ライフサイエンスコーパス: fucosylated

1 or a subset, of the EGF repeats need to be O-fucosylated.

2 orm with higher affinity for heparin was not fucosylated.

3 trast to expectations, PSGL-1 is not heavily fucosylated; a majority of the O-glycans are disialylate

4 e signals similar to cells treated only with fucosylated Ab.

5 er membrane protein that mediates binding to fucosylated ABH antigens of the ABO blood group.

6 ino acid residues as critical for binding to fucosylated ABH antigens.

7 Normal plasma IgG contains approximately 94% fucosylated Abs, but alloantibodies against, for example

8 Hypo-fucosylated adalimumab increased the number of CD206(+)

9 When hypo-fucosylated adalimumab was added to PBMCs, a larger numb

10 Susceptibility of [(14)C]fucosylated AGPs to alpha(1,2)fucosidase, and not to alp

11 pha2-3 glycans, including alpha2-3GalNAc and fucosylated alpha2-3 glycans (including sialyl Lewis x),

12 (b), and Le(y) determinants carried by their fucosylated analogues.

13 n strategy to separate functionally relevant fucosylated and afucosylated glycans on mononclonal anti

14 N-glycans are predominantly biantennary and fucosylated and contain varying levels of alpha2-6-linke

15 results in a form of the protein that is not fucosylated and has substantially weaker activity in cel

16 e tandem mass spectrometry; these are highly fucosylated and have a novel core that contains internal

17 sed 20 monosialylated and nonsialylated, and fucosylated and nonfucosylated complex- and hybrid-type

18 The minor fucosylated and polylactosamine species were well separa

19 n by sialyl transferases gave 12 differently fucosylated and sialylated compounds.

20 mannosamine (ManNAc), were incorporated into fucosylated and sialylated glycans in several cancer cel

21 Fucosylated and sialylated glycopeptides from human lact

22 h LAZ (P = 0.035), and relative abundance of fucosylated and sialylated HMOs with language at 18 mo (

23 taLAZ (P = 0.035), and relative abundance of fucosylated and sialylated HMOs with language at 18 mo (

24 gy that can give a library of differentially fucosylated and sialylated oligosaccharides starting fro

25 samine-type structures were found to be core fucosylated and some of them contained one to three lact

26 ogeneous polysaccharide composed of a highly fucosylated and xylosylated galactose backbone with arab

27 A mixture of afucosylated, fucosylated, and high mannose oligosaccharides was separ

28 were poorly galactosylated, not processively fucosylated, and negligibly inhibitory, whereas the fuco

29 linkage determination of neutral, branched, fucosylated, and sialylated oligosaccharides.

30 glycans but is modified with hybrid, highly fucosylated, and sialylated sugars.

31 The ligands must be sialylated, fucosylated, and sulfated for optimal recognition by L-s

32 Most human milk oligosaccharides are fucosylated, and their production depends on enzymes enc

33 of glycopeptides containing phosphorylated, fucosylated, and/or sialylated N-glycans.

34 Furthermore, they proposed that the non-fucosylated antenna mediated adherence to a peridontal p

35 core structures can be decorated with novel fucosylated antennae composed of Fucalpha(1-3)GlcNAc.

36 on its N-glycans, despite these lacking the fucosylated antennae typical of many other eukaryotes; s

37 nti-CD20 antibodies compared with fully core-fucosylated anti-CD20 antibodies, suggesting the presenc

38 Hypo-fucosylated anti-TNF might be more effective in patients

39 In mice with colitis, hypo-fucosylated anti-TNF significantly increased the number

40 We produced hypo-fucosylated antibodies against mouse and human TNF (adal

41 esidues and appear to be more effective than fucosylated antibodies in promoting phagocytosis of anti

42 ose transporter, resulting in a reduction of fucosylated antigens on the cell surface.

43 e form with lower heparin affinity being 97% fucosylated at this position, whereas the form with high

44 en animals given NFb12 and those given fully fucosylated b12, indicating that FcgammaR-mediated activ

45 tive N-glycans observed by MALDI-MSI, 2 core fucosylated bi-antennary N-glycans, m/z 1809.64; (Hex)(5

46 , together with the structures of another 12 fucosylated biantennary glycans.

