ライフサイエンスコーパス: glycoconjugate

1 ommon germline precursor when presented as a glycoconjugate.

2 from rabbits immunized with a trisaccharide glycoconjugate.

3 nt, suggesting that this antigen is likely a glycoconjugate.

4 and a comprehensive set of ganglioside-based glycoconjugates.

5 are used to assemble other bacterial surface glycoconjugates.

6 ty of PllA for alpha-galactoside-terminating glycoconjugates.

7 ith specific carbohydrate structures of MFGM glycoconjugates.

8 carbohydrate-centered and heteromultivalent glycoconjugates.

9 lipids and proteins on their surface, called glycoconjugates.

10 r the fragmentation of peptide backbones and glycoconjugates.

11 lex undertaking that requires access to pure glycoconjugates.

12 ilability and enhances desialylation of host glycoconjugates.

13 pon dehalogenation gave C-2 deoxy amino acid glycoconjugates.

14 as modular building blocks for more complex glycoconjugates.

15 els in glucose-containing polysaccharides or glycoconjugates.

16 e protein toward beta1-galactosyl-terminated glycoconjugates.

17 oval of sialic acid residues from sialylated glycoconjugates.

18 , yielding 'multicopy-multivalent' nanoscale glycoconjugates.

19 interacting with beta1-galactosyl-terminated glycoconjugates.

20 an affinity for beta-galactoside containing glycoconjugates.

21 nition sites on the cell surface or secreted glycoconjugates.

22 yse the removal of terminal sialic acid from glycoconjugates.

23 in order to provide monodisperse multivalent glycoconjugates.

24 ng end of the bulk of cell surface-expressed glycoconjugates.

25 upon microbiota, including growth-promoting glycoconjugates.

26 properties and protein binding functions of glycoconjugates.

27 c acids are essential components of membrane glycoconjugates.

28 known to be caused by impaired synthesis of glycoconjugates.

29 yranosyl 4,6-diols from oligosaccharides and glycoconjugates.

30 elected proteins, lipids, nucleic acids, and glycoconjugates.

31 of acrylamide directly from sugar-asparagine glycoconjugates.

32 responsible for the memory response to some glycoconjugates.

33 des without the context of other glycans and glycoconjugates.

34 to install non-natural monosaccharides into glycoconjugates.

35 ide applications in the synthesis of complex glycoconjugates.

36 is of oligosaccharides, polysaccharides, and glycoconjugates.

37 s of Glu-47 and Lys-50 do not restore GlcNAc glycoconjugates.

38 e for the synthesis of biologically relevant glycoconjugates.

39 allenge for glycobiology and the analysis of glycoconjugates.

40 r conjugation to bovine serum albumin (BSA), glycoconjugates 1 to 6 were used to develop individual i

41 erse range of novel regioselective triazolyl glycoconjugates 6a-u have been achieved in high yields v

42 The glycoconjugate 8 displayed excellent affinity and select

43 S1 overexpressing tumors, the diarylpyrazole glycoconjugate 8, derived from the potent NTS1 antagonis

44 -hexosaminidase with consequent clearance of glycoconjugates, alpha-synuclein and ubiquitinated prote

45 hat dictates the solution behaviour of these glycoconjugates, although the lower intrinsic viscositie

46 tion strategy based on immunization with the glycoconjugate and the subsequent administration of an i

47 thogen that encounters terminally sialylated glycoconjugates and free sialic acid (Sia) in the airway

48 quitous in biologically important classes of glycoconjugates and naturally occurring oligosaccharides

49 acid diester mediated coupling reactions for glycoconjugates and presents recent advances that aim to

50 sed for characterising, imaging or targeting glycoconjugates and, when printed on microarrays, they a

51 e lungs, we found extensive desialylation of glycoconjugates, and upregulation of sialidases.

52 esized and conjugated to proteins to provide glycoconjugate antigens and conjugate vaccines.

53 nt synthesis methods of oligosaccharides and glycoconjugates are a requisite.

54 Glycoconjugates are composed of carbohydrate building bl

55 L-Fucose-containing glycoconjugates are essential for a myriad of physiologi

56 Glycoconjugates are formed through a process called glyc

57 These glycoconjugates are involved in host-cell interactions a

58 eoxy amino l-sugars present in the bacterial glycoconjugates are not available from natural sources.

