ライフサイエンスコーパス: sialylated

1 l (RBC) surface receptors, many of which are sialylated.

2 retained the ability to bind fH when LOS was sialylated.

3 f polylactosamine alpha chains that could be sialylated.

4 s lipooligosaccharides (LOS) that are highly sialylated.

5 ave been reported to be complex and multiply sialylated.

6 clinical biomarkers but should also embrace sialylated Abeta standards to reveal specific sialylatio

7 anation for these findings is that levels of sialylated airway ligands for Siglec-F might be diminish

8 unotherapy in allergic patients also induced sialylated allergen-specific IgGs.

9 rmines that it binds to one or more alpha2,3-sialylated and alpha1,3-fucosylated glycan receptors tha

10 d glycine residues to interact with alpha2,3-sialylated and alpha1,3-fucosylated glycan receptors, in

11 on to and infection of neutrophils depend on sialylated and alpha1,3-fucosylated glycans.

12 udies, we obtained insights into the role of sialylated and fucosylated glycans in zebrafish hematopo

13 ological staining revealed that IAV binds to sialylated and non-sialylated glycans and binding is not

14 Both sialylated and nonsialytated FetA bind to LPS, but only

15 ity to detect labile glycans such as heavily sialylated and polysialic acid N-glycans, which are diff

16 ine specificity of Siglec-8 toward different sialylated and sulfated carbohydrate ligands and determi

17 Purified mucin preparations carried sialylated and sulfated glycans, bound to eosinophils an

18 that are expected to carry high densities of sialylated and sulfated O-linked glycans.

19 M. pneumoniae recognizes sialylated and sulfated oligosaccharide receptors to col

20 We demonstrate that H-ficolin is sialylated and that removal of sialic acid abrogates IAV

21 We generated one highly sialylated and two distinct more galactosylated 6-19 IgG

22 s related to its glycosylation consisting of sialylated and unsialylated Tn-antigens and core 1 and c

23 ed, showing a range of 26 neutral, sulfated, sialylated, and both sulfated and sialylated core 1 (Gal

24 ence of various fucosylated, phosphorylated, sialylated, and multiply sulfated moieties as modificati

25 ctive species of Panx3, likely glycosylated, sialylated, and phosphorylated, was highly expressed in

26 structural variants, including high mannose, sialylated, and terminal galactosylated species were stu

27 Two strategies for installation of sialylated antennae are explored, and both approaches co

28 gen-specific: only T cells responsive to the sialylated antigen become tolerized.

29 onstrating that immune complexes composed of sialylated antihemagglutinin antibodies and seasonal ina

30 and desialylated A2HSG, and depleted in mono-sialylated ApoC-III (ApoC-III1).

31 ents were enriched in SAA, LBP, ApoC-III, di-sialylated ApoC-III (ApoC-III2) and desialylated A2HSG.

32 an also be engaged by two potentially lethal sialylated bacterial pathogens of newborns and infants,

33 of 20 different saccharide compositions with sialylated bi-, tri-, and tetra-antennary structures.

34 ns, and mature IgD+ B cells were enriched in sialylated bone marrow niches.

35 typic Malawian diet with or without purified sialylated bovine milk oligosaccharides (S-BMO).

36 taining fluorophore at the reducing end were sialylated by a one-pot three-enzyme system to generate

37 een the TGN and the plasma membrane, was not sialylated by a sialyltransferase at the TGN and that th

38 e may explain the increased pathogenicity of sialylated C. jejuni and may be key to the initiation of

39 s CD14, and the amplified response of DCs to sialylated C. jejuni LOS is CD14 dependent.

40 lpha and IFN-beta responses to i.v.-injected sialylated C. jejuni.

41 of Sn showed greatly reduced phagocytosis of sialylated C. jejuni.

42 Surprisingly less sialylated, capacitated, sperm did not increase neutroph

43 Many CTCs express sialylated carbohydrate ligands on their surfaces that a

44 e demonstrate that JCPyV can engage numerous sialylated carbohydrate receptors.

