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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
5                                              Jacalin (a lectin) inhibits ookinete attachment by maski
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
11 hymal apoptosis that followed a reduction in jacalin and peanut agglutinin staining.
12 chain of the Artocarpus integrifolia lectin, jacalin, and to several proteins that contain multiple r
13 interactions between ABA, MIR842, MIR846 and jacalins are similar in A. lyrata.
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
19                    Subcutaneous injection of jacalin into neonatal mice drastically reduced PF IgG de
20 e mixtures of lectins concanavalin A (ConA), jacalin (JAC), and wheat germ agglutinin (WGA).
21     The carbohydrate-binding protein VER2, a jacalin lectin, promotes TaVRN1 upregulation by physical
22 e monoclonal antibodies HMFG-2 and OC125 and jacalin lectin, respectively.
23              In the cytosol, bGLU25 binds to JACALIN-LECTIN LIKE1 (AtJAC1), preventing the nuclear tr
24  previously cloned and characterized a novel jacalin-like lectin gene from wheat (Triticum aestivum)
25  proteins that contain multiple repeats of a jacalin-like sequence.
26                                     Although jacalin likely inhibited laminin-induced AChR clustering
27 by RNA interference abolished the effects of jacalin on PP2A activation and MEK inhibition.
28 n is not involved in the interaction of Dsg1/jacalin or Dsg1/PF IgG.
29                                         Like jacalin, peanut agglutinin lectin also binds the core 1
30 creased binding, which demonstrated that the jacalin probe binds specifically to O-linked glycans on
31 isease response or "dirigent" domain and the jacalin-related lectin (JRL) domain.
32                      The identification of a jacalin-related lectin in a true fern reveals for the fi
33                                  BanLec is a jacalin-related lectin isolated from the fruit of banana
34  is a conserved mitogenic motif in these two jacalin-related lectins BanLec and Malay BanLec, and fur
35 identity and showed structural similarity to jacalin-related lectins.
36 taining modular organizations of one or more jacalin repeat units and are implicated in defense again
37  a 128-to-139-substituted variant gp120 from jacalin-resistant SIV lacked O-linked carbohydrate.
38                               Selection of a jacalin-resistant SIVmac239 variant population resulted
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
42             The ability or inability to bind jacalin thus correlated with the presence of the serine-
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
46 ilibrium dissociation constants for ConA and jacalin toward mannose and galactose, respectively.
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
49 sequence predictions, two HIV-2 gp120s bound jacalin, while one did not.
50 e-fold pseudo-symmetry of the related lectin jacalin, with the 21-residue beta-chains in the center o