ライフサイエンスコーパス: sulfate

1 nite and the potential competitive effect of sulfate.

2 d in oocytes was gated open by extracellular sulfate.

3 tion pathway of dermatan sulfate and heparan sulfate.

4 erone antagonized the effect of pregnenolone sulfate.

5 reased decorin and production of chondroitin sulfate.

6 ced by oral administration of dextran sodium sulfate.

7 nt concentrations of selenate and competitor sulfate.

8 oxidase and converts H2S to thiosulfate and sulfate.

9 the addition of a primary amine to a cyclic sulfate.

10 relative availability of organic carbon and sulfate.

11 ing during colitis induced by dextran sodium sulfate.

12 fies H2S by converting it to thiosulfate and sulfate.

13 tmosphere as elemental sulfur is oxidised to sulfate.

14 olved enhanced specificity for selenate over sulfate.

15 calyx coverage, with preservation of heparan sulfate.

16 beneficial to crops naturally grown on high sulfate.

17 off through addition of the blocker dodecyl sulfate.

18 rrelated (R(2) = 0.96) with the reduction of sulfate.

19 ore specific in the detection of urinary bis-sulfates.

20 or enzymatic removal of cell surface heparan sulfates.

21 5 mg Fe as (57)FeFum+Na(58)FeEDTA or ferrous sulfate ((54)FeSO4).

22 SP-1 is inhibited by heparin and chondroitin sulfate A, indicating binding to the N-terminal globular

23 Here, we show that cholesterol sulfate, a molecule present in relatively high concentra

24 al enzymes that specifically degrade heparan sulfate, a sulfated glycosaminoglycan.

25 e VM) does not, instead exhibiting increased sulfate accumulation.

26 Abundant DOC and sulfate additionally supported some of the highest sulfa

27 anism of metals dissolution by highly acidic sulfate aerosol and the effect on particle oxidative pot

28 ge to the paler yellow tones with increasing sulfate amount.

29 re found when 0.5g mussel shell, 0.5g sodium sulfate and 5mL ethanol were used.

30 sed to water stress to investigate xylem sap sulfate and ABA, stomatal conductance, and sulfate trans

31 n a trash can was able to transform ammonium sulfate and ammonium nitrate into (MEA)2SO4 and (MEA)NO3

32 ation of naphthalene in the presence of iron sulfate and ammonium sulfate seed particles.

33 Copigmented complexes of chondroitin sulfate and anthocyanin were preloaded in CaCO3 scaffold

34 ositely charged micelles from sodium dodecyl sulfate and cetyltrimethylammonium bromide, respectively

35 alyzed with Fenton systems containing Fe(II)-sulfate and Fe(II)-Quin with and without buffer.

36 sponded with augmented extracellular heparan sulfate and glypican 4 levels.

37 he lysosomal degradation pathway of dermatan sulfate and heparan sulfate.

38 rongly protein-bound toxins, namely, indoxyl sulfate and p-cresyl sulfate, while for weakly bound tox

39 alpha-synuclein amyloid fibrils and heparan sulfate and show that overall sulfation of the heparan s

40 opic composition (delta(34)S) of sedimentary sulfate and sulfide phases over Earth history can be use

41 lycin is decorated with chondroitin/dermatan sulfate and that PF4 binds to these GAG chains.

42 ylogenetically related to known haloalkaline sulfate and thiosulfate reducers, thiosulfate-disproport

43 nstrate that S. rosetta produces chondroitin sulfate and thus extend the ancestry of this important g

44 data also implicate NCX-9 in a LON-2/heparan sulfate and UNC-6/netrin-mediated, RAC-dependent signali

45 eptor 1 was also found to bind two dianionic sulfate anions bridged by two water molecules in the sol

46 xation of chloride, nitrate, bicarbonate and sulfate anions via hydrogen bonding.

47 m metabolites (e.g., picolinic acid, indoxyl sulfate, anthranilate, (P < 0.01)).

