ライフサイエンスコーパス: sorbitol

1 r blackberry samples contained no detectable sorbitol).

2 tem that metabolizes the hexitol D-glucitol (sorbitol).

3 were negative for L-rhamnose and D-glucitol (sorbitol).

4 ose and trehalose) and polyols (glycerol and sorbitol).

5 sure to high concentrations of congo red and Sorbitol.

6 ng species such as hemoglobin, fructose, and sorbitol.

7 V40 in the presence of sucrose, but not with sorbitol.

8 d that the product of the LXR4 reaction is D-sorbitol.

9 zes the conversion of L-xylo-3-hexulose to D-sorbitol.

10 include galactitol, L-xylo-3-hexulose, and d-sorbitol.

11 PVP but the same sense in the presence of D-sorbitol.

12 in urea, and this effect was counteracted by sorbitol.

13 of SORD protein and increased intracellular sorbitol.

14 yeasts to overproduce xylitol, mannitol, and sorbitol.

15 interleukin-1beta, but not by ansiomycin or sorbitol.

16 is decreased by increasing concentrations of sorbitol.

17 ts), including sodium chloride, sucrose, and sorbitol.

18 ictive temperature by the osmotic stabilizer sorbitol.

19 om cheap and abundant bio-polyols, including sorbitol.

20 ed a major contribution to JNK activation by sorbitol.

21 th induced by environmental staurosporine or sorbitol.

22 athways in addition to converting glucose to sorbitol.

23 hydrogen from ethylene glycol, glycerol, and sorbitol.

24 ncreased bacterial growth in the presence of sorbitol.

25 spray aerosol composed of NaCl, CaCl(2), and sorbitol.

26 terized by accumulation of the sugar alcohol sorbitol.

27 rogenase, the key enzyme for biosynthesis of sorbitol.

28 esponse than infusion of hypertonic mannitol/sorbitol.

29 od pressure (ABP) than equi-osmotic mannitol/sorbitol.

30 uronal discharge frequency than equi-osmotic sorbitol.

31 ge and ABP than icv infusion of equi-osmotic sorbitol.

32 sorbitol, 1,3:2,4-bis-O-(p-methylbenzylidene)sorbitol, 1,3:2,4-bis-O-(3,4-dimethylbenzylidene)sorbito

33 larifying agents (1,3:2,4-bis-O-(benzylidene)sorbitol, 1,3:2,4-bis-O-(p-methylbenzylidene)sorbitol, 1

34 pple leaf tissue exposed to exogenous [(14)C]sorbitol, [(14)C]Suc, or (14)CO(2) did not accumulate ra

35 Finally, 2-deoxy-2-[F-18]fluoro-d-sorbitol ((18)F-FDS) can be easily synthesized from (18)

36 (SNA), adrenal SNA and ABP than equi-osmotic sorbitol (2.0 osmol l(-1) ).

37 oreover, the API was able to form films when sorbitol (30% (w/w)) was used as plasticizer and to form

38 1 from osmotically stressed HEK cells (0.2 M sorbitol; 30 min) revealed a persistent, 3.9 +/- 0.4-fol

39 ple plants were silenced or up-regulated for sorbitol-6-phosphate dehydrogenase by using the CaMV35S

40 Transgenic plants with suppressed sorbitol-6-phosphate dehydrogenase compensated by accumu

41 fructose and formate, and overexpression of sorbitol-6-phosphate dehydrogenase in lactate dehydrogen

42 PpeS6PDH encodes a NADPH-dependent sorbitol-6-phosphate dehydrogenase, the key enzyme for b

43 This work focuses on the role of sorbitol, a sugar alcohol, in flower development and pol

44 Consistently, sorbitol accumulates in dormant buds showing higher PpeS

45 lective uptake in S. aureus and E. coli; and sorbitol, accumulating only in E. coli None accumulated

46 mice also exhibited an impressive defect in sorbitol accumulation (88 +/- 9% less than wild type, p

47 , transcriptional regulation of PpeS6PDH and sorbitol accumulation in flower buds of peach.