45 n of increased surface expression of several sialylated cell adhesion molecules, including the known

46 rties in vivo Sialidase treatment of heavily sialylated CHO-sKlotho increased its co-receptor activit

47 evealed that Siglec-8 is partially masked by sialylated cis ligands.

48 catalysis and the rituximab glycoform with a sialylated complex-type biantennary glycan terminated wi

49 P1 of HPyV6 and HPyV7 does not interact with sialylated compounds in solution or on cultured human ce

50 sferases gave 12 differently fucosylated and sialylated compounds.

51 an studies revealed a pathological excess of sialylated conjugates as well as dermatan and heparan su

52 sulfated, sialylated, and both sulfated and sialylated core 1 (Galbeta1-3GalNAcalpha1-) and core 2 (

53 rm that was characterized by the presence of sialylated core 1 and core 2 O-glycans.

54 e CHO cells is glycosylated with the typical sialylated core 1 structure.

55 Furthermore, for the generation of sialylated core 1 structures constructs encoding human p

56 ry effect of SPN appeared to be dependent on sialylated core 2 O-glycosylation of the protein.

57 ts of eukaryotic plasma membranes, and their sialylated derivatives, gangliosides, are the major clas

58 y be mediated, at least in part, by alpha2-6-sialylated EGFR.

59 potential of a bTCE antibody that targets a sialylated epitope on CD43 in AML.

60 AT1413 binds CD43s, a unique sialylated epitope on CD43, which is weakly expressed on

61 rvation of an effective survival factor, the sialylated exopolysaccharide capsule.

62 This alpha2,6-sialylated Fc (sFc) has been reported to bind to the car

63 G subclass and Fc glycans, with abundance of sialylated Fc glycans (sFc) predicting quality of vaccin

64 eering of the IVIG's Fc glycans into a fully sialylated Fc glycoform, which may possess significantly

65 The efficacy of sialylated Fc has generated an incentive to modify the u

66 unctional P1 promoter, was unable to produce sialylated Fc in the systemic circulation, despite the p

67 parison of the structures of asialylated Fc, sialylated Fc, and F241A Fc, a mutant that displays incr

68 inflammatory status, pretreatment levels of sialylated FetA in the blood are indicative of the likel

69 y reveals that high levels of O-glycosylated sialylated FetA isoforms are found in patients exhibitin

70 ted Tn antigen (alphaGalNAc-Ser/Thr) and its sialylated form, the sialyl-Tn antigen.

71 odies made by p individuals recognize x2 and sialylated forms of x2, whereas x2 is lacking on P-defic

72 A lectin panel, distinguishing normally sialylated from hyposialylated glycans, used WGA, SNA, P

73 ma, during which a 55% increase of alpha-2,6-sialylated fucosylated N-glycans was revealed, demonstra

74 in which preferentially recognizes alpha-2,6 sialylated galactosides showed strong binding reactivity

75 on from Lewis(x)-type structures in mESCs to sialylated Galbeta1,3GalNAc-type glycans on differentiat

76 ialic acid precursor analogs to modulate the sialylated ganglioside-dependent interaction of MLV part

77 alylated PrP(C) contained greater amounts of sialylated gangliosides and cholesterol than membrane ra

78 PyV can both engage LSTc as well as multiple sialylated gangliosides.

79 Composed of a sialylated glycan attached to a ceramide lipid, the same

80 that each pathotype makes use of a different sialylated glycan ligand, with binding sites on opposite

81 ies on sialic acid recognition using a novel sialylated glycan microarray containing modified sialic

82 Our results demonstrate the utility of this sialylated glycan microarray to investigate the biologic

83 f its B subunit, PltB, with specific lumenal sialylated glycan packaging receptors.

