ライフサイエンスコーパス: glycerol

1 n sources (glucose, N-acetylglucosamine, and glycerol).

2 ly of aquaporins that conduct both water and glycerol.

3 le to replicate on propionamide, glucose, or glycerol.

4 3 in a lactose-based diluent, with 5% EY and glycerol.

5 dielectric constant upon addition of urea or glycerol.

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

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

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

9 tasis by enabling the transport of water and glycerol.

10 on numbers of glucose, fructose, maltose and glycerol.

11 lactose, cellobiose, lactose, and galactosyl-glycerol.

12 LSPR biosensor was verified by using aqueous glycerol (0-100 wt%) which showed that it is sufficientl

13 tivated protein kinase Hog1 (high-osmolarity glycerol 1), which regulates gene expression, metabolism

14 luding beta-d-galactofuranose (beta-Galf), d-glycerol 1-phosphate, d-glycero-d-talo-oct-2-ulosonic ac

15 ased-DES consists of betaine hydrochloride - glycerol (1:3) as extraction solvent and acetone as apro

16 ne glycol, 1,2-propanediol, 1,3-propanediol, glycerol, 1,4-butanediol, xylitol, and sorbitol), furano

17 -glycerol-3-phosphate, and LTA is made of sn-glycerol-1-phosphate.

18 form of an octahedral As(V) compound [As(V)-glycerol, 11876 eV].

19 ntrations of egg yolk (EY; 5, 10 or 15%) and glycerol (2, 5 or 10%), diluent types (SHOTOR, lactose,

20 diated by the endocannabinoid 2-arachidonoyl glycerol (2-AG) acting on a TRPV (transient receptor pot

21 levels of the endocannabinoid 2-arachidonoyl glycerol (2-AG) are protected from enteric infection by

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

23 substrate, the endocannabinoid 2-arachidonyl glycerol (2-AG), and elucidated a hitherto unknown canna

24 ivates the endocannabinoid 2-arachidonoyl-sn-glycerol (2-AG), exert anxiolytic-like effects in rodent

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

26 me for the endocannabinoid 2-arachidonoyl-sn-glycerol (2-AG).

27 long-chain fatty acids (LCFAs) and 2-oleoyl-glycerol (2-OG), but not medium-chain fatty acids (MCFAs

28 Here we show that exposing glycerol-2-phosphate to acylating agents leads to the fo

29 o from [1,2-(13)C(2)]glucose; by lowering of glycerol 3-phosphate an allosteric inhibitor of phosphof

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

31 and by overexpression of mGPDH, which lowers glycerol 3-phosphate and G6P and also mimics the G6pc re

32 rial lipopolysaccharide (LPS), mitochondrial glycerol 3-phosphate dehydrogenase (GPD2) regulates gluc

33 red for triacylglycerol (TAG) synthesis from glycerol 3-phosphate in most mammalian tissues.

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

35 he intermediates of the malate-aspartate and glycerol 3-phosphate shuttles.

36 FBP1) in association with a decrease in cell glycerol 3-phosphate, an inhibitor of PFK1, rather than

37 red for triacylglycerol (TAG) synthesis from glycerol 3-phosphate, lipin 1 has been the focus of most

38 e bisphosphatase-1, including AMP, P(i), and glycerol 3-phosphate.

39 e monophosphate, pyruvate, lactate, alanine, glycerol-3 phosphate, and isocitrate were significantly

40 going cardiac catheterization and identified glycerol-3-phosphate (G-3-P) as the most significant cor

41 Renal vein glycerol-3-phosphate (G-3-P) had the strongest correlati

42 Glycerol-3-phosphate (G3P) is a well-known mobile regula

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

44 lity to produce lactate by generating excess glycerol-3-phosphate (G3P), the production of which also

45 covery that the Escherichia coli periplasmic glycerol-3-phosphate (G3P)-binding protein UgpB can serv

46 G biosynthesis, including those that encoded glycerol-3-phosphate acyltransferase (GPAT), acyl-CoA:di

47 Two genes encoding glycerol-3-phosphate acyltransferase (GPAT), the first c

48 t a dual functionality of pathogen-inducible GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE 6 (GPAT6) in contro

49 opersicum 'Micro-Tom'; the wild type and the GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE [GPAT6] and CUTIN S

50 istent with this, inhibition of ER-localized glycerol-3-phosphate acyltransferase activity protected

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

52 c pathway, including fatty acid synthase and glycerol-3-phosphate acyltransferase.

