ライフサイエンスコーパス: sulphate

1 mg and >100 mg equivalents of oral morphine sulphate).

2 premix composition (with or without ferrous sulphate).

3 robial reduction in a system impoverished in sulphate.

4 as the increase due to the presence of zinc sulphate.

5 nd timing of the administration of magnesium sulphate.

6 flowers were precipitated with 60% ammonium sulphate.

7 rin is often used as an analogue for heparan sulphate.

8 compared to the blank containing no ferrous sulphate.

9 olved in the lysosomal catabolism of heparan sulphate.

10 e ferrielectric phase transition in ammonium sulphate.

11 and 21,606 M(-1) cm(-1) for ammonium ferrous sulphate.

12 mer when the neighboring residues are highly sulphated.

13 oke is constrained by inhibitory chondroitin sulphates.

14 that has two distinct atmospheric secondary sulphates.

15 eenhouse pollutants-black carbon, ozone, and sulphates.

16 ra of barbel by precipitation using ammonium sulphate (0-80%), Sephadex G-100, and Mono Q-Sepharose i

17 ndomized to receive either 4930 mg magnesium sulphate (= 20 mmol magnesium) or placebo 60 min before

18 ups (n = 10/group) to receive either ferrous sulphate (200 mg capsules containing 65 mg of iron) or p

19 Sulphate (39-278 mg/L) and phosphate (51-428 mg/L) were

20 nd Sulf2 that code for extracellular heparan sulphate 6-0-endosulphatases.

21 nated by gypsum (36%), plagioclase (16%), Na sulphates (8%), and Fe-S-O phases (8%) in the PM(10-2.5)

22 he IEs to adhere specifically to chondroitin sulphate A (CSA) in the placenta.

23 high immunoglobulin G response to chondrotin sulphate A-binding infected erythrocytes, parasite lysat

24 H (P<0.05) and plasma Cmax of hydroxytyrosol sulphate, a metabolite of OOPC 2h postprandial (P=0.05).

25 translocate dicarboxylate, tricarboxylate or sulphate across cell membranes, typically by utilizing t

26 We find that seven eruption-related sulphate aerosol deposition events have occurred during

27 y driven by anthropogenic greenhouse gas and sulphate aerosol emissions.

28 This highlights the high sensitivity of sulphate aerosol geoengineering detectability to the cho

29 ring techniques affects the detectability of sulphate aerosol geoengineering in annual-mean global-me

30 This does not imply sulphate aerosol geoengineering should be deployed, but

31 Loadings of sulphate aerosol in the troposphere are thought to have

32 Sulphate aerosol injection has been widely discussed as

33 methyl sulphide (DMS), the primary source of sulphate aerosol over remote ocean regions, potentially

34 idized to sulphate and can subsequently form sulphate aerosol, which can affect the Earth's radiation

35 sphere and geo-engineering plans to increase sulphate aerosol; and fertilization of the ocean with bi

36 enario for the twenty-first century in which sulphate aerosols decline before atmospheric CO(2) is st

37 g due to a mid-twentieth century increase of sulphate aerosols in the troposphere, or changes in the

38 interactions and anthropogenic emissions of sulphate aerosols.

39 of supplemental iron above 1 microM ferrous sulphate, although addition of iron is not needed for pl

40 HT-sulphate and 3,4-dihydroxyphenylacetic acid (DOPAC)-sulp

41 M2), which binds polyanions, such as dextran sulphate and bacterial LPS, and activates downstream sig

42 ding extracellular glutamate (OAT4), estrone-sulphate and bromosulphothalein (both OAT4 and OATP2B1)

43 SO(2) is oxidized to sulphate and can subsequently form sulphate aerosol, whi

44 rexpressing full-length ADAMTS6 lack heparan sulphate and focal adhesions, whilst depletion of ADAMTS

45 Accordingly, heparan sulphate and heparin oligomers compete with TrkC for RPT

46 cing of Papss2 led to undersulphated heparan sulphate and increased PrP(C) deposition at the ECM, con

47 Dihydrocoumaric acid sulphate and p-coumaric acid were identified as metaboli

48 aire was most discriminatory between ferrous sulphate and placebo groups were: heartburn, abdominal p

49 action by addition of a mixture of magnesium sulphate and primary secondary amine sorbent.