48 to NO donors also inhibited AR and prevented sorbitol accumulation in rat aortic vascular smooth musc

49 schemia-induced AR activation and myocardial sorbitol accumulation in rat hearts subjected to global

50 o-L-arginine methyl ester (L-NAME) increased sorbitol accumulation in the aorta of nondiabetic and di

51 development, but especially when growth and sorbitol accumulation rates are highest.

52 When incubated ex vivo with high glucose, sorbitol accumulation was increased by L-NAME and preven

53 r of NO) or nitroglycerine patches prevented sorbitol accumulation.

54 h there was a corresponding decrease in lens sorbitol accumulation.

55 hypothesis that these sugars (trehalose and sorbitol) act primarily as stress protectants for protei

56 d replication, was expelled within 30 min of sorbitol addition.

57 oic acid (PFOA) surfactant addition, and (3) sorbitol addition.

58 Sorbitol also rescues endocytic ingression defects of ce

59 Exposure to sorbitol also resulted in cleavage of the nuclear repair

60 Although sorbitol alters nucleotide levels, we show that invertin

61 vising against concomitant administration of sorbitol, an osmotic cathartic used to prevent SPS-induc

62 1 m sorbitol and 0.2 m NaCl, which induce the HOG pathway, r

63 The steady-state responses of JNK to sorbitol and anisomycin were found to be highly ultrasen

64 Sorbitol and citric acid may be partially responsible fo

65 cterized by high levels of aldose reductase, sorbitol and endogenous fructose.

66 coupled with the strain's ability to ferment sorbitol and express beta-glucuronidase have complicated

67 when compared with rats, did not accumulate sorbitol and fructose in the retina and were protected f

68 Glucose, sorbitol and fructose were markedly elevated in all AD b

69 ted cataract development, normalized retinal sorbitol and fructose, and protected the retina from abn

70 n +/- SD) showed increased retinal levels of sorbitol and fructose, attenuation of GFAP immunostainin

71 described (IC50, 1 nM; ED90 vs sciatic nerve sorbitol and fructose, respectively, 0.8 and 4.0 mg/kg).

72 High sorbitol and glycerol levels do not increase ROS or carb

73 ment failed to stimulate the accumulation of sorbitol and glycerol.

74 stream kinases were involved in responses to sorbitol and lipopolysaccharide.

75 tol have a tendency toward self-association; sorbitol and most other nonrenal osmolytes have a relati

76 components, decreased activation of OSR1 by sorbitol and reduced activity of the OSR1 substrate, the

77 Concomitant treatment with sorbitol and SB202190, a selective p38 inhibitor, preven

78 influenced the pH values and the contents of sorbitol and shikimic acid in the ice juices.

79 Sorbitol and sucrose are major products of photosynthesi

80 Sorbitol and sucrose significantly raised levels of bis-

81 the molecule, whereas for larger osmolytes, sorbitol and sucrose, Deltax(u) remains the same as that

82 accumulation of two cryoprotective polyols, sorbitol and threitol, is integral to the extraordinary

83 activated only by osmotic stresses, notably sorbitol and to a lesser extent NaCl.

84 tions were modulated using ligands (glucose, sorbitol and trehalose) and a thickener (maltodextrin).

85 We found that protecting osmolytes such as sorbitol and trimethylamine N-oxide can counteract the d

86 ind that two unrelated protective osmolytes, sorbitol and trimethylamine-n-oxide, function by margina

87 ation, and consequent elevation in fructose, sorbitol and/or uric acid, are important factors contrib

88 ormulations showed a variety of crystalline (sorbitol) and amorphous (sucrose, trehalose) structures,

89 cumulated radiolabel from [(14)C]Suc, [(14)C]sorbitol, and (14)CO(2).

90 ydration increased inner medullary inositol, sorbitol, and betaine concentrations in vivo by 85 +/- 1

91 umulation of the organic osmolytes inositol, sorbitol, and betaine in cultured mouse medullary inters

92 - 9, 57 +/- 12, and 96 +/- 10% for inositol, sorbitol, and betaine respectively, p < 0.05).

