.

7 organic chelators, such as nicotianamine and citrate.

8 r anaplerosis and reductive carboxylation to citrate.

9 imilar to the already known inhibitor sodium citrate.

10 HepG2 cells and decreases cellular levels of citrate.

11 tch between E. coli physiology and growth on citrate.

12 of water-soluble Fe(III)-mugineate, Fe(III)-(citrate)(2), and Fe(III)(2)-(phytate)(2).

13 rbonate (4.0g.L(-1)), chloride (5.0g.L(-1)), citrate (6.5g.L(-1)), hydroxide (4.0g.L(-1)), hypochlori

14 of sunflower pectin with 0.74% (w/v) sodium citrate (72 degrees C, 194 min) and different procedures

15 ing following treatment with oral sildenafil citrate, a phosphodiesterase type 5 (PDE5) inhibitor and

16 the succinate transporter NaDC-1 to control citrate absorption from the urinary lumen).

17 is responsible for TCA cycle alterations and citrate accumulation associated with polarization.

18 Risk of citrate accumulation during regional citrate anticoagula

19 rlactatemia (>/= 4 mmol/L), the frequency of citrate accumulation was 0.77%, 2.70%, and 6.33%, respec

20 gain a genome-wide view of the mechanism of citrate accumulation.

21 hould be considered in assessing the risk of citrate accumulation.

22 ificantly more patients randomized to ferric citrate achieved the primary end point (61 [52.1%] versu

23 carrier family 13 member 5, which transports citrate across cell membranes, halts liver cancer cell g

24 These data suggest that citrate acts on the IGF-1R-AKT-PTEN-eIF2a pathway.

25 We found that citrate administration inhibited A549 lung cancer growth

26 ats, chlorthalidone is superior to potassium citrate alone or combined with chlorthalidone in reducin

27 Potassium citrate, alone or with chlorthalidone, increased urine c

28 Citrate, alpha-ketoglutarate and succinate are TCA cycle

29 endogenous type I IFN controls the cellular citrate/alpha-ketoglutarate ratio and inhibits expressio

30 biomarkers [e.g., omega-3 (n-3) fatty acids, citrate, alpha1-acid glycoprotein, HDL, and MUFA] in the

31 tients, lower levels of urinary excretion of citrate, an endogenous inhibitor of calcium crystal form

32 ilability in the rhizosphere (as a result of citrate and acid phosphatase exudation) compared with ma

33 ve a 20-fold increase in signal-to-noise for citrate and an 8-fold increase for isocitrate as compare

34 with its mechanistically related metabolites citrate and aspartate, are widely reported as reduced in

35 on of citC and citS operons was dependent on citrate and CitAB, whose transcription was autorepressed

36 lytic mutant of ACLY in the presence of ATP, citrate and CoA substrates reveals a phospho-citryl-CoA

37 nd catalyses the ATP-dependent conversion of citrate and coenzyme A (CoA) to oxaloacetate and acetyl-

38 e transport of the metabolites succinate and citrate and hence are of paramount physiological importa

39 We illustrate the present approach with citrate and isocitrate, which are isomeric metabolites e

40 We demonstrate that fruit citrate and malate contents have been impacted by select

41 uces root secretion of organic acids such as citrate and malate.

42 ies identified included: iron complexes with citrate and malate: Fe(III)(Cit)(3)(Mal), Fe(III)(Cit)(2

43 eceptor MCP2201, which governs chemotaxis to citrate and other organic compounds in Comamonas testost

44 However, buffers (Citrate and phosphate) chelate iron ions (Fe (II)).

45 Chlorthalidone increased urine citrate and potassium citrate increased it even more; th

46 at pilot-scale by the extraction with sodium citrate and purification with membrane separation, eco-f

47 (4207) operon was induced in the presence of citrate and tartrate, perhaps by the activity of a diver

48 two surface chemistries that include anionic citrate and the cationic polyelectrolyte poly(allylamine

49 ) mice (previously shown to have low urinary citrate and to develop calcium oxalate stones) had a 40%

50 ide a fast and simple method to detect zinc, citrate, and aspartate levels as a biomarker signature f

51 Zinc, citrate, and aspartate were correlated with each other (

52 metabolite pools such as malate, fumarate or citrate, and flux calculations suggest the involvement o

53 the Krebs cycle intermediates succinate and citrate, and the Krebs cycle-derived metabolite itaconat

54 binding affinity of citrinin with diammonium citrate, and urea derived CD over Congo red in presence

55 In two re-refined structures a citrate anion forms an acyl-enzyme reaction intermediate

56 we present several examples of binding of a citrate anion to the active sites of E. coli L-asparagin

57 sp and L-Glu) and an opportunistic ligand, a citrate anion, were determined.

