ライフサイエンスコーパス: glycerol

1 cose, pyruvate/lactate, acetate, xylose, and glycerol).

2 bon sources glucose, gluconate, lactate, and glycerol.

3 atidylcholine liposomes with the addition of glycerol.

4 y enzymatic glycerolysis of sardine oil with glycerol.

5 o stimulate the accumulation of sorbitol and glycerol.

6 dielectric constant upon addition of urea or glycerol.

7 e brain generating arachidonic acid (AA) and glycerol.

8 cells, that can directly hydrolyze Gro3P to glycerol.

9 probes in the presence of all co-solutes but glycerol.

10 CHC), beta-glycerol phosphate (beta-GP), and glycerol.

11 graded by SMc01003 to another fatty acid and glycerol.

12 rdine pilchardus) in the central bond of the glycerol.

13 tasis by enabling the transport of water and glycerol.

14 g conditions, such as high concentrations of glycerol.

15 e key enzymes that catalyze their synthesis, glycerol-1-phosphate dehydrogenase and heptaprenylglycer

16 The structure of XEELCRD in complex with d-glycerol-1-phosphate, a residue present in microbe-speci

17 5 mM Pb(NO3)2-containing media amended with glycerol 2-phosphate (G2P) or phytic acid (PyA) as sole

18 show that the endocannabinoid 2-arachidonoyl glycerol (2-AG) can directly alter the properties of nat

19 ed increases in anandamide or 2-arachidonoyl glycerol (2-AG) levels, resulting in analgesic activity;

20 dogenous anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) on the permeability and inflammatory res

21 oduce the endocannabinoid, 2-arachidonoyl-sn-glycerol (2-AG) upon antigen activation.

22 cannabinoids, anandamide and 2-arachidonoyl glycerol (2-AG), are produced on demand from phospholipi

23 ndocannabinoids anandamide and 2-arachidonyl glycerol (2-AG), as well as the widely consumed plant (p

24 including the endocannabinoid 2-arachidonoyl glycerol (2-AG), for [35S]GTPgammaS binding and cAMP inh

25 and agonism, in particular by 2-arachidonyl glycerol (2-AG), have been shown to reduce somatic sympt

26 on of the endocannabinoid, 2-arachidonoyl-sn-glycerol (2-AG), in the amygdala.

27 lecules, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG), with stress exposure reducing AEA level

28 ion of the endocannabinoid 2-arachidonoyl-sn-glycerol (2AG), is tightly controlled by the cell's redo

29 cally hydrolyze glycerophosphodiesters to sn-glycerol 3-phosphate (Gro3P) and their corresponding alc

30 respectively, by 1.0 M phosphite dianion, d-glycerol 3-phosphate and d-erythritol 4-phosphate.

31 Therefore, we investigated the role of the glycerol 3-phosphate pathway in dietary lipid absorption

32 tly increased the dihydroxyacetone phosphate/glycerol 3-phosphate ratio in INS-1(832/13) cells, indic

33 Hence, the data support the glycerol 3-phosphate transporter-based homology model of

34 as not inhibited by either orthophosphate or glycerol 3-phosphate, indicating that either a glycerol

35 onical GPD enzymes catalyze the synthesis of glycerol-3-phosphate (G3P) by reduction of dihydroxyacet

36 The metabolism of glycerol-3-phosphate (G3P) is important for environmenta

37 the signaling molecules azelaic acid (AzA), glycerol-3-phosphate (G3P), and salicylic acid (SA).

38 FA cycle is regulated by the availability of glycerol-3-phosphate (Gro3P) and fatty acyl-CoA.

39 d storage triacylglycerols is catalyzed by a glycerol-3-phosphate acyltransferase (GPAT).

40 The expression of glycerol-3-phosphate acyltransferase (GPAT3) was examine

41 In this study, we targeted the glycerol-3-phosphate acyltransferase GPAM along with cho

42 xotrophs, and this lipid export requires the glycerol-3-phosphate acyltransferase RAM2, a direct targ

43 (lacs2), permeable cuticle1 (pec1), cyp77a6, glycerol-3-phosphate acyltransferase6 (gpat6), and defec

44 cy in a mutant thereafter named gpat6-a (for glycerol-3-phosphate acyltransferase6).