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

54 y the transfer of fatty acids to glycerol by glycerol-3-phosphate acyltransferases, which facilitate

55 of fructose-1,6-bisphosphate, production of glycerol-3-phosphate and competition that rods exert on

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

57 is shifted towards the pentose phosphate and glycerol-3-phosphate dehydrogenase pathways.

58 e (MAs(III)), which is a potent inhibitor of glycerol-3-phosphate dehydrogenase.

59 are enantiomeric polymers: WTA is made of sn-glycerol-3-phosphate, and LTA is made of sn-glycerol-1-p

60 identified, including glycerophosphocholine, glycerol-3-phosphate, L-carnitine, L-aspartate, glutathi

61 phatidylglycerol (DOPG), and 1,2-dioleoyl-sn-glycerol-3-phosphatidylcholine (DOPC) structurally stabi

62 We show here that the exolytic sn-glycerol-3-phosphodiesterase GlpQ can discriminate betwe

63 pecialised for de novo synthesis of TAG from glycerol-3-posphate only.

64 filtered air, propylene glycol and vegetable glycerol (50:50 PG/VG vehicle), or to PG/VG with 16 mg/m

65 new design strategies, e.g. the formation of glycerol, a novel product for C. ljungdahlii, thus broad

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

67 found that As(III) treatment did not induce glycerol accumulation and, in fact, blocked the accumula

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

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

70 The poly(carbonate) analogues degrade into glycerol, alcohol, and CO(2) in a time- and pH-dependent

71 is set to the influx obtained when grown on glycerol alone.

72 ng a liquid composed of propylene glycol and glycerol, also referred to as vegetable glycerin and col

73 in aqueous solution containing 20% (vol/vol) glycerol and 75 mM sodium phosphate.

74 om aerobic fermentation to respiration, with glycerol and acetate production.

75 rly-life stress (1) decreased 2-arachidonoyl glycerol and arachidonic acid in the cerebellar interpos

76 degradation, hydrolyzing monoglycerides into glycerol and fatty acids (FAs) and converting 2-arachido

77 with PTH, exhibited increased production of glycerol and fatty acids.

78 ogenic role of adipose tissue IR to increase glycerol and FFA availability to the liver in both recep

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

80 es: growth enrichment on alternative sugars, glycerol and galactose, and chemical overproduction of b

81 sm of mSOD1 in the presence of the viscogens glycerol and glucose.

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

83 quaporin 3 (AQP3) is a transporter of water, glycerol and hydrogen peroxide (H(2)O(2)) that is expres

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

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

86 Impact of glycerol and sorbitol on assembly of iron-bound ovotrans

87 Influence of glycerol and sorbitol on morphology of OVT nanofibrils w

88 way, leading to the abnormal accumulation of glycerol and subsequent cell lysis.

89 components of wine, alcohol, reduced sugar, glycerol and total acidity, in its viscosity.

90 of AQP1, AQP4 and AQP3 differentially affect glycerol and urea permeability in an AQP-specific manner

91 lp2 and Eglp4 show very high permeability to glycerol and urea.

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

93 (increased lactate, LPR; decreased glucose, glycerol) and cord inflammation (increased IL1beta, IL8,

94 solutions of identical RI containing small (glycerol) and large (bovine serum albumin; BSA) analyte

95 e/pyruvate ratio (LPR), glutamate; decreased glycerol) and markedly reduced cord inflammation (reduce

96 ines) to nonpolar (e.g., diacyl- and triacyl-glycerols), and they span 11 common metabolite classes.