50 rtitioning with addition of anhydrous sodium sulphate and sodium chloride, followed by dispersive SPE

51 n three phases comprising of water, ammonium sulphate and t-butanol, was explored for extraction of o

52 ions: chloride, phosphate, nitrate, nitrite, sulphate and the following organic acids: lactic, acetic

53 Reducing the levels of ferrous sulphate and xylenol orange in the FOX reagent enabled t

54 antioxidant and antibacterial activities of sulphated and crude polysaccharides were determined.

55 ed in the intestine and then in the liver to sulphated and glucuronidated forms that are exported to

56 d circulate in the organism as glucuronated, sulphated and methylated metabolites, displaying higher

57 iment and water, enriched with cellulose and sulphate, and allowed to develop over several months und

58 ry was transformed by delivery of oxygen and sulphate, and when a large part of Earth's ecology chang

59 cus thermophilus ASCC 1275 (ST1275 EPS) were sulphated, and antioxidant and antibacterial activities

60 h antibody contained the protruding tyrosine-sulphated, anionic antigen-binding loop (complementarity

61 it most from interventions such as magnesium sulphate, antihypertensives, or transportation to a high

62 olitis using the azoxymethane/dextran sodium sulphate (AOM/DSS) colitis-associated colon cancer model

63 because atmospheric black carbon, ozone, and sulphate are associated and could interact with related

64 LmPYK tetramer crystals grown with ammonium sulphate as precipitant adopt an active-like conformatio

65 content of standard hybrids due to enhanced sulphate assimilation and modifications in sulphur parti

66 buffer at pH 7.0 and 30 mM of sodium dodecyl sulphate at an applied voltage of 25 kV.

67 the administration of intravenous magnesium sulphate before and after ERCP reduces the incidence and

68 rritin synthesis in Caco-2 cells versus iron sulphate, beta-CN(1-25)4P being the most effective.

69 oscopy showed that nitration reduced heparan sulphate binding by CCL2.

70 Heparan sulphate binding is critical to neurite outgrowth, axon

71 hat is genetically controlled by the heparan sulphate biosynthetic pathway.

72 ample with 10 ml ethyl acetate (+10 g sodium sulphate) by homogenization at 15,000 rpm followed by ce

73 cherichia coli H7 flagella interacted with a sulphated carbohydrate (carrageenan) on a glycan array,

74 f the molecular (most commonly as sulphides, sulphates, carbonates, or oxides) form in which several

75 es act to post-synthetically remodel heparan sulphate chains, generating structural diversity of cell

76 Effects of sulphate, chloride, and thiocyanate salts on the heat-in

77 In the dextran sodium sulphate colitis model, PGE2, produced through cyclooxyg

78 to assess the effects of antenatal magnesium sulphate, compared with no magnesium treatment, given to

79 ) transcripts are consistent with pore-water sulphate concentration profiles.

80 y of gingerols and [6]-shogaol were ammonium sulphate concentration, ratio of t-butanol to slurry, so

81 was limited in the Precambrian period by low sulphate concentrations in sea water.

82 lactose and the gelling agent agar, with the sulphate content estimated as 51.01 mug/mg of polysaccha

83 nstrate that SLs, such as 8-deoxylactucin-15-sulphate, contribute most strongly to bitterness percept

84 rgely mitigated through microbially mediated sulphate-coupled methane oxidation, resulting in the pre

85 e extraction and purification of chondroitin sulphate (CS) from Prionace glauca head wastes.

86 lator controlling utilization of chondroitin sulphate (CS) in the mammalian gut symbiont Bacteroides

87 Here, we use the biopolymer chondroitin sulphate (CS), one of the major components of cartilage

88 ) and protic (DEAS = diethanolamine hydrogen sulphate; DEAP = diethanolamine hydrogen phosphate).