48 ar shorter than the residence time of marine sulfate, any change in the sulfur isotopic record preser

49 Sulfate application caused stomatal closure in excised l

50 erine over the normally preferred l-serine-O-sulfate ( approximately 1200-fold change in kcat/Km rati

51 levated levels of syndecan-1 and chondroitin sulfate are strongly associated with plasma leakage, and

52 s are metalloenzymes that oxidize sulfite to sulfate at a molybdenum active site.

53 nd Amplon (blend of sulfuric acid and sodium sulfate) at a poultry processing pilot plant scale, and

54 CI, 0.4 to 1.6 g/dL; P < .001) with ferrous sulfate (based on a linear mixed model).

55 le; this assumption may be well grounded for sulfate-bearing minerals but is less well established fo

56 because of the unique positioning of the 3-O-sulfated beta-galactose headgroup.

57 lude that the difference in the formation of sulfate between GDD and ATD particles is regulated mainl

58 molecular receptors with high-efficiency for sulfate binding still remains a significant challenge.

59 e compelling evidence that AgRP is a heparan sulfate-binding protein and localizes critical regions i

60 In membranes, dodecyl sulfate blocked chloride transport through the central c

61 When accounting for the neutralization of sulfate by ammonium, organic acid particles showed the g

62 ncorporated in the carrier materials calcium sulfate (CaSO4) and poly methyl methacrylate (PMMA).

63 Mincle activation by cholesterol sulfate causes the secretion of a range of proinflammato

64 B2 (SLC35B2) function in a common pathway to sulfate CCR5 on extracellular tyrosine residues, facilit

65 nin (CHL) or collagen IV + gelatin + heparan sulfate (CGH) demonstrated significantly higher expressi

66 d show that overall sulfation of the heparan sulfate chains is more important than sulfation at parti

67 itin in addition to low-sulfated chondroitin sulfate chains.

68 ions and increased concentrations of the non-sulfated chondroitin disaccharide D0a0 and the disacchar

69 This nematode produces large amounts of non-sulfated chondroitin in addition to low-sulfated chondro

70 non-sulfated chondroitin in addition to low-sulfated chondroitin sulfate chains.

71 for these complexes; indeed, for the highly sulfated chondroitin sulfate motifs, CS-E and CS-D, ther

72 tals such as bismuth stabilize labile Ti-oxo sulfate clusters in aqueous solution.[Ti22 Bi7 O41 (OH)(

73 In response to dextran sodium sulfate, colonic infiltration of neutrophils and inflamm

74 nutritional iron-deficiency anemia, ferrous sulfate compared with iron polysaccharide complex result

75 High sulfate concentrations in the solutions did not show a c

76 were identified in biological fluids, mainly sulfated conjugates of caffeic and ferulic/isoferulic ac

77 Versican is a large chondroitin sulfate-containing, hyaluronic acid-binding proteoglycan

78 pport the idea that abnormalities in heparan sulfate content and distribution contribute to alteratio

79 ferent isomeric disaccharides of chondroitin sulfate (CS) and heparan sulfate (HS), which are represe

80 ounts of hyaluronic acid (HA) or chondroitin sulfate (CS) did not directly increase indicators of dis

81 Chondroitin sulfate (CS) is a sulfated polysaccharide that plays ess

82 Chondroitin sulfate (CS) is the most abundant component in extracell

83 ration of N-glycolyl groups into chondroitin sulfate (CS) over other potential glycoconjugate product

84 (E)-caftaric acid (c), (E)-caftaric acid-4-O-sulfate (d) and (E)-caftaric acid-3-O-sulfate (e).

85 which could have been attributed to reduced sulfate deposition as increases in pH favor more diverse

86 This study examined sulfate deposition in Nova Scotia from 1999 to 2015, and

87 f the origin of large Hesperian-aged layered sulfate deposits on Mars.

88 er had significantly increased sodium lauryl sulfate deposits.

89 ccharide to be converted into 12 differently sulfated derivatives.