45 osphoserine phosphatase (PSP) motif fused to glycerol-3-phosphate dehydrogenase (GPD) domains.

46 The R269A mutation of glycerol-3-phosphate dehydrogenase (hlGPDH) results in a

47 , both the malate/oxaloacetate shuttle and a glycerol-3-phosphate dehydrogenase 1(Gpd1p)-dependent sh

48 co-imported with the PTS2-containing enzyme Glycerol-3-phosphate dehydrogenase 1, Gpd1.

49 production of the mature miRNA, derepresses glycerol-3-phosphate dehydrogenase 1-like enzyme (GPD1L)

50 The glycerol-producing PTS2 protein glycerol-3-phosphate dehydrogenase Gpd1p shows a tripart

51 rom NADL to glycolaldehyde (GA) catalyzed by glycerol-3-phosphate dehydrogenase were determined over

52 ntrations of glucose intermediates including glycerol-3-phosphate increased when simulating IR due to

53 data support roles for intermediates in the glycerol-3-phosphate pathway of triacylglycerol synthesi

54 inferred from the dihydroxyacetone phosphate:glycerol-3-phosphate ratio), mitochondrial membrane pote

55 duction by contributing to the production of glycerol-3-phosphate.

56 l (cholesterol) and Phos (1,2-dipalmitoyl-sn-glycerol-3-phospho-(1'rac-glycerol)) via disulfide bond

57 Conversely, addition of glycerol, a protein stabilizer, practically neutralizes

58 was analyzed at different concentrations of glycerol, accompanied by an investigation into the effec

59 Glycerol accumulation and melanization of the appressori

60 nt has increased and decreased trehalose and glycerol accumulation, respectively, suggesting SchA per

61 iacylglycerol to form 3-acetyl-1,2-diacyl-sn-glycerol (acetyl-TAG).

62 le the yield of CO2 remained unchanged; with glycerol, addition of D2 led not only to increased yield

63 e main metabolizing enzyme of 2-arachidonoyl glycerol, an endocannabinoid signaling lipid whose eleva

64 pids and it can be dephosphorylated to yield glycerol, an osmotic stabilizer and compatible solute un

65 orporating two immunomodulators (monomycolyl glycerol analog and polyinosinic-polycytidylic acid) tha

66 The minor secretion fluxes for glycerol and acetate are underestimated by our method, w

67 ficant amounts of ethyl acetate, arabinitol, glycerol and acetate in addition to ethanol, including f

68 rities in chemical structure, 2-arachidonoyl glycerol and anandamide are synthesized and degraded by

69 d endogenous cannabinoids are 2-arachidonoyl glycerol and arachidonoyl ethanolamide (anandamide).

70 nd pathway analyses predicted a link between glycerol and central energy metabolism that influences t

71 ght gain and hepatic glucose production from glycerol and elevates plasma HDL levels.

72 ion pathways in beta-cells possibly comprise glycerol and FFA formation and release extracellularly a

73 IHGW had elevated glycerol and gluconic acid amounts.

74 is electrode catalysed the oxidation of both glycerol and glyceraldehyde thus demonstrating a consecu

75 dehydrogenase (ADH) catalysing oxidation of glycerol and glyceraldehyde.

76 we discuss the physiological involvement of glycerol and HbXIP2;1 in water homeostasis and carbon st

77 fication of nonesterified hydroxyl groups of glycerol and hydroxy fatty acids was performed within cu

78 d formation of this hydrophobic polyester of glycerol and hydroxy/epoxy fatty acids has not been full

79 alanine, and also 2,3-butanediol, methanol, glycerol and isotopic variables were significant for cla

80 he development of the biosensors; the use of glycerol and lactitol as stabilisers resulted in a signi

81 This reaction releases glycerol and leads to the formation of oligomers with th

82 The endocannabinoids 2-arachidonoyl-glycerol and N-arachidonoyl-ethanolamine mediate an arra

83 We investigated glucose removal, lactate, glycerol and NEFA accumulation in media, and metabolic g

84 Adipose tissue lipolysis produces glycerol and nonesterified fatty acids (NEFA) that serve

85 y of fatty acid derivatives polymerized with glycerol and phenolics.

