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1 nks to hydroxyproline through the galactose (galactosylation).
2  of three IgGs, yielding 80.2-96.3% terminal galactosylation.
3  terminal sialylation, which is dependent on galactosylation.
4 f gene mutations that affect sialylation and galactosylation.
5 a configuration suspected to prevent beta1,3 galactosylation.
6   The epimerase is required for glycoprotein galactosylation.
7  considerable variation in the extent of LPG galactosylation.
8 , but which maintains normal levels of Golgi galactosylation.
9 ia ni TN-5B1-4 cells are capable of terminal galactosylation.
10 ontain LeX antigens that are masked by alpha-galactosylation.
11 ing group providing the most alpha-selective galactosylations.
12 ance to bacteriophage predation and that LTA galactosylation alters L. lactis resistance to bacterioc
13 ting antenna can be converted into LacNAc by galactosylation and can then be enzymatically modified i
14 t correlation between levels of aberrant IgG galactosylation and disease activity (Spearman's rho = 0
15                Correlations between aberrant galactosylation and disease activity were assessed in th
16 A of specific pathogen-free mice showed more galactosylation and much lower polymerization.
17 tween a donor substrate and acceptor in both galactosylation and N-acetylglucosaminylation, since a c
18  whilst long-term IgG Abs have low levels of galactosylation and sialylation and are most likely gene
19                Variations in their extent of galactosylation and sialylation could modulate IgG Fc-de
20 e 352 allele to be associated with decreased galactosylation and sialylation of apolipoprotein B100,
21 e (F241A, F243A, V262E, and V264E) increased galactosylation and sialylation of the Fc and, concomita
22          These results suggest that in vitro galactosylation and sialylation of therapeutic glycoprot
23 e (q < 0.01) and CRC mortality (q = 0.04 for galactosylation and sialylation).
24 d GN to define the relative contributions of galactosylation and sialylation, in relation to cryoglob
25 -protein interactions, rather than increased galactosylation and sialylation, modifies the Fc conform
26 all anti-S IgG subclasses with low levels of galactosylation and sialylation.
27 rend of increasing retention upon increasing galactosylation and sialylation.
28 d via stereoselective 1,2-cis- and 1,2-trans-galactosylations and beta-Kdosylation.
29                   Stereo- and site-selective galactosylations and mannosylations of a wide assortment
30 ble to distinguish differences in bisection, galactosylation, and sialylation in N-glycans derived fr
31 filing revealed a loss of core fucosylation, galactosylation, and sialylation in patient samples.
32 pressed in an Arabidopsis mutant lacking XyG galactosylation, and two of them resulted in the product
33           Roles for the gene products in WTA galactosylation are proposed.
34           Our findings identify aberrant IgG galactosylation as a dysregulated component of the humor
35 )-beta-D-galactosyl side chain and excessive galactosylation at an alternative xylose residue.
36    Cavities on the RiCE17 surface may accept galactosylations at the C6 positions of mannose adjacent
37        Our results demonstrated that lack of galactosylation, but not sialylation, enhanced the patho
38 alyltransferase ST6GalNAc-II, which prevents galactosylation by C1GalT1.
39   Acetyl groups at C4 ensure alpha-selective galactosylations by forming a covalent bond to the anome
40                                    Decreased galactosylation, decreased sialylation (of fucosylated I
41  for lectin resistance, were found to have a galactosylation defect.
42 ucosylation (tri-, core, and outer arm), and galactosylation (di-, tri-, and tetra-) between striatum
43 re independent of the state of intracellular galactosylation during spermatogenesis.
44 ered noncontiguous Hyp residues are sites of galactosylation, giving rise to the arabinogalactan hete
45             It was found that the pattern of galactosylation greatly influenced binding affinities, a
46                  Although the mere extent of galactosylation had no effect on either the cryogenic an
47 ed that biantennary oligosaccharides lacking galactosylation had slightly faster clearance rates than
48  in particular differences in the pattern of galactosylation have been noted.
49 tematically examined the requirement for WTA galactosylation in a mouse oral-virulent strain by first
50                On the basis of the decreased galactosylation in glycan chains, galactose was administ
51                                    That IgG1 galactosylation is a predictor of immune activation is s
52                                The degree of galactosylation is essential for the synthesis of the GG
53     The result is that the rate constant for galactosylation is increased but degalactosylation is sl
54  both core alpha1,6-fucosylation and beta1,4-galactosylation is the presence of a nonreducing termina
55  antibody displayed lower levels of terminal galactosylation leading to reduced asialoglycoprotein-re
56                                     Impaired galactosylation leads to a severe disorder with deformed
57 t oligoarabinosides (Hyp-arabinosides) while galactosylation leads to the addition of larger arabinog
58 thmatic children seemed to have reduced IgG1 galactosylation levels as well.
59                                    High IgG1 galactosylation levels correlated with low total IgE lev
60                     This indicates that IgG1 galactosylation levels could be used as a biomarker for
61  dependent on mannose glycan recognition and galactosylation levels in the IgG Fc domain.
62 ing antibodies (IgGs) characterized by lower galactosylation levels of the IgG fragment crystallizabl
63                                         IgG1 galactosylation levels were generally higher in more aff
64  was a significant predictor of reduced IgG1 galactosylation levels.