59 Polysaccharides and glycoconjugates are not encoded directly by genes; inste

60 tively, these results suggest that CPS-based glycoconjugates are promising candidates for the develop

61 Our results suggest that these glycoconjugates are promising candidates for vaccine for

62 The obtained glycoconjugates are related to fragments of exopolysacch

63 Cell surface glycoconjugates are used as markers for undifferentiated

64 r classes of biomolecules, carbohydrates and glycoconjugates are widely involved in numerous biologic

65 ggest that the shifting between the sulfated glycoconjugates as distinct targets of CTX A2, A3, and A

66 Using the organogels formed by the glycoconjugates as supramolecular catalysts, efficient c

67 fic and concomitant interaction with the two glycoconjugates as well as on dynamic avidity effects ty

68 e purification and characterization of other glycoconjugates as well.

69 via metabolic incorporation into endogenous glycoconjugates, as interactions with circulating anti-N

70 e-specific HIV-neutralizing antibodies using glycoconjugates based on the Rv3 LOS structure.

71 for the preparation of oligosaccharides and glycoconjugates bearing the 1,2-cis-2-amino glycosidic l

72 otocol has been developed for easy access to glycoconjugate benzothiazoles from protected carbohydrat

73 nsorgrams provides robust information of the glycoconjugate binding efficiency and real-time structur

74 umbers) are known to produce a wide range of glycoconjugate biopolymers with apparent benefits to hea

75 osamines, which are potential precursors for glycoconjugate biosynthesis.

76 e was assessed for a selected S. Typhimurium glycoconjugate by challenge with live Salmonella.

77 , it is now possible to generate tailor-made glycoconjugates by attaching polysaccharides derived fro

78 h direct engagement of specific cell surface glycoconjugates by traditional ligand-receptor binding.

79 . Typhimurium, we have synthesized different glycoconjugates, by linking O-antigen and core sugars (O

80 l versatility of glycan epitopes in cellular glycoconjugates calls for developing sensitive methods t

81 alyx associated with specific glycoforms and glycoconjugates can be monitored with quantitation using

82 that glycosylation and thus the function of glycoconjugates can be regulated by a protein that helps

83 Measurement of concentrations of selected glycoconjugates can be used to screen for many of these

84 Glycoconjugates can block such interactions and thereby

85 glycome describes the complete repertoire of glycoconjugates composed of carbohydrate chains, or glyc

86 Here, we evaluate the use of glycoconjugates consisting of these proteins and an ente

87 The glycoconjugates containing six branches showed significa

88 Glycoconjugates containing stable, monovalent synthetic

89 ormation has been available concerning their glycoconjugate content.

90 a family of glycosaminoglycan (GAG)-protein glycoconjugates, contribute to animal physiology through

91 nses against the OPS or CPS component of the glycoconjugates could be raised in BALB/c mice, only tho

92 can also be secreted to bind to cell surface glycoconjugate counterreceptors.

93 Various glycoconjugates decorate the sperm surface, including si

94 The formation of glycoconjugates depends on nucleotide sugars, which serv

95 The hydrophilic glycoconjugate derivative (12) showed improved inhibitio

96 uggests that DMAG may be an active cell wall glycoconjugate driving host-pathogen interactions and pa

97 obtaining the glycan's crystal structure in glycoconjugates due to its flexibility and heterogeneity

98 ation and on the obtention of lysine-glucose glycoconjugates during Maillard reaction (MR) has been s

99 ary is presented as a mixture of glycans and glycoconjugates, each of which is coded with a unique ol

100 esults of immunized studies showed all three glycoconjugates elicited antibodies that recognized all

101 ndard for the structural characterization of glycoconjugates, especially complex mixtures typical in

102 Terminal sialic acid residues of glycoconjugates exhibit remarkable functional and struct

103 atives, gangliosides, are the major class of glycoconjugates expressed by neurons.

104 ibitory concentration [IC(50)] = 32 nM), the glycoconjugate, FGlc-FAPI (IC(50) = 167 nM), showed slig

105 s known about the regulation of autophagy by glycoconjugates focusing on signaling mechanisms from th

106 baumannii strain 54149 (Ab-54149) to form a glycoconjugate for preparing anti-Ab-54149 EPS serum.

107 ogens' surface and use them to develop novel glycoconjugates for vaccine development.

