ライフサイエンスコーパス: sulfate

1 amino acids, vitamins, oxygen, nitrite, and sulfate.

2 einase, ADAM-10, in combination with heparan sulfate.

3 ral Salmonella Typhimurium or dextran sodium sulfate.

4 d binding was inhibited by competing dextran sulfate.

5 ydrogen sulfide (H(2)S), indole, and indoxyl sulfate.

6 the extracellular matrix component, heparan sulfate.

7 ddition of heparin, a GAG similar to heparan sulfate.

8 HS2ST1 mRNA and decreased or absent heparan sulfate 2-O-sulfotransferase 1 in two of three fibroblas

9 linker N, N'-bis (acryloyl) cystamine (BAC), sulfated 2-acrylamido-2-methyl-1-propanesulfonic acid (A

10 previously established collagen-chondroitin sulfate 3D scaffold.

11 e fluorogenic substrate 4-methylumbelliferyl sulfate (4-MUS) in a competition assay.

12 ulfoglycans containing sulfated-6-GlcNAc and sulfated-4-GalNAc residues.

13 ated and fucosylated sulfoglycans containing sulfated-6-GlcNAc and sulfated-4-GalNAc residues.

14 idinium (a destabilizing Hofmeister cation), sulfate (a stabilizing Hofmeister anion), and urea (a ne

15 AhR activation by indoxyl sulfate, a uremic toxin, leads to blood-brain barrier di

16 rc rocks have been attributed to significant sulfate addition by slab fluids.

17 Sulfate addition failed to increase Hg methylation rates

18 ington, USA), stimulated by both nitrate and sulfate addition.

19 c chemistry and a microphysical treatment of sulfate aerosol, used to assess the chemical and climate

20 This carbon, together with sulfate aerosols and dust, initiated an impact winter an

21 Atmospheric sulfate aerosols have important impacts on air quality,

22 The hgcAB(+) communities from higher sulfate amendments were less diverse and had relatively

23 y based on modifying the activity of heparan sulfate, an important regulator of a wide range of biolo

24 pike protein binding depends on both heparan sulfate and ACE2.

25 gomer length, and the number of incorporated sulfate and acetyl groups).

26 protein interacts with both cellular heparan sulfate and angiotensin-converting enzyme 2 (ACE2) throu

27 ts, represent the main source of chondroitin sulfate and are fundamental for the constitution of the

28 onding and interaction mechanisms between GR sulfate and As species [As(III) and As(V)] under anoxic

29 attice materials (composed of sodium dodecyl sulfate and beta-cyclodextrin) in a spatially resolved m

30 saminoglycans, including endothelial heparan sulfate and chondroitin sulfate E, but not with neutral

31 t and chemical agonists such as pregnenolone sulfate and CIM0216.

32 Heparan sulfate and heparin are highly acidic polysaccharides wi

33 Colistin sulfate and levofloxacin have a promising in vitro activ

34 Sulfate transporters and genes involved in sulfate and Met metabolism were upregulated, suggesting

35 and no pH differences were observed between sulfate and nitrate salts.

36 al site was frequently internally mixed with sulfate and nitrate, from multiphase chemical processing

37 ng and fuels AOM coupled to the reduction of sulfate and other electron acceptors.

38 , we determined the association between DHEA-sulfate and percentage predicted forced expiratory volum

39 A survey of salicin-7-sulfate and salirepin-7-sulfate in a subset of poplar (P

40 entified two sulfated salicinoids, salicin-7-sulfate and salirepin-7-sulfate, in black cottonwood (Po

41 convert salicin and salirepin into salicin-7-sulfate and salirepin-7-sulfate, respectively.

42 achment factors such as neuropilins, heparan sulfate and sialic acids and the putative alternative re

43 -based toolkit for the sequencing of heparan sulfate and structurally related biomolecules.

44 evels of its principal constituents, heparan sulfate and syndecan-1.

45 nated compounds were identified with dodecyl sulfate and tetradecyl sulfate the most abundant at 547.

