ライフサイエンスコーパス: oligosaccharide

1 lack of GlcpN residues in the defective core oligosaccharide.

2 syndrome do not have detectable IgG4 to the oligosaccharide.

3 ed to a lipid anchor through a conserved Kdo oligosaccharide.

4 relied on multivalent ligation of BCR sialyl-oligosaccharide.

5 ur dp6 isomers, and the observation of a dp3 oligosaccharide.

6 in both species, resulting in a shorter core oligosaccharide.

7 he synthesis of a library of 15 different CS oligosaccharides.

8 long, branched mannose and glucose types of oligosaccharides.

9 le receptors for a wide variety of mono- and oligosaccharides.

10 r the formation of dolichol-linked precursor oligosaccharides.

11 , LPS, fibronectin fragments, and hyaluronan oligosaccharides.

12 -acetamido-2-deoxyfucose (FucNAc) containing oligosaccharides.

13 tial in binding sucrose and beta(2-1)-linked oligosaccharides.

14 cificities of these proteins for ganglioside oligosaccharides.

15 alpha1-2, alpha1-3 and alpha1-4 fucosylated oligosaccharides.

16 n family harbors oxidases tuned for specific oligosaccharides.

17 rapidly provide a library of well-defined HS oligosaccharides.

18 ly of both heparin- and heparan sulfate-like oligosaccharides.

19 g thermodynamic preference relative to chito-oligosaccharides.

20 ential catalyst for the synthesis of various oligosaccharides.

21 sitivity to separate mixtures of digested HS oligosaccharides.

22 ind the progress in the synthesis of complex oligosaccharides.

23 LPG is capped by various oligosaccharides.

24 in degrading beechwood xylan to produce xylo-oligosaccharides.

25 olysis of flavonol beta-glucosides and cello-oligosaccharides.

26 insoluble plant polysaccharides and soluble oligosaccharides.

27 sizes and prebiotic functions of human milk oligosaccharides.

28 e this insoluble polymer into soluble chitin oligosaccharides.

29 Cyclic oligosaccharide 2-hydroxypropyl-beta-cyclodextrin (BCD)

30 three glycoside-hydrolases specific for xylo-oligosaccharides, a SusC/SusD tandem homolog and a MFS t

31 and in a ternary complex with GDP and a xylo-oligosaccharide acceptor (named XLLG).

32 limination of HCs from pathological HA by HA oligosaccharide administration would restore OPC maturat

33 nd molecular dynamics, reveal a diversity in oligosaccharide affinity and a requirement for accommoda

34 of human histo-blood group antigens and milk oligosaccharides, against an N-terminal fragment of the

35 aluate the isomeric heterogeneity of neutral oligosaccharide-alditols isolated from bovine submaxilla

36 ent, were examined and compared for selected oligosaccharide-alditols.

37 Pectic oligosaccharides also enhanced lactobacilli growth durin

38 ion to serving as a nutrient, chitin-derived oligosaccharides also induce natural genetic competence

39 These oligosaccharides also serve as an inducing cue for natur

40 e first sequencing of complex mixtures of HS oligosaccharides, an essential milestone in the analysis

41 We illustrate how stable, synthetic oligosaccharide analogs of labile CPS induce a specific

42 ates containing stable, monovalent synthetic oligosaccharide analogs of ST-5 CPS RU induced long-term

43 of a complex synthetic heparan sulfate (HS) oligosaccharide and biotin.

44 dy the in vitro modulating effects of fructo-oligosaccharide and five different monosaccharides on th

45 he apo-form and in complex with (xylo)glucan oligosaccharides and an active-site affinity label, toge

46 nd indicated a positive relationship between oligosaccharides and astringency.

47 cular interaction occurring between isomalto-oligosaccharides and domain V of the GH70 enzymes.

48 glycobiology, efficient synthesis methods of oligosaccharides and glycoconjugates are a requisite.