108 ntensity ultrasound efficiently promotes BLG-glycoconjugates formation by MR in aqueous solutions und

109 ple, the accumulation of volatile phenols in glycoconjugate forms following grapevine exposure to bus

110 hromatography (R-HPLC) to isolate and purify glycoconjugates from several natural sources.

111 cells per muL]) and received a 5 mug dose of glycoconjugate GBS vaccine (serotypes Ia, Ib, and III, w

112 dose of an investigational trivalent CRM197-glycoconjugate GBS vaccine (targeting serotypes Ia/Ib/II

113 dose of an investigational trivalent CRM197-glycoconjugate GBS vaccine (targeting serotypes Ia/Ib/II

114 l vaccination with an investigational CRM197-glycoconjugate GBS vaccine elicited higher GBS serotype-

115 mpare safety and immunogenicity of trivalent glycoconjugate GBS vaccine in pregnant women with and wi

116 This glycoconjugate generated titres of antibodies towards th

117 Glycoconjugates, glycans, carbohydrates, and sugars: the

118 the synthesis of therapeutically significant glycoconjugates (glycosaminoglycans, glycoproteins, glyc

119 Glycoconjugates had an approximately unimodal log-normal

120 Multivalent glycoconjugates have also been used for stimulating the

121 Many multivalent glycoconjugates have therefore been synthesized to study

122 ent data suggest that one mechanism by which glycoconjugates impact physiology is through the regulat

123 y a water-organic solvent interface than its glycoconjugates, important for the formulation in polyme

124 nly influences the physical behaviour of the glycoconjugate in solution.

125 nd enables cell imaging and visualization of glycoconjugates in alkynyl-saccharide-treated cells at e

126 are important for the assembly of essential glycoconjugates in all domains of life.

127 as inhibitors or MCRs of inositol-containing glycoconjugates in eukaryotic and mycobacterial systems.

128 ters (MCRs) for labeling inositol-containing glycoconjugates in eukaryotic cells and potentially in m

129 tigating the roles of C. jejuni cell surface glycoconjugates in host pathogen interactions.

130 nrecognized accumulation of a diverse set of glycoconjugates in NPC1-null and NPC2-deficient fibrobla

131 se UGTs may add to the production of further glycoconjugates in planta.

132 method for the synthesis of C-2 deoxy-2-iodo glycoconjugates in self-assembled structures was found u

133 dy investigated the accumulation of guaiacol glycoconjugates in the fruit, shoots and leaves of Monas

134 side hydrolases (GHs) catalyze hydrolyses of glycoconjugates in which the enzyme choreographs a serie

135 activated capsular polysaccharides and their glycoconjugates - in the form most relevant to their pot

136 These glycoconjugates include tumor-associated carbohydrate an

137 rivatized into C-glycoside analogues of beta-glycoconjugates, including C-disaccharide mimetics.

138 A series of cyclodextrin-based glycoconjugates, including glycoclusters and star glycop

139 dies have indicated a role for nonsialylated glycoconjugates, including histo-blood group antigens (H

140 ranose (Galf)-containing polysaccharides and glycoconjugates, including O-glycans, N-glycans, fungal-

141 to produce a diverse set of species-specific glycoconjugates, including ones heavily modified by fuco

142 eins, CaRe has the potential to purify other glycoconjugates, including proteoglycans.

143 , which when combined produce diastereomeric glycoconjugates indistinguishable by mass spectrometry.

144 mediate opsonophagocytic killing, the other glycoconjugates induced effective opsonic antibodies, wi

145 ing relocation in the heptamer and (ii) that glycoconjugates inhibited VCC by promoting its assembly

146 Thus, this semi-synthetic glycoconjugate is a lead for the development of a vaccin

147 detection of the carbohydrate components of glycoconjugates is critical for advancing glycobiology.

148 regarding the glycan structure of protonated glycoconjugates is hindered by the inability to differen

149 Dysregulation in biosynthesis of sialo-glycoconjugates is known to be associated with neurologi

150 and sialic acid, a major component of airway glycoconjugates, is identified as the host-derived metab

151 cleavage of terminal sialic acids from host glycoconjugates, is involved in both of these processes.

152 ith affinity for beta-galactoside-containing glycoconjugates, is upregulated upon infection, and it h

153 fluenzae type b (Hib), and the corresponding glycoconjugate made by conjugating this with the tetanus

154 reased protection over that obtained with TT glycoconjugates made using smaller OAgs.