47 ) and branched (sialylated, neutral and core fucosylated biantennary IgG glycans) carbohydrates.

48 Glycosylated human IgG contains fucosylated biantennary N-glycans with different modific

49 A core fucosylated biantennary oligosaccharide was converted to

50 e Fv region have three characteristics (core-fucosylated biantennary oligosaccharides with one or two

51 AZT) and a significant accumulation of core-fucosylated biantennary oligosaccharides.

52 after surgery with the decrease of most core-fucosylated biantennary structures, as well as the incre

53 d a larger proportion of sialylated and core-fucosylated biantennary, triantennary and tetra-antennar

54 Fc region contained typical Fc glycans (core-fucosylated, biantennary oligosaccharides with zero to t

55 conferred by the elaboration of sialylated, fucosylated binding determinants on N-glycans.

56 consisting predominantly of high-mannose and fucosylated/bisected structures.

57 enrichment of specific antigen responses for fucosylated bisecting glycoforms and the subsequent asso

58 ohydrates including high mannose structures, fucosylated blood group antigens, and glycans with termi

59 BabA adhesin of Helicobacter pylori binds to fucosylated blood group antigens, such as the Lewis(b) a

60 hilum infection of BMMCs depends on alpha1,3-fucosylated, but not sialylated, glycans.

61 that many proteins in human tissues are core-fucosylated, but their expression is localized to skin k

62 Both L-selectin ligands must be fucosylated by alpha(1,3)-fucosyltransferase (FucT)-IV o

63 Man5GlcNAc2 glycan could be efficiently core-fucosylated by FUT8 in an appropriate protein/peptide co

64 ary complex-type N-glycan also could be core-fucosylated by FUT8, albeit at much lower efficiency tha

65 PRR5 can be O-fucosylated by SPY in planta, while point mutation in th

66 The O-glycans and glycolipids were not fucosylated by the H-type alpha1, 2FT.

67 ggest that Sfrs proteins are responsible for fucosylated carbohydrate-dependent lung metastasis of ep

68 egulation and function of terminal alpha(1,2)fucosylated carbohydrates in these and other tissues, we

69 nteracts with several related sialylated and fucosylated carbohydrates.

70 t vaginitis, indicating a role for alpha(1,2)fucosylated cervical glycans in mucosal defense.

71 abundant glycoforms in HCC, including 3 core-fucosylated (CF) forms.

72 sulfation, some of which was located on the fucosylated chitobiose core.

73 Fucosylated chondroitin sulfate (fCS) extracted from the

74 eir highly modified glycosaminoglycans (e.g. fucosylated chondroitin sulfate and fucoidan), nothing i

75 zed holothurian glycosaminoglycan (DHG) is a fucosylated chondroitin sulfate with antithrombin-indepe

76 zed holothurian glycosaminoglycan (DHG) is a fucosylated chrondroitin sulfate that possesses antithro

77 a predominance of bi- and tri-antennary core-fucosylated complex type structures carrying one, two, a

78 ans in tACE to be mostly of the biantennary, fucosylated complex type.

79 abling a highly convergent synthesis of core-fucosylated, complex CD52 glycopeptide antigen.

80 od that distinguishes the outer arm and core fucosylated configurations of the N-glycopeptides.

81 the expression of sialyl Lewis X and sialyl-fucosylated core 2 O-glycan (CHO-131 antigen), respectiv

82 dified with tyrosine sulfate and sialylated, fucosylated, core-2 O-glycan(s).

83 ferases required to construct sialylated and fucosylated, core-2 O-glycans on PSGL-1.

84 d NK cells and cells activated only with its fucosylated counterpart.

85 In a recent study, we identified a fucosylated damage-associated ligand exposed by ischemia

86 d on the human receptor CD147/Basigin, while fucosylated derivatives of this N-glycan impaired bacter

87 finity binding epitope of SL2-1 was alpha1-6 fucosylated di-n-acetylchitobiose.