97 Citric acid, glycerol, and d-sorbitol are used as important food addi

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

99 ponse to CL316,243, circulating fatty acids, glycerol, and the phosphorylation of hormone-sensitive l

100 ethanolamide (anandamide) and 2-arachidonoyl glycerol, and the plant-derived Delta(9)-tetrahydrocanna

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

102 sonication) and transition-metal-free, using glycerol as a green solvent.

103 of phospholipids containing ethanolamine, or glycerol as phospholipid head group and in the number of

104 of nearly 0.6 g/L total monoterpenoids from glycerol as the sole carbon source.

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

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

107 due to the attachment of caffeic acid to the glycerol backbone of PC, which brings the antioxidant in

108 o define fatty acyl regiochemistry along the glycerol backbone or carbon-carbon double bond position(

109 at the middle (sn-2 or beta) position on the glycerol backbone, and there is evidence that triacylgly

110 ies having different sn-1/2 positions at the glycerol backbone, length of the hydrocarbon chain, and

111 hich contain a FAHFA group esterified to the glycerol backbone.

112 placing the sphingosine with a palmitoylated glycerol backbone.

113 tuents at the sn-1 and sn-2 positions of the glycerol backbone.

114 We used a panel of dendritic oligo-glycerol-based surfactants to demonstrate that a high de

115 ); and a redistribution of label from (14) C-glycerol between phosphoglycerides.

116 An improved glycerol biosensor was developed via direct attachment o

117 TAG estolides contain two non-hydroxylated, glycerol-bound fatty acids (FAs) and one dihydroxylated

118 are formed by the transfer of fatty acids to glycerol by glycerol-3-phosphate acyltransferases, which

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

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

121 We also found that glycerol can induce a rate-limiting enzyme of GNG, gluco

122 self-assembly of X-shaped polyphiles, where glycerol-capped terphenyl rods lie on the gyroid surface

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

124 , and chitosan-WPI conjugate were mixed with glycerol, casted for films at 60 +/- 2 degrees C and ass

125 buticaba peel (FJP) and the concentration of glycerol (CG) on the physicochemical, barrier, mechanica

126 cerol through closure of the plasma-membrane glycerol channel Fps1.

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

128 The gene hub Aquaporin-7 (Aqp7), a water and glycerol channel, was identified as a novel regulator of

129 ter + d-sorbitol + citric acid) and (water + glycerol + citric acid) were measured in mass fractions

130 that the lymphatics are a potential route of glycerol clearance.

131 gery and at a depth of approximately 2 mm in glycerol-cleared brain tissues.

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

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

134 al properties, the interactions of different glycerol concentrations and Ca(2+) ions in both steps of

135 Moreover, the addition of increasing glycerol concentrations to the protein solution induced

136 d metabolic changes required for acetate and glycerol cross feeding affect dozens of chemical reactio

137 etabolic modeling to ask whether acetate and glycerol cross-feeding are especially likely to evolve,

138 riptional repressor of factors that catalyze glycerol degradation.

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

140 lariciresinol diglucoside and 2-arachidonoyl glycerol, demonstrated protection by reducing inflammato

141 WT A2ML1 reacted with the hydroxyl substrate glycerol, demonstrating that His-1084 increases the hydr

142 oposed ionic hydrogenation intermediates for glycerol deoxygenation.

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

144 with excellent signal-to-noise ratio for the glycerol detection.

145 ed on distributions of soil fossil bacterial glycerol dialkyl glycerol tetraethers preserved in well-

146 ing bacterial cell membrane lipids (branched glycerol dialkyl glycerol tetraethers) and an aquatic pr

147 r of cyclopentyl and cyclohexyl rings in the glycerol dibiphytanyl glycerol tetraether (GDGT) Archaea

148 of cyclic moieties within the cores of their glycerol dibiphytanyl glycerol tetraether (GDGT) lipids.

149 Glycerol dibiphytanyl glycerol tetraethers (GDGTs) are d

150 ethane dimethacrylate (UDMA) or pyromellitic glycerol dimethacrylate.