58 s were randomized to receive either regional citrate anticoagulation (n = 300), which consisted of a

59 rrent guidelines suggest the use of regional citrate anticoagulation (which involves the addition of

60 Risk of citrate accumulation during regional citrate anticoagulation in a well-selected cohort of pat

61 fety and efficiency of heparin-free regional citrate anticoagulation of the dialysis circuit using a

62 ed the percentage of patients using regional citrate anticoagulation.

63 layer facing draw solution) using trisodium citrate as draw solute, most likely due to the unique sw

64 nc, in the form of ZnCl(3)(-), together with citrate, aspartate, and N-acetylaspartate on human prost

65 iendly alternatives, such as acetyl tributyl citrate (ATBC).

66 (originating from pyrite) > Au-NP-sulfate > citrate-Au-NP > Au-NP-arsenate > Au-NP-phosphate.

67 ention of citrate-coated gold nanoparticles (citrate-Au-NPs) were studied in partially saturated soil

68 he assay is based on inducing aggregation of citrate AuNPs decorated with a specific nucleic acid pro

69 iations in root surface area would overwhelm citrate benefits.

70 y to characterize Fe plaque using dithionite-citrate-bicarbonate (DCB) extraction and elemental analy

71 We show that upon citrate binding, the PAS domain contracts, resulting in

72 hanges in the enzyme that indirectly disrupt citrate binding.

73 ming that TM helix motions are linked to the citrate-binding event.

74 membrane-embedded CitA construct slows down citrate-binding kinetics by at least a factor of 60, con

75 age, thus suggesting a transformation of the citrate-binding mode during desorption.

76 urthermore, bioinformatics data, showing key citrate-binding motifs conserved across a broad range of

77 teric, mostly hydrophobic cavity next to the citrate-binding site, and requires extensive conformatio

78 However, the citrate-bound LBD revealed a four-helix bundle homotrime

79 Carrot powder (CP) in citrate-buffer (pH 5.20) was submitted to US-pretreatmen

80 Itch induced by acidic citrate, but not alpha-methyl-5-hydroxytryptamine, chlor

81 conclusion, black tea polyphenols and sodium citrate can be used as additives to inhibit TMAO-demethy

82 rameters such as the affinity of JWH-018 for citrate-capped gold nanospheres as well as the LOD.

83 owth of Escherichia coli in M9 medium with a citrate carbon source.

84 h potassium chloride (as control), potassium citrate, chlorthalidone (with potassium chloride to equa

85 We found that the contents of citrate, cis-aconitate and succinate were increased, whi

86 and IDH which may increase the synthesis of citrate, cis-aconitate and succinate.

87 e previously reported that aerobic growth on citrate (Cit(+)) evolved in an Escherichia coli populati

88 in size distributions have been observed for citrate- (cit) and polyvinylpyrrolidone- (PVP) capped si

89 its absorption in the small intestine, both citrate cleavage in hepatocytes and microorganism-derive

90 phosphate, and arsenate-on the retention of citrate-coated gold nanoparticles (citrate-Au-NPs) were

91 Following exposure of the citrate-coated nanoparticles to a suite of guest ligands

92 ity were observed with silver nanoparticles (citrate-coated) with an initial hydrodynamic diameter (D

93 To test whether chlorthalidone and potassium citrate combined would reduce calcium phosphate stone fo

94 ement therapy, anticoagulation with regional citrate, compared with systemic heparin anticoagulation,

95 genase, which are expected to alter cellular citrate concentrations.

96 of the dialysis circuit using a calcium-free citrate-containing dialysate, with calcium reinjected ac

97 3 m(2) 2:1 to receive a fixed dose of ferric citrate coordination complex (two tablets per meal, 210

98 To investigate whether fixed-dose ferric citrate coordination complex favorably affects multiple

99 pitalization, suggest that fixed-dose ferric citrate coordination complex has an excellent safety pro

100 The beneficial effects of fixed-dose ferric citrate coordination complex on biochemical parameters,

101 Ferric citrate coordination complex significantly increased hem

102 Compared with usual care, ferric citrate coordination complex treatment resulted in signi

103 Of the 133 patients randomized to ferric citrate coordination complex, 31 (23%) initiated dialysi

104 etabolism), malic acid and oxoglutaric acid (citrate cycle), carnitine (fatty acid metabolism), and p

105 g starch and sucrose metabolism, glycolysis, citrate cycle, amino acids synthesis, and plant hormones

106 transfer, detoxification of anion radicals, citrate cycle, and tetrapyrrole biogenesis.