89 ial chemical adulterants, including ammonium sulphate, dicyandiamide, melamine, and urea, were mixed

90 based on in vivo modification with dimethyl sulphate (DMS), which reacts with unpaired adenine and c

91 , whilst 15-p-hydroxylphenylacetyllactucin-8-sulphate does not contribute to bitter taste.

92 y established rabbit model of dextran sodium sulphate (DSS) induced colitis to study the efficacy, me

93 disease activity elicited by dextran sodium sulphate (DSS) through the modulation of leukocyte and p

94 type (WT) mice in response to dextran sodium sulphate (DSS) treatment, which is associated with incre

95 tal murine colitis induced by dextran sodium sulphate (DSS), and their paternal transmission to offsp

96 ward trend in anthropogenic black carbon and sulphate emissions.

97 high-risk patients treated with vincristine sulphate, etoposide phosphate, and carboplatin (VEC).

98 e oxygen isotope measurements of atmospheric sulphate extracted from tuffaceous deposits to investiga

99 ly, the co-administration of GDP and ferrous sulphate (FeSO4) ameliorated the turpentine-induced AI i

100 dition of lithium acetate and Sodium dodecyl sulphate, followed by centrifugation and alcohol precipi

101 crude extract by precipitation with ammonium sulphate, followed by gel filtration chromatography.

102 t A complexes was carried out using ammonium sulphate for precipitation.

103 Crystal soaking in sulphate-free buffers was found to induce major conforma

104 hat the triple oxygen isotope composition of sulphate from ancient evaporites and barites shows varia

105 oitinase ABC effectively removed chondroitin sulphate from the extracellular matrix and perineuronal

106 oluble fibre, mainly formed by carrageenans, sulphated-galactans of red seaweeds.

107 Sulphated-galactans seemed to be related to the antioxid

108 actans, 3,6-anhydro-alpha-L-galactopyranose, sulphated galactose and the gelling agent agar, with the

109 was purified by fractionation with ammonium sulphate, gel filtration, affinity and ion exchange chro

110 Antenatal magnesium sulphate given prior to preterm birth for fetal neuropro

111 nzyme that predominantly cleaves chondroitin sulphate glycans.

112 Cartilage sulphated glycosaminoglycan (sGAG) and collagen content

113 ative backscattered electron microscopy, and sulphated glycosaminoglycan levels with alcian blue stai

114 Human heparanase degrades heparan sulphate glycosaminoglycans and is up-regulated in prote

115 ex matrix composed of protein fibrils, hyper-sulphated glycosaminoglycans and serum amyloid P compone

116 Amounts of sulphated glycosaminoglycans, MMPs and TIMPs were assess

117 toms reported by participants in the ferrous sulphate group (4.6 +/- 2.0) appeared higher than for pa

118 toms reported by participants in the ferrous sulphate group (mean +/- SEM = 6.7 +/- 1.7) was signific

119 an enzyme that specifically removes the 6-O sulphate group from glucosamine in highly sulfated regio

120 on i.e. variation in glycosidic linkages and sulphate group orientation.

121 ic bands in FT-IR spectra indicated that the sulphate group was at the C6 position of the galactose s

122 first week of the study were in the ferrous sulphate group.

123 g one or more symptom(s) were in the ferrous sulphate group.

124 These results support the case for zinc sulphate having a specific effect on the navigational ab

125 Post-synthetic remodelling of heparan sulphate (HS) by Sulf1 has been shown to modulate these

126 m and peri-glomerulus via binding to heparan sulphate (HS) chains of proteoglycans and co-associated

127 red basic mutations interacting with heparin sulphate (HS); this virus is attenuated in natural infec

128 ase causes lysosomal accumulation of heparan sulphate in microglial cells followed by their activatio

129 to milk or peptides compared to free ferrous sulphate in solution.

130 upplied as an aqueous solution of gentamicin sulphate in vials or ampoules and requires health care w

131 als that the observed, isotopically discrete sulphates in sediments can be produced only in initially

132 uction and the development of dextran sodium sulphate-induced colitis in ILC-deficient mice.

