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1 changes in the conformation of gp120 and the antibody binding site.
2 d amino acid residues positioned outside the antibody binding site.
3 temperature and distal residues outside the antibody binding site.
4 peptides come close to each other to form an antibody-binding site.
5 s exposing the amino acid side chains of the antibody binding sites.
6 tory HA mutations can be located in distinct antibody binding sites.
7 wly identified sites not located in reported antibody binding sites.
8 ry that included CDR3 engineered to optimize antibody binding sites.
9 This region may have multiple antibody binding sites.
10 croscopic images of immunocomplexes show two antibody binding sites.
11 performance because of large numbers of free antibody binding sites.
12 4000-fold faster inactivation at 4.2 microM antibody binding sites.
13 analyte-tracer and the analyte (HSA) for the antibody binding sites.
14 mutations that truncate ATM upstream of the antibody binding sites.
15 H/gL/gO-, and Pentamer-specific neutralizing antibody binding sites.
16 ty and therefore are potentially part of the antibody binding sites.
17 f epidemic H3 strains were mainly located in antibody-binding sites A and B as compared with TX/12e.
18 determine the number of CD4, CCR5, and CXCR4 antibody-binding sites (ABS) on various T cell lines, T
19 human intestine expressed CD4 (14,530+/-7970 antibody-binding sites [ABSs]/cell), CCR5 (2730+/-1524 A
20 through an indirect interaction between the antibody binding site and the L1 loop (amino acids 112-1
21 tides and carbohydrates can bind to the same antibody-binding site and that peptides can structurally
22 Neither of these mutations lies within an antibody-binding site, and therefore the mechanism of im
23 regulatory region for DNA binding and PAb421 antibody binding site are replaced, and p53as is constit
24 ly employ this strategy since the individual antibody binding sites are not arranged with appropriate
26 ould induce a counter-charged residue in the antibody binding site at a locus suitable for it to depr
30 An algorithm was developed to identify the antibody binding site class automatically based on the d
31 b) tailored amino acid composition mimicking antibody binding-site composition at putative paratope p
32 taining the 2F5/4E10 neutralizing monoclonal antibody binding sites, displays no detectable HIV-neutr
33 oid structures with 2-3 amino-terminal Abeta antibody binding sites, distinct from previously charact
34 These observations identify IC3.4 as the antibody binding site for sera of OCP patients and sugge
35 and ligands and have successfully modulated: antibody binding sites for antigen; antigen binding site
36 liminating the CD33 IgV domain, which is the antibody-binding site for GO, as well as diagnostic immu
37 the binding sites of empty and of complexed antibody binding sites gave an indication of how the sha
39 ace plasmon resonance is used to identify an antibody binding site, HSA Peptide 40, on human serum al
40 ites identified in fibrillin-1, and on known antibody binding sites in fibrillin-1, a model is propos
42 nerates a comprehensive energetic map of the antibody-binding site in a facile and rapid manner and s
43 inal fragment of GRASP65, which contains the antibody binding site, into normal rat kidney cells prev
44 rticle and "intermediate" views, the primary antibody binding site is near the intersection between t
46 itivity to the antibody, consistent with the antibody binding site observed by x-ray crystallography.
47 fusion results in a steady-state gradient of antibody binding site occupancy transverse to convective
49 gion of the human herpesvirus 8 (HHV-8), the antibody-binding site of glycoprotein K8.1A, was mapped
54 g assays suggested the existence of multiple antibody binding sites on melanin-concentrating hormone
56 However, comparison of distances between antibody binding sites on the recombinant peptides and l
57 emonstrates the exposure of key neutralizing antibody binding sites on the surface of the postfusion
58 pressed (approximately 1000-7000 STRL33 ABS [antibody binding sites]) on specific subsets of natural
59 A dye-labeled TNT analogue prebound in the antibody binding site quenches the QD photoluminescence
60 establish the stereochemical features in the antibody binding site that confer specificity for cocain
62 inExA assay quantifies the fraction of total antibody binding sites that are unoccupied, regardless o
63 iscussed in the light of what is known about antibody binding sites, the high affinity of the 2C TCR,
64 ree-dimensional reconstructions revealed the antibody-binding sites to be on the so-called handle dom
65 s been used to measure the response of three antibody-binding sites to perturbation from electronic e
69 ructural model of this major epitope and its antibody binding site, which is independent of pH-induce
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