49 cids modification for the analysis of sialyl oligosaccharides and glycopeptides.

50 Three variable models built with A230, oligosaccharides and polysaccharides presented high R(2)

51 analysis (enological analysis, polyphenols, oligosaccharides and polysaccharides).

52 are categorized as monosaccharides (sugars), oligosaccharides and polysaccharides.

53 ynthetic access to extended fragments of K30 oligosaccharides and polysaccharides.

54 acterization of plant polysaccharide-derived oligosaccharides and their attachment to hydrophobic sel

55 ty to generate galacto- and galacto(arabino) oligosaccharides and their corresponding oligomers from

56 sing the xylan backbone for cleavage to xylo-oligosaccharides and xylose.

57 The recent applications of sugar (mono/oligosaccharides and/or polysaccharides) for the develop

58 e deoxystreptamine ring of the parent pseudo-oligosaccharide antibiotic.

59 Moreover, chemical approaches to synthesize oligosaccharide antigens have proven challenging.

60 llmark of many cancers, and tumor-associated oligosaccharides are actively investigated as targets fo

61 or the pathogenicity of S. scabies and cello-oligosaccharides are environmental triggers that induce

62 Galactomanno-oligosaccharides are further processed in the periplasm,

63 Mannose-6-phosphate (M6P)-terminated oligosaccharides are important signals for M6P-receptor-

64 How cello-oligosaccharides are sensed or transported in order to i

65 ynthetic precursors, the resulting microbial oligosaccharides are subjected to a greatly simplified p

66 Here we describe the synthesis of seven oligosaccharides as the minimal structures featuring all

67 glycoproteins by binding to Glc1Man9GlcNAc2 oligosaccharides as well as to the polypeptide chain.

68 centage of initial sucrose converted to each oligosaccharide, as monitored by HPLC.

69 Although the lectin-oligosaccharide association is well understood, the poly

70 howed that it produced arabinose substituted oligosaccharides (AXOS) having 2-10 xylose residues in t

71 e antioxidant capacity (AOC) of arabinoxylan oligosaccharides (AXOS) obtained from wheat aleurone was

72 itopes from parotid gland N-glycans and milk oligosaccharides based on fucosylated fragment ions with

73 tains an N-terminal globular oligonucleotide/oligosaccharide binding fold (OB-fold) and an intrinsica

74 strand telomeric DNA via two oligonucleotide/oligosaccharide binding folds (OB-folds).

75 Oligonucleotide/oligosaccharide-binding (OB) domain-containing proteins

76 tion between the ZnF and the oligonucleotide/oligosaccharide-binding domain, one of three domains con

77 nd the phosphodiesterase and oligonucleotide/oligosaccharide-binding domains of p59.

78 e structural features revealed it to have an oligosaccharide-binding protein fold, indicating that du

79 and an unexplained observation of synthetic oligosaccharide blocking of TV binding has been reported

80 eletion ofB. melitensis wadCremoves the core oligosaccharide branch not linked to the O-antigen causi

81 tractive technique for the rapid assembly of oligosaccharides, built up of repetitive elements.

82 tly more active than the Cel3B enzyme on the oligosaccharides but not disaccharides.

83 undant building block in naturally occurring oligosaccharides, but its incorporation by chemical glyc

84 s been shown to effectively resolve isobaric oligosaccharides, but the utility of IMS to obtain glyca

85 r patterns from the perception of lipochitin oligosaccharide by the LjNFR1/MtLYK3 and LjNFR5/MtNFP re

86 intracellularly and depends on the import of oligosaccharides by an outer membrane protein complex co

87 ion to consolidate peaks of the same type of oligosaccharides by removing heterogeneity and thus incr

88 t a role in the degradation of xylan-derived oligosaccharides by the fungus M. thermophila C1.

89 Detection and quantitation of low abundance oligosaccharides can also be achieved using a combinatio

90 Fortunately, structurally defined oligosaccharides can be used as models for the glycans,

91 of a backbone of sphingoid base and a polar oligosaccharide chain containing at least one sialic aci

92 and composition of their aglycone moiety and oligosaccharide chains.