151 bifunctional enzyme capable of synthesizing glycerol directly from DHAP.

152 the effect of an exogenous source of carbon (glycerol), energy (ATP), and an inhibitor of energy meta

153 reus secretes at least two lipases, Sal1 and glycerol ester hydrolase (Geh), with specificities for s

154 r leucocidin A (lukA, IC(50) 0.4-25 muM) and glycerol ester hydrolase or lipase (gehB, IC(50) 1.5-25

155 n, stigmasterol, and linoleic and oleic acid glycerol esters, together with 4-chlorobutyl oleate, ole

156 ines" (BW) had significantly higher alcohol, glycerol, extract, and polyphenol concentration.

157 Here, both aqueous and glycerol FeCl(3) solution surfaces are investigated with

158 e surface and in the near surface regions of glycerol FeCl(3) solutions, where glycerol is used as a

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

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

161 o-VD mice exhibited more rapid and increased glycerol flux from adipose tissue, suggesting that the l

162 s communis), followed by isotopic tracing of glycerol flux through the lipid metabolic network in dev

163 re-treated peels at 218 kJ/kg and in aqueous glycerol from pre-treated peels at 36 kJ/kg.

164 aprine muscles using sodium dodecyl sulphate glycerol gel electrophoresis (SDS-GGE).

165 diol, BuO(2), 3; 1,2-pentanediol, PeO(2), 4; glycerol, GlO(2), 5) and dabco is 1,4-diazo[2.2.2.]bicyc

166 terium tuberculosis, mycolic acids and their glycerol, glucose, and trehalose esters ("cord factor")

167 th various stabilizers (cholesterol (CHO) or glycerol (GLY)).

168 lene glycol (PG), dimethyl sulfoxide (DMSO), glycerol (GLY), and methanol (METH; listed in order from

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

170 nment, but only cross-feeding of acetate and glycerol has been experimentally observed.

171 The addition of glycerol has reduced the energy of the pre-treatment by

172 stidine kinase (HHK) and the high osmolarity glycerol (HOG) pathway.

173 The yeast high-osmolarity glycerol (HOG) stress-activated protein kinase Hog1 is a

174 in males only; (2) decreased 2-arachidonoyl glycerol in females only in cerebellar Crus I; and (3) i

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

176 g a new stress caused by the accumulation of glycerol in the absence of hyperosmotic stress condition

177 -palmitoyl-2-oleoyl-sn-glycero-3-phospho-rac-glycerol in the outer leaflet only was quantified by zet

178 on and, in fact, blocked the accumulation of glycerol induced by constitutive Hog1 activity.

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

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

181 of AKI following either I/R or intramuscular glycerol injection.

182 Lastly, we suggest that glycerol is a better substrate than pyruvate to test in

183 indicated that the abnormal accumulation of glycerol is not the primary cause of fludioxonil toxicit

184 Glycerol is present at high concentrations (up to molar

185 vate/lactate, and glutamine are all present, glycerol is responsible for over 75% of all glucose carb

186 After three-hour electrolysis, glycerol is selectively oxidized to glyceraldehyde with

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

188 In conclusion, glycerol is the major carbon source for GNG in vitro and

189 regions of glycerol FeCl(3) solutions, where glycerol is used as a high vacuum compatible proxy for w

190 lyxose, lyxitol (0.5 mo); mannose, ribitol, glycerol, isothreonic acid, lyxitol (2 mo); lyxitol and

191 Simultaneous inhibition of the trypanosomal glycerol kinase (TGK) and trypanosomal alternative oxida

192 l coumarins with dual inhibition of both the glycerol kinase and alternative oxidase of Trypanosoma b

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

194 lipidome, demonstrating molecular changes in glycerol lipid profiles.

195 itoyl-2-hydroxy-sn-glycero-3-phospho-(1'-rac-glycerol) (LPPG) micelles.

196 ne morphology, vacuole fusion, and growth on glycerol medium).