90 one, androstenedione, dehydroepiandrosterone sulfate (DHEAS)], sex hormone binding globulin (SHBG), a

91 Here we present dimethyl sulfate (DMS) mutational profiling with sequencing (DMS-

92 d then detects these events through dimethyl sulfate (DMS) probing and mutational profiling.

93 the lead chromates change as a result of the sulfate doping in such a way that the generation of elec

94 paclitaxel (PTX) to a dendritic polyglycerol sulfate (dPGS) nanocarrier.

95 Sulfate-driven metals dissolution may account for sulfat

96 elemental iron once daily as either ferrous sulfate drops or iron polysaccharide complex drops for 1

97 In proteomics, dodecyl sulfate (DS(-)) as sodium salt is commonly used in prote

98 Dextran sodium sulfate (DSS) and Citrobacter rodentium colitis (CC) was

99 zene sulfonic acid (TNBS) and dextran sodium sulfate (DSS) models of colitis.

100 after oral administration of dextran sodium sulfate (DSS).

101 id-4-O-sulfate (d) and (E)-caftaric acid-3-O-sulfate (e).

102 epresents another link between anthropogenic sulfate enrichment and MeHg production in the environmen

103 An unexplored implication of sulfate enrichment is alteration of the content and spec

104 effects of different PGs and their assorted sulfated epitopes.

105 rents, whereas the neurosteroid pregnenolone sulfate exerted similar effects as progesterone, likely

106 AFM pulling on glypican-1 and heparan sulfate for 10 min caused significantly increased NO pro

107 gene, dehydroepiandrosterone (DHEA) and its sulfated form (DHEA-S), and characteristics of attention

108 The maximum sulfate formation rate was reached at 25% RH and 45% for

109 imental results demonstrate the viability of sulfate formation under current Martian conditions, even

110 CD38+HLA-DR+ T cells, dehydroepiandrosterone sulfate, free testosterone, homeostatic model assessment

111 es, including the characterization of labile sulfated functional groups.

112 The sulfated GAG oligosaccharides derived from cartilage pos

113 Both the cartilage and skin sulfated GAG polysaccharides showed greater ferritin for

114 ) but not to the closely related chondroitin sulfate GAGs.

115 HSV-1 recognized all sulfated GAGs, but not the nonsulfated hyaluronan, indic

116 We report here on supramolecular sulfated glycopeptide nanostructures, which display a tr

117 Food grade sulfated glycosaminoglycan (GAG) polysaccharides were su

118 that specifically degrade heparan sulfate, a sulfated glycosaminoglycan.

119 , binds to heparin and brain-derived heparan sulfate glycosaminoglycans (GAGs) but not to the closely

120 resolution of IDA was higher in the ferrous sulfate group (29% vs 6%; P = .04).

121 n the iron complex group than in the ferrous sulfate group (58% vs 35%, respectively; P = .04).

122 on patterns depending on the position of the sulfate group in the heterocycle.

123 bin increased from 7.9 to 11.9 g/dL (ferrous sulfate group) vs 7.7 to 11.1 g/dL (iron complex group),

124 that binding is specific to the presence of sulfate groups.

125 te-driven metals dissolution may account for sulfate-health associations reported in past studies.

126 apable of being regenerated from its sulfite/sulfate heat stable salt, which enables the simultaneous

127 onal strategy on a library of 46 656 heparan sulfate hexasaccharides we identified a rare sequence co

128 glycosaminoglycans heparin (Hep) and heparan sulfate (HS) are high-priority carbohydrates for Bactero

129 ), a glycosyltransferase involved in heparan sulfate (HS) biosynthesis.