93 /- 5, 66 +/- 15, and 81 +/- 9% for inositol, sorbitol, and betaine, respectively, p < 0.05) by pretre

94 However, addition of quercetin, sorbitol, and chlorogenic acid to aronia anthocyanins in

95 luxes for sodium chloride, ammonium sulfate, sorbitol, and galactose are used to calculate droplet wa

96 of aqueous solutions of Erythritol, Xylitol, Sorbitol, and Maltitol were measured at 15 degrees C, 25

97 s can bind OSR1, block activation of OSR1 by sorbitol, and prevent the OSR1-induced enhancement of io

98 ytes glycerophosphorylcholine, myo-inositol, sorbitol, and taurine.

99 were osmotically challenged with 100-200 mm sorbitol, and the intranuclear distribution of nucleolin

100 cally sucrose, but not glucose, mannitol, or sorbitol, antiAtGLR1.1 seeds did not germinate, but germ

101 Exogenous sorbitol application during flower development partially

102 athways including dyslipidemia, hypoxia, and sorbitol are reviewed in this manuscript.

103 ysis measurements, confirming that Cl(-) and sorbitol are transported by a single-channel type.

104 Citric acid, glycerol, and d-sorbitol are used as important food additives.

105 itol, 1,3:2,4-bis-O-(3,4-dimethylbenzylidene)sorbitol) are presented for the native and trimethylsily

106 ression of SDH, allowing for accumulation of sorbitol as a compatible organic osmolyte.

107 In this study, we establish sorbitol as a novel physiological stressor that directs

108 s of ECO/pDNA nanoparticles using sucrose or sorbitol as a stablilizer to develop consistent and stab

109 dy, the solubility, density and viscosity of sorbitol as a sugar alcohol in the ([mmim](MeO)(2)PO(2))

110 ssava starch, casein, and gelatin, and using sorbitol as the plasticizer.

111 reas equivalent concentrations of xylitol or sorbitol, as osmotic controls, had no effect.

112 mixture of ethylglycerol, gulonolactone, and sorbitol (at 10, 1, and 1 mg/mL, respectively, in the in

113 e electron ionization mass spectra for three sorbitol-based nuclear clarifying agents (1,3:2,4-bis-O-

114 here is the mass spectral identification of sorbitol-based nuclear clarifying agents (NCAs) and the

115 Dyes that are soluble in molten sorbitol become oriented as the crystallization front pa

116 ein hydrolysate (FPH-2, FPH-8) or 8% sucrose-sorbitol blend (SuSo) were compared to control NAM befor

117 ter cryoprotection compared to an 8% sucrose-sorbitol blend, and a stabilizing effect of FPH on myosi

118 Millimolar added K(+), but not Na(+) or sorbitol, blocks the initiation or continuation of mutan

119 in organ culture increased the production of sorbitol by a degree similar to that observed in the rat

120 concern, however, that suspensions of SPS in sorbitol can be harmful.

121 , as well as ternary solutions of (water + d-sorbitol + citric acid) and (water + glycerol + citric a

122 wth, which were all closely related to lower sorbitol concentrations in stamens.

123 nce of these transporters and the high fruit sorbitol concentrations suggest that there is an apoplas

124 1 kinase, and impairs growth in high-salt or sorbitol conditions.

125 increased aldose reductase activity, higher sorbitol content and less accumulation of the toxic meta

126 fibrils, and the presence of 60% glycerol or sorbitol could increase thickness of OVT nanofibrils.

127 t indicated that the presence of glycerol or sorbitol could reduce the rate of OVT fibrillation.

128 de gel electrophoresis demonstrated that 60% sorbitol could retard hydrolysis of OVT completely for a

129 ves for the real-time monitoring of sucrose, sorbitol, d-glucose and d-fructose concentrations gave u

130 uencies for real-time monitoring of sucrose, sorbitol, d-glucose and d-fructose concentrations is rep

131 plied to the elaboration of biosensors for D-sorbitol, D-glucose and L-lactate with using D-sorbitol

132 bling system based on 1,3:2,4-dibenzyldene-D-sorbitol (DBS) derivatives which form gels as the pH is

133 1,3:2,4-Dibenzylidene-d-sorbitol (DBS), a simple, commercially relevant compound

134 ibed to be a potential negative regulator of sorbitol dehydrogenase (SDH) in hippocampal cells, we ex

135 Sorbitol dehydrogenase (SDH) is a polyol pathway enzyme

136 ythritol: alcohol dehydrogenase 1 (ADH1) and sorbitol dehydrogenase (SORD).

