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1 crystal structure of SBA cross-linked with a biantennary analog of the blood group I carbohydrate ant
2               Studies with monoantennary and biantennary analogs and mixtures suggest that Stx1, Stx2
3 sible, human IgG N-glycans are predominantly biantennary and fucosylated and contain varying levels o
4 d glycerophospholipid species, as well as in biantennary and GlcNAc-bisecting N-glycans, particularly
5                The results suggest that SLex biantennary and triantennary are N-linked oligosaccharid
6 inked oligosaccharides, with specificity for biantennary and triantennary complex glycans.
7 acokinetic profiles were identified for SLex biantennary and triantennary oligosaccharides but not fo
8 tribution studies established that both SLex biantennary and triantennary oligosaccharides distribute
9  type with the core-fucosylated disialylated biantennary and trisialylated triantennary structures pr
10 ealed an N-linked asialo, agalacto, bisected biantennary, and a core-fucosylated oligosaccharide in t
11  and nonfucosylated forms of hybrid, complex biantennary, and triantennary glycans account for 12% of
12 glycopeptide, including high-mannose/hybrid, biantennary, and triantennary with/without core fucose,
13 oss-linked with four isomeric analogs of the biantennary blood group I carbohydrate antigen.
14  relative affinities of the proteins for the biantennary carbohydrate.
15 aled nanotubes were covalently modified with biantennary carbohydrates, improving dispersibility and
16 st how DGL discriminates against binding the biantennary complex carbohydrate relative to ConA.
17 xy analogs of the core trimannoside and to a biantennary complex carbohydrate were determined by isot
18  show substantially reduced affinities for a biantennary complex carbohydrate with terminal GlcNAc re
19 ermodynamics of binding of DGL and ConA to a biantennary complex carbohydrate.
20 linked carbohydrates, but lower affinity for biantennary complex carbohydrates.
21   However, unlike ConA, DGL does not bind to biantennary complex carbohydrates.
22           This was confirmed by showing that biantennary complex glycopeptides do not bind to a DGL-S
23 he three carbohydrate structures were of the biantennary complex type, but only the ones from fetal b
24           Both glycans are xylose containing biantennary complex types that share the common core str
25 high mannose-type (33.3%), (ii) disialylated biantennary complex-type (19.2%), and (iii) alpha-galact
26 igosaccharide oxazoline corresponding to the biantennary complex-type N-glycan was synthesized and te
27 cNAcbeta1-O-pNP and to a GlcNAc-terminating, biantennary, complex N-glycan, with or without a core fu
28              One group represents sialylated biantennary compounds with an N-glycan core terminating
29  vitro from high mannose to hybrid and on to biantennary, core-fucosylated, complex structures by a p
30 characterization of a glycopeptide bearing a biantennary disialylated glycan.
31  2792.4 in AKC corresponding to a well-known biantennary, disialylated N-glycan.
32  with the alpha1-3Man branch of the complex, biantennary Fc glycan preferentially sialylated.
33 heir amino acid sequence and by the complex, biantennary Fc-associated N-linked glycan.
34 ns with little to no binding to galactose on biantennary forms.
35 ne-linked consensus motif, was modified with biantennary fucosylated oligosaccharide structures.
36 N-linked glycans in tACE to be mostly of the biantennary, fucosylated complex type.
37 lycan motifs expressed on CD11b/CD18 such as biantennary galactose could represent novel targets for
38 cognized by the Galanthus Nivalis lectin and biantennary galactosylated N-glycans recognized by the P
39 annose residues (Man(5)GlcNAc(2)), a complex biantennary galactosylated structure with core fucose (G
40  and glycopeptide acceptors, particularly to biantennary, GlcNAc-terminated acceptors.
41 ibody with alpha-2,6-sialylated complex type biantennary glycan (SCT) or its 3-fluorosialyl derivativ
42 ositional isomers of a single sialic acid on biantennary glycan antennae were resolved.
43             The most abundant compound was a biantennary glycan carrying sulfated GlcA on the 6-branc
44 on site on the Fc domain to which a complex, biantennary glycan is attached.