88 Six non-fucosylated diantennary complex type glycoforms were det

89 lycans are of the complex type with the core-fucosylated disialylated biantennary and trisialylated t

90 to be important for the recognition of an O-fucosylated EGF repeat by all three mammalian Fringes.

91 nants for the recognition of an individual O-fucosylated EGF repeat by the Fringe enzymes.

92 uences that will allow us to predict which O-fucosylated EGF repeats are modified by the Fringes.

93 laboratory have demonstrated that not all O-fucosylated EGF repeats of Notch are further modified by

94 It is probable that these highly fucosylated epitopes contribute to the immunosuppressive

95 , unexpected mucosal expression of alpha(1,2)fucosylated epitopes in nonsecretor individuals was freq

96 ression of Slc35c2 reduces expression of the fucosylated epitopes Lewis X and sialylated Lewis X in C

97 hat BambL could recognize a wide spectrum of fucosylated epitopes, albeit with a lower affinity for b

98 Fucosylated epitopes: the H-type-1 antigen and those rec

99 A hypo-fucosylated form of adalimumab bound human FcgammaRIIIa

100 A hypo-fucosylated form of anti-TNF binds FcgammaRIIIa with hig

101 N-glycans and milk oligosaccharides based on fucosylated fragment ions with characteristic CCSs.

102 Fucosylated (Fu)-Hp purified from SPs upregulates inflam

103 ution structures of both nonglycosylated and fucosylated FVII EGF-1 in the presence of CaCl2.

104 The overall structure of fucosylated FVII EGF-1 is very similar to the nonfucosyl

105 on constants (Kd) for the nonfucosylated and fucosylated FVII EGF-1 were found to be 16.4 +/- 1.8 and

106 toward a variety of sulfated, sialylated, or fucosylated Gal beta 1,3/4GlcNAc beta- or Gal beta 1,3Ga

107 discerned with sulfated, sialylated, and/or fucosylated Gal beta 1,3/4GlcNAc beta-based acceptor moi

108 resolution of all seven sets of sialylated, fucosylated galactosyllactose and lactosamine HMO buildi

109 rum albumin coupled with a common glycoform (fucosylated glycan lacking the alpha1,3-linked mannose)

110 Selectin interactions with fucosylated glycan ligands mediate leukocyte rolling in

111 for investigations into the role of specific fucosylated glycan motifs of schistosomes in parasite-ho

112 one or more alpha2,3-sialylated and alpha1,3-fucosylated glycan receptors that are unique from those

113 teract with alpha2,3-sialylated and alpha1,3-fucosylated glycan receptors, including 6-sulfo-sialyl L

114 od fluke Schistosoma mansoni produces highly fucosylated glycan structures on glycoproteins and glyco

115 lectively block the endogenous generation of fucosylated glycan structures.

116 orders was shown for twins with low level of fucosylated glycans and high level of non-fucosylated gl

117 that neither the FUT loci nor their cognate fucosylated glycans are essential to normal development.

118 CD43 lacks the fucosylated glycans found on PSGL-1 and is enriched for

119 f another locus that regulates production of fucosylated glycans in intestinal enterocytes.

120 DC-SIGN has high affinity for fucosylated glycans in several plant glycoproteins and p

121 ned insights into the role of sialylated and fucosylated glycans in zebrafish hematopoiesis.

122 The affinity of BambL for small fucosylated glycans is very high as demonstrated by micr

123 Fucosylated glycans on pathogens are known to shape the

124 Modeling of MsaFBP32 complexed with fucosylated glycans that are widely distributed in proka

125 etailed structures and roles of other highly fucosylated glycans that co-exist in the parotid gland a

126 Two fucosylated glycans were found to be up-regulated in hea

127 y that selectins and DC-SIGN bind to related fucosylated glycans, but the mechanism of the interactio

128 orhabditis elegans expresses a wide range of fucosylated glycans, including N-linked oligosaccharides

129 attack the human glycome, how it copes with fucosylated glycans, which are primarily histo-blood gro

130 eutrophils depend on sialylated and alpha1,3-fucosylated glycans.

