戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ffinities, not unlike those of some lectins (carbohydrate-binding proteins).
2 plays active-site properties unexpected of a carbohydrate-binding protein.
3 relaxation switch assay for the detection of carbohydrate binding proteins.
4 ates and glycoproteins to lectins, which are carbohydrate binding proteins.
5 imilarity to galectins, an ancient family of carbohydrate-binding proteins.
6 mains that are structurally similar to known carbohydrate-binding proteins.
7  is a member of a highly conserved family of carbohydrate-binding proteins.
8  to unveil new functions of both glycans and carbohydrate-binding proteins.
9 nges can influence the ligand specificity of carbohydrate-binding proteins.
10 logy with sugar recognition sites in several carbohydrate-binding proteins.
11 any of the conserved residues found in these carbohydrate-binding proteins.
12         C-Type lectins are a large family of carbohydrate-binding proteins.
13 lysis by cellulolytic enzymes and associated carbohydrate-binding proteins.
14 evolved from a particular family of cellular carbohydrate-binding proteins.
15 ohydrate ligands is demonstrated using three carbohydrate-binding proteins, a single chain antibody,
16                                         Most carbohydrate-binding proteins achieve tight binding thro
17 al platform for assessing the specificity of carbohydrate binding proteins, an important step in func
18 e "F-type" fold), which is shared with other carbohydrate-binding proteins and apparently unrelated p
19 Galectin-3 (Gal-3) is a member of a class of carbohydrate-binding proteins and plays a role in a numb
20 c parameters, (2) to capture efficiently the carbohydrate-binding protein, and (3) to identify the in
21 is of all predicted glycoside hydrolases and carbohydrate-binding proteins, and three-dimensional str
22        The relationships between AF(G)Ps and carbohydrate binding proteins are also discussed.
23                      These sequence-specific carbohydrate-binding proteins are in turn valuable tools
24 mechanism similar to other known hevein-like carbohydrate-binding proteins but differing in carbohydr
25                    Binding of raffinose to a carbohydrate-binding protein called LecA was the cause o
26                                              Carbohydrate binding proteins (CBPs) are attractive targ
27 out both glycan structure and recognition by carbohydrate-binding proteins (CBPs) and is now being ex
28 ct sugar sequences that can be recognized by carbohydrate-binding proteins (CBPs), such as antibodies
29                              Galectin-3 is a carbohydrate-binding protein central to regulating mecha
30                           The binding of the carbohydrate-binding proteins concanavalin A (ConA) and
31                                  Endothelial carbohydrate binding proteins, E- and P-selectins, are t
32  interacts with B-GRANULE CONTENT1 (BGC1), a carbohydrate-binding protein essential for normal B-type
33          Galectins are a family of mammalian carbohydrate-binding proteins expressed by many cell typ
34 ed N-glyco FASP protocol using an engineered carbohydrate-binding protein, Fbs1, to enrich N-glycosyl
35 he enhanced affinities of lectins, which are carbohydrate binding proteins, for multivalent carbohydr
36                                  Lectins are carbohydrate binding proteins found in plants, animals,
37              Galectin-3 is a multifunctional carbohydrate-binding protein found in the nucleus, cytop
38 nsible for creating concanavalin A (conA), a carbohydrate-binding protein from jack bean (Canavalia e
39       Here we investigate a new role for the carbohydrate-binding protein galectin-3 in stabilizing m
40  DX-52-1, reporting that the multifunctional carbohydrate-binding protein galectin-3 is a secondary t
41                   At the ocular surface, the carbohydrate-binding protein galectin-3 maintains barrie
42               Here, we demonstrated that the carbohydrate-binding protein galectin-3 stimulated micro
43 acterial secretion systems directs cytosolic carbohydrate-binding protein Galectin-3 to PVs and that
44 rface of the cells by an endogenous bivalent carbohydrate binding protein (galectin-1) leads to apopt
45             Recent studies have shown that a carbohydrate-binding protein, galectin-3, is a novel pro
46 eptide derived by digestion of a 15N-labeled carbohydrate-binding protein, galectin-3, is presented.
47 eratitis, we demonstrate the importance of a carbohydrate-binding protein, galectin-8 (Gal-8), in reg
48                  Here, we demonstrate that a carbohydrate-binding protein, galectin-8, promotes patho
49 nstrate for the first time the importance of carbohydrate-binding proteins galectins-3 and -7 in re-e
50 cleotide microarray that contains probes for carbohydrate-binding proteins, glycosyltransferases, and
51 hat are highly efficient in interacting with carbohydrate binding proteins, has been a goal of synthe
52  Galectin-1 (Gal-1), a member of a family of carbohydrate-binding proteins, has been shown to modulat
53                   Although a number of other carbohydrate-binding proteins have been shown to inhibit
54                                     Lectins, carbohydrate-binding proteins, have been regarded as pot
55          In this context, lectins, which are carbohydrate-binding proteins, have garnered attention d
56 ing monolayer containing lectin interface (a carbohydrate binding protein, herein ArtinM) as the bio-
57 zed directly on TentaGel beads interact with carbohydrate-binding proteins in a polyvalent manner.
