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1 acid, GlcN is D-glucosamine, and IdoUA is L-iduronic acid).
2 onic residues (sulfated rhamnose, glucuronic/iduronic acid).
3 rmational equilibrium is pH-dependent in the iduronic acid.
4 S C(5)-epimerase converts glucuronic acid to iduronic acid.
5 group to the 2-OH-position of glucuronic or iduronic acid.
6 d, primarily 4-O-sulfated, disaccharides and iduronic acid.
7 ry cell mutant defective in 2-O-sulfation of iduronic acid.
9 e contained significantly reduced amounts of iduronic acid and disulfated disaccharides DeltaDi-2,4S
11 nts of 6-O-sulfated glucosamine residues and iduronic acid and somewhat higher levels of N-sulfated g
12 sferases, which in turn lead to the higher L-iduronic acid and sulfate content of heparin versus hepa
14 e successfully applied to the synthesis of l-iduronic acid being an essential component of anticoagul
16 tain noncognate GAGs (including sulfated and iduronic acid-containing forms) are elongated by PmHAS (
19 NETD is also able to distinguish the epimers iduronic acid from glucuronic acid in heparan sulfate te
24 fers the sulfo group to the 2-OH position of iduronic acid (IdoA) or glucuronic acid (GlcA) within HS
31 unique oligosaccharide sequences containing iduronic acid (IdUA), N-sulfated glucosamine residues, a
32 ggesting that the disaccharide; 2-O-sulfated iduronic acid linked to 6-O-sulfated N-glucosamine, whic
33 saccharide consisting of glucuronic acid (or iduronic acid) linked to glucosamine carrying various su
34 all four anomeric and ring size isomers of l-iduronic acid methyl glycosides, including the first syn
36 tact with either the 2-O-sulfo groups of the iduronic acid monosaccharides or the N- and 6-O-sulfo gr
37 ddition to the alpha-linkage anticipated for iduronic acid nucleophiles, resulting in an inseparable
38 lfate consists of glucosamine and glucuronic/iduronic acid repeating disaccharides with various sulfa
39 enriched in MPSIH, representing the terminal iduronic acid residue capping the non-reducing end of th
41 catalyst to convert a glucuronic acid to an iduronic acid residue, displaying an "irreversible" cata
42 emonstrated that glucuronic acid rather than iduronic acid residues are important for IRBC binding.
43 ning a glypican 5 core protein and 2-O-sulfo-iduronic acid residues at the nonreducing ends of the gl
47 oss-peaks to the anomeric protons of the two iduronic acid residues, which overlap in normal two-dime
49 comprised predominantly of 2-O-sulfo-alpha-L-iduronic acid (the I ring) and 2-deoxy-2-sulfamido-6-O-s
50 rase converts some of the glucuronic acid to iduronic acid, thus becoming a substrate for 2OST Y94I.
51 s containing a glypican 5 core and 2-O-sulfo-iduronic acid to promote neural precursor proliferation.
52 rmediate that may be further elaborated into iduronic acid trichloroacetimidate glycosyl donors for t
53 ld be successfully converted into terminal l-iduronic acids via the syn addition of 2-furylzinc bromi
54 tion of D-glucuronic acid to its C5-epimer L-iduronic acid, which is essential for the function of he
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