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1 stitutions that include alpha-(1-->2)-linked glucuronosyl, 4-O-methyl glucuronosyl, and alpha-1,2- an
2 ed as a polysaccharide of alternating beta-D-glucuronosyl and N-acetyl-alpha-D-glucosaminyl residues
3 lpha-(1-->2)-linked glucuronosyl, 4-O-methyl glucuronosyl, and alpha-1,2- and alpha-1,3-arabinofurano
4 um leguminosarum were identified as encoding glucuronosyl-(B1-->4)-glucosyl transferases based on rec
5 se in Sphingomonas and that pssC codes for a glucuronosyl-(beta1-->4)-glucuronosyl transferase in R.
6 velopment of a non-radioactive NMR assay for glucuronosyl-C5-epimerase, and background-free quantific
7                                              Glucuronosyl diacylglycerides (GlcAGroAc2) are functiona
8 rium lacking monoglucosyl diacylglycerol and glucuronosyl diacylglycerol or all glycolipids are not i
9        Furthermore, this enzyme is the first glucuronosyl diacylglycerol synthase isolated.
10 ctroscopy as monoglucosyl diacylglycerol and glucuronosyl diacylglycerol.
11  and respond to the microbial antigen, alpha-glucuronosyl-diacylglycerol (alpha-GlcADAG) presented by
12  of its phospholipids with monoglucosyl- and glucuronosyl-diacylglycerols and by synthesizing new orn
13 precise, evenly spaced pattern of acetyl and glucuronosyl (MeGlcA) xylan substitutions in eudicots, w
14 n UGE4 of pectic (1-->4)-beta-D-galactan and glucuronosyl-modified AGP biosynthesis is exacerbated.
15                            A majority of the glucuronosyl residues are methyl-esterified at C-6.
16 e nonreducing termini with single 4-O-methyl-glucuronosyl residues via beta-(1-->6)-linkages.
17 tural features of GXM are single xylosyl and glucuronosyl side chains and O acetylation of the mannos
18 ed that each hydrolysis product has a single glucuronosyl substitution penultimate to the reducing te
19 thaliana) that is responsible for adding the glucuronosyl substitutions onto the xylan backbone.
20 ng Gunn rats, congenitally deficient in UGT1 glucuronosyl tranferases, and TR- rats, deficient in the
21                         Uridine-disphosphate glucuronosyl transferase (UGT) enzymes catalyze the form
22 ricted expression of human uridine diphospho-glucuronosyl transferase 1A1 in the Gunn rat, a model of
23  caused by a deficiency of uridine diphospho-glucuronosyl transferase 1A1.
24 at pssC codes for a glucuronosyl-(beta1-->4)-glucuronosyl transferase in R. leguminosarum.
25 e that spsL codes for a glucosyl-(beta1-->4)-glucuronosyl transferase in Sphingomonas and that pssC c
26      In mutant (Gunn) rats lacking bilirubin glucuronosyl transferase, 1 (like bilirubin) was not exc
27 on of human bilirubin-uridine 5'-diphosphate-glucuronosyl-transferase (BUGT) complementary DNA (SV-hB
28 1), epoxide hydrolase, heme oxygenase-1, UDP-glucuronosyl-transferase (Ugt) 1a6 and 2b5, and multidru
29 y cytochrome P450 and/or uridine diphosphate glucuronosyl transferases were simultaneously measured a
30 nd catalyzed the regiospecific transfer of a glucuronosyl unit from UDP-glucuronate to the 2''-hydrox
31 ss of EXTL3's GT47 domain to transfer beta-D-glucuronosyl units, and we observe that, in general, the