93 nting IalphaI heavy chain (HC) transfer), HA-oligosaccharides, cobalt, or Si bikunin prevented TSG-6

94 July to October) produced significantly less oligosaccharides compared to those nursing in the dry se

95 re of N-glycans significantly simplifies the oligosaccharide component enabling facile distinction of

96 ructo-oligosaccharides (FOS) are mixtures of oligosaccharides composed of fructose and glucose units.

97 Bacterial glycoproteins and oligosaccharides contain several rare deoxy amino l-suga

98 se, and their combination on microstructure, oligosaccharide content, crystalline order, pasting, gel

99 nd valency of the M6P moieties and the right oligosaccharide context are all critical for high-affini

100 pseudotuberculosis and Y. pestis produce an oligosaccharide core with a single O-antigen unit attach

101 Additionally, a four residue-long oligosaccharide could also be recognized by HS20 if an a

102 e number of carbohydrates, several mono- and oligosaccharides could be identified as substrates.

103 These oligosaccharides decreased from early lactation to almos

104 electivities for both anomers with mono- and oligosaccharides, deoxysugars, saccharides with free hyd

105 The sulfated GAG oligosaccharides derived from cartilage possessed the gr

106 Oligosaccharides differed between farming systems, with

107 Foods high in fermentable oligosaccharides, disaccharides, monosaccharides, and po

108 different peptide acceptor and lipid-linked oligosaccharide donor specificities, and trypanosomes do

109 plied to de novo sequencing of underivatized oligosaccharides.Establishing generic carbohydrate seque

110 th a mammalian-type high-mannose Man9GlcNAc2 oligosaccharide exhibited interaction with Manalpha1-2Ma

111 achinery are regulated by glycosylation, and oligosaccharide exposure in the cytosol triggers an auto

112 out the milking season and analysed for free oligosaccharides, fatty acids, major casein and whey pro

113 Vegetable/fruit juices provide polyphenols, oligosaccharides, fiber and nitrate (beet juice), which

114 ed motif located between the oligonucleotide/oligosaccharide fold (OB-fold) and A subdomain of Mcm2.

115 merizes large polysaccharide chains to small oligosaccharides followed by fast liquid chromatography

116 ration or late-stage modification of complex oligosaccharides for applications in glycobiology resear

117 m, and chemical synthesis of well-defined HS oligosaccharides for structure-activity relationship stu

118 he majority of polysaccharide hydrolysis and oligosaccharide formation occurred during enzymatic trea

119 t microbiome with prebiotics, such as fructo-oligosaccharides (FOS) and galacto-oligosaccharides (GOS

120 Fructo-oligosaccharides (FOS) are mixtures of oligosaccharides

121 Fructan-type inulin and fructo-oligosaccharides (FOS) are reserve polysaccharides that

122 biotic cranberry juice fortified with fructo-oligosaccharides (FOS).

123 egume roots respond to chitin and lipochitin oligosaccharides found in the heterogeneous mixture of c

124 moenzymatic approach for generating tailored oligosaccharide fractions ready for activation and coupl

125 Pure synthetic oligosaccharide fragments found in the side chains and b

126 ailed summaries of the chemical syntheses of oligosaccharide fragments of cellulose, hemicellulose, p

127 de galactomannan, producing comparably large oligosaccharide fragments.

128 olamine and sialic acid substitutions on the oligosaccharide from invasive compared with carrier isol

129 glycosylation, and an iterative synthesis of oligosaccharides from benchtop stable anomeric ester bui

130 es cerevisiae glycoproteins and lipid-linked oligosaccharides from glycoengineered Escherichia coli.