107 LIM), was matched in the cytosol by a lag in citrate cycling, as shown with a FRET reporter targeted

108 An acidified citrate cysteine medium (ACCM-2) has been developed whic

109 Diethylcarbamazine citrate (DEC) treatment of loiasis is complicated by adv

110 found that chlorthalidone, but not potassium citrate, decreased stone formation in these rats.

111 analyses showed that PFKFB3 is required for citrate-dependent H3K27 acetylation at enhancer sites of

112 nusual lipodepsipeptides containing a unique citrate-derived fatty acid and a rare dehydro-beta-alani

113 Here we describe a role for the citrate-derived metabolite malonyl-CoA in the effect of

114 gnostic solutions, we recently established a citrate-derived synthesis platform for the development o

115 nal group chemistry dictated the kinetics of citrate desorption, while the guest ligand concentration

116 Potassium citrate did not alter stone formation.

117 acid was added, whereas black tea and sodium citrate did not have a negative effect.

118 Trisodium citrate did not nonetheless influence the gel hardness e

119 than controls, whereas those given potassium citrate did not.

120 ation to a minimal glucose medium containing citrate (DM25).

121 at root structure plays an important role in citrate-enhanced uptake (additional phosphate uptake due

122 Quantifying citrate-enhanced uptake experimentally is difficult as v

123 A large variation of citrate-enhanced uptake over 11 root structures was obse

124 Citrate-enhanced uptake was correlated with morphologica

125 of citrate, resulting in a delayed spike in citrate-enhanced uptake.

126 er of exuding root tips correlated well with citrate-enhanced uptake.

127 ystems cannot entirely explain variations in citrate-enhanced uptake.

128 stem architecture plays an important role in citrate-enhanced uptake.

129 solute phosphate uptake, but did not explain citrate-enhanced uptake.

130 Citrate exhibited low resistance to replacement at high

131 the malate-aspartate shuttle, mitochondrial citrate export and complex I supply the substrates neede

132 Furthermore, we find that mitochondrial citrate export and the malate-aspartate shuttle promote

133 e malate-aspartate shuttle and mitochondrial citrate export are required to maintain synthesis of asp

134 Root citrate exudation is thought to be important for phospha

135 d uptake (additional phosphate uptake due to citrate exudation).

136 ms with many tips would benefit greatly from citrate exudation.

137 G2 hepatoma cells exposed to ferric ammonium citrate (FAC).

138 study, we explored regulatory mechanisms of citrate fermentation genes by global regulators ArcA and

139 can also directly regulate the expression of citrate fermentation genes in E. coli under anaerobic co

140 The putative anaerobic citrate fermentation genes in V. cholerae, consisting of

141 ctly regulated but also indirectly modulated citrate fermentation genes via controling CitA-CitB syst

142 ArcA indirectly controled the expression of citrate fermentation genes via regulating CitA-CitB syst

143 olerae can utilize citrate in vivo using the citrate fermentation pathway and that V. cholerae likely

144 In addition, citrate fermentation was under the control of catabolite

145 howed a sustained drug release of sildenafil citrate for over 24 h.

146 s a potential alternative of oral sildenafil citrate for treatment of PAH.

147 m baseline until week 50 as 40 mg per 0.4 mL citrate free subcutaneous injection.

148 e transporter, plays a key role in importing citrate from the circulation into liver cells.

149 ith the systemic heparin group, the regional citrate group had significantly fewer bleeding complicat

150 In the regional citrate group vs systemic heparin group, median filter l

151 ached statistical significance in the ferric citrate group, including the mean relative change in hem

152 ven chlorthalidone with or without potassium citrate had higher bone mineral density and better mecha

153 sts.Twenty patients received the taurolidine-citrate-heparin lock and 21 received the heparin lock, w

154 These findings reveal a succinate/citrate homeostatic pathway regulated by IRBIT that affe

155 Ferric citrate hydrate (FC) is an iron-based phosphate binder a

156 o be modulated by the Krebs cycle metabolite citrate in Escherichia coli.

157 overprescribing of omeprazole and maropitant citrate in hospitalised dogs, highlighting a need for in

158 The instructive role of citrate in inter-organ communication might be significan

159 r suggests that the role of surface-adsorbed citrate in nanomaterial fate and transport must be bette

160 ther members of the gut microbiota to access citrate in the gut.

