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1 ough splitting a domain from a Gram-positive bacterial adhesin.
2 C attachment to the gut by blocking the FimH bacterial adhesin.
3  cross-links are widespread in Gram-positive bacterial adhesins.
4 ivity that mediates protein glycosylation of bacterial adhesins.
5 ning the carbohydrate binding specificity of bacterial adhesins.
6 ory epithelia or exhibit similarity to known bacterial adhesins.
7 olved in UTI-induced preterm labor involving bacterial adhesins.
8 ink between the enzyme and the expression of bacterial adhesins.
9 ntrol molecular interactions with a range of bacterial adhesins.
10 s strains lacking expression of pertactin, a bacterial adhesin and vaccine target, are emerging.
11 rface involves specific interactions between bacterial adhesins and adsorbed salivary components.
12 pB) that had amino acid sequence homology to bacterial adhesins and structural homology to bacterial
13    To evaluate the relative contributions of bacterial adhesins and toxins to ciliary binding, we use
14 is a member of a diverse family of predicted bacterial adhesins, and although lacking a high degree o
15                      They are also important bacterial adhesins, and nonpiliated mutants of P. aerugi
16 ose encoded protein has characteristics of a bacterial adhesin; and implicated Ace in binding to coll
17 face proteins which are recurrent targets of bacterial adhesins at epithelial barriers.
18            This attachment is facilitated by bacterial adhesins at the cell surface.
19  In cocrystals with oligomannose-6, two FimH bacterial adhesins bind the Manalpha1,3Manalpha1 and Man
20 r hypotheses that some ligands recognized by bacterial adhesins change their compartmentalization and
21 invasion of heart tissue is dependent on the bacterial adhesin choline-binding protein A that binds t
22 h repeat glycoproteins (SRRPs) are important bacterial adhesins conserved in streptococci and staphyl
23  tissue fibronectin homing sequence from the bacterial adhesin CshA.
24 de O-linked to the serine-rich repeat of the bacterial adhesin, Fap1 of Streptococcus parasanguinis.
25 llosteric conformers of the mannose-specific bacterial adhesin FimH - the most common cell attachment
26                            Here we study the bacterial adhesin FimH to address the role of the inacti
27                           One example is the bacterial adhesin FimH, where the C-terminal pilin domai
28 nters around FimH antagonists that block the bacterial adhesin FimH, which would otherwise mediate bi
29 tylglucosamine-1-phosphotransferase, and the bacterial adhesin FimH.
30 ike serine-rich proteins are a new family of bacterial adhesins found in a variety of streptococci an
31 lycoproteins (SRRPs) are a growing family of bacterial adhesins found in many streptococci and staphy
32 s identified 19 genes with homology to known bacterial adhesin genes, virulence genes, genes involved
33 cterized, the interactions of defensins with bacterial adhesins have not.
34 ructural studies on a class of Gram-positive bacterial adhesins have revealed an intramolecular Cys-G
35 mate divergence plays a key role in limiting bacterial adhesin host tropism.
36 ns are mediated through the binding of other bacterial adhesins, in particular the Opa family of oute
37    This study tested the hypothesis that the bacterial adhesin intimin contributes to tissue specific
38 cing (A/E) pattern, which is mediated by the bacterial adhesin intimin.
39 in with similarity to the well-characterized bacterial adhesins intimin and invasin.
40 pathogen recognition receptors detecting the bacterial adhesin invasin (Inv).
41 ulosis internalization is interaction of the bacterial adhesins invasin and YadA with host cell beta1
42                             FadA is a unique bacterial adhesin/invasin in that it utilizes its own tw
43 ng this role is lacking, largely because the bacterial adhesins involved in this host-microbe associa
44    Adherence to host epithelium, mediated by bacterial adhesins, is one of the first steps in NTHi co
45  the identification of a yet uncharacterized bacterial adhesin, LabA, which specifically recognizes l
46 ibody-antigen, vascular selectin-ligand, and bacterial adhesin-ligand interactions.
47  is secreted in significant amounts and that bacterial adhesins may have other activities, prompted a
48                                     Distinct bacterial adhesins may mediate these cooperative interac
49                                              Bacterial adhesins mediate adhesion to substrates and bi
50  eukaryotic and bacterial viruses as well as bacterial adhesins might have a similar maturation mecha
51                                      FmlH, a bacterial adhesin of uropathogenic Escherichia coli (UPE
52 lt both because it is polyvalent and because bacterial adhesins often recognize more than one type of
53                                        Thus, bacterial adhesins (or other surface antigens) with the
54  IRF-1 expression depends on the presence of bacterial adhesin, our findings do not preclude the poss
55                                              Bacterial adhesins play an important role in the coloniz
56 cterial membrane vesicles containing YadA, a bacterial adhesin protein, were prepared.
57                                  Since these bacterial adhesins recognize their respective glycolipid
58 tyrin") that simultaneously targets multiple bacterial adhesins, resists proteolysis by bacterial pro
59 uggested a proteinaceous nature of potential bacterial adhesin(s) for hTSP-1.
60                                 However, the bacterial adhesin(s) remain elusive.
61 an E. faecalis sequence, ace, that encodes a bacterial adhesin similar to the collagen binding protei
62 Collectively, these findings establish a new bacterial adhesin structure that has in effect been hija
63  host cells, thus allowing interactions with bacterial adhesins such as intimin.
64  previously discovered a widespread group of bacterial adhesins, termed Multivalent Adhesion Molecule
65 h repeat glycoproteins (SRRPs) are important bacterial adhesins that are conserved in streptococci an
66 sinia adhesin A (YadA) belongs to a class of bacterial adhesins that form trimeric structures.
67                        SRRPs are a family of bacterial adhesins that have diverse roles in adhesion a
68 sents a new paradigm for target binding by a bacterial adhesin, the identification of which will info
69 ased at sites of inflammation, and allow the bacterial adhesin to selectively associate with surface-
70 We have developed a mouse model to study the bacterial adhesins which mediate the increased intestina
71 lecules and highlight the first example of a bacterial adhesin with two domains that participate in a
72 y infections initiated by the interaction of bacterial adhesins with carbohydrate receptors can be po
73 is aided by the interaction between numerous bacterial adhesins with components of the extracellular
74 onic acid capsule impedes the interaction of bacterial adhesins with keratinocyte receptors, (iii) mo
75 sruption or modulation of the interaction of bacterial adhesins with LR might engender unexpectedly b
76 ly interesting case is the complex formed by bacterial adhesins with their human peptide target.