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1 139-substituted SIVmac239 gp120 did not bind jacalin.
2 strain NL4-3 was resistant to inhibition by jacalin.
3 were resistant to the inhibitory effects of jacalin.
4 measured the binding and unbinding rates of jacalin (a lectin binding to O-linked glycans) to indivi
6 nd hOPSG from human retina are recognized by jacalin, a lectin that binds to O-glycans, preferentiall
7 .6 +/- 1.7 x 10(6) M(-)(1) were obtained for jacalin adsorbing to a galactose surface and ConA adsorb
8 emonstrating that the core 1-specific lectin jacalin almost completely abrogated laminin-induced AChR
9 ation (K(D)) constant for the interaction of jacalin and galactose was found to be 16 +/- 5 microM, a
10 O-glycosylation as detected by staining with jacalin and peanut agglutinin lectins after 30 min of tr
12 chain of the Artocarpus integrifolia lectin, jacalin, and to several proteins that contain multiple r
14 with accumulation of an ABA-inducible target jacalin At5g28520 mRNA, whose cleavage was shown by modi
15 that alpha-dystroglycan was the predominant jacalin-binding protein detected in C2C12 myotube lysate
16 ated that the O-glycan-specific plant lectin jacalin binds Dsg1 and inhibits the interaction of Dsg1/
17 g by directly binding to alpha-dystroglycan, jacalin had no effect on laminin binding to the myotube
18 hyposialylated glycans, used WGA, SNA, PNA, Jacalin, HPA, and VVA, indicating glomerular hyposialyla
21 The carbohydrate-binding protein VER2, a jacalin lectin, promotes TaVRN1 upregulation by physical
24 previously cloned and characterized a novel jacalin-like lectin gene from wheat (Triticum aestivum)
30 creased binding, which demonstrated that the jacalin probe binds specifically to O-linked glycans on
34 is a conserved mitogenic motif in these two jacalin-related lectins BanLec and Malay BanLec, and fur
36 taining modular organizations of one or more jacalin repeat units and are implicated in defense again
39 ements with A. thaliana and candidate target jacalins, similar primary transcript structures and intr
40 20s from four SIVmac and SIVsm strains bound jacalin strongly in an enzyme-linked immunosorbent assay
41 aminopeptidase N (AgAPN1) as the predominant jacalin target on the mosquito midgut luminal surface an
43 e-binding proteins concanavalin A (ConA) and jacalin to arrays composed of the monosaccharides mannos
44 y, these results suggest that the binding of jacalin to O-linked TF carbohydrate motifs on Dsg1 impai
45 n isotherms for the interactions of ConA and jacalin to the carbohydrate surfaces, (ii) monitor prote
47 how that lectin protein from jackfruit seed (jacalin), which binds to non- and monosialylated core 1
48 iproliferative effect of the dietary lectin, jacalin, which binds the Thomsen-Friedenreich antigen (g
50 e-fold pseudo-symmetry of the related lectin jacalin, with the 21-residue beta-chains in the center o