58 ge-like cells, but retain selectivity toward carbohydrate-binding proteins in protein-rich biological
59 ted that expression of galectin 3 (Gal-3), a carbohydrate binding protein is significantly upregulate
60 er is a difficult task, even for the natural carbohydrate-binding proteins known as lectins.
61                              Gliolectin is a carbohydrate-binding protein (lectin) that mediates cell
62 nized cross-linked lattices with multivalent carbohydrate binding proteins (lectins) together with th
63 esults obtained to date in the inhibition of carbohydrate binding proteins (lectins), but we will als
64 a major cause of nosocomial infections, uses carbohydrate-binding proteins (lectins) as part of its b
65 immobilized carbohydrates was confirmed with carbohydrate-binding proteins (lectins) detected by both
66                              We are pursuing carbohydrate-binding proteins (lectins) in a strategy ai
67                                              Carbohydrate-binding proteins (lectins) that recognize s
68 e functions of carbohydrates are mediated by carbohydrate-binding proteins, lectins, and the more the
69  structural similarity to some integrins and carbohydrate-binding proteins led to the hypothesis that
70                                          For carbohydrate-binding proteins, multivalency is important
71 of these structures to interact with various carbohydrate binding proteins or to stimulate immunity a
72    They are recognized by selectins or other carbohydrate-binding proteins or by complementary carboh
73                                              Carbohydrate binding proteins, or lectins, are engendere
74                                Galectins are carbohydrate-binding proteins overexpressed in bladder c
75                                              Carbohydrate-binding proteins, particularly mannose-bind
76            Increasing evidence suggests that carbohydrate-binding proteins play an essential role in
77                                              Carbohydrate-binding proteins play crucial roles across
78 in hydrolases and redox enzymes and contains carbohydrate-binding proteins potentially involved in ce
79                                  Lectins are carbohydrate-binding proteins produced by plants, algae,
80 e how galectins, a class of highly conserved carbohydrate-binding proteins, regulate liver homeostasi
81  regulated gene which encodes a cell surface carbohydrate binding protein, significantly reduced GAS
82                   Bacteria frequently employ carbohydrate-binding proteins, so-called lectins, to col
83                      Intelectins are ancient carbohydrate binding proteins, spanning chordate evoluti
84 can remodeling, and specificity studies with carbohydrate binding proteins such as lectins.
85       Interactions between glycopolymers and carbohydrate-binding proteins such as lectins, siglecs,
86 ng class of potential antivirals encompasses carbohydrate-binding proteins, such as antibodies and le
87                          Specifically, three carbohydrate binding proteins termed selectins (E-, P-,
88                      Galectin-3 (Gal-3) is a carbohydrate binding protein that has been implicated in
89 anovirin-N that represents a new tetravalent carbohydrate binding protein that is stable over a large
90                    Lectins are non-enzymatic carbohydrate binding proteins that all organisms employ
91                  Galectin-1 is an endogenous carbohydrate-binding protein that binds to specific glyc
92   Our findings indicate that Nesd is a novel carbohydrate-binding protein that functions together wit
93                  Galectin-1 is an endogenous carbohydrate-binding protein that induces death of leuke
94 tionarily ancient family of Ca(+2)-dependent carbohydrate-binding proteins that are involved in the i
95                                              Carbohydrate-binding proteins that bind their carbohydra
96                                  Lectins are carbohydrate-binding proteins that exert their biologica
97 wo-component system flanked by two predicted carbohydrate-binding proteins that is absolutely require
98                                  Lectins are carbohydrate-binding proteins that occur widely among pl
99                    Galectins are a family of carbohydrate-binding proteins that share a conserved seq
100  represents a first step in the evolution of carbohydrate-binding proteins that use a reactive unnatu
101 ba cyst wall proteins include Jacob lectins (carbohydrate-binding proteins) that crosslink chitin, ch
102 the shallow and hydrophilic binding sites of carbohydrate-binding proteins, the design of glycomimeti
103 creases binding of intelectin, an intestinal carbohydrate-binding protein, to V. cholerae in vivo Iva
104 atural glycosaminoglycans (GAG), and lectins/carbohydrate binding proteins using matrix-assisted lase
105                                          The carbohydrate-binding protein VER2, a jacalin lectin, pro
106     In addition, we have discovered that the carbohydrate-binding protein wheat germ agglutinin speci
107                     Galectin-3 is a chimeric carbohydrate-binding protein, which interacts with cell
108 teract highly specific with lectins, natural carbohydrate-binding proteins, which property is used in
109 ds that have not previously been observed in carbohydrate binding proteins, while LysM3 has a canonic
110                        Galectin-1 (Gal-1), a carbohydrate-binding protein whose secretion is enhanced
111         Galectin-3 is a family member of the carbohydrate-binding proteins widely expressed by many c
112                                Galectin-3, a carbohydrate-binding protein with affinity for beta-gala
113 ectin-1, a member of the conserved family of carbohydrate-binding proteins with affinity for beta-gal
114 y the observation that both KWL proteins are carbohydrate-binding proteins with distinct and likely t
115                                Galectin-3, a carbohydrate-binding protein, with specificity for type

 
Page Top