46 rat gut model, we found intact, methylated, sulfated and both methylated and sulfated quercetin soph

47 Expanded searches also revealed many sulfated and complex glycans that remained hidden to the

48 sociated with higher levels of three steroid sulfates and co-localized with expression levels of SLC5

49 Here, we identify heparins/heparan sulfates and Lewis antigens as receptors for different T

50 l aerosol consisting of an Aitken (potassium sulfate) and accumulation mode (aged alpha-pinene SOA) p

51 ds pregnanolone (3alpha5betaP), 3alpha5betaP sulfate, and beta-estradiol.

52 S267X) with three substrates (TCA, estrone-3-sulfate, and rosuvastatin).

53 , including ones heavily modified by fucose, sulfate, and sialic acid residues.

54 lity to distinguish among PE, sodium dodecyl sulfate, and stearates.

55 phase transformation to an anhydrous calcium sulfate, anhydrite, which was formed via reprecipitation

56 is acutely stressed by azoxymethane/dextran sulfate (AOM/DSS) exposure, both Xist-deleted and wild-t

57 ution and relative abundances of cholesterol sulfate are reported and correlated with the healing tim

58 Heparan sulfates are structurally diverse sulfated polysaccharid

59 lutions were prepared by mixing 1 M ammonium sulfate (AS), ammonium nitrate (AN), sodium sulfate (SS)

60 These systems contain ammonium sulfate (AS)/nitrate (AN) and C3-C5 dicarboxylic acids,

61 ons of all genes involved in heparin/heparan sulfate assembly uncovered a transcription factor-bindin

62 Barium sulfate (BaSO(4)) was considered to be poorly-soluble an

63 Heparan sulfate belongs to the group of glycosaminoglycans (GAGs

64 mpeting" co-occurring oxo-anions (phosphate, sulfate, bicarbonate, silicate, and nitrate) were select

65 ial origin (aromatic compounds, secondary or sulfated bile acids, and benzoate) and estrogen metaboli

66 results hint at the presence of a secondary sulfate-binding pocket that could be exploited in the de

67 The identification of membrane heparan sulfate-binding proteins is challenging because of their

68 Docking studies suggest a heparin/heparan sulfate-binding site adjacent to the ACE2-binding site.

69 hough some distinct pathways such as heparan sulfate biosynthesis showed differences.

70 obiome-derived tryptophan metabolite indoxyl sulfate, both of which increased by PDX.

71 on into terrestrial pyrite oxidation-derived sulfate, but a mechanistic understanding of pyrite oxida

72 acid CIF peptide ligands, which are tyrosine sulfated by the tyrosylprotein sulfotransferase TPST/SGN

73 sulfonic acids and homologues of alkyl ether sulfates (C(8)- and C(10)/EO(n), C(8)H(17)(C(2)H(4)O)(n)

74 nd delta(36)S, and the (34)S-(18)O "clumped" sulfate can be quantified simultaneously.

75 anaerobic microorganisms that do not reduce sulfate can produce MeHg as effectively as communities d

76 came clear that stearates and sodium dodecyl sulfates can cause substantial overestimation of PE.

77 utic proteins were studied in sodium dodecyl sulfate capillary gel electrophoresis (SDS-CGE) in the i

78 FPX is a valid model for the highly sulfated cell signalling molecule heparan sulfate (HS).

79 od cells and binds to specific chondroitin-4-sulfate chains of the placental proteoglycan receptor.

80 to be associated with fatty acid phosphate, sulfate, chloride, and carboxylate ions.

81 phosphorus reservoir, associated with rising sulfate concentrations and increased remineralization of

82 e-rich diet, we found an increase in indoxyl sulfate concentrations in serum associated with a strong

83 The modeled dispersal and higher sulfate concentrations recorded in Antarctic ice cores i

84 AMD discharges offer generally high sulfate concentrations, especially from the bituminous c

85 ot detected in laboratory cultures with high sulfate concentrations, one may suppose that conditions

86 o the low residual levels of free HP and its sulfate conjugate.

87 ents in leaves and roots, but did not affect sulfate contents significantly.