84 Crystal structures of EV-D68 in complex with sialylated glycan receptor analogues show that they bind

85 inding of QX-RBD is dependent on a different sialylated glycan receptor.

86 on surfaces, obstructing a groove that binds sialylated glycan receptors in many other polyomaviruses

87 stability and ionization bias experienced by sialylated glycan species.

88 Campylobacter jejuni expressing a GD1a-like, sialylated glycan.

89 itative binding affinity of HA to alpha2-->6 sialylated glycans (human receptors) is one of the impor

90 evealed that IAV binds to sialylated and non-sialylated glycans and binding is not concordant with re

91 Sialylated glycans and glycoproteins are involved in cel

92 in SK1 SRR adhesin affects interactions with sialylated glycans and glycoproteins, we determined high

93 During infection, sigma1 engages sialylated glycans and junctional adhesion molecule-A (J

94 The reovirus attachment protein sigma1 binds sialylated glycans and proteinaceous receptors to mediat

95 Sialylated glycans are found at elevated levels in many

96 Single-cell binding studies indicate that sialylated glycans are likely not required for initial a

97 demonstrate that different distributions of sialylated glycans are related to the metastatic propert

98 Sialylated glycans are synthesized in mammals by a singl

99 tissues and highlight a functional role for sialylated glycans as reovirus coreceptors in the CNS.

100 IL-6 secretion were enriched in ApoC-III, di-sialylated glycans at multiple A1AT glycosylation sites

101 The IgG1 Fc fragments containing complex sialylated glycans attached to the N-terminal Asn(221) s

102 ot only result in accurate identification of sialylated glycans but also improve the characterization

103 ows for linkage specific characterization of sialylated glycans directly from the precursor mass but

104 Lack of sialylated glycans due to genetic ablation of the Sia-ac

105 irus (IBV), require specific alpha2,3-linked sialylated glycans for attachment and entry.

106 Surprisingly, Gal6S is undetectable in sialylated glycans from eosinophils and BAL fluid analyz

107 A population of Fcs bearing sialylated glycans has been identified as contributing t

108 me, fluorescence and radionuclide imaging of sialylated glycans in a murine tumor model in vivo.

109 s revealed the importance of sialylation and sialylated glycans in breast cancer brain metastasis.

110 ring 3F-NeuAc to mice dramatically decreases sialylated glycans in cells of all tissues tested, inclu

111 The relative abundance of sialylated glycans in the S1 subunit compared to the ful

112 MS analysis of sialylated glycans is challenging due to their low ioniz

113 The analysis of sialylated glycans is critical for understanding the rol

114 ts viral envelope that interact with various sialylated glycans on a host cell.

115 serine-rich repeat (SRR) adhesins recognize sialylated glycans on human salivary, platelet, and plas

116 icity depends on toxin binding to terminally sialylated glycans on surface glycoproteins.

117 Sialylated glycans on the surface of mammalian cells act

118 Binding of sialylated glycans or other ligands triggers signals tha

119 s in ionization efficiency among neutral and sialylated glycans prevent direct quantitative compariso

120 in the expression of truncated core 1-based sialylated glycans rather than the core 2-based glycans

121 ed from the aqueous phase, while neutral and sialylated glycans remained in the DCM phase.

122 Sialylated glycans serve as cell surface attachment fact

123 DRAG), to quantitatively compare neutral and sialylated glycans simultaneously by MALDI-MS.

124 binding to sialyl Lewis x (sLe(x)) and other sialylated glycans that decorate P selectin glycoprotein

125 tiates viral entry by engaging host receptor sialylated glycans via its receptor-binding site (RBS).

126 and alkaline BGE systems, the mobilities of sialylated glycans were shifted relative to nonsialylate

127 for simultaneous profiling both neutral and sialylated glycans without derivatization or labeling.

128 high-mannose glycans, fucolsylated glycans, sialylated glycans, and hybrid structures were studied.