131 rTF(1-263) contain high mannose, hybrid, and fucosylated glycans.

132 (PSGL-1), as well as sialylated and alpha1,3-fucosylated glycans.

133 l tool to address functional questions about fucosylated glycans.

134 ctra and incorrect structural assignments of fucosylated glycans.

135 nants, including core beta-xylose and highly fucosylated glycans.

136 of fucosylated glycans and high level of non-fucosylated glycans.

137 as well as asymmetrically and symmetrically fucosylated, glycans were identified from HCCF in experi

138 m-free NMRI mice revealed that production of fucosylated glycoconjugates and an alpha1, 2-fucosyltran

139 The intracellular localization of fucosylated glycoconjugates was visualized by using fluo

140 ging but highly desirable; resolution of the fucosylated glycoforms is of particular interest due to

141 resented as relative abundance of individual fucosylated glycoforms normalized to the level of their

142 f the outer arm and total fucosylation of 12 fucosylated glycoforms of 9 glycopeptides in 7 plasma pr

143 line results in the production of fully core-fucosylated glycoforms of the oligomannose substrate Man

144 eported glycoforms of IgG1, including doubly fucosylated glycoforms.

145 utant animals are defective in production of fucosylated glycolipids and that bre-1 mutant animals ma

146 lular fucosylation and facilitate studies of fucosylated glycoproteins and glycolipids.

147 CTB-binding fucosylated glycoproteins are present in normal human in

148 n leukocyte CD11b/CD18 and basally expressed fucosylated glycoproteins followed by binding to desmoso

149 ttle is known about the distribution of core-fucosylated glycoproteins in mammalian tissues.

150 synthesis of structurally well-defined, core-fucosylated glycoproteins remains a challenging task due

151 Notably, fucosylated GSL such as Fuc-(n)Lc4Cer generally showed a

152 Moreover, fucosylated GSLs were recognized as potential tumor-asso

153 ted GSLs (e.g., Gb3Cer/Gb4Cer precursors and fucosylated GSLs) in tissue biopsies from three CRC pati

154 The presence of fucosylated HBGAs in saliva and stomach biopsy specimens

155 th the defucosylated pentasaccharide and the fucosylated hexasaccharide without a significant differe

156 he first example of production of fully core-fucosylated high-mannose glycoforms.

157 The capability to preferentially consume fucosylated HMO suggests a competitive advantage for the

158 A prominent fucosylated HMO, 2'-fucosyllactose, failed to elicit the

159 l gene cluster devoted to the utilization of fucosylated HMO, including genes for import of fucosylat

160 se, certain strains additionally metabolized fucosylated HMO.

161 ing revealed a preference for consumption of fucosylated HMO.

162 HMO diversity, (2) the sum of sialylated and fucosylated HMOs, (3) 6 a priori HMOs linked with infant

163 for general categories of HMOs (total HMOs, fucosylated HMOs, and sialylated HMOs), 51 individual HM

164 by the presence and near-absence of alpha1-2-fucosylated HMOs, respectively.

165 e fecal microbiota of Fut2(-) mice that lack fucosylated host glycans show decreased alpha diversity

166 wing intravascular administration into mice, fucosylated human CAR-T cells infiltrate marrow with 10-

167 Fucosyllactose (2'-FL), a major component of fucosylated human milk oligosaccharides, is beneficial t

168 These preclinical data indicate that fucosylated human Tregs is an effective strategy for pre

169 d galactosylation, decreased sialylation (of fucosylated IgG glycan structures) and increased bisecti

170 Fucosylated IgG were associated with Spike IgG, CSF prot

171 glycoforms, in which more than 50% were core-fucosylated, implicating a clear GnT I-independent core

172 e domain probes expressed nearly exclusively fucosylated LacdiNAc on bi-antennary complex-type chains

173 produce complex-type N-glycans with alpha1,3-fucosylated LDN (LDNF) GalNAcbeta1-4(Fucalpha1-3)GlcNAcb

174 hus, the HGE bacterium specifically bound to fucosylated leukocyte PSGL-1.