137 Sorbitol dehydrogenase activity was reduced in silenced

138 acological inhibition of aldose reductase or sorbitol dehydrogenase blocked JAK2 and STAT5 activation

139 Here we report biallelic mutations in the sorbitol dehydrogenase gene (SORD) as the most frequent

140 rbitol, D-glucose and L-lactate with using D-sorbitol dehydrogenase, D-glucose dehydrogenase and L-la

141 -fetoprotein, arginase-1, osteopontin (OPN), sorbitol dehydrogenase, fatty acid binding protein, cadh

142 By choosing a suitable sorbitol dehydrogenase, we designed yeast strains in whi

143 levels, and inhibiting the expression of the sorbitol dehydrogenase-1 SODH-1, a crucial sugar metabol

144 e may be similar to that described for human sorbitol dehydrogenase.

145 orted in the human sperm fibrous sheath, and sorbitol dehydrogenase.

146 mined the kinetic parameters of mannitol and sorbitol dehydrogenases encoded in the yeast genome, sho

147 Sorbitol density gradient analysis of membrane compartme

148 Using sorbitol density gradient fractionation, we show here th

149 Equi-osmotic sorbitol did not alter any variable.

150 blood pressure whereas equi-osmotic mannitol/sorbitol did not alter any variable.

151 hat hyperosmotic stress signaling induced by sorbitol disrupts the Ran protein gradient and reduces t

152 g the CaMV35S promoter to define the role of sorbitol distribution in fruit development.

153 Together, these results suggest that sorbitol distribution plays a key role in fruit carbon m

154 Binding studies of sugar alcohols mannitol, sorbitol, erythritol, adonitol, arabitol, galactitol, an

155 The resulted product, sorbitol ester of norbixin (SEN) was expected to be more

156 apoptosis induced by exogenous agents (e.g., sorbitol, Fas ligand, and BAD protein) or replication-in

157 Escherichia coli (EHEC) O157:H7 that are non-sorbitol fermenting (NSF) and beta-glucuronidase negativ

158 tor, enteropathogenic E. coli (EPEC) O55:H7 (sorbitol fermenting [SOR(+)] and beta-glucuronidase posi

159 cally similar to the O157:H7 serotype as non-sorbitol fermenting and negative for beta-glucuronidase

160 pO157 (>90,000 bp), whereas closely related sorbitol-fermenting (SF) E. coli O157:H(-) strains carry

161 ed that the loss of motility in these German sorbitol-fermenting (SF) O157 strains is due to a 12-bp

162 Between these events, sorbitol-fermenting E. coli O157:H(-) presumably diverge

163 polyols (glycerol, mannitol, erythritol, and sorbitol), five amino acids (glycine, alanine, sarcosine

164 es such as poly(vinylpyrrolidone) (PVP) or D-sorbitol, form ring-banded spherulites composed of hande

165 D-sorbitol forms so-called spherulites from under-cooled m

166 tions (8-12GPa compared to 0.05-11GPa), with sorbitol formulations showing a bimodal distribution of

167 trations of mannitol, sucrose, trehalose and sorbitol from 1:1 to 30:1 with carboxymethylcellulose (C

168 achieve nearly maximum theoretical yields of sorbitol from glucose.

169 R up-regulation and elevated AR metabolites (sorbitol, fructose, and uric acid), which correlated sig

170 diol, glycerol, 1,4-butanediol, xylitol, and sorbitol), furanoids (furfural and 5-hydroxymethylfurfur

171 se-fructose oxidoreductase, an enzyme in the sorbitol-gluconate pathway.

172 beta-d-glucose sodium salt, d-(+)-galactose, sorbitol, glycerol, and dextrose.