129 process, including initial binding of IAV to sialylated glycans, fusion between the viral envelope an

130 2)v showed a predominant binding to alpha2-6-sialylated glycans, similar to human-adapted influenza A

131 which bound almost exclusively to alpha-2,6 sialylated glycans, the seal H3 bound preferentially to

132 generally not microbial cell surfaces, have sialylated glycans.

133 hat lack coding nucleic acids but do possess sialylated glycans.

134 he seal H3 bound preferentially to alpha-2,3 sialylated glycans.

135 teroids, phospholipids, phosphopeptides, and sialylated glycans.

136 the ionization responses for all neutral and sialylated glycans.

137 mproved desorption of both large and heavily sialylated glycans.

138 protein exhibiting no detectable binding to sialylated glycans.

139 MCs depends on alpha1,3-fucosylated, but not sialylated, glycans.

140 -adapted pathogen that encounters terminally sialylated glycoconjugates and free sialic acid (Sia) in

141 Sialylated glycoconjugates on the surfaces of mammalian

142 genic tetrazine, allowing for the imaging of sialylated glycoconjugates within live zebrafish embryos

143 yze the removal of sialic acid residues from sialylated glycoconjugates.

144 sease mouse model, and find that an alpha2-3 sialylated glycoform designed to eliminate uptake by the

145 nflammation, depends on a specific alpha-2,6-sialylated glycoform of IgG Fc to induce Interleukin 4 (

146 Gangliosides (sialylated glycolipids) play an essential role in the CN

147 ive proteomics strategy in which we enriched sialylated glycopeptides by SNA, labeled them at the N-t

148 Fucosylated and sialylated glycopeptides from human lactoferrin served a

149 in the presence of m-NBA the charge state of sialylated glycopeptides increased and the chromatograph

150 can quantitatively and qualitatively enrich sialylated glycopeptides more than the commercially avai

151 aracteristic fragmentation of differentially sialylated glycopeptides.

152 A sialylated glycoprotein called serum amyloid P (SAP) inh

153 moniae hemadsorption (HA) and binding to the sialylated glycoprotein laminin by 95% failed to inhibit

154 processes; however, it is laborious to study sialylated glycoproteins due to the labile nature of sia

155 However, OpeRATOR is not fully active toward sialylated glycoproteins, and it has been suggested that

156 e to incorporate sialic acid precursors into sialylated glycoproteins.

157 Therefore, OmpA interacts with sialylated glycoproteins.

158 zymatic activity, with a special emphasis on sialylated glycosites.

159 ns leads to an increase in expression of the sialylated glycosphingolipid, GT1b.

160 Gangliosides, sialylated glycosphingolipids, found on all vertebrate c

161 ionally modified with N-linked glycans and a sialylated glycosylphosphatidylinositol (GPI) anchor.

162 e generated their degalactosylated or highly sialylated glycovariants and compared their pathogenic e

163 n FcgammaR-independent mechanism by which Fc-sialylated glycovariants might limit proinflammatory IgG

164 retions that can result in desialylation of (sialylated) gonococcal LOS.

165 ly at amino acid 1203 (N1203R) also bound to sialylated gonococci and restored killing.

166 ctional importance of Arg-1203 by incubating sialylated gonococci with normal human serum, in the pre

167 define amino acids important for binding to sialylated gonococci.

168 ain 20 of HufH contains the binding site for sialylated gonococci.

169 are consistent with the hypothesis that the sialylated GPI anchor attached to PrP(C) acts as a synap

170 tition studies showed that pretreatment with sialylated GPIs prevented the targeting of PrP(C) to syn

171 Convergent access to this key alpha(2,6)-sialylated hexasaccharide was also achieved through a [3

172 The total neutral and sialylated HMGs were derivatized with a bifunctional flu

173 The sialylated HMOs 3'SL and 3'SLN were associated with fast

174 atic activity to be confined to specific non-sialylated HMOs and synergistic with a number of convent

175 in two Malawian birth cohorts revealed that sialylated HMOs are significantly less abundant in those

176 ), and relative abundance of fucosylated and sialylated HMOs with language at 18 mo (P < 0.001 and P

177 s of HMOs (total HMOs, fucosylated HMOs, and sialylated HMOs), 51 individual HMOs, and 6 bioactive pr

178 s, yielding a selectivity factor of ~2.4 for sialylated host surfaces.