88 g that neither flooding itself, nor seawater sulfate, contributed greatly to stomatal closure.

89 de, suggesting that 1 mug m(-3) reduction in sulfate corresponds with at least ~0.5 mug m(-3) reducti

90 C is a type I protein carrying a chondroitin sulfate (CS) attached to serine 44.

91 r, efficient assembly of various chondroitin sulfate (CS)-based photoaffinity probes was developed.

92 Sulfate, cysteine, and some sulfur-containing secondary

93 The geologic application of sulfate Delta'(17)O as a proxy for past [Formula: see te

94 Sulfate Delta'(17)O decreases significantly when moving

95 strain CVO oxidized S(0) to thiosulfate and sulfate, demonstrating that soxCDY(2) Z(2) H genes alone

96 ain of LRRTM4 was found to engage in heparan-sulfate dependent binding with pikachurin.

97 the form of methylated, glucuronidated, and sulfated derivatives (in total, 21 derivatives were iden

98 Dehydroepiandrosterone (DHEA) and its sulfate, DHEAS, are the major adrenal androgen precursor

99 Efficient sulfate diester formation was achieved through systemati

100 Our calculations suggest that sulfate diester hydrolysis proceeds through loose transi

101 s of a variety of complex molecules carrying sulfate diesters at various positions, including monosac

102 ity of adenine-N1 to methylation by dimethyl sulfate (DMS) when in an A-T Watson-Crick versus Hoogste

103 ized by the individual 1 cell line lacks 2-O-sulfated domains but had an increase in N- and 6-O-sulfa

104 ed domains but had an increase in N- and 6-O-sulfated domains demonstrating functional impairment of

105 g units were converted into soluble forms by sulfate-driven acid dissolution.

106 ally in mice with infectious, dextran sodium sulfate (DSS)-, and T-cell-induced colitis.

107 2 in colitis, we employed the dextran sodium sulfate (DSS)-induced acute colitis model in mice with (

108 endothelial heparan sulfate and chondroitin sulfate E, but not with neutral or sialylated oligosacch

109 of PM2.5 and its major components [nitrates, sulfates, elemental carbon (EC), and organic carbon (OC)

110 curring minerals (e.g., silicate, phosphate, sulfate) follows energy-intensive chemical routes.

111 bent assays (ELISAs) and depended on heparan sulfate for efficient cell binding and infection, we obs

112 ecosystems and facilitation of anthropogenic sulfate for monoterpenes SOA.

113 1 [1%] of 20 819) or intramuscular magnesium sulfate for pre-eclampsia (198 [1%]), of whom most accep

114 hermoproteaceae were briefly reported to use sulfate for respiration but we were unable to detect DSR

115 s mechanism could provide an explanation for sulfate formation under some winter haze conditions.

116 desulfurization process on TiO(2), in which sulfate forms as a stable surface product that is known

117 phS2, NaphS3 and NaphS6) were transferred to sulfate-free medium, they released 2-naphthoate and [5,6

118 iron in mineral and road dust combined with sulfate from coal-fired electrical generating units were

119 dity (RH) and fast production of particulate sulfate from the oxidation of sulfur dioxide (SO(2)) emi

120 Heparinase treatment, which digests anionic sulfated glycan polymers, before exposure rendered cells

121 Heparan sulfate (HS) is a sulfated glycosaminoglycan abundant on the cell surface

122 This interaction is blocked by heparin, a sulfated glycosaminoglycan.

123 of glycans, sialylated oligosaccharides and sulfated glycosaminoglycans (GAGs).

124 cell surface glycocalyx with upregulation of sulfated glycosaminoglycans and charged glycoproteins.

125 scent stains indicated that sialic acids and sulfated glycosaminoglycans were present in the anammox

126 ents of sialic acids and 2.4% equivalents of sulfated glycosaminoglycans).

127 anular sludge, focussing on sialic acids and sulfated glycosaminoglycans.