197 mitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) membranes compared to OG micelles.

198 ylglycerols, with 1-(cis-9-octadecanoyl)-rac-glycerol (MO) being the most widely used lipid.

199 dentified an amide-linked 1,3-di-O-hexadecyl-glycerol moiety as the optimal lipid structure.

200 face (SURF-TG) are ordered like PLs with the glycerol moiety exposed to water, creating a significant

201 We investigated glycerol monolaurate (GML) in human milk versus bovine m

202 cid profile of broilers fed diets containing glycerol monolaurate (GML) in place of antimicrobials.

203 onooxy)ethyl methacrylate (P) with non-ionic glycerol monomethacrylate (G).

204 tension of a relatively short non-ionic poly(glycerol monomethacrylate) (PGMA) precursor block leads

205 d by a non-ionic water-soluble polymer, poly(glycerol monomethacrylate)(70) (G(70) ), which is chemic

206 Diblock designs of p(glycerol monomethacrylate)-b-p(Alkyl-TAF-methacrylate) a

207 hacrylate)-b-p(Alkyl-TAF-methacrylate) and p(glycerol monomethacrylate)-b-p(Benzyl-TAF-methacrylate)

208 synthesis of a series of silica-loaded poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacry

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

210 ent ratios of medium-chain-triglycerides and glycerol monostearate (lipid phase) were tested.

211 ction showed that the amount of solid lipid (glycerol monostearate) influences the melting, crystalli

212 Glycerol monosterate (GMS) and stearic acid (SA) share a

213 tion of riboflavin, L-asparagine, aspartate, glycerol, nicotinamide, and 3-hydroxy-3-methyglutarate i

214 g channel activation by 1-oleoyl-1-acetyl-sn-glycerol (OAG), the membrane-permeable analog of diacylg

215 f the e-liquid solvents propylene glycol and glycerol often generates multifunctional carbonyls that

216 deletion of cydAB, the detrimental effect of glycerol on the potency of Q203 was abrogated.

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

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

219 xtraction was performed in 20% (w/v) aqueous glycerol or in DES (lactic acid: glucose) instead of wat

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

221 ned OVT nanofibrils, and the presence of 60% glycerol or sorbitol could increase thickness of OVT nan

222 scence result indicated that the presence of glycerol or sorbitol could reduce the rate of OVT fibril

223 The presence of glycerol or sorbitol shortened OVT nanofibrils, and the

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

225 lesterol, and polyethylene glycol distearoyl glycerol (PEG-DSG).

226 ed that DFP00173 and Z433927330 inhibit AQP3 glycerol permeability in human erythrocytes.

227 r cross-sectional area predicts urea but not glycerol permeability.

228 ico comparisons of water-specific as well as glycerol-permeable human AQPs.

229 ), phosphatidylserine (PS), and phosphatidyl-glycerol (PG) can be unambiguously assigned based on 2D

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

231 2-AG) to produce prostaglandin E(2) (PGE(2))-glycerol (PGE(2)-G); PGE(2)-G is known to produce hypera

232 ous infusions of stable isotopes of glucose, glycerol, phenylalanine, tyrosine, and urea before and d

233 ce that monoscavenger therapy with sodium or glycerol phenylbutyrate was superior to sodium benzoate

234 Low protein diet and sodium or glycerol phenylbutyrate, two pillars of recommended long

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

236 anced synthesis of glycerolipids through the glycerol phosphate pathway, enhanced axon regeneration a

237 Therefore, GPD2 and the glycerol phosphate shuttle integrate the extent of micro

238 GPD2, a component of the glycerol phosphate shuttle, boosts glucose oxidation to

239 he reaction catalyzed by the enzyme indole-3-glycerol phosphate synthase (IGPS) starts with a condens

240 iate in the Sulfolobus solfataricus indole-3-glycerol phosphate synthase TIM barrel that appears with

241 were also up-regulated, as well as indole-3-glycerol phosphate synthase, an enzyme involved in the b