130 Expression of the heparan sulfate (HS) proteoglycan syndecan-1 is a hallmark of MM

131 EXTL3 regulates the biosynthesis of heparan sulfate (HS), important for both skeletal development an

132 ycans (GAGs), especially heparin and heparan sulfate (HS), modulate the functions of numerous cytokin

133 ides of chondroitin sulfate (CS) and heparan sulfate (HS), which are representatives of two major sub

134 Four new metabolites of PCMC (hydroxylated, sulfated/hydroxylated, sulfated PCMC, and glucuronidated

135 Accumulation of heparan sulfate in cultured astrocytes corresponded with augment

136 thiourea groups, initially encapsulates one sulfate in its thiourea-based outer cleft, followed by a

137 mately 0.4-0.5) suggest an important role of sulfate in tracer formation via both physical and chemic

138 ical analyses of sedimentary barites (barium sulfates) in the geological record have yielded fundamen

139 Dextran sodium sulfate-induced colitis model was established in C57BL/6

140 exposure, and exhibit severe dextran sodium sulfate-induced colitis, ameliorated by TNF inhibition.

141 sferred to CD1 nude mice with dextran sodium sulfate-induced colitis, with or without oral administra

142 (si)RNA to C57BL/6 mice with dextran sodium sulfate-induced colitis.

143 lpha, and IL-17) in mice with dextran sodium sulfate-induced colitis.

144 usions, volume resuscitation, and salbutamol sulfate inhalation, which resulted in an improvement of

145 Sulfate inputs to the Florida Everglades stimulate sulfi

146 Bis-sulfates ionized preferentially as the dianion ([M - 2H]

147 ronments supplied with additional barium and sulfate ions derived from heterotrophic remineralization

148 The results show that increased xylem sap sulfate is achieved upon drought by reduced xylem unload

149 Ferrous sulfate is the most commonly prescribed oral iron despit

150 We tested whether the uremic toxin indoxyl sulfate (IS), an endogenous ligand of the transcription

151 and solutes (e.g., indoxyl sulfate, p-cresol sulfate, kynurenine, creatinine, urate) include two "dru

152 orial ECMs composed of collagen IV + heparan sulfate + laminin (CHL) or collagen IV + gelatin + hepar

153 f the epithelial barrier with dextran sodium sulfate leads to increased IL-19 expression.

154 urface expression of CD138 increased heparan sulfate levels on ASCs, which are known to bind pro-surv

155 y led to the conclusion that the presence of sulfates limits formation of EPFRs due to inhibition or

156 nto the lymphatic system in a dextran sodium sulfate mediated model of inflammatory bowel disease.

157 eveloped for the analysis of glucuronide and sulfate metabolites of seven anabolic-androgenic steroid

158 nitiator, of linoleic acid in sodium dodecyl sulfate micelles, have been determined in terms of oxyge

159 Heparan sulfate modulates the activity and distribution of a set

160 s a precise molecular complementarity of the sulfate moieties on the GAG and charged residues display

161 Through heparan sulfate moieties, syndecans are thought to anchor AgRP n

162 indeed, for the highly sulfated chondroitin sulfate motifs, CS-E and CS-D, there are no structural d

163 sferase-1 (GlcNAc6ST-1) failed to synthesize sulfated N-glycans and exhibited abnormal myelination an

164 Here, we report that sulfated N-glycans are involved in peripheral nervous sy

165 Major sulfated N-glycans were identified in both porcine and m

166 myelin glycoproteins contain highly abundant sulfated N-glycans.

167 ie-Tooth neuropathy, has abundant GlcNAc-6-O-sulfated N-glycans.

168 n-6) polyunsaturated fatty acids (PUFAs), 2) sulfated neurosteroids, which play a role in brain devel

169 re essential for growth and development; low sulfated neurosteroids, which play a role in brain devel

170 AOM is known to be coupled to reductions of sulfate, nitrite, and nitrate, evidence that AOM is coup

171 fic sites, we show that the N-sulfate or 6-O-sulfate of glucosamine, but not the 2-O-sulfate of iduro

172 6-O-sulfate of glucosamine, but not the 2-O-sulfate of iduronate within heparin is required for 3Q b

173 Bis-sulfates of 23 steroid metabolites were synthesized and

174 Three sulfated oligosaccharides of natural origin were chosen

175 The grafting of chondroitin sulfate on the surface of the scaffold is able to induce

176 sive interactions with PI(4,5)P2 and heparan sulfates on opposing sides of the membrane.