175 nts can be difficult, in particular terminal fucosylated Lewis and blood group antigens present on N-

176 an outer membrane protein that binds to the fucosylated Lewis b histo-blood group antigen on the sur

177 of human adenocarcinomas express sialylated, fucosylated Lewis blood group antigens on cell surface a

178 IL-22 signaling regulates levels of the a1-3-fucosylated Lewis X (Le(x)) blood group antigen, and tha

179 2 signaling regulates levels of the alpha1-3-fucosylated Lewis X (Le(x)) blood group antigen, and tha

180 lly, that simultaneous DC-SIGN engagement by fucosylated ligands and TLR4 signaling was required for

181 participates in the generation of alpha(1,3)fucosylated ligands for L-selectin and provide further e

182 Thus, CD31 and fucosylated ligands of P-selectin seem to be the candida

183 ally could confer a distinct specificity for fucosylated ligands.

184 The production of the homogeneous core-fucosylated Man5GlcNAc2 glycoform of EPO in the FUT8-ove

185 ll surface oligosaccharides contain specific fucosylated moieties expressed in lineage- and/or tempor

186 Specific fucosylated moieties of oligosaccharides and related gly

187 1) and the alpha2,3-sialylated- and alpha1,3-fucosylated-moiety sialyl-Lewis x (sLe(x)), which modifi

188 a closely related sialylated and alpha-(1,3) fucosylated molecule, plays a key role in HGE infection,

189 ulations, confirmed by experiment, predicted fucosylated molecules that are restricted to librations

190 cosylated HMO, including genes for import of fucosylated molecules, fucose metabolism and two alpha-f

191 7 was conjugated to anti-mesothelin and anti-fucosylated monosialotetrahexosylganglioside (FucGM1) an

192 ter pylori, abnormal expression of alpha(1,2)fucosylated motifs and binding of GII.4 virus-like parti

193 ards a subset of glycans containing multiple-fucosylated motifs remained high until 6 weeks post-chal

194 nce to mucus-caused altered phage binding to fucosylated mucin glycans.

195 al alterations include an increase in large, fucosylated, mucin-type glycoproteins, changes in the ty

196 udies indicate that expression of sialylated fucosylated mucins by human carcinomas portends a poor p

197 ant animals, although viable, show a lack of fucosylated N- and O-glycans, based on mass spectrometri

198 the glycosylation reveals that only a single fucosylated N-acetyl glucosamine on N54 is required for

199 We found that Endo-D preferred core-fucosylated N-glycan for hydrolysis but favored nonfucos

200 To unravel the synthesis of highly fucosylated N-glycans by S. mansoni, we examined the abi

201 ine (PHN) labeling for structural studies of fucosylated N-glycans by tandem MALDI mass spectrometry

202 All types of core fucosylated N-glycans have produced two abundant ions co

203 e possible functional significance of highly fucosylated N-glycans is discussed in relation to their

204 d for selective capture and analysis of core fucosylated N-glycans present in complex glycan mixtures

205 rocainamide + H](+) in the tandem MS data of fucosylated N-glycans rapidly verifies core fucosylation

206 Asn623 and Asn752) are occupied with highly fucosylated N-glycans that possess unusual difucosylated

207 healthy human myelin, MOG is decorated with fucosylated N-glycans that support recognition by the C-

208 selective and quantitative profiling of core fucosylated N-glycans using UPLC-HILIC-FLR analysis was

209 which a 55% increase of alpha-2,6-sialylated fucosylated N-glycans was revealed, demonstrating the gr

210 strated its ability to bind to core alpha1-6 fucosylated N-glycans, but not to core alpha1-3 fucosyla

211 osylated N-glycans, but not to core alpha1-3 fucosylated N-glycans, or other alpha1-2, alpha1-3 and a

212 venue to a wide variety of homogeneous, core-fucosylated N-glycopeptides and N-glycoproteins that are

213 Surprisingly, fucosylated N-linked glycans and glycolipids, previously

214 tivity is mediated by sialylated, alpha(1,3) fucosylated, N-linked glycans.