86 C) films, plasticized with varying levels of glycerol and processed by compression molding, was exami

87 ion of the lipase ATGL, the lipolysis marker glycerol and release of fatty acids.

88 sugars (sucrose and trehalose) and polyols (glycerol and sorbitol).

89 increasingly secreting adiponectin, leptin, glycerol and total triglycerides.

90 suggesting SchA performs different roles for glycerol and trehalose accumulation during osmotic stres

91 the non-Maillard reactive characteristics of glycerol and trehalose.

92 egrees C and 65+/-2% relative humidity) lost glycerol and water over time, as determined by gas chrom

93 cultures growing on media supplemented with glycerol (and contained up to 189 mg glycerol g dry spor

94 Healthy subjects ingested [U-(13)C3]glycerol, and blood was drawn at multiple times.

95 values for hydrogen production from ethanol, glycerol, and glucose as high as 65%, 35%, and 6%, respe

96 together with increases in monoacylglycerol, glycerol, and medium- and long-chain free fatty acids, r

97 al chemical systems of aqueous NaCl, aqueous glycerol, and squalane at approximately 75% relative hum

98 es no major diffusion limitations for water, glycerol, and squalane core phases under humid condition

99 nover rate and circulating free fatty acids, glycerol, and triglycerides), lipid oxidation (LOx; by i

100 oocytes facilitated the permeation of water, glycerol, and urea.

101 Whole-body lipolysis (glycerol appearance rate [GlyRa], [(2)H5]glycerol at bas

102 onic cigarette solvents propylene glycol and glycerol are known to produce toxic byproducts such as f

103 docannabinoids anandamide and 2-arachidonoyl glycerol are terminated by enzymatic hydrolysis after cr

104 tion of POSS also affects the excess wing in glycerol arising from a secondary relaxation process, wh

105 r in media containing glucose, galactose, or glycerol as a carbon source.

106 tments, saponin as a natural surfactant, and glycerol as a co-surfactant, in the bicontinuous region

107 prolamin from maize, and in combination with glycerol as plasticizer have been investigated.

108 dy day, subjects received the same amount of glycerol as present in the Intralipid infusion.

109 yceroneogenesis and a switch from lactate to glycerol as substrate for gluconeogenesis, indicating an

110 nce of 1,8-diazabicyclo[5.4.0]undec-7-ene in glycerol at 120 degrees C.

111 is (glycerol appearance rate [GlyRa], [(2)H5]glycerol at baseline and during a hyperinsulinemic-eugly

112 ty acid located at the external bonds of the glycerol backbone and concentrated polyunsaturated fatty

113 tures, including acyl chain positions on the glycerol backbone and double bond positions within acyl

114 in both the positions of acyl chains on the glycerol backbone and the double bonds within the acyl c

115 oring of distribution of fatty acids (FA) in glycerol backbone is performed by enzymatic and chromato

116 red C16 over C18 in the sn-2 position of the glycerol backbone, but CrDGTT2 and CrDGTT3 preferred C18

117 tment of edible soybean oil, which generated glycerol-based polymer as a carbon source and fatty acid

118 and high zeta potential value were PW and BW+glycerol behenate samples, containing 10% oil and 6% sur

119 he electrochemical behavior of the FeS-based glycerol biosensor was analyzed at different concentrati

120 An improved glycerol biosensor was developed via direct attachment o

121 current responses generated by the FeS-based glycerol biosensor were also studied.

122 arachidonoyl-ethanolamine and 2-arachidonoyl-glycerol can be metabolized by cyclooxygenase-2 into PG-

123 Here we show that crude glycerol can be reacted with water over very simple basi

124 Here, we investigate whether glycerol can enhance xerophile germination under acute w

125 formation of products (lead carboxylates and glycerol) can be easily followed and quantified.

