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1 hich recognizes poly-N-acetylglucosamine and poly-N-acetyllactosamine.
2 ctures with increased branching and extended poly-N-acetyllactosamine.
3 beta1-3GalNAc termini, and some increases in poly-N-acetyllactosamines.
4 in adding a galactose to linear and branched poly-N-acetyllactosamines.
5 fficiently add N-acetyllactosamine to linear poly-N-acetyllactosamines.
6 of pro-MM factor, NGFR, implicating i-linear poly-N-acetyllactosamine and Gal-8 as biomarkers and the
7 verning the MM glycome by enforcing i-linear poly-N-acetyllactosamine and Gal-8 expression.
8 onstrated that itraconazole globally reduced poly-N-acetyllactosamine and tetra-antennary complex N-g
9                                              Poly-N-acetyllactosamines are attached to N-glycans, O-g
10 nsferases, which play important roles in how poly-N-acetyllactosamines are synthesized in different a
11 d on blood group H on a 6-linked branch of a poly-N-acetyllactosamine backbone.
12 found that 4-F-GlcNAc (putative inhibitor of poly-N-acetyllactosamine biosynthesis) was more potent t
13                                   I-branched poly-N-acetyllactosamine can carry bivalent functional o
14 bodies with IGHV4-34*01 heavy chains bind to poly-N-acetyllactosamine carbohydrates (I/i antigen) on
15 mannosyl core may carry predominantly linear poly-N-acetyllactosamine chains, whereas the Manalpha1-3
16 lpha1-3 arm may carry predominantly branched poly-N-acetyllactosamine chains.
17                   Both glycoproteins display poly-N-acetyllactosamines, consistent with virion assemb
18                Characterization of the large poly-N-acetyllactosamine containing N-glycans of the TbG
19  that TbGT8 influences the processing of the poly N-acetyllactosamine-containing asparagine-linked gl
20 ifically recognize a triantennary sialylated poly-N-acetyllactosamine-containing N-glycan exposed on
21  glycans, including some exceptionally large poly-N-acetyllactosamine-containing structures.
22 fferent classes of complex glycans including poly-N-acetyllactosamine derivatives, human milk oligosa
23  on T cells, indicating direct inhibition on poly-N-acetyllactosamine elongation and selectin-binding
24  enhancement of both beta(1,6) branching and poly-N-acetyllactosamine expression on N-cadherin.
25 poly-N-acetyllactosamine synthesis, allowing poly-N-acetyllactosamine extension mostly along the line
26                                              Poly-N-acetyllactosamine extension of core 4 branches is
27  the branched acceptor than the summation of poly-N-acetyllactosamines formed individually on each un
28 inyltransferase, was capable of synthesizing poly-N-acetyllactosamine in core 2 branched oligosacchar
29 irely consistent with previous findings that poly-N-acetyllactosamines in human erythrocytes, PA-1 em
30                                              Poly-N-acetyllactosamines in mucin-type O-glycans can be
31    In the present study, we first found that poly-N-acetyllactosamines in N-glycans are most efficien
32 in the presence of core 1 O-glycans, but not poly-N-acetyllactosamine, in apically targeted MUC1 and
33                                   I-branched poly-N-acetyllactosamine is a unique carbohydrate compos
34                                              Poly-N-acetyllactosamine is a unique carbohydrate compos
35                                              Poly-N-acetyllactosamine is a unique carbohydrate that c
36         It has been shown that the amount of poly-N-acetyllactosamine is increased in N-glycans, when
37                                              Poly-N-acetyllactosamine oligomer is a type-2 glycan cor
38 lular Gal-8 bound preferentially to i-linear poly-N-acetyllactosamines on N-glycans of the TIC marker
39 ely large complex-type N-glycans with linear poly-N-acetyllactosamine (PL) [-3Galbeta1-4GlcNAcbeta1-]
40 ing, core fucosylation, and the abundance of poly-N-acetyllactosamine (PL) [-3Galbeta1-4GlcNAcbeta1-]
41 tosamine (LN; Galbeta1-4GlcNAc) sequences on poly-N-acetyllactosamine (PL; (-3Galbeta1-4GlcNAcbeta1-)
42 sed in olfactory sensory neurons (OSNs) with poly-N-acetyllactosamine (PLN) oligosaccharides determin
43 in exhibited higher binding for glycans with poly-N-acetyllactosamine (poly(LacNAc)) sequences (Galbe
44                                              Poly-N-acetyllactosamine (poly-LacNAc) is ubiquitously e
45 ase that can participate in the synthesis of poly-N-acetyllactosamine (polyLacNAc) chains.