242 mitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (POPG) mediated by singlet oxygen at the air-w

243 In addition, several compatible solutes (glycerol, Pro, and Suc) accumulated to high levels in hi

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

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

246 We demonstrated that As(III) blocks glycerol production indirectly after its metabolic activ

247 In addition, when glycerol, pyruvate/lactate, and glutamine are all presen

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

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

252 tituted WTA, which lacks substituents at the glycerol residues, by sequentially removing glycerolphos

253 ellobiose, with either lactose or galactosyl-glycerol, revealed initially logarithmic growth on cello

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

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

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

257 track single Atto 647 N fluorophores in 90% glycerol solution with an average duration of ~16 s at c

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

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

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

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

262 pendent studies of food-spoilage fungi under glycerol stress (Aspergillus aculeatinus and A. scleroti

263 The negative effect of glycerol supplementation on Q203 potency correlated with

264 03 and related derivatives was alleviated by glycerol supplementation.

265 ermination rate for X. bisporus (FRR3443) in glycerol-supplemented media (r(2) = 0.012), nor to expon

266 consistent with the observed behavior at the glycerol surface.

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

268 This study explores the effect of ethanol, glycerol, tartaric acid and glucose/fructose on the refr

269 In Syrah wines, glycerol, tartaric acid, succinic acid and 2,3-butanedio

270 yclohexyl rings in the glycerol dibiphytanyl glycerol tetraether (GDGT) Archaeal lipids has been link

271 hin the cores of their glycerol dibiphytanyl glycerol tetraether (GDGT) lipids.

272 s between liposome made of glycerolmonoalkyl glycerol tetraether lipids with phosphatidic acid headgr

273 Glycerol dibiphytanyl glycerol tetraethers (GDGTs) are distinctive archaeal me

274 ns of soil fossil bacterial glycerol dialkyl glycerol tetraethers preserved in well-dated loess-paleo

275 l membrane lipids (branched glycerol dialkyl glycerol tetraethers) and an aquatic productivity indica

276 Hog1 promotes retention of glycerol through closure of the plasma-membrane glycerol

277 ic needs, adipocytes release fatty acids and glycerol through the action of neutral lipases.

278 te that P. syringae Lz4W can also synthesize glycerol to maintain flexibility of macromolecular syste

279 e show that mouse primary hepatocytes prefer glycerol to pyruvate/lactate in glucose production assay

280 ss, inducing the production and retention of glycerol to restore osmotic balance.

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

282 that inhibited AQP3-facilitated H(2)O(2) and glycerol transport, and prevented liver injury in experi

283 These lipid droplets stained positive for glycerol transporter aquaporin 7 and phosphorylated peri

284 The effects of glycerol/triacylglycerol molar ratio, enzyme concentrati

285 ycerol yields and oxidative stability were a glycerol/triacylglycerol ratio of 3/1, 9.0% (w/w) Lipase

286 Lipolysis (glycerol turnover), hepatic glucose production (HGP), gl

287 e change was relatively insensitive to added glycerol up to 60%, suggesting that solution viscosity i

288 s the upper-glycolytic flux and ensures that glycerol uptake defers to other glycolytic substrates bu

289 A detailed study of glycerol uptake finds that it is fully suppressed if the

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

291 Below this threshold, limited glycerol uptake is 'supplemented' such that the total ca

292 cylindracea followed by esterification with glycerol using Lipozyme RM1M.

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

294 ssociated with vehicle (polypropylene glycol/glycerol) vapor, suggesting low positive reinforcing eff

295 T-1 can also utilize lactose and galactosyl-glycerol via the cellobiose-PTS system together with a b

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

297 Deep eutectic solvents (DES) and aqueous glycerol were proposed as green alternatives to conventi

298 using over-accumulation of methylglyoxal and glycerol, which in turn impacts NO detoxification.

299 rast, however, neutral osmolytes sucrose and glycerol, which significantly stabilize proteins in bulk

300 ractive index, followed by tartaric acid and glycerol while ethanol had the smallest effect.