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1 involvement of wall teichoic acid but not of staphylococcal protein A.
2 tal NOESY data on the 58-residue Z domain of staphylococcal protein A.
3 with the binding of von Willebrand factor to staphylococcal protein A.
4 of the common model protein, the B domain of staphylococcal protein A.
5 2 plus CH3) to facilitate purification using staphylococcal protein A.
6 ach containing a VH domain and a B domain of staphylococcal protein A.
7 inhibited by fibronectin and did not bind to staphylococcal protein A.
8 ts the 46-residue segment from fragment B of staphylococcal protein A.
9 sferase, to IgG binding domains derived from staphylococcal protein A.
10 ons were further characterized by binding to staphylococcal protein A.
11 lococcal strains also secreted extracellular staphylococcal protein A.
12 tudy the folding pathways of the B-domain of staphylococcal protein A (1BDD (alpha; 46 residues)).
13 omains of streptococcal protein G (G(B)) and staphylococcal protein A (A(B)).
14 Fc mutation, or treatment with domain B from staphylococcal protein A), all of which reduced acute lu
15                                        Thus, staphylococcal protein A, alpha-toxin, and superantigeni
16 of surface proteins, we analyzed variants of staphylococcal protein A, an immunoglobulin binding prot
17 nce of the VH-restricted Fab binding site on staphylococcal protein A and demonstrate the diverse eff
18                                    Targeting staphylococcal protein A and stimulating the T-helper 17
19 t gC1qR as a novel cellular binding site for staphylococcal protein A and suggest an additional mecha
20                              The B domain of staphylococcal protein A (BdpA) is a small helical prote
21 A and B, and exfoliative toxin-A, as well as staphylococcal protein A, did not induce significant cyt
22  applied here to compute folding pathways of staphylococcal protein A, fragment B.
23                                              Staphylococcal protein A gene (spa) typing identified sp
24 cluded multilocus sequence typing (MLST) and staphylococcal protein A gene (spa) typing results as we
25 ace of the 10-55 fragment of the B-domain of staphylococcal protein A has been investigated by using
26               The folding of the B-domain of staphylococcal protein A has been studied by coarse-grai
27 utations on binding of Fc hinge fragments to staphylococcal protein A have also been analyzed and dem
28                   In this study we show that staphylococcal protein A induces T cell-independent huma
29 l, but not complete, overlap of the FcRn and staphylococcal protein A interaction sites on mouse IgG1
30                              The E-domain of staphylococcal protein A is one of five homologous IgG-b
31                              Microcolumns of staphylococcal protein A linked to Sepharose were used t
32  treated neonatal BALB/c mice with a form of staphylococcal protein A (MS) devoid of Fcgamma binding
33 he sGM-CSFRalpha-Fc was bound to immobilized staphylococcal protein A on the biosensor surface, and b
34 ied to the 10-55 fragment of the B-domain of staphylococcal protein A (protein A) and to a 75-residue
35 ion studies performed on serum samples using staphylococcal protein A-Sepharose indicated that antibo
36           Phenol-soluble modulins (PSMs) and Staphylococcal protein A (SpA) are key virulence determi
37           The antibody binding properties of staphylococcal protein A (SpA) can be attributed to the
38                                          The staphylococcal protein A (spa) gene was sequenced for al
39 eraction with virulence factor of S. aureus, staphylococcal protein A (SpA) in the presence of electr
40                                              Staphylococcal protein A (SPA) is a B cell superantigen
41                                              Staphylococcal protein A (SpA) is a cell-surface compone
42                                              Staphylococcal protein A (SpA) is a cell-wall-bound path
43                                              Staphylococcal protein A (Spa) is an important virulence
44                                              Staphylococcal protein A (SpA) is an important virulence
45                                              Staphylococcal protein A (SpA) is anchored to the cell w
46                                              Staphylococcal protein A (SpA) is representative of a ne
47                                              Staphylococcal protein A (SpA) is representative of a ne
48 lls and a murine model of RA, the ability of staphylococcal protein A (SPA) to interact with and modu
49 bility testing and characterization of their staphylococcal protein A (spa) type.
50     All S. aureus isolates were genotyped by staphylococcal protein A (spa) typing and with multilocu
51 enotype by pulsed-field gel electrophoresis, staphylococcal protein A (spa) typing, multilocus sequen
52 ntibiotic susceptibility, biofilm formation, Staphylococcal protein A (spa) typing, SCCmec typing, an
53 FGE), multilocus sequence typing (MLST), and staphylococcal protein A (spa) typing.
54                                              Staphylococcal protein A (SPA) was used to modify the si
55 3, V(H)3-30, or V(H)3-30.3), and/or modified staphylococcal protein A (SpA), a 45-kilodalton bacteria
56                                              Staphylococcal protein A (SpA), a bacterial membrane pro
57 d antigen presentation to CD4(+) T cells and staphylococcal protein A (SpA), a cell wall-anchored sur
58                  We previously reported that staphylococcal protein A (SpA), a key immune-evasion pro
59                                              Staphylococcal protein A (SpA), acting as a B cell super
60  the lactose operon (lac) and genes encoding staphylococcal protein A (spa), gamma hemolysin (hlg), a
61  The envelope of S. aureus is decorated with staphylococcal protein A (SpA), which captures the Fcgam
62 und that cytokine secretion was dependent on staphylococcal protein A (Spa), which was selectively ex
63 and neutralizes the abundant surface-exposed Staphylococcal protein A (SpA).
64 g salivary immunoglobulins was identified as staphylococcal protein A (SpA).
65 eins, including the lung inflammatory factor staphylococcal protein A (Spa).
66 e polypeptide (ELP) and the antibody-binding staphylococcal protein A (SpA).
67 duct was a fusion protein with a B domain of Staphylococcal protein A (SPA).
68 The cell surface of S. aureus is coated with Staphylococcal protein A (SpA).
69 4 fused to the soluble IgG-binding domain of staphylococcal protein A) suggest that the transmembrane
70 lates were found to express higher levels of staphylococcal protein A than the TSS isolates, another
71 as for the 46-residue N-terminal fragment of staphylococcal protein A, the native-like conformation w
72 s(-1)), the involvement of platelet gpIb and staphylococcal protein A through von Willebrand factor b
73  We have characterized the in vivo effect of staphylococcal protein A treatment on peripheral B cells
74                      Injection of homogenous staphylococcal protein A-V antigen fusion peptide into m
75 eviously showed that injection of homogenous staphylococcal protein A-V antigen fusion peptide into m
76 ted-residue force field, for the B domain of staphylococcal protein A, we are able to (i) provide the
77 laxation kinetics studies of the B-domain of staphylococcal protein A were performed to characterize
78 al pathogens produce virulence factors, like staphylococcal protein A, which interact at high frequen