46 ase that can participate in the synthesis of poly-N-acetyllactosamine (polyLacNAc) chains.
47               Enzymatic reduction in surface poly-N-acetyllactosamine (polyLacNAc) glycans in HL60 ce
48       However, one motif found in N-glycans, poly-N-acetyllactosamine (polyLacNAc), still poses a sub
49 essing moderate amounts of sialyl Lewis X in poly-N-acetyllactosamines produced large numbers of lung
50  a paucity of the Lewis(x) sequence based on poly-N-acetyllactosamine recognized by anti-SSEA-1; (ii)
51 n of N-acetylglucosamine residues within the poly(N-acetyllactosamine) repeat sequence and signals re
52 que LOS glycoforms containing di-, tri-, and poly-N-acetyllactosamine repeats added to the terminal r
53 n of branched oligosaccharides with multiple poly-N-acetyllactosamine repeats is nearly abolished by
54 ow here consists of (-6GalB1-4GlcNAcB1-)( 4) poly-N-acetyllactosamine repeats.
55 actosamine extension mostly along the linear poly-N-acetyllactosamine side chain.
56                             Galectin-3 binds poly-N-acetyllactosamine structures on glycoproteins, bu
57 ever, they produced extended GlcNAc-sulfated poly-N-acetyllactosamine structures with more than four
58  to longer carbohydrate substrates that have poly-N-acetyllactosamine structures, suggesting the invo
59                             B3GNT2 encodes a poly-N-acetyllactosamine synthase that targets >10 ligan
60 ndicate that beta4Gal-TIV is responsible for poly-N-acetyllactosamine synthesis in core 2 branched O-
61 These results, taken together, indicate that poly-N-acetyllactosamine synthesis in N-glycans and core
62 ta4Gal-TI was found to be most efficient for poly-N-acetyllactosamine synthesis in N-glycans.
63 branch is a rate-limiting step in I-branched poly-N-acetyllactosamine synthesis, allowing poly-N-acet
64 B3GNT1, an enzyme proposed to be involved in poly-N-acetyllactosamine synthesis, were causal for cong
65 To determine how this increased synthesis of poly-N-acetyllactosamines takes place, the branched acce
66 on at multiple internal GlcNAc of unbranched poly-N-acetyllactosamine, termed "myeloglycan," the phys
67 branched O-glycans contain fewer and shorter poly-N-acetyllactosamines than N-glycans in many cells.
68  express a unique glycome featuring i-linear poly-N-acetyllactosamines through the loss of I-branchin
69 tylglucosaminyltransferase, the formation of poly-N-acetyllactosamine was found to be extremely ineff
70               When a beta1,6-GlcNAc branched poly-N-acetyllactosamine was incubated with a mixture of
71                                Surprisingly, poly-N-acetyllactosamine was more efficiently formed on
72 rgeting when galectin-3, with preference for poly-N-acetyllactosamine, was depleted from polarized MD
73 cetyllactosamine branches attached to linear poly-N-acetyllactosamine, which is synthesized by I-bran
74  poorly to beta1,6-GlcNAc attached to linear poly-N-acetyllactosamines, while beta1, 3-N-acetylglucos