173 j 30, Span 20, Ecosurf EH-3, polyoxyethylene sorbitol hexaoleate, and R-95 rhamnolipid) were evaluate

174 rmination on both ionic (NaCl) and nonionic (sorbitol) hyperosmotic media.

175 f the rheological behavior revealed that the sorbitol/IL solution is Newtonian and the Arrhenius, Lit

176 both PGA1 and PGE1 reduced the formation of sorbitol in an ex-vivo model of diabetic cataract to an

177 s at 4 degrees C in 15 mg/mL dispase II with sorbitol in defined keratinocyte serum-free medium (KSFM

178 ldose reductase 2 (ALR2) and accumulation of sorbitol in eye lens which could have contributed to dia

179 We also suggest that apple leaves transport sorbitol in high concentrations to avoid the feedback li

180 ssfully applied to predict the solubility of sorbitol in IL.

181 ermination of glucose, fructose, sucrose and sorbitol in leaf and/or apple peel samples from nine app

182 ly efficient utilization of the co-substrate sorbitol in providing NADPH.

183 Including sorbitol in the sinapinic acid matrix was found to promo

184 nd glucose plateaued at the fourth week, but sorbitol increased 40% to the seventh harvest week.

185 rrant mitochondrial biogenesis and increased sorbitol-induced cell death.

186 a2 activity had no effect on contraction- or sorbitol-induced glucose transport.

187 ratinocyte growth, and to cellular stresses (sorbitol-induced hyperosmotic shock, UV irradiation, and

188 SORD is an enzyme that converts sorbitol into fructose in the two-step polyol pathway pr

189 locatable photosynthate in Rosaceae species, sorbitol is a widespread compatible solute and cryoprote

190 accumulation of polyols such as xylitol and sorbitol is associated with MI depletion in diabetic com

191 he exclusion limit for Cx46 channels whereas sorbitol is at the exclusion limit for Cx32E(1)43 channe

192 d show that ERK activation by TNF, IL-1, and sorbitol is attenuated in the absence of KSR1.

193 The results indicated that sorbitol is highly soluble in this IL.

194 We further characterize the impacts of NaCl, sorbitol, KCl and alkaline pH stresses on the cellular p

195 potent oral activity in normalizing elevated sorbitol levels and, more significantly, fructose levels

196 eductase inhibitors normalized intracellular sorbitol levels in patient-derived fibroblasts and in Dr

197 Furthermore, the serum fasting sorbitol levels in patients were dramatically increased.

198 , oxidative stress and optic neuropathy, and sorbitol levels were increased in LHON cybrids.

199 It lowers nerve and lens sorbitol levels with ED(50)'s of 1.9 and 4.5 mg/kg/d po,

200 ct plating of dilutions of bovine feces onto sorbitol MacConkey agar containing cefixime and tellurit

201 ess treated at a tertiary care center, i.e., sorbitol-MacConkey (SMAC) agar culture, enzyme immunoass

202 E. coli O157 can be detected by culture with sorbitol-MacConkey agar (SMAC), but non-O157 STEC cannot

203 d with LD-PCR findings in 25 (89%) of the 28 sorbitol-MacConkey agar culture-negative STEC cases.

204 ry metabolites, including fructose, glucose, sorbitol, malic acid were recorded among tested accessio

205 ts (n = 132) were randomized: controls (G1) (sorbitol/maltitol), or combinations giving xylitol 3.44

206 Sorbitol, mannitol, and galactitol were converted via 1,

207 furfural, 5-hydroxymethylfurfural, xylitol, sorbitol, mannitol, and gluconic acid as biorefinery pla

208 ased expression of MIOX, which is induced by sorbitol, mannitol, and xylitol in a porcine renal proxi

209 e hypothesize that osmolytes such as urea or sorbitol may modulate PC1 mechanical properties and may

210 th single PSAC patch-clamp recordings and in sorbitol-mediated osmotic lysis measurements, confirming

211 rowth of sto1 mutant plants on NaCl, but not sorbitol, medium was associated with a reduction in both

212 nase, we designed yeast strains in which the sorbitol metabolism yields a "surplus" of either NADPH o