45                                  A synthetic biantennary glycan precursor was (13)C-labeled on all fo
46 mab glycoform with a sialylated complex-type biantennary glycan terminated with 3F(ax)-Neu5Ac in the
47 ntennary glycans, and the relative amount of biantennary glycan versus tri- and tetraantennary glycan
48 The detailed structure of the trifucosylated biantennary glycan was confirmed, together with the stru
49 ar, we observed the increase of bisialylated biantennary glycan, A2G2S[3,6]2, 12 hours after surgery,
50         Previous studies examined binding to biantennary glycans expressing Pk trisaccharide mimics i
51 hat terminal sialic acid residues on complex biantennary glycans significantly enhance IgE's allergic
52 alylated glycopeptides identified carry more biantennary glycans than tri- and tetraantennary glycans
53 tyllactosamine oligosaccharide antennae from biantennary glycans using MS3, and the location of a bis
54 h, and the major complex-type structures are biantennary glycans with Lewisx (Galbeta1-4(Fucalpha1-3)
55 the FcgammaRIa receptor and IgG1s containing biantennary glycans with N-acetylglucosamine, galactose,
56 rom the FcyRIa receptor and IgG1s containing biantennary glycans with N-acetylglucosamine, galactose,
57 le in 72 h at 100 degrees C for glycans with biantennary glycans with or without sialic acids.
58 ally distributed, with N46 containing mostly biantennary glycans, N83 containing primarily tri- and t
59 ments showed GnT-III preferentially modifies biantennary glycans.
60 ary glycans, and N247 containing exclusively biantennary glycans.
61 ases in some nonfucosylated paucimannose and biantennary glycans.
62 ith the structures of another 12 fucosylated biantennary glycans.
63 fer to study the solution conformations of a biantennary glycopeptide and its partially trimmed produ
64 lcNAc preferentially to a GlcNAc-terminating biantennary glycopeptide that contains a core fucose res
65                                In the intact biantennary glycopeptide, the donor-acceptor distance di
66                         The major monosialyl biantennary glycopeptides (see below) were used as subst
67 ides were used for conformational studies of biantennary glycopeptides by energy transfer.
68                                              Biantennary glycopeptides from bovine fibrinogen were fl
69 lated Fc compared with similarly sialylated, biantennary glycoproteins, thus suggesting that a specif
70 It was found to be modified predominantly by biantennary hybrid structures.
71 ed (sialylated, neutral and core fucosylated biantennary IgG glycans) carbohydrates.
72 ve alpha-mannosidase trims some N-glycans to biantennary Man(3)GlcNAc(2).
73 on showed that TbSTT3A selectively transfers biantennary Man(5)GlcNAc(2) to specific glycosylation si
74 e showed that TbGnTI transfers UDP-GlcNAc to biantennary Man3GlcNAc2, but not to triantennary Man5Glc
75 ing that Pg 1 L-lysine binding sites and the biantennary, mannose-containing N-linked oligosaccharide
76 the positional isomers of monogalactosylated biantennary N-glycan and the monogalactosylated bisected
77 ion of the alpha2,6-sialylated terminus of a biantennary N-glycan by viscumin.
78 on linear tetrasaccharides versus on typical biantennary N-glycan core structures were compared regar
79 zed using the MS signal for the disialylated biantennary N-glycan derived from fetuin.
80              The assembly of an asymmetrical biantennary N-glycan from oligosaccharide fragments prep
81 cetylglucosaminyltransferase II activity for biantennary N-glycan production.
82         In this study, it was found that the biantennary N-glycan structure with two terminal alpha-2
83           This platform is based on a native biantennary N-glycan substrate attached to a glassy carb
84                                       With a biantennary N-glycan substrate, it exhibited a 5-fold pr
85                                            A biantennary N-glycan with terminal GlcNAc, beta-1,2 xylo
86 and reveals the presence of a mature complex biantennary N-glycan within the Fd segment.
87 alactose residue or to fully galactosylate a biantennary N-glycan.
88  composition of the agalactosylated bisected biantennary N-glycan.
89 cells was a dramatic reduction of sialylated biantennary N-glycans carrying the terminal NeuGcalpha2-
90  are primarily highly processed complex-type biantennary N-glycans linked to N-glycosylation sites th
91 e Gal(beta4)GlcNAc terminal structure of the biantennary N-glycans on the Fc domain.
92                                 Radiolabeled biantennary N-glycans synthesized by Pro(-)5Lec20 were p
93  Glycosylated human IgG contains fucosylated biantennary N-glycans with different modifications inclu
94 inds internal N-acetylglucosamine on complex biantennary N-glycans with select preference for L1CAM a
95 ary N-glycans and of O-glycans, 2) increased biantennary N-glycans, and 3) reduced LacNAc and sLe(X)
96 1-4GlcNAcbeta1-)(n)) sequences, complex-type biantennary N-glycans, or novel chitin-derived glycans m
97 culating blood glycoproteins are modified by biantennary N-glycans, rendering them unlikely to be lig
98 erize, resulting in the close proximation of biantennary N-glycans.
99 as discernible for a pentasaccharide and for biantennary N-glycans.
100 l galactose and for agalactosylated bisected biantennary N-glycans.