128 her validate that glycosaminoglycans but not sulfate groups are required for polyplex uptake and tran

129 rted onto the cell surface to liberate the 6-sulfate groups from the internal d-glucosamine residues

130 The importance of the sulfate groups was delineated by using desulfated analog

131 charides, notably including variants with 3O-sulfate groups.

132 izable syndrome and emphasize a role for 2-O-sulfated heparan sulfate in human neuronal, skeletal, an

133 eason lies in its ability to exploit heparan sulfate (HS) for attachment to cells.

134 Heparan sulfate (HS) is a sulfated glycosaminoglycan abundant on

135 mains of OPG is to bind cell surface heparan sulfate (HS), but the in vivo evidence was lacking.

136 IKV NS1 on expression and release of heparan sulfate (HS), hyaluronic acid (HA), and sialic acid on h

137 ude of cell-signaling events through heparan sulfate (HS)-protein interactions and are associated wit

138 iated by tau binding to cell surface heparan sulfate (HS).

139 ly sulfated cell signalling molecule heparan sulfate (HS).

140 y enriched in ADAM10-cleaved PrP and heparan sulfate (HS).

141 sion express Ndst1, a key enzyme for heparan sulfates (HS) synthesis.

142 survey of salicin-7-sulfate and salirepin-7-sulfate in a subset of poplar (Populus sp.) and willow (

143 R(-/-) knockout mice overloaded with indoxyl sulfate in drinking water.

144 ns directly bound to heparin and chondroitin sulfate in enzyme-linked immunosorbent assays (ELISAs) a

145 sulfate was likably interpreted as inorganic sulfate in field measurements using advanced instruments

146 , is a plausible contributor to the elevated sulfate in Greenland.

147 Sulfate in high-elevation headwaters is quantitatively s

148 nd emphasize a role for 2-O-sulfated heparan sulfate in human neuronal, skeletal, and renal developme

149 As human trypsins are post-translationally sulfated in the autolysis loop, we also assessed the eff

150 Greater deviations were observed for steroid sulfates in complex urine samples of adult bovines, show

151 licinoids, salicin-7-sulfate and salirepin-7-sulfate, in black cottonwood (Populus trichocarpa).

152 the increased transformation of organic S to sulfate indicates that the microbial activity in this zo

153 knockout mice were protected against indoxyl sulfate-induced blood-brain barrier disruption and cogni

154 ial cell-derived IL-33 during dextran sodium sulfate-induced colitis.

155 The putative uremic toxin indoxyl sulfate induces oxidative stress and dramatically alters

156 DHEA-sulfate is associated with FEV(1)PP and is suppressed wi

157 For example, less than 1 nmol sulfate is required to determine (18)O/(34)S ratios with

158 Indoxyl sulfate (IS) is one of the most potent uremic toxins.

159 r lake that were experimentally amended with sulfate levels from 7 to 300 mg L(-1).

160 M. pneumoniae also bound lactose 3'-sulfate ligated to an inert polymer scaffold, and bindin

161 truction of electron flow and energy gain by sulfate limitation offers an explanation for the occurre

162 ppose that conditions in reservoirs, such as sulfate limitation, trigger metabolite release.

163 e group of glycosaminoglycans (GAGs), highly sulfated linear polysaccharides.

164 characterized by soot internally mixed with sulfate (matching diesel soot) and organic carbon partic

165 profiles revealed decreases in acetaminophen-sulfate metabolite levels in both the amoxicillin and am

166 is (MOG) primarily occur at the depth of the sulfate-methane transition zone or underlying sediment r

167 nstrate a novel regulatory factor in heparan sulfate modification that could further advance the poss

168 As heparan sulfate modulates FGF-mediated signaling, we found a sig

169 fied by different patterns of N-acetyl and N-sulfate moieties.