155 and action mechanisms via distinct sulfated glycoconjugate-mediated processes.

156 ed the effects of meningococcal quadrivalent glycoconjugate (MenACWY-CRM) or serogroup B (4CMenB) vac

157 N. lactamica is even more potent than after glycoconjugate meningococcal vaccination.

158 the concise synthesis of naturally occurring glycoconjugate motifs containing N-acetylgalactosamine (

159 in fusion proteins to sialic acid-containing glycoconjugates, observed in enzyme-linked immunosorbent

160 ns revealed that binding of the two types of glycoconjugates occurs within different binding sites.

161 ne (3a-3x), 2-spiroquinazolinone (5, 7), and glycoconjugates of 2,3-dihydroquinazolin-4(1H)-one (10a,

162 the construction of glycosidic scaffolds and glycoconjugates of biological and chemical interest.

163 cessfully used for labeling azido-containing glycoconjugates of living cells.

164 Vaccination with glycoconjugates of MenA capsular polysaccharide led to a

165 The biosynthesis of the major cell envelope glycoconjugates of Mycobacterium tuberculosis is topolog

166 In this study, we use glycoconjugates of type 3 Streptococcus pneumoniae CPS (

167 Fucose is a sugar present in glycoconjugates often associated with recognition and ad

168 bing the galectin-induced multimerization of glycoconjugates on cultured cells.

169 negative charges provide high mobilities of glycoconjugates on polyacrylamide gel electrophoresis (P

170 mediated by lectins (adhesins) that bind to glycoconjugates on the surface of host cells.

171 Sialylated glycoconjugates on the surfaces of mammalian cells play

172 ha-GalNAc epitope and cross-link low valency glycoconjugates, only SBA showed a tendency to form inte

173 Glycoconjugates play a central role in several cellular

174 Indeed, carbohydrates and glycoconjugates play a major role in key biological even

175 of glycosidic bonds in oligosaccharides and glycoconjugates pose a bottleneck in enabling the remark

176 tereochemical isomers present in glycans and glycoconjugates poses a formidable challenge for compreh

177 HBGAs are genetically determined glycoconjugates present in mucosal secretions, epithelia

178 design and synthesis of a panel of 24 novel glycoconjugate primary sulfonamides that bind to the ext

179 independent microwells in which 64 spots of glycoconjugates probes are arrayed by using DNA Directed

180 hondroitin sulfate (CS) over other potential glycoconjugate products.

181 fter grapevine treatment; however, different glycoconjugate profiles were apparent.

182 ies recognising separate epitopes on a large glycoconjugate protein complex, is co-expressed with SOX

183 In this work, glycoconjugate prototypes were prepared by coupling S. s

184 tially directional resorcin[4]arene cavitand glycoconjugates (RCGs) have been applied as efficient re

185 dissect the mechanisms that underlie altered glycoconjugate recycling and storage in disease.

186 These reagents were applied to reveal the glycoconjugates regulating human myeloid cell adhesion t

187 d dissemination project for carbohydrate and glycoconjugate-related data retrieved from multiple inte

188 gical potential as these enzymes can produce glycoconjugates relevant to the pharmaceutical industry.

189 The uniquely modified glycoconjugates represent valuable tools for investigati

190 The addition of Sia to glycoconjugates requires metabolic activation to CMP-Sia

191 s spectrometry, to quantify guaiacol and its glycoconjugates, respectively.

192 nization with the synthetic hexasaccharide 1 glycoconjugate resulted in high titers of cross-reactive

193 display aberrant surface glycans and related glycoconjugate scaffolds.

194 h cellular cAMP and [Ca(2+)](i) to stimulate glycoconjugate secretion from CGCs, but the interaction

195 High molecular weight glycoconjugate secretion was measured with an enzyme-lin

196 s a cAMP-dependent increase in [Ca(2+)]i and glycoconjugate secretion, but not ERK1/2 activation.

197 .5 mug, 5.0 mug, or 20 mug) of each of three glycoconjugates (serotypes Ia, Ib and III).

198 of 0.5, 2.5, or 5.0 mug of each of 3 CRM197-glycoconjugates (serotypes Ia, Ib, and III), or placebo.