126 e (glucose or galactose) and nonfermentable (glycerol) carbon sources and were caused by mutations lo

127 orin-3 (AQP3) is a small transmembrane water/glycerol channel that may facilitate the membrane uptake

128 Aquaporin- (AQP) 3, a water and glycerol channel, plays an important role in epidermal f

129 ,2-dimyristoyl-sn-glycero-3-phospho- (1'-rac-glycerol)/cholesterol lipid bilayers using electron spin

130 Naringin-carrying CHC-beta-GP-glycerol colloidal hydrogel can be used to inhibit induc

131 swollen starch aggregations in lecithin and glycerol compared with those of potato puree and agar, c

132 temperature (TE) of 110 degrees C to remove glycerol completely and most of FFAs; and the second dis

133 osity; paste viscosity then increased as the glycerol concentration rose from 10 to 30%.

134 The effects of glycerol concentration, alkali concentration, ultrasonic

135 rowth and chlorophyll concentration, reduced glycerol concentration, and changes to lipid composition

136 its standard potential under a wide range of glycerol concentrations (0.001-1M).

137 For glycerol concentrations ranging from 1 to 25mM, a 77% in

138 concentrations, and attenuated fasting free glycerol concentrations versus PLA (P < 0.05).

139 vator of pyruvate carboxylase, and increased glycerol conversion to glucose.

140 solvents, DMSO-d6/glycerol (GL) and DMSO-d6/glycerol-d8 (GL-d8), is reported for the first time in o

141 riptional repressor of factors that catalyze glycerol degradation.

142 y) and structural similarity to the GRE-type glycerol dehydratase from Clostridium butyricum, we demo

143 pionibacterium jensenii, and two key enzymes-glycerol dehydrogenase and malate dehydrogenase-were ove

144 as developed via direct attachment of NAD(+)-glycerol dehydrogenase coenzyme-apoenzyme complex onto s

145 iques confirmed the concatenation of FeS and glycerol-dehydrogenase/nicotinamide-adenine-dinucleotide

146 oposed ionic hydrogenation intermediates for glycerol deoxygenation.

147 allowing them to synthesize primarily G3P or glycerol depending on environmental conditions and/or me

148 s extensively near the silica surface, while glycerol depletes there.

149 vations indicated a promising enhancement in glycerol detection using the novel FeS-based glycerol se

150 ucose, fructose, ethanol, and acetic acid in glycerol detection was studied.

151 ing novel species with >2 rings), as well as glycerol dialkanol diethers, GDDs (including novel speci

152 ere able to identify complete series of core glycerol dialkyl glycerol tetraethers (GDGTs with 0 to 8

153 focused on a small class of fully saturated glycerol dibiphytanyl glycerol tetraether (GDGT) homolog

154 Archaeal membrane lipids known as glycerol dibiphytanyl glycerol tetraethers (GDGTs) are t

155 ly similar and consist of membrane-spanning, glycerol dibiphytanyl glycerol tetraethers with monoglyc

156 Repeated addition of 1,2-dioctanoyl-sn-glycerol (DiC8) resulted in sustained plasma membrane as

157 ic cements were developed using pyromellitic glycerol dimethacrylate (PMGDM) and ethoxylated bispheno

158 bifunctional enzyme capable of synthesizing glycerol directly from DHAP.

159 de has been shown to promote chlorination of glycerol during thermal processing.

160 To prevent glycerol efflux, Hog1 action impedes the function of the

161 3 per g oil) were esterified with dicaprylic glycerol employing Novozyme 435.

162 d but also the biosynthesis of prostaglandin glycerol esters (PG-Gs) from 2-arachidonoylglycerol.

163 ified other, previously unreported groups of glycerol ether lipid species.

164 construction are focused on a limited set of glycerol ether lipids, mainly due to the lack of more co

165 ee main phases: a batch phase, followed by a glycerol fed-batch phase that increases cell density, an

166 two-phase strategy lacking the intermediate glycerol fed-batch phase.

167 owth and toxicity, a finding consistent with glycerol fermentation and reuterin production.

168 robiome, produces short-chain fatty acids by glycerol fermentation that can induce adipogenesis.

169 bolome (e.g., lactic acid, dihydroxyacetone, glycerol, fumarate) gives rise to almost limitless bioma

170 ed with glycerol (and contained up to 189 mg glycerol g dry spores(-1) ).