179 Human podocytes are highly sialylated; however, sialylation's role in podocyte home

180 allowed the generation of SM6 decorated with sialylated human-type oligosaccharides, comparable to pl

181 heir capacity to produce inhibitory IgG4 and sialylated IgG able to mediate anti-inflammatory mechani

182 Transfer of low amounts of antigen-specific sialylated IgG Abs was sufficient to inhibit B cell acti

183 Sialylated IgG Abs, which are immunosuppressive, and Tre

184 ry from murine studies, which states that Fc-sialylated IgG alters the balance between activating and

185 ghlighting the anti-inflammatory activity of sialylated IgG antibodies.

186 Sialylated IgG Fc (sFc) increases the activation thresho

187 Sialylated IgG Fc domains have antiinflammatory properti

188 nvolving basophils and the binding of highly sialylated IgG Fc to DC-SIGN-expressing myeloid cells.

189 on of IVIg, but unexpectedly, recombinant Fc-sialylated IgG or sialic acid-enriched IVIg were equally

190 Protective antibodies, including IgG4, Fc sialylated IgG, and IgA, have the capacity to modulate t

191 through the generation of immunosuppressive sialylated IgGs and may provide insight on the role of T

192 tory mechanism mediated by anti-inflammatory sialylated IgGs that are formed on TD tolerance inductio

193 se expression and secreted immunosuppressive sialylated IgGs that were sufficient to block antigen-sp

194 that TI immune responses induced suppressive sialylated IgGs, in contrast to TD proinflammatory Th1 a

195 alizing antibodies through immunization with sialylated immune complexes.

196 d to the discrimination of alpha2,3/alpha2,6-sialylated isomers, unambiguous identification of sialog

197 able process for generating a well-qualified sialylated IVIg drug candidate with maximum Fc sialylati

198 yer is an isoform of DMBT1 carrying O-linked sialylated keratan sulfate chains (DMBT1(S8)).

199 By linking of sialylated LAcNAc units to di- and trivalent scaffolds,

200 tion, with several isomers, corresponding to sialylated lacto-N-tetraose.

201 ted during HMO fermentation and is active on sialylated lacto-N-tetraose.

202 form of Lewis A (suLe(A)) trisaccharide and sialylated Lewis A and that fluoresceinated versions of

203 glycans initiated by GalNAc residues, but no sialylated Lewis A was detected.

204 immune encephalomyelitis, Sn interacted with sialylated ligands expressed selectively on CD4(+)Foxp3(

205 e (Mphi)-restricted receptor that recognizes sialylated ligands on host cells and pathogens.

206 Sialylated lipids serve as cellular receptors for polyom

207 Sialylated LOS also engages inhibitory Siglecs on host l

208 Highly sialylated LPS was ineffective in depleting bactericidal

209 Adding purified bovine sialylated milk oligosaccharides (S-BMO) with structures

210 tran show that the endosomal accumulation of sialylated molecules can be largely attributed to impair

211 nfluenza infection increases sialic acid and sialylated mucin availability and enhances desialylation

212 via multiple interactions involving terminal sialylated mucin glycans.

213 ion of virions bound to vesicles coated with sialylated mucin mimics was possible, the kinetics of fu

214 Therefore, sialylated N-glycan (Neu5Ac/Neu5Gc-terminal) is targeted

215 unoglobulin G (IgG) and the search for serum sialylated N-glycan biomarker candidates of hepatocellul

216 The alteration of sialylated N-glycan expressions is important to detect t

217 The LC method is capable of separating sialylated N-glycan isomers differing in alpha2-3 and al

218 first total synthesis of triantennary, fully sialylated N-glycan of complex type is described.