101 convergent synthesis of the sialic acid-rich biantennary N-linked glycan found in human glycoprotein
102 he composition of the complex, Fc-associated biantennary N-linked glycan.
103 2 binds selectively to galactose-terminated, biantennary N-linked glycans.
104 carbohydrates ranging from trisaccharides to biantennary N-linked glycans.
105  and tetraantennary N-linked glycoforms from biantennary N-linked glycoforms bearing terminal sialic
106 he baculovirus system typically lack complex biantennary N-linked oligosaccharide side chains contain
107 oduce recombinant glycoproteins with complex biantennary N-linked oligosaccharides structurally ident
108 e to select glycopeptides containing complex biantennary N-linked, hybrid, and high-mannose glycans,
109  acid appended to glycopeptides with complex biantennary N-linked, hybrid, and high-mannose glycans.
110 g human serum glycoproteins carrying complex biantennary N-linked, hybrid, and high-mannose oligosacc
111 neous compound containing an N-linked asialo biantennary nonasaccharide glycan moiety of defined cova
112 d the complex with its reaction product, the biantennary octasaccharide, Gal-beta(1-4)-GlcNAc-beta(1-
113                                  The complex biantennary oligosaccharide at Asn297 of IgG is essentia
114                               In an N-linked biantennary oligosaccharide chain, one antenna is attach
115 residues along one of the two antenna in the biantennary oligosaccharide has a small effect on the di
116 formational property for the 6' antenna of a biantennary oligosaccharide that is influenced by core f
117                           A core fucosylated biantennary oligosaccharide was converted to a glycosyla
118 ate moiety of both asialoglycopeptides was a biantennary oligosaccharide with a core alpha(1-->6)-lin
119 he conformation of each antenna of a complex biantennary oligosaccharide.
120 has high mannose-, hybrid-, and complex-type biantennary oligosaccharides including structures with f
121                      Our data indicated that biantennary oligosaccharides lacking galactosylation had
122        Using mass spectrometry, complex-type biantennary oligosaccharides were identified as major N-
123 have three characteristics (core-fucosylated biantennary oligosaccharides with one or two N-glycolyln
124 tained typical Fc glycans (core-fucosylated, biantennary oligosaccharides with zero to two Gal residu
125 ans present on rituximab are neutral complex biantennary oligosaccharides with zero, one, and two ter
126 saccharide is similar to that seen for other biantennary oligosaccharides, with the exception of two
127 significant accumulation of core-fucosylated biantennary oligosaccharides.
128 roduced in glycoengineered cells with either biantennary or higher valency triantennary and tetra-ant
129 teractions that are unique to complexes with biantennary or triantennary complex glycans.
130                  Simultaneous dosing of SLex biantennary or triantennary oligosaccharide with a mouse
131 es were conjugated to biotinylated mono- and biantennary platforms, allowing for the display of two t
132 he modular synthesis of robust, biotinylated biantennary sialylglycoconjugates and their ability to d
133 ol for the simultaneous installation of both biantennary side-chains of the dodecasaccharide as well
134 s at m/z 1907.0 (asialo, agalacto, bisected, biantennary structure-NGA2B) in CTRL MS profiles, at m/z
135  was shown to be a homogenous "complex type" biantennary structure.
136 alylated receptors other than a selection of biantennary structures and PL structures with or without
137 n64 of heavy chain 2: all these were complex biantennary structures composed of (Asn)-GlcNAc2-Man-(Ma
138                   The N-glycans were complex biantennary structures present in either a mono- or disi
139                              All are complex biantennary structures with a common N-linked pentasacch
140  carrying N-glycans revealed the presence of biantennary structures with terminal sialic acid residue
141 y with the decrease of most core-fucosylated biantennary structures, as well as the increase in sialy
142 d 2, which are required for the formation of biantennary structures.
143 spectrometry and found to contain sialylated biantennary structures.
144 oline-rich glycoproteins is a trifucosylated biantennary sugar with one difucosylated and one unfucos
145 from a small trisaccharide species to larger biantennary systems and is driven, in part, by the role
146 yses showed that SfSWT-1 cells could produce biantennary, terminally sialylated N-glycans.
147 roportion of sialylated and core-fucosylated biantennary, triantennary and tetra-antennary oligosacch
148 pha2-6-linked sialic acids were present with biantennary, triantennary, and tetraantennary N-glycans
149 plex N-glycans, including highly fucosylated biantennary, triantennary, tetra-antennary, and bisectin
150 erse complex glycans that were predominantly biantennary type with differential core fucosylation, bi
151 of the results obtained for the 6 antenna of biantennary with previous fluorescence energy transfer s

 
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