161 eriments showed that V. cholerae can utilize citrate in vivo using the citrate fermentation pathway a

162 Milk metabolomics revealed that citrate increased by HS, whereas choline, phosphocholine

163 lidone increased urine citrate and potassium citrate increased it even more; the combination did not

164 In the kidney, low urinary citrate increases the risk for developing kidney stones,

165 Citrate is a ubiquitous compound and can be utilized by

166 Citrate is known to suppress glycolysis by inhibiting ph

167 neurokinin-1 receptor antagonist maropitant citrate is licensed as an antiemetic drug.

168 es are essential for V. cholerae growth when citrate is the sole carbon source.

169 ld) and Krebs cycle intermediates, including citrate, isocitrate, succinate, and malate (1.4-3.9-fold

170 accumulation of the TCA cycle intermediates citrate, itaconate, and succinate.

171 lecules overcoated rather than displaced the citrate layer via electrostatic interaction.

172 bolism, including increased cytoplasmic (iso)citrate levels, reduced glycolytic flux, and functional

173 Uniform organic (primarily citrate ligands) layer on nAu was observable by TEM, and

174 Here we showed that ATP-citrate lyase (ACL), an enzyme converting citrate to ace

175 inherited variants in the genes encoding ATP citrate lyase (ACLY) and HMGCR to create instruments tha

176 cs and metabolite profiling, we identify ATP-citrate lyase (ACLY) as a distinctly mTORC2-sensitive AK

177 The ATP citrate lyase (ACLY) enzyme cleaves cytosolic citrate to

178 methylglutaryl-CoA reductase (HMGCR) and ATP-citrate lyase (ACLY) in a TGF-beta receptor/PI3K/protein

179 ATP-citrate lyase (ACLY) is a central metabolic enzyme and c

180 ATP-citrate lyase (ACLY) is a major source of nucleocytosoli

181 ATP-citrate lyase (ACLY) synthesizes cytosolic acetyl coenzy

182 Here, we show ATP citrate lyase (Acly) to be activated in inflammatory mac

183 anner involving fatty acid oxidation and ATP-citrate lyase activity.

184 Both forms of RuBisCO, together with ATP citrate lyase genes in the rTCA cycle, increase with dis

185 re bempedoic acid, an adenosine triphosphate-citrate lyase inhibitor that reduces cholesterol synthes

186 ate instruments that mimic the effect of ATP citrate lyase inhibitors and HMGCR inhibitors (statins),

187 enetic variants that mimic the effect of ATP citrate lyase inhibitors and statins appeared to lower p

188 ATP citrate lyase is an enzyme in the cholesterol-biosynthes

189 ATP-citrate lyase is an epigenetic regulator to promote obes

190 Whether the genetic inhibition of ATP citrate lyase is associated with deleterious outcomes an

191 tion, both processes being attenuated by ATP-citrate lyase knockdown.

192 Neither lifelong genetic inhibition of ATP citrate lyase nor lifelong genetic inhibition of HMGCR w

193 boxylase (ACCalpha), and increased FASN, ATP citrate lyase(ACLY), and malic enzyme (ME) protein expre

194 completed for bempedoic acid (targeting ATP-citrate lyase) and inclisiran (an interference RNA-based

195 ate transporter Slc25A1, and the nuclear ATP-citrate lyase, in association with intracellular accumul

196 own that bempedoic acid, an inhibitor of ATP citrate lyase, reduces levels of low-density lipoprotein

197 MyD88 and TRIF resulted in activation of ATP-citrate lyase, which in turn facilitated the induction o

198 yltransferase 1A and adenosine tri-phosphate citrate lyase, which, together, impart macrophages with

199 fat diet (HFD) results in suppression of ATP citrate-lyase levels in tissues such as adipose and live

200 ATP citrate-lyase produces acetyl-CoA in the nucleus and cyt

201 MED score was associated with higher urinary citrate, magnesium, oxalate, phosphate, uric acid, volum

202 ded by aralar deficiency, presumably through citrate-malate shuttle.

203 1 in comparison to those synthesized through citrate method.

204 mpare the safety and efficacy of oral ferric citrate (n=117) and placebo (n=115).

205 d trait refinement and adaptation to the new citrate niche, while also suggesting a recalcitrant mism

206 itions of the rigor-like conformation with a citrate of crystallization at the nucleotide binding sit

207 comparison to orally administered sildenafil citrate of the same dose.

