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1  < 0.0001) by rabbit anti-ASGR1 antibody and asialofetuin.
2 from ribonuclease B and linkage isomers from asialofetuin.
3 ch was inhibited by 3-27-fold by lactose and asialofetuin.
4 spherical shape with a diameter of 15-30 nm; asialofetuin, a natural ligand for the asialoglycoprotei
5 onventional liposomes (CL) were labeled with asialofetuin (AF), an asialoglycoprotein.
6 utant had a one and one-half log decrease in asialofetuin and cell binding relative to the parent dou
7 and cell supernatants were characterized for asialofetuin and cell binding, immunoreactivites, abilit
8 bdomains 1 alpha, 2 alpha, and 2 gamma bound asialofetuin and cells similarly to the parent 1 alpha,
9 d high affinities and specificities for both asialofetuin and T antigen in solution.
10  high riproximin binding, the NA3-presenting asialofetuin and the clustered Tn-rich asialo-bovine sub
11 variety of glycoproteins, including RNase B, asialofetuin, and transferrin, and the HIV envelope glyc
12 ated module can bind the plasma glycoprotein asialofetuin as well as the polysaccharide receptors pre
13 um albumin (Kd = 5 nM for MAP-P30 binding to asialofetuin) as well as free T-antigen disaccharide in
14 rtained by determining the IC(50) values for asialofetuin (ASF) and for bovine serum albumin derivati
15 isaccharide Galalpha1-3GalNAc (TF-AuNP), (2) asialofetuin (ASF) containing both LacNAc (Galbeta1-4Glc
16 ive cooperativity in the ITC binding data of asialofetuin (ASF), a glycoprotein that possesses nine L
17                   Preincubation of PHUECs in asialofetuin (ASF), an ASGP-R ligand, significantly redu
18 on of galectin-3 with the model glycoprotein asialofetuin (ASF), using a fluorescence anisotropy assa
19 chelate acceptor beads, whereas biotinylated asialofetuin (biotin-ASF), a galectin-3 nanomolar bindin
20  IgG, anti-RHL-1 IgG, asialoorosomucoid, and asialofetuin competitively blocked the binding of 125I-L
21                 As expected, when applied to asialofetuin (known to contain galactose only in the pyr
22 y the ability of both P30 and P10 to inhibit asialofetuin-mediated melanoma cell aggregation in vitro
23                                Additionally, asialofetuin, not fetuin, inhibited platelet phagocytosi
24 ies and affinities to T antigen displayed on asialofetuin or conjugated to bovine serum albumin (Kd =
25 e passage through two affinity columns, i.e. asialofetuin-Sepharose and invertase-Sepharose.
26                                              Asialofetuin, the beta1-galactosyl-terminated glycoprote
27 odel glycoproteins (RNase B, avidin, fetuin, asialofetuin, transferrin, and AGP) as well as a clade C
28  tetramethylrhodamine isothiocyanate labeled asialofetuin (TRITC-AF) as a ST substrate and fluorescei
29  and reduce the amount of toxin available to asialofetuin type II, which is used as a model to study
30 .01) by prior intravenous infusion of excess asialofetuin, which can selectively bind to the ASGP-R.

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