170 reverse transcription of long RNAs, dimethyl sulfate mutational profiling (DMS-MaP), selective 2'-hyd

171 We additionally performed dimethyl sulfate mutational profiling with sequencing (DMS-MaPseq

172 Here we use dimethyl sulfate mutational profiling with sequencing (DMS-MaPseq

173 The stable isotopes of sulfate, nitrate, and phosphate are frequently used to s

174 tracer ratios to provide new perspectives on sulfate, NO(x,) and particle acidity influencing isopren

175 M. pneumoniae recognizes sialylated and sulfated oligosaccharide receptors to colonize the respi

176 dology that can provide libraries of heparan sulfate oligosaccharides that have glucosamine residues

177 First, we used short heparan sulfate oligosaccharides to remove lipoproteins already

178 after in-community treatment with magnesium sulfate or during transport to facility.

179 atively modulated by 5beta-reduced steroids, sulfated or carboxylated steroids, and beta-estradiol, w

180 s were anionic, carrying either sialic acid, sulfate, or phosphate residues.

181 glyoxal and pinanediol by neutral and acidic sulfate particles is investigated.

182 Raman sulfate peak (~980 cm(-1)) intensity measurements and su

183 lude an endogenous neurosteroid pregnenolone sulfate (PES), but the binding site of PES on the NMDAR

184 as cholesterol and neurosteroid pregnenolone sulfate (PES).

185 We found that versican, a large chondroitin sulfate PG, promotes collagen fibrillogenesis in a turbi

186 infection with SBV, confirming that heparan sulfate plays an important role in cell attachment and e

187 homogeneity was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) an

188 Heparan sulfates are structurally diverse sulfated polysaccharides that reside at the surface of a

189 nds including dimethylsulfoniopropionate and sulfated polysaccharides.

190 nt heparin, heparin lyases, and lung heparan sulfate potently block spike protein binding and/or infe

191 5%) was obtained by the isoelectric-ammonium sulfate precipitation method.

192 Sulfate produced both the highly acidic aerosol (summer

193 nsport biogeochemical modelling of porewater sulfate profiles.

194 o paves the way for economical production of sulfated proteins as therapeutic agents in mammalian sys

195 d that Windpipe (Wdp) is a novel chondroitin sulfate proteoglycan (CSPG) in Drosophila.

196 that SLC35B2, as a key regulator of heparan sulfate proteoglycan (HSPG) biosynthesis, is essential f

197 Sulf-1 and Sulf-2) are extracellular heparan sulfate proteoglycan (HSPG)-specific 6-O-endosulfatases,

198 llin, the C-terminal fragment of the heparan sulfate proteoglycan perlecan, influences various signal

199 ellular matrix structure rich in chondroitin sulfate proteoglycans (CSPGs), which preferentially enca

200 s extracellularly and interacts with heparan sulfate proteoglycans (HSPG).

201 We now show that heparan sulfate proteoglycans (HSPGs) act as alternative co-rece

202 Glycosaminoglycan chains of keratan sulfate proteoglycans appear to be physiologically signi

203 ymers and negatively charged NG2 chondroitin sulfate proteoglycans of the SVZ extracellular matrix.

204 Heparan sulfate proteoglycans take part in crucial events of can

205 he cell surface level via binding to heparan sulfate proteoglycans, such as syndecans.

206 by the endogenous neurosteroid pregnenolone sulfate (PS) and heat, and altered response to ligand mo

207 methylated, sulfated and both methylated and sulfated quercetin sophoroside in the plasma following j

208 lglucoside, epicatechin, 8-hydroxyluteolin 8-sulfate, quercetin 3-(2''-galloyl-alpha-l-arabinopyranos

209 oxidation with hydroxyl radical (HO(*)) and sulfate radical (SO(4)(*-)) is often used to treat water

210 ate (PS) is a common method used to generate sulfate radicals (SO(4)(*-)), a powerful oxidant capable

211 Transformation of SMX was observed in both sulfate-reducing and methanogenic cultures, whereas nitr

212 Sulfate-reducing bacteria (SRB) are present in both type

213 th nano-porous sulfides (pyrite) produced by sulfate-reducing bacteria grown in the lab in the presen

214 We identified hgcA+ genomes derived from sulfate-reducing bacteria, but these accounted for only

215 d increased remineralization of organic P by sulfate-reducing bacteria.

216 in most cases form syntrophic consortia with sulfate-reducing bacteria.