131 In conclusion, neutral poly- and oligosaccharides from H. suaveolens have a prebiotic pot

132 he results presented herein demonstrate that oligosaccharides from lactulose can be used as prebiotic

133 tible dietary galacto- and gluco-alpha-(1,6)-oligosaccharides from legumes and starch, respectively,

134 zymes generate aldonic acid-terminated malto-oligosaccharides from retrograded starch and boost signi

135 d complete de-esterification of arabinoxylan oligosaccharides from wheat bran.

136 um, characterized by specific and recognized oligosaccharides, from as little as 0.1 mug of material.

137 Depolymerisation of GAG polysaccharides to oligosaccharides further improved ferritin formation by

138 Notably, both branches of the oligosaccharide GD1a can associate to botulinum neurotox

139 dhD-wzz O-antigen gene cluster, but not core oligosaccharide genes, was reduced in DeltarfaH mutants.

140 , with MOGS-CDG and biallelic MOGS (mannosyl-oligosaccharide glucosidase) mutations (GenBank: NM_0063

141 nd derivatives; fatty acids and derivatives; oligosaccharides; glycerolipids; purines; and retinoids.

142 in both form and function ranging from free oligosaccharides, glycoproteins, and proteoglycans, to g

143 Alginate-derived guluronate oligosaccharide (GOS) readily activates macrophages.

144 term effects of supplementation with galacto-oligosaccharides (GOS), an acetogenic fiber, on the comp

145 as fructo-oligosaccharides (FOS) and galacto-oligosaccharides (GOS), is an appealing but underinvesti

146 containing FeFum+NaFeEDTA and 7.5 g galacto-oligosaccharides (GOSs) (Fe+GOS group, n = 22) or the sa

147 c monoclonal antibodies (mAbs) for which the oligosaccharides have been remodelled to optimise effect

148 rometry (IM-MS) showed that the two isolated oligosaccharides have different conformations and both d

149 been linked to the utilization of human milk oligosaccharides (HMO).

150 due to its large concentration of human milk oligosaccharides (HMO).

151 The prebiotic nature of human milk oligosaccharides (HMOs) and increasing evidence of direc

152 identifying interactions between human milk oligosaccharides (HMOs) and their protein receptors.

153 Human milk oligosaccharides (HMOs) are a family of diverse unconjug

154 differences in the composition of human milk oligosaccharides (HMOs) correlate with infant growth and

155 The affinities of thirty-two free human milk oligosaccharides (HMOs) for four human galectin proteins

156 Analysis of human milk oligosaccharides (HMOs) from 6-month-postpartum mothers

157 Human milk oligosaccharides (HMOs) have important nutritional and b

158 Human milk oligosaccharides (HMOs) play an important role in the he

159 of 60 asymmetric, multiantennary human milk oligosaccharides (HMOs), which were used to develop a gl

160 plex carbohydrates referred to as human milk oligosaccharides (HMOs).

161 YKL-40 has been shown to bind chito-oligosaccharides; however, the production of chitin by t

162 sibility of polysaccharides, including cello-oligosaccharides, hyaluronan, heparan sulfate, heparin,

163 erine protease inhibitor blocked peptide and oligosaccharide hydrolysis by 18B7, and a putative serin

164 Both Hep and HS oligosaccharides imported into the periplasm were degrad

165 ovides a bridge between lipid A and the core oligosaccharide in all bacterial LPSs, whereas an oligos

166 d, unexplained increase in TV replication by oligosaccharide in cell-based blocking assays has been c

167 stand the behavior of the flatulence-causing oligosaccharides in cowpea seeds during isothermal water

168 er, these studies define a role for N-linked oligosaccharides in supporting the stability and functio

169 Maturation of Asn-linked oligosaccharides in the eukaryotic secretory pathway req

170 n the quantity, composition and structure of oligosaccharides in the finished wine.

171 -acting generating a more diverse mixture of oligosaccharides, including mannobiose.