208 Cit(+) variants can also grow in citrate-only medium (DM0), a novel environment for E. co

209 Caffeine citrate or placebo until drug therapy for apnea of prema

210 igate the relationship between succinate and citrate/oxalate levels, we assessed blood and urine leve

211 d isocitrate (p = 1.2 x 10(-3)), but reduced citrate (p = 5.0 x 10(-4)), were found to be associated

212 d analytical method for the determination of citrate, phosphate and sulfite in seafood by capillary z

213 influenced strongly vitamin C degradation in citrate-phosphate buffer but not in the apple puree seru

214 oot systems were used as the geometry for 3D citrate-phosphate solubilization models.

215 ith chlorthalidone, and rats given potassium citrate plus chlorthalidone had some stones but fewer th

216 rthalidone reduced it further, and potassium citrate plus chlorthalidone reduced it even more.

217 to equalize potassium intake), or potassium citrate plus chlorthalidone.

218 ative genomics and transcriptome analysis of citrate-producing strains-namely, A. niger H915-1 (citra

219 r influence on pH decrease nor difference in citrate production were observed.

220 ne and central carbon metabolism and reduces citrate production, leading to a decrease in the steady-

221 After brief tissue preparation, the glucose/citrate ratio can be recorded on a tissue sample in 1 mi

222 Potassium citrate reduced urine calcium compared with controls, ch

223 Citrate reduces the severity of the Mg(2+) toxicity phen

224 Interestingly, citrate regressed Ras-driven lung tumors.

225 ity could collectively exude high amounts of citrate, resulting in a delayed spike in citrate-enhance

226 leukocyte scintigraphy (LS), and Gallium-67 citrate scintigraphy for the diagnosis of CIED infection

227 No studies for (67)Ga citrate scintigraphy met the inclusion criteria.

228 ycolytic metabolism to sustain physiological citrate secretion, whereas prostate adenocarcinoma consu

229 , while the desorption mediated decay of the citrate signal followed a first-order model.

230 a testis-midgut interaction via cytokine and citrate signaling that regulates intestinal metabolism,

231 Indeed, supplying exogenous citrate significantly enhanced Ga tolerance.

232 oagulation (which involves the addition of a citrate solution to the blood before the filter of the e

233 ELT scavenges iron citrate species faster than deferasirox, but rapidly don

234 We measured the oxidation of citrate stabilized AgNPs by O(2) and hydrogen peroxide (

235 ch enables semiquantitative determination of citrate surface coverage.

236 h were consistent with the expression of ATP-citrate synthase (ACS) and isocitrate dehydrogenase (IDH

237 se reaction and anaplerotic pathways) and Re-citrate synthase (Ccar_06155) was a key enzyme in its tr

238 c selection unearthed the Krebs cycle enzyme citrate synthase (CitA) as a checkpoint regulator contro

239 The activities of the metabolic enzymes citrate synthase (CS), malate dehydrogenase, and strombi

240 companying the fall in CK flux, total CK and citrate synthase activities and the absolute activities

241 Although complex-IV and citrate synthase activities were similar in VOE platelet

242 Remarkably, re-acidification restores citrate synthase activity and ATP content in an insulin

243 Mitochondrial mass was analysed by citrate synthase activity and mitochondrial protein cont

244 d glucose tolerance, liver NAD(+) levels and citrate synthase activity in offspring.

245 eta2, insulin receptor, glycogen content and citrate synthase activity were similar among groups.

246 m and alterations in their respiratory rate, citrate synthase activity, and AMP/ATP ratio, while tryp

247 Mitochondrial oxygen consumption rate, citrate synthase activity, and ATP content are all reduc

248 ed adult neurogenesis, greater mitochondrial citrate synthase activity, and modulation of the adult h

249 analyzed for CK total activity, CK isoforms, citrate synthase activity, and total creatine.

250 ecreased mitochondrial ATP production and/or citrate synthase and cytochrome oxidase activities in th

251 moxia or hypoxia increased the activities of citrate synthase and cytochrome oxidase.

252 itofusin 2]), and oxidative phosphorylation (citrate synthase and electron transport chain complexes)

253 haB-crystallin with alcohol dehydrogenase or citrate synthase by applying thermal stress.

254 nted the muscle tricarboxylic acid cycle and citrate synthase facilitating energy expenditure.

255 um insulin concentrations (-53%) and hepatic citrate synthase flux (-38%), respectively.

