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1 levels of GalNAc, suggesting the absence of O-linked oligosaccharides.
2 oach may also be used to analyze both N- and O-linked oligosaccharides.
3 he structural characterization of mucin-type O-linked oligosaccharides.
4 which predominantly altered GAGs rather than O-linked oligosaccharides.
5 ase during the solid-phase permethylation of O-linked oligosaccharides.
8 inolysis was carried out at 60 degrees C for O-linked oligosaccharides and at 95 degrees C for total
17 hod is used to profile with quantitation the O-linked oligosaccharide (both neutral and anionic) comp
19 ains approximately 8 N- and approximately 11 O-linked oligosaccharide chains (but lacks glycosaminogl
23 proteins and assemble the core structures of O-linked oligosaccharides, constrained glycopeptides, co
25 ion and secretion of the fetal-like (rich in O-linked oligosaccharides) forms of decorin and biglycan
27 provides adequate measurements of important O-linked oligosaccharides glycans and their profiles, th
29 of catalyzing the transfer of sialic acid to O-linked oligosaccharides, human placental Galbeta-1,3Ga
31 It is also apparent that the presence of the O-linked oligosaccharides in the CTP sequence contribute
33 ate fertilization, mouse sperm bind to Ser- (O-) linked oligosaccharides located at the sperm combini
34 aminyltransferase, C2GnT, is a key enzyme in O-linked oligosaccharide (O-glycan) biosynthesis and the
38 uced by vascular cells that can binds N- and O-linked oligosaccharides of cell membrane glycoproteins
41 hr619 of heavy chain 1 and a cluster of four O-linked oligosaccharides on Thr612, Ser619, Thr621, and
42 of N-linked oligosaccharides as well as for O-linked oligosaccharides on yeast glycoproteins, and fo
43 binding of acrosome-intact sperm to specific O-linked oligosaccharides on zona pellucida glycoprotein
44 ots have been generated from the mixtures of O-linked oligosaccharides originated from bovine mucin a
47 dd GalNAc to beta1,6-linked GlcNAc in core 2 O-linked oligosaccharide structures to form Galbeta1,3(G
51 Mr 90 000 fragment, which carried primarily O-linked oligosaccharides, was subjected to reductive be
52 itope that is destroyed upon modification by O-linked oligosaccharides, we show that all post-endopla
55 co suspension-cultured cells are modified by O-linked oligosaccharides with terminal N-acetylglucosam
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