171 new highly viscous binary solvents, DMSO-d6/glycerol (GL) and DMSO-d6/glycerol-d8 (GL-d8), is report

172 with low molecular weight plasticizers (e.g. glycerol, glucose and trehalose) at different storage ti

173 a microdialysis catheter, to monitor hourly glycerol, glutamate, glucose, lactate, and pyruvate.

174 olize the solvents propylene glycol (PG) and glycerol (GLY), thereby affording unique product profile

175 mt- and h-DHFR separately indicate that the glycerol (GOL) binding site is likely to be critical for

176 ion of the 10S region (fractions 3-5) of the glycerol gradient with anti-galectin-3 antibodies.

177 eases had altered editosome sedimentation on glycerol gradients and substantial defects in overall ed

178 actionation of HeLa cell nuclear extracts on glycerol gradients revealed an endogenous approximately

179 e of 21% in the placebo group and 52% in the glycerol group (P < .001).

180 the segments of the acyl chain close to the glycerol group.

181 hydrophobic-hydrophilic interface, below the glycerol group.

182 l properties of potato puree in the order of glycerol>alginate>lecithin>agar, while at 1% concentrati

183 le at 1% concentration, the order changed to glycerol>lecithin>alginate, whereas 1% agar behaved diff

184 ffer and in buffers with specific amounts of glycerol, guanidine hydrochloride (GdnHCl), and sodium c

185 Both PKC and high osmolarity glycerol (HOG) MAPK pathways were shown previously to be

186 n, plays a vital role in the high-osmolarity glycerol (HOG) mitogen-activated protein kinase pathway

187 vated protein kinases of the high-osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillu

188 Naringin-carrying CHC-beta-GP-glycerol hydrogel sites showed significantly reduced per

189 We discuss the likely role of glycerol in expanding the water-activity limit for micro

190 ence that the radiation-induced formation of glycerol in low-temperature interstellar model ices is f

191 t plastid pathway for the rapid synthesis of glycerol in response to hyperosmotic stress.

192 important in fully understanding the role of glycerol in rice blast disease.

193 e discuss the potential metabolic sources of glycerol in the rice blast fungus and how appressorium t

194 pathway activity and metabolism of [U-(13)C3]glycerol in the tricarboxylic acid cycle prior to glucon

195 lipid assembly by [(14)C]acetate and [(14)C]glycerol incorporation into glycerolipids.

196 reatment with fructose, glucose, sucrose, or glycerol increased innate immunity against Pst DC3000 in

197 d infection, ischemia-reperfusion-injury and glycerol-induced acute kidney-injury.

198 otheses, we used the preterm rabbit model of glycerol-induced IVH and analyzed autopsy samples from p

199 tested these hypotheses in a rabbit model of glycerol-induced IVH and evaluated the expression of AMP

200 bial sepsis whereas glomerular damage due to glycerol-induced kidney-injury had strongest impact on D

201 ation has been observed in rat kidneys after glycerol-induced rhabdomyolysis, but the role of macroph

202 y mass index, received either a 6 h lipid or glycerol infusion in the setting of a concurrent hyperin

203 e conversion of phosphatidylethanolamine and glycerol into PG and is catalyzed by ClsB, a phospholipa

204 Utilization of this crude glycerol is important in improving the viability of the

205 Glycerol is present at high concentrations (up to molar

206 sorium-forming fungi which shed light on how glycerol is synthesized and how appressorium turgor is r

207 attributed to a null allele of Gk5, encoding glycerol kinase 5 (GK5), a skin-specific kinase expresse

208 In addition, GPD2 and a gene encoding glycerol kinase were up-regulated in Chlamydomonas cells

209 xidized horse cytochrome c in 1-decanoyl-rac-glycerol/lauryldimethylamine-N-oxide/hexanol reverse mic

210 ulating total cholesterol, triglycerides, or glycerol levels.