256 in assessing rates of hepatic mitochondrial citrate synthase flux (V CS) and pyruvate carboxylase fl

257 ition, there were striking increases in both citrate synthase gene expression and enzymatic activity

258 ACLY forms a homotetramer with a rigid citrate synthase homology (CSH) module, flanked by four

259 ht a novel and unique role of the C-terminal citrate synthase homology domain in ACLY function and ca

260 role of the uncharacterized ACLY C-terminal citrate synthase homology domain in the mechanism of ace

261 dispensable for CtrA control, and functional citrate synthase paralogs cannot replace CitA in promoti

262 Genetic knockdown of citrate synthase promotes increased nuclear acetyl-CoA l

263 d in higher OXPHOSCI+CII (pmol oxygen/s x mg/citrate synthase) in the cortex (6.00 +/- 0.28 vs 3.88 +

264 Inactivation of citrate synthase, but not down-stream enzymes suppressed

265 -catalyzed phosphorylation and inhibition of citrate synthase, elevated acetyl-CoA levels, and hypera

266 Corroborated by data referring to citrate synthase, these results confirm the transitory (

267 c acid esters to a single linkage block in a citrate synthase-like gene.

268 ACO2 promoted mitochondrial citrate synthesis to facilitate de novo lipogenesis, and

269 surand and the reducing agent of the Au(III)/citrate system in the flow network.

270 compared with frequently used Ca sources (Ca citrate tetrahydrate (CCT), tri-Ca phosphate (triCP) and

271 a substantial net uptake of both glucose and citrate that delivered exogenous energy and provided app

272 ation of alpha-ketoglutarate, aconitate, and citrate that is associated with reversal of the tricarbo

273 sociation with intracellular accumulation of citrate, the precursor for acetyl coenzyme A.

274 e-producing strains-namely, A. niger H915-1 (citrate titer: 157 g L(-1)), A1 (117 g L(-1)), and L2 (7

275 TP-citrate lyase (ACL), an enzyme converting citrate to acetyl-CoA, is highly induced in the kidney o

276 itrate lyase (ACLY) enzyme cleaves cytosolic citrate to generate acetyl-CoA, and is upregulated after

277 on, whereas prostate adenocarcinoma consumes citrate to power oxidative phosphorylation and fuel lipo

278 er the genomic mutations nor the addition of citrate to the medium overcomes ethanol toxicity or temp

279 : for Gu-0 membranes almost no phosphate and citrate transport could be detected, while the Gu-100 me

280 0 at pH 7, showing an enhanced phosphate and citrate transport for Gu-100 in comparison to Gu-0.

281 Likewise, MtMATE67-mediated citrate transport into the symbiosome space would increa

282 hibits the expression of the plasma membrane citrate transporter NaCT in HepG2 cells and decreases ce

283 We have characterized a nodule-specific citrate transporter of the multidrug and toxic compound

284 In sorghum, the root citrate transporter SbMATE confers Al tolerance by prote

285 :C increased expression of the mitochondrial citrate transporter Slc25A1, and the nuclear ATP-citrate

286 NaCT (SLC13A5; mINDY), a sodium-coupled citrate transporter, is the mammalian ortholog of Drosop

287 mily 13 member 5 (SLC13A5), a sodium-coupled citrate transporter, plays a key role in importing citra

288 Escherichia coli can utilize citrate under anaerobic conditions but not aerobic condi

289 Net citrate uptake from the CVVH circuit was 60 +/- 2 mg/min

290 In this study, we investigated citrate utilization and regulation in Vibrio cholerae, t

291 Genes involved in citrate utilization have been extensively studied in som

292 both ArcA and Fnr can indirectly control the citrate utilization via CitA-CitB system, while Fnr can

293 njected with streptozotocin (30-45 mg/kg) or citrate vehicle.

294 Citrate was found in five samples.

295 Phosphocreatine/creatine and citrate were identified at higher concentrations after c

296 g alpha-KG, succinate, fumarate, malate, and citrate were observed in TGF-beta1-differentiated myofib

297 lement thorium and counterions phosphate and citrate were separated effectively from the REEs in the

298 d metabolites (e.g., lactate, glutamine, and citrate) were mapped to pathways of glycolysis and the T

299 herefore, the decrease in cellular levels of citrate would stimulate glycolysis and inhibit gluconeog

300 cotianamine: Cu(II)(NA); zinc complexes with citrate: Zn(II)(Cit)(2) and nicotianamine Zn(II)(NA) and