65                       These data reveal high galactosylation like anti-D Ig (>60%) together with lowe
66  suggest that targeted modulation of protein galactosylation may represent a therapeutic approach to
67 h grants selective detection of sialylation, galactosylation, N-acetylglucosaminylation, and fucosyla
68 tance to both hexosaminidase and to in vitro galactosylation, O-GlcNAc moieties appear to be largely
69            Molecular modeling indicated that galactosylation occurred on the periphery of alpha2beta1
70                                 We find that galactosylation of 3F6-hIgG1 that favors C1q recruitment
71                            Glucosylation and galactosylation of a panel of representative alcohol acc
72 oups led to excellent stereocontrol of alpha-galactosylation of a variety of glycosyl acceptors with
73  GT31 glycosyltransferase likely involved in galactosylation of arabinogalactan proteins.
74                                              Galactosylation of B mAb-Ds was 57-83% but 15-58% for ro
75                                    Enzymatic galactosylation of chilled platelets blocks alphaMbeta2
76 e Golgi, (ii) secretion from the cell, (iii) galactosylation of chondroitin sulfate (CS) chains, (iv)
77 abinosylation of contiguous Hyp residues and galactosylation of clustered noncontiguous Hyp residues.
78 etylglucosamine was abolished, the degree of galactosylation of core alpha1,6-fucose increased, and a
79 nsible for 2-O-arabinopyranosylation and 2-O-galactosylation of GlcA side chains of xylan.
80 tion of the GPI precursor lipid or defective galactosylation of GPI intermediates in the endoplasmic
81             In contrast to the murine study, galactosylation of human platelets did not prevent the a
82                                          The galactosylation of Hyl(393) in alpha1(IV)382-393 and Hyl
83 ogether, these results strongly suggest that galactosylation of I-branch is a rate-limiting step in I
84             Our results confirm the aberrant galactosylation of IgG in RA patients as compared with h
85 ylation of the hydroxyproline residues and O-galactosylation of interspersed serine residues create a
86  essential for glycosylation of proteins and galactosylation of lipids and glycosaminoglycans.
87  respectively, whereas csdEF plays a role in galactosylation of lipoteichoic acid (LTA).
88  two genes gtlB and gttB are responsible for galactosylation of LTA and WTA respectively.
89 lgi lumen; this in turn results in selective galactosylation of macromolecules.
90 cells is accompanied by an increase in alpha-galactosylation of membrane glycoproteins and a decrease
91 beta4GalT-6 contributes only slightly to the galactosylation of N-glycans and is also not involved in
92 herefore, beta4GalT-1 is a key enzyme in the galactosylation of N-glycans, but is not involved in gly
93           Our understanding of the defective galactosylation of O-linked glycans in the hinge region
94                      These cytokines reduced galactosylation of the O-glycan substrate directly via d
95                                     In vitro galactosylation of the tGlcNAc proteins generated glycop
96 l elongation appears to be slightly reduced, galactosylation of the XyGs is not strictly required for
97 lytic anemia, we defined the contribution of galactosylation or sialylation to the pathogenic activit
98 ted that sialic acid modifications, alpha1-3-galactosylation, or sulfation did not mask epitopes for
99 duals did not produce IgA with the defective galactosylation pattern.
100 ity, and we propose that strain-specific LPG galactosylation patterns reflect differences in their ex
101 Although capping the beta-GlcNAc moieties by galactosylation prevents clearance of short-term-cooled
102 galactosyltransferase is used to enhance the galactosylation profile of three IgGs, yielding 80.2-96.
103                         However, the overall galactosylation profiles of plant PGT121 did not affect
104 ements of etiolated hypocotyls revealed that galactosylation rather than fucosylation of the side cha
105 eoselectivity of the cooperatively catalyzed galactosylation reaction.
106                                    The lipid galactosylation reactions are also fundamentally interes
107 ved in complex N-linked glycan formation and galactosylation, respectively, were reflected by increas
108 e cells, indicating that galactosyl(alpha1-3)galactosylation sensitizes these viruses as well as mamm
109 belong to three main glycosylation features: galactosylation, sialylation, and level of bisecting N-a
110       These features included differences in galactosylation, sialylation, bisection, fucosylation, a
111 ergy gradients, specifically in terms of the galactosylation/sialylation branching and linkage.
112 revious in vitro studies have shown that the galactosylation status of laminin directly influences it
113 ngineered by MAGTs reveal that the degree of galactosylation strongly affects the interaction with ce
114                        Further, aberrant IgG galactosylation substantially predated the onset of arth
115                                              Galactosylations using NIS/TfOH were generally alpha-sel
116 IgG-Fc glycoform with fucosylation and fully galactosylation was an independent factor for a total Kn
117 on, and C-reactive protein level on aberrant galactosylation was determined using multivariate analys
118 N-acetylglucosamine at the nonreducing ends, galactosylation was judged to be inefficient, prompting
119                           On the other hand, galactosylation was much more efficient on beta1,6-linke
120 of IgA1, probably taking the form of reduced galactosylation, was confirmed in IgAN in this study.
121                     Instead, alpha-selective galactosylations were observed with 4-O-benzoyl, 3,4-di-
122 ted galactosyltransferase produces efficient galactosylation when uridine diphosphate-galactose is ad
123 to the production of platelets with aberrant galactosylation, which in turn promote hepatic TPO synth
124 ith N-glycolyl neuraminic acid and extent of galactosylation (zero-, mono-, di-, and alpha(1-3)-galac

 
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