177 dified at specific sites, we show that the N-sulfate or 6-O-sulfate of glucosamine, but not the 2-O-s

178 umulation and less competitive inhibition by sulfate or by high-S pretreatment.

179 rminal steps are dominated by oxidation with sulfate or conversion into methane and CO2 The controls

180 interval [CI] = 1.001-1.007) and chondroitin sulfate (OR = 1.157; 95% CI = 1.025-1.307) had an adjust

181 ding studies, the receptor selectively binds sulfate over other oxoanions, forming a 1:2 stoichiometr

182 Of these 5 androgens, epiandrosterone sulfate (P = 0.0076) was most associated with 2-year inc

183 g metabolome-wide significance (androsterone sulfate, P = 0.000000029; epiandrosterone sulfate, P = 0

184 ne sulfate, P = 0.000000029; epiandrosterone sulfate, P = 0.0000040; 4-androsten-3beta,17beta-diol di

185 2, P = 0.000064; and dehydroepiandrosterone sulfate, P = 0.00011).

186 of uremic toxins and solutes (e.g., indoxyl sulfate, p-cresol sulfate, kynurenine, creatinine, urate

187 /dL [95% CI, -86 to -14 mug/dL] with ferrous sulfate; P < .001).

188 f PCMC (hydroxylated, sulfated/hydroxylated, sulfated PCMC, and glucuronidated PCMC) were identified

189 But only one metabolite, sulfated PCMC, was confirmed in wastewater and in urine.

190 foot process effacement following protamine sulfate perfusion.

191 Methods using sodium dodecyl sulfate poly acrylamide gel electrophoresis and immunobl

192 ophoretic mobility (shift) in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), w

193 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image den

194 leaf extract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immu

195 rotein 2 significantly more than the natural sulfated polysaccharide heparin, and promoted regenerati

196 Chondroitin sulfate (CS) is a sulfated polysaccharide that plays essential physiologic

197 with binding domains for the highly diverse sulfated polysaccharides are important growth factors in

198 imilar procedures can be applied to identify sulfated proteins in yeast and human proteome microarray

199 To confirm this finding, we prepared heparan sulfate proteoglycan (HSPG)-knockout (KO) cells by using

200 s from which they arise, express chondroitin sulfate proteoglycan 4 (NG2/CSPG4).

201 METHODS AND Expression of CSPG4 (chondroitin sulfate proteoglycan 4) was detected in epidermal kerati

202 annabinoid, in the modulation of chondroitin sulfate proteoglycan accumulation in Theiler's murine en

203 es neuroinflammation and reduces chondroitin sulfate proteoglycan deposition around demyelinated lesi

204 -mediated NO production and that the heparan sulfate proteoglycan glypican-1 is a primary mechanosens

205 Chondroitin sulfate proteoglycans (CSPGs) are important structural c

206 evious studies demonstrated that chondroitin sulfate proteoglycans (CSPGs) on apical surfaces of pala

207 virus-cell interaction by mimicking heparan sulfate proteoglycans (HSPG), the highly conserved targe

208 Heparan sulfate proteoglycans (HSPGs) critically modulate adhesi

209 Heparan sulfate proteoglycans and heparin derivatives further en

210 lasma membrane-bound heparan and chondroitin sulfate proteoglycans in cellular uptake of aggregates c

211 amin activity or remove cell surface heparan sulfate proteoglycans reduced infection efficiency.

212 r (GDNF), but not the removal of chondroitin sulfate proteoglycans, greatly enhanced the intraspinal

213 e reaction (r(2) approximately 0.4-0.7), and sulfate (r(2) approximately 0.4-0.5) suggest an importan

214 generation of highly reactive and selective sulfate radical (SO4(*-)).