213 GalOA in combination with the NADH-yielding sorbitol metabolism.

214 Poly(sorbitol methacrylate) appears to enhance activity by re

215 ogenase on a surface support displaying poly(sorbitol methacrylate) chains resulted in approximately

216 Enzymes in the glycolytic, sorbitol, methylglyoxal and mitochondrial pathways were

217 Following exposure of cells to sorbitol, MKK4 underwent ubiquitination and degradation

218 reated with various organic osmolytes, e.g., sorbitol, myoinositol, and glycerolphosphoryl-choline an

219 mmonly used stress-inducing agents mannitol, sorbitol, NaCl, and hydrogen peroxide impact shoot growt

220 lates of the M. fortuitum third biovariant D-sorbitol-negative group and porcine strains of M. porcin

221 solates of the M. fortuitum third biovariant sorbitol-negative group, of which 48 (70%) had the same

222 c transporters with similar affinities (K(m) sorbitol of 0.81 mM for PcSOT1 and 0.64 mM for PcSOT2).

223 l amounts (approximately 30% w/v) and types (sorbitol) of low molecular weight crowding agents.

224 Impact of glycerol and sorbitol on assembly of iron-bound ovotransferrin (OVT)

225 Influence of glycerol and sorbitol on morphology of OVT nanofibrils was studied us

226 In particular, a Y585C mutation in the sorbitol operon transcriptional regulator gutR was assoc

227 centrations of three inhibitors that abolish sorbitol or alanine uptake.

228 Adding sorbitol or alanine, permeant solutes that do not exhibi

229 the activation loop, whereas treatment with sorbitol or heat shock did not.

230 g cell integrity with the osmotic stabilizer sorbitol or via genetic suppression with the kre5(W1166X

231 w in the presence of trimethoprim plus added sorbitol parallels the catalytic efficiency of the DHFR

232 hyperglycemia, the mice displayed augmented sorbitol pathway activity in the peripheral nerve, as we

233 They also had increased sorbitol pathway activity in the sciatic nerve and incre

234 without diabetes, suggesting a role for the sorbitol pathway and the potential for ARIs to reduce in

235 oses that partially and completely inhibited sorbitol pathway hyperactivity) arrested diabetes-induce

236 To study aldose reductase and the sorbitol pathway in periodontitis and diabetes, rats wit

237 Nerve glucose and sorbitol pathway intermediate concentrations were simila

238 Sorbitol pathway intermediate, but not glucose, accumula

239 n glycolysis, pentose phosphate pathway, and sorbitol pathway, which may further exacerbate oxidative

240 induced by activated aldose reductase in the sorbitol pathway.

241 The polyol (sorbitol) pathway of glucose metabolism is activated in

242 mutagenesis of RMC26 produced defects in the sorbitol phosphotransferase system that prevented the tr

243 ing strategies of two species that transport sorbitol (Plantago major and apple [Malus domestica]), a

244 We conclude that sorbitol plays an essential role in stamen development a

245 Extracellular NaCl (100 mM), but not sorbitol, prevented vacuolar expansion and PI entry in c

246 hondrial uncoupler), muscle contraction, and sorbitol (producing hyperosmolar shock) did not increase

247 For arsenite, but not for sorbitol, quenching oxidative stress with N-acetylcystei

248 d carbon sources such as mannitol, fructose, sorbitol, raffinose and stachyose for growth.

249 me) with saline or various cell impermeants (sorbitol, raffinose, trehalose, gluconate, and polyethyl

250 lls with the non-permeant solutes sucrose or sorbitol, rapidly and robustly stimulated endogenous foc

251 't affect the transfection efficiency, while sorbitol resulted in a fluctuation of the in vitro trans

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

253 er), 1, 3, 5, 10, 20 and 30% w/w glycerol or sorbitol solution for 24h and adjusting the moisture con

254 Osmotic pretreatment was carried out in sorbitol solution of 35 degrees Brix at 55 degrees C for

255 Both genes encode proton-dependent, sorbitol-specific transporters with similar affinities (

256 The linear optical properties of sorbitol spherulites containing the azo dye amaranth wer

257 down of SNARK in C2C12 muscle cells impaired sorbitol-stimulated glucose transport.

