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1 Campylobacter jejuni expressing a GD1a-like, sialylated glycan.
2 und that conserved small noncoding RNAs bear sialylated glycans.
3  generally not microbial cell surfaces, have sialylated glycans.
4 hat lack coding nucleic acids but do possess sialylated glycans.
5 he seal H3 bound preferentially to alpha-2,3 sialylated glycans.
6 teroids, phospholipids, phosphopeptides, and sialylated glycans.
7 the ionization responses for all neutral and sialylated glycans.
8 mproved desorption of both large and heavily sialylated glycans.
9  protein exhibiting no detectable binding to sialylated glycans.
10 s as well as the growth of C. perfringens on sialylated glycans.
11 MCs depends on alpha1,3-fucosylated, but not sialylated, glycans.
12  mutation on HA resulted in a mixed alpha2-3 sialylated glycan (alpha2-3)/alpha2-6 binding virus (NY1
13 lutinin (HA) to long (chain length) alpha2-6 sialylated glycan (alpha2-6) receptors on the human uppe
14 evealed that IAV binds to sialylated and non-sialylated glycans and binding is not concordant with re
15 inding, with Gal-8N recognizing sulfated and sialylated glycans and Gal-8C recognizing blood group an
16                                              Sialylated glycans and glycoproteins are involved in cel
17 in SK1 SRR adhesin affects interactions with sialylated glycans and glycoproteins, we determined high
18             During infection, sigma1 engages sialylated glycans and junctional adhesion molecule-A (J
19 The reovirus attachment protein sigma1 binds sialylated glycans and proteinaceous receptors to mediat
20 --enables specific binding of HA to alpha2-6 sialylated glycans and that recognition of this topology
21 re substituted with a variety of neutral and sialylated glycans and the spectra obtained were such th
22 ereas Gal-1 bound alpha2-3- but not alpha2-6-sialylated glycans, and Gal-3 bound to some glycans term
23  high-mannose glycans, fucolsylated glycans, sialylated glycans, and hybrid structures were studied.
24 sm for a parietal cell-deficient niche where sialylated glycans are expressed by a narrow band of pit
25                                              Sialylated glycans are found at elevated levels in many
26    Single-cell binding studies indicate that sialylated glycans are likely not required for initial a
27 tory pathway in which host-specific alpha2,6-sialylated glycans are recognized as markers of self.
28  demonstrate that different distributions of sialylated glycans are related to the metastatic propert
29                              However, native sialylated glycans are suppressed or not detected during
30                                              Sialylated glycans are synthesized in mammals by a singl
31 glec) family that recognizes alpha2-6-linked sialylated glycans as ligands.
32  tissues and highlight a functional role for sialylated glycans as reovirus coreceptors in the CNS.
33 tein binds CD164 at acidic pH and requires a sialylated glycan at residue N104.
34 IL-6 secretion were enriched in ApoC-III, di-sialylated glycans at multiple A1AT glycosylation sites
35 s (SCS) in murine lymph nodes (LN) displayed sialylated glycans at particularly high densities.
36                                Composed of a sialylated glycan attached to a ceramide lipid, the same
37     The IgG1 Fc fragments containing complex sialylated glycans attached to the N-terminal Asn(221) s
38                                          Two sialylated glycans bearing N-acetylneuraminic acid were
39 ot only result in accurate identification of sialylated glycans but also improve the characterization
40                              Modification by sialylated glycans can affect protein functions, underly
41 O) structure, we show ABH antigens stabilize sialylated glycan clusters on erythrocyte membranes uniq
42 ows for linkage specific characterization of sialylated glycans directly from the precursor mass but
43                                      Lack of sialylated glycans due to genetic ablation of the Sia-ac
44 ated glycan library covering the most common sialylated glycan epitopes was prepared in high yield an
45                  Hemagglutinin (HA) binds to sialylated glycans exposed on the host cell surface in t
46 irus (IBV), require specific alpha2,3-linked sialylated glycans for attachment and entry.
47       Surprisingly, Gal6S is undetectable in sialylated glycans from eosinophils and BAL fluid analyz
48 process, including initial binding of IAV to sialylated glycans, fusion between the viral envelope an
49                  A population of Fcs bearing sialylated glycans has been identified as contributing t
50 itative binding affinity of HA to alpha2-->6 sialylated glycans (human receptors) is one of the impor
51 me, fluorescence and radionuclide imaging of sialylated glycans in a murine tumor model in vivo.
52 s revealed the importance of sialylation and sialylated glycans in breast cancer brain metastasis.