211 thyldioctadecylammonium bromide/monomycoloyl glycerol liposomes with polyinosinic:polycytidylic acid

212 istoyl-2-hydroxy-sn-glycero-3-phospho-1'-rac-glycerol (LMPG, anionic) than in 1-lauroyl-2-hydroxy-sn-

213 By contrast, films with 30% glycerol lost the most moisture and their elongation was

214 origin of a growth defect at 37 degrees C in glycerol medium, which is related to misregulation of th

215 ent the relaxation dynamics of glass-forming glycerol mixed with 1.1 nm sized polyhedral oligomeric s

216 We validate our method with standard water-glycerol mixtures, and then we apply this microfluidic d

217 action of (13)C labeling in glycogen and the glycerol moiety exceeded the possible contribution from

218 Glycerol Monolaurate (GML) is a naturally occurring fatt

219 Poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacry

220 More specifically, poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacry

221 croscopy (TEM) are used to characterize poly(glycerol monomethacrylate)55-poly(2-hydroxypropyl methac

222 patible polymers poly(caprolactone) and poly(glycerol monostearate carbonate-co-caprolactone), and a

223 of poly(epsilon-caprolactone) (PCL) and poly(glycerol monostearate-co-epsilon-caprolactone) (PGC-C18)

224 ounced than a commercial emulsifier known as glycerol monostearate.

225 The betaine monohydrate-glycerol NADES in a molar ratio of 1:8 was determined to

226 Endogenous glucose production, lipolysis (glycerol, nonesterified fatty acid), and glycogenolysis

227 Lipolysis (glycerol, nonesterified fatty acids) and endogenous gluc

228 diacylglycerol analogue 1-oleoyl-2-acetyl-sn-glycerol (OAG) reversed the inhibitory effect of candesa

229 The effects of agar, alginate, lecithin and glycerol on the rheological properties of commercial pot

230 effect of two biological osmolytes, urea and glycerol, on the surface charge of silica, an archetype

231 ycerol 3-phosphate, indicating that either a glycerol or ethanolamine headgroup is the chemical deter

232 l communities, whereas treatment with either glycerol or L. reuteri alone was ineffective.

233 ch in 0 (water), 1, 3, 5, 10, 20 and 30% w/w glycerol or sorbitol solution for 24h and adjusting the

234 tivities in DESs with those observed in pure glycerol or THF suggests a kinetic anionic activation of

235 mography, lipolysis (RaGly) with [U-(2) H5 ]-glycerol, oral glucose absorption (RaO) with [U-(13) C6

236 as a mediator of the TOR and high osmolarity glycerol pathways, and regulates vegetative differentiat

237 genase-2 into PG-ethanolamide (PG-EA) and PG-glycerol (PG-G), respectively.

238 carboxymethyl-hexanoyl chitosan (CHC), beta-glycerol phosphate (beta-GP), and glycerol.

239 phosphatidic acid, phosphatidylglycerol, and glycerol phosphate as specific ligands for 4E10 in the c

240 Imidazole glycerol phosphate synthase (IGPS) is a V-type allosteri

241 d using a model TIM barrel protein, indole-3-glycerol phosphate synthase (IGPS).

242 face polysaccharide d-galactan and the oligo(glycerol phosphate) backbone of the partially glycosylat

243 lomics analysis independently confirmed that glycerol precursor delivery with L. reuteri elicited cha

244 on rich media supplemented with d-glucose or glycerol produce H2 and simultaneously consume some of i

245 The glycerol-producing PTS2 protein glycerol-3-phosphate deh

246 oxidized, glucose was mainly metabolized via glycerol production and release and lipid synthesis (par

247 density, sugar consumption, and ethanol and glycerol production.

248 se uptake decreased, and the free fatty acid/glycerol ratio increased during the antagonist alone and

249 The theoretical model was validated using glycerol reference solutions.

250 and although young men demonstrated net leg glycerol release during exercise, older men showed net g

251 Lipolysis showed an early decrease in glycerol release in TB d 4 (TB4) rats in relation to the

252 ate upregulated Ucp1 expression and enhanced glycerol release, a dual effect that was abolished by th

253 However, glucose utilization, glycerol release, triglyceride and glycogen contents, fr

254 1, the critical component of high osmolarity glycerol response pathway, was mis-localized in the Delt

255 ated to misregulation of the high-osmolarity glycerol response.

256 acute kidney injury) or by IM injections of glycerol (rhabdomyolysis-induced acute kidney injury).