215 N-oxide (DMPO), hydroxyl radical ((*)OH) and sulfate radical anion (SO4(*-)) were measured from ultra

216 n were highly abundant, whereas the ammonium sulfate reactor contained nitrifiers and heterotrophs ca

217 The most abundant sulfate reducer in all cultures, related to Desulfotignu

218 Sulfate reducers coexisted with facultative nitrate redu

219 ctum silens' and identify it as a partner of sulfate reducers in marine sediments.

220 dustrial ecosystems, such as oil reservoirs, sulfate reducing microorganisms (SRM) produce hydrogen s

221 We tested the hypothesis that sulfate-reducing bacteria (SRB) are key drivers of arsen

222 ed by cyanobacteria and an anoxic state with sulfate-reducing bacteria and phototrophic sulfur bacter

223 y of anaerobic degradation of naphthalene by sulfate-reducing bacteria.

224 bacterium Geobacter sulfurreducens PCA and a sulfate-reducing bacterium Desulfovibrio desulfuricans N

225 Thioarsenates form from arsenite under sulfate-reducing conditions, e.g., in rice paddy soils,

226 continuous acetate amendment had resulted in sulfate-reducing conditions.

227 y for anaerobic naphthalene degradation by a sulfate-reducing enrichment culture.

228 ults show a direct experimental link between sulfate reduction and FDOM production, which impacts our

229 We found that delta(34)S, an indicator of sulfate reduction and habitat specific-foraging, was cor

230 is effect was unrelated to its inhibition of sulfate reduction and instead inhibited the methylation

231 ucture, but did not suppress fermentation or sulfate reduction as community functions, highlighting t

232 ation of organic matter in marine sediments, sulfate reduction coupled to fermentation plays a key ro

233 e additionally supported some of the highest sulfate reduction rates ever measured in terrestrial aqu

234 ate and monofluorophosphate as inhibitors of sulfate reduction to evaluate the contribution of SRB to

235 al samples and samples from a bioreactor for sulfate reduction to sulfide were measured and compared

236 le in anaerobic methane oxidation coupled to sulfate reduction, an important control on methane relea

237 hniques were used to perform measurements of sulfate reduction, methanogenesis, and acetate oxidation

238 naerobic dissimilatory nitrate reduction and sulfate reduction, suggesting a significant effect of lo

239 ne gene involved in CO2 fixation, aside from sulfate reduction.

240 pled both acetate- and hydrogen oxidation to sulfate reduction.

241 The activity of the sulfate reductive pathway key enzyme, adenosine 5'-phosp

242 cumulation in Salicornia and Sarcoconia: the sulfate reductive pathway that generates Cys and l-Cys d

243 y ocean that contained only trace amounts of sulfate remains controversial.

244 onsisting of consecutive glucuronic acid 2-O-sulfate residues as selectively targeting HCII.

245 eages capable of fermentative metabolism and sulfate respiration, indicating potential symbiont contr

246 ntrations of CCh and taurolithocholic acid 3-sulfate responded with trypsinogen activation, decreased

247 mediators, and s.c. injection of cholesterol sulfate results in a Mincle-mediated induction of a seve

248 A hypothetical 25% reduction of sulfate results in approximately 70% reduction of IEPOX

249 The accumulation of heparan sulfate results in neurological symptoms, culminating in

250 sphate buffer containing 2.0% sodium dodecyl sulfate (SDDS) were observed in HMT samples.

251 hromatography (MLC) employing sodium dodecyl sulfate (SDS) as surfactant, were determined.

252 The AS sodium dodecyl sulfate (SDS) denatures and unfolds globular proteins un

253 were treated with 0.1% or 1% sodium dodecyl sulfate (SDS) or 0.1% Triton X-100 and assayed for clini

254 ernary complex in presence of sodium dodecyl sulfate (SDS).

255 er with and without the presence of ammonium sulfate seed aerosol.

256 in the presence of iron sulfate and ammonium sulfate seed particles.