217 The transformation products in sulfate-reducing cultures were identified as the reduced

218 In sulfate-reducing cultures, up to 90% of an initial SMX c

219 Indeed, if naphthalene-grown cells of marine sulfate-reducing Deltaproteobacteria (strains NaphS2, Na

220 e associated with clades of Methanomicrobia, sulfate-reducing Deltaproteobacteria, Spirochaetes, and

221 g as effectively as communities dominated by sulfate-reducing populations.

222 ectron acceptors important to support AOM in sulfate-reducing sediment.

223 e the presence of a cryptic methane cycle in sulfate-reducing sediments from the continental shelf of

224 Methanogenesis can also occur in the sulfate-reducing sediments through the utilization of no

225 Here, we show that cryptic microbial sulfate reduction occurs in sinking particles from the e

226 addition, higher potential rates of AOM than sulfate reduction rates at in situ methane conditions we

227 Cooling the sediments induced sulfate reduction, coinciding with an enrichment of endo

228 analyses reveal a complex network involving sulfate reduction, sulfide oxidation and thiosulfate rea

229 Fe-Mn- and sulfate-reduction and cation-exchange processes may mobi

230 onfidence interval (CI): 5.703, 7.667] fewer sulfate-related CV deaths per 100,000 people.

231 is of complex bioactive molecules carrying O-sulfates remains challenging.

232 repin into salicin-7-sulfate and salirepin-7-sulfate, respectively.

233 ene-derived metabolites was also achieved in sulfate-rich medium upon addition of the protonophore ca

234 d-type and SOT1 knockdown trees suggest that sulfated salicinoids do not affect the feeding preferenc

235 x canescens) resulted in decreased levels of sulfated salicinoids in comparison to wild-type plants,

236 lar Lymantria dispar A potential role of the sulfated salicinoids in sulfur storage and homeostasis i

237 We identified two sulfated salicinoids, salicin-7-sulfate and salirepin-7-

238 samples, and X-ray results did not show any sulfate salt peaks.

239 organic carbon particles containing aminium sulfate salts.

240 tants: Tween 80, Triton X100, Sodium Dodecyl Sulfate (SDS) and Quillaja Saponin was evaluated against

241 fically, the intercalation of sodium dodecyl sulfate (SDS) bilayers in a PEM comprising poly(diallyld

242 Extensive use of Sodium Dodecyl Sulfate (SDS) in households, agricultural operations, an

243 ated, including the amount of sodium dodecyl sulfate (SDS), ethanol, and ionic strength in the releas

244 ohexanesulfonic acid (PFHxS); sodium dodecyl sulfate (SDS); and sodium tetradecyl sulfate (TDS).

245 Besides fluoride and sulfate, short-chain perfluorinated carboxylic acids (PF

246 n is characterized by diminished cholesterol sulfate signal along the stratum corneum toward the migr

247 reduced, S is increasingly transformed into sulfate (SO(4) (2-) ) and phosphorus (P) is increasingly

248 tributed by biomass pyrolysis, while abiotic sulfate (SO(4) (2-)) reduction produces large depletions

249 a (photo)degradation product of cysteine, to sulfate (SO(4)(2-)).

250 or colon permeability is shown using dextran sulfate sodium (DSS) and anti-CD40 murine colitis models

251 r and that Mn deficiency exacerbates dextran sulfate sodium (DSS)-induced colitis in mice.

252 In this study, using a dextran sulfate sodium (DSS)-induced colitis model in mice, we f

253 R(-/-) mice were more susceptible to dextran sulfate sodium (DSS)-induced colitis, manifested by incr

254 ed release compared to free 6-S in a dextran sulfate sodium (DSS)-induced mouse model of colitis.

255 is induced by oral administration of dextran sulfate sodium (DSS).

256 ulcerative colitis in response to 1% dextran sulfate sodium (DSS).

257 the VDR(DeltaPC) less vulnerable to dextran sulfate sodium colitis, suggesting the transmission of p

258 otected mice from colitis induced by dextran sulfate sodium in an inflammasome-dependent manner.