133 and Last Glacial NH eruptions, volcanogenic sulphate injections into the stratosphere cooled the NH

134 ut proteins with periodate amongst chloride, sulphate, iodide, phosphate, nitrate, nitrite, bromide,

135 tant adopt an active-like conformation, with sulphate ions at the active and effector sites.

136 ed at low pH in the presence of phosphate or sulphate ions.

137 Although sulphate is a cooling agent, black carbon and ozone coul

138 preserved in Martian meteoritic sulphide and sulphate is distinct from that observed in terrestrial a

139 If magnesium sulphate is found to be effective in preventing post-ERC

140 per limit for what is possible given in situ sulphate isotope data.

141 When coupled with observations and models of sulphate isotope dynamics and data-constrained model est

142 ter understand the physiological function of sulphated KPS, we isolated the sulphotransferase respons

143 which encodes an enzyme critical to heparan sulphate metabolism.

144 ing method, structure-seq, in which dimethyl sulphate methylation of unprotected adenines and cytosin

145 ilable for the effect of nebulised magnesium sulphate (MgSO(4)) in acute asthma in children.

146 suggested intravenous or nebulised magnesium sulphate (MgSO(4)) might improve respiratory function in

147 eroids (such as betamethasone) and magnesium sulphate (MgSO4) are administered to women in preterm la

148 sed in yeast mutants resistant to effects of sulphate-mimetics (like chromate or molybdate) on sulpha

149 tensively sampled ash beds display a similar sulphate mixing pattern that has two distinct atmospheri

150 ly reported the identification of an unusual sulphate-modified form of capsular polysaccharide (KPS)

151 between luteolin (L) and vanadium(IV) oxide sulphate monohydrate (VOSO4.H2O) was examined under UV-v

152 e system (ATPS) in combination with ammonium sulphate ((NH4)2SO4) precipitation was applied to fracti

153 detect the presence of phosphate compared to sulphate, nitrate and chloride.

154 The sulphates occupy positions similar to those of the phosp

155 utanol of 0.87 (v/v), saturation in ammonium sulphate of 49.46% (w/v) and a pH of 5.2.

156 The effects of vanadyl sulphate on the formation of acrylamide have been studie

157 eks' gestation) were randomised to magnesium sulphate or control treatment and where neurologic outco

158 s minimal rates of Cl(-) exchange for Cl(-), sulphate or formate, but rates of oxalate/Cl(-) exchange

159 reduction in GAG-side chains of chondroitin sulphate or heparan sulphate-PGs and 2.2-fold reduction

160 berately adulterated with melamine, ammonium sulphate or urea, which can be used to defraud milk prot

161 ation (MIC) for E. coli ATCC 25922, and both sulphated PEPS and sulphated ST1275 EPS had the lowest M

162 tested crude and sulphated polysaccharides, sulphated PEPS had the largest inhibition zone against E

163 Furthermore, sulphated PEPS had the lowest minimum inhibitory concent

164 de chains of chondroitin sulphate or heparan sulphate-PGs and 2.2-fold reduction in neurocan and brev

165 m citrate, potassium phosphate, and ammonium sulphate), pH, and NaCl, on the purification and selecti

166 anionic polysaccharides heparin and heparan sulphate play essential roles in the regulation of many

167 ht of 23 kDa as determined by sodium dodecyl sulphate-polyaccrylamide gel electrophoresis (SDS-PAGE).

168 roteins were characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE).

169 e fraction was carried out by sodium dodecyl sulphate polyacrylamide gel electrophoresis after pre-fr

170 f Fab to HRG was confirmed by sodium dodecyl sulphate polyacrylamide gel electrophoresis-Western blot

171 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) a

172 lterated samples by utilising sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) c

173 ic force microscopy (AFM) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) t

174 chromatography (SE-HPLC) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

175 f approximately 25 kDa on 12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis.

176 rigin of the sharp peaks to be due to sodium sulphate polymorphs.

177 ly important structural component in heparan sulphate polysaccharide for the biological functions.