219 ering approach led to secreted A1AT carrying sialylated N-glycan structures largely resembling its se

220 attributed to a decrease in neutral and mono-sialylated N-glycans and an increase in di-sialylated N-

221 Asn-145 and Asn-160 contain lower levels of sialylated N-glycans and higher levels of high-mannose N

222 NeuAcalpha2-6-terminated polylactosamine and sialylated N-glycans are important determinants for infl

223 that cell surface-associated VEGFR2 displays sialylated N-glycans at Asn-247 and, in contrast, that t

224 eceptors for binding to HA in the absence of sialylated N-glycans at the cell surface.

225 isomer-specific, quantitative comparison of sialylated N-glycans between bovine and rabbit immunoglo

226 l viruses tested interacted with one or more sialylated N-glycans but not O-glycans or glycolipid-der

227 and guinea pig erythrocytes contain complex sialylated N-glycans but that they differ with respect t

228 inhibitory activities, showing a key role of sialylated N-glycans in inducing the IgM-mediated immune

229 combination of enzymes and lectins to modify sialylated N-glycans in real time in the capillary so th

230 the syntheses of bi- and triantennary fully sialylated N-glycans is described.

231 n heterogeneity was identified of the highly sialylated N-glycans of rHuEPO by extensive acetylation,

232 Sialylated N-glycans play crucial roles in physiological

233 Sialylated N-glycans play pivotal role in several import

234 The key step to identify the sialylated N-glycans was to quantitatively neutralize th

235 ry appeared to be affected by the absence of sialylated N-glycans, dynamin-dependent entry was not af

236 uded the detection of a new class of heavily sialylated N-glycans, including polysialylated N-glycans

237 Highly sialylated N-glycans, which were up-regulated in brain-s

238 o-sialylated N-glycans and an increase in di-sialylated N-glycans.

239 ng binding to sialylated polylactosamine and sialylated N-glycans.

240 ntaining phosphorylated, fucosylated, and/or sialylated N-glycans.

241 PrP(C) has two sialylated N-linked carbohydrates.

242 Sialylated N-linked glycans have been reported to be ess

243 r knowledge, we show for the first time that sialylated N-linked glycans induce the internalization o

244 C1INH sialylated-N- and -O-glycans were not only essential for

245 Highly sialylated negatively charged glycans also exhibit high

246 linear (maltooligosaccharides) and branched (sialylated, neutral and core fucosylated biantennary IgG

247 ts and immunological responses to whole-cell sialylated NTHi were measured.

248 nto lymph nodes, indicating a requirement of sialylated O-glycans for proper trafficking.

249 Using bovine fetuin (because it contains the sialylated O-glycans most commonly found on biopharmaceu

250 We find that sialylated O-glycans on these novel PILRalpha ligands, a

251 ritic cartilage and has reduced affinity for sialylated O-glycans, a glycophenotype associated with i

252 k facilitate the OpeRATOR digestion of fully sialylated O-glycopeptides that are mass tagged to ident

253 er cells, it is decorated by multiple short, sialylated O-linked glycans (MUC1-ST).

254 Sialylated oligosaccharide epitopes found on a variety o

255 alpha1-acid glycoprotein (AGP) as well as of sialylated oligosaccharide reference standards and found

256 ires the engagement of two types of glycans, sialylated oligosaccharides and sulfated glycosaminoglyc

257 a library of differentially fucosylated and sialylated oligosaccharides starting from a single chemi

258 nce standards and found that for more highly sialylated oligosaccharides the loss is greater than the

259 ondroitin sulfate E, but not with neutral or sialylated oligosaccharides.

260 n vitro at residues 42, 66, and 74, becoming sialylated only at Asn-42.