53 ring 3F-NeuAc to mice dramatically decreases sialylated glycans in cells of all tissues tested, inclu
54 NAc), were incorporated into fucosylated and sialylated glycans in several cancer cell lines, allowin
55                    The relative abundance of sialylated glycans in the S1 subunit compared to the ful
56                              For example, 11 sialylated glycans including 28 isoforms were well profi
57                 This program is triggered by sialylated glycans, including those found in human milk
58                               MS analysis of sialylated glycans is challenging due to their low ioniz
59                              The analysis of sialylated glycans is critical for understanding the rol
60 that each pathotype makes use of a different sialylated glycan ligand, with binding sites on opposite
61 ies on sialic acid recognition using a novel sialylated glycan microarray containing modified sialic
62  Our results demonstrate the utility of this sialylated glycan microarray to investigate the biologic
63  often characterized by a hyperexpression of sialylated glycan moieties.
64 F(ab')(2) fragments and was dependent on the sialylated glycans of IgG.
65 ory signalling, which in turn implicates the sialylated glycans of the antigen as key suppressive det
66 ts viral envelope that interact with various sialylated glycans on a host cell.
67 ventional influenza A viruses (IAVs) bind to sialylated glycans on host cell surfaces for attachment
68  serine-rich repeat (SRR) adhesins recognize sialylated glycans on human salivary, platelet, and plas
69 icity depends on toxin binding to terminally sialylated glycans on surface glycoproteins.
70 lutinin, and Sambucus nigra agglutinin) with sialylated glycans on the same cell surface.
71       We propose that the densely clustered, sialylated glycans on the SCS floor LEC are a key compon
72                                              Sialylated glycans on the surface of mammalian cells act
73                                   Binding of sialylated glycans or other ligands triggers signals tha
74 f its B subunit, PltB, with specific lumenal sialylated glycan packaging receptors.
75                              In vertebrates, sialylated glycans participate in a wide range of biolog
76 ies of the first six reported siglecs, using sialylated glycans presented in multivalent form, on syn
77 s in ionization efficiency among neutral and sialylated glycans prevent direct quantitative compariso
78 dulated by HopZ, including hopP, which binds sialylated glycans produced by GEPs in vivo.
79  in the expression of truncated core 1-based sialylated glycans rather than the core 2-based glycans
80 Crystal structures of EV-D68 in complex with sialylated glycan receptor analogues show that they bind
81 inding of QX-RBD is dependent on a different sialylated glycan receptor.
82 pecificity of the viral hemagglutinin to the sialylated glycan receptors (in the human host) by use o
83 on surfaces, obstructing a groove that binds sialylated glycan receptors in many other polyomaviruses
84 go-potential gastric stem cells that express sialylated glycan receptors recognized by H. pylori adhe
85  sialylated glycans) to human-like (alpha2-6 sialylated glycans) receptors is believed to be associat
86  array approach to analyze the repertoire of sialylated glycans recognized by viruses from the same c
87 ed from the aqueous phase, while neutral and sialylated glycans remained in the DCM phase.
88 ay studies confirmed the binding of HMGB1 to sialylated glycan sequences typically found on plasma gl
89                                              Sialylated glycans serve as cell surface attachment fact
90 2)v showed a predominant binding to alpha2-6-sialylated glycans, similar to human-adapted influenza A
91 DRAG), to quantitatively compare neutral and sialylated glycans simultaneously by MALDI-MS.
92 stability and ionization bias experienced by sialylated glycan species.
93         Together, these results suggest that sialylated glycans, specifically glycolipids, facilitate
94 vealed that LEC from human skin express more sialylated glycans than the corresponding blood endothel
95 binding to sialyl Lewis x (sLe(x)) and other sialylated glycans that decorate P selectin glycoprotein
96  which bound almost exclusively to alpha-2,6 sialylated glycans, the seal H3 bound preferentially to
97  tested preferentially utilize NeuAcalpha2-6-sialylated glycans to infect SRECs.
98 hemagglutinin (HA) from avian-like (alpha2-3 sialylated glycans) to human-like (alpha2-6 sialylated g
99 cuous ligand of proteins with high levels of sialylated glycans typically produced by cancer cells.
100                   However, quantification of sialylated glycans using MS is not as reliable because o
101 tiates viral entry by engaging host receptor sialylated glycans via its receptor-binding site (RBS).
102 -R1 has not previously been shown to bind to sialylated glycans, we demonstrate that it preferentiall
103 entional IAVs rely on multivalent binding to sialylated glycans, we hypothesized that bat HA similarl
104  and alkaline BGE systems, the mobilities of sialylated glycans were shifted relative to nonsialylate
105 hibited significantly reduced binding to all sialylated glycans, whereas Gal-1 bound alpha2-3- but no
106 ly, we used a nonmetabolic approach to label sialylated glycans with an independent chemistry, enabli
107  viruses, specifically bind to long alpha2-6 sialylated glycans with this topology.
108  for simultaneous profiling both neutral and sialylated glycans without derivatization or labeling.

 
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