215 The structures of the fucosylated neoglycans in CHO(alpha1, 2)FT cells and the

216 teracting specifically with high mannose and fucosylated neutral carbohydrate structures, langerin ha

217 solated a nonfucosylated and three variously fucosylated neutral oligosaccharides from human milk tha

218 Fucosylated O- and N-linked glycans are essential recogn

219 ults demonstrate that PSGL-1 contains unique fucosylated O-glycans that are predicted to be critical

220 PSGL-1 requires sialylated, fucosylated O-linked glycans and tyrosine sulfate to bin

221 ressing cell line was found to be fully core-fucosylated oligomannose glycan (Man5GlcNAc2Fuc).

222 , agalacto, bisected biantennary, and a core-fucosylated oligosaccharide in the position of Asn B37 w

223 glycan moiety consisting of a sialylated and fucosylated oligosaccharide properly positioned on a cor

224 Fucosylated oligosaccharide structures were widely ident

225 nsensus motif, was modified with biantennary fucosylated oligosaccharide structures.

226 Fucosylated oligosaccharides and glycoconjugates have be

227 gests that the N-CRD recognizes more complex fucosylated oligosaccharides and with a relatively highe

228 -dimensional structure and dynamics of three fucosylated oligosaccharides are investigated using a co

229 Fucosylated oligosaccharides have been proposed to be in

230 combinant Sfrs1 protein bound to a series of fucosylated oligosaccharides in glycan array and plate-b

231 The expression of specific fucosylated oligosaccharides in milk thus varies in rela

232 Determination of fucosylated oligosaccharides is particularly important d

233 alpha(1,3)Fucosylated oligosaccharides represent components of leu

234 Additionally, administration of fucosylated oligosaccharides to C. rodentium-challenged

235 are the ancestral state in angiosperms, with fucosylated oligosaccharides transported across the plas

236 ed recombinantly and demonstrated to bind to fucosylated oligosaccharides with a preference for alpha

237 viding access to 6 selectively mono- and bis-fucosylated oligosaccharides.

238 is thus imperative for the synthesis of all fucosylated oligosaccharides.

239 ors but discriminates between differentially fucosylated oligosaccharides.

240 ns, or other alpha1-2, alpha1-3 and alpha1-4 fucosylated oligosaccharides.

241 fetal bovine serum acetylcholinesterase were fucosylated on the innermost N-acetylglucosamine residue

242 y oligosaccharides including structures with fucosylated or sialylated N, N'-diacetyllactosediamine (

243 Sf9 cells mainly processed the fucosylated paucomannosidic structure (GlcNAc)(2)(Mannos

244 appear to be caused by structural changes in fucosylated pectic components such as rhamnogalacturonan

245 hese analyses showed the presence of various fucosylated, phosphorylated, sialylated, and multiply su

246 d neutrophils, and a cell line devoid of the fucosylated platelet selectin glycoprotein ligand 1 (PSG

247 ls were co-administered with MSCs or ex vivo fucosylated prior to injection, respectively.

248 ccharides included sialylated, sulfated, and fucosylated products based on mass spectrometry.

249 Fucosylated proteins are shed into the lumen and fucose

250 oying CD11b/CD18 as a probe to blot T84 cell fucosylated proteins purified via fucose-specific lectin

251 he characteristic punctate localization of O-fucosylated proteins suggest that TgSPY controls the lev

252 on encodes an adhesin that binds an alpha1-2 fucosylated receptor(s) present in the cecal mucosa.

253 We showed that, compared to fully fucosylated (referred to as wild-type in the text) b12,

254 -Xaa(2)-(Ser/Thr)-Cys-Xaa-Xaa-Gly (where the fucosylated residue is underlined).

255 It is surprising that some of the fucosylated schistosome glycans contain the Lewis x (Le(

256 Fucosylated selectin ligands are essential for all inter

257 to express alpha2-3-sialylated and alpha1-3-fucosylated selectin ligands such as sialyl Lewis x (sLe

258 ed can allow rapid identification of various fucosylated, sialylated, sulfated glycotopes and definit

259 e chains - a key step in the biosynthesis of fucosylated sidechains of galactoxyloglucan.