257 Poly(glycerol sebacate)- poly(caprolactone) (PGS-PCL) blends

258 glycerol detection using the novel FeS-based glycerol sensing electrode compared to the conventional

259 SPC films plasticized with 40-50% glycerol showed a time-dependent increment of the elasti

260 l acyltransferase and mitochondrial acyl-CoA:glycerol-sn-3-phosphate acyltransferase and an increase

261 An increase in the concentration of glycerol solution from 1% to 5% resulted in a progressiv

262 roplets with highly viscous fluid, 75% (w/w) glycerol solution, were generated, half of which were se

263 r dynamics simulations of ubiquitin in water/glycerol solutions are used to test the suggestion by Ka

264 ture treated starches were more obvious when glycerol solutions were used instead of water.

265 When supplemented with glycerol, strains carrying the pocR gene locus were pote

266 [(14)C]glycerol studies demonstrated PC-derived DAG is the majo

267 eS-based bioanodes are capable of biosensing glycerol successfully and may be applicable for other en

268 umulation under nitrogen deprivation and for glycerol synthesis under high salinity.

269 ed by tangential flow filtration (TFF-DB) or glycerol tartrate gradient sedimentation (GT-DB) constit

270 ass of fully saturated glycerol dibiphytanyl glycerol tetraether (GDGT) homologues identified decades

271 recently identified butanetriol dibiphytanyl glycerol tetraethers (BDGT), which increased relatively

272 ify complete series of core glycerol dialkyl glycerol tetraethers (GDGTs with 0 to 8 alicyclic rings)

273 mbrane lipids known as glycerol dibiphytanyl glycerol tetraethers (GDGTs) are the basis of the TEX86

274 of membrane-spanning, glycerol dibiphytanyl glycerol tetraethers with monoglycosyl, diglycosyl, phos

275 in the exchange of amino acids, lipids, and glycerol than other eukaryotes.

276 When the growth medium was supplemented with glycerol, the expression of E. coli ClsB significantly i

277 sion (54% at 40 degrees C with 1:3M ratio of glycerol to CLA).

278 Human-derived L. reuteri bacteria convert glycerol to the broad-spectrum antimicrobial compound re

279 um generates enormous turgor by accumulating glycerol to very high concentrations within the cell.

280 hotocatalytic treatment of other wastewater (glycerol) to cogenerate H2 and clean water under both UV

281 ed, and their cutin contained a higher molar glycerol-to-dihydroxyhexadecanoic acid ratio.

282 ctural checkpoints by which HbXIP2;1 ensures glycerol transfer across the membrane.

283 2D, we also estimated lipolysis (from [(2)H5]glycerol turnover rate and circulating free fatty acids,

284 ersion with duodenal switch (DS), whole-body glycerol turnover was normalized and associated with low

285 se in AQP3 levels resulted in enhanced [(3)H]glycerol uptake in normal but not in AQP3-knockout kerat

286 elease during exercise, older men showed net glycerol uptake.

287 the effects of adjunctive dexamethasone and glycerol using clinical trial data from Malawi.

288 cylindracea followed by esterification with glycerol using Lipozyme RM1M.

289 cellulase expression, isobutanol production, glycerol utilization and acetic acid tolerance, and may

290 1,2-dipalmitoyl-sn-glycerol-3-phospho-(1'rac-glycerol)) via disulfide bond formation.

291 +/- 0.27% v/v) in combination with 1.49 g/L glycerol was achieved.

292 rated when the codelivery of L. reuteri with glycerol was effective against C. difficile colonization

293 method by complex formation of amylose with glycerol was employed for reducing the amylose content o

294 ication of both sn-1,3 and sn-2 positions of glycerol was impacted, and their cutin contained a highe

295 Using a solution of CsF in glycerol, we determine that 4 +/- 2 x 10(12 19)F spins i

296 Harmful effects of adjunctive glycerol were observed in groups with relatively low pre

297 comprises 65% SOS (1, 3-distearoyl-2-oleoyl-glycerol) which indicates potential to become a Cocoa Bu

298 -arachidonoylethanolamine and 2-arachidonoyl-glycerol, which derive from arachidonic acid, is influen

299 transform the fat into free fatty acids and glycerol, which elute at the end of the chromatogram aft

300 e-cigarette e-liquids (propylene glycol and glycerol), while the role of flavoring compounds has bee