172 Glycoconjugate vaccines based on synthetic oligosaccharides instead of isolated polysaccharides off

173 tly converting microbially-derived precursor oligosaccharides into structurally uniform human-type N-

174 The vibrational fingerprints of cold oligosaccharide ions exhibit a wealth of well-resolved a

175 gh the GlcN-O6 attachment point for the core oligosaccharide is buried in the combining site, which e

176 at the GlcN-O6 attachment point for the core oligosaccharide is buried in the combining site, which e

177 The HS oligosaccharide is functionally active, can restore prot

178 the construction of internal Galf containing oligosaccharide is limited, probably due to the difficul

179 OTase-dependent glycosylation mechanisms, an oligosaccharide is synthesized on a lipid carrier and su

180 A multistep regenerative synthesis of oligosaccharides is also reported.

181 The synthesis of complex oligosaccharides is often hindered by a lack of knowledg

182 challenges in structural characterization of oligosaccharides is the presence of many structural isom

183 Short alpha-(1,3)-oligosaccharides lacked the capacity to induce maturatio

184 Soaking with isomaltotriose or gluco-oligosaccharides led to structures in which isomaltosyl

185 es reveals that a close proximity of two M6P-oligosaccharide ligands is critical to achieve high affi

186 opriate ratios, suggesting the absence of an oligosaccharide linker.

187 The transfer of a glycan from a lipid-linked oligosaccharide (LLO) donor to the asparagine residue of

188 sociated with reduced levels of lipid-linked oligosaccharides (LLOs) and compensatory up-regulation o

189 Adding specific oligosaccharides may improve outcomes.

190 transport, are the protagonists of the cello-oligosaccharide mediated induction of thaxtomin producti

191 ion of this method allowed the separation of oligosaccharide mixtures with various degree of polymeri

192 ) have enabled compositional profiling of HS oligosaccharide mixtures, online separation and detailed

193 This finding does not correlate with the oligosaccharide moieties having a strong contribution to

194 ydrate-destroying chemical (NaIO4), mono- or oligosaccharides (N-acetylneuraminic acid, galactose, an

195 equence analysis by mass spectrometry of the oligosaccharides obtained after heparin lyase III digest

196 ce (STD)-NMR and X-ray crystallography using oligosaccharides obtained by synthetic and depolymerizat

197 saccharide in all bacterial LPSs, whereas an oligosaccharide of beta-Kdo residues links "group 2" cap

198 On the oligosaccharide of the LOS, the presence of phosphoethan

199 The simulations reveal that the oligosaccharides of LPS stabilize the extracellular loop

200 n shown to be antigenic when attached to Fab oligosaccharides of monoclonal antibodies (mAbs) , while

201 Three sulfated oligosaccharides of natural origin were chosen as repres

202 constitutes an innovative approach to access oligosaccharides of pharmacological importance.

203 specific for internalization of linear xylo-oligosaccharides of polymerization degree up to 3 and 4

204 The availability of structurally defined CS oligosaccharides offers a novel approach to investigate

205 and multi-enzymatic preparations to generate oligosaccharides/oligomers from potato RG I was evaluate

206 Sporadic and familial mutations in the oligosaccharide-oligonucleotide (OB) folds of POT1 have

207 e Mcm subunit DNA-binding loops, such as the oligosaccharide-oligonucleotide loops, helix 2 insertion

208 While the oligosaccharide-oligonucleotide-binding (OB)-fold domain

209 tein formula supplemented with nondigestible oligosaccharides on the prevention of eczema.

210 n of the method to screen small libraries of oligosaccharides, on the basis of human histo-blood grou

211 gnificant changes in polysaccharide (PS) and oligosaccharide (OS) base wine composition and concentra

212 ar polysaccharide arabinomannan (AM) and its oligosaccharide (OS) fragments in humans.

213 t ions corresponding to the lipid A and core oligosaccharide (OS) substructures.

214 The discovery of this novel oligosaccharide oxidase reveals that the VAO-type flavop

215 (VAO)-type flavoprotein oxidases, a putative oligosaccharide oxidase was identified.