199 The glycoconjugates showed >/=94% residual enzyme activity a

200 These glycoconjugates showed high affinity binding to the huma

201 Rabbit sera raised against these glycoconjugates showed Immunoglobulin G titers against t

202 novo sequencing of purified plant metabolite glycoconjugates, showing that the anomeric signature is

203 spite possessing high levels of GPI-anchored glycoconjugates, SMT-null mutants showed significantly a

204 Subsequently, we investigated glycoconjugate structure, activity, and stability.

205 structure and protein environment of natural glycoconjugate substrates influences CAZyme activity.

206 resent on their surfaces natural multivalent glycoconjugates such as lipopolysaccharides and S-layers

207 es miscellaneous applications of oxime-based glycoconjugates, such as enantioselective catalysis and

208 lockade of this receptor through multivalent glycoconjugates supposes a promising biological target t

209 ply may also be important for nucleotide and glycoconjugate syntheses in the insect host.

210 Glycoconjugate synthesis is a dynamic process that depen

211 s a simple, flexible biocatalytic method for glycoconjugate synthesis using PglB N-glycosylation mach

212 tomized native chemical ligation concept for glycoconjugates synthesis, utilizing a meticulously cont

213 All of the glycoconjugates tested induced Tcarb-dependent responses

214 riants had lower levels of GlcNAc-containing glycoconjugates than WT cells, indicating impaired UDP-G

215 This makes it difficult to design a glycoconjugate that can potently and specifically target

216 Here, we report the synthesis of a glycoconjugate that displays the so-called 'inner core'

217 ly on the availability of chemically defined glycoconjugates that can be selectively modified under o

218 Cell surfaces are often decorated with glycoconjugates that contain linear and more complex sym

219 may enhance turnover of N-cadherin and other glycoconjugates that determine junctional stability and

220 urfaces of bacteria are replete with diverse glycoconjugates that play pivotal roles in determining h

221 gands comprise a heterogeneous collection of glycoconjugates that share related glycan structures but

222 porter strategy for labeling of cell surface glycoconjugates that takes advantage of recombinant glyc

223 A key component of this structure is a glycoconjugate, the mycolyl-arabinogalactan-peptidoglyca

224 Our results suggest that the ability of a glycoconjugate to simultaneously block all binding sites

225 acteria that must secrete proteins and large glycoconjugates to grow, divide, and persist.

226 However, progress toward complex glycoconjugate total synthesis has been slowed by the ne

227 molecules, mimicking mammalian cell surface glycoconjugates triggering autoimmune responses.

228 Yariv reagents are glycoconjugate tris-azo dyes widely used in plant biolog

229 bolism in particular genes facilitating host glycoconjugates use.

230 tructure prediction/modeling of N-glycans of glycoconjugates using structure database could be effect

231 development of a candidate O-antigen-CRM197 glycoconjugate vaccine against S. Typhimurium.

232 idly, following the recent introduction of a glycoconjugate vaccine against serogroup A.

233 ously described a mechanism by which a model glycoconjugate vaccine can activate the adaptive immune

234 In conclusion, an O-antigen-CRM197 glycoconjugate vaccine can induce O-antigen-specific ant

235 ied this system to the characterization of a glycoconjugate vaccine candidate consisting of a genetic

236 ans were conjugated to DT protein to provide glycoconjugate vaccine candidates (DT-Hexa, DT-Hepta, an

237 -->2)-beta-mannans and to the viability of a glycoconjugate vaccine composed of a minimal length olig

238 y of all polysaccharides of a multicomponent glycoconjugate vaccine CRM197-MenACWY.

239 vaccine similar to that which occurs with a glycoconjugate vaccine despite a less robust reduction i

240 particularly advantageous in the context of glycoconjugate vaccine development.

241 (HMW)], and in a mouse model of tularemia, a glycoconjugate vaccine made with the HMW polysaccharide

242 umoniae Some components of the S. pneumoniae glycoconjugate vaccine Prevnar13 that contains CPS antig

243 chieved with other encapsulated pathogens, a glycoconjugate vaccine strategy was selected to elicit o

244 Therefore, a glycoconjugate vaccine targeting these 2 serotypes could

245 rst steps toward identifying components of a glycoconjugate vaccine to prevent E. faecium infection.

246 tularensis has been considered for use in a glycoconjugate vaccine, but conjugate vaccines tested so

247 the successful generation of an experimental glycoconjugate vaccine.