257 ( approximately 0.2 mug m(-3) ALW) ammonium sulfate seeds at exactly the same relative humidity (RH

258 Further browning in AS and methylammonium sulfate seeds was triggered by cloud events with chamber

259 In conclusion, xylem-derived sulfate seems to be a chemical signal of drought that in

260 ear to involve constitutive up-regulation of sulfate/selenate uptake and assimilation, associated wit

261 We used an mAb and/or a multimeric synthetic sulfated sialoglycan ligand recognizing Siglec-8 in comb

262 ring colonic regeneration in a mouse dextran sulfate sodium (DSS) colitis model, and we demonstrate t

263 r 1 week, SPF and GF mice were given dextran sulfate sodium (DSS) to induce colitis.

264 tis development was determined using dextran sulfate sodium (DSS)-induced acute and an Il10-deficienc

265 an antibiotic cocktail (ATB) and/or dextran sulfate sodium (DSS).

266 ck-out mice were orally administered dextran sulfate sodium for 7 days and were compared with wild-ty

267 fusion in the small intestine and by dextran sulfate sodium in the colon.

268 ) were administered azoxymethane and dextran sulfate sodium to induce colitis-associated dysplasia.

269 s disease following sub-pathological dextran sulfate sodium treatment.

270 ractions in colonic injury following dextran sulfate sodium treatment.

271 00f-deficient mice failed to resolve dextran sulfate sodium-induced colonic inflammation as a result

272 ents affected by acid mine drainage and acid sulfate soils.

273 on of aluminum-containing minerals in acidic sulfate solutions, such as those that could result from

274 centrations of aqueous uranium, nitrate, and sulfate species in groundwater together with their distr

275 fectiveness of adjunct sodium tanshinone IIA sulfate (STS) therapy on circulating inflammation marker

276 in two serotypes suggesting a propensity for sulfated-sugar binding.

277 cocornia than in Salicornia, especially upon sulfate supplementation.

278 proteins (including IgE, Bank1, chondroitin sulfate synthase 2, Cmip, and Fth1) were exclusively ide

279 roxysulfate mineral, which is common in acid sulfate systems.

280 S --> glutathione persulfide --> sulfite --> sulfate, than with a more convoluted route that would re

281 luoromethanesulfonate anions for hydrophilic sulfate; the resulting water-soluble cages could be rend

282 d, which in turn assist to adsorb the uranyl sulfates through hydrogen bonding thus facilitated elect

283 some mice by addition of 2.5% dextran sodium sulfate to drinking water for 5-9 consecutive days.

284 nosinic:polycytidylic acid or dextran sodium sulfate to induce colitis.

285 its incorporation by microalgae as inorganic sulfate to its biosynthesis and exudation as DMSP, and f

286 A second reactor was fed ammonium sulfate to mimic breakdown products of SCN(-).

287 nitrite as alternative electron acceptors to sulfate to support growth.

288 p sulfate and ABA, stomatal conductance, and sulfate transporter (SULTR) expression.

289 Sulfate up-regulated the expression of NCED3, a key step

290 ty decreased from 501 to 389 mug/dL (ferrous sulfate) vs 506 to 417 mug/dL (iron complex) (a greater

291 Accumulation of heparan sulfate was also detected in primary cultures of cortica

292 n lyase; although its substrate, chondroitin sulfate, was previously thought to be an animal synapomo

293 h) and the bile acid taurolithocholic acid 3-sulfate were also analyzed.

294 Eight steroid bis-sulfates were synthesized in high purity in order to qua

295 isulfate 1 and 2, and dehydroepiandrosterone sulfate, were the next most strongly associated of the 2

296 c-S accumulation in response to supplemental sulfate, whereas Sarcocornia fruticosa (ecotype VM) does

297 ot significantly affected by 100-fold excess sulfate, which reduced selenate uptake by 100% in S. ela

298 toxins, namely, indoxyl sulfate and p-cresyl sulfate, while for weakly bound toxins, namely, indole-3

299 In particular, the selective binding of sulfate with artificial receptors is important because o

300 hanges coincide with accumulation of heparan sulfate with characteristic non-reducing ends, which is