216 Partially acetylated chito-oligosaccharides (paCOS) have diverse bioactivities that

217 calorimetry indicated a stoichiometry of two oligosaccharides per CXCL5 dimer.

218 Plant-derived pectin and pectic-oligosaccharides (POS) have been considered as prebiotic

219 tilized agricultural by-product, into pectic oligosaccharides (POS), compounds with potential health

220 This was observed both for oligosaccharide precursor and product ions.

221 guanosine diphosphate mannose, lipid-linked oligosaccharide precursor and total cellular protein gly

222 in fragment bound to CCL5 indicated that the oligosaccharide preferred to interact simultaneously wit

223 OligoG CF-5/20 is an alginate oligosaccharide previously shown to have antimicrobial a

224 cation and quality-control protocols for the oligosaccharide products have been standardized.

225 ct of enzyme treatment and processing on the oligosaccharide profile of commercial pear juice samples

226 Oligosaccharide profiles showed that A. tequilana syrups

227 sAA9A bound to cellulosic and non-cellulosic oligosaccharides provide insight into the molecular dete

228 ment of these residues by the longer heparin oligosaccharide provides a rationalization for its effec

229 library covers 4-O-sulfated and 6-O-sulfated oligosaccharides ranging from trisaccharides to nonasacc

230 inverse correlation between monosaccharides/oligosaccharides ratio and ABTS radical-scavenging activ

231 Second, intraventricular injection of HA oligosaccharide reduced inflammation and enhanced myelin

232 s-links between phosphate groups on the core oligosaccharide regions.

233 We report the automated glycan assembly of oligosaccharides related to the arabinogalactan side cha

234 he anomeric alpha/beta glycan linkage within oligosaccharides remains a particular challenge.

235 s with functions related to raffinose family oligosaccharide (RFO) metabolism, late embryogenesis abu

236 Raffinose family oligosaccharides (RFOs) accumulate in seeds during matur

237 tty acid profiles, sucrose, raffinose family oligosaccharides (RFOs); phenolics, and free amino acids

238 h or without purified sialylated bovine milk oligosaccharides (S-BMO).

239 oaded aminopyrenetrisulfonate (APTS)-labeled oligosaccharide samples.

240 es efforts to study the relationship between oligosaccharide size and antigenicity.

241 Short cello- and xylo-oligosaccharides, sophorose and gentibiose, are among th

242 ing blocks, fragment mapping and sequence of oligosaccharide species, biological and biochemical assa

243 The marker compounds identified were oligosaccharide stachyose and the organic acid, succinic

244 s fragment-based hyphenated MS technology to oligosaccharide standards and to de novo sequencing of p

245 s hampered by a lack of well-defined complex oligosaccharide standards that are needed to fabricate t

246 We established that oligosaccharide stannanes could be prepared from monosac

247 Because some of these oligosaccharide structures are conserved across kingdoms

248 odifications involving many types of complex oligosaccharide structures, making structural analysis o

249 shield to comprise a network of interlocking oligosaccharides, substantially ordered by glycan crowdi

250 s and show that 18B7 is able to hydrolyze an oligosaccharide substrate, providing the first example o

251 tic analysis using a variety of well defined oligosaccharide substrates, revealed the structural dete

252 rmulas (IFs) are supplemented with prebiotic oligosaccharides, such as galactooligosaccharides (GOS)

253 Because nonenzymatic aqueous oligosaccharide syntheses are underdeveloped, mechanisti

254 y, is usually found as a byproduct of fructo-oligosaccharide synthesis from sucrose with fructosyltra

255 ally all common concepts for the expeditious oligosaccharide synthesis including selective, chemosele

256 perspective, solid-phase and chemoenzymatic oligosaccharide synthesis methods for GAG-derived motifs

257 , scalable, and transformative automation of oligosaccharide synthesis that easily interfaces with ex

258 The utility of the methodology for the oligosaccharide synthesis was demonstrated by the succes

259 z) imidates as versatile building blocks for oligosaccharide synthesis.