248 that differences in the design of OAg-based glycoconjugate vaccines against invasive African S. Typh

249 Here, we report the development of candidate glycoconjugate vaccines against MenX and preclinical dat

250 findings support the further development of glycoconjugate vaccines against MenX and their assessmen

251 operties which may affect the performance of glycoconjugate vaccines against serious disease are mola

252 are valuable targets for the development of glycoconjugate vaccines and diagnostics.

253 Glycoconjugate vaccines are among the most effective int

254 Pneumococcal glycoconjugate vaccines are expensive and provide limite

255 Although glycoconjugate vaccines are generally very efficacious,

256 Conventionally, glycoconjugate vaccines are manufactured using intricate

257 Glycoconjugate vaccines based on isolated capsular polys

258 s pave the way to the design of well-defined glycoconjugate vaccines based on short synthetic oligosa

259 Glycoconjugate vaccines based on synthetic oligosacchari

260 rotection against infection; therefore, O-PS glycoconjugate vaccines have proven useful against a num

261 n shown to potentiate the immune response to glycoconjugate vaccines in humans, we investigated if Al

262 However, the application of glycoconjugate vaccines in the animal health sector is l

263 However, the distribution of effective glycoconjugate vaccines in this region is limited by the

264 ents a proof of concept for the potential of glycoconjugate vaccines in veterinary medicine applicati

265 Glycoconjugate vaccines provide a safe and reliable stra

266 o prepare, purify and characterize two model glycoconjugate vaccines that can be used to generate Tca

267 ibe an alternative methodology for producing glycoconjugate vaccines whereby recombinant O-PS biosynt

268 Glycoconjugate vaccines, consisting of an antigenic carr

269 support the use of Alum-TLR7 as adjuvant for glycoconjugate vaccines.

270 signation 'Tcarbs') after stimulation by two glycoconjugate vaccines.

271 mulation of the immune system by alternative glycoconjugate vaccines.

272 rate, are operative in response to different glycoconjugate vaccines.

273 ride epitopes can aid in the design of novel glycoconjugate vaccines.

274 ion of CPSs with carrier proteins to produce glycoconjugate vaccines.

275 Functionality of the Cyt c glycoconjugates was determined by performing cell-free c

276 blet cell secretion of high molecular weight glycoconjugates was measured by an enzyme-linked lectin

277 Caspase 9 activation by the glycoconjugates was with 92 +/- 7% to 96 +/- 4% within t

278 The synthesized glycoconjugates were arrayed on streptavidin-coated plat

279 All glycoconjugates were compared for immunogenicity and abi

280 -galactosidase A, and these alpha-galactosyl glycoconjugates were found in corneal keratocytes, lens

281 Guaiacol glycoconjugates were observed in fruit and leaves in par

282 Solubility and emulsifying properties of glycoconjugates were significantly improved as compared

283 Different glycoconjugates were synthesized by coupling MenX oligos

284 Five neo-glycoconjugates were synthesized, Lac4-Cyt-c, Lac9-Cyt-c

285 he CRM197 carrier protein, and the resulting glycoconjugates were used to immunize rabbits.

286 but also the GLUT1 specificity of resulting glycoconjugates, where GLUT1 is glucose transporter 1.

287 ling intra- and extracellular azido-modified glycoconjugates, whereas S-DIBO 8 cannot pass the cell m

288 s concept and are devising a plethora of neo-glycoconjugates which can interfere with a series of pat

289 --> 2)-S-linked thiosaccharides and S-linked glycoconjugates, which are difficult to synthesize by cl

290 homogeneous samples of oligosaccharides and glycoconjugates, which could be accessed by chemical, en

291 y responses against the CPS component of the glycoconjugate, while immunization with Hcp1 and TssM pr

292 lity to quantitate individual glycoforms and glycoconjugates will find utility in a broad range of fu

293 A series of glycoconjugates with defined connectivity were synthesiz

294 t glucals and rhamnals into disaccharides or glycoconjugates with high alpha-selectivity and yields (

295 e the simulation system and input of various glycoconjugates with most sugar types and chemical modif

296 Dilignol glycoconjugates with reduced structures were found in th

297 and K(d) values provided similar ranking for glycoconjugates with respect to PA-IL binding thus affor

298 surface carbohydrates as well as of soluble glycoconjugates with their receptor proteins rule fundam

299 zine, allowing for the imaging of sialylated glycoconjugates within live zebrafish embryos.

300 study of the dynamic changes occurring among glycoconjugates within the cellular compartments.