258 P-43 modifications via oxidative stress, but sorbitol stimulates TDP-43 ubiquitylation and insolubili

259 Sorbitol stress also slowed RCC1 mobility in the nucleus

260 zation signal reporter protein revealed that sorbitol stress decreases the rate of nuclear import.

261 TP levels, which were reduced in response to sorbitol stress.

262 t increased susceptibility to osmotic (salt, sorbitol) stress and SDS.

263 ith the concentration of osmolytes (proline, sorbitol, sucrose, TMAO, and sarcosine).

264 MAO), sarcosine, betaine, proline, glycerol, sorbitol, sucrose, trehalose, and urea, using cyclic gly

265 Sorbitol suppresses the growth defect in the tps1 and tp

266 inhibition of the CWI pathway by addition of sorbitol, suppresses the ER inheritance defect in the pt

267 ic 'Greensleeves' apple trees with decreased sorbitol synthesis had abnormal stamen development, a de

268 SAGE: PpeS6PDH gene is postulated to mediate sorbitol synthesis in flower buds of peach concomitantly

269 in the acetate buffer solution containing 5% sorbitol than in the acetate buffer solution with 200-mM

270 at central fruitlets were better supplied in sorbitol than lateral fruitlets.

271 f GalA to the oxidation of the sugar alcohol sorbitol that has a higher reduction state compared to g

272 orodeoxysorbitol ((18)F-FDS) is an analog of sorbitol that is reported to be freely filtered at the r

273 sufficient NaCl or osmolytes, trehalose and sorbitol, the NFAT5 NTD undergoes a disorder-to-order sh

274 in; however, a premixed suspension of SPS in sorbitol, the only preparation stocked by many hospital

275 that they discriminate between mannitol and sorbitol to a much higher degree than the transporters.

276 pathway enzyme that catalyzes conversion of sorbitol to fructose.

277 The sorbitol to sucrose ratio in leaves was reduced by appro

278 xin, was enzymatically modified by appending sorbitol to the bixin scaffold.

279 Addition of sorbitol to the germination medium also partially restor

280 ed by the addition of 0.4 M sucrose or 0.4 M sorbitol to the growth medium.

281 Hyperosmotic stress, produced by addition of sorbitol to the incubation buffer, increased p38 phospho

282 of rat brain slices, produced by addition of sorbitol to the incubation buffer, produced prolonged ph

283 ing effective turgor pressure by addition of sorbitol to the media significantly accelerates early st

284 nimals or humans and no evidence that adding sorbitol to the resin increases its effectiveness as a t

285 gnificant differences in pathways related to sorbitol transport and breakdown.

286 viously for parasite-induced anion currents, sorbitol transport in infected RBCs was found to be sens

287 VA and MEP reprogrammed upon osmotic stress (sorbitol treatment) in Arabidopsis (Arabidopsis thaliana

288 lutamic Acid, m- Erythritol, D-Melezitose, D-Sorbitol) triggered the fungal metabolism in the co-inoc

289 Sorbitol uptake activities and other characteristics wer

290 Transport of the electroneutral solute sorbitol via the NPPs was found to increase by a small b

291 Postgermination growth of the sto1 plants on sorbitol was not improved.

292 .49 g/kg dry mass [DM], respectively), while sorbitol was predominant in leaves (40.66 g/kg DM).

293 A similar trend was observed when sorbitol was used as a plasticizer, but with a lesser ef

294 naling pathways of the osmotic shock inducer sorbitol, we could largely rule out the stress-activated

295 K(0.5) values for glucose and sorbitol were highly dependent on external pH.

296 nses to equi-osmotic infusions of hypertonic sorbitol were significantly smaller.

297 One product of aldose reductase is sorbitol, which has been linked to osmotic stress, oxida

298 diabetic conditions AR converts glucose into sorbitol, which is then converted to fructose.

299 t two major hexitols in nature, mannitol and sorbitol, with moderate affinities, by a facilitative me

300 nder combined stress of 25 mM NaCl and 50 mM sorbitol without subsequent mechanical stress had consid