178 Fucoidan is a sulphated polysaccharide that consists mainly of fucose,

179 ts and tocopherols in ethanolic extracts and sulphated polysaccharides, proteins or peptides in water

180 For tested crude and sulphated polysaccharides, sulphated PEPS had the larges

181 Using ammonium sulphate precipitation and affinity chromatography on pe

182 ail cardiac muscles, purified using ammonium sulphate precipitation and gel-filtration, and subjected

183 Following fractionation by using an ammonium sulphate precipitation method, three proteins (tropomyos

184 4.2-folds with 72.1% recovery using ammonium sulphate precipitation, gel filtration and ion exchange

185 Three-step purification - by ammonium sulphate precipitation, Sephadex G-100, and Q Sepharose

186 t, and chemical ligands such as pregnenolone sulphate (PregS) and CIM0216.

187 We propose that atmospheric secondary sulphate preserved in continental deposits represents an

188 molecule and melanoma-associated chondroitin sulphate proteoglycan and the tumor-initiating markers A

189 with nanomolar affinity to human chondroitin sulphate proteoglycan and with significantly weaker affi

190 city close, including changes in chondroitin sulphate proteoglycan core protein levels, changes in gl

191 The organization of chondroitin sulphate proteoglycan into perineuronal nets is therefor

192 the neurite outgrowth-inhibitory chondroitin sulphate proteoglycan NG2 was decreased in AAV-L1-treate

193 odomain shedding of the cell surface heparan sulphate proteoglycan syndecan-1 and elastin degradation

194 Syndecan-4 (Syn4) is a heparan sulphate proteoglycan that is able to bind to some growt

195 tion and the appearance of dense chondroitin sulphate proteoglycan-containing perineuronal nets aroun

196 , as well as parasite binding to chondroitin sulphate proteoglycan.

197 d that fixed negative charges on chondroitin sulphate proteoglycans (CSPGs) and other components of t

198 l cord injury, the expression of chondroitin sulphate proteoglycans (CSPGs) associated with the perin

199 an upregulation of glial-derived chondroitin sulphate proteoglycans (CSPGs) within the glial scar and

200 enetic studies have established that heparan sulphate proteoglycans (HSPGs) are required for signalli

201 ion of several growth inhibitory chondroitin sulphate proteoglycans and growth of adult sensory axons

202 nets, but the overall levels of chondroitin sulphate proteoglycans and their pattern of glycan sulph

203 paracrine regulator whose binding to heparan sulphate proteoglycans effectively precludes its circula

204 Chondroitin sulphate proteoglycans in the extracellular matrix restr

205 s type 1 and functions together with heparan sulphate proteoglycans to mediate adsorption to epitheli

206 ressing the levels of inhibitory chondroitin sulphate proteoglycans, decorin has the ability to suppr

207 quercetin 3-glucuronide (Q3G), quercetin 3'-sulphate (Q3'S) and isorhamnetin, followed by incubation

208 lated to anaerobic sulphur/iron reducers and sulphate reducers dominated libraries of expressed nifH

209 -) depletion because denitrifiers outcompete sulphate reducers.

210 Like other sulphate reducing bacteria, it can also protect itself a

211 Consortia of methane-oxidizing archaea and sulphate-reducing bacteria are a well-known environmenta

212 ociation, between methanotrophic archaea and sulphate-reducing bacteria, has been demonstrated in mar

213 ter prevented the proliferation of anaerobic sulphate-reducing bacteria, which were prevalent in the

214 anaerobic methanotrophic archaea (ANME) and sulphate-reducing bacteria.

215 phyla also contained distinct populations of sulphate-reducing bacteria.

216 niques, we validated the SahR regulon in the sulphate-reducing Deltaproteobacterium Desulfovibrio ala

217 favoured a 16S rRNA-phylotype related to the sulphate-reducing Desulfovibrio oxamicus DSM1925, wherea

218 d FloxABCD), was proposed to perform FBEB in sulphate-reducing organisms coupled with heterodisulfide

219 have formed within sediments where microbial sulphate reduction and methanogenesis converged.

