ライフサイエンスコーパス: sorbitol

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

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

3 enome), and biochemical tests (trehalose and sorbitol).

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

5 r blackberry samples contained no detectable sorbitol).

6 yeasts to overproduce xylitol, mannitol, and sorbitol.

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

8 is decreased by increasing concentrations of sorbitol.

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

10 ictive temperature by the osmotic stabilizer sorbitol.

11 ed a major contribution to JNK activation by sorbitol.

12 th induced by environmental staurosporine or sorbitol.

13 athways in addition to converting glucose to sorbitol.

14 hydrogen from ethylene glycol, glycerol, and sorbitol.

15 ng alcohols, including converting glucose to sorbitol.

16 tissues that accumulate large quantities of sorbitol.

17 M) containing 50 mg/mL dispase II and 100 mM sorbitol.

18 than twofold after exposure to hyperosmolar sorbitol.

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

20 se cells in media containing 1 m NaCl or 2 m sorbitol.

21 re rescued by osmotic stabilization with 1 m sorbitol.

22 uronal discharge frequency than equi-osmotic sorbitol.

23 ith sodium chloride, potassium chloride, and sorbitol.

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

25 rogenase, the key enzyme for biosynthesis of sorbitol.

26 sure to high concentrations of congo red and Sorbitol.

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

28 esponse than infusion of hypertonic mannitol/sorbitol.

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

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

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

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

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

34 plemented with either NaCl (0.4 or 0.5 m) or sorbitol (0.8 or 1.0 m) enhanced the subsequent growth o

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

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

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

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

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

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

41 1 from osmotically stressed HEK cells (0.2 M sorbitol; 30 min) revealed a persistent, 3.9 +/- 0.4-fol

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

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

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

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

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

47 nd activity and in the myocardial content of sorbitol, a unique product of AR catalysis.

48 Consistently, sorbitol accumulates in dormant buds showing higher PpeS

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

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

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

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

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

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

55 th L-arginine did not inhibit AR activity or sorbitol accumulation in the tissues of nondiabetic anim

56 or of NO synthesis, enhanced AR activity and sorbitol accumulation in tissues of nondiabetic rats.

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

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

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

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

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

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

63 Sorbitol also rescues endocytic ingression defects of ce

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

65 Although sorbitol alters nucleotide levels, we show that invertin

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

67 1 m sorbitol and 0.2 m NaCl, which induce the HOG pathway, r

68 rbinil prevented AR-mediated accumulation of sorbitol and abrogated the infarct-sparing effect of lat

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

70 re distinct with respect to motility and the sorbitol and beta-glucuronidase markers appear to have d

71 Sorbitol and citric acid may be partially responsible fo

72 d by PcSOT1 and PcSOT2 plays a major role in sorbitol and dry matter accumulation in sour cherry frui

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

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

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

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

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

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

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

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

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

82 Sorbitol and hydrogen peroxide each caused inhibition of

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

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

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

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

87 Sorbitol and sucrose are major products of photosynthesi

88 Sorbitol and sucrose significantly raised levels of bis-

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

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

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

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

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

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

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

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

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

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

99 - 9, 57 +/- 12, and 96 +/- 10% for inositol, sorbitol, and betaine respectively, p < 0.05).

100 /- 5, 66 +/- 15, and 81 +/- 9% for inositol, sorbitol, and betaine, respectively, p < 0.05) by pretre

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

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

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

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

105 ning flies on media containing NaCl, KCl, or sorbitol, and that this hypersensitivity is completely r

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

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

108 Exogenous sorbitol application during flower development partially

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 1 kinase, and impairs growth in high-salt or sorbitol conditions.

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

128 oglycerine patches decreased AR activity and sorbitol content in tissues of diabetic rats.