260 tructural modifications of carbohydrates and oligosaccharide synthesis.

261 ymatic approaches expanded the capability of oligosaccharide synthesis.

262 such that they disfavor the binding of malto-oligosaccharides that bear branches at their 6-positions

263 Here, the authors synthesize a series of oligosaccharides that mimic the lipopolysaccharides pres

264 h is required to liberate the soluble chitin oligosaccharides that serve as an inducing cue for compe

265 e is a decrease in 2- and 3-linked arabinose oligosaccharides, that contributes to around a 50% reduc

266 Using microarrays of synthetic oligosaccharides, the LM26 epitope has been identified a

267 -glycosylation involves the attachment of an oligosaccharide to selected asparagine residues in the s

268 Endo H was used to collapse high mannose oligosaccharides to a single peak of GlcNAc for ease of

269 d alpha-glucosidase that breaks down di- and oligosaccharides to absorbable monosaccharides.

270 hs and arabinose substitution pattern of the oligosaccharides to be recognized and hydrolyzed by the

271 erized the interaction of a panel of heparin oligosaccharides to CXCL5 using solution NMR, isothermal

272 the cell where a beta-xylosidase cleaves the oligosaccharides to fermentable sugars.

273 by characterizing the binding of GAG heparin oligosaccharides to hCXCL1 using NMR spectroscopy.

274 ith IVH; and depletion of HC-HA levels by HA oligosaccharide treatment reduced inflammation and enhan

275 Hence, hyaluronidase or HA oligosaccharide treatment represses inflammation, promot

276 The molecular details and impact of oligosaccharide uptake by distinct human gut microbiota

277 on anomer, linkage, and position isomers of oligosaccharides using conventional mass spectrometry (M

278 Here, we describe the rapid assembly of oligosaccharides using the commercially available Glycon

279 present the CTA-SAX purification of heparin oligosaccharides using volatile salt (VS) buffer.

280 cosyl units from sucroseto dextrans or gluco-oligosaccharides via the formation of alpha-(1-->2) gluc

281 on of the POS mixtures in terms of mono- and oligosaccharides was assessed at the molecular level.

282 tein formula supplemented with nondigestible oligosaccharides was closer to that of breast-fed infant

283 nt backbone compositions, a library of 47 HS-oligosaccharides was prepared and the resulting compound

284 afucosylated, fucosylated, and high mannose oligosaccharides was separated in the range of 15 to 45

285 total, acidic or neutral polysaccharides and oligosaccharides was tested using turbidity measurements

286 icroarrays to include probes derived from HS oligosaccharides, we found an unusually high content of

287 Oligosaccharides were distinguished on the basis of thei

288 Their respective oligosaccharides were obtained by bovine testicular hyal

289 The MS spectra of the oligosaccharides were performed on an AccuTOF mass spect

290 a glycan shield of approximately 90 N-linked oligosaccharides, which comprises roughly half its mass

291 Furthermore, similar oligosaccharides with 2-O, 6-O and 3-O-sulfations showed

292 tant enzymes synthesized polysaccharides and oligosaccharides with changed linkage composition.

293 antibody (HS20) and a panel of synthetic HS oligosaccharides with distinct lengths and sulfation mod

294 Main oligo-RG I products were oligosaccharides with DP of 2-12 (79.8-100%), while the

295 is, we devised a synthetic route to assemble oligosaccharides with natural and non-natural sequences.

296 I (RG I) was investigated as a new source of oligosaccharides with potential prebiotic properties.

297 The oligosaccharides with the greatest competitive effect fo

298 fficulties to access diverse heparan sulfate oligosaccharides with well-defined sulfation patterns.

299 h hydrolysis products are taken up mainly as oligosaccharides, with only one strain able to grow on g

300 ChiP is responsible for the uptake of chitin oligosaccharides, with particular selectivity for chitoh