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1 nt cells as well as in WT cells treated with xyloside.
2  or by treatment of WT cells with heparin or xyloside.
3 th 20 or 50 mM sodium chlorate, or 1 mM beta-xyloside.
4  case of the beta-mannoside than of the beta-xyloside.
5 epitopes at each antenna and containing core xyloside.
6              We previously reported that the xyloside 2-(6-hydroxynaphthyl) beta-d-xylopyranoside (Xy
7 porcine eyes with chlorate (3-fold) and beta-xyloside (3.5-fold) treatments.
8 erein we report the discovery of the novel O-xyloside 7c that inhibits SGLT2 in vitro and urinary glu
9 on of the main diastereoisomer of 3-methyl-1-xyloside-allene was determined for the first time by sin
10 uman gene C3ORF21 encodes a UDP-xylose:alpha-xyloside alpha1,3-xylosyltransferase, acting on xylose-a
11 the core proteins of proteoglycans by beta-d-xylosides also reduced incorporation of LTBP1 into the E
12 vity of the glycoside, we synthesized beta-D-xyloside analogs in which the hydroxyls were substituted
13 signing inhibitors of GAG synthesis based on xyloside analogs with reactive groups in key positions.
14  on fibrinogen were inhibited by both beta-d xyloside and after cleavage of chondroitin sulfate from
15 hat these differ in composition depending on xyloside and cell type, detailed knowledge regarding a s
16 ation, two more ACNs (cyanidin-3-galactoside-xyloside and cyanidin-3-galactoside-xyloside-glucoside-s
17 d as N-(4-methoxyphenyl)formamide 2-O-beta-D-xyloside and was revealed to have the potential to enhan
18 hydrolase specificity hint that, to enzymes, xylosides and arabinofuranosides are closely resemblant.
19 ontribute to the discrimination between beta-xylosides and beta-glucosides.
20 ns can be modified by bisecting GlcNAc, core xylosides and fucosides, and extended N-acetyl lactosami
21 ein glycoform, the addition of benzyl-beta-d-xyloside, and a UDP-xylose: core protein beta-d-xylosylt
22  sulfate side chain formation inhibitor beta-xyloside, and soluble heparin on the overexpression of p
23                        We surmise that click-xylosides are differentially recognized by the GAGOSOMES
24 ta-D-glucosides, beta-D-galactosides, beta-L-xylosides, beta-D-arabinosides), similar to the native e
25 by assaying the transfer of galactose to the xylosides by galactosyltransferase I (UDP-D-galactose:xy
26 highlighted a subnetwork including two novel xylosides (compounds 2 and 3).
27 ells also will assemble GAG chains on beta-D-xylosides containing hydrophobic aglycones.
28 l-beta-D-xyloside, reduced the amount of the xyloside-CS chains by 65.4 and 87.0%, respectively.
29                                  The size of xyloside-CS chains synthesized in the presence of 4-F-Gl
30 cterized by its unique capacity to take over xyloside derivatives linked to a hydrophobic aglycone as
31 -h incubation in 4-methylumbelliferyl-beta-D-xyloside did not attenuate the ability of LPL to reduce
32 inidin 3-O-glucoside, quercetin 3-O-glucosyl-xyloside, dihydroquercetin, and quercetin 3-O-glucuronid
33                        It revealed that core xyloside does not influence terminal epitope recognition
34 anthocyanin compound, followed by cyanidin-3-xyloside-galactoside (C3XG, 49.56-70.12mg/L).
35 nds from black carrot pomace with cyanidin-3-xyloside-galactoside-glucoside-ferrulic acid (C3XGGF, 60
36 ajor ACN, followed by cyanidin-3-galactoside-xyloside-glucoside-coumaric acid, and cyanidin-3-galacto
37 arified BCJ contained cyanidin-3-galactoside-xyloside-glucoside-ferulic acid as the major ACN, follow
38 actoside-xyloside and cyanidin-3-galactoside-xyloside-glucoside-sinapic acid) were also identified.
39 de-coumaric acid, and cyanidin-3-galactoside-xyloside-glucoside.
40  the PDGF effect, but not in the presence of xyloside, indicating that GAG synthesis that results fro
41            This conclusion was based on beta-xyloside inhibition of glycanation and specific glycosam
42       It was active on p-nitrophenyl-alpha-d-xyloside, isoprimeverose, xyloglucan heptasaccharide (XX
43 examined as well as protecting groups on the xyloside moiety and the influence of the substituents on
44 try revealed that the active principles were xylosides of dimethylated ellagic acid.
45                            These novel click-xylosides offer new avenues to profile the cell-specific
46                                 Second, beta-xyloside or monensin, reagents that inhibit the synthesi
47 paran sulfate side chain formation with beta-xyloside or the addition of soluble heparin prevented ER
48 lycan synthesis (4-methylumbelliferyl-beta-D-xyloside) or sulfation (sodium chlorate) enhanced the re
49            Treatment with either U0126, beta-xyloside, or heparin resulted in a reduction in the over
50 dications that this could be mediated by the xyloside-primed glycosaminoglycans (GAGs) and that these
51 of CS synthesis, 4-methylumbelliferyl-beta-D-xyloside, reduced the amount of the xyloside-CS chains b
52  treated with chlorate or substituted beta-D-xylosides, resulting in undersulfation or secretion of G
53  inhibition of endogenous PG biosynthesis by xyloside significantly attenuated exosome uptake.
54                     Priming by these unusual xylosides suggests the possibility of designing inhibito
55          We have utilized a library of click-xylosides that have various aglycones to decipher the me
56  OPCs and by treating demyelinated mice with xyloside to reduce the CSPG deposition that occurred fol
57 bronectin immunostaining was altered in beta-xyloside-treated eyes, whereas in cell culture, chlorate
58 Ac were only slightly larger than those with xyloside treatment alone (K(av) of 0.55 compared with th
59                             Finally, in vivo xyloside treatment to reduce CSPG synthesis in lysolecit
60 toside, peonidin-3-O-glucoside, cyanidin-3-O-xyloside were separated and identified by LC/DAD/MS and
61 hlorate, an inhibitor of sulfation, and beta-xyloside, which provides a competitive nucleation point
62 onation of differently substituted propargyl xylosides with s-BuLi/TMEDA followed by protonation with
63 -keto derivative) and benzyl-4-methyl-beta-D-xyloside, with a methyl group in place of an axial hydro
64  p-nitrophenyl beta-d xylopyranoside (beta-d xyloside), wound microvascular endothelial cells were ca
65 mbination of the food components vitexin-2-O-xyloside (X), raphasatin (4-methylsulphanyl-3-butenyl is
66                                  Vitexin-2-O-xyloside (XVX) from Beta vulgaris var. (BVc) seeds, beta
67                                  Vitexin-2-O-xyloside (XVX) from Beta vulgaris var. cicla L. (BVc) se
68 cubation of these cells with naphthol-beta-D-xyloside (Xylbeta-O-Np) resulted in accumulation of link
69                        Finally, a UDP-xylose:xyloside xylosyltransferase (Xxylt1) transfers xylose to
70       We have, therefore, renamed it XXYLT1 (xyloside xylosyltransferase 1).