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

134 disclosed hypothesis centered on the role of sorbitol dehydrogenase (SDH) in the second step of the p

135 Sorbitol dehydrogenase (SDH) is a polyol pathway enzyme

136 Sorbitol dehydrogenase activity was reduced in silenced

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

138 and pharmacology efforts to provide a potent sorbitol dehydrogenase inhibitor (SDI) as a tool to prob

139 Optimization of a previously disclosed sorbitol dehydrogenase inhibitor (SDI, II) for potency a

140 We report here a novel sorbitol dehydrogenase inhibitor, 16, that shows very hi

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

142 led and found to be a selective inhibitor of sorbitol dehydrogenase, with excellent pharmacodynamic/p

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

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

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

146 Sorbitol density gradient analysis of membrane compartme

147 Using sorbitol density gradient fractionation, we show here th

148 Equi-osmotic sorbitol did not alter any variable.

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

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

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

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

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

154 sses chosen, arsenite, hydrogen peroxide and sorbitol, exert their effects in quite different ways.

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

156 ss of physiological characteristics, such as sorbitol fermentation ability and beta-glucuronidase pro

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 logenetic relationship to populations of non-sorbitol-fermenting, beta-glucuronidase negative O157:H7

164 tinct subpopulations of the contemporary non-sorbitol-fermenting, beta-glucuronidase-negative O157:H7

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

166 ls were permeabilized by incubation in 0.8 M sorbitol followed by suspension in dilute buffer.

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

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

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

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

171 achieve nearly maximum theoretical yields of sorbitol from glucose.

172 nder six well-studied conditions: high salt, sorbitol, galactose, pH 8, minimal medium and nystatin t

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

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

175 motic stress induced by the organic osmolyte sorbitol, heat shock, ultraviolet irradiation, oxidative

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

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

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

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

180 ide (NO) donors prevent ex vivo synthesis of sorbitol in erythrocytes obtained from diabetic or nondi

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

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

183 articularly partitioning and accumulation of sorbitol in sink tissues, we have cloned two sorbitol tr

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

185 one) and a pathological stress (hyperosmolar sorbitol) in Xenopus laevis oocytes, a cell type that is

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

187 anion cells did not plasmolyze even in 1.2 M sorbitol, indicating that solute accumulates in the phlo

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

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

190 Thus, NaCl- or sorbitol-induced hyperosmotic shock causes a [Ca(2+)](cy

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

192 Hyperosmotic stress caused by NaCl, LiCl, or sorbitol induces an immediate and short duration ( appro

193 The acyclic polyol sorbitol is a primary photosynthetic product and the pri

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

226 t it is resistant to molar concentrations of sorbitol or KCl, indicating that it has normal osmoregul

227 wing in medium that is not supplemented with sorbitol or NaCl, providing evidence that transcription

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

229 with NaCl, an equi-osmolar concentration of sorbitol, or ABA, whereas AtNHX5 transcript abundance in

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

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

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

233 is, doses that completely inhibit increased sorbitol pathway activity) is an effective approach for

234 esulting in complete inhibition of increased sorbitol pathway activity.

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

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

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

238 Nerve glucose and sorbitol pathway intermediate concentrations were simila

239 Sorbitol pathway intermediate, but not glucose, accumula

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

241 induced by activated aldose reductase in the sorbitol pathway.

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

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

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

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

246 acterium fortuitum third biovariant complex (sorbitol positive), isolates of M. mageritense are likel

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

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

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

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

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

252 ociated with a weakened cell wall, including sorbitol-remedial temperature sensitivity and sensitivit

253 On the other hand, sorbitol requires expression of four MAP3Ks to cause max

254 omeostasis, but had no effect on the NaCl or sorbitol sensitivity of the osmotic hypersensitive hog1D

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

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

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

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

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 ents with 154 mM NaCl and either 0 or 300 mM sorbitol suggested that the changes in light scattering

266 Sorbitol suppresses the growth defect in the tps1 and tp

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

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

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

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

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

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

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

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

275 pathway enzyme that catalyzes conversion of sorbitol to fructose.

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

277 Addition of sorbitol to the germination medium also partially restor

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

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

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

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

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

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

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

285 sorbitol in sink tissues, we have cloned two sorbitol transporter genes (PcSOT1 and PcSOT2) from sour

286 In sorbitol-treated oocytes expressing a conditionally acti

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

295 sotonic to 154 mM NaCl by supplementing with sorbitol were progressively more transparent as NaCl inc

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

297 Mesophyll cells plasmolyzed in 600 mM sorbitol, whereas sieve elements and companion cells did

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

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

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