261 ferences in interactions with strains of the sialylated pathogen, group B Streptococcus, and with sia

262 strate that Sn plays a key role in capturing sialylated pathogens and promoting rapid proinflammatory

263 al Tfp specifically recognize a triantennary sialylated poly-N-acetyllactosamine-containing N-glycan

264 aining NeuAcalpha2-6, with strong binding to sialylated polylactosamine and sialylated N-glycans.

265 gG3 mAb are poorly galactosylated and hardly sialylated, possibly contributing to the pathogenic pote

266 red by the difficulty of generating suitable sialylated products for clinical use.

267 ae HA-negative mutant II-3 failed to bind to sialylated receptors but adhered to sulfatide in a tempe

268 uenza viruses to effectively bind human-like sialylated receptors is a major impediment to their effi

269 their capacity to bind nearly all canonical sialylated receptors other than a selection of biantenna

270 Airway epithelia express sialylated receptors that recognize exogenous danger sig

271 t unfavorable to bind any negatively charged sialylated receptors, consistent with the recombinant H1

272 To understand MERS-CoV engagement of sialylated receptors, we determined the cryo-EM structur

273 sting that EV-D68 can use multiple redundant sialylated receptors.

274 ed homogeneous glycoforms, including a fully sialylated (S2G2F) glycoform that may gain anti-inflamma

275 atic, scalable process to produce a tetra-Fc-sialylated (s4-IVIg) IVIg drug candidate and its qualifi

276 ic eosinophilic airway inflammation and less sialylated Siglec-F ligands in their airways.

277 use of in-source and metastable decay of the sialylated species.

278 trium and that these receptors interact with sialylated sperm.

279 orylated glycans, even as the recognition of sialylated structures is decreased through antigenic dri

280 enables the controlled in vivo synthesis of sialylated structures with different interlinkages and d

281 ycans from tissues and serum have mature and sialylated structures.

282 is strategy was not as effective with labile sialylated structures; instead, it was observed that the

283 tion mutant that lost the ability to grow on sialylated substrates, we showed that-in gnotobiotic mic

284 223 showed a decrease of high mannose versus sialylated sugars on N-glycoproteins such as the metallo

285 Siglec-F recognizes sialylated sulfated glycans in glycan-binding assays, bu

286 rapid identification of various fucosylated, sialylated, sulfated glycotopes and definitive determina

287 both the sialyl Lewis-X (sLe(X)) and the di-sialylated T-antigen (NeuAcalpha2,3Galbeta1,3(NeuAcalpha

288 counts for the accommodation of the alpha2,6-sialylated terminus of a biantennary N-glycan by viscumi

289 Three mono- and di-sialylated tetra-antennary N-glycans and one mono-sialyl

290 nnary structures, as well as the increase in sialylated tetraantennary and FA3G3S[3,3,3]3 structures.

291 As a result, spleen-derived PrP(Sc) is more sialylated than brain-derived PrP(Sc).

292 lated tetra-antennary N-glycans and one mono-sialylated tri-antennary N-glycan of rHuEPO are reported

293 eover, we observed a progressive increase of sialylated triantennary and tetraantennary structures tw

294 and 2-6 sialyllactose as well as 2-3 and 2-6 sialylated triantennary glycan.

295 The recognition of FITC-APBA to sialylated TRITC-AF leads to the FRET signal that is ana

296 We previously identified a series of sialylated Tyr-10 O-glycosylated Abeta peptides, 15-20 r

297 d terminal Galp residues that become readily sialylated upon addition of parasite trans-sialidases.

298 The highly sialylated vascular endothelial surface undergoes change

299 et endothelial cell adhesion molecule-1, was sialylated via alpha2,6-linkages, as shown by Sambucus n

300 t strains when lipooligosaccharide (LOS) was sialylated, whereas PorB molecules of lptA null mutants

301 Glycans at Asn-168 were predominantly sialylated with bi- to tetra-antennary branches, and Asn