260 Selectins bind to sialylated and fucosylated sLe(x) receptors, and two enzymes, fucosyltr

261 alter milk concentrations of HMO, including fucosylated species.

262 idase digestions, and co-chromatography with fucosylated standards, the product of the reaction with

263 ed nonfucosylated seed amyloid xyloglucan or fucosylated stem xyloglucan as a substrate with equal fa

264 glycans might be complicated by the partial fucosylated structure and the alpha-Gal (1-3)-beta-Gal o

265 Similar fucosylated structures are also commonly found in a vari

266 All fucosylated structures contained a core (alpha1-6-linked

267 Genetic deletion of these fucosylated structures in the mouse has been a powerful

268 The functional significance of these fucosylated structures is incompletely defined, although

269 We further show that fucosylated structures promote CTB entry into a colonic

270 mplying that as yet unidentified sialylated, fucosylated structures serve as physiologically relevant

271 es (10-15%) of extended SLex with internally fucosylated structures: NeuAc alpha 2-->3 Gal beta 1-->4

272 mprise a large enzyme family that recognizes fucosylated substrates with diverse alpha-linkages on th

273 Enzymatic synthesis of fucosylated sugars in milligram scale was successfully p

274 C-type lectins that bind certain sialylated, fucosylated, sulfated glycoprotein ligands.

275 somers, and regioisomers of afucosylated and fucosylated sulfoglycans containing sulfated-6-GlcNAc an

276 ent ADCC, even at very low Ag density, where fucosylated target Abs did not elicit ADCC.

277 nd similarly to alpha3-sialylated and alpha2-fucosylated terminal LN, but not to alpha6-sialylated an

278 LN, but not to alpha6-sialylated and alpha3-fucosylated terminal LN.

279 ding many species with highly charged and/or fucosylated termini.

280 studies have suggested that the sialylated, fucosylated tetrasaccharide sialyl Lewis X (sLex) is an

281 -galactosyl-capped trisaccharide and the two fucosylated tetrasaccharides.

282 A minority of the O-glycans are alpha-1,3-fucosylated that occur as two major species containing t

283 clinical data suggesting that use of ex vivo fucosylated third-party human regulatory T cells (Tregs)

284 e 2 O-linked glycans that are sialylated and fucosylated to bind P- and E-selectin.

285 Selectin ligands must be alpha1-3 fucosylated to form glycan determinants such as sialyl L

286 The DG9-glycan index, which is the ratio of fucosylated to nonfucosylated triantennary glycans, prov

287 he untreated Tregs, the murine recipients of fucosylated Tregs maintained weight, had ameliorated cli

288 In a xenogenic GVHD mouse model, fucosylated Tregs showed prolonged periods of in vivo pe

289 MALDI-MS data revealed several fucosylated tri- and tetra-antennary glycans which were

290 The level of core-alpha-1,6-fucosylated triantennary glycan (NA3Fb) increased both o

291 Glycopeptide 1 with the fucosylated trisaccharide, beta-d-GlcNAc(1-->4)[alpha-l-

292 e pd-A1PI, most glycans on recA1P1 were core fucosylated via alpha(1-6) linkage.

293 ures, sometimes methylated and core alpha1,6-fucosylated, with terminal beta1,3-linked galactose; a r

294 These results suggest that fucosylated XyG is a suitable substrate for at least one

295 ble genotypes all had substantial amounts of fucosylated XyGs and weakly ME-HGs, but lacked heavily M

296 s of PD-resistant grapevine genotypes lacked fucosylated XyGs and weakly methyl-esterified HGs (ME-HG

297 upport the conclusion that weakly ME-HGs and fucosylated XyGs are substrates of the pathogen's CWDEs

298 s) seeds, which produce large amounts of non-fucosylated xyloglucan as a seed storage polymer.

299 tain less than 2% of the wild-type amount of fucosylated xyloglucan because of a point mutation in th

300 polymer, XTR9 has a clear preference for non-fucosylated xyloglucan polymer.