259 ental colitis was induced in mice by dextran sulfate sodium salt.

260 fail to recover from and succumb to dextran sulfate sodium-induced colitis due to prolonged intestin

261 d colonic wounding and recovery from dextran sulfate sodium-induced colitis.

262 7BL/6 mice treated with azoxymethane-dextran sulfate sodium.

263 r5(ISC-/-) mice by administration of dextran sulfate sodium; disease severity was determined based on

264 of these tracers correlated with particulate sulfate spanning three orders of magnitude, suggesting t

265 sulfate (AS), ammonium nitrate (AN), sodium sulfate (SS), or sodium nitrate (SN) solutions with 1 M

266 tra of a systematic set of synthetic heparan sulfate stereoisomers were recorded in the fingerprint r

267 nternal d-glucosamine residues in the highly sulfated subdomains of HSPGs.

268 -) into the ettringite crystal structure via sulfate substitution when synthesized by aqueous precipi

269 each accommodate the 12-mer of chondroitin-4-sulfate, suggesting a model for receptor binding.

270 A syndrome caused by N-acetylgalactosamine-6-sulfate sulfatase (GALNS) deficiency.

271 e dominated by borates, sodium, thiosulfate, sulfate, sulfite, sulfide, bicarbonate, and other macrom

272 ut their responses to changes in methane and sulfate supplies remain poorly constrained.

273 Our data demonstrate that a heparan sulfate synthesis deficit causes a recognizable syndrome

274 The heparan sulfate synthesized by the individual 1 cell line lacks

275 dodecyl sulfate (SDS); and sodium tetradecyl sulfate (TDS).

276 d consumes [Formula: see text] and generates sulfate that is carried to the ocean by rivers.

277 entified with dodecyl sulfate and tetradecyl sulfate the most abundant at 547.8 and 496.4 mg/L, respe

278 synthesis are identical to those for heparan sulfate, the factors regulating these enzymes are not un

279 an enzyme which catalyzes the conversion of sulfate to adenosine 5'-phosphosulfate (APS), plays a si

280 easured; some mice were given dextran sodium sulfate to induce colitis and/or gavage with an antagoni

281 (control) diet and then given dextran sodium sulfate to induce colitis; we also studied Il10(-/-) mic

282 that slab-derived fluids provide negligible sulfate to oxidize the sub-arc mantle and cannot deliver

283 When we added indoxyl sulfate to the drinking water of rats fed an adenine-ric

284 High-affinity binding of heparin/heparan sulfate to the Ig-like domain may proceed from surface c

285 h as a strongly altered delivery of iron and sulfate to the ocean, or major shifts in marine producti

286 i.e., carbonate, chloride, phosphate [P], or sulfate) to convert native Pb species to PLJ and used a

287 Sulfate transporters and genes involved in sulfate and M

288 l protein sulfotransferase 1, we installed O-sulfated tyrosine in CDR H3 of both bNAbs.

289 t-translational modification (PTM), namely O-sulfated tyrosine in the heavy chain complementarity det

290 Homogenously sulfated variants of the proteins were efficiently assem

291 In contrast, tyrosine sulfated versions displayed equivalent neutralising acti

292 o the mammalian cell produced bNAbs, but non-sulfated versions showed loss of neutralisation breadth

293 emission regions that preindustrial aerosol sulfate was almost exclusively isoprene-derived organosu

294 entry, although to various degrees, heparan sulfate was also found to be important to initiate infec

295 Recent studies showed that organic sulfate was likably interpreted as inorganic sulfate in

296 : soxXY(1) Z(1) AB and soxCDY(2) Z(2) H, and sulfate was the sole metabolic end product.

297 rometer and the major contributor to organic sulfate was thought to be hydroxymethanesulfonate (HMS).

298 nt with its role in the synthesis of heparan sulfate, we show that this activity is required for effi

299 Sodium dodecyl sulfate, which is commonly applied in microplastic resea

300 utes-kynurenic acid, pyridoxic acid, indoxyl sulfate, xanthosine, isovalerylglycine, and cinnamoylgly