220 hate reduction to a combination of bacterial sulphate reduction and sulphide oxidation, largely bacte

221 Here we provide a new constraint for OMZ sulphate reduction based on isotopic profiles of oxygen

222 acterial clade are deficient in assimilatory sulphate reduction genes.

223 The dissimilatory sulphate reduction pathway uses this molecule as the ter

224 f sulphite is a key intermediate step in all sulphate reduction pathways.

225 fter injection indicate consistent microbial sulphate reduction through the geological record.

226 ent the evolution from single-step bacterial sulphate reduction to a combination of bacterial sulphat

227 arine bacteria are known to use assimilatory sulphate reduction to supply sulphur for biosynthesis, a

228 Most AOM activity may have been coupled to sulphate reduction, but other electron acceptors remain

229 t followed initial cellulose degradation and sulphate reduction.

230 oduct of both assimilatory and dissimilatory sulphate reduction.

231 ensitive metals and the growth of the marine sulphate reservoir in response to a widely oxygenated oc

232 AMTS10 and ADAMTS6 oppositely affect heparan sulphate-rich interfaces including focal adhesions.

233 l that ADAMTS6 causes a reduction in heparan sulphate-rich interfaces, and its expression is regulate

234 bolism, we selected three metabolites RV 3-O-sulphate, RV 3-O-glucuronide and RV 4'-O-glucuronide, an

235 t microgels were smallest in the presence of sulphate salts and showed that added ions, particularly

236 and relatively decreased in the presence of sulphate salts, indicating that the inverse Hofmeister s

237 tio of crude extract/t-butanol, the ammonium sulphate saturation and pH) were used.

238 e(IV) ions in the presence of sodium dodecyl sulphate (SDS) and Ponpe 7.5.

239 Proteins were denatured by sodium dodecyl-sulphate (SDS) and precipitated as potassium salts.

240 between the ionic surfactant sodium dodecyl sulphate (SDS) and the phenolic acid salicylic acid have

241 Sodium dodecyl sulphate (SDS) enhanced PPO activity, with pulp showing

242 e electrokinetic injection of sodium dodecyl sulphate (SDS) including sample (-10 kV, 20 s) was intro

243 rk, the stabilising effect of sodium dodecyl sulphate (SDS) micelles on pH-induced colour variations

244 fiers, lecithin, Tween-20 and sodium dodecyl sulphate (SDS) were tested.

245 ved by adding a cosurfactant (sodium dodecyl sulphate (SDS)).

246 hod using anionic surfactant, sodium dodecyl sulphate (SDS), as template to control the size of synth

247 id medium, in the presence of sodium dodecyl sulphate (SDS), producing a yellow compound (lambdamax=4

248 or 0, 2.5 and 5 min) on total sodium dodecyl sulphate (SDS)-soluble and sarcoplasmic proteins in froz

249 idation (400muM) in Tween- or sodium dodecyl sulphate (SDS)-stabilised hexadecane emulsions.

250 ual health effects difficult at present, but sulphate seems to have the most robust effects in multip

251 Cleaving heparan sulphate side chains from the exosome surface had no imp

252 hemical parameters namely, chloride (Cl(-)), sulphate (SO(4)(2-)) and magnesium (Mg) content and two

253 ed by oral treatment for 4 days with dextran sulphate sodium (DSS) followed by continuous infusion of

254 We used dextran sulphate sodium (DSS) to induce colitis in C57BL/6 N mic

255 GG containing beads and treated with dextran sulphate sodium (DSS) to induce intestinal injury and co

256 Dextran sulphate sodium (DSS)-induced colitis leads to accumulat

257 IFN and increased susceptibility to dextran sulphate sodium-induced colitis and failed to mount a pr

258 olyte complex gel membrane made of cellulose sulphate, sodium alginate and poly(methylene-co-guanidin

259 , partitioning step by addition of magnesium sulphate, sodium carbonate and sodium chloride, and clea

260 chips were soaked in the respective vanadyl sulphate solution before frying.

261 waters were either made anosmic with 4% zinc sulphate solution, magnetically impaired by attachment o

262 2 and Staphylococcus aureus CMCC 26003 while sulphated ST1275 EPS had the largest inhibition zone aga

263 coli ATCC 25922, and both sulphated PEPS and sulphated ST1275 EPS had the lowest MICs on S. aureus CM

264 by apolipoprotein E4 includes sodium dodecyl sulphate-stable dimers and trimers.

265 various oxidized sulphur compounds including sulphate, sulphite and thiosulphate.

266 e-effects associated with oral iron (ferrous sulphate) supplementation, and would be appropriate for

267 investigation into how SO(2) is oxidized to sulphate-the oxidation product preserved in the rock rec

268 rmed at high concentrations of phosphate (or sulphate), they remain stable in solution at 20-fold low

269 uman heparanase specifically cleaved heparan sulphate: this caused no change in trans-endothelial ele

270 lphur ((33)S/(32)S, (34)S/(32)S) in seawater sulphate through oxygenated open-ocean and OMZ-bearing w

271 alcium chloride, calcium citrate and calcium sulphate to 100g of raw homogenates of spinach to determ

272 cterially mediated fractionation of seawater sulphate to sulphide of Delta(34)S < 25 per thousand bef

273 possibility that administration of magnesium sulphate to women in preterm labor may aid in primary pr

274 echanisms, aminoglycosides and inhibition of sulphate transport cause errors in mRNA translation.

275 ate-mimetics (like chromate or molybdate) on sulphate transport.

276 lycoside antibiotics combined with different sulphate-transport inhibitors produced strong, synergist

277 by regulating the activity of SypA, a STAS (sulphate transporter and anti-sigma antagonist) domain p

278 ide from the C terminus of CFTR, the SLC26A3 sulphate transporter and antisigma factor antagonist (ST

279 nsport and assimilation, and a high-affinity sulphate transporter and three ATP sulfurylases (ATPS) w

280 The SLC26/SulP (solute carrier/sulphate transporter) proteins are a ubiquitous superfam

281 cterial members are frequently classified as sulphate transporters based on their homology with SulP

282 on in the risk of death or CP with magnesium sulphate treatment compared with no treatment (RR 0.86,

283 rall, there was no clear effect of magnesium sulphate treatment compared with no treatment on the pri

284 For cerebral palsy in survivors, magnesium sulphate treatment had a strong protective effect in bot

285 irth, the gestational age at which magnesium sulphate treatment was given, the total dose received, o

286 iven, the gestational age at which magnesium sulphate treatment was received, or the dose and timing

287 nal outcome potentially related to magnesium sulphate treatment, no events were recorded from the 2 t

288 In addition, cyprinol sulphate uptake, mediated by the putative zebrafish homo

289 eclinical trials, degradation of chondroitin sulphate using chondroitinase ABC reactivated neuroplast

290 were soaked in 0.001, 0.01 and 0.1 M vanadyl sulphate (VOSO(4)) solutions, respectively, for 60 min b

291 rees C for 30 min in the presence of vanadyl sulphate (VOSO(4)).

292 e specific oxidation pathways from which the sulphate was formed.

293 Lysosomal accumulation of heparan sulphate was observed in hepatocytes, splenic sinus endo

294 Tetrabutylammonium hydrogen sulphate was used as the ion-pair reagent in the eluent

295 ogenic anaeorobic oxidation of methane using sulphate, was limited in the Precambrian period by low s

296 , DOPAC-glucuronide, HVA-glucuronide and HVA-sulphate were also detected.

297 e and 3,4-dihydroxyphenylacetic acid (DOPAC)-sulphate were the main metabolites, followed by DOPAC an

298 sol metabolite called hydroxytyrosol acetate sulphate, which was determined using tandem MS, after in

299 Impact of zinc sulphate (ZnSO(4)) and zinc chloride (ZnCl(2)) on heat-i

300 Impacts of zinc sulphate (ZnSO4) (0-140 mumol/kg) on gel properties of y